<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Craig ME</submitter><funding>German Federal Ministry for Education and Research</funding><funding>Leona M. and Harry B. Helmsley Charitable Trust</funding><funding>NIDDK NIH HHS</funding><funding>Royal College of Paediatrics and Child Health</funding><funding>JDRF Australia</funding><funding>National Health and Medical Research Council</funding><pagination>1034-1040</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6463736</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>40(8)</volume><pubmed_abstract>&lt;h4>Objective&lt;/h4>Celiac disease (CD) has a recognized association with type 1 diabetes. We examined international differences in CD prevalence and clinical characteristics of youth with coexisting type 1 diabetes and CD versus type 1 diabetes only.&lt;h4>Research design and methods&lt;/h4>Data sources were as follows: the Prospective Diabetes Follow-up Registry (DPV) (Germany/Austria); the T1D Exchange Clinic Network (T1DX) (U.S.); the National Paediatric Diabetes Audit (NPDA) (U.K. [England/Wales]); and the Australasian Diabetes Data Network (ADDN) (Australia). The analysis included 52,721 youths &lt;18 years of age with a clinic visit between April 2013 and March 2014. Multivariable linear and logistic regression models were constructed to analyze the relationship between outcomes (HbA&lt;sub>1c&lt;/s</pubmed_abstract><journal>Diabetes care</journal><pubmed_title>Prevalence of Celiac Disease in 52,721 Youth With Type 1 Diabetes: International Comparison Across Three Continents.</pubmed_title><pmcid>PMC6463736</pmcid><funding_grant_id>APP1045777</funding_grant_id><funding_grant_id>T32 DK065522</funding_grant_id><funding_grant_id>17-2011-665</funding_grant_id><pubmed_authors>Jeandron D</pubmed_authors><pubmed_authors>Markman E</pubmed_authors><pubmed_authors>Wollam B</pubmed_authors><pubmed_authors>Starkman H</pubmed_authors><pubmed_authors>McGill J</pubmed_authors><pubmed_authors>Corathers S</pubmed_authors><pubmed_authors>Mawhorter C</pubmed_authors><pubmed_authors>Criego A</pubmed_authors><pubmed_authors>DuBose S</pubmed_authors><pubmed_authors>Fudge B</pubmed_authors><pubmed_authors>Schweiger M</pubmed_authors><pubmed_authors>Gandica R</pubmed_authors><pubmed_authors>Thornton H</pubmed_authors><pubmed_authors>Harwood K</pubmed_authors><pubmed_authors>Sinnott R</pubmed_authors><pubmed_authors>Fisher L</pubmed_authors><pubmed_authors>Meehan C</pubmed_authors><pubmed_authors>Sandstrom A</pubmed_authors><pubmed_authors>Young L</pubmed_authors><pubmed_authors>Holl RW</pubmed_authors><pubmed_authors>Howard N</pubmed_authors><pubmed_authors>Minnock P</pubmed_authors><pubmed_authors>Laffel L</pubmed_authors><pubmed_authors>Miller C</pubmed_authors><pubmed_authors>Monzavi R</pubmed_authors><pubmed_authors>Potter A</pubmed_authors><pubmed_authors>Quattrin T</pubmed_authors><pubmed_authors>Caldas-Vasquez M</pubmed_authors><pubmed_authors>White B</pubmed_authors><pubmed_authors>Kissel S</pubmed_authors><pubmed_authors>Brendle F</pubmed_authors><pubmed_authors>Deeb L</pubmed_authors><pubmed_authors>Tawa O</pubmed_authors><pubmed_authors>Dugdale DC</pubmed_authors><pubmed_authors>Bethin K</pubmed_authors><pubmed_authors>Dove 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Continents.</name><description>&lt;h4>Objective&lt;/h4>Celiac disease (CD) has a recognized association with type 1 diabetes. We examined international differences in CD prevalence and clinical characteristics of youth with coexisting type 1 diabetes and CD versus type 1 diabetes only.&lt;h4>Research design and methods&lt;/h4>Data sources were as follows: the Prospective Diabetes Follow-up Registry (DPV) (Germany/Austria); the T1D Exchange Clinic Network (T1DX) (U.S.); the National Paediatric Diabetes Audit (NPDA) (U.K. [England/Wales]); and the Australasian Diabetes Data Network (ADDN) (Australia). The analysis included 52,721 youths &lt;18 years of age with a clinic visit between April 2013 and March 2014. Multivariable linear and logistic regression models were constructed to analyze the relationship between outcomes (HbA&lt;sub>1c&lt;/s</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Aug</publication><modification>2026-07-17T01:39:21.405Z</modification><creation>2019-06-06T22:55:49Z</creation></dates><accession>S-EPMC6463736</accession><cross_references><pubmed>28546222</pubmed><doi>10.2337/dc16-2508</doi></cross_references></HashMap>