TY - JOUR
T1 - Accelerated coronary artery calcification in mildly reduced renal function of high-risk hypertensives
T2 - A 3-year prospective observation
AU - Bursztyn, Michael
AU - Motro, Michael
AU - Grossman, Ehud
AU - Shemesh, Joseph
PY - 2003/10
Y1 - 2003/10
N2 - Objective: To examine the effect of mild renal dysfunction on coronary artery calcifications. Methods: We examined the progression of coronary atherosclerosis, as measured by dual-section spiral computed tomography, using the total coronary artery calcium score as a quantitative measure of the burden of atherosclerosis. Of 547 high-risk Israeli hypertensive patients, who were participants of the prospective calcification study (a side-arm of the international INSIGHT study), 313 patients completed the 3-year follow-up. Subjects: were studied upon entry (on placebo) and again after 3 years of treatment (nifedipine or thiazide). Patients were divided into two groups depending on their creatinine clearance: (i) ≤ 60 ml/min, renal dysfunction (RD) (n = 53) and (ii) > 60 ml/min, normal renal function group (n = 263). Results: Blood pressure, hypercholesterolemia, and smoking did not differ between the groups. After 3 years of treatment, blood pressure control was similar, whereas the total coronary artery calcium score progression was two-fold greater in the RD than the normal group (156 ± 32 versus 64 ± 8, respectively) (P = 0.006). In a multiple logistic regression analysis, the odds ratio (OR) for total coronary artery calcium score progression was higher for the RD group (2.1) [95% confidence interval (CI) 1.2-3.7]. Gender, body mass index, smoking, cholesterol, family history of ischaemic heart disease and diabetes were not significant predictors. Thiazide-based antihypertensive therapy predicted a faster progression compared to nifedipine (OR 1.66, 95% CI 1.09-2.51). Conclusions: Mild renal dysfunction accelerates coronary artery calcifications, above and beyond conventional risk factors.
AB - Objective: To examine the effect of mild renal dysfunction on coronary artery calcifications. Methods: We examined the progression of coronary atherosclerosis, as measured by dual-section spiral computed tomography, using the total coronary artery calcium score as a quantitative measure of the burden of atherosclerosis. Of 547 high-risk Israeli hypertensive patients, who were participants of the prospective calcification study (a side-arm of the international INSIGHT study), 313 patients completed the 3-year follow-up. Subjects: were studied upon entry (on placebo) and again after 3 years of treatment (nifedipine or thiazide). Patients were divided into two groups depending on their creatinine clearance: (i) ≤ 60 ml/min, renal dysfunction (RD) (n = 53) and (ii) > 60 ml/min, normal renal function group (n = 263). Results: Blood pressure, hypercholesterolemia, and smoking did not differ between the groups. After 3 years of treatment, blood pressure control was similar, whereas the total coronary artery calcium score progression was two-fold greater in the RD than the normal group (156 ± 32 versus 64 ± 8, respectively) (P = 0.006). In a multiple logistic regression analysis, the odds ratio (OR) for total coronary artery calcium score progression was higher for the RD group (2.1) [95% confidence interval (CI) 1.2-3.7]. Gender, body mass index, smoking, cholesterol, family history of ischaemic heart disease and diabetes were not significant predictors. Thiazide-based antihypertensive therapy predicted a faster progression compared to nifedipine (OR 1.66, 95% CI 1.09-2.51). Conclusions: Mild renal dysfunction accelerates coronary artery calcifications, above and beyond conventional risk factors.
KW - Coronary artery disease
KW - Coronary atherosclerosis
KW - Creatinine clearance
KW - Double-helical computed tomography
KW - Hydrochlorothiazide
KW - Nifedipine
KW - Renal failure
UR - http://www.scopus.com/inward/record.url?scp=0142074207&partnerID=8YFLogxK
U2 - 10.1097/00004872-200310000-00024
DO - 10.1097/00004872-200310000-00024
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AN - SCOPUS:0142074207
SN - 0263-6352
VL - 21
SP - 1953
EP - 1959
JO - Journal of Hypertension
JF - Journal of Hypertension
IS - 10
ER -