Skip to main content

SYSTEMATIC REVIEW article

Front. Physiol., 28 June 2021
Sec. Exercise Physiology
This article is part of the Research Topic Exercise and Sport: Their Influences on Women's Health Across the Lifespan, Volume II View all 10 articles

Exercise During Pregnancy and Prenatal Depression: A Systematic Review and Meta-Analysis

  • 1AFIPE Research Group, Universidad Politécnica de Madrid, Madrid, Spain
  • 2Department of Education, Research Methods and Evaluation, Comillas Pontifical University, Madrid, Spain
  • 3Department of Physical Activity, Sports and Leisure Social Sciences, Universidad Politécnica de Madrid, Madrid, Spain
  • 4Department of Health and Human Performance, Universidad Politécnica de Madrid, Madrid, Spain
  • 5Department of Sports, Universidad Politécnica de Madrid, Madrid, Spain

Background: Prenatal depression is associated with an increased risk of physical, physiological, cardiovascular, and psychological diseases for mothers and future newborns. Prenatal depression and depressive symptoms could have negative effects on the cognitive, emotional, social, and behavioral development of children.

Objective: This study aimed to examine the influence of exercise during pregnancy on the prevalence of prenatal depression and depressive symptoms in the scientific literature.

Data Sources: A search was carried out examining different online databases up to November 2020.

Methods of Study Selection: A systematic review with random effects meta-analysis was performed. Only randomized controlled trials published in English or Spanish with pregnant populations and interventions with exercise programs carried out during pregnancy were included. The scores obtained by the tools that measured the emotional state and depressive symptoms as well as the number and percentage of depressed women of the study groups were analyzed.

Tabulation, Integration, and Results: We analyzed 15 studies and found a negative association between moderate exercise during pregnancy and prenatal depression (ES = −0.36, 95% CI = −0.58, −13, I2 = 80.2%, Pheterogeneity = 0.001). In addition, the studies also showed that women who were inactive during pregnancy had a 16% higher probability of suffering prenatal depression [RR = 0.84 (95% IC = 0.74, 0.96) I2 = 61.9%, Pheterogeneity = 0.010].

Conclusion: Supervised exercise during pregnancy may be useful for the prevention and reduction of prenatal depression and depressive symptoms.

Systematic Review Registration: Registered in PROSPERO (Registration No. CRD42020164819).

Introduction

Depression (major depressive disorder) is an important, common, and serious medical illness that negatively affects how a person feels, thinks, and acts. Depression causes different symptoms, such as feelings of sadness, loss of interest/energy, difficulty thinking/concentrating, and/or thoughts of death or suicide. All symptoms can vary from mild to severe (Bienvenu et al., 2013).

During the last 20 years, the World Health Organization (2004) has monitored diseases associated with depressive symptoms and the dangerous growth rate of the prevalence of these diseases within developed countries. Pregnant women are not exempt from depressive symptoms, and pregnancy is a particularly vulnerable time for depression to occur compared with other periods of a woman's life (Campagne, 2004).

Indeed, the physical and psychological changes that occur in pregnant women are the largest promoters of this type of emotional lability (Lederman et al., 1997). Symptoms that alter emotional balance and lead to sickness (in some women) usually appear at the beginning of pregnancy; these symptoms, together with the fear of not being able to cope with the baby, hormonal changes, transformation of the female body, and the possible presence of a history of psychological disorders, lead to a complex condition and may be responsible for the well-known emotional lability during pregnancy (Barakat, 2006; Austin et al., 2008).

It seems that the relationships between gestational alterations of a psychological and emotional nature (depression, changes in self-esteem, anxiety, stress, insecurity, etc.) and physiological parameters (longer deliveries and more instrumental labors, altered birth weights, etc.) have been scientifically confirmed (Field et al., 2006; Rahman et al., 2007; Grote et al., 2010). This negative association extends beyond the gestational period, causing postnatal complications for both mothers and offspring (Hammond and Crozier, 2007; Deave et al., 2008; Hay et al., 2010; Field, 2011). Undoubtedly, the intrauterine environment is decisive for the life of future humans.

Recent studies have estimated the prevalence of depression during pregnancy to be between 10 and 30% (Teixeira et al., 2009). It is closely associated with depression in the postpartum period, which has a prevalence of between 17 and 17.7% (Hahn-Holbrook et al., 2018; Shorey et al., 2018).

Drug treatment during pregnancy is difficult and often questioned due to the possible side effects of antidepressants in the mother and fetus (Hammond and Crozier, 2007). Depression is a difficult complication to control because it is necessary to implement an intervention that avoids the possible negative effects on the fetus and the mother, such as altered brain development (O'Connor et al., 2002; Lee et al., 2007), an increased risk of preterm birth or intrauterine growth restriction (Field et al., 2006; Li et al., 2009; Field, 2011). Notwithstanding the aforementioned difficulty, it is clear that it is necessary to establish strategies that prevent the already proven, dangerous, and increasing association between prenatal depression and postpartum depression, which is a more well-known type of depression that involves a series of related complications, such as mother–child bonding difficulties (Wisner et al., 2009), infant feeding difficulties and infant overweight problems (Ertel et al., 2010), low birth weight and long hospital stays.

