- Department of Psychiatry, New York University, New York, NY, United States
Transgender and gender-diverse (TGD) menstruators are individuals assigned female at birth (AFAB)*, who retain the capacity to menstruate and have a gender identity that differs from their natal sex. Reports indicate up to 1.6 million individuals in the US identify as TGD. Until recently, the mainstream menstrual discourse has failed to capture the experience of transmenstruators. However, a better understanding of the menstrual experiences of TGD-AFAB will allow for more individualized patient-centered care. In this review, we provide the relevant data necessary to inform the psychiatric management of menstruation in TGD-AFAB individuals, including experiences of menstruation, preferences for menstrual management, and the impact on mental health. Our review indicates that menstrual care in TGD patients must be tailored to the individual; clinicians should remain open-minded to the unique experience of transmenstruators; gender-affirming menstrual care is necessary to reduce psychological burden. It should not be assumed that TGD-AFAB menstruators are utilizing appropriate contraceptive methods and should receive contraceptive and fertility preservation counseling. We highlight the importance of having these conversations early in the reproductive arch, even before puberty onset. Keeping in mind the gender minority stress model, in the upcoming sections, we discuss the limited body of literature on mood disorders in TGD-AFAB individuals who menstruate, undergo menstrual suppression, or continue to ovulate. The psychological impact of hormonal therapies is also reviewed.
1 Introduction
Earlier estimates based on population-based surveys approximated that 0.3-0.6% of the United States population, or 1 million people, identify as transgender; however recent reports indicate that figure may be closer to 1.6 million (1, 2). Similarly, the DSM-V documents the prevalence of gender dysphoria as 0.005-0.014% for those assigned male at birth, and 0.002-0.003% for adults assigned female at birth, with recent reports indicating increasing numbers (3). Still, there is a lack of familiarity and competency around the medical and mental health needs of TGD individuals. According to the 2022 US Transgender Survey (USTS), amongst 92,329 respondents, 38% identified as nonbinary, 35% as transgender women (transwomen), and 25% as transgender men (transmen) (4). Of those respondents, 24% did not seek medical care, and 48% reported at least one negative experience due to their gender identity, including being misgendered; being refused care; being addressed with harsh or abusive language; or being subjected to physically rough treatment (4). Seelman et al., 2020 found that in the 2015 USTS, 54% of transmen found their routine healthcare providers knew very little (“nothing” or “some things”) about trans-related care (5).
Although some TGD individuals undergo medical transition, many do not (6). A social transition is when an individual changes their appearance and pronouns. A legal transition involves legally changing one’s name and documents to reflect this and their identified gender. Medical transition may involve gender-affirming hormone therapy (GAHT) and/or gender-affirming surgery. In TGD-AFAB individuals, common gender-affirming surgeries include masculinizing chest surgery (i.e., mastectomy), body contouring, and metoidioplasty, as well as non-surgical chest binding. Masculinizing GAHT in TGD-AFAB individuals is usually continued lifelong to maintain virilization independent of genital surgery. Testosterone is the mainstay of masculinization, which aims to induce secondary sex characteristics and suppress feminine physical features, and in most cases causes amenorrhea. At least 80% of TGD individuals have either taken, tried, or wanted to take GAHT at some point (7). Gender nonbinary or gender non-conforming individuals who do not identify as transgender may take hormones to develop more masculine sexual secondary characteristics. Although some gender-affirming treatments include a hysterectomy or oophorectomy, many TGD-AFAB menstruators wish to maintain their reproductive organs and childbearing potential (8–11).
Compared to other medical specialties, psychiatry has had a more fraught relationship with the TGD community. The Diagnostic and Statistical Manual of Mental Disorders (DSM) 3rd and 4th editions, for example, conceptualized gender identity disorder (GID) as pathologic. Although GID was subsequently reclassified as gender dysphoria (Supplementary Table 2) in DSM-V (3), literature continues to indicate a higher prevalence of mental health disorders among transgender individuals compared to the general population or cisgender individuals. TGD people experience a two-fold higher risk of receiving a psychiatric diagnosis compared to cisgender people and are diagnosed with a mood, anxiety, or psychotic disorder, with odd ratios of 1.5:1, 3.9:1, and 3.8:1 respectively (12). These disparities can be understood through the minority-stress framework, which describes the complex interaction between majority (cis-gender) and minoritized groups (transgender and nonbinary) communities.
Building on this, we aim to provide a comprehensive review of the experiential and clinical data necessary to inform the care of TGD-AFAB individuals. We review the gendered history of menstruation; the value of gender-inclusive menstrual dialogue; guidelines for transgender health around menstrual suppression, fertility preservation, and contraceptive counseling; and elucidate the interplay between gender dysphoria, menstruation, and hormone-related mood disorders in TGD-AFAB individuals.
2 Methods
We searched PubMed from March to July 2024 without date limitations for studies of TGD menstruators. We did not utilize any language restrictions and included historical and contemporary terms related to gender identity such as “transgender”, “transgender diverse”, “transmen”, “menstruators”, “assigned female at birth”, “nonbinary”, and “gender diverse”. We utilized similar terms through Google to locate magazine articles, books, government announcements, and websites.
3 Historical and social considerations
Menstruation is a biological process that is steeped in historical significance. In Greek mythology, menstrual blood is referred to as “the supernatural red wine,” conferring “miraculous power” to the gods (13). In Ancient Rome, menstruators were also thought to have “great powers,” and menstrual blood was recommended as a treatment for illnesses of all kinds, including rabies, malaria, and epilepsy (13). Many indigenous tribes emphasize the strength of menstruators and menstruation itself. The Cherokee Nation of Oklahoma believes that menstruation is powerful, a source of feminine strength, and a destructive force against evil and enemies (14). In Cherokee mythology, Stoneclad, a cannibalistic monster was undefeated by warriors until he was in the presence of seven menstruating virgins who took his strength away (13). To channel the power of menstruators, Cherokee men would also practice bloodletting before games and battles (14).
Menstruation has also been invoked as evidence of women’s inferiority, a notion that dates as far back as Aristotle (15). In biblical Jewish culture, menstruating women were required to remain separate from men for the duration of their menses. Orthodox Jewish women continue to use the ritual bath (mikvah) following menstruation and before engaging in intercourse after menses. The Roman Catholic Church of Thirteenth Century Europe perpetuated the “stigma of menstrual uncleanliness … [and] perceptions of menstrual blood as vile and polluting,” encouraging women to refrain from taking Holy Communion while menstruating (16). In Islamic culture, menstruating women are unable to pray, enter mosques, or touch the Quran; they are required to clean themselves through a spiritual bath (ghusl) each time menses concludes (17). Additionally, if menstruating, they are barred from completing the final ritual of Hajj, Tawaf-ul-Ziyarah, which involves circumnavigating the Kaaba to commemorate the end of the annual pilgrimage to Mecca (17).
By suggesting that menstruation was not a signifier of shame or weakness, but rather something that could be “managed,” the feminist movement of the 20th challenged the historical menstrual and reproductive rhetoric and through the lens of women’s empowerment, moved conversations around menstruation into the mainstream (18). More recently, conversations around menstruation have come to encompass an even wider range of perspectives, including those of transgender and non-binary menstruators. Kosher et al. (2023) refer to this as “the plurality of menstrual experiences,” encapsulating the increasingly common viewpoint that “not all women menstruate, and not all menstruators are women’’ (19, 20). Said differently, menstruation is a deeply nuanced and subjective experience for TGD-AFAB individuals (21, 22).
