Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
Metformin Does Not Significantly Alter Longitudinal Dynamics of Clonal Hematopoiesis.
СтатьяНазвание и аннотация: Перевод в очереди
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Pareek Eshani, Pershad Yash, Zhao Kun, Uddin Md Mesbah, Xue Liying, Vlasschaert Caitlyn, Mack Taralynn M, Haessler Jeffrey, Collins Jason M, Glick Elena, Glaser Veronica, Heise Rachel, Ling Wodan, Haring Bernhard, Shadyab Aladdin, Beydoun Hind, Wallace Robert, Jaiswal Siddhartha, Manson JoAnn E, Natarajan Pradeep, Honigberg Michael C, Kooperberg Charles, Whitsel Eric A, Kitzman Jacob O, Bick Alexander G, Reiner Alexander P, Desai Pinkal
Аннотация
PURPOSE: Early intervention in patients with clonal hematopoiesis (CH) is an area of intense investigation with no currently approved agents. With recent mechanistic data on metformin as a possible therapeutic agent in CH and its availability in clinical practice, we sought to investigate the clonal dynamics of CH mutations in metformin users.
EXPERIMENTAL DESIGN: We analyzed longitudinal targeted deep sequencing of 1,104 CH mutations in 863 metformin-treated type 2 diabetic participants in two longitudinal cohorts: the Women's Health Initiative (WHI) and BioVU, with blood collected at a median of 15.8 and 6.1 years apart, respectively.
RESULTS: Metformin duration (per 6 months) was not significantly associated with the overall CH growth rate in WHI [β = -0.05%/year; 95% confidence interval (CI), -0.11 to 0.01; P = 0.08; n = 543] and in BioVU (β = -0.09%/year; 95% CI, -0.22 to 0.05; P = 0.20; n = 561). Inverse variance-weighted random-effects meta-analysis demonstrated a small, statistically significant association (β = -0.06%/year; 95% CI, -0.11 to -0.002; P = 0.04; n = 1,104) without significant heterogeneity (P = 0.60). These results were similar when only considering DNMT3A and DNMT3A-R882 clones.
CONCLUSIONS: In our cohorts, the duration of metformin use among diabetic users was associated with a small reduction in CH growth rate (-0.06%/year), which is modest compared with typical DNMT3A clonal growth rates of 5% to 7% annually. Metformin's clinical utility for modulating clonal dynamics in real-world settings seems limited, and its clinical use for this indication requires further investigation in prospective studies.
EXPERIMENTAL DESIGN: We analyzed longitudinal targeted deep sequencing of 1,104 CH mutations in 863 metformin-treated type 2 diabetic participants in two longitudinal cohorts: the Women's Health Initiative (WHI) and BioVU, with blood collected at a median of 15.8 and 6.1 years apart, respectively.
RESULTS: Metformin duration (per 6 months) was not significantly associated with the overall CH growth rate in WHI [β = -0.05%/year; 95% confidence interval (CI), -0.11 to 0.01; P = 0.08; n = 543] and in BioVU (β = -0.09%/year; 95% CI, -0.22 to 0.05; P = 0.20; n = 561). Inverse variance-weighted random-effects meta-analysis demonstrated a small, statistically significant association (β = -0.06%/year; 95% CI, -0.11 to -0.002; P = 0.04; n = 1,104) without significant heterogeneity (P = 0.60). These results were similar when only considering DNMT3A and DNMT3A-R882 clones.
CONCLUSIONS: In our cohorts, the duration of metformin use among diabetic users was associated with a small reduction in CH growth rate (-0.06%/year), which is modest compared with typical DNMT3A clonal growth rates of 5% to 7% annually. Metformin's clinical utility for modulating clonal dynamics in real-world settings seems limited, and its clinical use for this indication requires further investigation in prospective studies.