Skip to main content

SYSTEMATIC REVIEW article

Front. Public Health, 24 January 2024
Sec. Infectious Diseases: Epidemiology and Prevention

How do socioeconomic determinants of health affect the likelihood of living with HTLV-1 globally? A systematic review with meta-analysis

  • 1School of Public Health, Imperial College London, London, United Kingdom
  • 2Section of Virology, Department of Infectious Disease, Faculty of Medicine, Imperial College London, London, United Kingdom
  • 3National Centre for Human Retrovirology, St Mary’s Hospital, Imperial College Healthcare NHS Trust, London, United Kingdom

Introduction: Human T Lymphotropic Virus type 1 (HTLV-1) is a neglected retrovirus associated with many clinical disorders, most notably Adult T-cell Leukemia/Lymphoma and HTLV-1-Associated Myelopathy (HAM). Found in endemic clusters across the world, high prevalence has been reported in minoritized groups who suffer from health inequities. This study investigates the association between HTLV-1 prevalence and the following socioeconomic determinants of health: education, income, and employment, which are markers of health inequity.

Methods: A systematic review was conducted by searching the following databases: Ovid/Medline, Embase, Global Health Database, Web of Science, LILACS and SciELO. Primary studies in English, Spanish and Portuguese mentioning HTLV-1 and one of education, income and/or employment were included. A random-effects meta-analysis was performed, and odds ratios (OR) were calculated to determine the association between these socioeconomic determinants of health and HTLV-1 prevalence.

Results: 42 studies were included. The likelihood of having HTLV-1 was higher in individuals with less than completed primary education compared to those who completed primary education (OR 1.86 [95% CI 1.34–2.57]; p < 0.01). This may be because individuals with low education have reduced access to and understanding of health information, thus increasing the prevalence of risk factors associated with HTLV-1 infection. No other determinants were found to be statistically significant.

Conclusion: Fewer years of schooling are associated with increased likelihood of contracting HTLV-1. Therefore, health promotion materials and public health policies regarding HTLV-1 must consider those with lower educational levels to effectively reduce disease transmission.

Systematic review registration: https://www.crd.york.ac.uk/prospero/display_record.php?RecordID=335004, identifier (CRD42022335004).

Introduction

Human T Lymphotropic virus type 1 (HTLV-1) is a human retrovirus that causes chronic lifelong infection, primarily of T-lymphocytes (1). First discovered in 1980 (2), it has been found in endemic clusters in many regions globally, such as West Africa, Brazil and Japan (3). In 2012 it was estimated that at least 5–10 million people were living with HTLV-1 worldwide (4), however this is thought to be an underestimate since reliable prevalence data is not available for many areas of the world (3). HTLV-1 infection is commonly associated with marginalized groups such as sex workers, immigrants, and First Nations communities (5). Furthermore, routes of transmission are varied, being through contaminated blood products, vertical transmission via prolonged breastfeeding, and condomless sexual intercourse (6).

HTLV-1 infection can cause severe and potentially fatal complications. The virus is associated with a wide variety of clinical disorders, most notably a severe leukemia and lymphoma, Adult T-cell Leukamia/Lymphoma (ATL) and a chronic and progressive neurological disease, known as HTLV-1-associated myelopathy (HAM) (7). Additionally, a meta-analysis revealed that HTLV-1 infection is associated with a 57% increase in all-cause mortality, as well as several inflammatory conditions such as uveitis, infective dermatitis and polyarthritis (5). No curative treatment exists for HTLV-1 and there is a lack of screening for the infection globally (7). Currently, prevention remains the best option to reduce HTLV-1 prevalence internationally.

HTLV-1 infection can impact quality of life significantly and lead to health inequities (8). The World Health Organization (WHO) defines health inequities as “systematic differences in the health status of different population groups. These inequities have significant social and economic costs both to individuals and societies” (9). By definition, health inequities are unjust and may be avoidable with the implementation of adequate health policies (9).

Health inequities are influenced by the social determinants of health, which are defined as “the non-medical factors that influence health outcomes” (10), and can include factors such as education, income and employment. The links between reduced access to such factors and increased prevalence of infectious diseases are well-described, in different populations and infections globally (11). Educational attainment is inversely correlated with the prevalence of several sexually transmitted infections, including HIV, Treponema pallidum, Chlamydia trachomatis, and Neisseria gonorrhea (1214). Low income is also associated with an increased susceptibility to a range of communicable diseases including HIV, tuberculosis, hepatitis, dengue, pneumonia, cholera, and diarrhoeal diseases (15). Unemployment is associated with a deterioration in physical and mental health (16) and has been seen to confer 2–3 times higher risk mortality from COVID-19 infection (17).

Scattered data indicates that HTLV-1 infection is also linked with many social determinants of health, including employment, income, education, sex work, intravenous drug use (IDU), homelessness, immigration, sexuality, and gender (3, 8, 18). However, to date there has been no systematic assessment of how the prevalence of HTLV-1 infection is affected by socioeconomic determinants of health. Therefore, this study aims to address this gap by exploring the association between HTLV-1 prevalence and three socioeconomic determinants of health: education, income and employment.

Methods

The Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA) reporting guidelines were followed throughout this study (Figure 1). The review was registered in the International Prospective Register of Systematic Reviews (PROSPERO) database (CRD42022335004) (19). The populations studied included blood donors, pregnant women, and the general population. The odds of having HTLV-1 according to different socioeconomic determinants of health were measured and compared to various control groups. These determinants of health included educational attainment, income, and employment.

Figure 1
www.frontiersin.org

Figure 1. PRISMA diagram. Of the 2068 papers screened, 175 were found by searching Ovid/MEDLINE, 156 were found in Embase, 344 were found in the Global Health database, 552 were found in Web of Science, 27 were found in Latin American and Caribbean Health Sciences Literature (LILACS) and 814 were found in SciELO.

Search strategy

A total of six databases were systematically searched by one reviewer (NR) on 23rd February 2022. These included Ovid/MEDLINE, Embase, The Global Health database, Web of Science, Latin American and Caribbean Health Sciences Literature (LILACS) and SciELO. The search strategy included the following groups of search terms: all key terms referring to HTLV-1, education, income, and employment. All search terms for HTLV-1 were combined with all search terms related to one socioeconomic determinant of health. This process was repeated for all three determinants of health. The search terms and examples of searches are outlined in Supplementary Tables S1, S2.

Eligibility criteria

Inclusion criteria

Studies considered for inclusion were those written in English, Spanish or Portuguese, containing primary research about HTLV-1 prevalence with mention of one or more of the following determinants: education, income or employment. The search was not restricted by date or study design.

