Korean J Nephrol.
1999 Mar;18(2):284-292.
Cardiac Disease and Its Risk Factors in Patients Starting Hemodialysis
- Affiliations
-
- 1Department of Internal Medicine, University of Ulsan, Korea.
- 2Department of Internal Medicine, Chungnam National University, Korea.
- 3Department of Internal Medicine, Hallym University, Korea.
Abstract
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To evaluate the prevalence of cardiac disease and its risk factors at the start of dialysis,
we analyzed the demographic, clinical, echocardiographic, and laboratory data including ACE
gene polymorphism of 111 end-stage renal disease(ESRD) patients who survived at least 6 months
and had an echocardiogram within 6 months from the initiation of hemodialysis Clinically,
24% of the patients had congestive heart failure and 14% had ischemic heart disease.
Congestive heart failure was associated with diabetes(56% vs. 32%, P=0.03), higher plasma
homocysteine(24.5 micromol/l vs. 20.7 micromol/l, P=0.01), and lower parathyroid
hormone(<60pg/ml; 46% vs. 14%, P= 0.004). Ischemic heart disease was associated with older
age(62 vs. 48, P=0.001), diabetes(67% vs. 33%, P=0.01), hypoalbuminemia(3.1g/dl vs. 3.4g/dl,
P=0.03) and lower parathyroid hormone(&60pg/ml; 47% vs. 18%, P=0.04).
Echocardiographically, left ventricular hypertrophy (LVH) was present in 89% of the patients
of whom in detail 70% had concentric left ventricular hypertrophy(CLVH), 18% had left
ventricular dilatation (LD), and 12% had systolic dysfunction(SD). The following associates
were found:LVH group-diabetes(41% vs. 9%, P=0.04) and smoking(34% vs. 2%, P=0.01),
CLVH group-hypoalbuminemia(3.3g/dl vs. 3.6g/dl, P=0.08), and diabetes(45% vs. 26%, P=0.048),
SD group-high cholesterolemia(205mg/dl vs. 168mg/ dl, P=0.01). High diastolic blood pressure
was an independent predictor of severe LVH in multivariate logistic analysis(relative risk=1.46,
P=0.05). In conclusion, LVH was highly prevalent in ESRD patients starting hemodialysis.
Diastolic hypertension was independently associated with severe LVH and there was no
association between ACE gene polymorphism and cardiovascular disease.