{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,15]],"date-time":"2026-07-15T00:06:25Z","timestamp":1784073985290,"version":"3.55.0"},"reference-count":43,"publisher":"The Endocrine Society","issue":"8","license":[{"start":{"date-parts":[[2026,3,12]],"date-time":"2026-03-12T00:00:00Z","timestamp":1773273600000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"funder":[{"DOI":"10.13039\/100009633","name":"National Institute of Child Health and Human Development","doi-asserted-by":"publisher","award":["R01 HD044876"],"award-info":[{"award-number":["R01 HD044876"]}],"id":[{"id":"10.13039\/100009633","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100000049","name":"National Institute on Aging","doi-asserted-by":"publisher","award":["R01AG053332"],"award-info":[{"award-number":["R01AG053332"]}],"id":[{"id":"10.13039\/100000049","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100012264","name":"NIH","doi-asserted-by":"publisher","id":[{"id":"10.13039\/501100012264","id-type":"DOI","asserted-by":"publisher"}]},{"name":"UCSF Clinical and Translational Science Institute","award":["UL1 RR024131"],"award-info":[{"award-number":["UL1 RR024131"]}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2026,7,15]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:sec>\n                    <jats:title>Context<\/jats:title>\n                    <jats:p>While the literature suggests women with diminished ovarian reserve may have increased metabolic risk, implications for long-term health are unknown.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Objective<\/jats:title>\n                    <jats:p>This work aimed to investigate the relationship between ovarian reserve markers at baseline with a subsequent measure of endothelial dysfunction, as a proxy for cardiovascular risk.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>This prospective cohort study was conducted in a community-based setting. Participants included 322 individuals from the Ovarian Aging Study (OVA), a National Institutes of Health\u2013funded study of ovarian aging (average age 35.4 years at the time of baseline ovarian reserve measurements, and age 45.1 years at the time of endothelial dysfunction measurement). This study investigated the association of ovarian reserve markers at baseline with a subsequent (average of 9.7 years) assessment of cardiovascular risk using the Endothelial and Peripheral Arterial Tone reactive hyperemia index (RHI) score of endothelial function. Secondary outcomes including the American Heart Association PREVENT score, metabolic syndrome, telomere length, and mitochondrial DNA were evaluated.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>RHI as a continuous outcome was significantly positively associated both with antim\u00fcllerian hormone (AMH) and antral follicle count (AFC) on fully adjusted models (AMH coefficient 0.052; 95% CI, 0.008-0.096; P = .02; AFC coefficient 0.017; 95% CI, 0.001-0.032; P = .04). For secondary outcomes, the only result that was statistically significant was the association of fully adjusted AFC with metabolic syndrome (odds ratio 0.92; 95% CI, 0.86-0.99; P = .02). A sensitivity analysis of the premenopausal cohort (N = 246) had similar findings.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusion<\/jats:title>\n                    <jats:p>In this longitudinal cohort of women with normal ovarian aging, baseline ovarian reserve markers of AMH and AFC were positively associated with endothelial function as a continuous outcome. Baseline ovarian reserve markers were not related to most secondary outcomes of cellular aging and metabolic risk.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1210\/clinem\/dgag105","type":"journal-article","created":{"date-parts":[[2026,3,10]],"date-time":"2026-03-10T12:39:21Z","timestamp":1773146361000},"page":"2190-2199","source":"Crossref","is-referenced-by-count":0,"title":["Ovarian reserve and endothelial health in healthy reproductive-age women"],"prefix":"10.1210","volume":"111","author":[{"given":"Ange","family":"Wang","sequence":"first","affiliation":[{"name":"Division of Reproductive Endocrinology & Infertility, University of California , San Francisco, CA 94158 ,","place":["USA"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Maria E","family":"Bleil","sequence":"additional","affiliation":[{"name":"Child, Family, & Population Health Nursing, University of Washington , Seattle, WA 98195 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