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Published on: July 3, 2013
[Left ventricular hypertrophy in patients with chronic kidney disease under conservative treatment]
Rachel Bregman1, Carla Lemos, Roberto Pecoits Filho
1Universidade do Estado do Rio de Janeiro, RJ, Brazil.
Insights
Left ventricular hypertrophy (LVH) affects over half of chronic kidney disease (CKD) patients before dialysis. Age, calcium, hemoglobin, and diastolic blood pressure are key predictors, highlighting the need for early LVH prevention in CKD.
Area of Science:
- Nephrology
- Cardiology
- Internal Medicine
Background:
- Cardiovascular disease (CVD) is the leading cause of mortality in chronic kidney disease (CKD) patients.
- Left ventricular hypertrophy (LVH) is highly prevalent in CKD, often appearing early.
- Limited data exists on LVH prevalence in predialysis CKD patients.
Purpose of the Study:
- To determine the prevalence of LVH in predialysis CKD patients.
- To identify independent determinants of LVH in this population.
Main Methods:
- Cross-sectional study of 309 clinically stable predialysis CKD patients across five Brazilian centers.
- Assessment of biochemical profiles, inflammatory markers, and demographic data.
- Multivariate logistic regression analysis to identify LVH predictors.
Main Results:
- LVH was present in 53% of patients, with 60% of those with LVH in CKD Stage 4.
- Independent predictors of LVH included older age, higher calcium levels, lower hemoglobin, and elevated diastolic blood pressure.
- Systolic blood pressure, lipids, and inflammatory markers did not correlate with LVH.
Conclusions:
- LVH is highly prevalent in predialysis CKD patients, even those on conservative treatment.
- LVH is associated with modifiable factors like calcium, hemoglobin, and diastolic blood pressure, alongside age.
- Early diagnosis and prevention of LVH in predialysis CKD are crucial for reducing CVD mortality.
Abstract:
Cardiovascular disease (CVD) remains the major cause of death in patients with chronic kidney disease (CKD). Left ventricular hypertrophy (LVH) is present in 75% of patients starting dialysis, suggesting that LVH might be present from an early stage of CKD. Few studies have addressed the predialysis prevalence of LVH. This study evaluated 309 clinically stable patients under treatment for at least three months at five Brazilian centers. Biochemical profile and inflammatory markers were assessed. Data were shown as mean ± SD. Left ventricular hypertrophy was present in 53% of the patients, whose mean age was 60 ± 13 years. The mean age of those without LVH was 55 ± 14 years. Diabetes mellitus was the underlying disease in 35% of the patients in both groups. Estimated glomerular filtration rate was 30 ± 11 and 32 ± 12 mL/min for patients with and without LVH, respectively (p = 0.19). The distribution of patients showed that 60% of those with LVH were in stage 4. Multivariate logistic regression analysis indicated the following independent determinants for LVH: age (p < 0.001); calcium (p < 0.001); hemoglobin (p < 0.048); and diastolic blood pressure (p < 0.001). Systolic blood pressure, lipids, and inflammatory markers showed no correlation with LVH. In conclusion, the incidence of LVH was high even among patients under conservative treatment, and, except for age, LVH correlated with reversible factors. The need for strictly diagnosing CKD and preventing LVH in the predialysis phase is emphasized to decrease mortality due to CVD in that population.
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