While the experience of menstruation among TGD individuals is conventionally understood as “the individual who was AFAB; identifies with masculinity; experiences intense dysphoria around menstruation because it is gendered feminine; and is actively undergoing intervention to suppress or eliminate menstruation,” the reality is much more complex (19). Fortunately, data examining TGD-AFAB individuals’ attitudes toward menstruation, considerations around menstrual management, and decisions about menstrual suppression are emerging. Chrisler et al. (2016) surveyed 150 TGD-AFAB individuals to examine attitudes toward menstruation and menstrual suppression (21). While some respondents expressed a positive view of menstruation, the majority reported “mixed or ambivalent attitudes.” Half of the participants reported that they would elect to suppress menstruation if suppression were possible without the use of testosterone. Fifty percent also agreed that “not menstruating would enhance their sense of their masculine identity” (21). More recently, Kosher et al. (2023) identified three major themes pertaining to menstruation in the TGD population: 1) dysphoria; 2) tensions between femininity and masculinity; and 3) transnormative pressures (19). A 2023 study by Schwartz et al. examined TGD adolescents’ (N=129) experiences of menstruation and found that a majority (93%) experienced menstrual-related dysphoria (23). A substantial number (88%) were interested in menstrual suppression, with the primary reason being a desire for a complete cessation of menses (97%) and the second to improve menstrual-related dysphoria (63%) (23).
Beyond menstrual bleeding itself, the management of menstruation can be a source of distress for TGD menstruators (24). Although femininity is neither a predicate for menstruation nor an outcome of menstruation, terms like “feminine hygiene product” or “feminine care” abound in the marketing and sale of menstrual products. Furthermore, TDG-AFAB individuals may experience aversion to vaginal penetration (21), and many menstrual products are designed for insertion into the vaginal opening. In 2016, the Thinx period product brand released its Boyshort style underwear with a series of video and print advertisements featuring trans male model, Sawyer DeVuyst. According to Miki Agrawal, Thinx’s Chief Executive Officer at the time, the Boyshort was “specifically designed with the trans male menstruating community in mind” and a deliberate step by Thinx to be part of “shifting [public] perspective” on the needs of the trans community (25). The introduction of the Boyshort to the period product market also came on the heels of a major shift in Thinx’s marketing strategy. Moving away from its original For Women with Periods advertising campaign, Thinx opted for a revised For People with Periods tagline. The goal, Thinx says, was an acknowledgment that menstruation “is not a trait of, nor a defining factor of, a specific gender. It is something that can occur amongst all people’’ (26).
However, the lack of inclusive period products is just one way in which TGD-AFAB individuals have been impacted by a menstrual landscape designed almost exclusively for cis-gender women. The issue of period poverty for menstruators is an underrecognized public health issue. Broadly, period poverty refers to a lack of access to menstrual education, menstrual products, and facilities that allow for proper menstrual hygiene and disposal of menstrual products (27). It also refers to “the increased economic vulnerability menstruating people face due to the financial burden posed by menstrual supplies….[and] costs accrued from pain medication and underwear used during the menstrual cycle (28). “ Period poverty also contributes to the cycle of generational poverty by adding to the marginalization of menstruators in the form of missed days of work, missed days of school, and diversion of monthly income to meet menstrual needs. TGD-AFAB communities are particularly vulnerable to the impact of period poverty. According to the University of Wisconsin-Madison Institute for Research on Poverty, nearly 34% of transmen and 24% of gender nonbinary individuals live in poverty, compared to 16% of cis-gendered individuals (29). In the 2022 USTS, TGD individuals reported facing substantially higher rates of housing instability compared to the general population (4).
To address issues of period poverty and menstrual inequity, at least 30 states and Washington D.C. have passed a combined total of 60 bills designed to improve access to menstrual health resources. While laws differ by state, they are generally aimed at improving access and affordability by eliminating sales tax for menstrual products and ensuring free menstrual products are available to individuals in public schools, correctional facilities, and homeless shelters (30). However, menstrual product availability in male-designated restrooms has become a topic of controversy in political and public discourse. Events that took place in a Connecticut (CT) High School made national headlines in 2024 after a tampon dispenser, affixed to the wall of a boys’ restroom, was torn down. The tampon dispenser was placed in the boys’ restroom in response to a relatively new CT state law that mandates public schools to provide free access to menstrual products for students. According to The Connecticut Department of Health “[t]he law was designed to affirm all genders in making empowered decisions about their health, including menstrual health. As a result, the law requires products to be provided in all-gender bathrooms, one men’s restroom per school, and all women’s restrooms in the building” (27).
However, such policies have not been applied uniformly across the United States. Nearly 47% of respondents in the 2022 USTS had thought of “moving to another state because their state government considered or passed laws that target transgender people for unequal treatment (such as banning access to bathrooms, health care, or sports), and 5% of respondents had moved out of state because of such state action” (4). In 2023, Florida signed House Bill 1521, barring TGD individuals from using locker rooms or public bathrooms consistent with their gender, highlighting continued barriers to menstrual management (31).
Unsurprisingly, research suggests that a majority of TGD-AFAB individuals feel “unsafe” or “very unsafe” managing menstruation in men’s restrooms (21). The risk of being ‘outed’ by the use of individually wrapped menstrual products (tampons, pads) appears to contribute, in part, to the preferential use of extended-use period products like menstrual cups, adult diapers, or period underwear (21). A study by Lane et al. (2022) also identified public restroom design as a “significant barrier to menstrual management” (32). Participants described large gaps between stalls, the “reflective gaze” of the mirrored sinks, high urinal-to-stall ratios, and lack of disposal sites for menstrual products as being some of the most fraught aspects of queer menstruation.
4 Applying consensus guidelines in gender-affirming medical care
A professional body spanning disciplines and geographic regions, the World Professional Association for Transgender Health (WPATH) tasks itself with promoting evidence-based care, education, research, public policy, and respect for transgender health. WPATH is associated with 7 regional organizations: United States, European, Canadian, Asia, Australia, Aotearoa (New Zealand, and Southern Africa. Since the organization’s formal inception in 1979, it has iteratively published standards of care (SOC). These documents have served as consensus guidelines and best practice recommendations for professionals caring for transgender and gender-diverse populations throughout the world (33). Within the last few years, there has been a shift in European countries with guideline implementation. The National Health Services England released the CASS Report in 2024, closed its Gender Identity Development Service, and recently banned puberty blockers for adolescents (34). Sweden, Finland, and Denmark continue to follow similar patterns.
While experiences of and feelings about menstruation among TGD-AFAB individuals are diverse, some may experience an exacerbation of incongruence between gender identity and perception of their bodies during menses. To address this, the most recent WPATH SOC-8 contains recommendations regarding the suppression of menstruation in adolescent and adult TGD-AFAB individuals (33). In most, GAHT with exogenous testosterone at adult physiologic doses will precipitate amenorrhea due to the sex steroid’s effect on the endometrium, and resultant endometrial atrophy (35). However, menstrual suppression with GnRH agonists, combined estrogen-progestin, or progestin-only methods can be indicated, especially in adolescent populations.
WPATH recommends considering menstrual suppression agents in adolescents only once they have reached the early stages of puberty. The Endocrine Society Guidelines from 2017 also recommend against puberty-blocking and GAHT in pre-pubertal children (36). Adolescents may wish to halt puberty to further explore gender expression and identity, take time to consider GAHT initiation with testosterone, or use adjunctive agents for breakthrough bleeding during the early stages of initiation of GAHT. Furthermore, if there is a delay in consensus about GAHT among the individual, provider, and/or guardian, menstrual suppression should be considered as an initial step (33). Engaging TGD-AFB individuals in conversations about menstrual suppression can also provide a forum to explore readiness for gender-affirming treatment and any associated mental health needs (37).
