Suppr超能文献

在一项大型多中心活动性狼疮肾炎患者队列中,第二次而不是第一次肾活检的临床和组织学发现可预测终末期肾病。

Clinical and histological findings at second but not at first kidney biopsy predict end-stage kidney disease in a large multicentric cohort of patients with active lupus nephritis.

机构信息

Unit of Rheumatology, Department of Medicine, DIMED, University of Padua, Padova, Italy.

Department of Medicine and Surgery, University of Milano Bicocca, Milan, Italy.

出版信息

Lupus Sci Med. 2022 May;9(1). doi: 10.1136/lupus-2022-000689.

Abstract

OBJECTIVE

To investigate second kidney biopsy as predictor of end-stage kidney disease (ESKD) in active lupus nephritis (LN).

METHODS

Patients with biopsy-proven LN (International Society of Nephrology/Renal Pathology Society 2003) who had undergone a second kidney biopsy between January 1990 and December 2018 were included. Clinical and histological findings at first and at second biopsy were analysed with Cox proportional hazard models to predict ESKD, defined as start of kidney replacement therapy. Survival curves were calculated with Kaplan-Meier method.

RESULTS

Ninety-two patients with LN were included, 87% females, mean follow-up 17.9±10.1 years. Reasons for second kidney biopsy encompassed nephritic flares (n=28, 30.4%), proteinuric flares (n=46, 50%) or lack of renal response (n=18, 19.5%). Class switch from first biopsy occurred in 50.5% of cases, mainly from non-proliferative towards proliferative classes. Class IV remained stable in over 50% of cases. Twenty-five patients (27.2%) developed ESKD, mostly belonging to the nephritic flare group (17/28, 60.7%). Independent predictors of ESKD at second biopsy were activity index (AI; (HR 95% CI) 1.20 (1.03 to 1.41), p=0.022), chronicity index (CI; 1.41 (1.09 to 1.82), p=0.008) and 24h-proteinuria (1.22 (1.04 to 1.42), p=0.013). AI≥2 (log-rank p=0.031), CI >4 (log-rank p=0.001) or proteinuria ≥3.5 g/day (log-rank=0.009) identified thresholds for higher ESKD risk. In a subgroup analysis, glomerular activity and tubular chronicity mostly accounted for AI and CI association with ESKD. No histological or laboratory predictors emerged at first biopsy (95% CI): AI: 0.88 to 1.19; CI: 0.66 to 1.20; proteinuria 0.85 to 1.08.

CONCLUSIONS

Findings at second but not at first kidney biopsy in patients with persistently active or relapsing LN inform about ESKD development in a long-term follow-up.

摘要

目的

探讨在活动性狼疮肾炎(LN)中,第二次肾活检作为终末期肾病(ESKD)预测指标的价值。

方法

纳入 1990 年 1 月至 2018 年 12 月间接受第二次肾活检的活检证实的 LN 患者。使用 Cox 比例风险模型分析第一次和第二次肾活检时的临床和组织学发现,以预测 ESKD,定义为开始肾脏替代治疗。使用 Kaplan-Meier 方法计算生存曲线。

结果

共纳入 92 例 LN 患者,女性占 87%,平均随访 17.9±10.1 年。第二次肾活检的原因包括肾炎性发作(n=28,30.4%)、蛋白尿性发作(n=46,50%)或肾脏无反应(n=18,19.5%)。50.5%的病例发生了从第一次活检的类型转换,主要是从非增殖性向增殖性类型转换。超过 50%的病例 IV 级保持稳定。25 例(27.2%)患者发展为 ESKD,主要来自肾炎性发作组(17/28,60.7%)。第二次肾活检发生 ESKD 的独立预测因素是活动指数(AI;HR 95%CI 为 1.20(1.03 至 1.41),p=0.022)、慢性指数(CI;1.41(1.09 至 1.82),p=0.008)和 24 小时蛋白尿(1.22(1.04 至 1.42),p=0.013)。AI≥2(对数秩检验 p=0.031)、CI>4(对数秩检验 p=0.001)或蛋白尿≥3.5 g/天(对数秩检验=0.009)确定了 ESKD 风险较高的阈值。在亚组分析中,肾小球活性和肾小管慢性主要导致 AI 和 CI 与 ESKD 相关。在第一次肾活检时,没有出现任何组织学或实验室预测因素(95%CI):AI:0.88 至 1.19;CI:0.66 至 1.20;蛋白尿:0.85 至 1.08。

结论

在持续活动或复发的 LN 患者中,第二次而非第一次肾活检的结果可在长期随访中提供 ESKD 发展的信息。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验