Luca Salhöfer, Gregor Jost, Mathias Holtkamp, Jannis Straus, Marcel Opitz, Sebastian Zensen, Rene Hosch, Johannes Harmes, Lale Umutlu, Michael Forsting, Felix Nensa, Hubertus Pietsch, Johannes Haubold
{"title":"Intravenous contrast medium impairs CT-based muscle quality but not quantity assessment: a translational study.","authors":"Luca Salhöfer, Gregor Jost, Mathias Holtkamp, Jannis Straus, Marcel Opitz, Sebastian Zensen, Rene Hosch, Johannes Harmes, Lale Umutlu, Michael Forsting, Felix Nensa, Hubertus Pietsch, Johannes Haubold","doi":"10.3389/fradi.2026.1746296","DOIUrl":null,"url":null,"abstract":"<p><strong>Objectives: </strong>CT-based body composition analysis (BCA) provides imaging biomarkers, including muscle volume and surrogates of muscle quality. Concerns over the comparability of Non-contrast and contrast-enhanced CT scans have limited their clinical application. This study aims to assess the influence of various contrast phases on a volumetric CT-based BCA.</p><p><strong>Materials and methods: </strong>20 Göttingen minipigs were subjected to a Non-contrast (NC) and five contrast-enhanced [Early Arterial, Late Arterial, Vascular Portal Venous, Parenchymal Portal Venous (PPV), Late] CT scans. 114 tri-phasic (Non-Contrast, Arterial, Venous) CT scans were analyzed for human validation. A volumetric BCA network [Body and Organ Analysis (BOA)] extracted muscle radiodensity and the following features as volumes: Muscle, Subcutaneous Adipose Tissue (SAT), Inter- and Intramuscular Adipose Tissue (IMAT), Visceral Adipose Tissue (VAT), and Total Adipose Tissue (TAT). Significance was assessed by a one-way ANOVA with Tukey's multiple comparisons test.</p><p><strong>Results: </strong>In the animal model, there was a tendency toward reduced IMAT volumes after CM injection [NC = 245 ml (±105 ml), e.g., PPV = 241 ml (±105 ml)]. Muscle radiodensity was significantly higher following CM administration [Non-contrast: 51.1 HU (±1.9 HU), e.g., Late: 56.6 HU (±2.4 HU), <i>p</i> < 0.001]. The human validation analysis showed similar tendencies for the IMAT volume [Non-contrast: 1750ml (±729 ml), Venous: 1,552 ml (±696 ml), <i>p</i> = 0.10] and significantly higher muscle radiodensity [Venous: 39.2 HU (±9.1 HU), Non-contrast: 35.6 HU (±7.8), <i>p</i> = 0.007].</p><p><strong>Conclusion: </strong>Myosteatosis surrogates, such as muscle radiodensity or IMAT, are susceptible to interference by CM, while quantification of muscle tissue and extramuscular fat remains robust.</p>","PeriodicalId":73101,"journal":{"name":"Frontiers in radiology","volume":"6 ","pages":"1746296"},"PeriodicalIF":4.0000,"publicationDate":"2026-05-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13195011/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Frontiers in radiology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3389/fradi.2026.1746296","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/1/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Objectives: CT-based body composition analysis (BCA) provides imaging biomarkers, including muscle volume and surrogates of muscle quality. Concerns over the comparability of Non-contrast and contrast-enhanced CT scans have limited their clinical application. This study aims to assess the influence of various contrast phases on a volumetric CT-based BCA.
Materials and methods: 20 Göttingen minipigs were subjected to a Non-contrast (NC) and five contrast-enhanced [Early Arterial, Late Arterial, Vascular Portal Venous, Parenchymal Portal Venous (PPV), Late] CT scans. 114 tri-phasic (Non-Contrast, Arterial, Venous) CT scans were analyzed for human validation. A volumetric BCA network [Body and Organ Analysis (BOA)] extracted muscle radiodensity and the following features as volumes: Muscle, Subcutaneous Adipose Tissue (SAT), Inter- and Intramuscular Adipose Tissue (IMAT), Visceral Adipose Tissue (VAT), and Total Adipose Tissue (TAT). Significance was assessed by a one-way ANOVA with Tukey's multiple comparisons test.
Results: In the animal model, there was a tendency toward reduced IMAT volumes after CM injection [NC = 245 ml (±105 ml), e.g., PPV = 241 ml (±105 ml)]. Muscle radiodensity was significantly higher following CM administration [Non-contrast: 51.1 HU (±1.9 HU), e.g., Late: 56.6 HU (±2.4 HU), p < 0.001]. The human validation analysis showed similar tendencies for the IMAT volume [Non-contrast: 1750ml (±729 ml), Venous: 1,552 ml (±696 ml), p = 0.10] and significantly higher muscle radiodensity [Venous: 39.2 HU (±9.1 HU), Non-contrast: 35.6 HU (±7.8), p = 0.007].
Conclusion: Myosteatosis surrogates, such as muscle radiodensity or IMAT, are susceptible to interference by CM, while quantification of muscle tissue and extramuscular fat remains robust.