This situation constitutes an interesting incentive to investigate alternative treatments for depression (Hammond and Crozier, 2007). According to a review of studies about the effects of exercise on the non-pregnant population, previous studies report beneficial antidepressant effects (Barbour et al., 2007; Blumenthal et al., 2007; Martinsen, 2008). Furthermore, the results of previous investigations, involving psychological variables during an exercise program carried out in pregnant women are encouraging (Koniak-Griffin, 1994; Goodwin et al., 2000; Nordhagen and Sundgot-Borgen, 2002; Orr et al., 2006).

Over the last 30 years, exercise has been shown to have many benefits for pregnant women without a risk of adverse effects for maternal–fetal well-being provided that the activity is of a moderate intensity and is supervised by a professional. Although the scientific literature is not fully conclusive, there are many investigations indicating the positive effects of moderate exercise on the prevention of complications, including the adequate control of certain maternal, fetal, and newborn parameters (Barakat et al., 2015, 2016; Klein et al., 2018). However, due to fear, ignorance, or other factors, the prevalence of women who achieve the minimum weekly recommendation of exercise during pregnancy is ~15–20% (Mottola et al., 2018; Barakat et al., 2019).

The purpose of this systematic review and meta-analysis was to synthesize the literature and determine the effect of exercise during pregnancy on the prevalence of prenatal depression.

Methods

This review was performed in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines (Moher et al., 2015) and was registered with PROSPERO, the International Prospective Register of Systematics Reviews (Registration No. CRD42020164819).

Eligibility Criteria

For this systematic review, the PICOS framework (population, intervention, comparison, outcome, study design) was used, and the nature of the interventions included in this research (Moher et al., 2015) was analyzed. Only articles written in English or Spanish and published between 2010 and 2020 were selected.

Population

The chosen population was pregnant women without any contraindication during pregnancy to undergo an exercise intervention during this period. Women suffering any absolute (e.g., heart failure, multiple pregnancy, or premature labor) or relative (e.g., essential arterial hypertension, cardiac arrhythmia, or anemia) contraindication were excluded from analyses.

Intervention

The following characteristics of the interventions were analyzed: (i) intensity: except for one study, all of the included studies had a light-to-moderate intensity of the load, which was prescribed using 55–65% of maximum maternal heart rate and in some cases by means of the perception of effort (range 12–14 of the Borg Scale); (ii) duration of the program; (iii) type of exercise (e.g., aerobic, strength, balance, or pelvic floor training); (iv) weekly frequency of the sessions; (v) duration of the sessions; (vi) whether the exercise program was supervised by a professional; (vii) adherence of the sample to the exercise program; and (viii) in some studies analyzed, a complementary intervention with different outcomes was carried out, and so this was classified as “exercise + cointervention” as shown in Table 1.

TABLE 1
www.frontiersin.org

Table 1. Characteristics of the studies analyzed.

Comparison

Women who engaged in exercise or physical activity were compared with those who did not. Additionally, the intervention characteristics were reviewed (shown in Table 1) to enrich our understanding of each study: no exercise intervention; weekly frequency, duration (both the program and sessions) or supervision of the program by a professional; mode of exercise; or if depression was a primary or secondary variable.

Outcomes

Target outcomes were the number of pregnant women with depression in both groups (to compare both the control and intervention groups) and the prenatal depression score of each depression questionnaire administered. The questionnaires dealing with prenatal depression among the selected articles were, in order of relevance, the Center for Epidemiologic Studies Depression Scale (CES-D), Edinburgh Postnatal Depression Scale (EPDS), The Short Form 36 Health Survey (SF-36) and Hospital Anxiety and Depression Scale (HADS).

Study Design, Information Sources, and Search Strategy

To perform this review, the SPORTDiscus, ClinicalTrials.gov, and MEDLINE (PubMed) databases were searched at the Universidad Politécnica de Madrid. The search began in October 2019 and the study was last updated between February and March 2020.

• English: exercise OR physical activity OR sport OR fitness AND pregnancy OR prenatal depression OR depression OR emotional OR emotional factors AND randomized clinical trial.

• Spanish: ejercicio O ejercicio físico O actividad física O deportes Y embarazo O depresión prenatal O depresión O emocional O factores emocionales Y ensayo clínico aleatorizado.

Study Selection

The inclusion criteria of the studies were randomized clinical trials whose intervention involved measurable or quantifiable activity or exercise (studies in which only advice to have an active pregnancy was provided were not selected), prenatal depression outcomes (depression symptoms or diagnosed depression) measured, and different characteristics of an exercise program provided. The selection process followed for the reviewed articles is captured in Figure 1 (Page et al., 2021).

FIGURE 1
www.frontiersin.org

Figure 1. Flow chart of the retrieved and analyzed articles.

Regarding the parameters studied, prenatal maternal depression expressed quantitatively (scale) and/or categorically (maternal depression yes/no) was the primary outcome extracted from the included studies. To determine the extent of the effects of exercise on the health of pregnant women, other pregnancy outcomes were examined as secondary outcomes (sociodemographic and physiological maternal variables and newborn outcomes, among others).

The data extracted from each of the included studies were the author(s) and publication year, country in which the study was conducted, number of participants, details of the type of exercise program, primary and secondary variable(s) analyzed and cointervention, if applicable (Table 1).

