{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,3]],"date-time":"2026-10-03T03:28:31Z","timestamp":1790998111023,"version":"4.1.0"},"reference-count":39,"publisher":"American Medical Association (AMA)","issue":"8","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["JAMA Netw Open"],"abstract":"<jats:sec id=\"ab-zoi260848-4\">\n                    <jats:title>Importance<\/jats:title>\n                    <jats:p>Earlier menopause has been linked to increased cognitive decline, but longitudinal data regarding corresponding volumetric brain changes are scarce, and the lasting associations of menopause timing on brain atrophy rates that accompany cognitive decline in women remain unknown.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi260848-5\">\n                    <jats:title>Objective<\/jats:title>\n                    <jats:p>To evaluate whether menopause age is associated with cognitive decline, Alzheimer disease (AD) onset, and brain volume trajectories in older women and whether this differs by menopause type.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi260848-6\">\n                    <jats:title>Design, Setting, and Participants<\/jats:title>\n                    <jats:p>Longitudinal cohort study using the Religious Orders Study and Rush Memory and Aging Project with up to 18 years of follow-up. Religious Orders Study enrollment began January 1994 and Rush Memory and Aging Project enrollment ran September 1997 to April 2005; follow-up is ongoing in both. Data were extracted and analyzed in August 2025. Analyses included 2603 women with cognitive data, 1287 with neuropathology at autopsy, and 774 with serial 3T magnetic resonance imaging.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi260848-7\">\n                    <jats:title>Exposures<\/jats:title>\n                    <jats:p>Age at menopause, examined overall and stratified by menopause type (spontaneous vs surgical).<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi260848-8\">\n                    <jats:title>Main Outcomes and Measures<\/jats:title>\n                    <jats:p>Global and domain-specific cognitive decline, time to AD diagnosis, AD neuropathologic change at autopsy, and brain volume trajectories including total brain volume and white matter hyperintensity volume, modeled using linear mixed-effects, accelerated failure time, proportional odds, and inverse-probability-weighted generalized additive mixed models with a prespecified 3-family Benjamini-Hochberg correction.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi260848-9\">\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      From a total of 2603 women (mean [SD] age of enrollment, [78.30 [7.85], ; 172 [6.6%] Black or African American and 2400 [92.2%] White non-Hispanic), earlier menopause age was associated with faster global cognitive decline (\u03b2\u2009=\u2009\u20130.0009 SD per year earlier menopause age; SE\u2009=\u20090.0004; false-discovery rate [FDR]\u2013corrected\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      \u2009=\u2009.04), faster episodic memory decline (\u03b2\u2009=\u2009\u20130.0014; SE\u2009=\u20090.0005; FDR-corrected\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      \u2009=\u2009.03), and earlier AD diagnosis in the full cohort (time ratio\u2009=\u20090.998; 95% CI, 0.997\u20130.999; FDR-corrected\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      \u2009=\u2009.02); associations were directionally stronger in surgical menopause (time ratio\u2009=\u20091.000; 95% CI, 0.998-1.000;\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      \u2009=\u2009.008). Earlier menopause age was associated with substantially faster white matter hyperintensity volume accumulation in women with spontaneous menopause (\n                      <jats:italic toggle=\"yes\">f<\/jats:italic>\n                      <jats:sup>2<\/jats:sup>\n                      \u2009=\u20090.30; FDR-corrected\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      \u2009&amp;amp;lt;\u2009.001), an association that increased with advancing age and was absent in surgical menopause, indicating specificity to the gradual hormonal trajectory of spontaneous menopause.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi260848-10\">\n                    <jats:title>Conclusions and Relevance<\/jats:title>\n                    <jats:p>In this cohort study of older women, earlier menopause was associated with less favorable functional and structural neurological outcomes, with associations persisting and intensifying decades after the menopausal transition. These findings position menopause age as a midlife-identifiable marker for risk stratification, offering a window for targeted prevention before structural or cognitive changes become apparent.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1001\/jamanetworkopen.2026.30973","type":"journal-article","created":{"date-parts":[[2026,8,25]],"date-time":"2026-08-25T15:01:28Z","timestamp":1787670088000},"page":"e2630973","source":"Crossref","is-referenced-by-count":2,"title":["Age at Menopause and Brain Atrophy Among Older Women"],"prefix":"10.1001","volume":"9","author":[{"given":"M. Pia","family":"Campagna","sequence":"first","affiliation":[{"name":"University of California San Francisco Weill Institute for Neuroscience, Department of Neurology, University of California San Francisco"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Julie A.","family":"Schneider","sequence":"additional","affiliation":[{"name":"Rush Alzheimer\u2019s Disease Center, Rush University Medical Center, Chicago, Illinois"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Lisa L.","family":"Barnes","sequence":"additional","affiliation":[{"name":"Rush Alzheimer\u2019s Disease Center, Rush University Medical Center, Chicago, Illinois"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Konstantinos","family":"Arfanakis","sequence":"additional","affiliation":[{"name":"Rush Alzheimer\u2019s Disease Center, Rush University Medical Center, Chicago, Illinois"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Galit Levi","family":"Dunietz","sequence":"additional","affiliation":[{"name":"Department of Neurology, Division of Sleep Medicine, University of Michigan, Ann Arbor"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"David A.","family":"Bennett","sequence":"additional","affiliation":[{"name":"Rush Alzheimer\u2019s Disease Center, Rush University Medical Center, Chicago, Illinois"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Riley M.","family":"Bove","sequence":"additional","affiliation":[{"name":"University of California San Francisco Weill Institute for Neuroscience, Department of Neurology, University of California San Francisco"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"10","published-online":{"date-parts":[[2026,8,25]]},"reference":[{"issue":"12","key":"zoi260848r1","doi-asserted-by":"publisher","first-page":"1966","DOI":"10.1002\/alz.12362","article-title":"Population estimate of people with clinical Alzheimer\u2019s disease and 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