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The association between diet and glucocorticoid treatment in patients with SLE

BACKGROUND: Some studies suggest that the risk for and severity of systemic lupus erythematosus (SLE) can be modified by certain nutrients. The aim of this study was to investigate the association between diet and glucocorticoid (GC) treatment, as a proxy for disease activity, in patients with SLE....

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Autores principales: Lourdudoss, Cecilia, Hafström, Ingiäld, Frostegård, Johan, van Vollenhoven, Ronald
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4731837/
https://www.ncbi.nlm.nih.gov/pubmed/26848399
http://dx.doi.org/10.1136/lupus-2015-000135
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author Lourdudoss, Cecilia
Hafström, Ingiäld
Frostegård, Johan
van Vollenhoven, Ronald
author_facet Lourdudoss, Cecilia
Hafström, Ingiäld
Frostegård, Johan
van Vollenhoven, Ronald
author_sort Lourdudoss, Cecilia
collection PubMed
description BACKGROUND: Some studies suggest that the risk for and severity of systemic lupus erythematosus (SLE) can be modified by certain nutrients. The aim of this study was to investigate the association between diet and glucocorticoid (GC) treatment, as a proxy for disease activity, in patients with SLE. METHODS: We included 111 patients with SLE from the SLE Vascular Impact Cohort (SLEVIC). Dietary data were linked with data on GC treatment during a 2-year period. The association between diet and GC treatment was analysed with logistic regression. GC treatment and unchanged/increased doses were considered a proxy for active SLE. RESULTS: During the 2-year period, 54 patients (48.6%) had continued GC treatment. Dietary vitamin D was associated with GC treatment (OR=2.70–2.85 (95% CI 1.00 to 8.11)), whereas alcohol was inversely associated with GC treatment (OR=0.28–0.39 (95% CI 0.10 to 98)). Beta-carotene, fatty acid C18:2 and vitamin B(6) were inversely associated with unchanged/increased GC dose (OR=0.29–0.30 (95% CI 0.10 to 0.90)). Finally, total energy intake was associated with GC doses >5.0 mg/day and >7.5 mg/day, explaining a direct association between 35 nutrients and higher GC dose levels (OR=2.98–23.82 (95% CI 1.01 to 203.88)). DISCUSSION: Dietary vitamin D did not protect against lupus activity. Beta-carotene, fatty acid C18:2 and vitamin B(6) may protect against increased GC dose. The inverse association between alcohol intake and GC treatment/lupus activity may provide a partial explanation for the link between moderate alcohol intake and reduced risk of SLE. The association between higher dietary intake and higher GC dose levels indicated GC's influence on increasing appetite.
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spelling pubmed-47318372016-02-04 The association between diet and glucocorticoid treatment in patients with SLE Lourdudoss, Cecilia Hafström, Ingiäld Frostegård, Johan van Vollenhoven, Ronald Lupus Sci Med Epidemiology and Outcomes BACKGROUND: Some studies suggest that the risk for and severity of systemic lupus erythematosus (SLE) can be modified by certain nutrients. The aim of this study was to investigate the association between diet and glucocorticoid (GC) treatment, as a proxy for disease activity, in patients with SLE. METHODS: We included 111 patients with SLE from the SLE Vascular Impact Cohort (SLEVIC). Dietary data were linked with data on GC treatment during a 2-year period. The association between diet and GC treatment was analysed with logistic regression. GC treatment and unchanged/increased doses were considered a proxy for active SLE. RESULTS: During the 2-year period, 54 patients (48.6%) had continued GC treatment. Dietary vitamin D was associated with GC treatment (OR=2.70–2.85 (95% CI 1.00 to 8.11)), whereas alcohol was inversely associated with GC treatment (OR=0.28–0.39 (95% CI 0.10 to 98)). Beta-carotene, fatty acid C18:2 and vitamin B(6) were inversely associated with unchanged/increased GC dose (OR=0.29–0.30 (95% CI 0.10 to 0.90)). Finally, total energy intake was associated with GC doses >5.0 mg/day and >7.5 mg/day, explaining a direct association between 35 nutrients and higher GC dose levels (OR=2.98–23.82 (95% CI 1.01 to 203.88)). DISCUSSION: Dietary vitamin D did not protect against lupus activity. Beta-carotene, fatty acid C18:2 and vitamin B(6) may protect against increased GC dose. The inverse association between alcohol intake and GC treatment/lupus activity may provide a partial explanation for the link between moderate alcohol intake and reduced risk of SLE. The association between higher dietary intake and higher GC dose levels indicated GC's influence on increasing appetite. BMJ Publishing Group 2016-01-27 /pmc/articles/PMC4731837/ /pubmed/26848399 http://dx.doi.org/10.1136/lupus-2015-000135 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/ This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
spellingShingle Epidemiology and Outcomes
Lourdudoss, Cecilia
Hafström, Ingiäld
Frostegård, Johan
van Vollenhoven, Ronald
The association between diet and glucocorticoid treatment in patients with SLE
title The association between diet and glucocorticoid treatment in patients with SLE
title_full The association between diet and glucocorticoid treatment in patients with SLE
title_fullStr The association between diet and glucocorticoid treatment in patients with SLE
title_full_unstemmed The association between diet and glucocorticoid treatment in patients with SLE
title_short The association between diet and glucocorticoid treatment in patients with SLE
title_sort association between diet and glucocorticoid treatment in patients with sle
topic Epidemiology and Outcomes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4731837/
https://www.ncbi.nlm.nih.gov/pubmed/26848399
http://dx.doi.org/10.1136/lupus-2015-000135
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