Induction of cardiac FGF23/FGFR4 expression is associated with left ventricular hypertrophy in patients with chronic kidney disease
Language English Country England, Great Britain Media print-electronic
Document type Comparative Study, Journal Article
Grant support
R01 HL128714
NHLBI NIH HHS - United States
PubMed
26681731
PubMed Central
PMC6388939
DOI
10.1093/ndt/gfv421
PII: gfv421
Knihovny.cz E-resources
- Keywords
- Klotho, chronic kidney disease, fibroblast growth factor 23, fibroblast growth factor receptor 4, left ventricular hypertrophy,
- MeSH
- Biomarkers metabolism MeSH
- Renal Insufficiency, Chronic complications MeSH
- Child MeSH
- Fibroblast Growth Factors metabolism MeSH
- Fibroblast Growth Factor-23 MeSH
- Hypertrophy, Left Ventricular etiology metabolism pathology MeSH
- Humans MeSH
- Receptor, Fibroblast Growth Factor, Type 4 metabolism MeSH
- Retrospective Studies MeSH
- Case-Control Studies MeSH
- Check Tag
- Child MeSH
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Comparative Study MeSH
- Names of Substances
- Biomarkers MeSH
- FGF23 protein, human MeSH Browser
- FGFR4 protein, human MeSH Browser
- Fibroblast Growth Factors MeSH
- Fibroblast Growth Factor-23 MeSH
- Receptor, Fibroblast Growth Factor, Type 4 MeSH
BACKGROUND: In chronic kidney disease (CKD), serum concentrations of fibroblast growth factor 23 (FGF23) increase progressively as glomerular filtration rate declines, while renal expression of the FGF23 coreceptor Klotho decreases. Elevated circulating FGF23 levels are strongly associated with mortality and with left ventricular hypertrophy (LVH), which is a major cause of cardiovascular death in CKD patients. The cardiac FGF23/FGF receptor (FGFR) system and its role in the development of LVH in humans have not been addressed previously. METHODS: We conducted a retrospective case-control study in 24 deceased patients with childhood-onset end-stage renal disease (dialysis: n = 17; transplanted: n = 7), and 24 age- and sex-matched control subjects. Myocardial autopsy samples of the left ventricle were evaluated for expression of endogenous FGF23, FGFR isoforms, Klotho, calcineurin and nuclear factor of activated T-cells (NFAT) by immunohistochemistry, immunofluorescence microscopy, qRT-PCR and western blotting. RESULTS: The majority of patients presented with LVH (67%). Human cardiomyocytes express full-length FGF23, and cardiac FGF23 is excessively high in patients with CKD. Enhanced myocardial expression of FGF23 in concert with Klotho deficiency strongly correlates with the presence of LVH. Cardiac FGF23 levels associate with time-averaged serum phosphate levels, up-regulation of FGFR4 and activation of the calcineurin-NFAT signaling pathway, an established mediator of cardiac remodelling and LVH. These changes are detected in patients on dialysis but not in those with a functioning kidney transplant. CONCLUSIONS: Our results indicate a strong association between LVH and enhanced expression levels of FGF23, FGFR4 and calcineurin, activation of NFAT and reduced levels of soluble Klotho in the myocardium of patients with CKD. These alterations are not observed in kidney transplant patients.
Department of Pediatrics University Hospital Rostock Ernst Heydemann Str 8 18057 Rostock Germany
Institute for Forensic Medicine Hannover Medical School Carl Neuberg Str 1 30625 Hannover Germany
Institute of Pathology University Hospital Cologne Kerpener Str 62 50937 Cologne Germany
Institute of Pathology University Hospital Rostock Strempelstr 14 18055 Rostock Germany
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