{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,26]],"date-time":"2026-10-26T20:33:31Z","timestamp":1793046811917,"version":"4.5.0"},"reference-count":72,"publisher":"American Medical Association (AMA)","issue":"1","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["JAMA Netw Open"],"abstract":"<jats:sec id=\"ab-zoi251450-4\">\n                    <jats:title>Importance<\/jats:title>\n                    <jats:p>Sex differences in Alzheimer disease (AD) neuropathology have not been examined extensively across multiple pathological constructs within broadly representative samples.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi251450-5\">\n                    <jats:title>Objective<\/jats:title>\n                    <jats:p>To examine sex differences in neuroimaging biomarkers of AD-related pathologies in a racially and ethnically diverse cohort.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi251450-6\">\n                    <jats:title>Design, Setting, and Participants<\/jats:title>\n                    <jats:p>Data for this cross-sectional study were collected from a community-based sample of adults without cognitive impairment aged 60 to 69 years in New York City from March 1, 2016, to September 31, 2022, and analyzed in March 2025.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi251450-7\">\n                    <jats:title>Exposure<\/jats:title>\n                    <jats:p>The primary exposure was self-reported sex (women or men).<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi251450-8\">\n                    <jats:title>Main Outcomes and Measures<\/jats:title>\n                    <jats:p>\n                      The outcomes were global amyloid burden measured with florbetaben labeled with fludeoxyglucose 18 (\n                      <jats:sup>18<\/jats:sup>\n                      F) positron emission tomography (PET), tau burden in Braak stages I to VI measured with\n                      <jats:sup>18<\/jats:sup>\n                      F-MK-6240 PET, and magnetic resonance imaging (MRI)\u2013derived AD signature cortical thickness and white matter hyperintensity volumes. Linear regression analyses were performed to examine sex differences in the outcomes. Covariates included demographics,\n                      <jats:italic toggle=\"yes\">APOE<\/jats:italic>\n                      \u03b54 status, and vascular health\u2013related factors. Sex\u2009\u00d7\u2009age, sex\u2009\u00d7\u2009\n                      <jats:italic toggle=\"yes\">APOE<\/jats:italic>\n                      \u03b54, and sex\u2009\u00d7\u2009race and ethnicity interactions were additionally examined on the outcomes. False discovery rate (FDR) correction for multiple comparisons were also performed.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi251450-9\">\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      A total of 503 participants (mean [SD] age, 64.6\u2009[2.8] years; 321 [63.8%] women; 305 [60.6%] Hispanic, 120 [23.9%] non-Hispanic Black, and 78 [15.5%] non-Hispanic White) with A\u03b2 PET, MRI (n\u2009=\u2009501), and tau PET (n\u2009=\u2009355) data were studied. Compared with men, women had greater amyloid burden (B\u2009=\u20090.05; 95% CI, 0.02-0.07;\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      \u2009&amp;amp;lt;\u2009.001), Braak stages III and IV (B\u2009=\u20090.05; 95% CI, 0.02-0.08;\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      \u2009=\u2009.003) and Braak stages V and VI (B\u2009=\u20090.09; 95% CI, 0.06-0.12;\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      \u2009&amp;amp;lt;\u2009.001) tau burden, and AD signature thickness (B = 0.04; 95% CI, 0.02-0.05;\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      \u2009&amp;amp;lt;\u2009.001). A significant sex\u2009\u00d7\u2009\n                      <jats:italic toggle=\"yes\">APOE<\/jats:italic>\n                      \u03b54 interaction was observed, with women showing greater Braak stages I and II (B\u2009=\u20090.15; 95% CI, 0.04-0.25;\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      \u2009=\u2009.006) and Braak stages III and IV (B\u2009=\u20090.08; 95% CI, 0.02-0.14;\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      \u2009=\u2009.01) tau burden than men among\n                      <jats:italic toggle=\"yes\">APOE<\/jats:italic>\n                      \u03b54 carriers. All findings remained statistically significant after FDR correction. No significant sex\u2009\u00d7\u2009age or sex\u2009\u00d7\u2009race and ethnicity interactions were observed on any outcome.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi251450-10\">\n                    <jats:title>Conclusions and Relevance<\/jats:title>\n                    <jats:p>\n                      This cross-sectional study of community-based adults found greater AD pathology yet better preserved structural brain integrity in women compared with men. Sex differences in tau burden across early to middle Braak stages were more pronounced among\n                      <jats:italic toggle=\"yes\">APOE<\/jats:italic>\n                      \u03b54 carriers compared with noncarriers. These findings were not modified by age or race and ethnicity. Overall, the results underscore sex-specific distinctions in AD pathology burden and brain structure at the cross-sectional level.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1001\/jamanetworkopen.2025.54524","type":"journal-article","created":{"date-parts":[[2026,1,27]],"date-time":"2026-01-27T16:00:25Z","timestamp":1769529625000},"page":"e2554524","source":"Crossref","is-referenced-by-count":8,"title":["Sex Differences in Alzheimer Disease Imaging Biomarkers in a Diverse, Community-Based Cohort"],"prefix":"10.1001","volume":"9","author":[{"given":"Muge","family":"Akinci","sequence":"first","affiliation":[{"name":"Department of Medicine, College of Physicians and Surgeons, Columbia University Irving Medical Center, New York, New York"},{"name":"Department of Epidemiology, Joseph P. 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