Exclusion criteria

Duplicate studies, studies about HTLV-2, HIV, and those that did not contain primary research were also excluded.

Study selection

One reviewer (NR) screened the title and abstracts of all eligible studies using Covidence (Veritas Health Innovation, Melbourne, Australia), a screening tool designed to assist with systematic reviews. Duplicates and studies which did not fit the eligibility criteria were excluded. A second reviewer (BC) screened 10% of the title and abstracts randomly selecting papers using an online random number generator. After the initial screening, one reviewer (NR) screened all remaining papers in full for the final selection, whilst a second reviewer (BC) screened the full texts of 10% of randomly selected papers. The concordance rate between both reviewers at both stages was found to be 99.7 and 98.7% respectively, so no additional duplicate screening was deemed necessary. Any discrepancies were resolved by a third reviewer (CR).

Statistical analysis

The data were analyzed using RevMan 5.4. The prevalence of HTLV-1 within each population was used to calculate the odds ratios (OR) for dichotomous determinants. Each determinant was analyzed using the random effects Mantel–Haenszel model to determine if the association between HTLV-1 and any determinant was statistically significant. Heterogeneity was also calculated and represented as I2.

Education was further divided into three categories: did not complete primary education, did not complete secondary education, and completed secondary education and above. There was overlap between these classifications, therefore separate subgroup analyzes were carried out to understand the isolated effect that each level of education had on HTLV-1 prevalence. Similarly, income was divided into two categories: low and middle/high income, and low/middle and high income to again determine if differing levels of income impacted results.

There was no standardized way to categorize education across all studies, therefore for the purpose of this review, it was classified as the following: primary education 1–8 years, secondary education 9–12 years, higher education 12+ years. This was adapted from school systems in Brazil, where many of the selected studies took place (20). The classification of income and employment were derived from the definitions used in the selected studies (See Supplementary Table S3).

Where data were available, subgroup analysis was conducted for each determinant, according to the populations studied: blood donors, pregnant women, and the general population. Additionally, analysis including studies with only explicit confirmatory testing for HTLV-1 was carried out for all determinants. This had no impact on the findings; therefore, these data are not shown. Forest plots for each socioeconomic determinant of health were created.

Due to the nature of the topic, the existing literature mainly consisted of observational studies. Therefore, no specific quality assessment was undertaken for the papers in this study.

Research ethics approval

Ethics approval was not required as this was a systematic review with meta-analysis and did not include patient involvement.

Patient and public involvement

Patients were not involved in the study design, data collection, data analysis, data interpretation or writing of the report.

Results

The search strategy yielded 2068 papers in total (Figure 1). Of these, 175 were found by searching Ovid/MEDLINE, 156 were found in Embase, 344 were found in The Global Health database, 552 were found in Web of Science, 27 were found in Latin American and Caribbean Health Sciences Literature (LILACS) and 814 were found in SciELO.

After screening, 2022 papers were excluded, and 42 studies were included for meta-analysis (Figure 1). Reasons for exclusion include wrong comparator, wrong patient population or irrelevant data. Data were included from over 500,000 participants in 11 countries. Thirty-six studies (86%) took place in LMICs, with 16 (38%) taking place in Brazil (2, 2135) and the rest being carried out in Peru (3638), Guadeloupe (39, 40), Mozambique (41), Nigeria (42, 43), Iran (4450), Jamaica (51), Gabon (52) and Panama (53) (Supplementary Table S3). Thirty-seven papers assessed level of education in relation to HTLV-1 infection (2139, 41, 42, 4451, 5461). Eighteen papers assessed income (23, 2630, 33, 35, 39, 40, 43, 47, 48, 50, 51, 53, 56, 62), and six assessed employment status (42, 47, 50, 52, 55, 59). The characteristics of selected studies are summarized in Supplementary Table S3.

Thirty-seven papers assessed level of education in relation to HTLV-1 infection (2139, 41, 42, 4451, 5461). Of these, twelve papers found a statistically significant association between education and the likelihood of having HTLV-1 (21, 31, 34, 36, 39, 45, 48, 50, 54, 57, 58, 60). Eighteen papers assessed income (23, 2630, 33, 35, 39, 40, 43, 47, 48, 50, 51, 53, 56, 62), and of these, only four papers found a statistically significant association between income and the likelihood of having HTLV-1 (39, 40, 47, 48). Lastly, six papers assessed employment (42, 47, 50, 52, 55, 59) and none found a statistically significant association for this variable. The characteristics of selected studies are summarized in Supplementary Table S3.

Individuals with less than primary education were almost twice as likely to be infected with HTLV-1, compared to those who had completed primary education (OR 1.86 [95% Confidence Interval (CI) 1.34–2.57]; p < 0.01) (Figure 2) or had completed secondary education (OR 2.46 [95% CI 1.43–4.23]; p < 0.01) (Figure 3). Considerable heterogeneity was observed for both variables, with I2 = 78% and I2 = 96% for primary and secondary education, respectively. To determine whether primary or secondary education was predominantly influencing the results, the prevalence of HTLV-1 among those who had not completed secondary education was compared with those having completed secondary education (Supplementary Figure S1). Having completed secondary education was associated with a significantly lower rate of HTLV-1 infection (OR 0.47 [95% CI 0.35–0.61]; p < 0.01, I2 = 0%). In a subgroup analysis only the results for blood donors were statistically significant (OR 0.44 [95% CI 0.32–0.59]; p < 0.01, I2 = 0%) (Supplementary Figure S1). These results suggest that completing secondary education is associated with low odds of being seropositive for HTLV-1.

Figure 2
www.frontiersin.org

Figure 2. Forest plot comparing the level of primary education and HTLV-1 prevalence, subdivided into the groups of general population, blood donors and pregnant women.

Figure 3
www.frontiersin.org

Figure 3. Forest plot comparing the level of secondary education and HTLV-1 prevalence, subdivided into the groups of general population, blood donors and pregnant women.

Subgroup analysis for those who had incomplete and complete primary education found that the results for the general population (OR 1.58 [95% CI 1.12–2.25]; p < 0.01, I2 = 61%) and blood donors (OR 3.88 [95% CI 2.11–7.14]; p < 0.01, I2 = 78%) remained statistically significant, whereas that for pregnant women (OR 1.23 [95% CI 0.42–3.56]; p = 0.71, I2 = 83%) were no longer significant (Figure 2).

