Evidence map›Paper›PMID 41357184›Full record

SynthesisFrontiers in immunology2025

Prevalence of histopathological subtypes associated with steroid-resistant nephrotic syndrome in children: a systematic review and meta-analysis.

Sen Lin, Shanshan Zheng, Wanying Dong, Yangyang Tian, Hao Li, Xinyuan Gao, Fang Qin, Chaoqun Ma, Yipeng Liu

Abstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Sen LinDepartment of Nephrology, The First Affiliated Hospital of Shandong First Medical University & Shandong Provincial Qianfoshan Hospital, Shandong Institute of Nephrology, Jinan, China.
Shanshan ZhengDepartment of Nephrology, The First Affiliated Hospital of Shandong First Medical University & Shandong Provincial Qianfoshan Hospital, Shandong Institute of Nephrology, Jinan, China.
Wanying DongDepartment of Nephrology, Shandong Second Provincial General Hospital, Jinan, China.
Yangyang TianDepartment of Nephrology, The First Affiliated Hospital of Shandong First Medical University & Shandong Provincial Qianfoshan Hospital, Shandong Institute of Nephrology, Jinan, China.
Hao LiDepartment of Nephrology, The First Affiliated Hospital of Shandong First Medical University & Shandong Provincial Qianfoshan Hospital, Shandong Institute of Nephrology, Jinan, China.
Xinyuan GaoDepartment of Nephrology, The First Affiliated Hospital of Shandong First Medical University & Shandong Provincial Qianfoshan Hospital, Shandong Institute of Nephrology, Jinan, China.
Fang QinDepartment of Nephrology, The First Affiliated Hospital of Shandong First Medical University & Shandong Provincial Qianfoshan Hospital, Shandong Institute of Nephrology, Jinan, China.
Chaoqun Ma *Department of Emergency Medicine, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, China.
Yipeng Liu *Department of Nephrology, The First Affiliated Hospital of Shandong First Medical University & Shandong Provincial Qianfoshan Hospital, Shandong Institute of Nephrology, Jinan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Steroid-resistant nephrotic syndrome (SRNS) in children is associated with various histopathological subtypes;however, the prevalence of these subtypes remains insufficiently defined. These subtypes often demonstrate variable responses to identical therapeutic regimens and are indicative of distinct clinical outcomes. This systematic review and meta-analysis seeks to comprehensively elucidate the prevalence of the most common histopathological subtypes in pediatric SRNS, offering valuable insights that may inform future therapeutic strategies and improve prognostic predictions for affected patients. Methods: We conducted a comprehensive literature search across four major databases: PubMed, Embase, Web of Science, and Cochrane, with coverage extending from the inception of these databases up to December 2023. Two independent researchers screened the identified studies, selecting only cross-sectional and longitudinal studies that reported the prevalence of histopathological subtypes in pediatric SRNS. The quality of the studies was assessed using the Joanna Briggs Institute Critical Appraisal Checklist, and only those meeting the required quality criteria were included. Data were extracted from the selected studies using a standardized data extraction form. Meta-analysis was performed with Stata software to estimate the prevalence of different histopathological subtypes in pediatric SRNS. Subgroup analyses were conducted to explore potential sources of heterogeneity. Publication bias was assessed using funnel plots and the Begg test, and sensitivity analysis was also conducted. Results: The most commonly reported histopathological subtypes associated with SRNS in children are focal segmental glomerulosclerosis (FSGS), membranous nephropathy (MN), minimal change disease (MCD), mesangioproliferative glomerulonephritis (MesPGN), and membranoproliferative glomerulonephritis (MPGN). Among these, the subtype with the highest average prevalence is FSGS, at 39%, followed by MCD (27%), MesPGN (23%), MPGN (18%), and MN (4%). Conclusion: FSGS exhibits a notably high prevalence in SRNS and remains the most frequently observed histopathological lesion associated with this condition. Systematic review registration: https://www.crd.york.ac.uk/PROSPERO/view/CRD420251000869, identifier CRD420251000869.

Indexed as

Nephrotic SyndromeChildDrug ResistanceGlomerulosclerosis, Focal SegmentalHumansPrevalenceSteroidsSteroidsfocal segmental glomerulosclerosis (FSGS)histopathologic subtypesimmune-mediatedprevalencesteroid-resistant nephrotic syndrome in children

Identifiers

PMID41357184
PMCPMC12675457

What Socratic holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

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 Socratic graph.