TY - JOUR
T1 - Effect of Clonal Hematopoiesis on Cardiovascular Disease in People Living with HIV
AU - Wiley, Brian
AU - Parsons, Tyler M.
AU - Burkart, Samantha
AU - Young, Andrew L.
AU - Erlandson, Kristine M.
AU - Tassiopoulos, Katherine K.
AU - Wu, Kunling
AU - Gurnett, Christina
AU - Presti, Rachel M.
AU - Bolton, Kelly L.
AU - Challen, Grant A.
N1 - Publisher Copyright:
© 2022 ISEH – Society for Hematology and Stem Cells
PY - 2022/10
Y1 - 2022/10
N2 - Hematopoietic stem cells (HSCs) with age-associated somatic mutations that disproportionally contribute to hematopoiesis generate the condition known as clonal hematopoiesis (CH). While CH conveys increased risk of hematologic cancer, there is also strong association between CH and cardiovascular disease (CVD). Accumulating evidence suggests that inflammation mechanistically links CH to CVD, and we hypothesized that CH may be a predictive biomarker of CVD in conditions of chronic inflammation. One such patient population comprises people living with HIV (PLWH) who also have substantially increased incidences of CVD and CH. We studied the association between CH and CVD in PLWH using samples from ACTG Study A5001 (or ALLRT), a prospective clinical trial of HIV-infected persons with long-term follow-up. We observed a positive association between CH and CVD in PLWH independent of traditional CVD risk factors. Moreover, in CVD cases, the CH clone was identifiable in the blood years before CVD diagnosis, unlike in PLWH with CH who did not have CVD. With the life span of PLWH increasing because of advances in treatment, our results indicate that the presence of CH and its clonal dynamics could be used as a prognostic biomarker of the risk for CVD in PLWH.
AB - Hematopoietic stem cells (HSCs) with age-associated somatic mutations that disproportionally contribute to hematopoiesis generate the condition known as clonal hematopoiesis (CH). While CH conveys increased risk of hematologic cancer, there is also strong association between CH and cardiovascular disease (CVD). Accumulating evidence suggests that inflammation mechanistically links CH to CVD, and we hypothesized that CH may be a predictive biomarker of CVD in conditions of chronic inflammation. One such patient population comprises people living with HIV (PLWH) who also have substantially increased incidences of CVD and CH. We studied the association between CH and CVD in PLWH using samples from ACTG Study A5001 (or ALLRT), a prospective clinical trial of HIV-infected persons with long-term follow-up. We observed a positive association between CH and CVD in PLWH independent of traditional CVD risk factors. Moreover, in CVD cases, the CH clone was identifiable in the blood years before CVD diagnosis, unlike in PLWH with CH who did not have CVD. With the life span of PLWH increasing because of advances in treatment, our results indicate that the presence of CH and its clonal dynamics could be used as a prognostic biomarker of the risk for CVD in PLWH.
UR - http://www.scopus.com/inward/record.url?scp=85137040544&partnerID=8YFLogxK
U2 - 10.1016/j.exphem.2022.07.304
DO - 10.1016/j.exphem.2022.07.304
M3 - Article
C2 - 35940373
AN - SCOPUS:85137040544
SN - 0301-472X
VL - 114
SP - 18
EP - 21
JO - Experimental Hematology
JF - Experimental Hematology
ER -