儿童期狼疮性肾炎患者早期不良预后的临床和实验室危险因素——单中心回顾性研究

IF 3.1 4区 医学 Q3 IMMUNOLOGY
Wei Qijiao, Huang Fujia, Yang Bing, Wang Changyan, Zhong Linqing, Dong Yanqing, Wang Wei, Song Hongmei
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引用次数: 0

摘要

目的儿童期狼疮性肾炎(LN)较成人更为严重。在成人中,诱导治疗3个月时的缓解和3年后的缓解之间存在显著的相关性。而对儿童LN早期预后不良的危险因素研究较少。因此,本研究探讨早期不良反应的危险因素,以帮助医生制定有效的治疗策略。方法回顾性分析2012年1月至2018年1月北京协和医院收治的99例LN患儿的临床资料。在本研究中,完全缓解(CR)定义为实验室检查结果完全正常,包括血常规、肾功能、白蛋白、补体和红细胞沉降率,24小时尿总蛋白(24小时UTP)小于150mg。治疗3个月后,15例患儿达到CR,归预后良好组(n = 15)。84例未达到CR,属于预后不良组(n = 84)。比较两组患者临床及实验室指标的差异。结果根据纳入和排除标准,116例LN患儿中有99例纳入本研究。预后良好组15例。预后不良组84例。预后不良组皮疹(32.1% vs. 6.7%, p = 0.036)、口腔溃疡(81.0% vs. 53.3%, p = 0.027)发生率高于预后良好组。不良预后组24 h UTP (g)[2.46(1.41, 4.86)比0.56 (0.30,0.66),p <; 0.001]和血清肌酐(umol/L)[53.0(40.3, 65.0)比39.0 (29.8,51.5),p = 0.017]较高。预后不良组白蛋白(g/L)(28.7±8.1∶34.5±5.3,p = 0.003)较预后不良组低。Logistic回归分析显示,皮疹(p = 0.036)、口腔溃疡(p = 0.027)、高24 h UTP (p < 0.001)、高肌酐(p = 0.017)和低血清白蛋白(p = 0.003)与儿童期LN早期预后不良显著相关。结论皮疹的发生不容忽视,尤其对于口腔溃疡患儿,应对各系统进行综合评价,以免造成治疗不积极,影响预后。高24小时UTP对儿童期起病LN的早期不良预后有积极的预测价值。积极控制蛋白尿和实现快速肾脏缓解是良好预后的关键。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Clinical and Laboratory Risk Factors of Early Poor Outcome in Patients With Childhood-Onset Lupus Nephritis—A Single-Center Retrospective Study

Clinical and Laboratory Risk Factors of Early Poor Outcome in Patients With Childhood-Onset Lupus Nephritis—A Single-Center Retrospective Study

Objective

Childhood-onset lupus nephritis (LN) tends to be more severe than in adults. A significant correlation between remission at 3 months of induction therapy and remission after 3 years was found in adults. While few studies on the risk factors of poor early prognosis in children with LN were made. Thus, this study investigated the risk factors of early poor response to help doctors develop effective treatment strategies.

Methods

A total of 99 LN children at Peking Union Medical College Hospital from January 2012 to January 2018 were evaluated and clinical data were retrospectively collected. In the study, a complete remission (CR) was defined as laboratory test results were completely normal, including blood routine, renal function, albumin, complement, and erythrocyte sedimentation rate, and the 24-h urinary total protein (24 h UTP) was less than 150 mg. After 3 months of treatment, 15 children achieved CR, and they were in good prognosis group (n = 15). While 84 did not achieve CR, and they were in poor prognosis group (n = 84). We compared the differences of clinical and laboratory indicators between the two groups.

Results

According to inclusion and exclusion criteria, 99 of 116 children with LN were included in this study. And 15 LN children were in good prognosis group. While 84 patients were in poor prognosis group. The incidence of rash (32.1% vs. 6.7%, p = 0.036) and oral ulcer (81.0% vs. 53.3%, p = 0.027) in poor prognosis group is higher than that in the good prognosis group. The 24 h UTP (g) [2.46 (1.41, 4.86) vs. 0.56 (0.30, 0.66), p < 0.001] and the serum creatinine (umol/L) [53.0 (40.3, 65.0) vs. 39.0 (29.8, 51.5), p = 0.017] were higher in poor prognosis group. The albumin (g/L) (28.7 ± 8.1 vs. 34.5 ± 5.3, p = 0.003) is lower in poor prognosis group. Logistic regression analysis showed that rash (p = 0.036), oral ulcer (p = 0.027), high 24 h UTP (p < 0.001), high creatinine (p = 0.017), and low serum albumin (p = 0.003) were significantly associated with poor early prognosis in childhood-onset LN.

Conclusion

The occurrence of rash cannot be ignored, especially for children with oral ulcers, a comprehensive evaluation of each system should be carried out, so as not to cause inactive treatment and affect the prognosis. High 24 h UTP have a positive predictive value for the early poor outcome of childhood-onset LN. Active control of proteinuria and achieving rapid renal remission is crucial for good prognosis.

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来源期刊
Immunity, Inflammation and Disease
Immunity, Inflammation and Disease Medicine-Immunology and Allergy
CiteScore
3.60
自引率
0.00%
发文量
146
审稿时长
8 weeks
期刊介绍: Immunity, Inflammation and Disease is a peer-reviewed, open access, interdisciplinary journal providing rapid publication of research across the broad field of immunology. Immunity, Inflammation and Disease gives rapid consideration to papers in all areas of clinical and basic research. The journal is indexed in Medline and the Science Citation Index Expanded (part of Web of Science), among others. It welcomes original work that enhances the understanding of immunology in areas including: • cellular and molecular immunology • clinical immunology • allergy • immunochemistry • immunogenetics • immune signalling • immune development • imaging • mathematical modelling • autoimmunity • transplantation immunology • cancer immunology
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