TY - JOUR
T1 - Angiotensin-converting enzyme inhibitors and change in aortic valve calcium
AU - O'Brien, Kevin D.
AU - Probstfield, Jeffrey L.
AU - Caulfield, Michael T.
AU - Nasir, Khurram
AU - Takasu, Junichiro
AU - Shavelle, David M.
AU - Wu, Audrey H.
AU - Zhao, Xue Qiao
AU - Budoff, Matthew J.
PY - 2005/4/25
Y1 - 2005/4/25
N2 - Background: Calcium accumulation in the aortic valve is a hallmark of aortic sclerosis and aortic stenosis. Because lipoproteins, angiotensin- converting enzyme, and angiotensin II colocalize with calcium in aortic valve lesions, we hypothesized an association between angiotensin-converting enzyme inhibitor (ACEI) use and lowered aortic valve calcium (AVC) accumulation, as measured by electron beam computed tomography. Methods: Rates of change in volumetric AVC scores were determined retrospectively for 123 patients who had undergone 2 serial electron beam computed tomographic scans. The mean (±SD) interscan interval was 2.5 (±1.7) years; 80 patients did not receive ACEIs and 43 received ACEIs. The relationship of ACEI use to median rates of AVC score change (both unadjusted and adjusted for baseline AVC scores and coronary heart disease risk factors) was determined. We also examined the relationship of ACEI use to the likelihood of and adjusted odds ratio for definite progression (AVC change >2 times the median interscan variability). Results: Unadjusted and adjusted median rates of AVC score change were significantly higher in the no-ACEI group than in the ACEI group (adjusted median AVC changes [95% confidence interval]: relative, 28.7%/y [18.9%-38.5%/y] vs 11.0%/y [-1.9% to 24.0%/y], P=.04; absolute: 25.1/y [19.7-30.5/y] vs 12.2/y [4.5-19.9/y], P=.02). The adjusted odds ratio (95% confidence interval) for definite AVC progression was significantly lower for patients who received ACEIs (0.29 [0.11-0.75],P=.01). Conclusions: This retrospective study finds a significant association between ACEI use and a lower rate of AVC accumulation. The results support the need for prospective, randomized trials of ACEIs in calcific aortic valve disease.
AB - Background: Calcium accumulation in the aortic valve is a hallmark of aortic sclerosis and aortic stenosis. Because lipoproteins, angiotensin- converting enzyme, and angiotensin II colocalize with calcium in aortic valve lesions, we hypothesized an association between angiotensin-converting enzyme inhibitor (ACEI) use and lowered aortic valve calcium (AVC) accumulation, as measured by electron beam computed tomography. Methods: Rates of change in volumetric AVC scores were determined retrospectively for 123 patients who had undergone 2 serial electron beam computed tomographic scans. The mean (±SD) interscan interval was 2.5 (±1.7) years; 80 patients did not receive ACEIs and 43 received ACEIs. The relationship of ACEI use to median rates of AVC score change (both unadjusted and adjusted for baseline AVC scores and coronary heart disease risk factors) was determined. We also examined the relationship of ACEI use to the likelihood of and adjusted odds ratio for definite progression (AVC change >2 times the median interscan variability). Results: Unadjusted and adjusted median rates of AVC score change were significantly higher in the no-ACEI group than in the ACEI group (adjusted median AVC changes [95% confidence interval]: relative, 28.7%/y [18.9%-38.5%/y] vs 11.0%/y [-1.9% to 24.0%/y], P=.04; absolute: 25.1/y [19.7-30.5/y] vs 12.2/y [4.5-19.9/y], P=.02). The adjusted odds ratio (95% confidence interval) for definite AVC progression was significantly lower for patients who received ACEIs (0.29 [0.11-0.75],P=.01). Conclusions: This retrospective study finds a significant association between ACEI use and a lower rate of AVC accumulation. The results support the need for prospective, randomized trials of ACEIs in calcific aortic valve disease.
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U2 - 10.1001/archinte.165.8.858
DO - 10.1001/archinte.165.8.858
M3 - Article
C2 - 15851635
AN - SCOPUS:17644373433
SN - 0003-9926
VL - 165
SP - 858
EP - 862
JO - Archives of Internal Medicine
JF - Archives of Internal Medicine
IS - 8
ER -