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Evaluation of Mineralocorticoid Receptor Antagonism on Changes in NT-proBNP Among Persons With HIV.
Srinivasa, Suman; deFilippi, Christopher; Fitch, Kathleen V; Iyengar, Sanjna; Shen, Grace; Burdo, Tricia H; Walpert, Allie R; Thomas, Teressa S; Adler, Gail K; Grinspoon, Steven K.
Affiliation
  • Srinivasa S; Metabolism Unit, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114, USA.
  • deFilippi C; INOVA Heart and Vascular Institute, Falls Church, VA 22042, USA.
  • Fitch KV; Metabolism Unit, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114, USA.
  • Iyengar S; Metabolism Unit, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114, USA.
  • Shen G; Metabolism Unit, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114, USA.
  • Burdo TH; Department of Neuroscience, Lewis Katz School of Medicine at Temple University, Philadelphia, PA 19140, USA.
  • Walpert AR; Metabolism Unit, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114, USA.
  • Thomas TS; Metabolism Unit, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114, USA.
  • Adler GK; Division of Endocrinology, Diabetes, and Hypertension, Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115, USA.
  • Grinspoon SK; Metabolism Unit, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114, USA.
J Endocr Soc ; 6(1): bvab175, 2022 Jan 01.
Article in En | MEDLINE | ID: mdl-34909518
Subclinical myocardial dysfunction is prevalent among well-treated persons with HIV (PWH). We have previously demonstrated unique renin-angiotensin-aldosterone system physiology among PWH with metabolic dysregulation. Mineralocorticoid receptor blockade may be a targeted treatment strategy for subclinical heart disease in PWH. Forty-six PWH were randomized to receive either eplerenone 50 mg daily or placebo in a 6-month randomized, double-blinded, placebo-controlled trial. We assessed changes in N-terminal pro-B-type natriuretic peptide (NT-proBNP), a biomarker of cardiac stretch, under controlled posture and dietary conditions. The eplerenone- and placebo-treated groups demonstrated a long duration of HIV with good immunological control. NT-proBNP levels were similar between the groups at baseline (41.1 [20.2, 97.9] vs 48.9 [29.2, 65.4] ng/L, P = .80) and decreased significantly more in the eplerenone- vs placebo-treated groups after 6 months (change NT-proBNP -9.6 [-46.8, 0.3] vs -3.0 [-17.0, 39.9] ng/L, P = .02 for comparison of change between groups). Decreases in NT-proBNP were independent of changes in systolic and diastolic blood pressure, and related to decreases in high-sensitivity C-reactive protein (ρ = 0.32, P = .05) and inversely to increases in serum aldosterone (ρ = -0.33, P = .04) among all participants. Treatment with eplerenone for 6 months vs placebo significantly decreases NT-proBNP levels among PWH, independent of eplerenone's known blood pressure-lowering effects. Further studies should elucidate whether lowering NT-proBNP in this at-risk metabolic population with subclinical heart disease will offer cardioprotection. CLINICAL TRIAL REGISTRATION: NCT01405456.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Clinical_trials Language: En Journal: J Endocr Soc Year: 2022 Document type: Article Affiliation country: United States Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Clinical_trials Language: En Journal: J Endocr Soc Year: 2022 Document type: Article Affiliation country: United States Country of publication: United States