Key result
HIV infection is linked to ~2-fold higher prevalence of CHIP compared to controls.
Why the study?
People living with HIV have increased cardiovascular risk potentially linked to inflammation and immune dysregulation, and the prevalence of clonal hematopoiesis of indeterminate potential (CHIP) in this population was unknown.
Do people living with HIV have a greater prevalence of clonal hematopoiesis of indeterminate potential (CHIP) compared to controls?
Case-Control (n=8,711)
Yes
Do people living with HIV have a greater prevalence of clonal hematopoiesis of indeterminate potential (CHIP) compared to controls?
Absolute Event Rate: 7% vs 3%
p-value: p=0.005
People living with HIV have a significantly higher prevalence of CHIP, which may contribute to their excess cardiovascular risk.
People living with human immunodeficiency virus (PLWH) have significantly increased risk for cardiovascular disease in part due to inflammation and immune dysregulation. Clonal hematopoiesis of indeterminate potential (CHIP), the age-related acquisition and expansion of hematopoietic stem cells due to leukemogenic driver mutations, increases risk for both hematologic malignancy and coronary artery disease (CAD). Since increased inflammation is hypothesized to be both a cause and consequence of CHIP, we hypothesized that PLWH have a greater prevalence of CHIP. We searched for CHIP in multi-ethnic cases from the Swiss HIV Cohort Study (SHCS, n = 600) and controls from the Atherosclerosis Risk in the Communities study (ARIC, n = 8111) from blood DNA-derived exome sequences. We observed that HIV is associated with a twofold increase in CHIP prevalence, both in the whole study population and in a subset of 230 cases and 1002 matched controls selected by propensity matching to control for demographic imbalances (SHCS 7%, ARIC 3%, p = 0.005). We also observed that ASXL1 is the most commonly mutated CHIP-associated gene in PLWH. Our results suggest that CHIP may contribute to the excess cardiovascular risk observed in PLWH.
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Bick et al. (2022) conducted a case-control in HIV (n=8,711). HIV infection vs. Controls without HIV was evaluated on Prevalence of clonal hematopoiesis of indeterminate potential (CHIP) (p=0.005). HIV infection was associated with a significantly higher prevalence of clonal hematopoiesis of indeterminate potential compared to matched controls (7% vs 3%, p=0.005).
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