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Left ventricular hypertrophy in nondiabetic predialysis CKD
Ernesto Paoletti1, Diego Bellino, Paolo Cassottana
1Divisionse di Nefrologia, Dialisi e Trapianto and Cardiologia, Azienda Ospedaliera Universitaria S Martino, Genova, Italy. ernesto.paoletti@hsanmartino.it
Insights
Left ventricular hypertrophy (LVH) is common in patients with chronic kidney disease (CKD) before dialysis, with arterial hypertension and elevated pulse pressure being key factors. Early detection and management of LVH in CKD are crucial for improving patient outcomes.
Area of Science:
- Nephrology
- Cardiology
- Internal Medicine
Background:
- Left ventricular hypertrophy (LVH) is a significant predictor of mortality in end-stage renal disease patients.
- Limited data exists on LVH prevalence in chronic kidney disease (CKD) patients before initiating dialysis.
- This study investigates LVH in nondiabetic CKD patients not yet on renal replacement therapy.
Purpose of the Study:
- To determine the prevalence of LVH in nondiabetic predialysis CKD patients.
- To identify clinical factors associated with LVH in this population.
- To explore the role of arterial stiffness in LVH development in early-stage CKD.
Main Methods:
- Studied 244 nondiabetic CKD patients (stages 1-5) and 52 healthy controls.
- Assessed left ventricular mass index (LVMi) via echocardiography and 24-hour ambulatory blood pressure monitoring.
- Measured creatinine clearance, hemoglobin, lipids, and urinary protein excretion.
Main Results:
- Overall LVH prevalence was 74%, with 51% in early CKD stages (1-2) and 78% in advanced stages (3-5).
- LVH correlated with age, hypertension duration, 24-hour systolic BP, pulse pressure, and urinary protein excretion.
- Pulse pressure was a significant predictor of LVMi in advanced CKD, suggesting increased arterial stiffness.
Conclusions:
- LVH is highly prevalent in predialysis CKD patients, even in early stages.
- Arterial hypertension is strongly associated with LVH in CKD.
- Elevated pulse pressure and arterial stiffness may contribute to LVH development before dialysis initiation.
Background:
Although left ventricular hypertrophy (LVH) is a strong predictor of mortality in patients with end-stage renal disease, few studies are available before the start of dialysis treatment. The purpose of this study is to evaluate the prevalence and clinical correlates of LVH in nondiabetic patients with chronic kidney disease (CKD) not yet undergoing renal replacement therapy.
Methods:
We investigated 244 nondiabetic patients with CKD; 57 patients (42 men; age, 20 to 78 years) had stages 1 to 2 CKD and 187 patients (122 men; age, 18 to 77 years) had stages 3 to 5 CKD. Fifty-two normotensive healthy subjects served as controls. Each patient had blood pressure (BP) measured by means of 24-hour ambulatory BP monitoring and left ventricular mass index (LVMi) assessed by means of M-mode echocardiography. Creatinine clearance was estimated by means of the Cockcroft-Gault formula, and hemoglobin, serum lipid, and intact parathyroid hormone concentrations and daily urinary protein excretion were assessed by using routine methods.
Results:
In the overall group, prevalences of arterial hypertension and LVH were 66% and 74%, respectively. LVMi was 160 +/- 50 g/m2 body surface area and associated directly with age (P = 0.0013), duration of arterial hypertension (P = 0.0075), 24-hour systolic BP (P = 0.0113), pulse pressure (P = 0.0003), daytime (P = 0.0206) and nighttime systolic BP (P = 0.0059), and urinary protein excretion (P < 0.05) and inversely with creatinine clearance (P = 0.0103) and hemoglobin level (P = 0.0276). In patients with CKD stages 1 to 2 (LVH prevalence, 51%), age, duration of arterial hypertension, pulse pressure, and urinary protein excretion were significant predictors of LVMi (P < 0.00002) by using stepwise regression analysis, whereas in those with CKD stages 3 to 5 (LVH prevalence, 78%), pulse pressure emerged as the sole predictor of LVMi (P = 0.0011).
Conclusion:
The prevalence of LVH in nondiabetic predialysis patients with CKD is greater than previously reported, and there is evidence that LVH already is present in the early stages of renal disease. Arterial hypertension is associated with LVH in patients with CKD, and the strong relationship between elevated pulse pressure and LVH in those with more advanced CKD suggests that increased arterial stiffness might have a role for LVH well before the start of dialysis therapy.
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