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Published on: June 14, 2016
Fibroblast growth factor 23 is associated with cardiac disease severity in transthyretin amyloid cardiomyopathy
Mahshid Eslami1, Nikita Ermolaev1, Christina Kronberger1
1Department of Internal Medicine II, Division of Cardiology, Medical University of Vienna, Vienna, Austria.
Insights
Fibroblast growth factor 23 (FGF23) is linked to cardiac and kidney markers in transthyretin amyloid cardiomyopathy (ATTR-CM). Higher FGF23 levels correlate with advanced disease stages, suggesting its potential as a complementary biomarker for ATTR-CM risk stratification.
Area of Science:
- Cardiology
- Endocrinology
- Biomarker Discovery
Background:
- Fibroblast growth factor 23 (FGF23) is a hormone primarily produced by bone cells.
- FGF23 is increasingly recognized for its role in cardiovascular disease.
- The significance of FGF23 in transthyretin amyloid cardiomyopathy (ATTR-CM) is not well understood.
Purpose of the Study:
- To investigate the association between circulating FGF23 levels and markers of cardiac and renal function in patients with ATTR-CM.
- To explore the relationship between FGF23 levels and disease severity in ATTR-CM.
Main Methods:
- Intact FGF23 levels were measured in 114 patients with confirmed ATTR-CM using a chemiluminescent immunoassay.
- Associations between FGF23 levels, cardiac biomarkers (N-terminal pro-B-type natriuretic peptide [NT-proBNP], troponin T), and National Amyloidosis Centre (NAC) stages were analyzed.
- Statistical analyses included evaluation across FGF23 tertiles and adjustments for estimated glomerular filtration rate (eGFR).
Main Results:
- Elevated FGF23 levels were significantly associated with higher NT-proBNP and troponin T levels.
- Higher FGF23 levels correlated with advanced NAC stages, indicating a link to disease progression.
- FGF23 remained significantly associated with NT-proBNP after adjusting for eGFR, though the association with troponin T showed a non-significant trend.
Conclusions:
- This study provides the first evidence of a significant association between FGF23 and cardiac injury markers in ATTR-CM.
- FGF23 may serve as a valuable complementary biomarker for risk stratification in patients with ATTR-CM.
- Further research is warranted to elucidate the precise role of FGF23 in the pathophysiology and progression of ATTR-CM.
Abstract:
Fibroblast growth factor 23 (FGF23), a bone-derived hormone, is emerging as a potential biomarker in cardiovascular disease. However, its role in transthyretin amyloid cardiomyopathy (ATTR-CM), a progressive infiltrative cardiomyopathy, remains poorly defined. This study examined the relationship between circulating FGF23 levels and cardiac and renal function markers in patients with ATTR-CM. In 114 patients with confirmed ATTR-CM, intact FGF23 levels were measured in venous ethylenediaminetetraacetic acid blood samples using a chemiluminescent immunoassay on the DiaSorin LIAISON XL system. Associations between FGF23 levels, cardiac biomarker levels, and disease severity were evaluated across FGF23 tertiles and National Amyloidosis Centre (NAC) stages. N-terminal pro-B-type natriuretic peptide (NT-proBNP) and troponin T levels were significantly associated with FGF23 tertiles. NT-proBNP medians across tertiles were 1,608, 2,920, and 1,948.5 pg/mL, respectively (P = 0.0084). Higher FGF23 levels were significantly associated with advanced NAC classification, and cumulative probability modeling supported its association with disease stage. After adjustment for eGFR, FGF23 remained significantly associated with NT-proBNP (Spearman's ρ = 0.16; p = 0.084). However, the association with troponin T did not reach statistical significance (ρ = 0.19; p = 0.043), representing a non-significant trend. This is the first study to demonstrate a significant association between FGF23 and established markers of cardiac injury and disease staging in ATTR-CM, supporting FGF23 as a potential complementary biomarker for risk stratification.
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