Association between exposure to polycyclic aromatic hydrocarbons and reproductive health outcomes: a systematic review and meta-analysis.

backgroundPolycyclic aromatic hydrocarbons (PAHs) are widespread environmental pollutants with known harmful effects on human health. However, their specific impact on reproductive outcomes, both cancer-related and non-cancer-related, has not been comprehensively assessed. This study systematically reviews and synthesizes existing evidence on PAH exposure and reproductive health in men and women.

methodsA comprehensive literature search was conducted in Web of Science, Cochrane Library, PubMed/MEDLINE, ProQuest, and Scopus through May 31, 2024, following PRISMA guidelines. Study quality was assessed using the Newcastle-Ottawa Scale, and the strength of evidence was evaluated using the GRADE framework. The certainty of evidence was rated as moderate for male reproductive organ cancers and low for female reproductive organ cancers, based on GRADE assessment, primarily due to imprecision in the latter.

resultsOf the 4,546 articles screened, 30 met the inclusion criteria for the systematic review. Among these, 9 studies were included in a meta-analysis. In men, PAH exposure was consistently associated with reduced semen quality, including lower sperm count, motility, viability, and morphology, as well as increased DNA damage and hormone disruption. The meta-analysis of seven studies found a 13% increased risk of male reproductive cancers, primarily prostate cancer, associated with PAH exposure (standardized incidence ratio [SIR]: 1.13; 95% CI: 1.04-1.23; P < 0.001). For women, PAH metabolites were linked to infertility and possibly endometriosis, but these associations were weakened after controlling for confounders. No significant association was found between PAH exposure and female reproductive cancers (SIR: 1.01; 95% CI: 0.91-1.12; P = 0.91).

conclusionPAH exposure may be associated with adverse male reproductive outcomes, including impaired semen quality and a potential increase in reproductive cancer risk. However, the evidence is limited by methodological heterogeneity, observational designs, and imprecision. In contrast, evidence in females is sparse and of very low certainty, underscoring the need for more rigorous, targeted research on female reproductive outcome.