Calcitriol for bone disease in patients with cirrhosis of the liver

被引:31
作者
Shiomi, S
Masaki, K
Habu, D
Takeda, T
Nishiguchi, S
Kuroki, T
Tanaka, T
Ochi, H
机构
[1] Osaka City Univ, Dept Internal Med 3, Sch Med, Abeno Ku, Osaka 5458585, Japan
[2] Osaka City Univ, Dept Publ Hlth, Sch Med, Abeno Ku, Osaka 5458585, Japan
[3] Osaka City Univ, Div Nucl Med, Sch Med, Abeno Ku, Osaka 5458585, Japan
关键词
bone disease; calcitriol; cirrhosis of the liver; dual-energy X-ray absorptiometry;
D O I
10.1046/j.1440-1746.1999.01913.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Osteoporosis is associated with cirrhosis of the liver, but the effects of therapy for osteoporosis associated with cirrhosis are still controversial. Methods: We evaluated the effects of calcitriol (1 alpha,25-dihydroxyvitamin D-3) on bone mineral density (BMD) in 76 patients (26 men and 50 women) with cirrhosis who were assigned randomly to receive calcitriol (0.5 mg twice per day) or not. The BMD of the lumbar vertebrae was measured by dual-energy X-ray absorptiometry at least twice, 12-57 months apart. Results: For men, the mean annual change in BMD was 1.1% in the treated group and -0.4% in the control group. The median (25th and 75th percentiles) annual change in BMD was 0.6 (-0.1, 2.1%) in the treated group and -1.4 (-1.9, 1.6%) in the control group. The difference in the median annual change between the two groups was significant (P = 0.013). For women, the mean annual change in BMD was -0.5% in the treated group and -2.3% in the control group. The median (25th and 75th percentiles) annual change in BMD was -0.5 (-1.8, 1.3%) in the treated group and -1.5 (-3.8, -0.7%) in the control group. This difference was significant (P = 0.011). Conclusions: Our results suggest that calcitriol can prevent bone loss and, therefore, may be useful for the treatment of bone disease in patients with cirrhosis of the liver. (C) 1999 Blackwell Science Asia Pty Ltd.
引用
收藏
页码:547 / 552
页数:6
相关论文
共 19 条
[1]   BONE-DISEASE IN ALCOHOL-ABUSE [J].
BIKLE, DD ;
GENANT, HK ;
CANN, C ;
RECKER, RR ;
HALLORAN, BP ;
STREWLER, GJ .
ANNALS OF INTERNAL MEDICINE, 1985, 103 (01) :42-48
[2]   SERUM VITAMIN-D METABOLITES AND THEIR BINDING-PROTEIN IN PATIENTS WITH LIVER-CIRRHOSIS [J].
BOUILLON, R ;
AUWERX, J ;
DEKEYSER, L ;
FEVERY, J ;
LISSENS, W ;
DEMOOR, P .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1984, 59 (01) :86-89
[3]   HEPATIC OSTEODYSTROPHY - VITAMIN-D METABOLISM IN PATIENTS WITH LIVER-DISEASE [J].
COMPSTON, JE .
GUT, 1986, 27 (09) :1073-1090
[4]   VITAMIN-D PROPHYLAXIS AND OSTEOMALACIA IN CHRONIC CHOLESTATIC LIVER-DISEASE [J].
COMPSTON, JE ;
CROWE, JP ;
WELLS, IP ;
HORTON, LWL ;
HIRST, D ;
MERRETT, AL ;
WOODHEAD, JS ;
WILLIAMS, R .
DIGESTIVE DISEASES AND SCIENCES, 1980, 25 (01) :28-32
[5]   RECOMBINANT INTERFERON-ALFA THERAPY FOR CHRONIC HEPATITIS-C - A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED TRIAL [J].
DIBISCEGLIE, AM ;
MARTIN, P ;
KASSIANIDES, C ;
LISKERMELMAN, M ;
MURRAY, L ;
WAGGONER, J ;
GOODMAN, Z ;
BANKS, SM ;
HOOFNAGLE, JH .
NEW ENGLAND JOURNAL OF MEDICINE, 1989, 321 (22) :1506-1510
[6]  
HERLONG HF, 1982, GASTROENTEROLOGY, V83, P103
[7]   RANDOMIZED, CONTROLLED TRIAL OF RECOMBINANT HUMAN ALPHA-INTERFERON IN PATIENTS WITH CHRONIC HEPATITIS-B [J].
HOOFNAGLE, JH ;
PETERS, M ;
MULLEN, KD ;
JONES, DB ;
RUSTGI, V ;
DIBISCEGLIE, A ;
HALLAHAN, C ;
PARK, Y ;
MESCHIEVITZ, C ;
JONES, EA .
GASTROENTEROLOGY, 1988, 95 (05) :1318-1325
[8]  
IMAWARI M, 1979, J LAB CLIN MED, V93, P171
[9]  
KANDA T, 1995, JPN PHARMACOL THER, V23, P191
[10]   INTERFERON-ALPHA AND INTERFERON-GAMMA INHIBIT INTERLEUKIN-1-BETA-STIMULATED OSTEOCLAST-LIKE CELL-FORMATION IN LONG-TERM HUMAN MARROW CULTURES [J].
KURIHARA, N ;
ROODMAN, GD .
JOURNAL OF INTERFERON RESEARCH, 1990, 10 (05) :541-547