For those who had incomplete and complete secondary education, subgroup analysis found that the results for blood donors (OR 2.02 [95% CI 1.58–2.58]; p < 0.01, I2 = 74%) remained significant, whereas the results for the general population (OR 4.01 [95% CI 0.89–18.10]; p = 0.07, I2 = 96%) and pregnant women (OR 1.72 [95% CI 0.69–4.31]; p = 0.24, I2 = 63%) were no longer significant (Figure 3).

Income (OR 1.1 [95% CI 0.87–1.47]; p = 0.36, I2 = 65%) (Figure 4) and employment status (OR 0.59 [95% CI 0.23–1.48] p = 0.26, I2 = 74%) (Figure 5) were not found to be associated with HTLV-1 infection. However, the subgroup analysis for income found that amongst blood donors, low income was associated with increased odds of being infected by HTLV-1 (OR 1.41 [95% CI 1.15–1.71]; p < 0.01, I2 = 24%) (Figure 4). No other subgroup analysis had an impact on the overall result (Figures 4, 5).

Figure 4
www.frontiersin.org

Figure 4. Forest plot comparing low and middle/high income and HTLV-1 prevalence, subdivided into the groups of general population, blood donors and pregnant women.

Figure 5
www.frontiersin.org

Figure 5. Forest plot comparing employment status and HTLV-1 prevalence, subdivided into the groups of general population, blood donors and pregnant women.

Discussion

HTLV-1 is a neglected infection that mainly affects vulnerable groups. However, there is little systematic data on the impact of socioeconomic determinants of health on HTLV-1 prevalence globally. Some existing studies touch on the relationship between HTLV-1 prevalence and education, socioeconomic status, social class, age at first intercourse, parity, and race/ethnicity, however, there has been inadequate action by governing bodies in response to these results (6365).

The present study revealed that lower education is associated with higher likelihood of having HTLV-1 infection. Initially it appeared that having completed secondary education (including those who had some degree of higher education) was associated with reduced prevalence of HTLV-1 infection, but further analysis demonstrated that incomplete primary education, i.e., not completing at least 8 years of education, contributed most to the likelihood of having HTLV-1 infection. This has major implications for effective public health education. No other socioeconomic determinant of health analyzed (income and employment status) was found to be significant overall, except for low income among blood donors in the subgroup analysis.

Level of schooling is an important social determinant of health since less education can lead to social and health inequities. Education level is just one measure of socioeconomic status and is closely linked with various determinants of health, making it difficult to establish the isolated effect on HTLV-1 prevalence. Despite this, several studies have confirmed that fewer years of education are associated with poorer health literacy (6672). Health literacy is defined as the ability to find, understand, and use health information (73). Reduced access to and understanding of health promotion materials can directly impact an individual’s risk of acquiring HTLV-1 infection (30). Indeed, Nunes et al. (30), found illiteracy to be associated with lower rates of condom use.

Furthermore, fewer employment opportunities are available for individuals with lower levels of education (74). This can restrict the type of work available, potentially worsening health inequities, as well as restricting individuals to types of work which may increase their risk of HTLV-1 transmission, such as condomless sex work (75).

Fewer years of schooling can not only reduce employment opportunities but also associated income. Low income may affect access to healthcare and may lead to individuals being more reliant on financial support from partner(s). This support may be more assured in the context of sexual relationships, particularly condomless sex and childbearing (76, 77). Condomless sex, especially with multiple partners, is a risk factor for acquiring infection, and can increase HTLV-1 prevalence (78). Moreover, low education level and financial dependency are both independently associated with higher rates of violence against women (79), and this in turn has also been linked to a 9-fold increased risk of having HTLV-1 (80). Additionally, it is possible that low parental income may predispose children to low education levels, which our study found is associated with increased risk of HTLV-1 prevalence (81).

Our study found no statistically significant impact of income and employment status on the prevalence of HTLV-1 infection. However, low income was associated with the increased likelihood of blood donors being seropositive for HTLV-1. The lack of overall association was surprising as low income is usually associated with low education level, the determinant of health assessed in this study that was found to be significant. Sampaio et al. (82) recently compared HTLV-1 prevalence and Human Development Index (HDI) of various countries globally and found that HTLV-1 prevalence was three times higher in countries with low HDI than in countries with high HDI (82). HDI is calculated using education level and GDP per capita, confirming that these determinants of health influence HTLV-1 prevalence globally. As our study assessed the impact on an individual level, differences in methodologies including the variety of countries that were included in the studies, may have influenced the results.

The results of our study will have been impacted by the limited number of studies available, particularly from countries other than Brazil, the wide period of time that the studies were performed, with some of which being done more than three decades ago, and the heterogeneity observed. Information on education was collated for over 500,000 individuals, representing 84% of the total data which increased the likelihood of detecting an association (See Figure 1). Furthermore, much of the evidence used differing methodologies, and measured variables differently. Additionally, there was limited access to the raw data from each study, making it difficult to standardize the way in which the different determinants of health were classified for this analysis. This contributed greatly towards heterogeneity within the data and limited depth. In addition to this, many studies did not account for confounding factors. Therefore, although some studies have found a significant association between HTLV-1 prevalence and low income (27, 39, 47, 48) and employment status (47), this was not confirmed by this meta-analysis. Thus, further research in this area is needed.

Upcoming studies on HTLV-1 should therefore aim to investigate various factors affecting the prevalence of infection globally, such as immigration and race, and detailed information on socioeconomic determinants of health should be included in every future prevalence study. These results will be important in solidifying our understanding of the topic and may aid both clinicians and policy makers in improving access to HTLV-1 prevention strategies and care.

Since HTLV-1 affects many marginalized populations across the world, an improved understanding of the virus’ epidemiology in diverse populations is necessary, to try and reduce the impact of the infection on these groups. This further reinforces the need for research in other areas of the world with high HTLV-1 prevalence to consider the structural inequities associated with the infection. Our findings emphasize the importance of ensuring that health promotion strategies, including those to reduce HTLV-1 prevalence, are designed to be accessible to those with poor health literacy. For example, this could be achieved by using minimal text on posters (63), via art (83), or video-based campaigns (84).

This concept is hardly new, since there are many examples of successful health promotion strategies that focus on providing information to at-risk populations. In particular, public communication campaigns regarding COVID-19 and national lockdowns were successful in significantly reducing mortality from SARS-CoV-2 in New Zealand (85). With information about the importance of handwashing and staying at home being relayed to the population in an accessible way, a high degree of national support for the intervention emerged, despite the disruption to people’s lives (85). Furthermore, the introduction of school-based sex education in the United Kingdom, in which information was delivered using appropriate language, was found to be effective at reducing the risk of contracting sexually transmitted infections in early adulthood (86). These studies further strengthen our findings and emphasize the importance of accessible health information, especially in relation to HTLV-1.

