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Clonal hematopoiesis is associated with protection from Alzheimer's disease.
Bouzid, Hind; Belk, Julia A; Jan, Max; Qi, Yanyan; Sarnowski, Chloé; Wirth, Sara; Ma, Lisa; Chrostek, Matthew R; Ahmad, Herra; Nachun, Daniel; Yao, Winnie; Beiser, Alexa; Bick, Alexander G; Bis, Joshua C; Fornage, Myriam; Longstreth, William T; Lopez, Oscar L; Natarajan, Pradeep; Psaty, Bruce M; Satizabal, Claudia L; Weinstock, Joshua; Larson, Eric B; Crane, Paul K; Keene, C Dirk; Seshadri, Sudha; Satpathy, Ansuman T; Montine, Thomas J; Jaiswal, Siddhartha.
Afiliação
  • Bouzid H; Department of Pathology, Stanford University School of Medicine, Stanford, CA, USA.
  • Belk JA; Department of Computer Science, Stanford University, Stanford, CA, USA.
  • Jan M; Department of Pathology, Massachusetts General Hospital, Boston, MA, USA.
  • Qi Y; Department of Pathology, Stanford University School of Medicine, Stanford, CA, USA.
  • Sarnowski C; Department of Epidemiology, Human Genetics and Environmental Sciences, The University of Texas Health Science Center at Houston, School of Public Health, Houston, TX, USA.
  • Wirth S; Department of Pathology, Stanford University School of Medicine, Stanford, CA, USA.
  • Ma L; Department of Pathology, Stanford University School of Medicine, Stanford, CA, USA.
  • Chrostek MR; Department of Pathology, Stanford University School of Medicine, Stanford, CA, USA.
  • Ahmad H; Department of Pathology, Stanford University School of Medicine, Stanford, CA, USA.
  • Nachun D; Department of Cardiology, Charité Universitätsmedizin, Berlin, Germany.
  • Yao W; Department of Pathology, Stanford University School of Medicine, Stanford, CA, USA.
  • Bick AG; Department of Biostatistics, Boston University School of Public Health, Boston, MA, USA.
  • Bis JC; Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
  • Fornage M; Cardiovascular Health Research Unit, Department of Medicine, University of Washington, Seattle, WA, USA.
  • Longstreth WT; Brown Foundation Institute of Molecular Medicine, McGovern Medical School, University of Texas Health Science Center at Houston, Houston, TX, USA.
  • Lopez OL; Departments of Neurology and Epidemiology, University of Washington, Seattle, WA, USA.
  • Natarajan P; Department of Neurology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
  • Psaty BM; Medical and Population Genetics and Cardiovascular Disease Initiative, Broad Institute of Harvard and MIT, Cambridge, MA, USA.
  • Satizabal CL; Cardiovascular Research Center, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
  • Weinstock J; Cardiovascular Health Research Unit, Departments of Medicine, Epidemiology, and Health Systems and Population Health, University of Washington, Seattle, WA, USA.
  • Larson EB; Glenn Biggs Institute for Alzheimer's & Neurodegenerative Diseases, University of Texas Health Science Center, San Antonio, TX, USA.
  • Crane PK; Department of Population Health Sciences, University of Texas Health Science Center, San Antonio, TX, USA.
  • Keene CD; Department of Neurology, Boston University School of Medicine, Boston, MA, USA.
  • Seshadri S; Center for Statistical Genetics, Department of Biostatistics, University of Michigan School of Public Health, Ann Arbor, MI, USA.
  • Satpathy AT; Kaiser Permanente Washington Health Research Institute, Seattle, WA, USA.
  • Montine TJ; Department of Medicine, University of Washington, Seattle, WA, USA.
  • Jaiswal S; Department of Laboratory Medicine and Pathology, University of Washington, Seattle, WA, USA.
Nat Med ; 29(7): 1662-1670, 2023 07.
Article em En | MEDLINE | ID: mdl-37322115
ABSTRACT
Clonal hematopoiesis of indeterminate potential (CHIP) is a premalignant expansion of mutated hematopoietic stem cells. As CHIP-associated mutations are known to alter the development and function of myeloid cells, we hypothesized that CHIP may also be associated with the risk of Alzheimer's disease (AD), a disease in which brain-resident myeloid cells are thought to have a major role. To perform association tests between CHIP and AD dementia, we analyzed blood DNA sequencing data from 1,362 individuals with AD and 4,368 individuals without AD. Individuals with CHIP had a lower risk of AD dementia (meta-analysis odds ratio (OR) = 0.64, P = 3.8 × 10-5), and Mendelian randomization analyses supported a potential causal association. We observed that the same mutations found in blood were also detected in microglia-enriched fraction of the brain in seven of eight CHIP carriers. Single-nucleus chromatin accessibility profiling of brain-derived nuclei in six CHIP carriers revealed that the mutated cells comprised a large proportion of the microglial pool in the samples examined. While additional studies are required to validate the mechanistic findings, these results suggest that CHIP may have a role in attenuating the risk of AD.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Lesões Pré-Cancerosas / Doença de Alzheimer Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Lesões Pré-Cancerosas / Doença de Alzheimer Idioma: En Ano de publicação: 2023 Tipo de documento: Article