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269例抗中性粒细胞胞浆抗体相关性血管炎患者的临床特征及预后

Clinical characteristics and prognosis in 269 patients with antineutrophil cytoplasimc antibody associated vasculitis.

作者信息

Wu Ting, Zhong Yong, Zhou Ya'ou, Chen Jinbiao, Yang Yingqiang, Tang Rong, Meng Ting, Xiao Zhou, Xiao Xiangcheng, Zhou Qiaoling, Xiao Ping

机构信息

Department of Nephrology, Xiangya Hospital, Central South University, Changsha 410008.

Department of Rheumatology and Immunology, Xiangya Hospital, Central South University, Changsha 410008.

出版信息

Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2020 Aug 28;45(8):916-922. doi: 10.11817/j.issn.1672-7347.2020.190436.

Abstract

OBJECTIVES

To investigate the clinic-pathological characteristics, prognosis and its risk factors for antineutrophil cytoplasimc antibody (ANCA)-associated vasculitis (AAV).

METHODS

The basic information and clinic-pathological characteristics of AAV patients, who was diagnosed from January 2010 to January 2018 in Xiangya Hospital, Central South University, were retrospectively collected. The renal survival and patient survival were regular followed up, and their clinical pathological, prognosis data and risk factors for renal were analyzed.

RESULTS

Among 269 AAV patients, 225 patients (83.64%) were microscopic polyangiitis (MPA), 33 patients (12.27%) were granulomatosis with polyangiitis (GPA), and 11 patients (4.09%) were eosinophilic granulomatosis with polyangiitis (EGPA). Male-to-female ratio was almost 1∶1 for MPA (147/122), but GPA and EGPA was more frequent among man. The medium time from disease onset to diagnosis was 64.0 (32.5, 148.5) days, 65 patients (24.16%) were diagnosed within 30 days. A total of 94.67% patients had kidney involvement in MPA patients, which was significantly higher than that in patients with GPA (63.63%), but ear, nose, and throat manifestations were more frequent in GPA patients. The 1-year kidney survival rates of GPA and MPA patients in this study were 75% and 59.3%, respectively. The 1-year death rates were 16.7% and 16.9%, respectively. The multivariable logistic regression analysis revealed that the low platelet level, low globulin level, low immunoglobin G, and high serum creatinine level were independent risk factors for the 1-year renal survival rate in AAV patients. Multiple factor logistic regression analysis showed that the serum creatinine level was an independent risk factor for all-cause mortality.

CONCLUSIONS

MPA is the priority in the AAV patients. The proportion of patients with advanced end-stage renal disease and mortality is still high, and the early diagnosis and treatment in time is crucial for the improvement of prognosis for AAV.

摘要

目的

探讨抗中性粒细胞胞浆抗体(ANCA)相关性血管炎(AAV)的临床病理特征、预后及其危险因素。

方法

回顾性收集2010年1月至2018年1月在中南大学湘雅医院确诊的AAV患者的基本信息和临床病理特征。定期随访肾脏生存率和患者生存率,并分析其临床病理、预后数据及肾脏危险因素。

结果

269例AAV患者中,显微镜下多血管炎(MPA)225例(83.64%),肉芽肿性多血管炎(GPA)33例(12.27%),嗜酸性肉芽肿性多血管炎(EGPA)11例(4.09%)。MPA患者男女比例约为1∶1(147/122),但GPA和EGPA在男性中更为常见。从发病到诊断的中位时间为64.0(32.5,148.5)天,65例(24.16%)患者在30天内确诊。MPA患者中共有94.67%有肾脏受累,显著高于GPA患者(63.63%),但GPA患者耳、鼻、喉表现更为常见。本研究中GPA和MPA患者的1年肾脏生存率分别为75%和59.3%。1年死亡率分别为16.7%和16.9%。多变量logistic回归分析显示,血小板水平低、球蛋白水平低、免疫球蛋白G低和血清肌酐水平高是AAV患者1年肾脏生存率的独立危险因素。多因素logistic回归分析显示,血清肌酐水平是全因死亡率的独立危险因素。

结论

MPA是AAV患者中的主要类型。晚期终末期肾病患者比例和死亡率仍较高,及时进行早期诊断和治疗对改善AAV预后至关重要。

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