Australia and New Zealand Dialysis and Transplant Registry, Adelaide, Australia.
Clin J Am Soc Nephrol. 2013 May;8(5):773-80. doi: 10.2215/CJN.08770812. Epub 2013 Jan 24.
This study aimed to evaluate dialysis and transplant outcomes of patients with ESRD secondary to ANCA-associated vasculitis (AAV).
DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: All ESRD patients who commenced renal replacement therapy in Australia and New Zealand between 1996 and 2010 were included. Outcomes were assessed by Kaplan-Meier, multivariable Cox regression, and competing-risks regression survival analyses.
Of 36,884 ESRD patients, 228 had microscopic polyangiitis (MPA) and 221 had granulomatosis with polyangiitis (GPA). Using competing-risks regression, compared with other causes of ESRD, MPA patients (hazard ratio [HR], 0.89; 95% confidence interval [95% CI], 0.73-1.08; P=0.24) and GPA patients (HR, 0.94; 95% CI, 0.74-1.19; P=0.62) experienced comparable survival on dialysis. Forty-six MPA patients (21%) and 47 GPA (20%) patients received 98 renal allografts. Respective 10-year first graft survival rates in MPA, GPA, and non-AAV patients were 50%, 62%, 70%, whereas patient survival rates were 68%, 85% and 83%, respectively. Compared with non-AAV patients, MPA transplant recipients had higher risks of graft failure (HR, 1.87; 95% CI, 1.07-3.25; P=0.03) and death (HR, 1.94; 95% CI, 1.02-3.69; P=0.04), whereas GPA transplant recipients experienced comparable renal allograft survival (HR, 0.91; 95% CI, 0.43-1.93; P=0.81) and patient survival (HR, 0.58; 95% CI, 0.23-2.27; P=0.58). AAV recurrence was observed in two renal allografts (2%).
Compared with ESRD patients without AAV, those with GPA have comparable renal replacement therapy outcomes, whereas MPA patients have comparable dialysis survival but poorer renal transplant allograft and patient survival rates.
本研究旨在评估继发于抗中性粒细胞胞浆抗体(ANCA)相关性血管炎(AAV)的终末期肾病(ESRD)患者的透析和移植结局。
设计、地点、参与者和测量:纳入了 1996 年至 2010 年期间在澳大利亚和新西兰开始肾脏替代治疗的所有 ESRD 患者。通过 Kaplan-Meier、多变量 Cox 回归和竞争风险回归生存分析评估结局。
在 36884 名 ESRD 患者中,228 名患有显微镜下多血管炎(MPA),221 名患有肉芽肿性多血管炎(GPA)。通过竞争风险回归,与其他 ESRD 病因相比,MPA 患者(风险比 [HR],0.89;95%置信区间 [95%CI],0.73-1.08;P=0.24)和 GPA 患者(HR,0.94;95%CI,0.74-1.19;P=0.62)的透析期间生存情况相似。46 名 MPA 患者(21%)和 47 名 GPA 患者(20%)接受了 98 个肾脏同种异体移植物。MPA、GPA 和非 AAV 患者的 10 年首次移植物存活率分别为 50%、62%和 70%,而患者存活率分别为 68%、85%和 83%。与非 AAV 患者相比,MPA 移植受者的移植物失败风险更高(HR,1.87;95%CI,1.07-3.25;P=0.03)和死亡风险更高(HR,1.94;95%CI,1.02-3.69;P=0.04),而 GPA 移植受者的肾脏同种异体移植物和患者存活率相似(HR,0.91;95%CI,0.43-1.93;P=0.81)和患者存活率(HR,0.58;95%CI,0.23-2.27;P=0.58)。两个肾移植(2%)中观察到 AAV 复发。
与无 AAV 的 ESRD 患者相比,GPA 患者的肾脏替代治疗结局相似,而 MPA 患者的透析生存情况相似,但肾脏移植移植物和患者存活率较低。