Clonal hematopoiesis is associated with protection from Alzheimer’s disease

Hind Bouzid(Stanford University), Julia A. Belk(Stanford University), Max Jan(Massachusetts General Hospital), Yanyan Qi(Stanford University), Chloé Sarnowski(The University of Texas Health Science Center at Houston), Sara A. Wirth(Stanford University), Lisa Ma(Stanford University), Matthew R. Chrostek(Stanford University), Herra Ahmad(Charité - Universitätsmedizin Berlin), Daniel Nachun(Stanford University), Winnie Yao(Stanford University), Joshua C. Bis(University of Washington), Bruce M. Psaty(University of Washington), Alexa Beiser(Boston University), Alexander G. Bick(Vanderbilt University Medical Center), Joshua C. Bis(University of Washington), Myriam Fornage(Brown Foundation), W.T. Longstreth(University of Washington), Oscar L. López(University of Pittsburgh), Pradeep Natarajan(Broad Institute), Bruce M. Psaty(University of Washington), Claudia L. Satizábal(Boston University), Joshua S. Weinstock(University of Michigan), Eric B. Larson(Kaiser Permanente Washington Health Research Institute), Paul K. Crane(University of Washington), C. Dirk Keene(University of Washington), Sudha Seshadri(The University of Texas at San Antonio Health Science Center), Ansuman T. Satpathy(Stanford University), Thomas J. Montine(Stanford University), Siddhartha Jaiswal(Neurosciences Institute)
Nature Medicine
June 15, 2023
Cited by 145Open Access
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Abstract

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.


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