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Association of cystatin C with left ventricular structure and function: the Dallas Heart Study
Parag C Patel1, Colby R Ayers, Sabina A Murphy
1Division of Cardiology, Donald W. Reynolds Cardiovascular Clinical Research Center, University of Texas Southwestern Medical Center, Dallas, TX 75390-9047, USA.
Insights
Elevated cystatin C levels are linked to preclinical heart abnormalities, specifically increased left ventricular (LV) mass and concentric hypertrophy, even in younger adults. This finding suggests cystatin C may help identify early structural heart changes.
Area of Science:
- Cardiology
- Nephrology
- Biomarker Research
Background:
- Cystatin C is a emerging marker for kidney function.
- Previous studies linked cystatin C to heart failure and mortality in older adults.
- The association with preclinical cardiac changes in younger populations is less understood.
Purpose of the Study:
- To investigate the relationship between cystatin C levels and subclinical cardiac structural and functional abnormalities.
- To test if cystatin C is associated with preclinical cardiac changes in a younger, population-based sample.
Main Methods:
- The Dallas Heart Study cohort (ages 30-65) was analyzed.
- Cardiac magnetic resonance imaging (MRI) assessed left ventricular (LV) mass, volumes, ejection fraction, and wall thickness.
- Associations between cystatin C and cardiac parameters were evaluated using multivariable regression.
Main Results:
- Higher cystatin C levels correlated with increased LV mass, concentricity, and LV wall thickness.
- These associations remained significant after adjusting for traditional risk factors and estimated glomerular filtration rate (eGFR).
- The findings were consistent regardless of the eGFR calculation method used (MDRD or Cockcroft-Gault).
Conclusions:
- Elevated cystatin C is associated with increased LV mass and a concentric LV hypertrophy phenotype.
- These associations are independent of standard renal function measures.
- Cystatin C may serve as a valuable tool for identifying individuals with early, preclinical structural heart disease.
Background:
Cystatin C, a novel marker of renal function, has been associated with heart failure and cardiovascular mortality in older individuals. We tested the hypothesis that cystatin C is associated with preclinical cardiac structural and functional abnormalities in a younger population-based sample.
Methods And Results:
The study included participants in the Dallas Heart Study (ages 30 to 65 years) who had measurements of cystatin C and cardiac MRI. The associations of cystatin C with left ventricular (LV) mass, LV end-systolic and -diastolic volumes, concentricity (LV mass/LV end-diastolic volume), LV wall thickness, and LV ejection fraction were evaluated. Cystatin C levels ranged from 0.46 to 6.55 mg/L. In univariable analyses, increasing levels of cystatin C correlated with higher LV mass, concentricity, and wall thickness (P<0.001), but not with LV end-systolic volume, LV end-diastolic volume, or LV ejection fraction. After adjustment with traditional covariates and estimated glomerular filtration rate by the modification of diet in renal disease formula, log-transformed cystatin C remained independently associated with LV mass (P<0.001), concentricity (P=0.027), and wall thickness (P<0.001). These associations persisted when creatinine or estimated glomerular filtration rate by the Cockcroft-Gault formula were included in the models.
Conclusions:
Higher levels of cystatin C were associated with increased LV mass and a concentric LV hypertrophy phenotype. These findings were independent of potential confounding variables including standard measurements of renal function, supporting the hypothesis that cystatin C may be useful to identify individuals with preclinical structural heart abnormalities.
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