The choice of menstrual suppression agent (between GnRH agonist and progestin-only or combined estrogen-progestin methods more commonly used as contraceptive agents) is dictated largely by the developmental status of the individual, consideration of individual medical risk factors (specifically venous thromboembolism in estrogen-containing methods), potential dysphoria caused by estrogen-containing agents, cost, and availability. While GnRH agonists can delay further progression of puberty and cause the regression of some early secondary sex characteristics, these agents are costly, and not always covered by insurance (33). In cases where GnRH agonists are not reasonably available, progestin agents (available as depot injection, oral pill, intrauterine device, subdermal implant) or combined estrogen-progestin agents (available as oral pill, transdermal patch, vaginal ring) can be used. Between 55-97% of transmasculine adults achieve amenorrhea within the first 6 months of testosterone therapy (38, 39). Lower rates of amenorrhea have been described in TGD-AFAB adolescents using testosterone (59% at 6 months) and higher success rates with NETA or DMPA monotherapy (40). Breakthrough bleeding requires clinical investigation to determine etiology and most commonly requires adjustment of testosterone dosage or additional hormonal intervention. Compared to individuals who initiated treatment with GnRHa at a later age, those who initiated at an earlier age (average age 11) had lower rates of depression, anxiety, suicidal ideation, and suicide attempts (41).
Ultimately, a third of TGD-AFAB individuals surveyed desired a hysterectomy, which would obviate the need for pelvic examinations and stop menses (5). TGD-AFAB individuals may seek a hysterectomy in response to pelvic pain (42). While pelvic pain has a prevalence of 25% among cis-gender women, higher rates have been reported in adult trans cohorts (43). In a 2020 cross-sectional survey of 486 AFAB trans participants, 72.2% reported pelvic pain after initiation of GAHT with testosterone, with most pain localizing to the suprapubic region and being characterized as “crampy” in nature (44). Additionally, this study found an association of pelvic pain after initiation of testosterone therapy with a personal history of PTSD, continued menstruation, and experiences of pain with orgasm (44). In another survey conducted between 2015-2017, 69.4% of respondents reported abdominopelvic pain specifically onset since initiation of GAHT (45). All respondents who reported curative treatment of this pelvic pain identified hysterectomy as the treatment method (43, 45).
5 Contraception and fertility preservation
WPATH and the Ethics Committee of the American Society for Reproductive Medicine (ASRM) recommend discussing fertility preservation and family planning before initiation of GAHT (46). The impact of testosterone on fertility depends on duration and timing of use; if started before puberty and concurrently with puberty blockers, the individual may never develop reproductive function. If GAHT is initiated after puberty, reproductive function can be restored. The use of exogenous testosterone can have lasting effects on fertility (43). While testosterone does not affect ovarian reserve, testosterone can induce gonadal suppression through its action on the hypothalamic-pituitary axis, preventing ovulation and follicle development (44). Ovarian exposure to exogenous testosterone can cause ovarian capsule thickening, which can also impair fertility (45). While most TGD-AFAB individuals on testosterone will achieve amenorrhea and ovarian suppression, it is still possible to ovulate and become pregnant while amenorrheic (47). A study of TGD-AFAB individuals on testosterone found evidence of breakthrough ovulatory events by monitoring hormonal levels.
Studies have found that a majority of TGD-AFAB individuals express parental desire and that a quarter fear infertility (8, 10, 11). Fertility preservation options include embryo, oocyte cryopreservation, and experimental ovarian tissue banking, which can be used before gender-affirming surgery or the initiation of GAHT regardless of puberty status (43). Many TGD-AFAB individuals choose to forgo fertility preservation to avoid delaying GAHT. A majority also report fears that hormone injections and the pelvic procedures required for egg retrievals will worsen gender dysphoria (9, 23, 48). Overall, utilization of fertility preservation remains low in TGD communities. In a survey of TGD menstruators referred to a community health clinic in Tel Aviv, Alpern et al. found that while 61.9% wanted a child, only 5.8% accessed fertility preservation (9). There are many barriers to access to fertility preservation, including the high out-of-pocket expense of cryopreservation and assisted reproductive technologies and lack of adequate insurance coverage; provider discomfort in discussing fertility preservation with TGD-AFAB patients; fears of discrimination for the transgender parent as well as the child; and legislation barring gender-affirming care (9, 11, 35, 43).
Among TGD-AFAB individuals, 30% of pregnancies are unintended (47). Therefore, discussing contraception options is imperative, especially given the potential teratogenicity of testosterone. The teratogenic risks of testosterone in animal studies are well documented; however, the literature on human outcomes is sparse. In utero exposure to testosterone can result in abnormal development of genitalia including labial fusion and clitoromegaly, and several hypotheses that these exposures contribute to anorexia nervosa and autism in offspring (49). However, a longitudinal pregnancy cohort study failed to confirm this association (50). In a sample of 25 TGD-AFAB individuals who were on testosterone prior to pregnancy, 20% were on testosterone for at least some portion of their pregnancies. Among this sample size, rates of fetal anomalies, developmental disorders, or disorders of sexual development were equivalent to rates in TGD-AFAB individuals not on testosterone (47). More research is needed to identify long-term neurodevelopmental impacts of perinatal testosterone exposure.
Contraception in this specific population is inconsistently reported; however, estimates are between 20-60% (51). Contraceptive methods may be underutilized due to several factors, including the lack of education provided by medical providers, lack of access, as well as the frequent misconception by both transmen and providers that testosterone provides reliable contraception (51, 52). Furthermore, the irregular nature of ovulation while on GAHT may make pregnancy harder to anticipate; this places TGD-AFAB menstruators at high risk for unplanned pregnancy, especially coupled with limited access and inconsistent contraceptive use. And just as menstruation can worsen gender dysphoria by the repetitive reminder of natal sex, contraceptive methods, and fertility preservation may too (48). Oral Contraceptive Pills (OCPs) are marketed to women and can serve as daily reminders of anatomy; longer-term options, such as IUDs are invasive, painful, and require a pelvic exam and manipulation, exposing transmen to dysphoria-based discomfort. Other barriers to contraceptive use include concerns that hormones from OCPs can counteract the effects of testosterone by increasing sex hormone-binding globulin which binds to testosterone (51).
6 Psychiatric and psychosocial considerations
In understanding mood disorders among TGD-AFB individuals, we consider biological and psychosocial contributors. Biologically, GAHT with exogenous testosterone in TGD-AFAB individuals is known to increase total brain volume, total gray matter volume, thalamus volume, and cortical thickness, specifically in frontal and parietal brain areas (46, 47, 52). Kiyar et al. (2022) found that the neural profile of TGD individuals assigned male at birth (AMAB) shifted from natal sex to their gender identity after 6-10 months of GAHT on fMRI. This confirmed that total testosterone is involved with the neural processing of emotions (51). However, it remains unclear how testosterone-driven neural profiles change with menstrual-related mood disorders.
The gender minority stress model outlines psychological processes that ultimately lead to mental health conditions and mood disorders (49). Chronic exposure to gender-based rejection; gender victimization; lack of gender affirmation; violence targeting TGD individuals; and legislation barring gender expression leads to the internalization of negative self-concept, fosters negative anticipation of upcoming experiences, and delays engagement in gender-affirming care. Internalization of negative self-concept may also contribute to gender dysphoria and a variety of mental health conditions (49).