In conclusion, HTLV-1 is a severely neglected infection in both medical research and practice, despite affecting millions of people worldwide and having a significant impact on their quality of life. It is associated with marginalized populations, who disproportionally suffer from the consequences of chronic HTLV-1 infection due to the wider consequences of living with health inequities. This study found that individuals with less primary education were more likely to have HTLV-1 infection, compared to those with higher levels of education. This highlights the importance of ensuring health promotion materials regarding HTLV-1 are accessible to people of all education levels. This will be helpful to reduce HTLV-1 transmission and the significant morbidity and mortality associated with the infection.

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

NR: Conceptualization, Data curation, Formal analysis, Methodology, Writing – original draft. BC: Conceptualization, Data curation, Methodology, Supervision, Writing – review & editing. GT: Conceptualization, Supervision, Writing – review & editing. CR: Conceptualization, Methodology, Supervision, Writing – review & editing.

Funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. BC is an Academic Clinic Fellow (ACF-2019-21-009). GT is supported by the NIHR Imperial Biomedical Research Centre.

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/fpubh.2024.1298308/full#supplementary-material

References

1. Schierhout, G, McGregor, S, Gessain, A, Einsiedel, L, Martinello, M, and Kaldor, J. Association between HTLV-1 infection and adverse health outcomes: a systematic review and meta-analysis of epidemiological studies. Lancet Infect Dis. (2020) 20:133–43. doi: 10.1016/S1473-3099(19)30402-5

PubMed Abstract | Crossref Full Text | Google Scholar

2. Poiesz, B, Ruscetti, F, Gazdar, A, Bunn, P, Minna, J, and Gallo, R. Detection and isolation of type C retrovirus particles from fresh and cultured lymphocytes of a patient with cutaneous T-cell lymphoma. Proc Natl Acad Sci. (1980) 77:7415–9. doi: 10.1073/pnas.77.12.7415

PubMed Abstract | Crossref Full Text | Google Scholar

3. Gessain, A, and Cassar, O. Epidemiological aspects and world distribution of HTLV-1 infection. Front Microbiol. (2012) 3:3 10.3389/fmicb.2012.00388. doi: 10.3389/fmicb.2012.00388

Crossref Full Text | Google Scholar

4. World Health Organisation. Human T-lymphotropic virus type 1. Available at: https://www.who.int/news-room/fact-sheets/detail/human-t-lymphotropic-virus-type-1 (accessed September 9, 2022).

Google Scholar

5. Rosadas, C, Assone, T, Yamashita, M, Adonis, A, Puccioni-Sohler, M, Santos, M, et al. Health state utility values in people living with HTLV-1 and in patients with HAM/TSP: the impact of a neglected disease on the quality of life. PLoS Negl Trop Dis. (2020) 14:e0008761. doi: 10.1371/journal.pntd.0008761

Crossref Full Text | Google Scholar

6. Souza, LS, Lins-Silva, DH, Dorea-Bandeira, I, Barouh, JL, Tolentino, A, Bandeira, ID, et al. Prevalence and factors associated with depression and anxiety in people living with HTLV-1: a systematic review with meta-analysis and meta-regression. Gen Hosp Psychiatry. (2021) 73:54. doi: 10.1016/j.genhosppsych.2021.08.012

PubMed Abstract | Crossref Full Text | Google Scholar

7. Caron, M, Besson, G, Padilla, C, Makuwa, M, Nkoghe, D, Leroy, E, et al. Revisiting human T-cell lymphotropic virus types 1 and 2 infections among rural population in Gabon, Central Africa thirty years after the first analysis. PLoS Negl Trop Dis. (2018) 12:e0006833. doi: 10.1371/journal.pntd.0006833

Crossref Full Text | Google Scholar

8. Rosadas, C, and Taylor, GP. Health inequities and HTLV-1. Lancet Microbe. (2022) 3:e164. doi: 10.1016/S2666-5247(21)00330-X

PubMed Abstract | Crossref Full Text | Google Scholar

9. World Health Organisation. Health inequities and their causes. Available at: https://www.who.int/news-room/facts-in-pictures/detail/health-inequities-and-their-causes (accessed September 9, 2022).

Google Scholar

10. World Health Organisation. Social determinants of health. Available at: https://www.who.int/health-topics/social-determinants-of-health#tab=tab_1 (accessed September 9, 2022).

Google Scholar

11. Butler-Jones, D, and Wong, T. Infectious disease, social determinants and the need for intersectoral action. Can Commun Dis Rep. (2016) 42:S1-18–20. doi: 10.14745/ccdr.v42is1a04

Crossref Full Text | Google Scholar

12. Solomon, MM, Smith, MJ, and Del Rio, C. Low educational level: a risk factor for sexually transmitted infections among commercial sex workers in Quito, Ecuador. Int J STD AIDS. (2008) 19:264–7. doi: 10.1258/ijsa.2007.007181

PubMed Abstract | Crossref Full Text | Google Scholar

13. Slurink, IA, Götz, HM, van Aar, F, and van Benthem, BH. Educational level and risk of sexually transmitted infections among clients of Dutch sexual health Centres. Int J STD AIDS. (2021) 32:1004–13. doi: 10.1177/09564624211013670

PubMed Abstract | Crossref Full Text | Google Scholar

14. Mmbaga, EJ, Leyna, GH, Mnyika, KS, Hussain, A, and Klepp, K-I. Education attainment and the risk of HIV-1 infections in rural Kilimanjaro region of Tanzania, 1991–2005: a reversed association. Sex Transm Dis. (2007) 34:947–53. doi: 10.1097/olq.0b013e31813e0c15

PubMed Abstract | Crossref Full Text | Google Scholar

15. Health Inequalities, the Financial Crisis, and Infectious Disease in Europe. (2013). Available at: https://www.ecdc.europa.eu/en/publications-data/health-inequalities-financial-crisis-and-infectious-disease-europe

Google Scholar

16. Janlert, U. Unemployment as a disease and diseases of the unemployed. Scand J Work Environ Health. (1997) 23:79–83.

Google Scholar

17. Mirahmadizadeh, A, Shamooshaki, MT, Dadvar, A, Moradian, MJ, and Aryaie, M. Unemployment and covid-19-related mortality: a historical cohort study of 50,000 COVID-19 patients in Fars, Iran. Epidemiology and Health. (2022) 44:44. doi: 10.4178/epih.e2022032

PubMed Abstract | Crossref Full Text | Google Scholar

18. National Academies of Sciences, Engineering, Division HaM, Practice, Board on Population Health and Public Health, States, Committee on Community-Based Solutions to Promote Health Equity in the UnitedBaciu, A, and Negussie, Y. The Root Causes of Health Inequity. Washington, DC: National Academies Press (2017).

