Progression rate of Chinese herb nephropathy:: impact of Aristolochia fangchi ingested dose

被引:89
作者
Martinez, MCM [1 ]
Nortier, J [1 ]
Vereerstraeten, P [1 ]
Vanherweghem, JL [1 ]
机构
[1] Free Univ Brussels, Hop Erasme, Dept Nephrol, B-1070 Brussels, Belgium
关键词
Aristolochia species; Chinese herbs; chronic interstitial nephropathy; renal fibrosis; toxic nephropathy;
D O I
10.1093/ndt/17.3.408
中图分类号
R3 [基础医学]; R4 [临床医学];
学科分类号
1001 ; 1002 ; 100602 ;
摘要
Background. Renal failure after ingestion of Chinese herbs between 1990 and 1992 was related to the replacement of Stephania tetrandra by Aristolochia fangchi (ST-AF), containing nephrotoxic and carcinogenic aristolochic acids. However, the relationship between ST-AF and renal failure is still a matter of debate. We therefore tested the impact of the ST-AF ingested dose on the progression of renal function deterioration. Methods. Analysis of medical charts and prescriptions between 1990 and 1992 was carried out to determine the presence of risk factors for kidney failure and the cumulative dose of pill components. Individual progression rate of renal impairment was studied by the time-course of the inverse of blood creatinine level (1/P-creat). Results. Patients were divided into an end-stage renal disease (ESRD) group (n = 44) and a chronic renal failure (CRF) group (n = 27) according to their P-creat at the time of this study. The mean number of risk factors (+/-SD) was equally distributed within both groups (1.50 +/- 0.18 vs 1.59 +/- 0.17, P = 0.74). Patients from the ESRD group ingested significantly higher cumulative doses of ST-AF (192 +/- 13.1 g vs 138 +/- 16.3 g), Magnolia officinalis, (80.1 +/- 6.3 g vs 59.8 +/- 11.7 g), diethylpropion (14.7 +/- 1.4 g vs 10.0 +/- 1.4 g) and fenfluramine (14.1 +/- 1.6 g vs 8.7 +/- 1.3 g). In the ESRD group, some patients who had received steroids had a slower progression to ESRD than the others. In multiple regression analysis, ST-AF emerged as the only significant drug predicting the slope of the progression of renal failure. Moreover. hypothesizing a linear dose-response relationship, the risk of developing ESRD linearly increased with ST-AF doses. Conclusions. The relationship between the cumulative ST-AF dose and the renal failure progression rate confirms that regular ingestion of Aristolochia sp. extracts is causally involved in the onset of chronic interstitial nephropathy leading to ESRD.
引用
收藏
页码:408 / 412
页数:5
相关论文
共 19 条
[1]  
Colson Conny R., 1998, Journal of the American Society of Nephrology, V9, p593A
[2]   Chinese herbs nephropathy-associated slimming regimen induces tumours in the forestomach but no interstitial nephropathy in rats [J].
Cosyns, JP ;
Goebbels, RM ;
Liberton, V ;
Schmeiser, HH ;
Bieler, CA ;
Bernard, AM .
ARCHIVES OF TOXICOLOGY, 1998, 72 (11) :738-743
[3]   Chronic aristolochic acid toxicity in rabbits: A model of Chinese herbs nephropathy? [J].
Cosyns, JP ;
Dehoux, JP ;
Guiot, Y ;
Goebbels, RM ;
Robert, A ;
Bernard, AM ;
de Strihou, CV .
KIDNEY INTERNATIONAL, 2001, 59 (06) :2164-2173
[4]   PATHOLOGICAL ASPECTS OF A NEWLY DESCRIBED NEPHROPATHY RELATED TO THE PROLONGED USE OF CHINESE HERBS [J].
DEPIERREUX, M ;
VANDAMME, B ;
HOUTE, KV ;
VANHERWEGHEM, JL .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1994, 24 (02) :172-180
[5]  
LEWIS CJ, 2000, COMMUNICATION 0531
[6]   Nephropathy caused by Chinese herbs in the Uh [J].
Lord, GM ;
Tagore, R ;
Cook, T ;
Gower, P ;
Pusey, CD .
LANCET, 1999, 354 (9177) :481-482
[7]   Chinese herbs: Risk, side effects, and poisoning: The case for objective reporting and analysis reveals serious misrepresentation [J].
McIntyre, M .
JOURNAL OF ALTERNATIVE AND COMPLEMENTARY MEDICINE, 1998, 4 (01) :15-16
[8]   ACUTE TOXICITY OF ARISTOLOCHIC ACID IN RODENTS [J].
MENGS, U .
ARCHIVES OF TOXICOLOGY, 1987, 59 (05) :328-331
[9]   THE CARCINOGENIC ACTION OF ARISTOLOCHIC ACID IN RATS [J].
MENGS, U ;
LANG, W ;
POCH, JA .
ARCHIVES OF TOXICOLOGY, 1982, 51 (02) :107-119
[10]   Urothelial carcinoma associated with the use of a Chinese herb (Aristolochia fangchi). [J].
Nortier, JL ;
Martinez, MM ;
Schmeiser, HH ;
Arlt, VM ;
Bieler, CA ;
Petein, M ;
Depierreux, MF ;
De Pauw, L ;
Abramowicz, D ;
Vereerstraeten, P ;
Vanherweghem, JL .
NEW ENGLAND JOURNAL OF MEDICINE, 2000, 342 (23) :1686-1692