6.1 Premenstrual disorder and premenstrual dysphoric disorder
There is limited data on premenstrual disorders amongst TGD-AFAB individuals as this population is often excluded from studies about menstruation (50). PMD symptoms are categorized as predominantly physical, emotional, or mixed (48). The prevalence rate of PMD among cisgender women is estimated at around 20-40 %, with around 5% of cisgender women experiencing PMDD, a severe form of PMD that was added to the DSM-V in 2013 (48, 53). An exclusion criterion of PMDD is an exacerbation of an underlying psychiatric disorder, which can include gender dysphoria. Undoubtedly, comorbid gender dysphoria and the inherent worsening of dysphoria for many TGD-AFAB individuals with the onset of menses complicates the diagnosis of underlying PMDD (50). Despite diagnostic challenges, anyone with a menstrual cycle, including a TGD-AFAB person, is susceptible to PMD and PMDD.
Treatment for PMDD, which often includes cycle suppression, can dovetail with gender-affirming care. Low-dose selective serotonin reuptake inhibitors (SSRIs), with either luteal or continuous dosing, remain a first-line treatment option (48, 54). Other treatments include herbal supplements, such as chasteberry which is supported by data from a systematic review, and vitamins, including Vitamin B6, Calcium, and Magnesium (48, 55).
People with PMDD are also at high risk for suicidality; a recent systematic literature review found that 7-16% of people with PMDD have attempted suicide (56) compared to 0.7% of the general population in the most recent CDC data. Given the high baseline rate of suicide attempts (between 32-50%) in transgender people (57), screening for PMDD and suicidality in TGD-AFAB menstruators merits increased clinical attention (58, 59). At the time of this writing, we could not find data on the prevalence rates of PMDD among TGD-AFAB menstruators.
6.2 Depression and anxiety
There is limited literature on depression and anxiety among transmen, as most studies combine transgender identities. In a review of the literature published between 2013-2018, Nguyen et al. (2018) found lower depressive symptoms in TGD-AFAB individuals receiving GAHT across all studies (60). They also found that transgender men and women over the age of 50 receiving GAHT experienced a reduction of anxiety symptoms, as well as decreased cortisol awakening response and perceived stress (60). Although they found ongoing self-reports of high stress, 70 TGD individuals had a decrease in cortisol awakening response, which has been linked to decreased anticipation of stress (61, 62).
6.3 Post-traumatic stress disorder, post-traumatic stress symptoms and discrimination
TGD individuals report higher rates of exposure to traumatic events, including abuse in childhood, physical assault, intimate partner violence, and sexual assault (63–65). They also experience pervasive discrimination, discrete traumatic events linked to discrimination, and anti-TGD bias (66). In a national sample, up to 63% of TGD individuals reported discriminatory events leading to eviction, job loss, losing stable housing, denial of medical care, or losing an intimate relationship (67). Despite this, the wide range of PTSD prevalence within the TGD community suggests that there may either be varying detection strategies for PTSD or an over-pathologizing of responses to trauma and discrimination. Studies linking symptoms to specific traumatic events found lower rates of PTSD diagnosis when compared to studies that assessed PTSD symptoms generally (64, 65, 68, 69). Given this, it is important to delineate trauma from discrimination in TGD individuals, as conflation of the two may result in over-pathologizing responses from discrimination-based psychological distress (66).
6.4 Bipolar disorder, mania
There is limited to no data to guide the management of bipolar affective disorder in patients undergoing GAHT. Studies that associate manic symptoms with exogenous testosterone are often reported in cisgender men with supraphysiologic levels of anabolic androgenic steroids (70, 71). This contrasts with GAHT in TGD-AFAB individuals, where the dosing of testosterone targets physiologic levels. There is limited data on the association of mania in transmen with exogenous testosterone administration (36). Thus far, there is no data to indicate that appropriate GAHT dosing of testosterone would lead to an induction of mania, but close monitoring during testosterone initiation in at-risk individuals is warranted.
6.5 Psychosis
Current literature indicates an increased prevalence of schizophrenia spectrum disorders and psychosis amongst TGD individuals (72). In a review of 254 million discharges in the United States National Inpatient Sample database in 2019, Hanna et al. (2019) found that 14.5% of TGD patients were diagnosed with psychosis, compared to 4.3% of cis-gendered patients, and 14.2% of TGD patients were diagnosed with schizophrenia, compared to 2.8% of cis-gendered patients (57). In their literature review, Barr et al. (2021) found variability in the reported rates of psychotic illness among TGD individuals, which they attributed to varying recruitment strategies, racial bias in diagnosis, and demographic differences, as TGD study participants were on average 17 years or younger (72). Through a cohort study examining birth certificates and national insurance data in the Netherlands from 2006-2020, Termorshuizen et al. (2023) found that of 5,564 TGD individuals, the TGD-AFAB cohort was substantially more likely to be diagnosed with a non-affective psychotic disorder when compared to TGD-AMAB (73). They also found that up to 50% of TGD individuals were diagnosed with psychosis after the first registration of data indicative of TGD status, and up to 83.7% were documented at the same time (73). These results, coupled with the historical classification of gender dysphoria as symptomatology within the realm of psychotic spectrum illness, suggest a continued risk of diagnostic bias of psychosis amongst TGD individuals.
6.6 Aggression
Although WPATH SOC Version 7 listed destabilization of psychiatric disorders as a potential side effect of testosterone, this was removed in WPATH SOC Version 8 (33). There is no documented consistent association or correlation between anger and serum testosterone levels; however, if irritability, mood changes, or anger do occur, these symptoms are more likely during the first year of initiation of GAHT (74, 75). Of the literature linking anger expression with testosterone in TGD-AFAB individuals, there was no increased risk for psychiatric hospitalization or self-harm (76, 77). Self-report measures of irritability and aggression decreased after gender-affirming surgical intervention, perhaps reflecting a decrease in depressive symptom burden (78). If mood changes occur with testosterone treatment, then it may be helpful to consider dose adjustments; changing from short-acting to long-acting intramuscular injections, or changing to gel formulations (79).
6.7 Quality of life, body satisfaction, and self-esteem
Several studies indicate a statistically significant improvement in self-reported quality of life and self-esteem in TGD-AMAB and TGD-AFAB individuals receiving GAHT (80–82). Silve et al. (2021) interviewed 113 people (60 TGD-AMAB and 53 TGD-AFAB) using quality of life questionnaires and found that in transmen, improved quality of life was associated with employment, being in a stable relationship, physical activity, and increased body hair (83). However, in a systematic review of 32 articles looking at TGD individuals on GAHT, not all studies reported a consistent improvement in body satisfaction when cross-sectional data was analyzed. They also noted that the literature on quality of life was inconsistent, ranging from improved, neutral, and worsened quality of life (82).
6.8 Sexual desire
One year of GAHT treatment in TGD-AFAB individuals is associated with an improvement in sexual function, specifically masturbation frequency, arousal, sexual fantasies, and desire (78). Additionally, increased libido is also linked to the earlier treatment with GAHT (84). In a cross-sectional analysis of data from the PRIDE study in 2021-2023, TGD-AFAB individuals on GAHT reported increased sexual desire (85). They theorized that GAHT increases the quality of life and self-image, which in turn positively impacts other areas of their life, including sexual desire (85).
