髓样
造血
体细胞
生物
癌症的体细胞进化
免疫学
谱系(遗传)
干细胞
癌症
基因
遗传学
作者
Abhishek Niroula,Aswin Sekar,Mark A. Murakami,Mark Trinder,Mridul Agrawal,Waihay J. Wong,Alexander G. Bick,Md Mesbah Uddin,Christopher J. Gibson,Gabriel K. Griffin,Michael C. Honigberg,Seyedeh M. Zekavat,Kaavya Paruchuri,Pradeep Natarajan,Benjamin L. Ebert
出处
期刊:Nature Medicine
[Nature Portfolio]
日期:2021-10-18
卷期号:27 (11): 1921-1927
被引量:281
标识
DOI:10.1038/s41591-021-01521-4
摘要
Clonal hematopoiesis (CH) results from somatic genomic alterations that drive clonal expansion of blood cells. Somatic gene mutations associated with hematologic malignancies detected in hematopoietic cells of healthy individuals, referred to as CH of indeterminate potential (CHIP), have been associated with myeloid malignancies, while mosaic chromosomal alterations (mCAs) have been associated with lymphoid malignancies. Here, we analyzed CHIP in 55,383 individuals and autosomal mCAs in 420,969 individuals with no history of hematologic malignancies in the UK Biobank and Mass General Brigham Biobank. We distinguished myeloid and lymphoid somatic gene mutations, as well as myeloid and lymphoid mCAs, and found both to be associated with risk of lineage-specific hematologic malignancies. Further, we performed an integrated analysis of somatic alterations with peripheral blood count parameters to stratify the risk of incident myeloid and lymphoid malignancies. These genetic alterations can be readily detected in clinical sequencing panels and used with blood count parameters to identify individuals at high risk of developing hematologic malignancies. Genomic analyses in the UK Biobank show that clonal hematopoiesis of indeterminate potential in the lymphoid lineage is associated with a higher risk of developing lymphoid malignancies
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