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    <Identifier>25dkou192</Identifier>
    <IdentifierDoi>10.3205/25dkou192</IdentifierDoi>
    <IdentifierUrn>urn:nbn:de:0183-25dkou1920</IdentifierUrn>
    <ArticleType>Meeting Abstract</ArticleType>
    <TitleGroup>
      <Title language="en">Paraspinal muscle atrophy and lumbar disc degeneration: Independent or interconnected processes&#63;</Title>
    </TitleGroup>
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      <Creator>
        <PersonNames>
          <Lastname>Schoennagel</Lastname>
          <LastnameHeading>Schoennagel</LastnameHeading>
          <Firstname>Lukas</Firstname>
          <Initials>L</Initials>
        </PersonNames>
        <Address>
          <Affiliation>Charit&#233; Universit&#228;tsmedizin Berlin, Berlin, Deutschland</Affiliation>
        </Address>
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      <Creator>
        <PersonNames>
          <Lastname>Hoehl</Lastname>
          <LastnameHeading>Hoehl</LastnameHeading>
          <Firstname>Bernhard</Firstname>
          <Initials>B</Initials>
        </PersonNames>
        <Address>
          <Affiliation>Charit&#233; Universit&#228;tsmedizin Berlin, Berlin, Deutschland</Affiliation>
        </Address>
        <Creatorrole corresponding="no" presenting="no">author</Creatorrole>
      </Creator>
      <Creator>
        <PersonNames>
          <Lastname>Berndt</Lastname>
          <LastnameHeading>Berndt</LastnameHeading>
          <Firstname>Anna</Firstname>
          <Initials>A</Initials>
        </PersonNames>
        <Address>
          <Affiliation>Charit&#233; Universit&#228;tsmedizin Berlin, Berlin, Deutschland</Affiliation>
        </Address>
        <Creatorrole corresponding="no" presenting="no">author</Creatorrole>
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      <Creator>
        <PersonNames>
          <Lastname>Reitmaier</Lastname>
          <LastnameHeading>Reitmaier</LastnameHeading>
          <Firstname>Sandra</Firstname>
          <Initials>S</Initials>
        </PersonNames>
        <Address>
          <Affiliation>Charit&#233; Universit&#228;tsmedizin Berlin, Berlin, Deutschland</Affiliation>
        </Address>
        <Creatorrole corresponding="no" presenting="no">author</Creatorrole>
      </Creator>
      <Creator>
        <PersonNames>
          <Lastname>Pumberger</Lastname>
          <LastnameHeading>Pumberger</LastnameHeading>
          <Firstname>Matthias</Firstname>
          <Initials>M</Initials>
        </PersonNames>
        <Address>
          <Affiliation>Charit&#233; Universit&#228;tsmedizin Berlin, Berlin, Deutschland</Affiliation>
        </Address>
        <Creatorrole corresponding="no" presenting="no">author</Creatorrole>
      </Creator>
      <Creator>
        <PersonNames>
          <Lastname>Schmidt</Lastname>
          <LastnameHeading>Schmidt</LastnameHeading>
          <Firstname>Hendrik</Firstname>
          <Initials>H</Initials>
        </PersonNames>
        <Address>
          <Affiliation>Charit&#233; Universit&#228;tsmedizin Berlin, Berlin, Deutschland</Affiliation>
        </Address>
        <Creatorrole corresponding="no" presenting="no">author</Creatorrole>
      </Creator>
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    <PublisherList>
      <Publisher>
        <Corporation>
          <Corporatename>German Medical Science GMS Publishing House</Corporatename>
        </Corporation>
        <Address>D&#252;sseldorf</Address>
      </Publisher>
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    <SubjectGroup>
      <SubjectheadingDDB>610</SubjectheadingDDB>
    </SubjectGroup>
    <DatePublishedList>
      <DatePublished>20251031</DatePublished>
    </DatePublishedList>
    <Language>engl</Language>
    <License license-type="open-access" xlink:href="http://creativecommons.org/licenses/by/4.0/">
      <AltText language="en">This is an Open Access article distributed under the terms of the Creative Commons Attribution 4.0 License.</AltText>
      <AltText language="de">Dieser Artikel ist ein Open-Access-Artikel und steht unter den Lizenzbedingungen der Creative Commons Attribution 4.0 License (Namensnennung).</AltText>