6.9 Gender dysphoria
Although the literature indicates a decrease in gender dysphoria with GAHT, long-term affirmation is also impacted by social gender recognition, discrimination, and other variables. In a cross-sectional survey of 359 TGD individuals (219 TGD-AMAB and 140 TGD-AFAB), higher levels of dysphoria were related to sociological indicators of identity (ex: legally changing sex on identification) in those utilizing masculinizing GAHT compared to those who were not, suggesting that gender dysphoria may be related to sociological indicators of identity rather than just the hormones themselves (86). In that same study, the AFAB individuals who ultimately initiated GAHT noted global gender dysphoria decreased at 3 months and subsequently increased at 6, 12, and 24 months (86). When delineated further, it seems that subjective dysphoria was decreased, but dysphoria impacted by social and sociolegal factors had increased (86). In another study from Australia, TGD-AFAB individuals undergoing GAHT were found to have a significant reduction in gender dysphoria within the first few months of treatment, however, over 2 years had an increase in dysphoria related to social and sociolegal factors (87).
7 Age-related considerations
Despite the expectation that the number of Americans aged 65 and older will surpass children in 2023 and an estimation of at least 700,000 senior TGD individuals, there is limited literature on older TGD individuals in the United States (88). Most data and knowledge about TGD individuals come from European cohorts, with a larger proportion documented as transgender women. Under-representation of TGD-AFAB seniors in the literature makes it difficult to determine the long-term impact of hormonal and GAHT interventions on TGD-AFAB menstruators (89, 90).
Studies on cis-gendered individuals with a prostate, and post-menopausal women on hormone replacement therapy (HRT) suggest that sex hormones can be neuroprotective and improve cognition (91, 92). Cognitive changes in menopause are believed to be related to decreased estrogen availability, and androgen receptors in the hippocampus and prefrontal cortex (93). However, it remains unclear if these studies can be extrapolated to TGD-AFAB menstruators.
Data drawn from health insurance companies and ICD codes indicates TGD individuals had a statistically significant elevated probability of being diagnosed with dementia when compared to cis-gendered individuals (94). Furthermore, TGD-AFAB individuals aged 45+ who identified as ethnically minoritized reported more memory loss and confusion in the past year when compared to their cis-gender counterparts (95). It is important to note that these studies combine transgender men and women, and often do not ask further questions about non-binary and fluid identities.
When gender identity is parsed out, the findings change. Heesewijk et al. (2023) found that transgender men had an increased risk of dementia compared only to cis-gender women; later research in 2021 found that transgender men had a similar cognitive functioning profile when compared to cisgender men and cisgender women (96). It has been theorized that the reported increased rate of dementia may be associated with delayed gender affirmation, repeated dysphoric episodes when menstruating, as well as limited social support (97).
Currently, a link between GAHT and impaired cognition has not been consistently described in the literature (97). Although there is little to no published literature on lifestyle factors impacting cognitive decline in TGD-AFAB individuals, when compared to cis-gender people, there is an overall increased prevalence of known risk factors, including higher rates of cigarette and alcohol consumption and lower physical activity (97). A higher burden of depressive symptoms may also impact cognition; rates of clinically significant depressive symptoms in older transgender individuals have been reported as high as 48%, which is pointedly higher than the general population of 6-8% (98, 99).
8 Conclusions
The language of TGD healthcare continues to evolve towards improving inclusivity. Medical providers should engage patients in discussions about their gender identity, how they relate to it, and what it means to them, as it can vary greatly. An example is the variability of preferred pronouns- she/her/he/him/they/them. WPATH guidelines recommend providers use active listening to encourage exploration in those uncertain about their gender identity. Rather than impose their narratives or preconceptions, providers should assist people in determining their paths. These conversations should also include the changing legislation for TGD-affirming care. Supplementary Table 4 provides examples of how to address topics discussed in this review.
Limitations to our review include an emphasis on North American data and Euro-centric experiences. To extrapolate this to other cultures and ethnicities requires sensitivity to their specific identities and contexts. There are also significant limitations in the current global literature on TGD-AFAB individuals. Survey language often omits TGD-AFAB as a gender category or groups all TGD individuals into one category, which excludes the diversity and spectrum range of gender. This has led to limited literature on the impact of menstruation, menstrual-related disorders, pregnancies, fertility, and exogenous testosterone exposure among TGD-AFAB individuals.
Our review indicates that the WPATH SOC-8 has moved beyond a focus on surgery and hormones, now including sexual, reproductive, mental, and primary health care services. There remains a need for additional research on the reduction of barriers to OBGYN care, contraception, and fertility preservation in TGD-AFAB individuals. These barriers can be addressed through their inclusion in medical, psychiatric, and menstruation-related research, as well as in medical, graduate, and residency-level curricula. Doing so may allow more comfort in treating this increasingly prevalent patient population.
Author contributions
AA: Conceptualization, Writing – original draft, Writing – review & editing. SM: Writing – original draft, Writing – review & editing. SP: Writing – original draft, Writing – review & editing. MA: Conceptualization, Supervision, Writing – original draft, Writing – review & editing. AD: Conceptualization, Supervision, Writing – original draft, Writing – review & editing.
Funding
The author(s) declare that no financial support was received for the research, authorship, and/or publication of this article.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Supplementary material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fpsyt.2024.1422333/full#supplementary-material
References
1. Kachen A, Pharr JR. Health care access and utilization by transgender populations: a United States transgender survey study. Transgender Health. (2020) 5:141–8. doi: 10.1089/trgh.2020.0017
2. Flores AR, Herman J, Gates GJ, Brown TN. How many adults identify as transgender in the United States? Washington DC, USA: Williams Institute Los Angeles, CA (2016).
3. Association AP. DIagnostic and Statistical Manual of Mental Disorders. 5th ed. Washington DC: American Psychiatric Association (2013).
4. James SE, Herman JL, Durso LE, Heng-Lehtinen R. Early Insights: A Report of the 2022 US Transgender Survey. Washington DC, USA: National Center for Transgender Equality (2024).
5. Seelman KL, Kattari SK, Harvey P, Bakko M. Trans men’s access to knowledgeable providers and their experiences in health care settings: differences by demographics, mental health, and degree of being “out” to providers. Health Soc Work. (2020) 45:229–39. doi: 10.1093/hsw/hlaa030
6. Margulies IG, Chuang C, Travieso R, Zhu V, Persing JA, Steinbacher DM, et al. Preferences of transgender and gender-nonconforming persons in gender-confirming surgical care: A cross-sectional study. Ann Plast surg. (2021) 86:82–8. doi: 10.1097/SAP.0000000000002351
7. Grant J, Mottet L, Tanis J, Herman JL, Harrison J, Keisling M. National transgender discrimination survey report on health and health care. (2010).
