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Association between Cystatin C and MRI Measures of Left Ventricular Structure and Function: Multi-Ethnic Study of
Subhashish Agarwal1, Vinay Thohan, Michael G Shlipak
1Department of Cardiology, Wake Forest University, Winston-Salem, NC 27157, USA.
Insights
Elevated cystatin C, a marker of kidney dysfunction, is linked to reduced left ventricular volumes (LVEDV and LVESV). This pattern of concentric remodeling may explain how kidney issues contribute to heart failure.
Area of Science:
- Cardiology
- Nephrology
- Biomarkers
Background:
- Reduced kidney function is associated with heart failure and cardiovascular mortality.
- The mechanisms linking kidney dysfunction to cardiac issues remain unclear.
- Cystatin C is a marker for kidney function.
Purpose of the Study:
- To investigate the relationship between cystatin C and subclinical left ventricular (LV) remodeling.
- To explore these associations across diverse ethnic populations.
Main Methods:
- Utilized data from the Multi-Ethnic Study of Atherosclerosis (MESA) cohort (N=4,970).
- Measured cystatin C and LV parameters (LVEDV, LVESV, LVM, concentricity, LVEF) via MRI.
- Employed nested linear models, adjusting for demographics and cardiovascular risk factors.
Main Results:
- Higher cystatin C quartiles showed a linear association with lower LV end-diastolic volume (LVEDV) and LV end-systolic volume (LVESV).
- A significant inverse relationship was found between cystatin C and LV concentricity.
- No association was observed between cystatin C and LV mass (LVM) or LV ejection fraction (LVEF).
Conclusions:
- Cystatin C levels are inversely associated with LVEDV and LVESV.
- A disproportionate decrease in LVEDV relative to LVM suggests concentric left ventricular remodeling.
- This remodeling pattern may partially explain the link between kidney dysfunction and heart failure.
Abstract:
Introduction. Reduced kidney function, approximated by elevated cystatin C, is associated with diastolic dysfunction, heart failure, and cardiovascular mortality; however, the precise mechanism(s) that account for these relationships remains unclear. Understanding the relationship between cystatin C and subclinical left ventricular (LV) remodeling, across ethnically diverse populations, may help explain the mechanisms underlying the association of kidney dysfunction with heart failure and cardiovascular mortality. Methods. Measures of cystatin C and LV parameters were obtained from the multi-ethnic study of atherosclerosis (MESA) cohort at baseline (N = 4, 970 with complete data on cystatin C and LV parameters). LV parameters; LV end-diastolic (LVEDV) and end-systolic volumes (LVESV), LV mass (LVM), concentricity (LV mass/LV end-diastolic volume), and LV ejection fraction (LVEF) were measured using magnetic resonance imaging. Nested linear models were used to examine the relationship between higher quartiles of cystatin C and LV parameters, with and without adjustment for demographics, height, and weight, and traditional cardiovascular risk factors. Similar analyses were performed stratified by ethnicity and gender. Results. A fully adjusted model demonstrated a linear relationship between higher quartiles of cystatin C and lower LVEDV, (Mean ± SE, 128 ± 0.7, 128 ± 0.7, 126 ± 0.7, 124 ± 0.8 mL; P = 0.0001). Associations were also observed between higher quartiles of cystatin C and lower LVESV (P = 0.04) and concentricity (P = 0.0001). In contrast, no association was detected between cystatin C and LVM or LVEF. In analyses stratified by race and gender, the patterns of association between cystatin C quartiles and LV parameters were qualitatively similar to the overall association. Conclusion. Cystatin C levels were inversely associated with LVEDV and LVESV with a disproportionate decrease in LVEDV compared to LVM in a multi-ethnic population. This morphometric pattern of concentric left ventricular remodeling, may in part explain the process by which kidney dysfunction leads to diastolic dysfunction, heart failure and cardiovascular mortality.
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