The use of electronic nicotine delivery systems (ENDS) is increasing rapidly across Sub-Saharan Africa (SSA), particularly among young women, while endometriosis remains substantially underdiagnosed in the region. Emerging evidence suggests that vaping may influence hormonal, inflammatory, and oxidative pathways relevant to endometriosis. This scoping review followed PRISMA guidelines and searched PubMed, Web of Science, Scopus, African regional databases, and grey literature to identify studies examining vaping exposure in relation to reproductive or hormonal outcomes and gynecologic pathology. Eligible studies were appraised using the Newcastle–Ottawa Scale and STROBE criteria, and findings were narratively synthesized due to methodological heterogeneity. Across epidemiologic and mechanistic domains, the evidence indicates that nicotine-product use is associated with higher odds of dysmenorrhea and suspected endometriosis; disrupts the hypothalamic–pituitary–gonadal axis and estrogen–progesterone signaling; induces oxidative stress, mitochondrial dysfunction, and NF-κB activation; and may drive epigenetic and immune alterations that promote endometrial adhesion, angiogenesis, and impaired fertility. Contextual vulnerabilities in SSA including environmental co-exposures, infectious disease burden, limited diagnostic capacity, and dual use of vaping with alcohol may further amplify these risks. Although direct causal data from SSA remain limited, the convergence of biological plausibility and emerging epidemiologic signals highlights vaping as a potential reproductive health concern, underscoring the need to integrate vaping into sexual and reproductive health guidelines and to prioritize region-specific research.
| Published in | Journal of Gynecology and Obstetrics (Volume 14, Issue 1) |
| DOI | 10.11648/j.jgo.20261401.12 |
| Page(s) | 13-29 |
| Creative Commons |
This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited. |
| Copyright |
Copyright © The Author(s), 2026. Published by Science Publishing Group |
Vaping, Endometriosis, Sub-Saharan Africa, Women of Reproductive Age, Public Health
Domain / Focus Area | Mechanism or Observation | Key Findings (Study Type / Evidence Source) | Subgroup / Regional Relevance (SSA Context) |
|---|---|---|---|
Epidemiologic associations | Vaping exposure ↔ endometriosis prevalence/severity | Case–control & cross-sectional studies from mixed settings suggest higher odds of dysmenorrhea and diagnosis among nicotine product users; heterogeneity prevents meta-analysis. | Underdiagnosis due to limited laparoscopy, stigma; rising youth e-cigarette uptake in urban Nigeria, Ghana; peri-urban mining zones (heavy metals) may interact with vaping exposures. |
Nicotine & hormonal dysregulation | Nicotine → HPG axis disruption, altered ER/PR signaling | Experimental and human biomarker studies show increased inflammatory markers and disrupted progesterone signaling after nicotine exposure. | In West Africa, contraceptive access gaps and high adolescent pregnancies may amplify hormonal vulnerability. |
Oxidative stress & inflammation | E-cig aerosols → ROS, mitochondrial damage | In vitro & animal studies show ROS, NF-κB activation; human studies link biomarkers to vaping/alcohol co-use. | Malnutrition and infectious comorbidities (e.g., malaria) could worsen oxidative damage in West African populations. |
Epigenetic / miRNA | Altered DNA methylation, miR expression (HOXA10, miR-200) | Smoking literature robust; early vaping epigenetic signals emerging. | Environmental pollutants (artisanal mining) + vaping may create cumulative epigenetic risk in coastal and inland mining communities. |
Immune & angiogenic pathways | Flavors → macrophage polarization, ↑VEGF | Preclinical pro-angiogenic findings; early human inflammatory marker elevation in young initiators. | High rates of pelvic infection could mask or modify immune signals from vaping. |
Fertility & implantation | Nicotine delays implantation, reduces receptivity | Animal and limited human fertility studies show implantation delays and poorer outcomes. | Fertility services are limited; such effects could have large social impact in contexts where family size is highly valued. |
Duration & intensity | Long-term / high-nicotine use → worse symptoms | Observational correlation between use duration and menstrual pain severity. | Young urban professionals and students increasingly use high-nicotine pods; occupational exposure (mining) matters. |
