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Left ventricular myocardial mass index associated with cardiovascular and renal prognosis in IgA nephropathy
Balázs Sági1,2, István Késői3, Tibor Vas1
1Medical School, Clinical Center, 2Nd. Dep. of Internal Medicine and Nephrology, Diabetes Center, University of Pécs, 1 Pacsirta street, 7624, Pécs, Hungary.
Insights
Left ventricular mass index (LVMI) predicts worse outcomes in IgA nephropathy (IgAN) patients. Higher LVMI is linked to increased risk of cardiovascular events and kidney disease progression, highlighting its role in risk stratification.
Area of Science:
- Nephrology
- Cardiology
- Internal Medicine
Background:
- Chronic kidney disease (CKD), including IgA nephropathy (IgAN), significantly elevates cardiovascular (CV) mortality and morbidity.
- Left ventricular hypertrophy (LVH) is a known independent risk factor for CV disease in CKD patients.
Purpose of the Study:
- To investigate the association between left ventricular mass index (LVMI) and renal or cardiovascular outcomes in IgAN patients.
- To determine if LVMI can serve as a predictor for adverse events in this population.
Main Methods:
- A prospective follow-up study involving 118 IgAN patients.
- Echocardiography was used to assess LVMI and LV geometry.
- Primary endpoints included total mortality, major CV events, and end-stage renal disease.
Main Results:
- LVMI inversely correlated with estimated glomerular filtration rate (eGFR).
- Patients with LVH showed a significantly worse prognosis for primary, renal, and CV endpoints.
- Independent predictors for LVMI included gender and eGFR; for the primary endpoint, they included LVMI, eGFR, gender, obesity, hypertension, diabetes, and metabolic syndrome.
Conclusions:
- Increased LVMI is a potential predictor of progression to end-stage renal disease and CV events in IgAN.
- LVMI determination can aid in stratifying both cardiovascular and renal risk in CKD patients.
Introduction:
In chronic kidney disease (CKD), like in IgA nephropathy (IgAN), cardiovascular (CV) mortality and morbidity are many times higher than in the general population, and left ventricular hypertrophy (LVH) is an independent risk factor for CV disease. This follow-up study investigated the association between left ventricular mass index (LVMI) and renal or cardiovascular outcomes.
Methods:
We examined 118 IgAN patients prospectively. LVMI and LV geometry was investigated using echocardiography. The primary combined endpoints were total mortality, major CV events, and end-stage renal disease. Secondary endpoints, i.e.-cardiovascular or renal endpoints,-were also examined separately.
Results:
Sixty seven percent were males, mean age 53.5 ± 13.5. Mean follow-up time: 184 months. LVMI inversely correlated with eGFR (corr. coefficient: -0.365; p < 0.01). We divided the patients into two groups based on the LVMI cut-off suggested by the literature. The presence of LVH caused a worse prognosis in primary (p < 0.001), renal endpoints (p = 0.01), and also in CV endpoints (p = 0.001). The higher LVMI in men significantly worsened the prognosis in all endpoints. Concentric hypertrophy meant a worse prognosis. Independent predictors of LVMI were gender and eGFR in uni- and multivariate regression and hemoglobin levels only in logistic regression. Independent predictors of the primary endpoint were LVMI, eGFR, gender, obesity, HT, DM, and metabolic syndrome in Cox regression analysis.
Conclusion:
Increased LVMI may predict the progression to end-stage renal disease and CV events in IgAN. Determining LVMI may be a useful parameter not only in CV risk but also in the stratification of renal risk in CKD.
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