螺内酯
医学
内科学
心力衰竭
心脏病学
队列
射血分数
人口
生物标志物
射血分数保留的心力衰竭
内分泌学
利钠肽
生物
生物化学
环境卫生
作者
Masatake Kobayashi,João Pedro Ferreira,Kévin Duarte,Emmanuel Bresso,Olivier Huttin,Erwan Bozec,Hans‐Peter Brunner‐La Rocca,Christian Delles,Andrew L. Clark,Frank Edelmann,Arantxa González,Stéphane Heymans,Pierpaolo Pellicori,Johannes Petutschnigg,Job A.J. Verdonschot,Patrick Rossignol,John G.F. Cleland,Faı̈ez Zannad,Nicolas Girerd
摘要
Aims High left ventricular filling pressure increases left atrial volume and causes myocardial fibrosis, which may decrease with spironolactone. We studied clinical and proteomic characteristics associated with left atrial volume indexed by body surface area (LAVi), and whether LAVi influences the response to spironolactone on biomarker expression and clinical variables. Methods and results In the HOMAGE trial, where people at risk of heart failure were randomized to spironolactone or control, we analysed 421 participants with available LAVi and 276 proteomic measurements (Olink) at baseline, month 1 and 9 (mean age 73 ± 6 years; women 26%; LAVi 32 ± 9 ml/m 2 ). Circulating proteins associated with LAVi were also assessed in asymptomatic individuals from a population‐based cohort (STANISLAS; n = 1640; mean age 49 ± 14 years; women 51%; LAVi 23 ± 7 ml/m 2 ). In both studies, greater LAVi was significantly associated with greater left ventricular masses and volumes. In HOMAGE, after adjustment and correction for multiple testing, greater LAVi was associated with higher concentrations of matrix metallopeptidase‐2 (MMP‐2), insulin‐like growth factor binding protein‐2 (IGFBP‐2) and N‐terminal pro‐B‐type natriuretic peptide (NT‐proBNP) (false discovery rates [FDR] <0.05). These associations were externally replicated in STANISLAS (all FDR <0.05). Among these biomarkers, spironolactone decreased concentrations of MMP‐2 and NT‐proBNP, regardless of baseline LAVi ( p interaction > 0.10). Spironolactone also significantly reduced LAVi, improved left ventricular ejection fraction, lowered E/e', blood pressure and serum procollagen type I C‐terminal propeptide (PICP) concentration, a collagen synthesis marker, regardless of baseline LAVi ( p interaction > 0.10). Conclusion In individuals without heart failure, LAVi was associated with MMP‐2, IGFBP‐2 and NT‐proBNP. Spironolactone reduced these biomarker concentrations as well as LAVi and PICP, irrespective of left atrial size.
科研通智能强力驱动
Strongly Powered by AbleSci AI