开发用于预测 IgA 肾病患者慢性肾病进展风险的提名图模型,并进行内部和外部验证。

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
ACS Applied Bio Materials Pub Date : 2024-10-30 eCollection Date: 2024-01-01 DOI:10.7717/peerj.18416
Ying Zhang, Zhixin Wang, Wenwu Tang, Xinzhu Yuan, Xisheng Xie
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引用次数: 0

摘要

背景:IgA肾病(IgAN)是慢性肾脏病(CKD)中最常见的原发性肾小球疾病,其临床和病理表现均具有显著的异质性。我们旨在探索影响短期预后(≥90 天)的风险因素,并构建一个提名图模型,用于评估 IgAN 患者 CKD 进展的风险:方法:回顾性收集两个中心通过活检确诊的 IgAN 患者的临床和病理资料。采用逻辑回归分析训练队列数据集,确定独立预测因子,并根据最终变量构建提名图模型。预测模型经过了内部和外部验证,并使用曲线下面积(AUC)、校准曲线和决策曲线分析对其性能进行了评估:在建模组的患者中,有 129 人(41.6%)在接受 3 个月治疗后病情没有得到缓解,这表明他们面临着 CKD 进展的高风险。多变量逻辑回归分析表明,体重指数、尿蛋白排泄量和肾小管萎缩/间质纤维化是风险分层的独立预测因素。利用最终变量建立了一个提名图模型。训练集、内部验证集和外部验证集的 AUC 分别为 0.746(95% 置信区间 (CI) [0.691-0.8])、0.764(95% CI [0.68-0.85])和 0.749(95% CI [0.65-0.85])。亚组分析的验证也显示了令人满意的AUC:本研究开发并验证了一种实用的提名图,可单独预测 IgAN 患者的短期治疗效果(≥90 天)和 CKD 进展风险。它为及时的个性化干预和治疗策略提供了可靠的指导。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development and internal and external validation of a nomogram model for predicting the risk of chronic kidney disease progression in IgA nephropathy patients.

Background: IgA nephropathy (IgAN) is the most common primary glomerular disease in chronic kidney disease (CKD), exhibiting significant heterogeneity in both clinical and pathological presentations. We aimed to explore the risk factors influencing short-term prognosis (≥90 days) and to construct a nomogram model for evaluating the risk of CKD progression in IgAN patients.

Methods: Clinical and pathological data of patients diagnosed with IgAN through biopsy at two centers were retrospectively collected. Logistic regression was employed to analyze the training cohort dataset and identify the independent predictors to construct a nomogram model based on the final variables. The predictive model was validated both internally and externally, with its performance assessed using the area under the curve (AUC), calibration curves, and decision curve analysis.

Results: Out of the patients in the modeling group, 129 individuals (41.6%) did not achieve remission following 3 months of treatment, indicating a high risk of CKD progression. A multivariate logistic regression analysis demonstrated that body mass index, urinary protein excretion, and tubular atrophy/interstitial fibrosis were identified as independent predictors for risk stratification. A nomogram model was formulated utilizing the final variables. The AUCs for the training set, internal validation set, and external validation set were 0.746 (95% confidence intervals (CI) [0.691-0.8]), 0.764 (95% CI [0.68-0.85]), and 0.749 (95% CI [0.65-0.85]), respectively. The validation of the subgroup analysis also demonstrated a satisfactory AUC.

Conclusion: This study developed and validated a practical nomogram that can individually predict short-term treatment outcomes (≥90 days) and the risk of CKD progression in IgAN patients. It provides reliable guidance for timely and personalized intervention and treatment strategies.

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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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