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Published on: June 14, 2016
Association between elevated fibrosis markers and heart failure in the elderly: the cardiovascular health study
Eddy Barasch1, John S Gottdiener, Gerard Aurigemma
1Department of Research and Education, St Francis Hospital/SUNY at Stony Brook, Roslyn, NY 11576, USA. eddy.barasch@chsli.org
Insights
Serum fibrosis markers are elevated in elderly individuals with heart failure (HF). These findings highlight potential biomarkers for HF in older populations.
Area of Science:
- Cardiology
- Biomarkers
- Geriatrics
Background:
- Myocardial fibrosis, characterized by excess collagen in the left ventricular matrix, is linked to heart failure (HF).
- Previous research has not explored the relationship between fibrosis biomarkers and HF specifically in elderly populations.
Purpose of the Study:
- To investigate the association between serum fibrosis biomarkers and heart failure (HF) in an elderly cohort.
- To determine if these biomarkers differ between systolic HF, diastolic HF, and healthy controls.
Main Methods:
- Serum samples from 880 elderly participants (mean age 77) in the Cardiovascular Health Study were analyzed for fibrosis markers.
- Participants were categorized into systolic HF, diastolic HF, and control groups.
- Logistic regression analysis was performed, adjusting for multiple covariates relevant to aging and cardiovascular health.
Main Results:
- Elevated levels of carboxyl-terminal telopeptide of collagen type I and amino-terminal peptide of procollagen type III were significantly associated with both systolic and diastolic HF.
- These associations remained significant after adjusting for various clinical factors.
- Carboxyl-terminal peptide of procollagen type I did not show a significant association with HF.
Conclusions:
- Serum fibrosis markers are significantly elevated in elderly individuals diagnosed with either diastolic or systolic heart failure.
- These elevated markers persist even after accounting for other relevant covariates in the aging process.
Background:
Myocardial fibrosis reflects excess collagen deposition in the extracellular left ventricular matrix, which has been associated with heart failure (HF). No studies have addressed the relation between fibrosis biomarkers and HF in the elderly.
Methods And Results:
Serum fibrosis markers were measured in 880 participants of the Cardiovascular Health Study (mean age 77+/-6 years, 48% women). Participants with systolic HF (n=131, left ventricular ejection fraction <55%) and those with diastolic HF (n=179, left ventricular ejection fraction > or =55%) were compared with controls (280 with cardiovascular risk factors, and 279 healthy individuals) using a nested case-control design. Fibrosis markers included carboxyl-terminal peptide of procollagen type I, carboxyl-terminal telopeptide of collagen type I, and amino-terminal peptide of procollagen type III. Echocardiography was used to document systolic and diastolic function parameters. Analysis of variance and logistic regression analysis (per tertile odds ratios [OR]), adjusted by age, gender, race, hypertension, atrial fibrillation, coronary heart disease, baseline serum glucose, serum cystatin C, serum creatinine, C-reactive protein, any angiotensin-converting enzyme inhibitor, spironolactone or any diuretic, NT-proBNP, and total bone mineral density were performed. Systolic HF was associated with significantly elevated carboxyl-terminal telopeptide of collagen type I (OR=2.6; 95% CI=1.2 to 5.7) and amino-terminal peptide of procollagen type III (OR=3.3; 95% CI=1.6 to 5.8), when adjusting for covariates. Associations of diastolic HF were significant for carboxyl-terminal telopeptide of collagen type I (OR=3.9; 95% CI=1.9 to 8.3) and amino-terminal peptide of procollagen type III (OR=2.7; 95% CI=1.4 to 5.4). HF was not associated with elevated carboxyl-terminal peptide of procollagen type I (P>0.10), and fibrosis markers did not significantly differ between HF with diastolic versus those with systolic dysfunction (P>0.10) whereas NT-proBNP mean values were higher in systolic heart failure than in diastolic heart failure (P<0.0001).
Conclusions:
Fibrosis markers are significantly elevated in elderly individuals with diastolic or systolic HF. These associations remained significant when adjusting for covariates relevant to the aging process.
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