Zoledronic acid to prevent bone loss in the first 6 months after renal transplantation

被引:101
作者
Haas, M
Leko-Mohr, Z
Roschger, P
Kletzmayr, J
Schwarz, C
Mitterbauer, C
Steininger, R
Grampp, S
Klaushofer, K
Delling, G
Oberbauer, R
机构
[1] Univ Vienna, Dept Internal Med 3, Div Nephrol, Vienna, Austria
[2] Hanusch Hosp & UKH Meidling, Dept Med 4, Vienna, Austria
[3] Hanusch Hosp & UKH Meidling, Ludwig Boltzmann Inst Osteol, Vienna, Austria
[4] Univ Vienna, Dept Radiol, Div Osteoradiol, A-1010 Vienna, Austria
[5] Univ Vienna, Dept Surg, Div Transplant Surg, A-1010 Vienna, Austria
[6] Univ Hamburg, Hosp Eppendorf, Dept Osteopathol, Inst Pathol, D-20246 Hamburg, Germany
关键词
zoledronic acid; renal transplantation; biopsy; bone mineralization; morphometry;
D O I
10.1046/j.1523-1755.2003.00816.x
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Background. Bisphosphonates can prevent bone mineral density loss after renal transplantation, but their effect on trabecular mineralization and bone morphology, two key factors of bone stability, remains unknown. Methods. In a 6-month, randomized, placebo-controlled study, 20 kidney transplant recipients received either 4 mg zoledronic acid or placebo twice within 3 months after engraftment. At transplantation and after 6 months, mean trabecular calcium concentration and trabecular morphometry were measured in bone biopsies. Bone mineral density (BMD) of the femoral neck and the lumbar spine were evaluated by dual-energy x-ray absorptiometry, and serum biochemical markers of bone metabolism were determined monthly. Results. Trabecular calcium content increased significantly in the zoledronic acid group, but remained unchanged in the placebo group. BMD at femoral neck showed no change in the zoledronic acid group, but decreased in the placebo group. BMD of the lumbar spine was increased in the zoledronic acid group without change in the placebo group. High-turnover bone disease resolved similarly in both groups, as evidenced by a significant decrease of eroded bone surface, osteoclast and osteoblast surface. Serologic markers of bone formation and resorption were significantly lower in zoledronic acid-treated patients throughout the study. Kidney transplant function was stable after zoledronic acid therapy. Conclusions. Our results show that administration of zoledronic acid improves the calcium content of cancellous bone after kidney transplantation. The beneficial effect of bisphosphonate therapy is further evidenced by an increase of lumbar spine BMD, and stabilization of femur BMD.
引用
收藏
页码:1130 / 1136
页数:7
相关论文
共 36 条
[1]
Intermittent etidronate therapy to prevent corticosteroid-induced osteoporosis [J].
Adachi, JD ;
Bensen, WG ;
Brown, J ;
Hanley, D ;
Hodsman, A ;
Josse, R ;
Kendler, DL ;
Lentle, B ;
Olszynski, W ;
SteMarie, LG ;
Tenenhouse, A ;
Chines, AA .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 337 (06) :382-387
[2]
3-DIMENSIONAL ANALYSIS OF THE SPINE IN AUTOPSY CASES WITH RENAL OSTEODYSTROPHY [J].
AMLING, M ;
GROTE, HJ ;
VOGEL, M ;
HAHN, M ;
DELLING, G .
KIDNEY INTERNATIONAL, 1994, 46 (03) :733-743
[3]
A comparison of quantitative computed tomography and dual x-ray absorptiometry for evaluation of bone mineral density in patients on chronic hemodialysis [J].
Barnas, U ;
Schmidt, A ;
Seidl, G ;
Kaider, A ;
Pietschmann, P ;
Mayer, G .
AMERICAN JOURNAL OF KIDNEY DISEASES, 2001, 37 (06) :1247-1252
[4]
Berenson JR, 2001, CANCER, V91, P1191, DOI 10.1002/1097-0142(20010401)91:7<1191::AID-CNCR1119>3.0.CO
[5]
2-0
[6]
BORDIER P, 1964, PATHOL BIOL, V12, P1238
[7]
PREVENTION OF CANCELLOUS BONE LOSS BUT PERSISTENCE OF RENAL BONE-DISEASE DESPITE NORMAL 1,25 VITAMIN-D LEVELS 2 YEARS AFTER KIDNEY-TRANSPLANTATION [J].
BRINER, VA ;
THIEL, G ;
MONIERFAUGERE, MC ;
BOGNAR, B ;
LANDMANN, J ;
KAMBER, V ;
MALLUCHE, HH .
TRANSPLANTATION, 1995, 59 (10) :1393-1400
[8]
Bone disease in patients with long-term renal transplantation and normal renal function [J].
Carlini, RG ;
Rojas, E ;
Weisinger, JR ;
Lopez, M ;
Martinis, R ;
Arminio, A ;
Bellorin-Font, E .
AMERICAN JOURNAL OF KIDNEY DISEASES, 2000, 36 (01) :160-166
[9]
Zoledronic acid [J].
Cheer S.M. ;
Noble S. .
Drugs, 2001, 61 (6) :799-805
[10]
Duarte M E, 1998, Sao Paulo Med J, V116, P1790