<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Liu D</submitter><funding>the "Shu-Guang Scholar Programme" from Shanghai Municipal Education Commission, the "Shanghai Municipal Education Commission-Gaofeng Clinical Medicine Grant Support" from Shanghai Jiao Tong University School of Medicine</funding><funding>National Key R&amp;D Program of China</funding><funding>Noncommunicable Chronic Diseases-National Science and Technology Major Project</funding><funding>National Natural Science Foundation of China</funding><pagination>170</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12008983</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>24(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Delineating the causal chain effects of reproductive traits and fat- and muscle-related traits on cardiovascular disease (CVD) is essential for optimizing precision prevention and control of cardiovascular health in women.&lt;h4>Methods&lt;/h4>In this study, we applied the two-sample Mendelian randomization (MR) analyses and two-step MR framework to investigate the causal chain effects and the mediating effect pathways among reproductive factors and fat- and muscle-related traits on CVD outcomes in women, applying the genome-wide association study summary statistics of 16 women's reproductive traits across puberty and pre-pregnancy, pregnancy and postpartum, and menopausal transition stages, 16 women's fat- and muscle-related traits, and five CVD outcomes of coronary artery di</pubmed_abstract><journal>Cardiovascular diabetology</journal><pubmed_title>Chain effect of lifecourse reproductive characteristics and body fat and muscle on cardiovascular disease in women: a Mendelian randomization study.</pubmed_title><pmcid>PMC12008983</pmcid><funding_grant_id>20171901 Round 2</funding_grant_id><funding_grant_id>82370820, 82088102, and 81930021</funding_grant_id><funding_grant_id>2023ZD0508603</funding_grant_id><funding_grant_id>2023YFC2506700</funding_grant_id><pubmed_authors>Kong L</pubmed_authors><pubmed_authors>Xu M</pubmed_authors><pubmed_authors>Zhu Z</pubmed_authors><pubmed_authors>Ye C</pubmed_authors><pubmed_authors>Chen M</pubmed_authors><pubmed_authors>Zhao Z</pubmed_authors><pubmed_authors>Li M</pubmed_authors><pubmed_authors>Ning G</pubmed_authors><pubmed_authors>Zheng J</pubmed_authors><pubmed_authors>Lu J</pubmed_authors><pubmed_authors>Wang T</pubmed_authors><pubmed_authors>Chen Y</pubmed_authors><pubmed_authors>Wang W</pubmed_authors><pubmed_authors>Liu D</pubmed_authors><pubmed_authors>Dou C</pubmed_authors><pubmed_authors>Xu Y</pubmed_authors><pubmed_authors>Bi Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Chain effect of lifecourse reproductive characteristics and body fat and muscle on cardiovascular disease in women: a Mendelian randomization study.</name><description>&lt;h4>Background&lt;/h4>Delineating the causal chain effects of reproductive traits and fat- and muscle-related traits on cardiovascular disease (CVD) is essential for optimizing precision prevention and control of cardiovascular health in women.&lt;h4>Methods&lt;/h4>In this study, we applied the two-sample Mendelian randomization (MR) analyses and two-step MR framework to investigate the causal chain effects and the mediating effect pathways among reproductive factors and fat- and muscle-related traits on CVD outcomes in women, applying the genome-wide association study summary statistics of 16 women's reproductive traits across puberty and pre-pregnancy, pregnancy and postpartum, and menopausal transition stages, 16 women's fat- and muscle-related traits, and five CVD outcomes of coronary artery di</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Apr</publication><modification>2025-07-03T03:04:53.163Z</modification><creation>2025-07-03T03:04:53.163Z</creation></dates><accession>S-EPMC12008983</accession><cross_references><pubmed>40251560</pubmed><doi>10.1186/s12933-025-02681-0</doi></cross_references></HashMap>