8. Light A, Wang L-F, Zeymo A, Gomez-Lobo V. Family planning and contraception use in transgender men. Contraception. (2018) 98:266–9. doi: 10.1016/j.contraception.2018.06.006
9. Alpern S, Yaish I, Wagner-Kolasko G, Greenman Y, Sofer Y, Lifshitz DP, et al. Why fertility preservation rates of transgender men are much lower than those of transgender women. Reprod BioMedicine Online. (2022) 44:943–50. doi: 10.1016/j.rbmo.2022.01.003
10. Stolk T, Asseler J, Huirne J, Van Den Boogaard E, Van Mello N. Desire for children and fertility preservation in transgender and gender-diverse people: A systematic review. Best Pract Res Clin Obstetrics Gynaecol. (2023) 87:102312. doi: 10.1016/j.bpobgyn.2023.102312
11. Defreyne J, Van Schuylenbergh J, Motmans J, Tilleman KL, T’Sjoen GGR. Parental desire and fertility preservation in assigned female at birth transgender people living in Belgium. Fertility Sterility. (2020) 113:149–57.e2. doi: 10.1016/j.fertnstert.2019.09.002
12. Holmgren E, Raaska H, Lapinleimu H, Elovainio M. Bullying among international adoptees: testing risks and protective factors. Violence Vict. (2019) 34:930–51. doi: 10.1891/0886-6708.VV-D-18-00157
13. Tan DA, Haththotuwa R, Fraser IS. Cultural aspects and mythologies surrounding menstruation and abnormal uterine bleeding. Best Pract Res Clin Obstetrics Gynaecol. (2017) 40:121–33. doi: 10.1016/j.bpobgyn.2016.09.015
14. Sturm C. Blood politics: Race, culture, and identity in the Cherokee Nation of Oklahoma. California, USA: Univ of California Press (2002).
15. Nicolson P. The menstrual cycle, science and femininity: assumptions underlying menstrual cycle research. Soc Sci Med. (1995) 41:779–84. doi: 10.1016/0277-9536(95)00044-8
16. Ott MF. Impure blood: The menstrual taboo in the Christian church during the thirteenth century. (2018).
17. Islam N, Ayaz A, Farooq MU. Awareness and experiences of female pilgrims about menstrual suppression during Hajj 1437 Hijrah: A cross-sectional study. Saudi J Health Sci. (2019) 8:12–6. doi: 10.4103/sjhs.sjhs_104_18
18. Becknuss K. The Female Stigma: Menstruation Attitudes in the Women's Liberation Movement. Utah, USA: AWE (A Woman’s Experience (2022) 8:13.
19. Kosher RB, Houghton LC, Winkler IT. MANstruation: A cyberethnography of linguistic strategies of trans and nonbinary menstruators. Soc Sci Med. (2023) 328:115974. doi: 10.1016/j.socscimed.2023.115974
20. Bobel C. New blood: Third-wave feminism and the politics of menstruation. New Jersey, USA: Rutgers University Press (2020).
21. Chrisler JC, Gorman JA, Manion J, Murgo M, Barney A, Adams-Clark A, et al. Queer periods: attitudes toward and experiences with menstruation in the masculine of centre and transgender community. Culture Health sexuality. (2016) 18:1238–50. doi: 10.1080/13691058.2016.1182645
22. Persdotter J. Introducing menstrunormativity: Toward a complex understanding of ‘menstrual monsterings. In: The Palgrave handbook of critical menstruation studies. Singapore: Palgrave Macmillen (2020). p. 357–73.
23. Schwartz BI, Bear B, Kazak AE. Menstrual management choices in transgender and gender diverse adolescents. J Adolesc Health. (2023) 72:207–13. doi: 10.1016/j.jadohealth.2022.09.023
24. Lowik A. Just because I don't bleed, doesn't mean I don't go through it”: Expanding knowledge on trans and non-binary menstruators. Int J Transgender Health. (2020) 22:113–25.
25. Puckett L. These genius advertisements are a reminder that transgender men can get periods too. Teen Vogue. (2016) 18:2016.
26. Navarro A. This period-friendly underwear brand just showed major support for trans men. Teen Vogue. (2015) 17:2015.
28. Sacca L, Markham CM, Gupta J, Peskin M. Period poverty. Front Media SA;. (2023), 1140981. doi: 10.3389/frph.2023.1140981
29. Siers-Poisson J. The Complexity of LGBT Poverty in the United States Institute for Resarch on Poverty website2021(2021). Available online at: https://www.irp.wisc.edu/resource/the-complexity-of-lgbt-poverty-in-the-united-states/ (accessed March 28, 2024).
30. Fouladi F. Online: national conference of state legislators(2023). Available online at: https://www.ncsl.org/health/state-actions-to-increase-access-to-menstrual-products (accessed March 27, 2024).
31. Migdon B. Hill T, editor. The Hill. (2023). Available online at: https://thehill.com/homenews/state-watch/4008737-desantis-signs-transgender-bathroom-bill-bans-gender-affirming-care-expands-dont-say-gay-law (accessed March 28, 2024).
32. Lane B, Perez-Brumer A, Parker R, Sprong A, Sommer M. Improving menstrual equity in the USA: perspectives from trans and non-binary people assigned female at birth and health care providers. Culture Health sexuality. (2022) 24:1408–22. doi: 10.1080/13691058.2021.1957151
33. Coleman E, Radix AE, Bouman WP, Brown GR, De Vries AL, Deutsch MB, et al. Standards of care for the health of transgender and gender diverse people, version 8. Int J transgender Health. (2022) 23:S1–S259. doi: 10.1080/26895269.2022.2100644
34. Ghorayshi A. Youth Gender Medications Limited in England, Part of Big Shift in Europe. London, UK: New York Times (2024). Available at: https://www.nytimes.com/2024/04/09/health/europe-transgender-youth-hormone-treatments.html.
35. Carswell JM, Roberts SA. Induction and maintenance of amenorrhea in transmasculine and nonbinary adolescents. Transgender Health. (2017) 2:195–201. doi: 10.1089/trgh.2017.0021
36. Hembree WC, Cohen-Kettenis PT, Gooren L, Hannema SE, Meyer WJ, Murad MH, et al. Endocrine treatment of gender-dysphoric/gender-incongruent persons: an endocrine society clinical practice guideline. J Clin Endocrinol Metab. (2017) 102:3869–903. doi: 10.1210/jc.2017-01658
37. Rew L, Young CC, Monge M, Bogucka R. Puberty blockers for transgender and gender diverse youth—a critical review of the literature. Child Adolesc Ment Health. (2021) 26:3–14. doi: 10.1111/camh.12437
38. Irwig MS. Testosterone therapy for transgender men. Lancet Diabetes endocrinol. (2017) 5:301–11. doi: 10.1016/S2213-8587(16)00036-X
39. Ahmad S, Leinung M. The response of the menstrual cycle to initiation of hormonal therapy in transgender men. Transgender Health. (2017) 2:176–9. doi: 10.1089/trgh.2017.0023
40. Alaniz V, Sheeder J, Whitmore G, Wilde M, Hutchens K, Nokoff N, et al. Menstrual suppression in adolescent and young adult transgender males. J Pediatr Adolesc Gynecol. (2023) 36:116–21. doi: 10.1016/j.jpag.2022.10.007