Concurrent exposures | Vaping + alcohol/tobacco → synergistic harm | Mixed-exposure studies show amplified oxidative/hormonal disruption. | Social nightlife culture in cities like Lagos/Accra increases dual exposures among women. |
Policy & interventions | Weak regulation, low reproductive education | WHO/AU recommend action; few region-specific guidelines exist. | Need to integrate vaping education in adolescent reproductive health programs and mining occupational health policies. |
Domain / Focus Area | Mechanism or Observation | Key Findings (Study Type / Evidence Source) | Subgroup / Regional Relevance (SSA Context) |
|---|---|---|---|
Epidemiologic associations | Rising urban vaping ↔ endometriosis symptoms | Cross-sectional surveys in tertiary clinics indicate associations between nicotine exposure and pelvic pain but limited diagnostics. | Kenya/Uganda show increasing e-cig uptake among youth; rural healthcare access gaps lead to late presentation. |
Nicotine & hormones | Nicotine alters estrogen/progesterone signaling | Lab and clinical biomarker studies show upregulated inflammatory pathways, aromatase activity. | Limited hormone monitoring capacity and contraceptive counseling in peripheral facilities. |
Oxidative stress | Aerosol constituents cause ROS and lipid peroxidation | In vitro and animal evidence; human biomarker studies show higher oxidative markers in dual-users. | High burden of infectious diseases (HIV/TB) could amplify oxidative pathways. |
Epigenetics | miRNA shifts regulating endometrial adhesion | Early evidence from smokers; vaping epigenetic evidence emerging. | Urban pollution (traffic) + vaping may have combined epigenetic impacts in cities like Nairobi and Dar es Salaam. |
Immune & angiogenesis | Flavored condensates → VEGF, macrophage shift | Animal models show pro-angiogenic changes relevant to lesion growth. | High STI prevalence and pelvic inflammation could confound diagnosis of endometriosis. |
Fertility | Reduced uterine receptivity after nicotine | Mouse models + small human cohorts show implantation issues. | Assisted reproduction limited; fertility impacts have outsized social consequences. |
Duration/intensity | Chronic use → severe dysmenorrhea | Observational link between years of vaping and pain scores. | University students and young professionals in capital cities are an at-risk group. |
Concurrent use | Alcohol/Tobacco/vaping interactions | Synergistic oxidative & endocrine disruption reported. | Cultural alcohol consumption patterns at social events may increase joint exposures. |
Policy | Few reproductive guidelines referencing vaping | Regional health policy lags behind use trends. | Opportunities for school-based prevention and adolescent SRH programming. |
Domain / Focus Area | Mechanism or Observation | Key Findings | Subgroup / Regional Relevance |
|---|---|---|---|
Epidemiology | Sparse data; probable underestimation of vaping-related gynecologic disease | Clinic case series suggest links but diagnostic capacity limited. | DRC, CAR: few laparoscopies; artisanal mining exposures (lead, mercury) common — potential synergists. |
Nicotine & hormones | Nicotine → endocrine disruption demonstrated experimentally | Limited human biomarker work; animal studies generalizable. | Nutritional deficiencies and anemia prevalent — could worsen hormonal effects. |
Oxidative stress | Aerosol-induced ROS exacerbated by infections | Preclinical evidence strong; human data limited. | High infectious disease burden may amplify oxidative/inflammatory pathways. |
Epigenetics | Environmental pollutants + vaping may change epigenome | Smoking literature strong; vaping not well-studied. | Mining towns (Lubumbashi) are priority areas to study combined exposures. |
Immune pathways | Proinflammatory shifts with flavored aerosols | Animal studies: macrophage polarization and angiogenesis. | Coexisting pelvic infections increase diagnostic complexity. |
Fertility | Nicotine harms implantation in animal models | Relevant but poorly documented in human Central African cohorts. | Social importance of fertility and very limited ART services increase impact of subfertility. |
