Julien Lagarde MD, PhD, Piyush Maiti MS, Daniel R. Schonhaut PhD, Ganna Blazhenets PhD, Jiaxiuxiu Zhang MS, Ani Eloyan PhD, Maryanne Thangarajah MS, Alexander Taurone MS, Isabel Elaine Allen PhD, David N. Soleimani-Meigooni MD, Ehud Zeltzer MD, Charles Windon MD, Maison Abu Raya MD, Agathe Vrillon MD, PhD, Karen Smith BS, Ranjani Shankar BS, Alinda Amuiri BS, Salma Rocha BA, Dustin B. Hammers PhD, Jeffrey L. Dage PhD, Kelly N. Nudelman PhD, Kala Kirby BS, Paul Aisen MD, Robert Koeppe PhD, Susan M. Landau PhD, Maria C. Carrillo PhD, Alexandra Touroutoglou PhD, Michael Brickhouse BS, Prashanthi Vemuri PhD, Laurel Beckett PhD, Rema Raman PhD, Alireza Atri MD, PhD, Gregory S. Day MD, Ranjan Duara MD, Neill R. Graff-Radford MD, Lawrence S. Honig MD, PhD, David T. Jones MD, Joseph C. Masdeu MD, PhD, Mario F. Mendez MD, PhD, Kyle Womack MD, Erik Musiek MD, PhD, Chiadi U. Onyike MD, Meghan Riddle MD, Ian M. Grant MD, Emily Rogalski PhD, Erik C. B. Johnson MD, PhD, Stephen Salloway MD, Sharon Sha MD, R. Scott Turner MD, PhD, Thomas S. Wingo MD, David A. Wolk MD, Bradford C. Dickerson MD, Liana G. Apostolova MD, Renaud La Joie PhD, Gil D. Rabinovici MD, the LEADS Consortium for the Alzheimer's Disease Neuroimaging Initiative
{"title":"Amyloid PET in Sporadic Early- Versus Late-Onset Alzheimer's Disease: Comparison of the LEADS and ADNI Cohorts","authors":"Julien Lagarde MD, PhD, Piyush Maiti MS, Daniel R. Schonhaut PhD, Ganna Blazhenets PhD, Jiaxiuxiu Zhang MS, Ani Eloyan PhD, Maryanne Thangarajah MS, Alexander Taurone MS, Isabel Elaine Allen PhD, David N. Soleimani-Meigooni MD, Ehud Zeltzer MD, Charles Windon MD, Maison Abu Raya MD, Agathe Vrillon MD, PhD, Karen Smith BS, Ranjani Shankar BS, Alinda Amuiri BS, Salma Rocha BA, Dustin B. Hammers PhD, Jeffrey L. Dage PhD, Kelly N. Nudelman PhD, Kala Kirby BS, Paul Aisen MD, Robert Koeppe PhD, Susan M. Landau PhD, Maria C. Carrillo PhD, Alexandra Touroutoglou PhD, Michael Brickhouse BS, Prashanthi Vemuri PhD, Laurel Beckett PhD, Rema Raman PhD, Alireza Atri MD, PhD, Gregory S. Day MD, Ranjan Duara MD, Neill R. Graff-Radford MD, Lawrence S. Honig MD, PhD, David T. Jones MD, Joseph C. Masdeu MD, PhD, Mario F. Mendez MD, PhD, Kyle Womack MD, Erik Musiek MD, PhD, Chiadi U. Onyike MD, Meghan Riddle MD, Ian M. Grant MD, Emily Rogalski PhD, Erik C. B. Johnson MD, PhD, Stephen Salloway MD, Sharon Sha MD, R. Scott Turner MD, PhD, Thomas S. Wingo MD, David A. Wolk MD, Bradford C. Dickerson MD, Liana G. Apostolova MD, Renaud La Joie PhD, Gil D. Rabinovici MD, the LEADS Consortium for the Alzheimer's Disease Neuroimaging Initiative","doi":"10.1002/ana.27233","DOIUrl":null,"url":null,"abstract":"<div>\n \n <section>\n \n <h3> Objective</h3>\n \n <p>Early-onset Alzheimer's disease (EOAD) and late-onset Alzheimer's disease (LOAD) differ in many respects. Here, we address the issue of possible differences in fibrillar amyloid pathology as measured by positron emission tomography (PET), which remains unresolved due to the lack of large-scale comparative studies.</p>\n </section>\n \n <section>\n \n <h3> Methods</h3>\n \n <p>Three hundred ninety-nine cognitively impaired participants younger than 65 years of age from the multicenter Longitudinal Early-onset Alzheimer's Disease Study (LEADS) and 450 cognitively impaired participants older than 65 years from the Alzheimer's Disease Neuroimaging Initiative (ADNI) underwent clinical assessment, brain magnetic resonance imaging (MRI), and amyloid PET and were included in this study. We compared amyloid PET outcomes (positivity rate based on visual read and quantified tracer uptake expressed as Centiloids [CLs]) between the 2 cohorts and studied their association with age, sex, <i>APOE</i> genotype, and cognition.