TY - JOUR
T1 - Non-malignant gynaecological disease and risk of cardiovascular or cerebrovascular disease
T2 - A systematic review and meta-analysis
AU - Colombo, Giorgia Elisabeth
AU - Mahamat-Saleh, Yahya
AU - Armour, Mike
AU - Madan, Kedar
AU - Sabag, Angelo
AU - Kvaskoff, Marina
AU - Missmer, Stacey A.
AU - Condous, George
AU - Pathan, Faraz
AU - Leonardi, Mathew
N1 - Publisher Copyright:
© Author(s) (or their employer(s)) 2025.
PY - 2025/5/1
Y1 - 2025/5/1
N2 - Background Cardiovascular disease is the leading cause of death globally. Non-malignant gynaecological diseases (NMGD) significantly affect patient health and well-being and may be associated with cardiovascular or cerebrovascular disease (C/CVD). Methods Seven databases were searched for relevant studies up to 21 April 2024. Observational studies reporting risk estimates and 95% CIs for the association between NMGD and C/CVD were included. Data were extracted by two independent reviewers. Random effects models were used to calculate summary relative risk (SRR) with 95% CI. Composite C/CVD outcome was defined as a combination of ischaemic heart disease, cerebrovascular disease, heart failure, and peripheral vascular disease. The ROBINS-I tool defined study quality and risk of bias. Results We screened 6639 studies, of which 59 were eligible for full-Text review and 28 were included in our analysis, comprising a total of 3 271 242 individuals. The majority (53.5%) of the studies were scored as having a â € serious'/â € critical' risk of bias. Overall, individuals with an NMGD had a significantly greater risk of composite C/CVD with low heterogeneity among contributing studies (SRR 1.28, 95% CI 1.20 to 1.37; n=16 studies, I 2 =65.3%), ischaemic heart disease (SRR 1.41, 95% CI 1.31 to 1.51; n=21 studies, I 2 =73.7%), and cerebrovascular disease (SRR 1.33, 95% CI 1.18 to 1.51; n=16 studies, I 2 =91.5%). In NMGD-specific analyses, the risk of C/CVD and its components was greater among those with a history of endometriosis or polycystic ovary syndrome. Conclusions We found an overall association between NMGD and C/CVD across all studies. However, estimates from individual studies varied substantially.
AB - Background Cardiovascular disease is the leading cause of death globally. Non-malignant gynaecological diseases (NMGD) significantly affect patient health and well-being and may be associated with cardiovascular or cerebrovascular disease (C/CVD). Methods Seven databases were searched for relevant studies up to 21 April 2024. Observational studies reporting risk estimates and 95% CIs for the association between NMGD and C/CVD were included. Data were extracted by two independent reviewers. Random effects models were used to calculate summary relative risk (SRR) with 95% CI. Composite C/CVD outcome was defined as a combination of ischaemic heart disease, cerebrovascular disease, heart failure, and peripheral vascular disease. The ROBINS-I tool defined study quality and risk of bias. Results We screened 6639 studies, of which 59 were eligible for full-Text review and 28 were included in our analysis, comprising a total of 3 271 242 individuals. The majority (53.5%) of the studies were scored as having a â € serious'/â € critical' risk of bias. Overall, individuals with an NMGD had a significantly greater risk of composite C/CVD with low heterogeneity among contributing studies (SRR 1.28, 95% CI 1.20 to 1.37; n=16 studies, I 2 =65.3%), ischaemic heart disease (SRR 1.41, 95% CI 1.31 to 1.51; n=21 studies, I 2 =73.7%), and cerebrovascular disease (SRR 1.33, 95% CI 1.18 to 1.51; n=16 studies, I 2 =91.5%). In NMGD-specific analyses, the risk of C/CVD and its components was greater among those with a history of endometriosis or polycystic ovary syndrome. Conclusions We found an overall association between NMGD and C/CVD across all studies. However, estimates from individual studies varied substantially.
UR - http://www.scopus.com/inward/record.url?scp=85219089155&partnerID=8YFLogxK
U2 - 10.1136/heartjnl-2024-324675
DO - 10.1136/heartjnl-2024-324675
M3 - Article
C2 - 39993911
AN - SCOPUS:85219089155
SN - 1355-6037
VL - 111
SP - 402
EP - 411
JO - Heart
JF - Heart
IS - 9
M1 - heartjnl-2024-324675
ER -