Statistical Analysis

Meta-analysis was performed separately by a different expression of depression variable. First, when the depression variable was expressed as a continuous variable, such as a score obtained by a questionnaire, the overall confidence interval (CI) was calculated using the standardized mean difference (Hedges et al., 2010).

Second, when depression was expressed as a categorical variable (yes/no), the number of events present in each study group and its relative risk (RR) were recorded, and the total sum of the RR was calculated using a random effects model (Higgins and Thompson, 2002).

In both analyses (dichotomous and continuous) the compensated average was established by assigning each study a weight relative to its sample size or number of events that contributed to the entire study (weight) or, in short, the information burden that each of them contributes. To quantify the heterogeneity present in the results, the I2 statistic was used, which indicates the proportion of variability observed in the effect of the intervention (between studies) that is due to the heterogeneity between studies and is not random. The following thresholds were used for the I2 statistic: low = 25%, moderate = 50%, and high = 75% (Daley et al., 2018).

One approach previously used to solve the problem of high heterogeneity has been to split the studies into subgroups based on some characteristics that could explain the variability of the studies (Ferreira González et al., 2011). However, in our case, given the limited number of the studies identified for the review, we have opted to present all of the examined studies in each analysis as we understand that this approach provides a more comprehensive view of the study.

Quality of Evidence Assessment and Risk of Bias

Despite being often mistaken as interchangeable terms, “quality” and “risk of bias” are, in fact, distinct but related concepts that should, thus, be differently addressed (Gunnell et al., 2020). In the present study, the assessment of quality (i.e., the degree to which studies are conducted in alignment with the highest possible standards) was performed by means of the Grading of Recommendations Assessment, Development and Evaluation (GRADE) technique (Guyatt et al., 2008), and studies that were rated as having high or moderate quality were included.

On the other hand, risk of bias (i.e., the degree to which potential biases may have led to underestimation or overestimation of an effect) was assessed following the Cochrane Handbook (Higgins et al., 2020).

Results

From a total of 827 retrieved articles, 727 were excluded for not meeting any of the inclusion criteria (Figure 1). In addition, 85 articles were excluded because they were not completely randomized clinical trials (i.e., they lacked a randomization process). Finally, 15 studies were included for analysis. Thirteen of them reported participants' depression or depression symptoms as a continuous variable (i.e., a score obtained in a questionnaire), and these studies are presented in Figure 2. On the other hand, in eight of them, depression was treated as a categorical variable reporting the number of women showing depression symptoms in each group (control and intervention). These studies are displayed in Figure 3. Last, six studies reported information about depression as both a continuous variable (score obtained in a questionnaire) and a dichotomous variable (suffering/not suffering depression). These works have, thus, been included in both Figures 2, 3 (Perales et al., 2014, 2015; Ussher et al., 2015; Haakstad et al., 2016; Uebelacker et al., 2016; Daley et al., 2018).

FIGURE 2
www.frontiersin.org

Figure 2. Effect of exercise on the score obtained for the participants on the administered questionnaires.

FIGURE 3
www.frontiersin.org

Figure 3. Effect of exercise programs during pregnancy on the probability of experiencing prenatal depression.

Among the 15 articles included in the meta-analysis, 14 included sessions supervised by professionals in the field. The exercise sessions (both supervised and not) were designed for low-to-moderate intensity or moderate-to-high intensity exercise and were not performed more than three times per week. The session durations varied from 20 to a maximum of 75 min for a session.

Effect of Exercise on the Score Obtained for the Participants on the Administered Questionnaires

Thirteen studies were included in this analysis. The results revealed a negative association between exercise practice during pregnancy and the scores obtained for the questionnaires that were used to measure depression in pregnant women (ES = −0.36, 95% CI = −0.58, −13, I2 = 80.2%, Pheterogeneity = 0.001). Figure 2 shows the forest plot corresponding to the present meta-analysis.

Effect of Exercise on the Number and Percentage of Depressed Pregnant Women in the Study Groups

A total of eight studies were included in this analysis. The global effect of exercise was evident in the number and percentage of pregnant women when those who were considered depressed in the intervention groups were compared with those in the control groups. Specifically, the total RR compensated was 0.84 (95% CI = 0.74, 0.96, I2 = 61.9%, Pheterogeneity = 0.010). These outcomes indicate that women who remain inactive present a 16% greater probability of experiencing prenatal depression. Figure 3 shows the forest plot corresponding to the present meta-analysis.

Risk of Bias Assessment

Overall, the quality of evidence ranged from low to high (see Figure 4; Table 2).

FIGURE 4
www.frontiersin.org

Figure 4. Risk of bias summary.

TABLE 2
www.frontiersin.org

Table 2. Risk of bias of reviewed studies.

Most of the studies exhibited low selection and attrition bias. There was a reasonable number of studies whose risk of detection bias was found to be unclear because studies reported whether outcome assessors had not been blinded to participants. The most common sources of risk of bias were (a) the low likelihood that either study participants or personnel were blinded to the experimental condition (performance bias) and (b) the fact that findings of some outcomes appearing in the protocol of the studies were not published in the analyzed studies (reporting bias).

