Evidence map›Paper›PMID 41126366›Full record

ArticleEuropean journal of medical research2025

Novel inflammation biomarkers in adult minimal change disease: predicting steroid-resistance and relapse.

Weiwei Zhang, Wei Lin, Huipeng Ge, Wenbin Tang, Zhangzhe Peng, Qiongjing Yuan, Xiangcheng Xiao

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Article in European journal of medical research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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7 authors.

Weiwei ZhangDepartment of Nephrology, Xiangya Hospital of Central South University, Changsha, China.
Wei LinDepartment of Pathology, Xiangya Hospital of Central South University, Changsha, China.
Huipeng GeDepartment of Nephrology, Xiangya Hospital of Central South University, Changsha, China.
Wenbin TangHealth Management Center, Xiangya Hospital of Central South University, Changsha, China.
Zhangzhe PengDepartment of Nephrology, Xiangya Hospital of Central South University, Changsha, China.
Qiongjing YuanDepartment of Nephrology, Xiangya Hospital of Central South University, Changsha, China. yuanqiongjing@csu.edu.cn.
Xiangcheng XiaoDepartment of Nephrology, Xiangya Hospital of Central South University, Changsha, China. xiaoxc@csu.edu.cn.

Funding

General Programs of National Natural Science Foundation of China 82173877Key Research and Development Program of Hunan Province 2021SK2015Major Program of National Natural Science Foundation of China 82090024National Key R&D Program of China 2020YFC2005004National Natural Science Foundation of China 82070717Natural Science Foundation of Hunan province China 2020JJ5942 and 2019JJ40515
6 · The paper itself

Abstract

introductionThe novel systemic inflammation markers are a class of indicators combining clinically common laboratory indices, reflecting the underlying immune and inflammatory status. Minimal change disease (MCD) is an important cause of idiopathic nephrotic syndrome (INS) in adults. Novel systemic inflammation markers were evaluated for their ability to predict treatment response to steroids and subsequent relapse in adult-onset MCD.

methodsThis unicentric, retrospective study included the clinical data of adult-onset INS patients who were pathologically diagnosed with MCD at Xiangya Hospital of Central South University from January 2010 to December 2021 and followed up with the patients' remission after adequate steroid treatment, starting from the time of initial complete remission to May 31, 2022, with recurrence as the end-point event. Eight common and associated novel systemic inflammation markers were collected, and univariate analysis of these markers was performed using dummy variable assignment or maximally selected rank statistics. Multivariate logistic regression and Cox regression statistics identified the independent risk factors for steroid resistance and relapse after initial remission in adult-onset MCD, respectively.

resultsA total of 121 patients were included; the median age was 22 (19,40) years, and there were 92 (76%) men. Adequate corticosteroids were the initial treatment: 98 (81%) patients achieved remission, and 23 (19%) developed steroid resistance. Of the 98 patients with remission, the median age was 25 (19, 44) years, 76 (77.6%) were male, the median follow-up time was 11.4 (6.3, 33.4) months, and 46 (46.9%) experienced relapse. The multivariate analysis showed that elevated C-reactive protein to albumin ratio (CAR) (≥ 0.196) and derived neutrophil/ (leukocyte minus neutrophil) ratio (dNLR) (≥ 1.32) were independent predictors of steroid resistance and relapse in adult-onset MCD, respectively.

conclusionsThe novel systemic inflammation markers CAR and dNLR may play significant roles in steroid treatment and the prognosis of MCD in adults, and deeper clinical studies in the future are warranted.

Indexed as

Adrenal Cortex HormonesDrug ResistanceInflammationNephrosis, LipoidAdultBiomarkersFemaleHumansMalePrognosisRecurrenceRetrospective StudiesSteroidsYoung AdultAdrenal Cortex HormonesBiomarkersSteroidsIndependent risk factorMinimal change diseaseNovel systemic inflammation markersRelapseSteroid resistance

Identifiers

PMID41126366
PMCPMC12542185

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