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与单阳性患者相比,同时出现抗中性粒细胞胞浆抗体(ANCA)和抗肾小球基底膜(GBM)抗体双阳性的患者具有不同的肾脏存活率、复发频率和结局。

Patients double-seropositive for ANCA and anti-GBM antibodies have varied renal survival, frequency of relapse, and outcomes compared to single-seropositive patients.

机构信息

Renal and Vascular Inflammation Section, Department of Medicine, Imperial College London, London, UK.

Renal and Vascular Inflammation Section, Department of Medicine, Imperial College London, London, UK.

出版信息

Kidney Int. 2017 Sep;92(3):693-702. doi: 10.1016/j.kint.2017.03.014. Epub 2017 May 12.

DOI:10.1016/j.kint.2017.03.014
PMID:28506760
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5567410/
Abstract

Co-presentation with both ANCA and anti-GBM antibodies is thought to be relatively rare. Current studies of such 'double-positive' cases report small numbers and variable outcomes. To study this further we retrospectively analyzed clinical features and long-term outcomes of a large cohort of 568 contemporary patients with ANCA-associated vasculitis, 41 patients with anti-GBM disease, and 37 double-positive patients with ANCA and anti-GBM disease from four European centers. Double-positive patients shared characteristics of ANCA-associated vasculitis (AAV), such as older age distribution and longer symptom duration before diagnosis, and features of anti-GBM disease, such as severe renal disease and high frequency of lung hemorrhage at presentation. Despite having more evidence of chronic injury on renal biopsy compared to patients with anti-GBM disease, double-positive patients had a greater tendency to recover from being dialysis-dependent after treatment and had intermediate long-term renal survival compared to the single-positive patients. However, overall patient survival was similar in all three groups. Predictors of poor patient survival included advanced age, severe renal failure, and lung hemorrhage at presentation. No single-positive anti-GBM patients experienced disease relapse, whereas approximately half of surviving patients with AAV and double-positive patients had recurrent disease during a median follow-up of 4.8 years. Thus, double-positive patients have a truly hybrid disease phenotype, requiring aggressive early treatment for anti-GBM disease, and careful long-term follow-up and consideration for maintenance immunosuppression for AAV. Since double-positivity appears common, further work is required to define the underlying mechanisms of this association and define optimum treatment strategies.

摘要

同时存在抗中性粒细胞胞质抗体 (ANCA) 和抗肾小球基底膜 (GBM) 抗体被认为相对罕见。目前对这类“双阳性”病例的研究报告数量较少且结果不一。为了进一步研究这一问题,我们回顾性分析了来自四个欧洲中心的 568 例当代抗中性粒细胞胞质抗体相关性血管炎患者、41 例抗 GBM 病患者和 37 例抗中性粒细胞胞质抗体和抗 GBM 病双阳性患者的临床特征和长期结局。双阳性患者具有抗中性粒细胞胞质抗体相关性血管炎(AAV)的特征,如年龄分布较老,诊断前症状持续时间较长,以及抗 GBM 病的特征,如严重的肾脏疾病和高频率的肺出血。尽管与抗 GBM 病患者相比,双阳性患者的肾活检更有慢性损伤的证据,但与单阳性患者相比,双阳性患者在治疗后从透析依赖中恢复的趋势更大,且具有中间的长期肾脏存活率。然而,所有三组患者的总体生存率相似。患者生存率差的预测因素包括年龄较大、严重肾功能衰竭和肺出血。没有单阳性抗 GBM 患者出现疾病复发,而大约一半的存活 AAV 患者和双阳性患者在中位随访 4.8 年后出现疾病复发。因此,双阳性患者具有真正的混合疾病表型,需要积极早期治疗抗 GBM 病,并仔细长期随访和考虑维持免疫抑制治疗 AAV。由于双阳性似乎很常见,需要进一步研究以确定这种关联的潜在机制并定义最佳治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e61f/5567410/32be06077773/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e61f/5567410/cca1fee03e5e/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e61f/5567410/0a9388a12534/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e61f/5567410/186bae6ea9e6/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e61f/5567410/32be06077773/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e61f/5567410/cca1fee03e5e/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e61f/5567410/0a9388a12534/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e61f/5567410/186bae6ea9e6/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e61f/5567410/32be06077773/gr4.jpg

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