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>The amyloid positivity rate was higher in LEADS (78%, 95% confidence interval [CI] = 74–82) than in ADNI (71%, 95% CI = 67–75, <i>p</i> = 0.02). Lower Mini-Mental State Examination (MMSE) and APOE4 genotype increased the odds of amyloid positivity in both cohorts. Visually positive scans had higher CLs in LEADS (EOAD, mean = 95.3 ± 26.1) than in ADNI (LOAD, mean = 80.9 ± 36.8, <i>p</i> < 0.0001), predominantly in parietal cortex/precuneus, superior temporal, and frontal cortices. In amyloid-positive patients, (1) CLs were higher in female patients in both cohorts; (2) APOE4 carriership was associated with <i>lower</i> CLs in EOAD, which was not observed in LOAD; and (3) correlations between CLs and MMSE scores were significantly stronger in EOAD than in LOAD.</p>\n </section>\n \n <section>\n \n <h3> Interpretation</h3>\n \n <p>Differences in the burden of amyloid pathology may contribute to differences in clinical and anatomic patterns in sporadic EOAD and LOAD, and have implications for optimizing therapeutic strategies in each group. ANN NEUROL 2025;98:236–248</p>\n </section>\n </div>","PeriodicalId":127,"journal":{"name":"Annals of Neurology","volume":"98 2","pages":"236-248"},"PeriodicalIF":7.7000,"publicationDate":"2025-03-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Annals of Neurology","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/ana.27233","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Objective
Early-onset Alzheimer's disease (EOAD) and late-onset Alzheimer's disease (LOAD) differ in many respects. Here, we address the issue of possible differences in fibrillar amyloid pathology as measured by positron emission tomography (PET), which remains unresolved due to the lack of large-scale comparative studies.
Methods
Three hundred ninety-nine cognitively impaired participants younger than 65 years of age from the multicenter Longitudinal Early-onset Alzheimer's Disease Study (LEADS) and 450 cognitively impaired participants older than 65 years from the Alzheimer's Disease Neuroimaging Initiative (ADNI) underwent clinical assessment, brain magnetic resonance imaging (MRI), and amyloid PET and were included in this study. We compared amyloid PET outcomes (positivity rate based on visual read and quantified tracer uptake expressed as Centiloids [CLs]) between the 2 cohorts and studied their association with age, sex, APOE genotype, and cognition.
Results
The amyloid positivity rate was higher in LEADS (78%, 95% confidence interval [CI] = 74–82) than in ADNI (71%, 95% CI = 67–75, p = 0.02). Lower Mini-Mental State Examination (MMSE) and APOE4 genotype increased the odds of amyloid positivity in both cohorts. Visually positive scans had higher CLs in LEADS (EOAD, mean = 95.3 ± 26.1) than in ADNI (LOAD, mean = 80.9 ± 36.8, p < 0.0001), predominantly in parietal cortex/precuneus, superior temporal, and frontal cortices. In amyloid-positive patients, (1) CLs were higher in female patients in both cohorts; (2) APOE4 carriership was associated with lower CLs in EOAD, which was not observed in LOAD; and (3) correlations between CLs and MMSE scores were significantly stronger in EOAD than in LOAD.
Interpretation
Differences in the burden of amyloid pathology may contribute to differences in clinical and anatomic patterns in sporadic EOAD and LOAD, and have implications for optimizing therapeutic strategies in each group. ANN NEUROL 2025;98:236–248
期刊介绍:
Annals of Neurology publishes original articles with potential for high impact in understanding the pathogenesis, clinical and laboratory features, diagnosis, treatment, outcomes and science underlying diseases of the human nervous system. Articles should ideally be of broad interest to the academic neurological community rather than solely to subspecialists in a particular field. Studies involving experimental model system, including those in cell and organ cultures and animals, of direct translational relevance to the understanding of neurological disease are also encouraged.