Relationship of recipient age and development of chronic allograft failure

被引:109
作者
Meier-Kriesche, HU [1 ]
Ojo, AO [1 ]
Cibrik, DM [1 ]
Hanson, JA [1 ]
Leichtman, AB [1 ]
Magee, JC [1 ]
Port, FK [1 ]
Kaplan, B [1 ]
机构
[1] Univ Michigan, Dept Med, Ann Arbor, MI 48109 USA
关键词
D O I
10.1097/00007890-200007270-00012
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. The elderly are the fastest growing segment of the end stage renal disease (ERSD) population, Older renal transplant recipients experience fewer acute rejection episodes than do younger patients, Despite this, death censored graft survival is no better in these older transplant recipients than in younger recipients. We examined the United States Renal Data System (USRDS) database to determine whether recipient age itself has an independent effect on the development of chronic allograft failure (CAF). Methods. Ne analyzed 59,509 patients from the files of the USRDS. To determine whether age was an independent risk factor for CAF, the population was analyzed separately for Caucasians, African-Americans, and other ethnic groups. All renal transplant recipients from 1988 to 1997 were examined. Both univariate and multivariate analysis were performed using chronic allograft failure as the outcome of interest. Results. Actuarial 8-year censored graft survival was significantly decreased in the older age groups 67% for ages 18-49 vs. 61.8% for ages 50-64 vs. 50.7% for ages 65+ (P<0.001). In the multivariate analysis, recipient age was a strong and independent risk factor for the development of chronic allograft failure in Caucasians (RR 1.29 for ages 50-64, RR 1.67 for ages older than 65). These findings mere reinforced by an analysis that was restricted to living donor transplants without acute rejection. Conclusion, In Caucasians increased recipient age is an independent risk factor for the development of chronic renal allograft failure.
引用
收藏
页码:306 / 310
页数:5
相关论文
共 27 条
[1]  
ABRASS CK, 1995, AM J PATHOL, V146, P742
[2]  
Becker BN, 1996, SEMIN NEPHROL, V16, P353
[3]   Differential distribution of apolipoprotein E in young and aged spontaneously hypertensive and stroke-prone rats [J].
Chiang, AN ;
Chang, CP ;
Chou, YC ;
Huang, KY ;
Hu, HH .
JOURNAL OF HYPERTENSION, 1999, 17 (06) :793-800
[4]   An antibody specific for interleukin-6 reverses age-associated changes in spontaneous and induced cytokine production in mice [J].
Gorczynski, RM ;
Cinader, B ;
Ramakrishna, V ;
Terzioglu, E ;
Waelli, T ;
Westphal, O .
IMMUNOLOGY, 1997, 92 (01) :20-25
[5]   Medullary injury in the ageing rat kidney: Functional-morphometric correlations [J].
Greenfeld, Z ;
Stillman, IE ;
Brezis, M ;
Rosen, S .
EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 1997, 27 (04) :346-351
[6]  
Halloran PF, 1999, J AM SOC NEPHROL, V10, P167
[7]   Hyperhomocysteinemia in high-aged subjects: relation of B-vitamins, folic acid, renal function and the methylenetetrahydrofolate reductase mutation [J].
Herrmann, W ;
Quast, S ;
Ullrich, M ;
Schultze, H ;
Bodis, M ;
Geisel, J .
ATHEROSCLEROSIS, 1999, 144 (01) :91-101
[8]  
HESTIN D, 1994, CLIN NEPHROL, V42, P232
[9]  
ISMAIL N, 1994, AM J KIDNEY DIS, V23, P1