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Psoriatic arthritis is associated with adverse body composition predictive of greater coronary heart disease and type 2 diabetes propensity – a cross-sectional study

"V体育安卓版" Ferguson, Lyn D. ORCID logoORCID: https://orcid.org/0000-0002-6136-8349, "VSports" Linge, Jennifer, Leinhard, Olof Dahlqvist, Woodward, Rosemary, Hall Barrientos, Pauline, Roditi, Giles (VSports), Radjenovic, Aleksandra ORCID logoORCID: https://orcid.org/0000-0002-1742-6863, McInnes, Iain B. ORCID logoORCID: https://orcid.org/0000-0002-6462-4280, "V体育安卓版" Siebert, Stefan ORCID logoORCID: https://orcid.org/0000-0002-1802-7311 and "VSports app下载" Sattar, Naveed ORCID logoORCID: https://orcid.org/0000-0002-1604-2593 (2021) Psoriatic arthritis is associated with adverse body composition predictive of greater coronary heart disease and type 2 diabetes propensity – a cross-sectional study. Rheumatology, 60(4), pp. 1858-1862. (doi: 10.1093/rheumatology/keaa604) (PMID:33147607)

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Abstract

Objectives: To compare body composition in PsA with metabolic disease free (MDF) controls and type 2 diabetes and assess body-composition predicted propensity for cardiometabolic disease. Methods: Detailed MRI body composition profiles of 26 PsA participants from the IMAPA study were compared with 130 age, sex and BMI-matched MDF controls and 454 individuals with type 2 diabetes from UK Biobank. The body-composition predicted propensity for coronary heart disease (CHD) and type 2 diabetes was compared between PsA and matched MDF controls. Results: PsA participants had a significantly greater visceral adipose tissue (VAT) volume [mean 5. 89 l (S. D. 2. 10 l)] compared with matched-MDF controls [mean 4. 34 l (S. D. 1. 83 l)] (P <0. 001) and liver fat percentage [median 8. 88% (interquartile range 4. 42–13. 18%)] compared with MDF controls [3. 29% (1. 98–7. 25%)] (P <0. 001). These differences remained significant after adjustment for age, sex and BMI. There were no statistically significant differences in VAT, liver fat or muscle fat infiltration (MFI) between PsA and type 2 diabetes. PsA participants had a lower thigh muscle volume than MDF controls and those with type 2 diabetes. Body composition-predicted propensity for CHD and type 2 diabetes was 1. 27 and 1 VSports app下载. 83 times higher, respectively, for PsA compared with matched-MDF controls. Conclusion: Individuals with PsA have an adverse body composition phenotype with greater visceral and ectopic liver fat and lower thigh muscle volume than matched MDF controls. Body fat distribution in PsA is more in keeping with the pattern observed in type 2 diabetes and is associated with greater propensity to cardiometabolic disease. These data support the need for greater emphasis on weight loss in PsA management to lessen CHD and type 2 diabetes risk.

Item Type:Articles
Status:Published
Refereed:Yes
Glasgow Author(s) Enlighten ID:McInnes, Professor Iain and Ferguson, Dr Lyn and Hall Barrientos, Dr Pauline and Roditi, Dr Giles and Siebert, Professor Stefan and Sattar, Professor Naveed and Woodward, Miss Rosie and Radjenovic, Dr Aleksandra
Authors: Ferguson, L. D., Linge, J., Leinhard, O. D., Woodward, R., Hall Barrientos, P., Roditi, G., Radjenovic, A., McInnes, I. B., Siebert, S., and Sattar, N.
College/School:College of Medical Veterinary and Life Sciences > School of Cardiovascular & Metabolic Health
College of Medical Veterinary and Life Sciences > School of Infection & Immunity
College of Medical Veterinary and Life Sciences > School of Medicine, Dentistry & Nursing
Research Centre:College of Medical Veterinary and Life Sciences > School of Infection & Immunity > Centre for Immunobiology
Journal Name:Rheumatology
Publisher:Oxford University Press
ISSN:1462-0324
ISSN (Online):1462-0332
Published Online:04 November 2020
Copyright Holders:Copyright © 2020 The Authors
First Published:First published in Rheumatology 60(4):1858–1862
Publisher Policy:Reproduced under a Creative Commons License

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Project Code
Award No
Project Name
Principal Investigator
Funder's Name
Funder Ref
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BHF centre of excellence
Rhian Touyz
RE/13/5/30177
Institute of Cardiovascular & Medical Sciences

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