<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Sauer CG</submitter><funding>National Center for Advancing Translational Sciences</funding><funding>NCATS NIH HHS</funding><funding>NIDDK NIH HHS</funding><funding>National Institute of Diabetes and Digestive and Kidney Diseases</funding><funding>National Institutes of Health</funding><pagination>641-650</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6176888</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>24(3)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Vitamin D regulates intestinal epithelial and immune functions, and vitamin D receptor deficiency increases the severity of murine colitis. Bioavailable 25-hydroxyvitamin D (25(OH)D) is available to target tissues and may be a driver of immune function. The aim is to evaluate the relationship of bioavailable 25(OH)D to the clinical expression of treatment naive pediatric ulcerative colitis (UC).&lt;h4>Methods&lt;/h4>The PROTECT (Predicting Response to Standardized Pediatric Colitis Therapy) study enrolled children ≤17 years newly diagnosed with UC. Free and total 25(OH)D were directly measured and 25(OH)D fractions were compared with disease activity measures.&lt;h4>Results&lt;/h4>Data were available on 388 subjects, mean age 12.7 years, 49% female, 84% with extensive/pancolitis. Th</pubmed_abstract><journal>Inflammatory bowel diseases</journal><pubmed_title>Free and Bioavailable 25-Hydroxyvitamin D Concentrations are Associated With Disease Activity in Pediatric Patients With Newly Diagnosed Treatment Naive Ulcerative Colitis.</pubmed_title><pmcid>PMC6176888</pmcid><funding_grant_id>UL1TR000454</funding_grant_id><funding_grant_id>T32 DK007727</funding_grant_id><funding_grant_id>UL1 TR002378</funding_grant_id><funding_grant_id>UL1 TR000454</funding_grant_id><funding_grant_id>P30 DK078392</funding_grant_id><funding_grant_id>5U01DK095745</funding_grant_id><pubmed_authors>Walters T</pubmed_authors><pubmed_authors>Davis S</pubmed_authors><pubmed_authors>Wang J</pubmed_authors><pubmed_authors>Denson LA</pubmed_authors><pubmed_authors>Marquis A</pubmed_authors><pubmed_authors>Kugathasan S</pubmed_authors><pubmed_authors>Baldassano RN</pubmed_authors><pubmed_authors>Spada KL</pubmed_authors><pubmed_authors>Loop MS</pubmed_authors><pubmed_authors>Hyams JS</pubmed_authors><pubmed_authors>Patel S</pubmed_authors><pubmed_authors>Bonkowski E</pubmed_authors><pubmed_authors>Griffiths AM</pubmed_authors><pubmed_authors>Venkateswaran S</pubmed_authors><pubmed_authors>Baker SS</pubmed_authors><pubmed_authors>Rosh J</pubmed_authors><pubmed_authors>Boyle B</pubmed_authors><pubmed_authors>Keljo DJ</pubmed_authors><pubmed_authors>Leleiko NS</pubmed_authors><pubmed_authors>Dhawan A</pubmed_authors><pubmed_authors>Tangpricha V</pubmed_authors><pubmed_authors>Markowitz J</pubmed_authors><pubmed_authors>McCall C</pubmed_authors><pubmed_authors>Sauer CG</pubmed_authors><pubmed_authors>Mack DR</pubmed_authors><pubmed_authors>Ziegler TR</pubmed_authors></additional><is_claimable>false</is_claimable><name>Free and Bioavailable 25-Hydroxyvitamin D Concentrations are Associated With Disease Activity in Pediatric Patients With Newly Diagnosed Treatment Naive Ulcerative Colitis.</name><description>&lt;h4>Background&lt;/h4>Vitamin D regulates intestinal epithelial and immune functions, and vitamin D receptor deficiency increases the severity of murine colitis. Bioavailable 25-hydroxyvitamin D (25(OH)D) is available to target tissues and may be a driver of immune function. The aim is to evaluate the relationship of bioavailable 25(OH)D to the clinical expression of treatment naive pediatric ulcerative colitis (UC).&lt;h4>Methods&lt;/h4>The PROTECT (Predicting Response to Standardized Pediatric Colitis Therapy) study enrolled children ≤17 years newly diagnosed with UC. Free and total 25(OH)D were directly measured and 25(OH)D fractions were compared with disease activity measures.&lt;h4>Results&lt;/h4>Data were available on 388 subjects, mean age 12.7 years, 49% female, 84% with extensive/pancolitis. Th</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Feb</publication><modification>2025-04-18T16:10:35.49Z</modification><creation>2019-08-04T07:59:27Z</creation></dates><accession>S-EPMC6176888</accession><cross_references><pubmed>29462384</pubmed><doi>10.1093/ibd/izx052</doi></cross_references></HashMap>