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Glucocorticoid-associated blood glucose response and MS relapse recovery

OBJECTIVE: To determine the relationship between MS relapse recovery and blood glucose (BG) response to IV methylprednisolone (IVMP) treatment. METHODS: We retrospectively identified 36 patients with MS admitted for IVMP treatment of acute relapse who had adequate data to characterize BG response, r...

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Autores principales: Goldman, Myla D., Koenig, Scott, Engel, Casey, McCartney, Christopher R., Sohn, Min-Woong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5515601/
https://www.ncbi.nlm.nih.gov/pubmed/28761902
http://dx.doi.org/10.1212/NXI.0000000000000378
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author Goldman, Myla D.
Koenig, Scott
Engel, Casey
McCartney, Christopher R.
Sohn, Min-Woong
author_facet Goldman, Myla D.
Koenig, Scott
Engel, Casey
McCartney, Christopher R.
Sohn, Min-Woong
author_sort Goldman, Myla D.
collection PubMed
description OBJECTIVE: To determine the relationship between MS relapse recovery and blood glucose (BG) response to IV methylprednisolone (IVMP) treatment. METHODS: We retrospectively identified 36 patients with MS admitted for IVMP treatment of acute relapse who had adequate data to characterize BG response, relapse severity, and recovery. The relationship between glucocorticoid-associated nonfasting BG (NFBG) and relapse recovery was assessed. RESULTS: Highest recorded nonfasting BG (maximum NFBG [maxNFBG]) values were significantly higher in patients with MS without relapse recovery compared with those with recovery (271 ± 68 vs 209 ± 48 mg/dL, respectively; p = 0.0045). After adjusting for relapse severity, MS patients with maxNFBG below the group median were 6 times (OR = 6.01; 95% CI, 1.08–33.40; p = 0.040) more likely to experience relapse recovery than those with maxNFBG above the group median. In a multiple regression model adjusting for age, sex, and relapse severity, a 1-mg/dL increase in the maxNFBG was associated with 4.5% decrease in the probability of recovery (OR = 0.955; 95% CI, 0.928–0.983; p = 0.002). CONCLUSIONS: These findings suggest that higher glucocorticoid-associated NFBG values in acutely relapsing patients with MS are associated with diminished probability of recovery. This relationship could reflect steroid-associated hyperglycemia and/or insulin resistance, defects in non–steroid-associated (e.g., prerelapse) glucose metabolism, or both. This study included only those admitted for an MS relapse, and it is this subset of patients for whom these findings may be most relevant. A prospective study to evaluate glucose regulation and MS relapse recovery in a broader outpatient MS population is under way.
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spelling pubmed-55156012017-07-31 Glucocorticoid-associated blood glucose response and MS relapse recovery Goldman, Myla D. Koenig, Scott Engel, Casey McCartney, Christopher R. Sohn, Min-Woong Neurol Neuroimmunol Neuroinflamm Article OBJECTIVE: To determine the relationship between MS relapse recovery and blood glucose (BG) response to IV methylprednisolone (IVMP) treatment. METHODS: We retrospectively identified 36 patients with MS admitted for IVMP treatment of acute relapse who had adequate data to characterize BG response, relapse severity, and recovery. The relationship between glucocorticoid-associated nonfasting BG (NFBG) and relapse recovery was assessed. RESULTS: Highest recorded nonfasting BG (maximum NFBG [maxNFBG]) values were significantly higher in patients with MS without relapse recovery compared with those with recovery (271 ± 68 vs 209 ± 48 mg/dL, respectively; p = 0.0045). After adjusting for relapse severity, MS patients with maxNFBG below the group median were 6 times (OR = 6.01; 95% CI, 1.08–33.40; p = 0.040) more likely to experience relapse recovery than those with maxNFBG above the group median. In a multiple regression model adjusting for age, sex, and relapse severity, a 1-mg/dL increase in the maxNFBG was associated with 4.5% decrease in the probability of recovery (OR = 0.955; 95% CI, 0.928–0.983; p = 0.002). CONCLUSIONS: These findings suggest that higher glucocorticoid-associated NFBG values in acutely relapsing patients with MS are associated with diminished probability of recovery. This relationship could reflect steroid-associated hyperglycemia and/or insulin resistance, defects in non–steroid-associated (e.g., prerelapse) glucose metabolism, or both. This study included only those admitted for an MS relapse, and it is this subset of patients for whom these findings may be most relevant. A prospective study to evaluate glucose regulation and MS relapse recovery in a broader outpatient MS population is under way. Lippincott Williams & Wilkins 2017-07-18 /pmc/articles/PMC5515601/ /pubmed/28761902 http://dx.doi.org/10.1212/NXI.0000000000000378 Text en Copyright © 2017 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits downloading and sharing the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Article
Goldman, Myla D.
Koenig, Scott
Engel, Casey
McCartney, Christopher R.
Sohn, Min-Woong
Glucocorticoid-associated blood glucose response and MS relapse recovery
title Glucocorticoid-associated blood glucose response and MS relapse recovery
title_full Glucocorticoid-associated blood glucose response and MS relapse recovery
title_fullStr Glucocorticoid-associated blood glucose response and MS relapse recovery
title_full_unstemmed Glucocorticoid-associated blood glucose response and MS relapse recovery
title_short Glucocorticoid-associated blood glucose response and MS relapse recovery
title_sort glucocorticoid-associated blood glucose response and ms relapse recovery
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5515601/
https://www.ncbi.nlm.nih.gov/pubmed/28761902
http://dx.doi.org/10.1212/NXI.0000000000000378
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