Duration & intensity | Chronic users show worse menstrual outcomes elsewhere; local data lacking | Need longitudinal tracking. | Young urban migrants to mining towns may be high-risk group. |
Concurrent exposures | High prevalence of multi-toxin exposures (smoke, mining pollutants) | Likely synergistic but under-researched. | Occupational exposures create unique exposure profiles. |
Policy & interventions | Minimal e-cig regulation, limited SRH integration | Public health priorities often focus on infectious disease. | Integrate vaping topics into maternal/occupational health guidance for mining regions. |
Domain / Focus Area | Mechanism or Observation | Key Findings | Subgroup / Regional Relevance |
|---|---|---|---|
Epidemiology | Rising urban vaping (SA) with some clinic data on pelvic pain associations | Case–control and hospital series from South Africa more numerous than other SSA regions. | South Africa leads in vaping prevalence and diagnostic capacity; neighboring countries show emerging uptake. |
Nicotine & hormones | Robust experimental evidence for endocrine disruption | Human biomarker studies available; vaping data building. | Better lab capacity (Cape Town, Johannesburg) enables mechanistic studies. |
Oxidative stress | Aerosols cause ROS & mitochondrial damage | Both in vitro and small clinical studies support this. | Intersection with high HIV prevalence and TB could magnify impacts. |
Epigenetics | Smoking and vaping associated with methylation changes | South African cohorts feasible for epigenetic studies. | Urban industrial pollution + vaping → cumulative exposures. |
Immune & angiogenesis | Flavors → angiogenic pathways in animal models | Mechanistic signals present. | Pelvic infection patterns may complicate diagnosis. |
Fertility | Nicotine reduces implantation in models; limited human data | Feasible to study at fertility clinics in major cities. | Fertility clinics concentrated in SA enable cohort studies. |
Duration & intensity | Chronic, high-nicotine users experience worse symptoms | Observational data align with global findings. | University student cohorts and nightlife cultures are clear target groups. |
Concurrent exposures | Alcohol + vaping common in nightlife settings | Synergistic damage observed in mixed-use studies. | Strong nightlife economy in SA increases dual exposures among young women. |
Policy & interventions | Some regulatory movement but gaps remain | South Africa has some policy activity; regional harmonization lacking. | Opportunity to pilot reproductive-health integration into tobacco control programs. |
AJOL | African Journals Online |
AU | African Union |
CAR | Central African Republic |
DRC | Democratic Republic of the Congo |
ENDS | Electronic Nicotine Delivery Systems |
ER | Estrogen Receptor |
GnRH | Gonadotropin-Releasing Hormone |
HPO Axis | Hypothalamic–Pituitary–Ovarian Axis |
HPG Axis | Hypothalamic–Pituitary–Gonadal Axis |
HIV | Human Immunodeficiency Virus |
LMICs | Low- and Middle-Income Countries |
NF-κB | Nuclear Factor Kappa-Light-Chain-Enhancer of Activated B Cells |
NOS | Newcastle–Ottawa Scale |
PR | Progesterone Receptor |
PRISMA | Preferred Reporting Items for Systematic Reviews and Meta-Analyses |
ROS | Reactive Oxygen Species |
Scopus | Scientific Citation Index Database (Elsevier) |
SSA | Sub-Saharan Africa |
SRH | Sexual and Reproductive Health |
VEGF | Vascular Endothelial Growth FactorSTI – Sexually Transmitted Infection |
STROBE | Strengthening the Reporting of Observational Studies in Epidemiology |
TB | Tuberculosis |
VOCs | Volatile Organic Compounds |
WHO | World Health Organization |
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APA Style
Kabuya, K. E., Sangany, M. C. (2026). The Potential Role of Vaping in the Increasing Burden of Endometriosis Among Women of Reproductive Age in Sub-Saharan Africa: A Public Health Concern. Journal of Gynecology and Obstetrics, 14(1), 13-29. https://doi.org/10.11648/j.jgo.20261401.12
ACS Style
Kabuya, K. E.; Sangany, M. C. The Potential Role of Vaping in the Increasing Burden of Endometriosis Among Women of Reproductive Age in Sub-Saharan Africa: A Public Health Concern. J. Gynecol. Obstet. 2026, 14(1), 13-29. doi: 10.11648/j.jgo.20261401.12
@article{10.11648/j.jgo.20261401.12,
author = {Kalala Elisee Kabuya and Mukasa Charline Sangany},
title = {The Potential Role of Vaping in the Increasing Burden of Endometriosis Among Women of Reproductive Age in Sub-Saharan Africa: A Public Health Concern},