Despite the risk of bias findings, it was decided to not disregard any study in our analyses. First, with regard to performance bias, because it is acknowledged in the Cochrane Collaboration's Tool (Higgins et al., 2020), blinding is not possible in certain situations (it is usually impossible to blind people to whether a PA program has been followed). Second, relating to the reporting bias, based on data extracted from the included studies, it is unlikely that the remaining outcomes of interest (biological rather than social data) were significantly associated with depression.

Discussion

The present study aimed to determine the effects of exercise during pregnancy on maternal prenatal depression. The results show a trend toward a small reduction in both the scores of the instruments (questionnaires) that measured the prevalence of depressive symptoms in pregnant women and the number and percentage of women with diagnosed prenatal depression in the intervention groups (physical exercise). It is important to clarify that, during pregnancy, a woman may present depressive symptoms and increased emotional lability but not be diagnosed with prenatal depression although obviously both conditions are closely associated.

Because all the studies investigated healthy pregnant women, the results obtained in these studies are related to depressive symptoms rather than to diagnosed depression. Therefore, from a global perspective, the findings of the present study could be used and have an important clinical application to prescribe groups and supervised exercise during pregnancy as a preventive factor against emotional lability and associated complications. The results of the present study allow us to conclude that supervised exercise during pregnancy constitutes a powerful tool for preventing and reducing prenatal depression.

Regarding the impact of exercise during pregnancy, the results suggest that there is a positive association between an active pregnancy and a more balanced and adequate emotional state. Because depressive symptoms begin early in pregnancy (first trimester), the supervised exercise program designed for healthy pregnant women should also begin early, once it is known that there are no obstetric contraindications to exercise during pregnancy.

The study designed by Perales et al. (2014) deserves particular attention; the article included 167 pregnant women and noted that, although depression levels were similar in both groups (slightly higher in the intervention group) at the beginning of pregnancy, by the end of pregnancy there was a significant difference (reduction) in favor of the intervention group (exercise) compared with the control group in relation to both the questionnaire values (CES-D questionnaire) and the number and percentage of pregnant women considered depressed. Overall, this result confirms the positive impact of a supervised exercise program during pregnancy on the emotional state of pregnant women.

It is interesting to analyze what factors present in exercise programs can be associated with the emotional response of pregnant women and determine an improvement in emotional state. In this sense, we find that both the supervision of exercise by a professional and the adherence of the participants to the program were relevant factors to increase the positive impact of exercise on improving emotional state. This positive association between exercise and the prevention of maternal prenatal depression has been demonstrated by some studies with supervised exercise programs and high adherence of the participants (Field et al., 2012; Perales et al., 2014, 2015, 2016; Ussher et al., 2015; Haakstad et al., 2016; Uebelacker et al., 2016; Vargas-Terrones et al., 2019).

The other important aspects seem to include the type of exercise and the activities implemented in the sessions. Thus, some studies include a combined practice with mixed activities (aerobic resistance, muscle strengthening, coordination, pelvic floor, flexibility) and show good results (Mosquera-Valderrama et al., 2012; Robledo-Colonia et al., 2012; Perales et al., 2014, 2015, 2016; Haakstad et al., 2016; Vargas-Terrones et al., 2019). Additionally, there was a reduction in prenatal depression in studies that used yoga (Davis et al., 2015) or tai-chi (Field et al., 2013a) as an intervention program; however, it is important to highlight that there is no absolute consensus as to which type of exercise reduces these symptoms the most.

In a recent RS-MA, Davenport et al. (2018) found a positive influence of supervised exercise on the reduction of depressive symptoms during pregnancy. Similarly, there are other recent systematic reviews that conclude that supervised exercise with low-to-moderate intensity is a preventive measure against postpartum depression as well as gestational depression (Shivakumar et al., 2011; Daley et al., 2015; Gong et al., 2015).

As it is been shown that women who were inactive during pregnancy were 16% more likely to suffer prenatal depression, future studies will focus on comparing the effect of antidepressants during pregnancy with exercise during the same period. However, more studies examining the effect of exercise during pregnancy are needed to contribute to understanding our research question.

The limitations of this study were the scarcity of scientific literature about exercise and prenatal depression because there are more papers that study postnatal depression than prenatal depression, the lack of consensus on the depression scales used (there were four different scales with four different measured scores), and the variability of the exercise programs performed in all studies. The results of the present study demonstrate that aerobic and supervised exercise during pregnancy could be a tool to prevent depressive symptoms as well as diagnosed prenatal depression.

Data Availability Statement

The original contributions presented in the study are included in the article/supplementary material, further inquiries can be directed to the corresponding author.

Author Contributions

MS-P was responsible for the design of the review study, contributed to the data selection and analysis, and the preparation of the manuscript. EF led data selection and analysis and contributed to manuscript writing. CS-J and JG-A contributed to the data selection and analysis. JP-T contributed to the data selection and analysis and the preparation of the manuscript. RB contributed to the design of the study and the manuscript writing. IR was mainly responsible for the design of the review study and the data analysis and led the manuscript writing. All authors contributed to the article and approved the submitted version.

Funding

This work was partially supported by the Program CSD-16/UPB/19, Consejo Superior de Deportes (Ministerios de Cultura y Deporte), Spain.

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.