Google Scholar

19. Ramesh, N, Cockbain, B, Rosadas, C, and Taylor, G P. How do socioeconomic determinants of health affect the prevalence of HTLV-1 globally? A systematic review with meta-analysis. PROSPERO 2022 CRD42022335004. Available at: https://www.crd.york.ac.uk/prospero/display_record.php?ID=CRD42022335004

Google Scholar

20. The Education System in Brazil. Available at: https://www.studycountry.com/guide/BR-education.htm (accessed May 22, 2022).

Google Scholar

21. Carneiro-Proietti, ABF, Sabino, EC, Leao, S, Salles, NA, Loureiro, P, Sarr, M, et al. Human T-lymphotropic virus type 1 and type 2 seroprevalence, incidence, and residual transfusion risk among blood donors in Brazil during 2007-2009. AIDS Res Hum Retrovir. (2012) 28:1265–72. doi: 10.1089/aid.2011.0143

PubMed Abstract | Crossref Full Text | Google Scholar

22. de Fatima Castro Mendes, M, de Ribamar Oliveira Lima, J, de Oliveira de Melo, B, de Maria Fernandes da Silva Pinto, C, Maia, HS, TAF, F, et al. Molecular detection of human T cell lymphotropic virus type 1 in pregnant women from Maranhao state, Brazil. Braz J Microbiol. (2020) 51:637–45. doi: 10.1007/s42770-020-00233-0

PubMed Abstract | Crossref Full Text | Google Scholar

23. Costa, GB, de Oliveira, MC, Gadelha, SR, Albuquerque, GR, Teixeira, M, Raiol, MRDS, et al. Infectious diseases during pregnancy in Brazil: Seroprevalence and risk factors. J Infect Dev Ctries. (2018) 12:657–65. doi: 10.3855/JIDC.9492

PubMed Abstract | Crossref Full Text | Google Scholar

24. Fabbro, D, Maria, M, Janini, F, Cunha, RV, Bóia, MN, Portela, P, et al. Infecção pelo HTLV 1/2: atuação no pré-natal como estratégia de controle da doença no Estado de Mato Grosso do Sul. Rev Soc Bras Med Trop. (2008) 41:148–51. doi: 10.1590/S0037-86822008000200003

PubMed Abstract | Crossref Full Text | Google Scholar

25. de Morais, MPE, Gato, CM, Maciel, LA, Lalwani, P, Costa, CA, and Lalwani, JDB. Prevalence of human T-lymphotropic virus type 1 and 2 among blood donors in Manaus, Amazonas state, Brazil. Rev Inst Med Trop São Paulo. (2017) 59:e80. doi: 10.1590/S1678-9946201759080

PubMed Abstract | Crossref Full Text | Google Scholar

26. Dourado, I, Alcantara, LCJ, Barreto, ML, da Gloria, TM, and Galvão-Castro, B. HTLV-I in the general population of Salvador, Brazil: a city with African ethnic and sociodemographic characteristics. J Acquir Immune Defic Syndr. (1999) 34:527–31. doi: 10.1097/00126334-200312150-00013

Crossref Full Text | Google Scholar

27. Magno Falcão, LF, Fuzii, HT, Feio Libonati, RM, Aarão, d S, Leila, T, Moura Guimarães, AG, et al. Environmental impact and seroepidemiology of HTLV in two communities in the eastern Brazilian amazon. J Med Virol. (2013) 85:1585–90. doi: 10.1002/jmv.23620

PubMed Abstract | Crossref Full Text | Google Scholar

28. Mello, M, da Conceicao, AF, Sousa, S, Alcantara, LC, Marin, LJ, Raiol, M, et al. HTLV-1 in pregnant women from the southern Bahia, Brazil: a neglected condition despite the high prevalence. Virol J. (2014) 11:11. doi: 10.1186/1743-422X-11-28

Crossref Full Text | Google Scholar

29. Moxoto, I, Boa-Sorte, N, Nunes, C, Mota, A, Dumas, A, Dourado, I, et al. Perfil sociodemográfico, epidemiológico e comportamental de mulheres infectadas pelo HTLV-1 em Salvador-Bahia, uma área endêmica para o HTLV. Rev Soc Bras Med Trop. (2007) 40:37. doi: 10.1590/S0037-86822007000100007

PubMed Abstract | Crossref Full Text | Google Scholar

30. Nunes, D, Boa Sorte, N, Grassi, MFR, Taylor, GP, Teixeira, MG, Barreto, ML, et al. HTLV-1 is predominantly sexually transmitted in Salvador, the city with the highest HTLV-1 prevalence in Brazil. PLoS One. (2017) 12:e0171303. doi: 10.1371/journal.pone.0171303

Crossref Full Text | Google Scholar

31. Pessoni, LL, Aquino, ECD, and Alcantara, KCD. Prevalence and trends in transfusion-transmissible infections among blood donors in Brazil from 2010 to 2016. Hematol Transfus Cell Ther. (2019) 41:310–5. doi: 10.1016/j.htct.2019.03.009

PubMed Abstract | Crossref Full Text | Google Scholar

32. Sequeira, CG, Tamegao-Lopes, BP, dos Santos, E, Ventura, A, Moraes-Pinto, MI, and Succi, R. Descriptive study of HTLV infection in a population of pregnant women from the state of Para, northern Brazil. Rev Soc Bras Med Trop. (2012) 45:453–6. doi: 10.1590/S0037-86822012005000007

PubMed Abstract | Crossref Full Text | Google Scholar

33. Silva, IC, Pinheiro, BT, Nobre, AFS, Coelho, JL, Pereira, CCC, Ferreira, LSC, et al. Moderate endemicity of the human T-lymphotropic virus infection in the metropolitan region of Belem, Para, Brazil. Rev Bras Epidemiol. (2018) 21:e180018. doi: 10.1590/1980-549720180018

PubMed Abstract | Crossref Full Text | Google Scholar

34. Soares, BC, Proietti, AB, Carneiro, F, and Proietti, FA. HTLV-I/II and blood donors: determinants associated with seropositivity in a low-risk population. Rev Saude Publica. (2003) 37:470–6. doi: 10.1590/s0034-89102003000400012

PubMed Abstract | Crossref Full Text | Google Scholar

35. Sodre Barmpas, D, Monteiro, D, Taquette, SR, Rodrigues, N, Trajano, A, Cunha, JD, et al. Pregnancy outcomes and mother-to-child transmission rate in HTLV-1/2 infected women attending two public hospitals in the metropolitan area of Rio de Janeiro. PLoS Negl Trop Dis. (2019) 13:e0007404. doi: 10.1371/journal.pntd.0007404

