Body composition profiling in a Dutch sarcoidosis population

Body composition profiling in a Dutch sarcoidosis population

Authors

  • Johanna P Cremers Dept. of Interstitial Lung Diseases, Gelderse Vallei Hospital, Ede
  • Marjolein Drent Dept. of Interstitial Lung Diseases, Gelderse Vallei Hospital, Ede; Dept. of Toxicology, Faculty of Health, Medicine and Life Sciences (FHML), University Maastricht, Maastricht
  • Marjon D Elfferich Dept. of Interstitial Lung Diseases, Gelderse Vallei Hospital, Ede
  • Patty J Nelemans Dept. of Epidemiology, University Maastricht, Maastricht
  • Petal A Wijnen Dept. of Clinical Chemistry, Maastricht University Medical Centre+ (MUMC+), Maastricht
  • Ben J Witteman Division of Gastroenterology, Dept. of Internal Medicine, Gelderse Vallei Hospital, Ede
  • Annemie M Schols Dept. of Respiratory Medicine, MUMC+, Maastricht; Nutrim School for Nutrition, Toxicology and Metabolism, FHML, University Maastricht, Maastricht, the Netherlands

Keywords:

Sarcoidosis, Body composition, Muscle atrophy, Cachexia, Lung function, Exercise capacity.

Abstract

Muscle atrophy is a common problem in many chronic inflammatory diseases. It may occur as part of a generalized wasting process (cachexia) or be hidden due to preservation of fatmass (sarcopenia, sarcopenic obesity). Objectives: The aim of this study was to assess the prevalence of cachexia and muscle atrophy in sarcoidosis and their association with disease activity and severity. Methods: A cross-sectional study was performed in 423 sarcoidosis patients. Fat-free mass was assessed as an indirect measure of muscle mass by bioelectrical impedance analysis. Patients were stratified based on body mass index (BMI) and fat-free mass index (FFMI).Muscle atrophy was defined as FFMI <15 kg/m2 for women and <17 kg/m2 for men corresponding to <10th percentile of current reference values; cachexia as BMI <20 combined with muscle atrophy.Multivariate linear regression models were used to adjust for potential confounders. Results: Of the patients examined, 58% were categorized as overweight (37%) or obese (21%), whereas 7% were underweight.Muscle atrophy was present in 25% and cachexia in 5%. Patients with muscle atrophy showed significantly worse lung function (DLCO, FEV1, FVC, all p-values <0.01) and impaired exercise capacity (VO2max, p<0.001). The associations were most pronounced in patients with cachexia. Associations remained significant after adjustment for potential confounders. Conclusions: Muscle atrophy was present in 25% of sarcoidosis patients and was associated withmore severe pulmonary disease. Prospective studies with longitudinal design are needed to assess the association between muscle atrophy and disease severity in sarcoidosis.

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Published

17-12-2013

Issue

Section

Original Articles: Clinical Research

How to Cite

1.
Cremers JP, Drent M, Elfferich MD, Nelemans PJ, Wijnen PA, Witteman BJ, et al. Body composition profiling in a Dutch sarcoidosis population. Sarcoidosis Vasc Diffuse Lung Dis [Internet]. 2013 Dec. 17 [cited 2025 May 20];30(4):289-9. Available from: https://mattioli1885journals.com/index.php/sarcoidosis/article/view/2951