References

Austin, M. P., Priest, S. R., and Sullivan, E. A. (2008). Antenatal psychosocial assessment for reducing perinatal mental health morbidity. Cochrane Database Syst. Rev. Cd005124. doi: 10.1002/14651858.CD005124.pub2

PubMed Abstract | CrossRef Full Text | Google Scholar

Barakat, R. (2006). El ejercicio físico durante el embarazo. Madrid: Pearson Alhambra.

Google Scholar

Barakat, R., Díaz-Blanco, A., Franco, E., Rollán-Malmierca, A., Brik, M., Vargas, M., et al. (2019). Guías clínicas para el ejercicio físico durante el embarazo. Prog. Obstet. Gynecol. 62, 464–471. doi: 10.20960/j.pog.00231

CrossRef Full Text | Google Scholar

Barakat, R., Pelaez, M., Cordero, Y., Perales, M., Lopez, C., Coteron, J., et al. (2016). Exercise during pregnancy protects against hypertension and macrosomia: randomized clinical trial. Am. J. Obstet. Gynecol. 214, 649.e1–649.e8. doi: 10.1016/j.ajog.2015.11.039

PubMed Abstract | CrossRef Full Text | Google Scholar

Barakat, R., Perales, M., Garatachea, N., Ruiz, J. R., and Lucia, A. (2015). Exercise during pregnancy. A narrative review asking: what do we know? Br. J. Sports Med. 49, 1377–1381. doi: 10.1136/bjsports-2015-094756

PubMed Abstract | CrossRef Full Text | Google Scholar

Barbour, K. A., Edenfield, T. M., and Blumenthal, J. A. (2007). Exercise as a treatment for depression and other psychiatric disorders: a review. J. Cardiopulm. Rehabil. Prev. 27, 359–367. doi: 10.1097/01.HCR.0000300262.69645.95

PubMed Abstract | CrossRef Full Text | Google Scholar

Bienvenu, O. J., Needham, D. M., and Hopkins, R. O. (2013). Diagnostic and statistical manual of mental disorders, and the impact of events scale-revised: response. Chest 144, 1974–1975. doi: 10.1378/chest.13-1940

CrossRef Full Text | Google Scholar

Blumenthal, J. A., Babyak, M. A., Doraiswamy, P. M., Watkins, L., Hoffman, B. M., Barbour, K. A., et al. (2007). Exercise and pharmacotherapy in the treatment of major depressive disorder. Psychosom. Med. 69, 587–596. doi: 10.1097/PSY.0b013e318148c19a

PubMed Abstract | CrossRef Full Text | Google Scholar

Campagne, D. M. (2004). The obstetrician and depression during pregnancy. Eur. J. Obstet. Gynecol. Reprod. Biol. 116, 125–130. doi: 10.1016/j.ejogrb.2003.11.028

CrossRef Full Text | Google Scholar

Daley, A., Riaz, M., Lewis, S., Aveyard, P., Coleman, T., Manyonda, I., et al. (2018). Physical activity for antenatal and postnatal depression in women attempting to quit smoking: randomised controlled trial. BMC Pregnancy Childbirth 18:156. doi: 10.1186/s12884-018-1784-3

PubMed Abstract | CrossRef Full Text | Google Scholar

Daley, A. J., Foster, L., Long, G., Palmer, C., Robinson, O., Walmsley, H., et al. (2015). The effectiveness of exercise for the prevention and treatment of antenatal depression: systematic review with meta-analysis. BJOG Int. J. Obstet. Gynaecol. 122, 57–62. doi: 10.1111/1471-0528.12909

PubMed Abstract | CrossRef Full Text | Google Scholar

Davenport, M. H., McCurdy, A. P., Mottola, M. F., Skow, R. J., Meah, V. L., Poitras, V. J., et al. (2018). Impact of prenatal exercise on both prenatal and postnatal anxiety and depressive symptoms: a systematic review and meta-analysis. Br. J. Sports Med. 52, 1376–1385. doi: 10.1136/bjsports-2018-099697

PubMed Abstract | CrossRef Full Text | Google Scholar

Davis, K., Goodman, S. H., Leiferman, J., Taylor, M., and Dimidjian, S. (2015). A randomized controlled trial of yoga for pregnant women with symptoms of depression and anxiety. Complement. Ther. Clin. Pract. 21, 166–172. doi: 10.1016/j.ctcp.2015.06.005

PubMed Abstract | CrossRef Full Text | Google Scholar

Deave, T., Heron, J., Evans, J., and Emond, A. (2008). The impact of maternal depression in pregnancy on early child development. BJOG Int. J. Obstet. Gynaecol. 115, 1043–1051. doi: 10.1111/j.1471-0528.2008.01752.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Ertel, K. A., Koenen, K. C., Rich-Edwards, J. W., and Gillman, M. W. (2010). Antenatal and postpartum depressive symptoms are differentially associated with early childhood weight and adiposity. Paediatr. Perinat. Epidemiol. 24, 179–189. doi: 10.1111/j.1365-3016.2010.01098.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Ferreira González, I., Urrútia, G., and Alonso-Coello, P. (2011). Systematic reviews and meta-analysis: scientific rationale and interpretation. Rev. Esp. Cardiol. 64, 688–696. doi: 10.1016/j.rec.2011.03.027

