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Genetic architecture of cardiometabolic risks in people living with HIV.
Cheng, Haoxiang; Sewda, Anshuman; Marquez-Luna, Carla; White, Sierra R; Whitney, Bridget M; Williams-Nguyen, Jessica; Nance, Robin M; Lee, Won Jun; Kitahata, Mari M; Saag, Michael S; Willig, Amanda; Eron, Joseph J; Mathews, W Christopher; Hunt, Peter W; Moore, Richard D; Webel, Allison; Mayer, Kenneth H; Delaney, Joseph A; Crane, Paul K; Crane, Heidi M; Hao, Ke; Peter, Inga.
Affiliation
  • Cheng H; Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, 1425 Madison Avenue, New York, NY, 10029, United States of America.
  • Sewda A; Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, 1425 Madison Avenue, New York, NY, 10029, United States of America.
  • Marquez-Luna C; Institute of Health Management Research, IIHMR University, Jaipur, Rajasthan, India.
  • White SR; The Charles Bronfman Institute for Personalized Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, United States of America.
  • Whitney BM; Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, 1425 Madison Avenue, New York, NY, 10029, United States of America.
  • Williams-Nguyen J; Department of Epidemiology, University of Washington School of Public Health, Seattle, WA, United States of America.
  • Nance RM; Department of Epidemiology, University of Washington School of Public Health, Seattle, WA, United States of America.
  • Lee WJ; Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, 1425 Madison Avenue, New York, NY, 10029, United States of America.
  • Kitahata MM; Department of Medicine, University of Washington School of Medicine, Seattle, WA, United States of America.
  • Saag MS; Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, 1425 Madison Avenue, New York, NY, 10029, United States of America.
  • Willig A; Department of Medicine, University of Washington School of Medicine, Seattle, WA, United States of America.
  • Eron JJ; Center for AIDS Research, University of Washington, Seattle, WA, United States of America.
  • Mathews WC; School of Medicine, University of Alabama at Birmingham, Birmingham, AL, United States of America.
  • Hunt PW; School of Medicine, University of Alabama at Birmingham, Birmingham, AL, United States of America.
  • Moore RD; Department of Medicine, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC, 27514, United States of America.
  • Webel A; Department of Medicine, University of California San Diego, San Diego, CA, United States of America.
  • Mayer KH; Division of Experimental Medicine, University of California San Francisco, San Francisco, CA, United States of America.
  • Delaney JA; Department of Medicine, Johns Hopkins University, Baltimore, MD, United States of America.
  • Crane PK; Department of Epidemiology, |Johns Hopkins University, Baltimore, MD, United States of America.
  • Crane HM; Frances Payne Bolton School of Nursing, Case Western Reserve University, Cleveland, OH, United States of America.
  • Hao K; The Fenway Institute at Fenway Health, Boston, MA, United States of America.
  • Peter I; Department of Epidemiology, University of Washington School of Public Health, Seattle, WA, United States of America.
BMC Med ; 18(1): 288, 2020 10 28.
Article in En | MEDLINE | ID: mdl-33109212
ABSTRACT

BACKGROUND:

Advances in antiretroviral therapies have greatly improved the survival of people living with human immunodeficiency virus (HIV) infection (PLWH); yet, PLWH have a higher risk of cardiovascular disease than those without HIV. While numerous genetic loci have been linked to cardiometabolic risk in the general population, genetic predictors of the excessive risk in PLWH are largely unknown.

METHODS:

We screened for common and HIV-specific genetic variants associated with variation in lipid levels in 6284 PLWH (3095 European Americans [EA] and 3189 African Americans [AA]), from the Centers for AIDS Research Network of Integrated Clinical Systems cohort. Genetic hits found exclusively in the PLWH cohort were tested for association with other traits. We then assessed the predictive value of a series of polygenic risk scores (PRS) recapitulating the genetic burden for lipid levels, type 2 diabetes (T2D), and myocardial infarction (MI) in EA and AA PLWH.

RESULTS:

We confirmed the impact of previously reported lipid-related susceptibility loci in PLWH. Furthermore, we identified PLWH-specific variants in genes involved in immune cell regulation and previously linked to HIV control, body composition, smoking, and alcohol consumption. Moreover, PLWH at the top of European-based PRS for T2D distribution demonstrated a > 2-fold increased risk of T2D compared to the remaining 95% in EA PLWH but to a much lesser degree in AA. Importantly, while PRS for MI was not predictive of MI risk in AA PLWH, multiethnic PRS significantly improved risk stratification for T2D and MI.

CONCLUSIONS:

Our findings suggest that genetic loci involved in the regulation of the immune system and predisposition to risky behaviors contribute to dyslipidemia in the presence of HIV infection. Moreover, we demonstrate the utility of the European-based and multiethnic PRS for stratification of PLWH at a high risk of cardiometabolic diseases who may benefit from preventive therapies.
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Full text: 1 Database: MEDLINE Main subject: HIV Infections / Genome-Wide Association Study / Cardiometabolic Risk Factors Type of study: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Female / Humans / Male / Middle aged Language: En Year: 2020 Type: Article

Full text: 1 Database: MEDLINE Main subject: HIV Infections / Genome-Wide Association Study / Cardiometabolic Risk Factors Type of study: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Female / Humans / Male / Middle aged Language: En Year: 2020 Type: Article