Evidence map›Paper›PMID 36472788›Full record

ArticleJournal of nephrology2023

The spectrum and changes of biopsy-proven kidney diseases in Chinese children.

Guohua He, Liyuan Tao, Chenglong Li, Xuhui Zhong, Haibo Wang, Jie Ding

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Article in Journal of nephrology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.4field-weighted citation impact, top 19% of its field
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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6 citing papers in PubMed, 10 citations in OpenAlex.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors at 4 institutions in 1 country.

Guohua HeDepartment of Pediatrics, Peking University First Hospital, Beijing, China.
Liyuan TaoResearch Center of Clinical Epidemiology, Peking University Third Hospital, Beijing, China.
Chenglong LiPeking University Clinical Research Institute, Peking University First Hospital, Beijing, China.
Xuhui ZhongDepartment of Pediatrics, Peking University First Hospital, Beijing, China.
Haibo WangClinical Trial Unit, The First Affiliated Hospital, Sun Yat-Sen University, Guangzhou, China.
Jie DingDepartment of Pediatrics, Peking University First Hospital, Beijing, China. djnc_5855@126.com.
Peking University · CNPeking University First Hospital · CNPeking University Third Hospital · CNSun Yat-sen University · CN

Funding

Beijing Natural Science Foundation Z190023Fundamental Research Funds for Central Universities of the Central South University BMU2018MI015the Beijing Key Laboratory of Molecular Diagnosis and Study on Pediatric Genetic Diseases BZ0317the Capital Characteristic Clinical Application Research supported by Beijing Municipal Science & Technology Commission Z181100001718134
6 · The paper itself

Abstract

aimThe study aimed to investigate the spectrum of biopsy-proven kidney disease in Chinese children.

methodsRecords of children 0-17 years old who underwent native kidney biopsy from June 1st, 2013 to December 31st, 2018 in the national inpatients' database of China were analyzed. Biopsy-proven kidney diseases of different sex, age groups, and diagnosis, and the changing patterns of kidney disease compared with the previous study were analyzed.

resultsA total of 21,311 patients from 232 hospitals with a median age of 11.34 years were included. Immunoglobulin A vasculitis with nephritis (IgAVN) was the most common pathological finding [29.17%, 95% confidence interval (confidence interval, CI) = 28.56-29.78], followed by IgA nephropathy (IgAN) (22.70%, 95% CI = 22.14-23.27). IgAN was the most common finding in patients with hematuria (60.75%, 95% CI = 58.83-62.65], proteinuria (33.43%, 95% CI = 30.54-36.42), and hematuria plus proteinuria (62.77%, 95% CI = 56.19-69.02). Minimal change disease was the most common finding (40.69%, 95% CI = 39.41-41.98) in nephrotic syndrome. The proportion of IgAVN in patients with biopsy-proven glomerular disease increased year by year during 2013-2018 (p for trend < 0.001) and was higher than that of 2004-2014 [29.41% (95% CI = 29.10-29.72) in 2013-2018 vs. 13.35% (95% CI = 12.97-13.73) 2004-2014, p < 0.001]. The proportion of hepatitis B virus associated nephritis during 2013-2018 was lower than that of  2004-2014 [0.44% (95% CI = 0.36-0.54) in 2013-2018 vs. 0.87% (95% CI = 0.67-1.10) in 2004-2014, p < 0.001].

conclusionsIgAVN and IgAN were the most common types of pathological findings in children who underwent kidney biopsies from 2013 to 2018. The pathological spectrum of kidney biopsy changed over time.

Indexed as

Glomerulonephritis, IGAIgA VasculitisKidney DiseasesAdolescentBiopsyChildChild, PreschoolEast Asian PeopleHematuriaHumansInfantInfant, NewbornKidneyProteinuriaRetrospective StudiesBiopsyChildrenPathology

Identifiers

PMID36472788
OpenAlexW4310774830

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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.