Evidence map›Paper›PMID 41260879›Full record

ArticleLupus science & medicine2025

Development and validation of nomograms for predicting activity index and tubulointerstitial lesions in lupus nephritis: a multicentre study.

Zishan Lin, Bingjing Jiang, Fan Wu, Wenfeng Wang, Yufeng Liang, Shidong Xie, Hong Chen, Jianxin Wan, Caiming Chen, Yanfang Xu

Abstract readMulticenter StudyValidation Study
In one paragraph

Article in Lupus science & medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Zishan Lin *Department of Nephrology, Blood Purification Research Center, the First Affiliated Hospital, Fujian Medical University, Fuzhou, Fujian, China.ORCID 0000-0003-3513-6939
Bingjing Jiang *Department of Nephrology, Blood Purification Research Center, the First Affiliated Hospital, Fujian Medical University, Fuzhou, Fujian, China.
Fan WuDepartment of Nephrology, the Affiliated Hospital of Putian University, Putian, Fujian, China.
Wenfeng WangDepartment of Nephrology, Blood Purification Research Center, the First Affiliated Hospital, Fujian Medical University, Fuzhou, Fujian, China.
Yufeng LiangDepartment of Nephrology, The Second Hospital of Longyan, Longyan, Fujian, China.
Shidong XieDepartment of Nephrology, Blood Purification Research Center, the First Affiliated Hospital, Fujian Medical University, Fuzhou, Fujian, China.
Hong ChenDepartment of Pathology, the First Affiliated Hospital, Fujian Medical University, Fuzhou, Fujian, China.
Jianxin WanDepartment of Nephrology, Blood Purification Research Center, the First Affiliated Hospital, Fujian Medical University, Fuzhou, Fujian, China.
Caiming ChenDepartment of Nephrology, Blood Purification Research Center, the First Affiliated Hospital, Fujian Medical University, Fuzhou, Fujian, China chencm419@163.com xuyanfang99@hotmail.com.
Yanfang XuDepartment of Nephrology, Blood Purification Research Center, the First Affiliated Hospital, Fujian Medical University, Fuzhou, Fujian, China chencm419@163.com xuyanfang99@hotmail.com.ORCID 0000-0002-6207-545X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveLupus nephritis (LN) is a prevalent renal manifestation in patients with SLE, with kidney biopsy remaining the gold standard for evaluating disease activity. However, the invasive nature of biopsy and associated risks highlight the need for a non-invasive predictive tool. This study aimed to construct and validate predictive models for the activity index (AI) and tubulointerstitial lesions (TIL) in patients with LN as an alternative tool to assist clinicians in decision-making when kidney biopsy is not feasible.

methodsWe enrolled 266 patients with LN diagnosed by kidney biopsy from three centres, divided into a training cohort (n=213) and a validation cohort (n=53). Patients were stratified by AI and TIL scores: high AI (AI >4), low AI (AI ≤4), high TIL (TIL >4) and low TIL (TIL ≤4). Clinicopathological data were systematically collected. Multivariate logistic regression was employed to identify significant risk factors for high AI and TIL, and nomograms for individualised assessment were constructed. Model performance was evaluated using receiver operating characteristic curves, decision curve analysis, calibration plots and the Hosmer-Lemeshow test.

resultsThe key independent risk factors for high AI included lymphocyte count, haematuria, albumin, serum creatinine, complement 4 and antihistone antibodies. For high TIL, the risk factors included age, haemoglobin, platelet count, blood urea nitrogen and antiribosomal P antibodies. Both nomograms demonstrated favourable performance in terms of discrimination and calibration across both cohorts.

conclusionThe developed nomograms provide reliable, non-invasive tools for identifying patients with LN with high AI and TIL, which can improve clinical risk assessment and help guide more personalised management strategies.

Indexed as

KidneyLupus NephritisNomogramsAdultBiopsyCreatinineFemaleHumansLogistic ModelsMaleMiddle AgedRisk FactorsROC CurveSeverity of Illness IndexYoung AdultCreatinineAutoimmune DiseasesLupus NephritisSystemic Lupus Erythematosus

Identifiers

PMID41260879
PMCPMC12636907

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.