Weiner Maria, Goh Su Mein, Mohammad Aladdin J, Hruskova Zdenka, Tanna Anisha, Bruchfeld Annette, Selga Daina, Chocova Zdenka, Westman Kerstin, Eriksson Per, Pusey Charles D, Tesar Vladimir, Salama Alan D, Segelmark Mårten
Departments of Nephrology and Medical and Health Sciences and
University College London Centre for Nephrology, Royal Free Hospital, London, United Kingdom;
Clin J Am Soc Nephrol. 2015 Jul 7;10(7):1128-35. doi: 10.2215/CJN.00480115. Epub 2015 Jun 22.
ANCA-associated vasculitis is commonly found in elderly patients, but there are few data concerning outcome and treatment in the highest age groups.
DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: Consecutive patients (N=151) presenting between 1997 and 2009 were retrospectively included from local registries in six centers in Sweden, the United Kingdom, and the Czech Republic if diagnosed with microscopic polyangiitis or granulomatosis with polyangiitis at age ≥75 years during the study period. Patients were followed until 2 years from diagnosis or death. Data on survival and renal function were analyzed with respect to age, sex, ANCA specificity, renal function, C-reactive protein, comorbidities, and Birmingham Vasculitis Activity Score at diagnosis as well as treatment during the first month.
Median follow-up was 730 days (interquartile range, 244-730). Overall 1-year survival was 71.5% and 2-year survival was 64.6%. Older age, higher creatinine, and lower Birmingham Vasculitis Activity Score were associated with higher mortality in multivariable analysis. Patients who were not treated with standard immunosuppressive therapy had significantly worse survival. Renal survival was 74.8% at 1 year. No new cases of ESRD occurred during the second year. High creatinine at diagnosis was the only significant predictor of renal survival in multivariable analysis.
ANCA-associated vasculitis is a disease with substantial mortality and morbidity among elderly patients. This study showed a better prognosis for those who received immunosuppressive treatment and those who were diagnosed before having developed advanced renal insufficiency.
抗中性粒细胞胞浆抗体(ANCA)相关血管炎常见于老年患者,但关于最高年龄组的预后和治疗的数据较少。
设计、地点、参与者及测量方法:对1997年至2009年间连续就诊的患者(N = 151例)进行回顾性研究,这些患者来自瑞典、英国和捷克共和国六个中心的本地登记处,若在研究期间年龄≥75岁且被诊断为显微镜下多血管炎或肉芽肿性多血管炎,则纳入研究。对患者进行随访直至确诊后2年或死亡。分析了生存和肾功能数据,涉及年龄、性别、ANCA特异性、肾功能、C反应蛋白、合并症、确诊时的伯明翰血管炎活动评分以及第一个月的治疗情况。
中位随访时间为730天(四分位间距,244 - 730天)。总体1年生存率为71.5%,2年生存率为64.6%。在多变量分析中,年龄较大、肌酐水平较高以及伯明翰血管炎活动评分较低与较高的死亡率相关。未接受标准免疫抑制治疗的患者生存率明显较差。1年时肾脏生存率为74.8%。第二年未出现新的终末期肾病病例。在多变量分析中,确诊时肌酐水平高是肾脏生存的唯一显著预测因素。
ANCA相关血管炎是一种在老年患者中具有较高死亡率和发病率的疾病。本研究表明,接受免疫抑制治疗的患者以及在出现晚期肾功能不全之前被诊断的患者预后较好。