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Survival Association of Angiotensin Inhibitors in Heart Failure With Reduced Ejection Fraction: Comparisons Using Self-Identified Race and Genomic Ancestry.
Luzum, Jasmine A; Edokobi, Ozioma; Dorsch, Michael P; Peterson, Edward; Liu, Bin; Gui, Hongsheng; Williams, L Keoki; Lanfear, David E.
Afiliación
  • Luzum JA; From the Department of Clinical Pharmacy, University of Michigan College of Pharmacy, Ann Arbor, Michigan; Center for Individualized and Genomic Medicine Research, Henry Ford Hospital, Detroit, Michigan. Electronic address: jluzum@umich.edu.
  • Edokobi O; From the Department of Clinical Pharmacy, University of Michigan College of Pharmacy, Ann Arbor, Michigan.
  • Dorsch MP; From the Department of Clinical Pharmacy, University of Michigan College of Pharmacy, Ann Arbor, Michigan.
  • Peterson E; Department of Public Health Sciences, Henry Ford Hospital, Detroit, Michigan.
  • Liu B; Department of Public Health Sciences, Henry Ford Hospital, Detroit, Michigan.
  • Gui H; Center for Individualized and Genomic Medicine Research, Henry Ford Hospital, Detroit, Michigan.
  • Williams LK; Center for Individualized and Genomic Medicine Research, Henry Ford Hospital, Detroit, Michigan; Department of Internal Medicine, Henry Ford Hospital, Detroit, Michigan.
  • Lanfear DE; Center for Individualized and Genomic Medicine Research, Henry Ford Hospital, Detroit, Michigan; Heart and Vascular Institute, Henry Ford Health System, Detroit, Michigan.
J Card Fail ; 28(2): 215-225, 2022 02.
Article en En | MEDLINE | ID: mdl-34425222
BACKGROUND: It remains unclear whether there is a racial disparity in the response to angiotensin inhibitors in patients with heart failure with reduced ejection fraction (HFrEF) and whether the role of genomic ancestry plays a part. Therefore, we compared survival rates associated with angiotensin inhibitors in patients with HFrEF by self-identified race and proportion of West African genomic ancestry. METHODS: Three datasets totaling 1153 and 1480 self-identified Black and White patients, respectively, with HFrEF were meta-analyzed (random effects model) for race-based analyses. One dataset had genomic data for ancestry analyses (416 and 369 self-identified Black and White patients, respectively). Cox proportional hazards regression, adjusted for propensity scores, assessed the association of angiotensin inhibitor exposure with all-cause mortality by self-identified race or proportion of West African genomic ancestry. RESULTS: In meta-analysis of self-identified race, adjusted hazard ratios (95% CI) for exposure to angiotensin inhibitors were similar in self-identified Black and White patients with HFrEF: 0.52 (0.31-0.85) P = 0.006 and 0.54 (0.42-0.71) P = 0.001, respectively. Results were similar when the proportion of West African genomic ancestry was > 80% or < 5%: 0.66 (0.34-1.25) P = 0.200 and 0.56 (0.26-1.23) P = 0.147, respectively. CONCLUSIONS: Among self-identified Black and White patients with HFrEF, reduction in all-cause mortality associated with exposure to angiotensin inhibitors was similar regardless of self-identified race or proportion of West African genomic ancestry.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Insuficiencia Cardíaca Tipo de estudio: Prognostic_studies / Risk_factors_studies / Systematic_reviews Límite: Humans Idioma: En Revista: J Card Fail Asunto de la revista: CARDIOLOGIA Año: 2022 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Insuficiencia Cardíaca Tipo de estudio: Prognostic_studies / Risk_factors_studies / Systematic_reviews Límite: Humans Idioma: En Revista: J Card Fail Asunto de la revista: CARDIOLOGIA Año: 2022 Tipo del documento: Article