Which vitamin D derivative to prescribe for renal patients

被引:20
作者
Drüeke, TB
机构
[1] INSERM, Unite 507, F-75743 Paris, France
[2] Hop Necker Enfants Malad, Serv Nephrol, F-75743 Paris, France
关键词
calcium; parathyroid hormone; phosphorus; renal; osteodystrophy; secondary hyperparathyroidism; vitamin D analogs;
D O I
10.1097/01.mnh.0000172720.34229.39
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 ; 100201 ;
摘要
Purpose of review It is possible to control the secondary hyperparathyroiism and osteitis fibrosa of patients with chronic kidney disease I, by calcitriol when given early and in appropriate doses. However, this control is often achieved at the price of unacceptably high plasma calcium and phosphorus levels, the induction of adynamic bone disease, and soft tissue calcification. To avoid these side effects, so-called nonhypercalcemic' vitamin 0 analogs have been developed. Their possible advantages and their precise place in the treatment and prevention of secondary i hyperparathyroidism remain a matter of debate. Recent findings A large US multicenter study showed that the administration of the vitamin D analog paricalcitol to hemodialysis patients, as compared with calcitriol, was associated with better survival. In a subsequent large US multicenter study paricalcitol-treated hemodialysis patients experienced fewer hospitalizations and hospital days compared with calcitriol-treated patients, In a third, smaller study from Japan, regular alfacalcidol users among hemodialysis patients had better cardiovascular survival than nonusers. Finally, in a recent historical control study the mortality of a large hemodialysis patient cohort was analyzed as a i function of previous vitamin D treatment. Patients on active vitamin D compounds at any time had a 2-year survival advantage over vitamin D-naive patients. It must be pointed out, however, that all four studies were retrospective in nature. Summary The development of vitamin D analogs with less side effects than with calcitriol is of major theoretical interest. Practically speaking, however, we still need to be convinced that this goal can be achieved in chronic kidney disease patients.
引用
收藏
页码:343 / 349
页数:7
相关论文
共 59 条
[21]   Dendritic cell modulation by 1α,25 dihydroxyvitamin D3 and its analogs:: A vitamin D receptor-dependent pathway that promotes a persistent state of immaturity in vitro and in vivo [J].
Griffin, MD ;
Lutz, W ;
Phan, VA ;
Bachman, LA ;
McKean, DJ ;
Kumar, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (12) :6800-6805
[22]   Arterial stiffening and vascular calcifications in end-stage renal disease [J].
Guérin, AP ;
London, GM ;
Marchais, SJ ;
Metivier, F .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 2000, 15 (07) :1014-1021
[23]   EFFECT OF ALFACALCIDOL ON NATURAL COURSE OF RENAL BONE-DISEASE IN MILD-TO-MODERATE RENAL-FAILURE [J].
HAMDY, NAT ;
KANIS, JA ;
BENETON, MNC ;
BROWN, CB ;
JUTTMANN, JR ;
JORDANS, JGM ;
JOSSE, S ;
MEYRIER, A ;
LINS, RL ;
FAIREY, IT .
BRITISH MEDICAL JOURNAL, 1995, 310 (6976) :358-363
[24]   Comparison of the effects of calcitriol and maxacalcitol on secondary hyperparathyroidism in patients on chronic haemodialysis: a randomized prospective multicentre trial [J].
Hayashi, M ;
Tsuchiya, Y ;
Itaya, Y ;
Takenaka, T ;
Kobayashi, K ;
Yoshizawa, M ;
Nakamura, R ;
Monkawa, T ;
Ichihara, A .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 2004, 19 (08) :2067-2073
[25]   COMPARISON OF INTERMITTENT AND CONTINUOUS ORAL-ADMINISTRATION OF CALCITRIOL IN DIALYSIS PATIENTS - A RANDOMIZED PROSPECTIVE TRIAL [J].
HERRMANN, P ;
RITZ, E ;
SCHMIDTGAYK, H ;
SCHAFER, I ;
GEYER, J ;
NONNASTDANIEL, B ;
KOCH, KM ;
WEBER, U ;
HORL, W ;
HAASWORLE, A ;
KUHN, K ;
BIERTHER, B ;
SCHNEIDER, P .
NEPHRON, 1994, 67 (01) :48-53
[26]   The parathyroid-bone axis in uremia: New insights into old questions [J].
Hory, B ;
Drueke, TB .
CURRENT OPINION IN NEPHROLOGY AND HYPERTENSION, 1997, 6 (01) :40-48
[27]   EFFECT OF 22-OXA-CALCITRIOL ON CALCIUM-METABOLISM IN RATS WITH SEVERE SECONDARY HYPERPARATHYROIDISM [J].
KUBRUSLY, M ;
GAGNE, ER ;
URENA, P ;
HANROTEL, C ;
CHABANIS, S ;
LACOUR, B ;
DRUEKE, TB ;
JEHENNE, G ;
DUCHAMBON, P ;
BANIDE, H ;
PACHER, N .
KIDNEY INTERNATIONAL, 1993, 44 (03) :551-556
[28]  
KWAN JTC, 1992, NEPHROL DIAL TRANSPL, V7, P829
[29]   Vitamin D: a negative endocrine regulator of the renin-angiotensin system and blood pressure [J].
Li, YC ;
Qiao, GL ;
Uskokovic, M ;
Xiang, W ;
Zheng, W ;
Kong, J .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 2004, 89-90 (1-5) :387-392
[30]   Suppression of parathyroid hormone secretion in hemodialysis patients by a novel vitamin D analogue:: 19-nor-1,25-dihydroxyvitamin D2 [J].
Llach, F ;
Keshav, G ;
Goldblat, MV ;
Lindberg, JS ;
Sadler, R ;
Delmez, J ;
Arruda, J ;
Lau, A ;
Slatopolsky, E .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1998, 32 (02) :S48-S54