Association between growth differentiation factor-15 and adverse outcomes among patients with heart failure: A systematic literature review
Growth differentiation factor-15 (GDF-15) is an emerging biomarker in several conditions. This SLR, conducted following PRISMA guidelines, examined the association between GDF-15 concentration and range of adverse outcomes in patients with heart failure (HF). Publications were identified from Embase® and Medline® bibliographic databases between January 1, 2014, and August 23, 2022 (congress abstracts: January 1, 2020, to August 23, 2022). Sixty-three publications met the eligibility criteria (55 manuscripts and 8 abstracts; 45 observational studies and 18 post hoc analyses of randomized controlled trials [RCTs]). Of the 19 outcomes identified, the most frequently reported longitudinal outcomes were mortality (n = 32 studies; all-cause [n = 27] or cardiovascular-related [n = 6]), composite outcomes (n = 28; most commonly mortality ± hospitalization/rehospitalization [n = 19]), and hospitalization/re-hospitalization (n = 11). The most common cross-sectional outcome was renal function (n = 22). Among longitudinal studies assessing independent relationships with outcomes using multivariate analyses (MVA), a significant increase in risk associated with higher baseline GDF-15 concentration was found in 22/24 (92 %) studies assessing all-cause mortality, 4/5 (80 %) assessing cardiovascular-related mortality, 13/19 (68 %) assessing composite outcomes, and 4/8 (50 %) assessing hospitalization/rehospitalization. All (7/7; 100 %) of the cross-sectional studies assessing the relationship with renal function by MVA, and 3/4 (75 %) assessing exercise capacity, found poorer outcomes associated with higher baseline GDF-15 concentrations. This SLR suggests GDF-15 is an independent predictor of mortality and other adverse but nonfatal outcomes in patients with HF. A better understanding of the prognostic role of GDF-15 in HF could improve clinical risk prediction models and potentially help optimize treatment regimens.
Authors
- Ali Javaheri (ORCID: https://orcid.org/0000-0001-6657-331X)
- John D. Groarke (ORCID: https://orcid.org/0000-0002-5277-8696)
- Mualla Özcan (ORCID: https://orcid.org/0000-0002-1763-5454)
- Michelle I. Rossulek (ORCID: https://orcid.org/0009-0002-4478-9501)
- Karen E. Smoyer
- James H. Revkin (ORCID: https://orcid.org/0009-0000-5383-9879)
- Mikhail Kosiborod (ORCID: https://orcid.org/0000-0002-3750-9789)
- Lisa C. Tarasenko
- Lauren Moubarak
Institutions
- Pfizer (United States) (US)
- Washington University in St. Louis (US)
- Saint Luke's Hospital (US)
- John Cochran VA Medical Center (US)
- University of Missouri–Kansas City (US)
Publication Details
- Journal
- Heliyon
- Published
- 2024-08-01
- DOI
- https://doi.org/10.1016/j.heliyon.2024.e35916
- Citations
- 9
- Primary Topic
- GDF15 and Related Biomarkers
- Type
- article
- Field-Weighted Citation Impact
- 4.23
Funders
- Longer Life Foundation
- Pfizer
- St. Louis Children's Hospital
- Children's Discovery and Innovation Institute, University of California, Los Angeles