Ontology highlight
ABSTRACT: Purpose
Solid organ transplant recipients comprise a unique population of immunosuppressed patients with increased risk of malignancy, including hematologic neoplasms. Clonal hematopoiesis of indeterminate potential (CHIP) represents a known risk factor for hematologic malignancy and this study describes the prevalence and patterns of CHIP mutations across several types of solid organ transplants.Experimental design
We use two national biobank cohorts comprised of >650,000 participants with linked genomic and longitudinal phenotypic data to describe the features of CHIP across 2,610 individuals who received kidney, liver, heart, or lung allografts.Results
We find individuals with an allograft before their biobank enrollment had an increased prevalence of TET2 mutati
SUBMITTER: Silver AJ
PROVIDER: S-EPMC12129112 | biostudies-literature | 2024 Jun
REPOSITORIES: biostudies-literature