PubMed Abstract | CrossRef Full Text | Google Scholar

Field, T. (2011). Prenatal depression effects on early development: a review. Infant Behav. Dev. 34, 1–14. doi: 10.1016/j.infbeh.2010.09.008

PubMed Abstract | CrossRef Full Text | Google Scholar

Field, T., Diego, M., Delgado, J., and Medina, L. (2013a). Tai chi/yoga reduces prenatal depression, anxiety, and sleep disturbances. Complement. Ther. Clin. Pract. 19, 6–10. doi: 10.1016/j.ctcp.2012.10.001

PubMed Abstract | CrossRef Full Text | Google Scholar

Field, T., Diego, M., Delgado, J., and Medina, L. (2013b). Yoga and social support reduce prenatal depression, anxiety, and cortisol. J. Bodyw. Mov. Ther. 17, 397–403. doi: 10.1016/j.jbmt.2013.03.010

PubMed Abstract | CrossRef Full Text | Google Scholar

Field, T., Diego, M., and Hernandez-Reif, M. (2006). Prenatal depression effects on the fetus and newborn: a review. Infant Behav. Dev. 29, 445–455. doi: 10.1016/j.infbeh.2006.03.003

PubMed Abstract | CrossRef Full Text | Google Scholar

Field, T., Diego, M., Hernandez-Reif, M., Medina, L., Delgado, J., and Hernandez, A. (2012). Yoga and massage therapy reduce prenatal depression and prematurity. J. Bodyw. Mov. Ther. 16, 204–209. doi: 10.1016/j.jbmt.2011.08.002

PubMed Abstract | CrossRef Full Text | Google Scholar

Gong, H., Ni, C., Shen, X., Wu, T., and Jiang, C. (2015). Yoga for prenatal depression: a systematic review and meta-analysis. BMC Psychiatry 15:14. doi: 10.1186/s12888-015-0393-1

PubMed Abstract | CrossRef Full Text | Google Scholar

Goodwin, A., Astbury, J., and McMeeken, J. (2000). Body image and psychological well-being in pregnancy. A comparison of exercisers and non-exercisers. Aust. N. Z. J. Obstet. Gynaecol. 40, 442–447. doi: 10.1111/j.1479-828X.2000.tb01178.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Grote, N. K., Bridge, J. A., Gavin, A. R., Melville, J. L., Iyengar, S., and Katon, W. J. (2010). A meta-analysis of depression during pregnancy and the risk of preterm birth, low birth weight, and intrauterine growth restriction. Arch. Gen. Psychiatry 67, 1012–1024. doi: 10.1001/archgenpsychiatry.2010.111

PubMed Abstract | CrossRef Full Text | Google Scholar

Gunnell, K., Poitras, V. J., and Tod, D. (2020). Questions and answers about conducting systematic reviews in sport and exercise psychology. Int. Rev. Sport Exerc. Psychol. 13, 297–318. doi: 10.1080/1750984X.2019.1695141

CrossRef Full Text | Google Scholar

Guyatt, G. H., Oxman, A. D., Vist, G. E., Kunz, R., Falck-Ytter, Y., Alonso-Coello, P., et al. (2008). GRADE: an emerging consensus on rating quality of evidence and strength of recommendations. BMJ 336, 924–926. doi: 10.1136/bmj.39489.470347.AD

PubMed Abstract | CrossRef Full Text | Google Scholar

Haakstad, L. A., Torset, B., and Bø, K. (2016). What is the effect of regular group exercise on maternal psychological outcomes and common pregnancy complaints? an assessor blinded RCT. Midwifery 32, 81–86. doi: 10.1016/j.midw.2015.10.008

PubMed Abstract | CrossRef Full Text | Google Scholar

Hahn-Holbrook, J., Cornwell-Hinrichs, T., and Anaya, I. (2018). Economic and health predictors of national postpartum depression prevalence: a systematic review, meta-analysis, and meta-regression of 291 studies from 56 countries. Front. Psychiatry 8:248. doi: 10.3389/fpsyt.2017.00248

PubMed Abstract | CrossRef Full Text | Google Scholar

Hammond, S., and Crozier, K. (2007). Depression: assessing the causes. R. Coll. Midwives 10, 365–368.

Google Scholar

Hay, D. F., Pawlby, S., Waters, C. S., Perra, O., and Sharp, D. (2010). Mothers' antenatal depression and their children's antisocial outcomes. Child Dev. 81, 149–165. doi: 10.1111/j.1467-8624.2009.01386.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Hedges, L. V., Tipton, E., and Johnson, M. C. (2010). Robust variance estimation in meta-regression with dependent effect size estimates. Res. Synth. Methods 1, 39–65. doi: 10.1002/jrsm.5

PubMed Abstract | CrossRef Full Text | Google Scholar

Higgins, J. P., Savovíc, J., Page, M. J., Elbers, R. G., and Sterne, J. A. C. (2020). “Chapter 8: assessing risk of bias in a randomized trial,” in Cochrane Handbook for Systematic Reviews of Interventions Version 6.1, eds J. P. Higgins, J. Thomas, J. Chandler, M. Cumpston, T. Li, M. J. Page, and V. A. Welch (London: Cochrane), 1539–1558.

