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However, few studies have examined how these features relate to AD biomarkers in cognitively unimpaired (CU) older adults.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>METHODS<\/jats:title>\n                    <jats:p>\n                      Meta\u2010analyses were performed using cross\u2010sectional data from nine cohorts (\n                      <jats:italic>n<\/jats:italic>\n                      \u00a0=\u00a07219, mean age (SD): 71.17 (5.9), 56.5% female) to determine associations of SCD\u2010\n                      <jats:italic>plus<\/jats:italic>\n                      features with positron emission tomography (PET)\u2013 or cerebrospinal fluid (CSF)\u2013derived amyloid beta (A\u03b2) and tau biomarkers.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>RESULTS<\/jats:title>\n                    <jats:p>\n                      Participants with preclinical AD (community\u2010based only) were more likely to fulfill SCD\u2010\n                      <jats:italic>plus<\/jats:italic>\n                      features. The presence of self\u2010reported memory decline, associated concern\/worry, and a higher number of fulfilled features were all associated with high A\u03b2 levels. Only the latter was associated with abnormal tau.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>DISCUSSION<\/jats:title>\n                    <jats:p>\n                      Simultaneous endorsement of multiple SCD\u2010\n                      <jats:italic>plus<\/jats:italic>\n                      features is a robust indicator of abnormal AD biomarkers in CU older adults, whereas isolated SCD features seem only sensitive to elevated A\u03b2, supporting their value as early behavioral markers of preclinical AD.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Highlights<\/jats:title>\n                    <jats:p>\n                      <jats:list list-type=\"bullet\">\n                        <jats:list-item>\n                          <jats:p>About two\u2010tenths of our sample had abnormal amyloid beta (A\u03b2) levels with evidence of subjective cognitive decline (SCD).<\/jats:p>\n                        <\/jats:list-item>\n                        <jats:list-item>\n                          <jats:p>\n                            Preclinical AD subsamples (community\u2010based) had a higher percentage of participants meeting SCD\u2010\n                            <jats:italic>plus<\/jats:italic>\n                            features. Self\u2010reported memory decline and concern\/worry were the sole features associated with high A\u03b2, but not tau, burden.\n                          <\/jats:p>\n                        <\/jats:list-item>\n                        <jats:list-item>\n                          <jats:p>\n                            A higher number of fulfilled SCD\u2010\n                            <jats:italic>plus<\/jats:italic>\n                            features are linked to high A\u03b2 and tau burden.\n                          <\/jats:p>\n                        <\/jats:list-item>\n                        <jats:list-item>\n                          <jats:p>\n                            Use of multiple SCD\u2010\n                            <jats:italic>plus<\/jats:italic>\n                            features may help identify early stages of biological AD.\n                          <\/jats:p>\n                        <\/jats:list-item>\n                      <\/jats:list>\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1002\/alz.14307","type":"journal-article","created":{"date-parts":[[2025,2,22]],"date-time":"2025-02-22T07:39:02Z","timestamp":1740209942000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":15,"title":["SCD\u2010\n                    <i>plus<\/i>\n                    features and AD biomarkers in cognitively unimpaired samples: A meta\u2010analytic approach for nine cohort studies"],"prefix":"10.1002","volume":"21","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-3744-1155","authenticated-orcid":false,"given":"Elizabeth","family":"Kuhn","sequence":"first","affiliation":[{"name":"German Center for Neurodegenerative Diseases (DZNE) Bonn  Bonn Germany"},{"name":"Department of Cognitive Disorders and Old Age Psychiatry University Hospital Bonn  Bonn Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0009-0006-5633-2954","authenticated-orcid":false,"given":"Hannah M.","family":"Klinger","sequence":"additional","affiliation":[{"name":"Department of Neurology Massachusetts General Hospital  Boston Massachusetts USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Rebecca E.","family":"Amariglio","sequence":"additional","affiliation":[{"name":"Department of Neurology Massachusetts General Hospital  Boston Massachusetts USA"},{"name":"Center for Alzheimer Research and Treatment (CART) Brigham &amp; 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