Predictors of the progression of renal insufficiency in patients with insulin-dependent diabetes and overt diabetic nephropathy

被引:189
作者
Breyer, JA
Bain, RP
Evans, JK
Nahman, NS
Lewis, EJ
Cooper, M
McGill, J
Berl, T
Rohde, R
Hunsicker, LG
Lachin, J
Greenhouse, SW
Verme, DA
Turlington, TR
Burrows, PK
Wish, J
Sheehan, J
Pohl, M
Berl, T
Santiago, G
Hunsicker, L
Kern, EFO
Lemann, J
Blementhal, S
Bresnahan, BS
Hebert, L
Goldfarb, S
Kobrin, S
Rodby, R
Levey, A
McLaughlin, M
Williams, M
McGill, J
Whittler, F
Rutecki, G
Cattran, D
Lietz, S
Valaitis, D
Hano, J
Maxwell, D
Porush, J
Spitalewitz, S
Shapiro, K
Adler, S
Tolchin, N
Hoy, W
Bernstein, R
Svetkey, L
Sharon, Z
Rausenbaum, B
机构
[1] UNIV COLORADO, SCH MED, DENVER, CO 80262 USA
[2] GEORGE WASHINGTON UNIV, CTR BIOSTAT, WASHINGTON, DC USA
[3] VANDERBILT UNIV, MED CTR, NASHVILLE, TN USA
[4] RUSH PRESBYTERIAN ST LUKES MED CTR, CHICAGO, IL 60612 USA
[5] BRISTOL MYERS SQUIBB, CLIN RES, PRINCETON, NJ USA
[6] WASHINGTON UNIV, ST LOUIS, MO USA
关键词
D O I
10.1038/ki.1996.481
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
We designed a prospective, double-blind controlled trial to determine predictors of loss of renal function in patients with insulin dependent diabetes and established nephropathy. A total of 409 insulin-dependent diabetic patients with established nephropathy enrolled in a trial on the effect of Captopril on the rate of progression of renal disease. Baseline demographic, clinical (history and physical) and laboratory parameters were analyzed as risk factors for time to progression. Dichotomous characteristics were compared by Fisher's exact test and continuous characteristics with the Wilcoxon rank-sum test. Univariate proportional hazards regression analysis was used to estimate relative risk of nephropathy progression, and bivariate proportional hazard regression to identify interactions with the treatment group assignment. Multivariate proportional hazard regression was employed to determine which characteristics were independent risk factors. We found that a number of demographic and clinical characteristics were significantly associated with nephropathy progression even after adjustment for treatment group. However, after multivariate analysis, the risk factors that independently predicted progression were onset of IDDM later in life, parental diagnosis of IDDM, the presence of edema, increased mean arterial pressure, and an abnormal electrocardiogram. Likewise, a number of laboratory characteristics were also predictive of nephropathy progression. A low hematocrit, high blood sugar, and higher protein excretion predicted nephropathy progression as did a higher serum creatinine, particularly in the face of a normal serum albumin. In conclusion, this study identifies a number of clinical and laboratory risk factors that can predict which patients with insulin-dependent diabetes with established nephropathy are more likely to sustain a clinically important decrease in renal function over a median follow-up of three years.
引用
收藏
页码:1651 / 1658
页数:8
相关论文
共 44 条
[1]  
ANDERSEN AR, 1983, DIABETOLOGIA, V25, P496
[2]  
[Anonymous], 1989, Analysis of binary data
[3]  
APPERLOO AJ, 1994, KIDNEY INT, V45, pS174
[4]   BENEFICIAL-EFFECTS OF ANGIOTENSIN CONVERTING ENZYME-INHIBITION ON RENAL-FUNCTION IN PATIENTS WITH DIABETIC NEPHROPATHY [J].
BJORCK, S ;
NYBERG, G ;
MULEC, H ;
GRANERUS, G ;
HERLITZ, H ;
AURELL, M .
BMJ-BRITISH MEDICAL JOURNAL, 1986, 293 (6545) :471-474
[5]  
COGGINS CH, UNPUB WOMEN MEN MDRD
[6]   GLOMERULOPATHY IN SPONTANEOUSLY DIABETIC RAT - IMPACT OF GLYCEMIC CONTROL [J].
COHEN, AJ ;
MCGILL, PD ;
ROSSETTI, RG ;
GUBERSKI, DL ;
LIKE, AA .
DIABETES, 1987, 36 (08) :944-951
[7]  
DAMICO G, 1986, Q J MED, V59, P363
[8]  
DIAMOND JR, 1992, ANNU REV MED, V43, P83, DOI 10.1146/annurev.me.43.020192.000503
[9]   RELATIONSHIP OF MICROVASCULAR DISEASE IN DIABETES TO METABOLIC CONTROL [J].
ENGERMAN, R ;
BLOODWORTH, JMB ;
NELSON, S .
DIABETES, 1977, 26 (08) :760-769
[10]   END-STAGE RENAL-DISEASE IN US MINORITY-GROUPS [J].
FELDMAN, HI ;
KLAG, MJ ;
CHIAPELLA, AP ;
WHELTON, PK .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1992, 19 (05) :397-410