Circulating bone morphogenetic protein 10 as a novel marker of atrial stress and remodelling in heart failure

医学 心力衰竭 内科学 心脏病学 比例危险模型 心房颤动 队列 利钠肽 队列研究 生物标志物 骨形态发生蛋白 基因 生物化学 化学
作者
Daan Ceelen,Valentina Bračun,Bart J van Essen,Adriaan A. Voors,Rudolf A. de Boer,Jozine M. ter Maaten,Serge Masson,Peter Kastner,Chim C. Lang,Navin Suthahar
出处
期刊:Heart [BMJ]
卷期号:: heartjnl-324486
标识
DOI:10.1136/heartjnl-2024-324486
摘要

Background We evaluated the potential of circulating bone morphogenetic protein 10 (BMP10) as a biomarker for atrial stress and remodelling in patients with heart failure (HF), in comparison to N-terminal pro-B-type natriuretic peptide (NT-proBNP). We also assessed the predictive value of BMP10 for adverse clinical outcomes. Methods BMP10 levels were quantified in 2085 chronic HF patients from the European BIOlogy Study to TAilored Treatment in Chronic Heart Failure (BIOSTAT-CHF) cohort and in 1487 patients from the Scottish validation cohort. Multivariable linear regression identified independent associates of BMP10. Proteomic analysis of 6369 proteins with subsequent gene set enrichment analysis was used to explore biological pathways associated with elevated BMP10. Cox proportional hazards models adjusting for established risk factors were used to associate BMP10 levels with clinical outcomes, including all-cause mortality and HF hospitalisation. Results In a multivariable model including clinical and echocardiographic parameters, log-transformed and standardised BMP10 levels were significantly associated with a history of atrial fibrillation (Sβ=0.419; p<0.001), and with echocardiographic features reflecting atrial stress, such as increased left atrial diameter (Sβ=0.075; p=0.048). By contrast, these were not among the strongest associates of NT-proBNP levels. Gene set enrichment analysis showed significant overrepresentation in pathways of muscle contraction and extracellular matrix organisation. Higher log-transformed and standardised BMP10 levels predicted a combined outcome of 2-year all-cause mortality and HF rehospitalisation (HR=1.10, 95% CI=1.02–1.19), with the validation cohort yielding comparable results. Conclusion BMP10 emerges as a novel biomarker reflecting atrial stress and remodelling in chronic HF patients. Its additional predictive value for adverse outcomes underscores its potential utility in enhancing risk stratification and guiding therapeutic interventions in HF management.

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