41. Chen D, Abrams M, Clark L, Ehrensaft D, Tishelman AC, Chan Y-M, et al. Psychosocial characteristics of transgender youth seeking gender-affirming medical treatment: Baseline findings from the Trans Youth Care Study. J Adolesc Health. (2021) 68:1104–11. doi: 10.1016/j.jadohealth.2020.07.033
42. Blakemore JK, Quinn GP, Fino ME. A discussion of options, outcomes, and future recommendations for fertility preservation for transmasculine individuals. Urologic Clinics. (2019) 46:495–503. doi: 10.1016/j.ucl.2019.07.014
43. Moussaoui D, Elder CV, O’Connell MA, Mclean A, Grover SR, Pang KC. Pelvic pain in transmasculine adolescents receiving testosterone therapy. Int J Transgender Health. (2024) 25:10–8. doi: 10.1080/26895269.2022.2147118
44. Zwickl S, Burchill L, Wong AFQ, Leemaqz SY, Cook T, Angus LM, et al. Pelvic pain in transgender people using testosterone therapy. LGBT Health. (2023) 10:179–90. doi: 10.1089/lgbt.2022.0187
45. Grimstad FW, Boskey E, Grey M. New-onset abdominopelvic pain after initiation of testosterone therapy among trans-masculine persons: a community-based exploratory survey. LGBT Health. (2020) 7:248–53. doi: 10.1089/lgbt.2019.0258
46. Zubiaurre-Elorza L, Junque C, Gómez-Gil E, Guillamon A. Effects of cross-sex hormone treatment on cortical thickness in transsexual individuals. J sexual Med. (2014) 11:1248–61. doi: 10.1111/jsm.12491
47. Pol HEH, Cohen-Kettenis PT, Van Haren NE, Peper JS, Brans RG, Cahn W, et al. Changing your sex changes your brain: influences of testosterone and estrogen on adult human brain structure. Eur J Endocrinol. (2006) 155:S107–S14. doi: 10.1530/eje.1.02248
48. Cary E, Simpson P. Psychological issues and hormone therapy. Best Pract Res Clin Endocrinol Metab. (2023) 101858. doi: 10.1089/lgbt.2014.0009
49. Hendricks ML, Testa RJ. A conceptual framework for clinical work with transgender and gender nonconforming clients: An adaptation of the Minority Stress Model. Prof Psychology: Res Practice. (2012) 43:460. doi: 10.1037/a0029597
50. Weiselberg E. Menstrual considerations for transgender male and gender diverse adolescents who were assigned female at birth. Curr Problems Pediatr Adolesc Health Care. (2022) 52:101239. doi: 10.1016/j.cppeds.2022.101239
51. Kiyar M, Kubre M-A, Collet S, Van Den Eynde T, T’Sjoen G, Guillamon A, et al. Gender-affirming hormonal treatment changes neural processing of emotions in trans men: an fMRI study. Psychoneuroendocrinology. (2022) 146:105928. doi: 10.1016/j.psyneuen.2022.105928
52. Seiger R, Hahn A, Hummer A, Kranz GS, Ganger S, Woletz M, et al. Subcortical gray matter changes in transgender subjects after long-term cross-sex hormone administration. Psychoneuroendocrinology. (2016) 74:371–9. doi: 10.1016/j.psyneuen.2016.09.028
53. Halbreich U, Borenstein J, Pearlstein T, Kahn LS. The prevalence, impairment, impact, and burden of premenstrual dysphoric disorder (PMS/PMDD). Psychoneuroendocrinology. (2003) 28:1–23. doi: 10.1016/S0306-4530(03)00098-2
54. Pearlstein T. Perinatal depression: treatment options and dilemmas. J Psychiatry Neurosci. (2008) 33:302–18. doi: 10.1037/pas0001215
55. Dante G, Facchinetti F. Herbal treatments for alleviating premenstrual symptoms: a systematic review. J Psychosomatic Obstetrics Gynecol. (2011) 32:42–51. doi: 10.3109/0167482X.2010.538102
56. Osborn E, Brooks J, O’Brien P, Wittkowski A. Suicidality in women with Premenstrual Dysphoric Disorder: a systematic literature review. Arch women's Ment Health. (2021) 24:173–84. doi: 10.1007/s00737-020-01054-8
57. Hanna B, Desai R, Parekh T, Guirguis E, Kumar G, Sachdeva R. Psychiatric disorders in the US transgender population. Ann Epidemiol. (2019) 39:1–7.e1. doi: 10.1016/j.annepidem.2019.09.009
58. James S, Herman J, Rankin S, Keisling M, Mottet L, Anafi Ma. The report of the 2015 US transgender survey. (2016). doi: 10.1080/26895269.2022.2147118
59. Virupaksha H, Muralidhar D, Ramakrishna J. Suicide and suicidal behavior among transgender persons. Indian J psychol Med. (2016) 38:505–9. doi: 10.4103/0253-7176.194908
60. Nguyen HB, Chavez AM, Lipner E, Hantsoo L, Kornfield SL, Davies RD, et al. Gender-affirming hormone use in transgender individuals: impact on behavioral health and cognition. Curr Psychiatry Rep. (2018) 20:1–9. doi: 10.1007/s11920-018-0973-0
61. Colizzi M, Costa R, Pace V, Todarello O. Hormonal treatment reduces psychobiological distress in gender identity disorder, independently of the attachment style. J sexual Med. (2013) 10:3049–58. doi: 10.1111/jsm.12155
62. Elder GJ, Wetherell MA, Barclay NL, Ellis JG. The cortisol awakening response–applications and implications for sleep medicine. Sleep medicine reviews. (2014) 18:215–24.
63. Foundation HRC. Dismantling a culture of violence: Understanding anti-transgender violence and ending the crisis. Report. (2018). doi: 10.1016/j.psychres.2021.114272
64. Reisner SL, White JM, Bradford JB, Mimiaga MJ. Transgender health disparities: comparing full cohort and nested matched-pair study designs in a community health center. LGBT Health. (2014) 1:177–84. doi: 10.1089/lgbt.2014.0009
65. Reisner SL, White Hughto JM, Gamarel KE, Keuroghlian AS, Mizock L, Pachankis JE. Discriminatory experiences associated with posttraumatic stress disorder symptoms among transgender adults. J Couns Psychol. (2016) 63:509. doi: 10.1037/cou0000143
66. Valentine SE, Smith AM, Miller K, Hadden L, Shipherd JC. Considerations and complexities of accurate PTSD assessment among transgender and gender diverse adults. psychol assessment. (2023) 35:383. doi: 10.1037/pas0001215
67. Grant JM, Mottet LA, Tanis J, Min D. Transgender discrimination survey Vol. 1. . Washington, DC, USA: National Center for Transgender Equality and National Gay and Lesbian Task Force (2011) p. 2–7.
68. McDowell MJ, Hughto JM, Reisner SL. Risk and protective factors for mental health morbidity in a community sample of female-to-male trans-masculine adults. BMC Psychiatry. (2019) 19:1–12. doi: 10.1371/journal.pone.0261039
69. Shipherd JC, Maguen S, Skidmore WC, Abramovitz SM. Potentially traumatic events in a transgender sample: Frequency and associated symptoms. Traumatology. (2011) 17:56–67. doi: 10.1177/1534765610395614
70. Franey DG, Espiridion ED. Anabolic steroid-induced mania. Cureus. (2018) 10. doi: 10.7759/cureus.3163
71. Pope H, Phillips KA, Olivardia R. The Adonis complex: The secret crisis of male body obsession. Bristol, UK: Simon and Schuster (2000).
