Victoria L. Fleming, Brian C. Helsel, Lauren T. Ptomey, Benjamin L. Handen, Sharon J. Krinsky-McHale, Christy L. Hom, Matthew Zammit, Davneet Minhas, Weiquan Luo, Charles Laymon, Joseph H. Lee, Ira Lott, Annie Cohen, Beau M. Ances, Adam M. Brickman, Margaret Pulsifer, Isabel C. H. Clare, H. Diana Rosa, Florencia Lai, Jordan Harp, Fredrick Schmitt, Julie Price, Shahid H. Zaman, Elizabeth Head, Mark Mapstone, Bradley T. Christian, Ozioma Okonkwo, Sigan L. Hartley, Alzheimer's Biomarkers Consortium–Down Syndrome
{"title":"Longitudinal study of body mass index in relation to Alzheimer's disease pathology and symptomatology in Down syndrome","authors":"Victoria L. Fleming, Brian C. Helsel, Lauren T. Ptomey, Benjamin L. Handen, Sharon J. Krinsky-McHale, Christy L. Hom, Matthew Zammit, Davneet Minhas, Weiquan Luo, Charles Laymon, Joseph H. Lee, Ira Lott, Annie Cohen, Beau M. Ances, Adam M. Brickman, Margaret Pulsifer, Isabel C. H. Clare, H. Diana Rosa, Florencia Lai, Jordan Harp, Fredrick Schmitt, Julie Price, Shahid H. Zaman, Elizabeth Head, Mark Mapstone, Bradley T. Christian, Ozioma Okonkwo, Sigan L. Hartley, Alzheimer's Biomarkers Consortium–Down Syndrome","doi":"10.1002/alz.70387","DOIUrl":null,"url":null,"abstract":"<div>\n \n \n <section>\n \n <h3> INTRODUCTION</h3>\n \n <p>Weight loss has been linked to early Alzheimer's disease (AD) pathology, possibly through metabolic dysregulation. We examined changes in body mass index (BMI) in relation to AD biomarkers (amyloid beta [Aβ] and tau) and cognitive decline in adults with Down syndrome (DS). We hypothesized that BMI decline would track with early AD pathology and cognitive decline.</p>\n </section>\n \n <section>\n \n <h3> METHODS</h3>\n \n <p>Adults with DS (<i>N</i> = 467; <i>M<sub>age </sub></i>= 43.67 ± 10.06) completed one to four data cycles (≈16 months apart). Linear mixed models examined BMI change over time by age, positron emission tomography (PET) Aβ and tau, and changes in memory and dementia symptoms.</p>\n </section>\n \n <section>\n \n <h3> RESULTS</h3>\n \n <p>BMI declined with age-by-time (<i>β</i> = −0.014, <i>p</i> = 0.002) and baseline PET Aβ-by-time (<i>β</i> = −0.005, <i>p</i> = 0.002). On average, BMI decline began in the early 40s and was related to decline in memory and overall cognitive functioning.</p>\n </section>\n \n <section>\n \n <h3> DISCUSSION</h3>\n \n <p>Weight loss is associated with the presence of Aβ and cognitive decline in adults with DS. Longitudinal studies need to clarify directionality and biological mechanisms.</p>\n </section>\n \n <section>\n \n <h3> Highlights</h3>\n \n <div>\n <ul>\n \n <li>Adults with Down syndrome (DS) are at an elevated risk for Down Syndrome assocaited Alzheimer's disease (DSAD).</li>\n \n <li>On average, adults with DS experience body mass index (BMI) decline beginning in their early 40s.</li>\n \n <li>Positron emission tomography amyloid beta deposition is associated with greater decline in BMI in adults with DS.</li>\n \n <li>Across time, AD-related memory declines are associated with BMI decline.</li>\n \n <li>BMI decline should be part of DSAD screening tools, as it is an important part of DSAD clinical disease expression.</li>\n </ul>\n </div>\n </section>\n </div>","PeriodicalId":7471,"journal":{"name":"Alzheimer's & Dementia","volume":"21 6","pages":""},"PeriodicalIF":13.0000,"publicationDate":"2025-06-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/alz.70387","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Alzheimer's & Dementia","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/alz.70387","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
INTRODUCTION
Weight loss has been linked to early Alzheimer's disease (AD) pathology, possibly through metabolic dysregulation. We examined changes in body mass index (BMI) in relation to AD biomarkers (amyloid beta [Aβ] and tau) and cognitive decline in adults with Down syndrome (DS). We hypothesized that BMI decline would track with early AD pathology and cognitive decline.
METHODS
Adults with DS (N = 467; Mage = 43.67 ± 10.06) completed one to four data cycles (≈16 months apart). Linear mixed models examined BMI change over time by age, positron emission tomography (PET) Aβ and tau, and changes in memory and dementia symptoms.
RESULTS
BMI declined with age-by-time (β = −0.014, p = 0.002) and baseline PET Aβ-by-time (β = −0.005, p = 0.002). On average, BMI decline began in the early 40s and was related to decline in memory and overall cognitive functioning.
DISCUSSION
Weight loss is associated with the presence of Aβ and cognitive decline in adults with DS. Longitudinal studies need to clarify directionality and biological mechanisms.
Highlights
Adults with Down syndrome (DS) are at an elevated risk for Down Syndrome assocaited Alzheimer's disease (DSAD).
On average, adults with DS experience body mass index (BMI) decline beginning in their early 40s.
Positron emission tomography amyloid beta deposition is associated with greater decline in BMI in adults with DS.
Across time, AD-related memory declines are associated with BMI decline.
BMI decline should be part of DSAD screening tools, as it is an important part of DSAD clinical disease expression.
期刊介绍:
Alzheimer's & Dementia is a peer-reviewed journal that aims to bridge knowledge gaps in dementia research by covering the entire spectrum, from basic science to clinical trials to social and behavioral investigations. It provides a platform for rapid communication of new findings and ideas, optimal translation of research into practical applications, increasing knowledge across diverse disciplines for early detection, diagnosis, and intervention, and identifying promising new research directions. In July 2008, Alzheimer's & Dementia was accepted for indexing by MEDLINE, recognizing its scientific merit and contribution to Alzheimer's research.