Crossref Full Text | Google Scholar

36. Blas, MM, Alva, IE, Garcia, PJ, Carcamo, C, Montano, SM, Mori, N, et al. High prevalence of human T-Lymphotropic virus infection in indigenous women from the Peruvian Amazon. PLoS One. (2013) 8:e73978. doi: 10.1371/journal.pone.0073978

Crossref Full Text | Google Scholar

37. Gotuzzo, E, Sánchez, J, Escamilla, J, Carrillo, C, Phillips, IA, Moreyra, L, et al. Human T cell lymphotropic virus type I infection among female sex workers in Peru. J Infect Dis. (1994) 169:754–9. doi: 10.1093/infdis/169.4.754

PubMed Abstract | Crossref Full Text | Google Scholar

38. Laguna Torres, VA, Perez Bao, J, Chauca, G, Sovero, M, Blichtein, D, Chunga, A, et al. Epidemiology of transfusion-transmitted infections among multi-transfused patients in seven hospitals in Peru. J Clin Virol. (2005) 34:S61–8. doi: 10.1016/s1386-6532(05)80036-8

PubMed Abstract | Crossref Full Text | Google Scholar

39. Courouble, G, Rouet, F, Herrmann-Storck, C, Nicolas, M, Candolfi, E, Deloumeaux, J, et al. Epidemiologic study of the association between human T-cell lymphotropic virus type 1 and Strongyloides stercoralis infection in female blood donors (Guadeloupe, French West Indies). West Indian Med J. (2004) 53:3–6.

PubMed Abstract | Google Scholar

40. Rouet, F, Herrmann Storck, C, Courouble, G, Deloumeaux, J, Madani, D, and Strobel, M. A case-control study of risk factors associated with human T-cell lymphotrophic virus type-I seropositivity in blood donors from Guadeloupe, French West Indies. Vox Sang. (2002) 82:61–6. doi: 10.1046/j.0042-9007.2001.00143.x

PubMed Abstract | Crossref Full Text | Google Scholar

41. Cunha, L, Plouzeau, C, Ingrand, P, Gudo, JPS, Ingrand, I, Mondlane, J, et al. Use of replacement blood donors to study the epidemiology of major blood-borne viruses in the general population of Maputo, Mozambique. J Med Virol. (2007) 79:1832–40. doi: 10.1002/jmv.21010

PubMed Abstract | Crossref Full Text | Google Scholar

42. Hananiya, HS, Ella, EE, Aminu, M, and Anyanwu, NCJ. Prevalence of human T-cell lymphotropic virus and the socio-demographic and risk factors associated with the infection among post-natal clinics women in Zaria, Nigeria. J Immunoass Immunochem. (2019) 40:485–94. doi: 10.1080/15321819.2019.1636817

Crossref Full Text | Google Scholar

43. Olusanya, O, Lawoko, A, and Blomberg, J. Seroepidemiology of human retroviruses in Ogun state of Nigeria. Scand J Infect Dis. (1990) 22:155–60. doi: 10.3109/00365549009037896

PubMed Abstract | Crossref Full Text | Google Scholar

44. Azarpazhooh, MR, Hasanpour, K, Ghanbari, M, Rezaee, SAR, Mashkani, B, Hedayati-Moghaddam, MR, et al. Human T-lymphotropic virus type 1 prevalence in northeastern Iran, Sabzevar: an epidemiologic-based study and phylogenetic analysis. AIDS Res Hum Retrovir. (2012) 28:1095–101. doi: 10.1089/aid.2011.0248

Crossref Full Text | Google Scholar

45. Emadi, B, Rezaieh, MG, and Sedighi, M. Seroprevalence and trends of transfusion transmissible infections among retrospective blood donors in Western Azerbaijan regional blood transfusion center, Iran: a ten-years evaluation. Transfus Apher Sci. (2021) 60:103132. doi: 10.1016/j.transci.2021.103132

Crossref Full Text | Google Scholar

46. Ghaffari, J, Naghshvar, F, Nazari, Z, Farid, R, Torabizadeh, J, and Madani, F. Seroprevalence of human T-cell lymphotropic virus type 1 infection (HTLV1) in different patients in the north of Iran. Afr J Biotechnol. (2011) 10:10752–5. doi: 10.5897/AJB11.177

Crossref Full Text | Google Scholar

47. Hedayati-Moghaddam, MR, Fathimoghadam, F, Mashhadi, IE, Soghandi, L, and Bidkhori, HR. Epidemiology of HTLV-1 in Neyshabour, northeast of Iran. Iran Red Crescent Med J. (2011) 13:424–7.

PubMed Abstract | Google Scholar

48. Hedayati-Moghaddam, MR, Tehranian, F, and Bayati, M. Human T-Lymphotropic virus type I (HTLV-1) infection among Iranian blood donors: first case-control study on the risk factors. Viruses-Basel. (2015) 7:5736–45. doi: 10.3390/v7112904

PubMed Abstract | Crossref Full Text | Google Scholar

49. Maghsudlu, M, Safabakhsh, H, and Jamili, P. Seroepidemiology of human T-cell lymphotropic virus type-I in blood donors of northeastern Iran, Sabzevar. Asian J Transfus Sci. (2015) 9:203–6. doi: 10.4103/0973-6247.154255

PubMed Abstract | Crossref Full Text | Google Scholar

50. Rafatpanah, H, Hedayati Moghaddam, MR, Fathimoghadam, F, Bidkhori, HR, Shamsian, SK, Ahmadi, S, et al. High prevalence of HTLV-I infection in Mashhad, Northeast Iran: a population-based seroepidemiology survey. J Clin Virol. (2011) 52:172–6. doi: 10.1016/j.jcv.2011.07.004

PubMed Abstract | Crossref Full Text | Google Scholar

51. Murphy, EL, Wilks, R, Hanchard, B, Cranston, B, Figueroa, JP, Gibbs, WN, et al. A case-control study of risk factors for seropositivity to human T-lymphotropic virus type I (HTLV-I) in Jamaica. Int J Epidemiol. (1996) 25:1083–9. doi: 10.1093/ije/25.5.1083

Crossref Full Text | Google Scholar

52. Pegha Moukandja, I, Ngoungou, EB, Lemamy, GJ, Bisvigou, U, Gessain, A, Toure Ndouo, FS, et al. Non-malarial infectious diseases of antenatal care in pregnant women in Franceville, Gabon. BMC Pregnancy Childbirth. (2017) 17:185:185. doi: 10.1186/s12884-017-1362-0