Google Scholar

Higgins, J. P., and Thompson, S. G. (2002). Quantifying heterogeneity in a meta-analysis. Stat. Med. 21, 1539–1558. doi: 10.1002/sim.1186

CrossRef Full Text | Google Scholar

Klein, C. P., dos Santos Rodrigues, K., Hözer, R. M., de Sá Couto-Pereira, N., Saccomori, A. B., Dal Magro, B. M., et al. (2018). Swimming exercise before and during pregnancy: promising preventive approach to impact offspring's health. Int. J. Dev. Neurosci. 71, 83–93. doi: 10.1016/j.ijdevneu.2018.08.009

CrossRef Full Text | Google Scholar

Koniak-Griffin, D. (1994). Aerobic exercise, psychological well-being, and physical discomforts during adolescent pregnancy. Res. Nurs. Health 17, 253–263. doi: 10.1002/nur.4770170404

PubMed Abstract | CrossRef Full Text | Google Scholar

Lederman, S. A., Paxton, A., Heymsfield, S. B., Wang, J., Thornton, J., and Pierson, R. N. Jr. (1997). Body fat and water changes during pregnancy in women with different body weight and weight gain. Obstet. Gynecol. 90(4 Pt 1), 483–488. doi: 10.1016/S0029-7844(97)00355-4

PubMed Abstract | CrossRef Full Text | Google Scholar

Lee, A. M., Lam, S. K., Sze Mun Lau, S. M., Chong, C. S., Chui, H. W., and Fong, D. Y. (2007). Prevalence, course, and risk factors for antenatal anxiety and depression. Obstet. Gynecol. 110, 1102–1112. doi: 10.1097/01.AOG.0000287065.59491.70

PubMed Abstract | CrossRef Full Text | Google Scholar

Li, D., Liu, L., and Odouli, R. (2009). Presence of depressive symptoms during early pregnancy and the risk of preterm delivery: a prospective cohort study. Hum. Reprod. 24, 146–153. doi: 10.1093/humrep/den342

PubMed Abstract | CrossRef Full Text | Google Scholar

Martinsen, E. W. (2008). Physical activity in the prevention and treatment of anxiety and depression. Nord. J. Psychiatry 62(Suppl. 47), 25–29. doi: 10.1080/08039480802315640

PubMed Abstract | CrossRef Full Text | Google Scholar

Moher, D., Shamseer, L., Clarke, M., Ghersi, D., Liberati, A., Petticrew, M., et al. (2015). Preferred reporting items for systematic review and meta-analysis protocols (PRISMA-P) 2015 statement. Syst. Rev. 4, 1–9. doi: 10.1186/2046-4053-4-1

PubMed Abstract | CrossRef Full Text | Google Scholar

Mosquera-Valderrama, Y. F., Robledo-Colonia, A. F., and Ramírez-Vélez, R. (2012). Ensayo clínico controlado de la influencia del entrenamiento aeróbico en la tolerancia al ejercicio y los síntomas depresivos en primigestantes colombianas. Prog. Obstet. Ginecol. 55, 385–392. doi: 10.1016/j.pog.2012.03.010

CrossRef Full Text | Google Scholar

Mottola, M. F., Davenport, M. H., Ruchat, S. M., Davies, G. A., Poitras, V., Gray, C., et al. (2018). 2019 Canadian guideline for physical activity throughout pregnancy. Br. J. Sports Med. 52, 1339–1346. doi: 10.1136/bjsports-2018-100056

PubMed Abstract | CrossRef Full Text | Google Scholar

Nordhagen, I. H., and Sundgot-Borgen, J. (2002). Physical activity among pregnant women in relation to pregnancy-related complaints and symptoms of depression. J. Nor. Med. Assoc. 122, 470–474.

PubMed Abstract | Google Scholar

O'Connor, T. G., Heron, J., Golding, J., Beveridge, M., and Glover, V. (2002). Maternal antenatal anxiety and children's behavioural/emotional problems at 4 years. Report from the avon longitudinal study of parents and children. Br. J. Psychiatry 180, 502–508. doi: 10.1192/bjp.180.6.502

PubMed Abstract | CrossRef Full Text | Google Scholar

Orr, S. T., James, S. A., Garry, J., and Newton, E. (2006). Exercise participation before and during pregnancy among low-income, urban, Black women: the Baltimore Preterm Birth Study. Ethn. Dis. 16, 909–913.

PubMed Abstract | Google Scholar

Page, M. J., Moher, D., Bossuyt, P. M., Boutron, I., Hoffmann, T. C., Mulrow, C. D., et al. (2021). PRISMA 2020 explanation and elaboration: updated guidance and exemplars for reporting systematic reviews. BMJ 372:n160. doi: 10.31222/osf.io/gwdhk

PubMed Abstract | CrossRef Full Text | Google Scholar

Perales, M., Cordero, Y., Vargas, M., Lucia, A., and Barakat, R. (2015). Exercise and depression in overweight and obese pregnant women: a randomised controlled trial. Arch. Med. Deporte 32, 156–163.

