biostudies-literatureZuriaga MAAEIPRTRNHLBI NIH HHSPro CNIC FoundationERDF/EUMICIUNational Human Genome Research InstituteESF Investing in your future‘La Marató TV3’American Heart Association'la CaixaMICINInstituto de Salud Carlos IIIMinisterio de Ciencia, Innovación y UniversidadesNHGRI NIH HHSLeducq FoundationEuropean Union NextGenerationEUSevero Ochoa Center of ExcellenceU.S. National Heart, Lung, and Blood Institute'La Marató TV3'‘la CaixaJapan Society for the Promotion of Science4601-4615https://www.ebi.ac.uk/biostudies/studies/S-EPMC11560281biostudies-literatureUnknown45(43)<h4>Background and aims</h4>Somatic mutations in the TET2 gene that lead to clonal haematopoiesis (CH) are associated with accelerated atherosclerosis development in mice and a higher risk of atherosclerotic disease in humans. Mechanistically, these observations have been linked to exacerbated vascular inflammation. This study aimed to evaluate whether colchicine, a widely available and inexpensive anti-inflammatory drug, prevents the accelerated atherosclerosis associated with TET2-mutant CH.<h4>Methods</h4>In mice, TET2-mutant CH was modelled using bone marrow transplantations in atherosclerosis-prone Ldlr-/- mice. Haematopoietic chimeras carrying initially 10% Tet2-/- haematopoietic cells were fed a high-cholesterol diet and treated with colchicine or placebo. In humans, whole-exome sequencing data and clinical data from 37 181 participants in the Mass General Brigham Biobank and 437 236 participants in the UK Biobank were analysed to examine the potential modifying effect of colchicine prescription on the relationship between CH and myocardial infarction.<h4>Results</h4>Colchicine prevented accelerated atherosclerosis development in the mouse model of TET2-mutant CH, in parallel with suppression of interleukin-1β overproduction in conditions of TET2 loss of function. In humans, patients who were prescribed colchicine had attenuated associations between TET2 mutations and myocardial infarction. This interaction was not observed for other mutated genes.<h4>Conclusions</h4>These results highlight the potential value of colchicine to mitigate the higher cardiovascular risk of carriers of somatic TET2 mutations in blood cells. These observations set the basis for the development of clinical trials that evaluate the efficacy of precision medicine approaches tailored to the effects of specific mutations linked to CH.European heart journalColchicine prevents accelerated atherosclerosis in TET2-mutant clonal haematopoiesis.PMC11560281K08HL166687FJC2020-042841-IR01 HL148050PID2021-126580OB-I00K99HL165024LCF/PR/HR17/52150007TNE-18CVD04FPU18/02913K99HG012956940166R01HL148050PRE2019-087829CEX2020-001041-SPLEC2021-008194202314-31LCF/PR/HR22/52420011K08 HL166687RYC-2016-20026K99 HG012956979465Amoros-Perez MZuriaga MAFuster JJMatesanz NNakao TMoro REbert BLTruong BZorita VHonigberg MCPascual-Figal DAsensio-Lopez MCUddin MMNiroula AYu ZNatarajan PRamos-Neble BLfalseColchicine prevents accelerated atherosclerosis in TET2-mutant clonal haematopoiesis.<h4>Background and aims</h4>Somatic mutations in the TET2 gene that lead to clonal haematopoiesis (CH) are associated with accelerated atherosclerosis development in mice and a higher risk of atherosclerotic disease in humans. Mechanistically, these observations have been linked to exacerbated vascular inflammation. This study aimed to evaluate whether colchicine, a widely available and inexpensive anti-inflammatory drug, prevents the accelerated atherosclerosis associated with TET2-mutant CH.<h4>Methods</h4>In mice, TET2-mutant CH was modelled using bone marrow transplantations in atherosclerosis-prone Ldlr-/- mice. Haematopoietic chimeras carrying initially 10% Tet2-/- haematopoietic cells were fed a high-cholesterol diet and treated with colchicine or placebo. In humans, whole-exome sequencing data and clinical data from 37 181 participants in the Mass General Brigham Biobank and 437 236 participants in the UK Biobank were analysed to examine the potential modifying effect of colchicine prescription on the relationship between CH and myocardial infarction.<h4>Results</h4>Colchicine prevented accelerated atherosclerosis development in the mouse model of TET2-mutant CH, in parallel with suppression of interleukin-1β overproduction in conditions of TET2 loss of function. In humans, patients who were prescribed colchicine had attenuated associations between TET2 mutations and myocardial infarction. This interaction was not observed for other mutated genes.<h4>Conclusions</h4>These results highlight the potential value of colchicine to mitigate the higher cardiovascular risk of carriers of somatic TET2 mutations in blood cells. These observations set the basis for the development of clinical trials that evaluate the efficacy of precision medicine approaches tailored to the effects of specific mutations linked to CH.2024-01-01T00:00:00Z2024 Nov2025-04-04T00:38:39.807Z2025-04-04T00:38:39.807ZS-EPMC115602813921293310.1093/eurheartj/ehae546