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Left ventricular diastolic dysfunction in peritoneal dialysis: a forgotten risk factor
Cho-Kai Wu1, Jen-Kuang Lee, Yi-Fan Wu
1From the Division of Cardiology (C-KW, J-KL, C-TT, F-TC, J-JH, J-LL, J-WL), Department of Internal Medicine, National Taiwan University College of Medicine and Hospital; Cardiovascular Center (C-KW, J-KL, C-TT, F-TC, J-JH, J-LL), National Taiwan University Hospital; Department of Family Medicine (Y-FW), Taipei City Hospital, Renai Branch; Division of Nephrology (K-YH, J-WH), Department of Internal Medicine, National Taiwan University College of Medicine and Hospital; Department of Internal Medicine (J-WL), National Taiwan University College of Medicine and Hospital, Yun-Lin Branch, Yun-Lin, Taipei, Taiwan.
Insights
Left ventricular diastolic dysfunction (LVDD) in peritoneal dialysis (PD) patients is linked to inflammation and visceral fat. LVDD independently predicts major adverse cardiovascular events (MACE) and mortality in PD patients.
Area of Science:
- Cardiology
- Nephrology
- Internal Medicine
Background:
- Left ventricular diastolic dysfunction (LVDD) is prevalent in patients undergoing peritoneal dialysis (PD).
- Understanding LVDD's impact on cardiovascular outcomes and mortality in PD patients is crucial.
Purpose of the Study:
- To investigate the relationship between LVDD, major adverse cardiovascular events (MACE), and mortality in PD patients.
- To explore the association of LVDD with systemic inflammation and visceral adipose tissue in PD patients.
Main Methods:
- 149 PD patients with preserved systolic function were followed for 3.5 years.
- LVDD diagnosed via echocardiography; serum high-sensitivity C-reactive protein (hsCRP) and visceral fat (CT scan) were measured.
- Multivariate Cox regression analysis assessed LVDD and hsCRP as predictors of MACE and mortality.
Main Results:
- LVDD patients exhibited higher hsCRP, visceral, and peritoneal fat.
- LVDD was a significant, independent predictor of MACE (HR: 1.71) and mortality (HR: 2.25) in PD patients.
- Systemic inflammation (hsCRP) also independently predicted MACE (HR: 2.03) and mortality (HR: 2.16).
Conclusions:
- LVDD is associated with systemic inflammation and increased visceral fat in PD patients.
- LVDD serves as a sensitive, independent indicator for predicting future MACE and mortality in PD patients.
- Managing LVDD and inflammation is critical for improving cardiovascular outcomes in PD patients.
Abstract:
Left ventricular diastolic dysfunction (LVDD) is common among patients undergoing peritoneal dialysis (PD). We examined the relationship between LVDD, major adverse cardiovascular events (MACE), and mortality in PD patients. A total of 149 patients undergoing PD with preserved left ventricular systolic function were included and followed for 3.5 years. LVDD was diagnosed (according to the European Society of Cardiology guidelines) by conventional and tissue Doppler echocardiography. Serum high-sensitivity C-reactive protein (hsCRP) was measured. The location and volume of adipose tissue were assessed by computed tomography (CT) at the level of the fourth lumbar vertebra. Subjects with LVDD had higher levels of hsCRP, and more visceral and peritoneal fat than controls. The relationship between adjusted visceral adipose tissue and LVDD became nonsignificant when hsCRP and baseline demographic data were introduced into the logistic regression model (odds ratio = 1.52, P = 0.07). Subsequent hierarchical multivariate Cox regression analysis showed that LVDD was one of the most powerful determinants of MACE and mortality after adjusting for all confounding factors (hazard ratio [HR]: 1.71, 95% confidence interval [CI]: 1.43-3.51, P = 0.02 and HR: 2.25, 95% CI: 1.45-2.91, P = 0.04, respectively). Systemic inflammation (hsCRP) was also significantly associated with MACE and mortality (HR: 2.03, P = 0.03 and HR: 2.16, P = 0.04, respectively). LVDD is associated with systemic inflammation and increased visceral fat in patients undergoing PD. LVDD is also a sensitive, independent indicator of future MACE and mortality in PD patients.
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