The Novel Biomarker Growth Differentiation Factor-15 in Patients with Chronic Heart Failure at a Heart Failure Clinic in the Asia-Pacific Region: A Prospective Observational Study

Author:

Cham Yee Ling1ORCID,Fong Alan Yean Yip2ORCID,Chung Joshua Bui Kiong1ORCID,Ling Hwei Sung3ORCID,Pang Ing Xiang3ORCID,Thien Lee Karl1ORCID,Chow Han Bin3ORCID,Chan Issac En Zhe3ORCID,Shu Francis Eng Pbeng1ORCID,Tan Chen Ting1ORCID,Koh Keng Tat1ORCID,Oon Yen Yee1ORCID,Said Asri3ORCID,Ong Tiong Kiam1ORCID

Affiliation:

1. Department of Cardiology, Sarawak Heart Center, Kota Samarahan, Sarawak, Malaysia

2. Department of Cardiology, Sarawak Heart Center, Kota Samarahan, Sarawak, Malaysia; Clinical Research Center, Sarawak General Hospital, Kuching, Sarawak, Malaysia

3. Department of Medicine, University Malaysia Sarawak, Kota Samarahan, Sarawak, Malaysia

Abstract

Background: Growth differentiation factor-15 (GDF-15) is an emerging prognostic biomarker in heart failure (HF). However, there are limited data on its role in HF patients in southeast Asia. This prospective observational study investigated the association between GDF-15 and various clinical parameters, and its role in predicting all-cause mortality. Methods: 160 patients with chronic HF and reduced left ventricular ejection fraction (LVEF) enrolled between October 2020 and April 2021. At study entry, baseline GDF-15 and N-terminal pro B-type natriuretic peptide (NT-proBNP) were evaluated. Patients were followed up per clinical routine. Results: The median GDF-15 was 1,715 ng/l. Patients were divided into two groups: GDF-15 <2,000 or ≥2,000 ng/l. This cut-off has been shown to represent prognostic threshold in previous studies. The GDF-15 ≥2,000 group was older, had more severe HF and higher comorbidity burden, and lower use of renin–angiotensin–aldosterone system inhibitors (RAASi). GDF-15 was positively correlated with a history of MI, diabetes, chronic kidney disease and use of loop diuretics, but negatively correlated with RAAsi use. GDF-15 ≥2,000 was not associated with all-cause mortality at 60 weeks. The pooled stratum of GDF-15 ≥2,000/NT-proBNP ≥1,000 pg/ml had significantly higher mortality than GDF-15 <2,000/NT-proBNP <1,000 pg/ml. NT-proBNP and the Meta-Analysis Global Group In Chronic risk score but not GDF-15, were independently predictive of all-cause mortality. Conclusion: In our cohort of chronic HF patients with reduced LVEF who were relatively younger than the cohorts studied in previous GDF-15 in HF trials, well-managed and largely asymptomatic, GDF-15 did not independently predict all-cause mortality. The prognostic cut-off of GDF-15 ≥2,000 ng/l was not significantly associated with higher all-cause mortality at 60 weeks.

Publisher

Radcliffe Media Media Ltd

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