The effect of maintenance immunosuppression medication on the change in kidney allograft function

被引:40
作者
Gill, JS
Tonelli, M
Mix, CH
Johnson, N
Pereira, BJG
机构
[1] St Pauls Hosp, Div Nephrol, Vancouver, BC V6Z 1Y6, Canada
[2] Tufts Univ New England Med Ctr, Div Nephrol, Boston, MA USA
[3] Univ Alberta, Div Nephrol, Edmonton, AB, Canada
关键词
transplantation; immunosuppression; glomerular filtration rate;
D O I
10.1111/j.1523-1755.2004.00431.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 ; 100201 ;
摘要
Background. The optimum maintenance immunosuppression regimen for kidney transplant recipients is uncertain. In this study we determined the effect of maintenance immunosuppression medications on the rate of kidney allograft function loss defined by the annualized change in glomerular filtration rate (GFR). Methods. We studied 40,963 first kidney only transplant recipients between 1987 and 1996 with allograft survival of at least two years in the United States Renal Data System. Linear regression methods were applied to serial GFR estimates after transplantation to determine the annualized change in GFR. Patients were classified according to the type of maintenance calcineurin and purine metabolism inhibitor received after transplantation. Multiple linear regression was used to determine the independent effect of maintenance immunosuppression medications on the annualized change in GFR (mL/min/1.73m(2)/year). Results. Compared to patients who received cyclosporine microemulsion (Neoral), a slower decline in GFR was observed in tacrolimus-treated patients (1.60 mL/min/1.73m(2)/year, 95% CI 1.22- 1.97, P < 0.001) and patients who did not receive calcineurin inhibitors (0.82 mL/ min/1.73m(2)/year, 95% CI 0.08-1.56, P = 0.03). In contrast, compared to compared to patients who received Neoral, a faster decline in GFR was observed in patients who received the original oil-based formulation of cyclosporine (Sandimmune) (- 0.16 mL/min/1.73m(2)/year, 95% CI 0.003 to 0.32, P = 0.04) and patients with unknown calcinuerin inhibitor exposure (- 2.11 mL/min/ 1.73m(2) /year, 95% CI 2.27 to 1.95, P < 0.001). Compared to patients who received azathioprine, patients who received mycophenolate mofetil (MMF) had a slower decline in GFR(0.61 mL/min/1.73m(2)/year, 95% CI 0.14- 1.08, P = 0.01) and patients with unknown purine metabolism inhibitor exposure had a faster decline in GFR (-0.61 mL/min/ 1.73m(2)/year, 95% CI 0.75 to 0.47, P < 0.001.) In a subgroup analysis of patients who received a transplant after 1993, the decline in GFR was slower for tacrolimus compared to neoral treated patients (1.64 mL/min/1.73m(2)/year, 95% CI 1.15- 2.14, P < 0.001) but was not different for MMF compared to azathioprine-treated patients (0.24 mL/min/ 1.73m(2) /year, 95% CI 0.38- 0.85, P = 0.45). Conclusion. Tacrolimus and MMF were the calcineurin inhibitor and purine metabolism inhibitor associated with the most favorable effects on rates of change in allograft function. Because most transplant recipients establish a low baseline level of allograft function, the effect of immunosuppression medication on GFR decline should be considered when selecting a maintenance immunosuppression regimen.
引用
收藏
页码:692 / 699
页数:8
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