Prevalence, Risk Factors and Association with Clinical Outcomes of Malnutrition and Sarcopenia in Inflammatory Bowel Disease: A Prospective Study
- PMID: 39683376
- PMCID: PMC11643262
- DOI: 10.3390/nu16233983
Prevalence, Risk Factors and Association with Clinical Outcomes of Malnutrition and Sarcopenia in Inflammatory Bowel Disease: A Prospective Study
Abstract
Introduction: The prevalences of malnutrition and sarcopenia in patients with IBD are not precisely known, and nutritional assessment is not standardized. We assessed the prevalence and risk factors of these conditions in outpatients and their impact on clinical outcomes.
Methods: This prospective longitudinal study considered patients who had IBD for at least one year, were attending a tertiary IBD center, and were followed for the subsequent year.
Results: In a sample of 158 consecutive patients (96 with Crohn's disease and 62 with ulcerative colitis), the prevalence of malnutrition, according to GLIM criteria, was 13.3%. For identifying patients at risk of malnutrition, the Malnutrition Universal Screening Tool demonstrated better accuracy, (sensitivity 88.9 (65.3-98.6) and specificity 90.2 (83.8-93.4)) than the SaskIBD-NR questionnaire (sensitivity 69.3 (41.1-86.7) and specificity 60.9 (60.9-76.8)). The prevalence of sarcopenia was 34.2%. Considering clinical outcomes, sarcopenia at baseline was significantly associated with hospital admission within a year (p = 45.2% vs. 20.3%, 0.026).
Conclusions: Malnutrition and sarcopenia were present in about one-third of IBD patients. Awareness should be raised among physicians caring for IBD patients about the need to evaluate patients' nutritional statuses to help patients achieve a better quality of life.
Keywords: Crohn; GLIM; MUST; SaskIBD; ulcerative colitis.
Conflict of interest statement
C.B. served as a consultant or received lecture fees from AbbVie, Alfasigma, Celltrion, Eli Lilly, Ferring, Fresenius Kabi, Galapagos, Lionhealth, Johnson & Johnson, MSD, Pfizer, and Takeda. S.S. received lecture fees from Janssen Pharmaceuticals and Takeda Pharmaceuticals and served as a consultant and advisory board member for AbbVie and Janssen Pharmaceuticals. D.G.R. received fees for consultancies from Biogen, Celltrion, Galapagos, Janssen, and Takeda. M.C. has received lecture fees and served as an Advisory Board Member for AbbVie, Biogen, Ferring, Galapagos, Janssen, Kedrion, Takeda, and Pfizer. M.V. received lecture fees from Abbvie, Takeda, and AgPharma. L.L. and D.G.R. received fees for consultancies from Celltrion, Galapagos, Janssen, and Takeda. The other authors declare no conflicts of interest.
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