Ahlmen M, Ahlmen J, Svalander C, Bucht H
Clin Rheumatol. 1987 Mar;6(1):27-38. doi: 10.1007/BF02200997.
Twenty-two patients with amyloidosis secondary to rheumatoid arthritis were randomised and followed prospectively in order to determine whether treatment with cytotoxic drugs could postpone the development of end-stage renal failure. The diagnosis of amyloidosis was based on albuminuria, amyloid-positive rectal and/or abdominal fat aspiration and/or renal biopsies. Renal function was followed by repeated 51Cr-EDTA measurements of the glomerular filtration rate (GFR). Urinary albumin and serum-creatinine were found unreliable as predictors of renal function. GFR declined more rapidly in the patient group receiving only symptomatic drugs and no cytotoxic drugs (NT-group). After an initial decline, the GFR in the cytotoxic drug treatment group (T-group), mean treatment quotient 79%, levelled off and remained constant for a considerable time. The mean observation time was 45.7 months in the NT-group and 53.5 months in the T-group. Seven out of eleven patients in the NT-group developed end-stage renal disease, compared to two out of eleven patients in the T-group. The cumulative proportion of survivors in the NT-group at 36 and 60 months was 71% and 27% respectively. The corresponding figures in the T-group were 89% and 89%. The difference in favour of the cytotoxic drug-treated group was significant (p less than 0.04).
22例类风湿关节炎继发淀粉样变性患者被随机分组并进行前瞻性随访,以确定细胞毒性药物治疗是否能延缓终末期肾衰竭的发生。淀粉样变性的诊断基于蛋白尿、淀粉样蛋白阳性的直肠和/或腹部脂肪抽吸及/或肾活检。通过重复进行51Cr-EDTA测量肾小球滤过率(GFR)来跟踪肾功能。发现尿白蛋白和血清肌酐作为肾功能预测指标不可靠。仅接受对症药物而非细胞毒性药物治疗的患者组(非治疗组)的GFR下降更快。在初始下降后,细胞毒性药物治疗组(治疗组)的GFR,平均治疗商数为79%,趋于平稳并在相当长一段时间内保持稳定。非治疗组的平均观察时间为45.7个月,治疗组为53.5个月。非治疗组11例患者中有7例发展为终末期肾病,而治疗组11例患者中有2例。非治疗组在36个月和60个月时的累积存活比例分别为71%和27%。治疗组的相应数字分别为89%和89%。细胞毒性药物治疗组的优势差异具有显著性(p小于0.04)。