Clonal hematopoiesis is associated with protection from Alzheimer’s disease

痴呆 生物 疾病 孟德尔随机化 髓系白血病 造血 小胶质细胞 髓样 DNA甲基化 免疫学 医学 遗传学 干细胞 基因型 内科学 基因 基因表达 炎症 遗传变异
作者
Hind Bouzid,Julia A. Belk,Max Jan,Yanyan Qi,Chloé Sarnowski,Sara Wirth,Lisa Ma,Matthew R. Chrostek,Herra Ahmad,Daniel Nachun,Winnie Yao,Joshua C. Bis,Bruce M. Psaty,Alexa S. Beiser,Alexander G. Bick,Joshua C. Bis,Myriam Fornage,W.T. Longstreth,Oscar L. López,Pradeep Natarajan,Bruce M. Psaty,Claudia L. Satizábal,Joshua S. Weinstock,Eric B. Larson,Paul K. Crane,C. Dirk Keene,Sudha Seshadri,Ansuman T. Satpathy,Thomas J. Montine,Siddhartha Jaiswal
出处
期刊:Nature Medicine [Nature Portfolio]
卷期号:29 (7): 1662-1670 被引量:65
标识
DOI:10.1038/s41591-023-02397-2
摘要

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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