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Published on: November 29, 2024
Independent associations between resistin and left ventricular mass and myocardial dysfunction in a community sample
Glenda Norman1, Gavin R Norton1, Carlos D Libhaber2
1Cardiovascular Pathophysiology and Genomics Research Unit, School of Physiology, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.
Insights
Resistin, a hormone, is linked to increased left ventricular mass and impaired systolic function in heart failure, independent of other factors. These findings clarify resistin's role in cardiac remodeling and dysfunction.
Area of Science:
- Cardiovascular Research
- Endocrinology
- Biomarkers
Background:
- The adipokine resistin's role in heart failure is not fully understood.
- Mechanisms linking resistin to left ventricular mass (LVM) and function require clarification.
Purpose of the Study:
- To investigate the association between circulating resistin concentrations and LVM, inappropriate LVMI (LVMinappr), and left ventricular systolic and diastolic function.
- To determine if these associations persist independently of confounders such as blood pressure, BMI, and insulin resistance.
Main Methods:
- Cross-sectional study of 739 community participants.
- Assessed circulating resistin concentrations via assays.
- Evaluated LVM index (LVMI), LVMinappr, and LV systolic/diastolic function using echocardiography.
- Statistical analysis included partial correlations, adjusting for multiple confounders.
Main Results:
- Resistin concentrations were independently associated with LVMI, LVMinappr, and LV hypertrophy, independent of BP, BMI, and insulin resistance.
- Associations remained significant after adjusting for C-reactive protein.
- Resistin was the sole independent predictor of LV midwall fractional shortening, with enhanced relations at higher CRP levels.
- No independent association was found between resistin and LV diastolic function indices.
Conclusions:
- Resistin partially explains variations in LVM, hypertrophy, and myocardial systolic dysfunction.
- These effects are independent of insulin resistance and general inflammatory processes.
- Resistin emerges as a significant factor in cardiac remodeling and systolic dysfunction.
Background:
Although the adipokine resistin may play a role in heart failure, the mechanisms of this effect are uncertain. Relations with left ventricular mass (LVM) and function are uncertain.
Methods:
In 739 randomly selected participants from a community sample (43.6% obese), we assessed relations between circulating resistin concentrations and LVM index (LVMI), LVM beyond that predicted by stroke work (inappropriate LVMI [LVMinappr]) and systolic and diastolic LV function (echocardiography).
Results:
Resistin concentrations were not independently associated with blood pressure (BP). However, resistin concentrations were associated with LVMI (partial r=0.12, p<0.0005), LVMinappr (partial r=0.18, p<0.0001) and LV hypertrophy (partial r=0.13, p<0.001) independent of BP, BMI, the homeostasis model of insulin resistance and additional confounders. Independent relations between resistin concentrations and LVMI and LVMinappr persisted with further adjustments for C-reactive protein concentrations. Resistin concentration (partial r=-0.12, p<0.002 in all and partial r=-0.15, p<0.0005 in untreated) was the only factor independently associated with LV midwall fractional shortening and these relations were enhanced at incremental concentrations of CRP. Resistin was not independently associated with transmitral and myocardial tissue Doppler indices of LV diastolic function.
Conclusions:
Resistin in-part explains variations in LVM, hypertrophy and myocardial systolic dysfunction, and these effects are independent of insulin resistance and general inflammatory changes.
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