﻿<?xml version="1.0" encoding="UTF-8"?>
<ArticleSet>
  <Article>
    <Journal>
      <PublisherName>Society of Diabetic Nephropathy Prevention</PublisherName>
      <JournalTitle>Journal of Nephropharmacology</JournalTitle>
      <Issn>2345-4202</Issn>
      <Volume>13</Volume>
      <Issue>2</Issue>
      <PubDate PubStatus="ppublish">
        <Year>2024</Year>
        <Month>06</Month>
        <DAY>29</DAY>
      </PubDate>
    </Journal>
    <ArticleTitle>Comparative histological and clinical differences between children and adults in IgA nephropathy</ArticleTitle>
    <FirstPage>e12705</FirstPage>
    <LastPage>e12705</LastPage>
    <ELocationID EIdType="doi">10.34172/npj.2024.12705</ELocationID>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Samaneh</FirstName>
        <LastName>Zandifar</LastName>
        <Identifier Source="ORCID">https://orcid.org/0009-0008-5316-8241</Identifier>
      </Author>
      <Author>
        <FirstName>Azadeh</FirstName>
        <LastName>Khayyat</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0002-1867-1609</Identifier>
      </Author>
      <Author>
        <FirstName>Arefeh</FirstName>
        <LastName>Zahmatkesh</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0001-5745-1513</Identifier>
      </Author>
      <Author>
        <FirstName>Mohammad Ali</FirstName>
        <LastName>Esmaeil pour</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0002-0393-3928</Identifier>
      </Author>
    </AuthorList>
    <PublicationType>Journal Article</PublicationType>
    <ArticleIdList>
      <ArticleId IdType="doi">10.34172/npj.2024.12705</ArticleId>
    </ArticleIdList>
    <History>
      <PubDate PubStatus="received">
        <Year>2024</Year>
        <Month>02</Month>
        <Day>20</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2024</Year>
        <Month>06</Month>
        <Day>25</Day>
      </PubDate>
    </History>
    <Abstract>IgA nephropathy (IgAN), as an autoimmune-mediated kidney disease worldwide, is considered an important cause of end-stage renal disease in adults. The most important diagnostic method in the patients is the evaluation of the biopsy findings. To date, several studies have examined different histopathological findings in patients with IgAN with an attempt to find out the relationship between morphologic findings with outcome and disease progression. Although there have been limited reports of IgAN in children, the Oxford scoring system is currently the most widely used IgAN classification and is validated for use in children and adults. In this review, we examined the most frequently published pathological findings on IgAN with a focus on Oxford classification between adults and children and attempted to highlight the key differences. The main purpose of this study was to assess the prognosis of patients with IgAN in childhood and adulthood, with emphasis on pathological risk factors for disease progression. Our results indicated that acute glomerulonephritis in children was predominantly reported more than chronic lesions. In addition, mesangial and endocapillary lesions were more common in children than in adults. In contrast, glomerular sclerosis, tubular atrophy/interstitial fibrosis, and atherosclerotic lesions were more common in older individuals.</Abstract>
    <ObjectList>
      <Object Type="keyword">
        <Param Name="value">Immunoglobulin A nephropathy</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Pediatrics</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">IgA nephropathy</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Oxford classification</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">End-stage renal disease</Param>
      </Object>
    </ObjectList>
  </Article>
</ArticleSet>