72. Barr SM, Roberts D, Thakkar KN. Psychosis in transgender and gender non-conforming individuals: A review of the literature and a call for more research. Psychiatry Res. (2021) 306:114272. doi: 10.1016/j.psychres.2021.114272
73. Termorshuizen F, De Vries AL, Wiepjes CM, Selten J-P. The risk of psychosis for transgender individuals: a Dutch national cohort study. psychol Med. (2023) 53:7923–32. doi: 10.1017/S0033291723002088
74. Kristensen TT, Christensen LL, Frystyk J, Glintborg D, T'sjoen G, Roessler KK, et al. Effects of testosterone therapy on constructs related to aggression in transgender men: a systematic review. Hormones behavior. (2021) 128:104912. doi: 10.1016/j.yhbeh.2020.104912
75. Davis SA, St. Amand C. Effects of testosterone treatment and chest reconstruction surgery on mental health and sexuality in female-to-male transgender people. Int J Sexual Health. (2014) 26:113–28. doi: 10.1080/19317611.2013.833152
76. Turban JL, King D, Kobe J, Reisner SL, Keuroghlian AS. Access to gender-affirming hormones during adolescence and mental health outcomes among transgender adults. PloS One. (2022) 17:e0261039. doi: 10.1371/journal.pone.0261039
77. Defreyne J, Kreukels B, t'Sjoen G, Staphorsius A, Den Heijer M, Heylens G, et al. No correlation between serum testosterone levels and state-level anger intensity in transgender people: Results from the European Network for the Investigation of Gender Incongruence. Hormones Behavior. (2019) 110:29–39. doi: 10.1016/j.yhbeh.2019.02.016
78. Costantino A, Cerpolini S, Alvisi S, Morselli PG, Venturoli S, Meriggiola MC. A prospective study on sexual function and mood in female-to-male transsexuals during testosterone administration and after sex reassignment surgery. J sex marital Ther. (2013) 39:321–35. doi: 10.1080/0092623X.2012.736920
79. Madsen MC, den Heijer M, Pees C, Biermasz NR, Bakker LE. Testosterone in men with hypogonadism and transgender males: a systematic review comparing three different preparations. Endocrine Connections. (2022) 11. doi: 10.1530/EC-22-0112
80. Gorin-Lazard A, Baumstarck K, Boyer L, Maquigneau A, Penochet J-C, Pringuey D, et al. Hormonal therapy is associated with better self-esteem, mood, and quality of life in transsexuals. J nervous Ment disease. (2013) 201:996–1000. doi: 10.1097/NMD.0000000000000046
81. Gómez-Gil E, Zubiaurre-Elorza L, Esteva de Antonio I, Guillamon A, Salamero M. Determinants of quality of life in Spanish transsexuals attending a gender unit before genital sex reassignment surgery. Qual Life Res. (2014) 23:669–76. doi: 10.1007/s11136-013-0497-3
82. van Leerdam TR, Zajac JD, Cheung AS. The effect of gender-affirming hormones on gender dysphoria, quality of life, and psychological functioning in transgender individuals: a systematic review. Transgender Health. (2023) 8:6–21. doi: 10.1089/trgh.2020.0094
83. Silva ED, Fighera TM, Allgayer RM, Lobato MIR, Spritzer PM. Physical and sociodemographic features associated with quality of life among transgender women and men using gender-affirming hormone therapy. Front Psychiatry. (2021) 12:621075. doi: 10.3389/fpsyt.2021.621075
84. Kirisawa T, Ichihara K, Sakai Y, Morooka D, Iyoki T, Masumori N. Physical and psychological effects of gender-affirming hormonal treatment using intramuscular testosterone enanthate in Japanese transgender men. Sexual Med. (2021) 9:100306–. doi: 10.1016/j.esxm.2020.100306
85. Tordoff DM, Lunn MR, Chen B, Flentje A, Dastur Z, Lubensky ME, et al. Testosterone use and sexual function among transgender men and gender diverse people assigned female at birth. Am J Obstetrics Gynecol. (2023) 229:669.e1–.e17. doi: 10.1016/j.ajog.2023.08.035
86. Fisher AD, Castellini G, Ristori J, Casale H, Cassioli E, Sensi C, et al. Cross-sex hormone treatment and psychobiological changes in transsexual persons: two-year follow-up data. J Clin Endocrinol Metab. (2016) 101:4260–9. doi: 10.1210/jc.2016-1276
87. Foster Skewis L, Bretherton I, Leemaqz SY, Zajac JD, Cheung AS. Short-term effects of gender-affirming hormone therapy on dysphoria and quality of life in transgender individuals: A prospective controlled study. Front Endocrinol. (2021) 12. doi: 10.1016/j.jsxm.2021.05.013
88. Witten TM, Eyler AE. Gay, lesbian, bisexual, and transgender aging: Challenges in research, practice, and policy. London, UK: JHU Press (2012).
89. Feldman J, Brown GR, Deutsch MB, Hembree W, Meyer W, Meyer-Bahlburg HF, et al. Priorities for transgender medical and healthcare research. Curr Opin Endocrinol Diabetes Obes. (2016) 23:180–7. doi: 10.1097/MED.0000000000000231
90. van Heesewijk JO, Dreijerink KM, Wiepjes CM, Kok AA, van Schoor NM, Huisman M, et al. Long-term gender-affirming hormone therapy and cognitive functioning in older transgender women compared with cisgender women and men. J sexual Med. (2021) 18:1434–43. doi: 10.1016/j.jsxm.2021.05.013
91. Siddiqui AN, Siddiqui N, Khan RA, Kalam A, Jabir NR, Kamal MA, et al. Neuroprotective role of steroidal sex hormones: an overview. CNS Neurosci Ther. (2016) 22:342–50. doi: 10.1111/cns.2016.22.issue-5
92. Navarro-Pardo E, Holland CA, Cano A. Sex hormones and healthy psychological aging in women. Front Aging Neurosci. (2018) 9:439. doi: 10.3389/fnagi.2017.00439
93. Yeap BB, Alfonso H, Chubb SP, Handelsman DJ, Hankey GJ, Almeida OP, et al. In older men an optimal plasma testosterone is associated with reduced all-cause mortality and higher dihydrotestosterone with reduced ischemic heart disease mortality, while estradiol levels do not predict mortality. J Clin Endocrinol Metab. (2014) 99:E9–E18. doi: 10.1210/jc.2013-3272
94. Hughto JM, Varma H, Babbs G, Yee K, Alpert A, Hughes L, et al. Disparities in health condition diagnoses among aging transgender and cisgender medicare beneficiaries, 2008-2017. Front Endocrinol. (2023) 14:1102348. doi: 10.3389/fendo.2023.1102348
95. Cicero EC, Lett E, Flatt JD, Benson GP, Epps F. Transgender adults from minoritized ethnoracial groups in the US Report Greater Subjective Cognitive Decline. Journals Gerontol: Ser B. (2023) 78:1051–9. doi: 10.1093/geronb/gbad012
96. van Heesewijk JO, Dreijerink KM, Wiepjes CM, Kok AA, Geurtsen GJ, van Schoor NM, et al. Cognitive functioning in older transgender individuals receiving long-term gender-affirming hormone therapy. Int J Transgender Health. (2023), 1–17. doi: 10.1080/26895269.2023.2289069
97. Iwamoto SJ, Defreyne J, Kaoutzanis C, Davies RD, Moreau KL, Rothman MS. Gender-affirming hormone therapy, mental health, and surgical considerations for aging transgender and gender diverse adults. Ther Adv Endocrinol Metab. (2023) 14:20420188231166494. doi: 10.1177/20420188231166494
Keywords: menstruation, transgender, transmen, mood disorder, gender diverse, menstruator, gender dysphoria
Citation: Arshed A, Madanes S, Pottinger S, Ackerman MG and Deutch AB (2024) Menstrual management in transgender and gender diverse individuals: psychiatric and psychosocial considerations. Front. Psychiatry 15:1422333. doi: 10.3389/fpsyt.2024.1422333
Received: 23 April 2024; Accepted: 09 September 2024;
Published: 29 October 2024.
Edited by:
Leah Susser, Cornell University, United StatesReviewed by:
Nimali Jayasinghe, Cornell University, United StatesAnna Dickerman, Cornell University, United States
Copyright © 2024 Arshed, Madanes, Pottinger, Ackerman and Deutch. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Arslaan Arshed, arslaan.arshed@nyulangone.org
†These authors share last authorship