PubMed Abstract | Crossref Full Text | Google Scholar

53. Reeves, WC, Saxinger, C, Brenes, MM, Quiroz, E, Clark, JW, Hoh, MW, et al. Human T-cell lymphotropic virus type I (HTLV-I) seroepidemiology and risk factors in metropolitan Panamá. Am J Epidemiol. (1988) 127:532–9. doi: 10.1093/oxfordjournals.aje.a114828

PubMed Abstract | Crossref Full Text | Google Scholar

54. Barcellos, NT, Fuchs, SC, Mondini, LG, and Murphy, EL. Human T lymphotropic virus type I/II infection: prevalence and risk factors in individuals testing for HIV in counseling centers from southern Brazil. Sex Transm Dis. (2006) 33:302–6. doi: 10.1097/01.olq.0000194598.47821.b6

Crossref Full Text | Google Scholar

55. Cj, C, Sf, H, and Cs, Y. Seroepidemiology of human T-Lymphotropic virus type-I infection among intravenous drug-abusers in Taiwan. J Med Virol. (1994) 42:264–7. doi: 10.1002/jmv.1890420312

PubMed Abstract | Crossref Full Text | Google Scholar

56. De Vita, DA, White, MC, Zhao, X, Kaidarova, Z, and Murphy, EL. Determinants of subject visit participation in a prospective cohort study of HTLV infection. BMC Med Res Methodol. (2009) 9:9 19. doi: 10.1186/1471-2288-9-19

PubMed Abstract | Crossref Full Text | Google Scholar

57. Murphy, EL, Glynn, S, Watanabe, K, Fridey, J, Smith, J, Sacher, R, et al. Laboratory test differences associated with HTLV-I and HTLV-II infection. Retrovirus epidemiology donor study investigators. J Acquir Immune Defic Syndr Hum Retrovirol. (1998) 17:332–8. doi: 10.1097/00042560-199804010-00007

PubMed Abstract | Crossref Full Text | Google Scholar

58. Schreiber, GB, Murphy, EL, Horton, JA, Wright, DJ, Garfein, R, Co Chien, H, et al. Risk factors for human T-cell lymphotropic virus types I and II (HTLV-I and -II) in blood donors: the retrovirus epidemiology donor study. J Acquir Immune Defic Syndr Hum Retrovirol. (1997) 14:263–71. doi: 10.1097/00042560-199703010-00011

PubMed Abstract | Crossref Full Text | Google Scholar

59. Udeze, AO, Odebisi Omokanye, MB, Faneye, A, Olusola, BA, Ogunsemowo, O, Iwuoha, C, et al. Serological detection of human T-cell lymphotropic virus types I and II among pregnant women in Ilorin, Nigeria. J Immunoass Immunochem. (2018) 39:428–38. doi: 10.1080/15321819.2018.1500374

PubMed Abstract | Crossref Full Text | Google Scholar

60. Wang, CH, Chen, CJ, Hu, CY, You, SL, Chu, CT, Chou, MJ, et al. Seroepidemiology of human T-cell lymphotropic virus type I infection in Taiwan. Cancer Res. (1988) 48:5042–4.

PubMed Abstract | Google Scholar

61. Yousefi, M, Sharifzadeh, GR, Ebrahimzadeh, A, Azarkar, Z, Namaei, MH, Azarkar, G, et al. Prevalence and associated risk factors of htlv-1 and co-infections of blood-borne viruses in Birjand, iran's eastern border. Arch Iran Med. (2020) 23:672–7. doi: 10.34172/aim.2020.85

PubMed Abstract | Crossref Full Text | Google Scholar

62. Murphy, EL, Glynn, SA, Fridey, J, Smith, JW, Sacher, RA, Nass, CC, et al. Increased incidence of infectious diseases during prospective follow-up of human T-lymphotropic virus type II- and I-infected blood donors. Arch Intern Med. (1999) 159:1485–91. doi: 10.1001/archinte.159.13.1485

PubMed Abstract | Crossref Full Text | Google Scholar

63. Kamphuis, DJ, Martina, IS, Keli, SO, Balentien, EG, and Top, C. Seroprevalence of human T-cell lymphotropic virus type I in Curaçao and predictive variables for that infection. Ned Tijdschr Geneeskd. (1998) 142:89–92.

PubMed Abstract | Google Scholar

64. Sanchez-Palacios, C, Gotuzzo, E, Vandamme, A-M, and Maldonado, Y. Seroprevalence and risk factors for human T-cell lymphotropic virus (HTLV 1) infection among ethnically and geographically diverse Peruvian women. Int J Infect Dis. (2003) 7:132–7. doi: 10.1016/s1201-9712(03)90009-9

PubMed Abstract | Crossref Full Text | Google Scholar

65. Courouble, G, Rouet, F, Herrmann-Storck, C, Nicolas, M, Candolfi, E, Strobel, M, et al. Human T-cell lymphotropic virus type I association with strongyloïdes stercoralis: a case control study among Caribbean blood donors from Guadeloupe (French west indies). J Clin Microbiol. (2000) 38:3903–4. doi: 10.1128/jcm.38.10.3903-3904.2000

PubMed Abstract | Crossref Full Text | Google Scholar

66. Gilder, M, Moo, P, Hashmi, A, Praisaengdet, N, Wai, K, Pimanpanarak, M, et al. “I can’t read and don’t understand”: health literacy and health messaging about folic acid for neural tube defect prevention in a migrant population on the Myanmar-Thailand border. PLoS One. (2019) 14:e0218138. doi: 10.1371/journal.pone.0218138

PubMed Abstract | Crossref Full Text | Google Scholar

67. Cavanaugh, KL, Wingard, RL, Hakim, RM, Eden, S, Shintani, A, Wallston, KA, et al. Low health literacy associates with increased mortality in ESRD. J Am Soc Nephrol. (2010) 21:1979–85. doi: 10.1681/asn.2009111163

PubMed Abstract | Crossref Full Text | Google Scholar

68. Hanchate, AD, Ash, AS, Gazmararian, JA, Wolf, MS, and Paasche-Orlow, MK. The demographic assessment for health literacy (dahl): a new tool for estimating associations between health literacy and outcomes in national surveys. J Gen Intern Med. (2008) 23:1561–6. doi: 10.1007/s11606-008-0699-5

PubMed Abstract | Crossref Full Text | Google Scholar

69. Hoffman-Goetz, L, Meissner, HI, and Thomson, MD. Literacy and cancer anxiety as predictors of health status: an exploratory study. J Cancer Educ. (2009) 24:218–24. doi: 10.1080/08858190902910871