journal = {Journal of Gynecology and Obstetrics},
volume = {14},
number = {1},
pages = {13-29},
doi = {10.11648/j.jgo.20261401.12},
url = {https://doi.org/10.11648/j.jgo.20261401.12},
eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.jgo.20261401.12},
abstract = {The use of electronic nicotine delivery systems (ENDS) is increasing rapidly across Sub-Saharan Africa (SSA), particularly among young women, while endometriosis remains substantially underdiagnosed in the region. Emerging evidence suggests that vaping may influence hormonal, inflammatory, and oxidative pathways relevant to endometriosis. This scoping review followed PRISMA guidelines and searched PubMed, Web of Science, Scopus, African regional databases, and grey literature to identify studies examining vaping exposure in relation to reproductive or hormonal outcomes and gynecologic pathology. Eligible studies were appraised using the Newcastle–Ottawa Scale and STROBE criteria, and findings were narratively synthesized due to methodological heterogeneity. Across epidemiologic and mechanistic domains, the evidence indicates that nicotine-product use is associated with higher odds of dysmenorrhea and suspected endometriosis; disrupts the hypothalamic–pituitary–gonadal axis and estrogen–progesterone signaling; induces oxidative stress, mitochondrial dysfunction, and NF-κB activation; and may drive epigenetic and immune alterations that promote endometrial adhesion, angiogenesis, and impaired fertility. Contextual vulnerabilities in SSA including environmental co-exposures, infectious disease burden, limited diagnostic capacity, and dual use of vaping with alcohol may further amplify these risks. Although direct causal data from SSA remain limited, the convergence of biological plausibility and emerging epidemiologic signals highlights vaping as a potential reproductive health concern, underscoring the need to integrate vaping into sexual and reproductive health guidelines and to prioritize region-specific research.},
year = {2026}
}
TY - JOUR T1 - The Potential Role of Vaping in the Increasing Burden of Endometriosis Among Women of Reproductive Age in Sub-Saharan Africa: A Public Health Concern AU - Kalala Elisee Kabuya AU - Mukasa Charline Sangany Y1 - 2026/01/20 PY - 2026 N1 - https://doi.org/10.11648/j.jgo.20261401.12 DO - 10.11648/j.jgo.20261401.12 T2 - Journal of Gynecology and Obstetrics JF - Journal of Gynecology and Obstetrics JO - Journal of Gynecology and Obstetrics SP - 13 EP - 29 PB - Science Publishing Group SN - 2376-7820 UR - https://doi.org/10.11648/j.jgo.20261401.12 AB - The use of electronic nicotine delivery systems (ENDS) is increasing rapidly across Sub-Saharan Africa (SSA), particularly among young women, while endometriosis remains substantially underdiagnosed in the region. Emerging evidence suggests that vaping may influence hormonal, inflammatory, and oxidative pathways relevant to endometriosis. This scoping review followed PRISMA guidelines and searched PubMed, Web of Science, Scopus, African regional databases, and grey literature to identify studies examining vaping exposure in relation to reproductive or hormonal outcomes and gynecologic pathology. Eligible studies were appraised using the Newcastle–Ottawa Scale and STROBE criteria, and findings were narratively synthesized due to methodological heterogeneity. Across epidemiologic and mechanistic domains, the evidence indicates that nicotine-product use is associated with higher odds of dysmenorrhea and suspected endometriosis; disrupts the hypothalamic–pituitary–gonadal axis and estrogen–progesterone signaling; induces oxidative stress, mitochondrial dysfunction, and NF-κB activation; and may drive epigenetic and immune alterations that promote endometrial adhesion, angiogenesis, and impaired fertility. Contextual vulnerabilities in SSA including environmental co-exposures, infectious disease burden, limited diagnostic capacity, and dual use of vaping with alcohol may further amplify these risks. Although direct causal data from SSA remain limited, the convergence of biological plausibility and emerging epidemiologic signals highlights vaping as a potential reproductive health concern, underscoring the need to integrate vaping into sexual and reproductive health guidelines and to prioritize region-specific research. VL - 14 IS - 1 ER -