Google Scholar

Perales, M., Refoyo, I., Coteron, J., Bacchi, M., and Barakat, R. (2014). Exercise during pregnancy attenuates prenatal depression: a randomized controlled trial. Eval. Health Prof. 38, 59–72. doi: 10.1177/0163278714533566

CrossRef Full Text | Google Scholar

Perales, M., Santos-Lozano, A., Sanchis-Gomar, F., Luaces, M., Pareja-Galeano, H., Garatachea, N., et al. (2016). Maternal cardiac adaptations to a physical exercise program during pregnancy. Med. Sci. Sports Exerc. 48, 896–906. doi: 10.1249/MSS.0000000000000837

PubMed Abstract | CrossRef Full Text | Google Scholar

Rahman, A., Bunn, J., Lovel, H., and Creed, F. (2007). Association between antenatal depression and low birthweight in a developing country. Acta Psychiatr. Scand. 115, 481–486. doi: 10.1111/j.1600-0447.2006.00950.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Robledo-Colonia, A. F., Sandoval-Restrepo, N., Mosquera-Valderrama, Y. F., Escobar-Hurtado, C., and Ramírez-Vélez, R. (2012). Aerobic exercise training during pregnancy reduces depressive symptoms in nulliparous women: a randomised trial. J. Physiother. 58, 9–15. doi: 10.1016/S1836-9553(12)70067-X

PubMed Abstract | CrossRef Full Text | Google Scholar

Satyapriya, M., Nagarathna, R., Padmalatha, V., and Nagendra, H. R. (2013). Effect of integrated yoga on anxiety, depression, and well being in normal pregnancy. Complement. Ther. Clin. Pract. 19, 230–236. doi: 10.1016/j.ctcp.2013.06.003

PubMed Abstract | CrossRef Full Text | Google Scholar

Shivakumar, G., Brandon, A. R., Snell, P. G., Santiago-Muñoz, P., Johnson, N. L., Trivedi, M. H., et al. (2011). Antenatal depression: a rationale for studying exercise. Depress. Anxiety 28, 234–242. doi: 10.1002/da.20777

PubMed Abstract | CrossRef Full Text | Google Scholar

Shorey, S., Chee, C. Y. I., Ng, E. D., Chan, Y. H., Tam, W. W. S., and Chong, Y. S. (2018). Prevalence and incidence of postpartum depression among healthy mothers: a systematic review and meta-analysis. J. Psychiatr. Res. 104, 235–248. doi: 10.1016/j.jpsychires.2018.08.001

PubMed Abstract | CrossRef Full Text | Google Scholar

Teixeira, C., Figueiredo, B., Conde, A., Pacheco, A., and Costa, R. (2009). Anxiety and depression during pregnancy in women and men. J. Affect. Disord. 119, 142–148. doi: 10.1016/j.jad.2009.03.005

PubMed Abstract | CrossRef Full Text | Google Scholar

Uebelacker, L. A., Battle, C. L., Sutton, K. A., Magee, S. R., and Miller, I. W. (2016). A pilot randomized controlled trial comparing prenatal yoga to perinatal health education for antenatal depression. Arch. Womens Ment. Health 19, 543–547. doi: 10.1007/s00737-015-0571-7

PubMed Abstract | CrossRef Full Text | Google Scholar

Ussher, M., Lewis, S., Aveyard, P., Manyonda, I., West, R., Lewis, B., et al. (2015). Physical activity for smoking cessation in pregnancy: randomised controlled trial. BMJ 350:h2145. doi: 10.1136/bmj.h2145

PubMed Abstract | CrossRef Full Text | Google Scholar

Vargas-Terrones, M., Barakat, R., Santacruz, B., Fernandez-Buhigas, I., and Mottola, M. F. (2019). Physical exercise programme during pregnancy decreases perinatal depression risk: a randomised controlled trial. Br. J. Sports Med. 53, 348–353. doi: 10.1136/bjsports-2017-098926

PubMed Abstract | CrossRef Full Text | Google Scholar

Wisner, K. L., Sit, D. K. Y., Hanusa, B. H., Moses-Kolko, E. L., Bogen, D. L., Hunker, D. F., et al. (2009). Major depression and antidepressant treatment: impact on pregnancy and neonatal outcomes. Am. J. Psychiatry 166, 557–566. doi: 10.1176/appi.ajp.2008.08081170

PubMed Abstract | CrossRef Full Text | Google Scholar

World Health Organization (2004). Invertir en salud mental. Available online at: https://apps.who.int/iris/handle/10665/42897 (accessed December 5, 2020).

Google Scholar

Keywords: exercise, pregnancy, prenatal depression, model, fetus

Citation: Sánchez-Polán M, Franco E, Silva-José C, Gil-Ares J, Pérez-Tejero J, Barakat R and Refoyo I (2021) Exercise During Pregnancy and Prenatal Depression: A Systematic Review and Meta-Analysis. Front. Physiol. 12:640024. doi: 10.3389/fphys.2021.640024

Received: 10 December 2020; Accepted: 24 May 2021;
Published: 28 June 2021.

Edited by:

Angelica Lindén Hirschberg, Karolinska Institute (KI), Sweden

Reviewed by:

Giancarlo Condello, University of Taipei, Taiwan
Andrew McKune, University of Canberra, Australia

Copyright © 2021 Sánchez-Polán, Franco, Silva-José, Gil-Ares, Pérez-Tejero, Barakat and Refoyo. 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: Javier Gil-Ares, javier.gil@upm.es

Disclaimer: 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.