PubMed Abstract | Crossref Full Text | Google Scholar

70. Diviani, N, van den Putte, B, Giani, S, and van Weert, JC. Low health literacy and evaluation of online health information: a systematic review of the literature. J Med Internet Res. (2015) 17:e112. doi: 10.2196/jmir.4018

PubMed Abstract | Crossref Full Text | Google Scholar

71. Martin, LT, Ruder, T, Escarce, JJ, Ghosh-Dastidar, B, Sherman, D, Elliott, M, et al. Developing predictive models of health literacy. J Gen Intern Med. (2009) 24:1211–6. doi: 10.1007/s11606-009-1105-7

PubMed Abstract | Crossref Full Text | Google Scholar

72. Mackenbach, JP, Stirbu, I, Roskam, A-JR, Schaap, MM, Menvielle, G, Leinsalu, M, et al. Socioeconomic inequalities in health in 22 European countries. N Engl J Med. (2008) 358:2468–81. doi: 10.1056/nejmsa0707519

Crossref Full Text | Google Scholar

73. Health Literacy. NHS digital service manual. England: NHS (2022).

Google Scholar

74. van Zon, S, Reijneveld, S, Mendes de Leon, C, and Bültmann, U. The impact of low education and poor health on unemployment varies by work life stage. Int J Public Health. (2017) 62:997–1006. doi: 10.1007/s00038-017-0972-7

PubMed Abstract | Crossref Full Text | Google Scholar

75. Roucoux, DF, Wang, B, Smith, D, Nass, CC, Smith, J, Hutching, ST, et al. A prospective study of sexual transmission of human T lymphotropic virus (HTLV)-I and HTLV-II. J Infect Dis. (2005) 191:1490–7. doi: 10.1086/429410

PubMed Abstract | Crossref Full Text | Google Scholar

76. Cox, CM, Babalola, S, Kennedy, CE, Mbwambo, J, Likindikoki, S, and Kerrigan, D. Determinants of concurrent sexual partnerships within stable relationships: a qualitative study in Tanzania. BMJ Open. (2014) 4:e003680. doi: 10.1136/bmjopen-2013-003680

PubMed Abstract | Crossref Full Text | Google Scholar

77. Harrison, A, Cleland, J, and Frohlich, J. Young People's sexual partnerships in KwaZulu-Natal, South Africa: patterns, contextual influences, and HIV risk. Stud Fam Plan. (2008) 39:295–308. doi: 10.1111/j.1728-4465.2008.00176.x

PubMed Abstract | Crossref Full Text | Google Scholar

78. Figueroa, JP, Morris, J, Brathwaite, A, Ward, E, Peruga, A, Hayes, R, et al. Risk factors for HTLV-I among heterosexual STD clinic attenders. J Acquir Immune Defic Syndr Hum Retrovirol. (1995) 9:81–8. doi: 10.1097/00042560-199505010-00012

PubMed Abstract | Crossref Full Text | Google Scholar

79. Izugbara, C. Spousal age differences and violence against women in Nigeria and Tanzania. Health Care Women Int. (2018) 39:872–87. doi: 10.1080/07399332.2018.1426001

PubMed Abstract | Crossref Full Text | Google Scholar

80. Rosadas, C, Menezes, MLB, Galvão-Castro, B, Assone, T, Miranda, AE, Aragón, MG, et al. Blocking HTLV-1/2 silent transmission in Brazil: current public health policies and proposal for additional strategies. PLoS Negl Trop Dis. (2021) 15:e0009717. doi: 10.1371/journal.pntd.0009717

PubMed Abstract | Crossref Full Text | Google Scholar

81. Chevalier, A, Harmon, C, O’Sullivan, V, and Walker, I. The impact of parental income and education on the schooling of their children. IZA. J Labor Econ. (2013) 2:8. doi: 10.1186/2193-8997-2-8

Crossref Full Text | Google Scholar

82. Sampaio, GC, Ribeiro, JR, de Almeida, CN, Boa-Sorte, N, Galvão-Castro, B, Grassi, MF, et al. Human T cell lymphotropic virus type 1 global prevalence associated with the human development index: systematic review with meta-analysis. AIDS Res Hum Retrovir. (2023) 39:145–65. doi: 10.1089/aid.2021.0230

PubMed Abstract | Crossref Full Text | Google Scholar

83. Darivemula, S, and Rutter, A (2022). Health literacy of HPV and HTLV Infection pathophysiologies in Shipibo-Konibo women: A traditional arts-based study. APHA - APHA's 2018 Annual Meeting & Expo.

Google Scholar

84. Treffry-Goatley, A, Lessells, R, Moletsane, R, de Oliveira, T, and Gaede, B. Community engagement with HIV drug adherence in rural South Africa: a transdisciplinary approach. Med Humanit. (2018) 44:239–46. doi: 10.1136/medhum-2018-011474

PubMed Abstract | Crossref Full Text | Google Scholar

85. Collins, T, Akselrod, S, Bloomfield, A, Gamkrelidze, A, Jakab, Z, and Placella, E. Rethinking the covid-19 pandemic: Back to public health. Ann Glob Health. (2020) 86:133. doi: 10.5334/aogh.3084

PubMed Abstract | Crossref Full Text | Google Scholar

86. Vivancos, R, Abubakar, I, Phillips-Howard, P, and Hunter, PR. School-based sex education is associated with reduced risky sexual behaviour and sexually transmitted infections in young adults. Public Health. (2013) 127:53–7. doi: 10.1016/j.puhe.2012.09.016

PubMed Abstract | Crossref Full Text | Google Scholar

Keywords: HTLV-1, education, income, employment, social determinant of health

Citation: Ramesh N, Cockbain B, Taylor GP and Rosadas C (2024) How do socioeconomic determinants of health affect the likelihood of living with HTLV-1 globally? A systematic review with meta-analysis. Front. Public Health. 12:1298308. doi: 10.3389/fpubh.2024.1298308

Received: 21 September 2023; Accepted: 09 January 2024;
Published: 24 January 2024.

Edited by:

Miguel Angel Sanchez-Aleman, National Institute of Public Health, Mexico

Reviewed by:

Mahamadou Diakite, Université des Sciences, des Techniques et des Technologies de Bamako, Mali
Luciane Amorim Santos, Bahiana School of Medicine and Public Health, Brazil

Copyright © 2024 Ramesh, Cockbain, Taylor and Rosadas. 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: Carolina Rosadas, c.rosadas-de-oliveira@imperial.ac.uk

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.