﻿<?xml version="1.0" encoding="UTF-8"?>
<ArticleSet>
  <Article>
    <Journal>
      <PublisherName>Nickan Research Institute</PublisherName>
      <JournalTitle>Journal of Renal Injury Prevention</JournalTitle>
      <Issn>2345-2781</Issn>
      <Volume>14</Volume>
      <Issue>3</Issue>
      <PubDate PubStatus="ppublish">
        <Year>2025</Year>
        <Month>09</Month>
        <DAY>01</DAY>
      </PubDate>
    </Journal>
    <ArticleTitle>Exploring the correlation of remnant-like particle cholesterol levels with CKD developing risk: a comprehensive systematic review and meta-analysis</ArticleTitle>
    <FirstPage>e38437</FirstPage>
    <LastPage>e38437</LastPage>
    <ELocationID EIdType="doi">10.34172/jrip.2025.38437</ELocationID>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Halime</FirstName>
        <LastName>Aali</LastName>
        <Identifier Source="ORCID">https://orcid.org/0009-0007-2587-7676</Identifier>
      </Author>
      <Author>
        <FirstName>Sara</FirstName>
        <LastName>Bazgiri</LastName>
        <Identifier Source="ORCID">https://orcid.org/0009-0004-1105-7309</Identifier>
      </Author>
      <Author>
        <FirstName>Zahra</FirstName>
        <LastName>Jamalafrouz</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0001-8955-8147</Identifier>
      </Author>
      <Author>
        <FirstName>Seyed Saied</FirstName>
        <LastName>Rajaei Ramsheh</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0003-4770-9634</Identifier>
      </Author>
      <Author>
        <FirstName>Mahboobeh</FirstName>
        <LastName>Askarizade</LastName>
        <Identifier Source="ORCID">https://orcid.org/0009-0006-2532-6818</Identifier>
      </Author>
      <Author>
        <FirstName>Zahra</FirstName>
        <LastName>Bazargani</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0003-1943-5752</Identifier>
      </Author>
      <Author>
        <FirstName>Fariba</FirstName>
        <LastName>Asadi Noghabi</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0003-1862-1166</Identifier>
      </Author>
      <Author>
        <FirstName>Erfan</FirstName>
        <LastName>Shafiei</LastName>
        <Identifier Source="ORCID">https://orcid.org/0009-0009-2484-763X</Identifier>
      </Author>
      <Author>
        <FirstName>Dadkhoda</FirstName>
        <LastName>Soofi</LastName>
        <Identifier Source="ORCID">https://orcid.org/0000-0002-8582-4783</Identifier>
      </Author>
    </AuthorList>
    <PublicationType>Journal Article</PublicationType>
    <ArticleIdList>
      <ArticleId IdType="doi">10.34172/jrip.2025.38437</ArticleId>
    </ArticleIdList>
    <History>
      <PubDate PubStatus="received">
        <Year>2025</Year>
        <Month>01</Month>
        <Day>08</Day>
      </PubDate>
      <PubDate PubStatus="accepted">
        <Year>2025</Year>
        <Month>03</Month>
        <Day>28</Day>
      </PubDate>
    </History>
    <Abstract>Introduction: Chronic kidney disease (CKD) is a progressing illness worldwide and the relationship between remnant-C and CKD is still uncertain. Indeed, this study aims to evaluate the relationship between remnant-C and the risk of CKD development in a systematic review and meta-analysis study. Materials and Methods: This study surveyed databases like Web of Science, Cochrane, ProQuest, PubMed, Embase, and Google Scholar up to December 17, 2024. Data analysis was performed by STATA 14 software, and the test confidential level was P&lt;0.05. Results: Remnant-C causes a higher risk of CKD (OR: 1.31, 95% CI: 1.22, 1.41). In addition, the remnant-C in second quartile (R:1.20, 95% CI: 1.13, 1.27), third quartile (OR:1.26, 95% CI: 1.13, 1.40), 4th quartile (OR:1.62, 95% CI: 1.42, 1.86), second tertile (OR:1.12, 95% CI: 1.06, 1.19) and 3rd tertile (OR:1.23, 95% CI: 1.16, 1.31) further increased CKD risk. According to the subgroup analysis, remnant-C in the group with the range of 40 to 49 years (OR:1.32, 95% CI: 1.18, 1.48), 50 to 59 years (OR:1.26, 95% CI: 1.14, 1.40), 60 to 69 years (OR:1.39, 95% CI: 1.14, 1.69), in men (OR:1.23, 95% CI: 1.13, 1.33) and women (OR:1.51, 95% CI: 1.25, 1.82) lead to higher risk of CKD. Additionally, remnant-C in diabetic patients (OR: 1.35, 95% CI: 1.22, 1.48), individuals with body mass index (BMI) &lt;25 (OR: 1.28, 95% CI: 1.15, 1.43), and individuals with BMI&gt;25 (OR:1.39, 95% CI: 1.20, 1.60) lead to a higher risk of CKD, either. Conclusion: Our study reveals that remnant-C causes a higher risk of CKD, and a higher level of remnant-C leads to a higher risk of CKD. Notably, remnant-C causes CKD in women more than men and in individuals with BMI &gt;25 kg/m2 more than ones with BMI&lt;25 kg/m2 , shedding new light on the gender and BMI-specific risks associated with remnant-C. Registration: This study has been compiled based on the PRISMA checklist, and its protocol was registered on the PROSPERO (ID: CRD42025632075) and Research Registry (UIN: reviewregistry1936) websites.  </Abstract>
    <ObjectList>
      <Object Type="keyword">
        <Param Name="value">Renal insufficiency</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Chronic kidney disease</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Chronic renal disease</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Remnant-like particle cholesterol</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">RLP-C cholesterol</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Remnant cholesterol</Param>
      </Object>
    </ObjectList>
  </Article>
</ArticleSet>