Association between pelvic inflammatory disease and risk of ovarian, uterine, cervical, and vaginal cancers—a meta-analysis

Background and aim The present meta-analysis aims to investigate a potential link between pelvic inflammatory disease (PID) and an increased risk of genitourinary cancers (ovarian, cervical, uterus, and vagina cancers). While previous research has hinted at a possible link, this meta-analysis seeks...

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Veröffentlicht in:Archives of gynecology and obstetrics 2024-11, Vol.310 (5), p.2577-2585
Hauptverfasser: Syed Khaja, Azharuddin Sajid, Saleem, Mohd, Zafar, Mubashir, Moursi, Soha, Mohammed, Ghorashy Eltayeb Yousif, Shahid, Syed Monowar Alam, Hammam, Sahar, Moussa, Safia, Alharbi, Mohammed Salem, Alshammari, Ahmed Nawi
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Sprache:eng
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Zusammenfassung:Background and aim The present meta-analysis aims to investigate a potential link between pelvic inflammatory disease (PID) and an increased risk of genitourinary cancers (ovarian, cervical, uterus, and vagina cancers). While previous research has hinted at a possible link, this meta-analysis seeks to delve deeper into the available evidence. Understanding this association is crucial for preventive strategies and improving clinical management practices. Methodology A comprehensive literature search was conducted across various databases, covering studies published between 2016 and 2024. We included 13 observational studies meeting stringent criteria, followed by meticulous data extraction and quality assessment. Meta-analytical techniques were then employed to calculate pooled odds ratios (ORs), adjusted hazard ratios (HRs), and 95% confidence intervals (CIs), with heterogeneity assessed using the I 2 statistic. Results Our analysis revealed significant findings, underscoring the association between PID and increased risks of genitourinary cancers. Specifically, individuals with a history of PID demonstrated notably higher odds of developing ovarian cancer (OR = 1.477, 95% CI 1.033–2.207), uterine cancer (OR = 1.263, 95% CI 0.827–2.143), cervical cancer (OR = 1.000, 95% CI 0.900–1.100), and vaginal cancer (OR = 2.500, 95% CI 1.400–4.000) compared to those without such a history. The overall heterogeneity across studies was high ( I 2  = 82.92%), suggesting varying trends across different populations and study designs. Conclusion This meta-analysis provides updated evidence supporting a significant association between PID and an increased risk of cervical, ovarian, and uterine cancers. Early detection and management of PID are crucial in potentially mitigating the risk of these cancers.
ISSN:1432-0711
0932-0067
1432-0711
DOI:10.1007/s00404-024-07748-z