Novel Endocrine Signaling Axis in Cardiovascular‐Kidney‐Metabolic Syndrome: Interactions and Therapeutic Potential of FGF21 and GDF15
Cardiovascular-Kidney-Metabolic Syndrome (CKM) is a multisystem disorder characterized by interdependent cardiovascular, renal, and metabolic dysfunction. It commonly involves metabolic conditions such as type 2 diabetes and obesity and is associated with substantial morbidity and mortality Recently, stress-induced hormone-like cytokines, fibroblast growth factor 21 (FGF21) and growth differentiation factor 15 (GDF15), are emerging as the central two-controllers of the pathophysiological network of CKM. This review is a systemic summary of the biological functions and mechanism of interaction between FGF21 and GDF15 in CKM with a focus on the functions of these two hormones in regulating energy metabolism, insulin sensitivity, inflammation, fibrosis, and cardiovascular protection. We examine their clinical relevance as disease biomarkers and discuss their prospective potential as newer therapeutic targets, in addition to discussing the obstacles that are still in the way of our translations of these findings into therapeutic application. This article will elucidate shared and distinct actions of FGF21 and GDF15 and thereby offer a thorough comprehension of integrative endocrine signaling axis output, as well as its implication to further the development of CKM management.
Authors
- Yi Ma (ORCID: https://orcid.org/0000-0003-2351-9537)
- Hong Xiao
- Changlong Yang
- Jiafei Liang
- Wanghang Wei (ORCID: https://orcid.org/0009-0000-8776-7076)
- Tao Yang
- Lei Chen
- Tao Chen
Institutions
- Guangzhou University of Chinese Medicine (CN)
- Zunyi Medical University (CN)
- Chinese University of Hong Kong, Shenzhen (CN)
- University of Hong Kong - Shenzhen Hospital (CN)
- Affiliated Hospital of Zunyi Medical College (CN)
- Shenzhen Second People's Hospital (CN)
Publication Details
- Journal
- Journal of Cellular Biochemistry
- Published
- 2026-07-28
- DOI
- https://doi.org/10.1002/jcb.70113
- Primary Topic
- GDF15 and Related Biomarkers
- Type
- article
- Field-Weighted Citation Impact
- 0.00