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Predictors of vitamin D deficiency in inflammatory bowel disease and health: A Mississippi perspective

AIM: To identify the predictors of vitamin D deficiency in patients with and without inflammatory bowel disease (IBD). METHODS: Patients with ulcerative colitis (UC) or Crohn’s disease (CD) related diagnostic codes who received medical care at University of Mississippi Medical Center between July 20...

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Autores principales: Pallav, Kumar, Riche, Daniel, May, Warren L, Sanchez, Patrick, Gupta, Nitin K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5292337/
https://www.ncbi.nlm.nih.gov/pubmed/28216970
http://dx.doi.org/10.3748/wjg.v23.i4.638
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author Pallav, Kumar
Riche, Daniel
May, Warren L
Sanchez, Patrick
Gupta, Nitin K
author_facet Pallav, Kumar
Riche, Daniel
May, Warren L
Sanchez, Patrick
Gupta, Nitin K
author_sort Pallav, Kumar
collection PubMed
description AIM: To identify the predictors of vitamin D deficiency in patients with and without inflammatory bowel disease (IBD). METHODS: Patients with ulcerative colitis (UC) or Crohn’s disease (CD) related diagnostic codes who received medical care at University of Mississippi Medical Center between July 2012 and 2015 were identified. After thorough chart review, we identified patients with biopsy proven IBD who had also been tested for serum 25-hydroxyvitamin D [25(OH)D] concentration. We compared these patients to a previously studied cohort of healthy controls who also had vitamin D concentration checked. Logistic regression analysis was performed to determine the association between vitamin d deficiency and UC, CD, race, age, gender and body mass index (BMI). RESULTS: We identified 237 patients with confirmed IBD. Of these, only 211 had a serum 25(OH)D concentrations available in the medical record. The group of healthy controls consisted of 98 individuals with available serum 25(OH)D concentration. 43% of IBD patients were African American (AA). Patients with CD were more likely to have vitamin D concentration checked. Bivariate analysis showed that AA (51% vs 21%, P = 0.00001), subjects with BMI >30 kg/m(2) (39% vs 23% P = 0.01) and CD (40% vs 26%, P = 0.04) were more likely to be vitamin D deficient than vitamin D sufficient. Those with Age > 65 were more likely to be vitamin D sufficient (46% vs 15%, P = 0.04). Multiple regression showed that only BMI > 30 kg/m(2) and AA race are associated with vitamin D deficiency. CONCLUSION: BMI > 30 kg/m(2) and AA race are predictive of vitamin D deficiency. Gender, age and diagnosis of IBD are not predictive of vitamin D deficiency.
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spelling pubmed-52923372017-02-17 Predictors of vitamin D deficiency in inflammatory bowel disease and health: A Mississippi perspective Pallav, Kumar Riche, Daniel May, Warren L Sanchez, Patrick Gupta, Nitin K World J Gastroenterol Retrospective Study AIM: To identify the predictors of vitamin D deficiency in patients with and without inflammatory bowel disease (IBD). METHODS: Patients with ulcerative colitis (UC) or Crohn’s disease (CD) related diagnostic codes who received medical care at University of Mississippi Medical Center between July 2012 and 2015 were identified. After thorough chart review, we identified patients with biopsy proven IBD who had also been tested for serum 25-hydroxyvitamin D [25(OH)D] concentration. We compared these patients to a previously studied cohort of healthy controls who also had vitamin D concentration checked. Logistic regression analysis was performed to determine the association between vitamin d deficiency and UC, CD, race, age, gender and body mass index (BMI). RESULTS: We identified 237 patients with confirmed IBD. Of these, only 211 had a serum 25(OH)D concentrations available in the medical record. The group of healthy controls consisted of 98 individuals with available serum 25(OH)D concentration. 43% of IBD patients were African American (AA). Patients with CD were more likely to have vitamin D concentration checked. Bivariate analysis showed that AA (51% vs 21%, P = 0.00001), subjects with BMI >30 kg/m(2) (39% vs 23% P = 0.01) and CD (40% vs 26%, P = 0.04) were more likely to be vitamin D deficient than vitamin D sufficient. Those with Age > 65 were more likely to be vitamin D sufficient (46% vs 15%, P = 0.04). Multiple regression showed that only BMI > 30 kg/m(2) and AA race are associated with vitamin D deficiency. CONCLUSION: BMI > 30 kg/m(2) and AA race are predictive of vitamin D deficiency. Gender, age and diagnosis of IBD are not predictive of vitamin D deficiency. Baishideng Publishing Group Inc 2017-01-28 2017-01-28 /pmc/articles/PMC5292337/ /pubmed/28216970 http://dx.doi.org/10.3748/wjg.v23.i4.638 Text en ©The Author(s) 2017. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Retrospective Study
Pallav, Kumar
Riche, Daniel
May, Warren L
Sanchez, Patrick
Gupta, Nitin K
Predictors of vitamin D deficiency in inflammatory bowel disease and health: A Mississippi perspective
title Predictors of vitamin D deficiency in inflammatory bowel disease and health: A Mississippi perspective
title_full Predictors of vitamin D deficiency in inflammatory bowel disease and health: A Mississippi perspective
title_fullStr Predictors of vitamin D deficiency in inflammatory bowel disease and health: A Mississippi perspective
title_full_unstemmed Predictors of vitamin D deficiency in inflammatory bowel disease and health: A Mississippi perspective
title_short Predictors of vitamin D deficiency in inflammatory bowel disease and health: A Mississippi perspective
title_sort predictors of vitamin d deficiency in inflammatory bowel disease and health: a mississippi perspective
topic Retrospective Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5292337/
https://www.ncbi.nlm.nih.gov/pubmed/28216970
http://dx.doi.org/10.3748/wjg.v23.i4.638
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