Impact of the angiotensin II receptor antagonist, losartan, on myocardial fibrosis in patients with end-stage renal disease: Assessment by ultrasonic integrated backscatter and biochemical markers
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作者:
Shibasaki, Y
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机构:Kansai Med Univ, Dept Med 2, Moriguchi, Osaka 5708507, Japan
Shibasaki, Y
Nishiue, T
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机构:Kansai Med Univ, Dept Med 2, Moriguchi, Osaka 5708507, Japan
Nishiue, T
Masaki, H
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机构:Kansai Med Univ, Dept Med 2, Moriguchi, Osaka 5708507, Japan
Masaki, H
Tamura, K
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机构:Kansai Med Univ, Dept Med 2, Moriguchi, Osaka 5708507, Japan
Tamura, K
Matsumoto, N
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机构:Kansai Med Univ, Dept Med 2, Moriguchi, Osaka 5708507, Japan
Matsumoto, N
Mori, Y
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机构:Kansai Med Univ, Dept Med 2, Moriguchi, Osaka 5708507, Japan
Mori, Y
Nishikawa, M
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机构:Kansai Med Univ, Dept Med 2, Moriguchi, Osaka 5708507, Japan
Nishikawa, M
Matsubara, H
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机构:Kansai Med Univ, Dept Med 2, Moriguchi, Osaka 5708507, Japan
Matsubara, H
Iwasaka, T
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机构:Kansai Med Univ, Dept Med 2, Moriguchi, Osaka 5708507, Japan
Iwasaka, T
机构:
[1] Kansai Med Univ, Dept Med 2, Moriguchi, Osaka 5708507, Japan
angiotensin II type 2 receptor;
myocardial fibrosis;
hemodialysis;
ultrasonic integrated backscatter;
collagen turnover;
D O I:
10.1291/hypres.28.787
中图分类号:
R6 [外科学];
学科分类号:
1002 ;
100210 ;
摘要:
Myocardial fibrosis commonly occurs in patients with end-stage renal disease (ESRD) and has proven to be an important predictor for cardiovascular events. In experimental settings, angiotensin 11 type 1 receptor (AT1-R) antagonists have been shown to have anti-fibrotic effects on the myocardium independent of their anti hypertensive effects. In this study, to investigate whether the AT1-R antagonist losartan would have such anti-fibrotic effects in patients, we administered losartan or, for purpose of comparison, the angiotensin-converting enzyme enalapril or Ca2+-antagonist amlodipine to patients with ESRD. Thirty-nine ESRD patients with hypertension were randomly assigned to receive losartan (n=13), enalapril (n=13), or amlodipine (n=13). Ultrasonic integrated backscatter (IBS) and serological markers of collagen type I synthesis and degradation were used to assess the degree of myocardial fibrosis just before and after 6 months of treatment. There were no significant differences in anti hypertensive effects among the three agents. In the enalapril- and amlodipine-treated groups, the mean calibrated IBS values increased significantly after 6 months of treatment (enalapril: -31.6 +/- 1.3 to -29.4 +/- 1.2 dB, p=0.011; amlodipine: -30.6 +/- 1.4 to -27.2 +/- 1.2 dB, p=0.012). However, the mean calibrated IBS values in the losartan-treated group did not increase after 6 months of treatment (-31.2 +/- 1.7 to -31.3 +/- 1.4 dB, p=0.88). The ratio of the serum concentration of procollagen type I carboxy-terminal peptide to the serum concentration of collagen type I pyridinoline cross-linked carboxy-terminal telopeptide was significantly reduced in the losartan-treated group (42.6 +/- 4.6 to 34.4 +/- 3.6, p=0.038). The present study indicates that losartan more effectively suppresses myocardial fibrosis in patients with ESRD than does enalapril or amlodipine despite a comparable anti hypertensive effect among the three drugs.
机构:
KANSAI MED UNIV,DEPT INTERNAL MED 2,FUMIZONOCHO 1,MORIGUCHI,OSAKA 570,JAPANKANSAI MED UNIV,DEPT INTERNAL MED 2,FUMIZONOCHO 1,MORIGUCHI,OSAKA 570,JAPAN
SUZUKI, J
;
MATSUBARA, H
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KANSAI MED UNIV,DEPT INTERNAL MED 2,FUMIZONOCHO 1,MORIGUCHI,OSAKA 570,JAPANKANSAI MED UNIV,DEPT INTERNAL MED 2,FUMIZONOCHO 1,MORIGUCHI,OSAKA 570,JAPAN
MATSUBARA, H
;
URAKAMI, M
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KANSAI MED UNIV,DEPT INTERNAL MED 2,FUMIZONOCHO 1,MORIGUCHI,OSAKA 570,JAPANKANSAI MED UNIV,DEPT INTERNAL MED 2,FUMIZONOCHO 1,MORIGUCHI,OSAKA 570,JAPAN
URAKAMI, M
;
INADA, M
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KANSAI MED UNIV,DEPT INTERNAL MED 2,FUMIZONOCHO 1,MORIGUCHI,OSAKA 570,JAPANKANSAI MED UNIV,DEPT INTERNAL MED 2,FUMIZONOCHO 1,MORIGUCHI,OSAKA 570,JAPAN
机构:
KANSAI MED UNIV,DEPT INTERNAL MED 2,FUMIZONOCHO 1,MORIGUCHI,OSAKA 570,JAPANKANSAI MED UNIV,DEPT INTERNAL MED 2,FUMIZONOCHO 1,MORIGUCHI,OSAKA 570,JAPAN
SUZUKI, J
;
MATSUBARA, H
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KANSAI MED UNIV,DEPT INTERNAL MED 2,FUMIZONOCHO 1,MORIGUCHI,OSAKA 570,JAPANKANSAI MED UNIV,DEPT INTERNAL MED 2,FUMIZONOCHO 1,MORIGUCHI,OSAKA 570,JAPAN
MATSUBARA, H
;
URAKAMI, M
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KANSAI MED UNIV,DEPT INTERNAL MED 2,FUMIZONOCHO 1,MORIGUCHI,OSAKA 570,JAPANKANSAI MED UNIV,DEPT INTERNAL MED 2,FUMIZONOCHO 1,MORIGUCHI,OSAKA 570,JAPAN
URAKAMI, M
;
INADA, M
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KANSAI MED UNIV,DEPT INTERNAL MED 2,FUMIZONOCHO 1,MORIGUCHI,OSAKA 570,JAPANKANSAI MED UNIV,DEPT INTERNAL MED 2,FUMIZONOCHO 1,MORIGUCHI,OSAKA 570,JAPAN