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      <Meeting>
        <MeetingId>M0634</MeetingId>
        <MeetingSequence>192</MeetingSequence>
        <MeetingCorporation>Deutsche Gesellschaft f&#252;r Orthop&#228;die und Unfallchirurgie</MeetingCorporation>
        <MeetingCorporation>Deutsche Gesellschaft f&#252;r Orthop&#228;die und Orthop&#228;dische Chirurgie</MeetingCorporation>
        <MeetingCorporation>Deutsche Gesellschaft f&#252;r Unfallchirurgie</MeetingCorporation>
        <MeetingCorporation>Berufsverband f&#252;r Orthop&#228;die und Unfallchirurgie</MeetingCorporation>
        <MeetingName></MeetingName>
        <MeetingTitle>Deutscher Kongress f&#252;r Orthop&#228;die und Unfallchirurgie (DKOU 2025)</MeetingTitle>
        <MeetingSession>Posterpreise experimentell</MeetingSession>
        <MeetingCity>Berlin</MeetingCity>
        <MeetingDate>
          <DateFrom>20251028</DateFrom>
          <DateTo>20251031</DateTo>
        </MeetingDate>
      </Meeting>
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    <ArticleNo>AB28-4438</ArticleNo>
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      <MainHeadline>Text</MainHeadline><Pgraph><Mark1>Objectives and questions: </Mark1>Paraspinal muscle atrophy and disc degeneration are hallmarks of spinal aging, yet their interaction remains unclear. To better define their interplay, this study aims to investigate the association between paraspinal muscle atrophy and lumbar disc degeneration in individuals with and without chronic low back pain (cLBP).</Pgraph><Pgraph><Mark1>Material and methods: </Mark1>Participants aged 18 to 64 with and without chronic low back pain (cLBP) were prospectively enrolled from the general population. Paraspinal muscle atrophy was assessed on T2-weighted axial MRI by measuring fat infiltration (FI) and functional cross-sectional area (fCSA) of the multifidus (MF) and erector spinae (ES) at each lumbar level. FI and fCSA values were averaged across all lumbar levels to reflect overall muscle condition. Lumbar disc degeneration was classified according to the Pfirrmann Classification at each level, and a mean lumbar value was calculated. The association between muscle and disc degeneration was analyzed in participants with and without cLBP using multivariable linear regression models, adjusted for age, sex, Body Mass Index (BMI), physical activity, measured by the International Physical Activity Questionnaire (IPAQ), and smoking.</Pgraph><Pgraph><Mark1>Results: </Mark1>A total of 726 participants (55.5&#37; female). Patients characteristics are summarized in Table 1 <ImgLink imgNo="1" imgType="table" />. The unadjusted association between disc degeneration and FI is shown in Figure 1 <ImgLink imgNo="1" imgType="figure" />. In the multivariable analysis, FI of the MF and ES were associated with increased levels of disc degeneration in both groups (p &#60; 0.05). However, the association was stronger in the cLBP group (Table 2 <ImgLink imgNo="2" imgType="table" />). In contrast to the no cLBP group, a significant negative association between disc degeneration and fCSA of the erector spinae was observed in the cLBP group (&#946;: -0.24, 95&#37; CI: -0.47 to -0.01, p &#61; 0.044), with a similar, though not significant trend, for MF fCSA (&#946;: -0.55, 95&#37; CI: -1.10 to 0.00, p &#61; 0.051). </Pgraph><Pgraph><Mark1>Discussion and conclusions: </Mark1>This study confirms an independent association between paraspinal muscle atrophy and lumbar disc degeneration, with a stronger association in cLBP patients. While FI was significantly linked to disc degeneration in both groups, the association was more pronounced than the fCSA, highlighting its potential as a key marker of muscle degeneration. These findings suggest that assessing FI may provide valuable insights into spinal degeneration and warrant further investigation into its role in disease progression and potential therapeutic targets.</Pgraph></TextBlock>
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          <Caption><Pgraph><Mark1>Table 2</Mark1></Pgraph></Caption>
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