{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,17]],"date-time":"2026-08-17T14:07:20Z","timestamp":1786975640712,"version":"build-2736575974"},"reference-count":29,"publisher":"American Medical Association (AMA)","issue":"4","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["JAMA Netw Open"],"abstract":"<jats:sec id=\"ab-zoi230262-4\">\n                    <jats:title>Importance<\/jats:title>\n                    <jats:p>Cerebrospinal fluid (CSF) and plasma biomarkers can detect biological evidence of Alzheimer disease (AD), but their use in low-resource environments and among minority ethnic groups is limited.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi230262-5\">\n                    <jats:title>Objective<\/jats:title>\n                    <jats:p>To assess validated plasma biomarkers for AD among adults of Caribbean Hispanic ethnicity.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi230262-6\">\n                    <jats:title>Design, Setting, and Participants<\/jats:title>\n                    <jats:p>In this decision analytical modeling study, adults were recruited between January 1, 2018, and April 30, 2022, and underwent detailed clinical assessments and venipuncture. A subsample of participants also consented to lumbar puncture. Established CSF cut points were used to define AD biomarker-positive status, allowing determination of optimal cut points for plasma biomarkers in the same individuals. The performance of a panel of 6 plasma biomarkers was then assessed with respect to the entire group. Data analysis was performed in January 2023.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi230262-7\">\n                    <jats:title>Main Outcomes and Measures<\/jats:title>\n                    <jats:p>\n                      Main outcomes were the association of plasma biomarkers amyloid-\u03b2 1-42 (A\u03b242), amyloid-\u03b2 1-40 (A\u03b240), total tau (T-tau), phosphorylated tau181 (P-tau181), glial fibrillary acidic protein (GFAP), and neurofilament light chain (NfL) with AD diagnosis. These biomarkers allow assessment of amyloid (A), neurofibrillary degeneration (T), and neurodegeneration (N) aspects of AD. Statistical analyses performed included receiver operating characteristics, Pearson and Spearman correlations,\n                      <jats:italic>t<\/jats:italic>\n                      tests, and Wilcoxon rank-sum, chi-square, and Fisher exact tests.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi230262-8\">\n                    <jats:title>Exposures<\/jats:title>\n                    <jats:p>\n                      Exposures included age, sex, education, country of residence, apolipoprotein-\u03b54 (\n                      <jats:italic>APOE-\u03b54<\/jats:italic>\n                      ) allele number, serum creatinine, blood urea nitrogen, and body mass index.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi230262-9\">\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      This study included 746 adults. Participants had a mean (SD) age of 71.0\u2009(7.8) years, 480 (64.3%) were women, and 154 (20.6%) met clinical criteria for AD. Associations were observed between CSF and plasma P-tau181 (\n                      <jats:italic>r<\/jats:italic>\n                      \u2009=\u2009.47 [95% CI, 0.32-0.60]), NfL (\n                      <jats:italic>r<\/jats:italic>\n                      \u2009=\u20090.57 [95% CI, 0.44-0.68]), and P-tau181\/A\u03b242 (\n                      <jats:italic>r<\/jats:italic>\n                      \u2009=\u20090.44 [95% CI, 0.29-0.58]). For AD defined by CSF biomarkers, plasma P-tau181 and P-tau181\/A\u03b242 provided biological evidence of AD. Among individuals judged to be clinically healthy without dementia, biomarker-positive status was determined by plasma P-tau181 for 133 (22.7%) and by plasma P-tau181\/A\u03b242 for 104 (17.7%). Among individuals with clinically diagnosed AD, 69 (45.4%) had plasma P-tau181 levels and 89 (58.9%) had P-tau181\/A\u03b242 levels that were inconsistent with AD. Individuals with biomarker-negative clinical AD status tended to have lower levels of education, were less likely to carry\n                      <jats:italic>APOE-\u03b54<\/jats:italic>\n                      alleles, and had lower levels of GFAP and NfL than individuals with biomarker-positive clinical AD.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec id=\"ab-zoi230262-10\">\n                    <jats:title>Conclusions and Relevance<\/jats:title>\n                    <jats:p>In this cross-sectional study, plasma P-tau181 and P-tau181\/A\u03b242 measurements correctly classified Caribbean Hispanic individuals with and without AD. However, plasma biomarkers identified individuals without dementia with biological evidence of AD, and a portion of those with dementia whose AD biomarker profile was negative. These results suggest that plasma biomarkers can augment detection of preclinical AD among asymptomatic individuals and improve the specificity of AD diagnosis.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1001\/jamanetworkopen.2023.8214","type":"journal-article","created":{"date-parts":[[2023,4,20]],"date-time":"2023-04-20T12:33:10Z","timestamp":1681993990000},"page":"e238214","source":"Crossref","is-referenced-by-count":39,"title":["Evaluation of Plasma Biomarkers for A\/T\/N Classification of Alzheimer Disease Among Adults of Caribbean Hispanic Ethnicity"],"prefix":"10.1001","volume":"6","author":[{"given":"Lawrence S.","family":"Honig","sequence":"first","affiliation":[{"name":"Taub Institute for Research on Alzheimer\u2019s Disease and the Aging Brain, Vagelos College of Physicians and Surgeons, Columbia University, New York, New York"},{"name":"G. H. Sergievsky Center, Vagelos College of Physicians and Surgeons, Columbia University, New York, New York"},{"name":"Universidad Pedro Henr\u00edquez Urena, Santo Domingo, Dominican Republic"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Min Suk","family":"Kang","sequence":"additional","affiliation":[{"name":"Taub Institute for Research on Alzheimer\u2019s Disease and the Aging Brain, Vagelos College of Physicians and Surgeons, Columbia University, New York, New York"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Annie J.","family":"Lee","sequence":"additional","affiliation":[{"name":"G. H. Sergievsky Center, Vagelos College of Physicians and Surgeons, Columbia University, New York, New York"},{"name":"Universidad Pedro Henr\u00edquez Urena, Santo Domingo, Dominican Republic"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Dolly","family":"Reyes-Dumeyer","sequence":"additional","affiliation":[{"name":"Taub Institute for Research on Alzheimer\u2019s Disease and the Aging Brain, Vagelos College of Physicians and Surgeons, Columbia University, New York, New York"},{"name":"G. H. Sergievsky Center, Vagelos College of Physicians and Surgeons, Columbia University, New York, New York"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Angel","family":"Piriz","sequence":"additional","affiliation":[{"name":"Taub Institute for Research on Alzheimer\u2019s Disease and the Aging Brain, Vagelos College of Physicians and Surgeons, Columbia University, New York, New York"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Belisa","family":"Soriano","sequence":"additional","affiliation":[{"name":"Universidad Pedro Henr\u00edquez Urena, Santo Domingo, Dominican Republic"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yahaira","family":"Franco","sequence":"additional","affiliation":[{"name":"Cl\u00ednica Corominas, Santiago, Dominican Republic"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Zoraida Dominguez","family":"Coronado","sequence":"additional","affiliation":[{"name":"Cl\u00ednica Gregorio Hernandez, Puerto Plata, Dominican Republic"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Patricia","family":"Recio","sequence":"additional","affiliation":[{"name":"Center for Diagnosis, Advanced Medicine and Telemedicine, Santo Domingo, Dominican Republic"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Diones Rivera","family":"Mej\u00eda","sequence":"additional","affiliation":[{"name":"Universidad Pedro Henr\u00edquez Urena, Santo Domingo, Dominican Republic"},{"name":"Center for Diagnosis, Advanced Medicine and Telemedicine, Santo Domingo, Dominican Republic"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Martin","family":"Medrano","sequence":"additional","affiliation":[{"name":"Pont\u00edficia Universidad Cat\u00f3lica Madre y Maestra, Santiago, Dominican Republic"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Rafael A.","family":"Lantigua","sequence":"additional","affiliation":[{"name":"Taub Institute for Research on Alzheimer\u2019s Disease and the Aging Brain, Vagelos College of Physicians and Surgeons, Columbia University, New York, New York"},{"name":"Department of Medicine, Vagelos College of Physicians and Surgeons, New York Presbyterian Hospital, Columbia University, New York, New York"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Andrew F.","family":"Teich","sequence":"additional","affiliation":[{"name":"Taub Institute for Research on Alzheimer\u2019s Disease and the Aging Brain, Vagelos College of Physicians and Surgeons, Columbia University, New York, New York"},{"name":"Department of Neurology, Vagelos College of Physicians and Surgeons, New York Presbyterian Hospital, Columbia University, New York, New York"},{"name":"Department of Pathology and Cell Biology, Vagelos College of Physicians and Surgeons, Columbia University, New York, New York"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jeffrey L.","family":"Dage","sequence":"additional","affiliation":[{"name":"Department of Neurology, Indiana University School of Medicine, Indianapolis"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Richard","family":"Mayeux","sequence":"additional","affiliation":[{"name":"Taub Institute for Research on Alzheimer\u2019s Disease and the Aging Brain, Vagelos College of Physicians and Surgeons, Columbia University, New York, New York"},{"name":"G. H. Sergievsky Center, Vagelos College of Physicians and Surgeons, Columbia University, New York, New York"},{"name":"Universidad Pedro Henr\u00edquez Urena, Santo Domingo, Dominican Republic"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"10","published-online":{"date-parts":[[2023,4,20]]},"reference":[{"issue":"3","key":"zoi230262r1","doi-asserted-by":"publisher","first-page":"131","DOI":"10.1038\/nrneurol.2010.4","article-title":"Cerebrospinal fluid and plasma biomarkers in Alzheimer disease.","volume":"6","author":"Blennow","year":"2010","journal-title":"Nat Rev Neurol"},{"issue":"1","key":"zoi230262r2","doi-asserted-by":"publisher","first-page":"1683","DOI":"10.1038\/s41467-020-15436-0","article-title":"Cerebrospinal fluid p-tau217 performs better than p-tau181 as a biomarker of Alzheimer\u2019s disease.","volume":"11","author":"Janelidze","year":"2020","journal-title":"Nat 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