<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Scully KJ</submitter><funding>National Institute of Diabetes and Digestive and Kidney Diseases</funding><funding>NIDDK NIH HHS</funding><funding>National Institutes of Health</funding><funding>Cystic Fibrosis Foundation Clinical Research Award</funding><pagination>e1444-e1454</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8947309</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>107(4)</volume><pubmed_abstract>&lt;h4>Context&lt;/h4>The clinical utility and implications of continuous glucose monitoring (CGM) in cystic fibrosis (CF) are unclear.&lt;h4>Objective&lt;/h4>We examined the correlation between CGM measures and clinical outcomes in adults with CF, investigated the relationship between hemoglobin A1c (HbA1c) and CGM-derived average glucose (AG), and explored CGM measures that distinguish cystic fibrosis-related diabetes (CFRD) from normal and abnormal glucose tolerance.&lt;h4>Methods&lt;/h4>This prospective observational study included 77 adults with CF who had CGM and HbA1c measured at 2 to 3 time points 3 months apart.&lt;h4>Results&lt;/h4>Thirty-one of the 77 participants met American Diabetes Association-recommended diagnostic criteria for CFRD by oral glucose tolerance testing and/or HbA1c. In all participan</pubmed_abstract><journal>The Journal of clinical endocrinology and metabolism</journal><pubmed_title>Continuous Glucose Monitoring and HbA1c in Cystic Fibrosis: Clinical Correlations and Implications for CFRD Diagnosis.</pubmed_title><pmcid>PMC8947309</pmcid><funding_grant_id>PUTMAN16A0</funding_grant_id><funding_grant_id>T32 DK007699</funding_grant_id><funding_grant_id>5T32DK007699</funding_grant_id><pubmed_authors>Sherwood JS</pubmed_authors><pubmed_authors>Wexler DJ</pubmed_authors><pubmed_authors>Ruazol M</pubmed_authors><pubmed_authors>Sawicki GS</pubmed_authors><pubmed_authors>Uluer A</pubmed_authors><pubmed_authors>Marchetti P</pubmed_authors><pubmed_authors>Larkin M</pubmed_authors><pubmed_authors>Zheng H</pubmed_authors><pubmed_authors>Putman MS</pubmed_authors><pubmed_authors>Martin K</pubmed_authors><pubmed_authors>Yonker LM</pubmed_authors><pubmed_authors>Sicilian L</pubmed_authors><pubmed_authors>Neuringer I</pubmed_authors><pubmed_authors>Scully KJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Continuous Glucose Monitoring and HbA1c in Cystic Fibrosis: Clinical Correlations and Implications for CFRD Diagnosis.</name><description>&lt;h4>Context&lt;/h4>The clinical utility and implications of continuous glucose monitoring (CGM) in cystic fibrosis (CF) are unclear.&lt;h4>Objective&lt;/h4>We examined the correlation between CGM measures and clinical outcomes in adults with CF, investigated the relationship between hemoglobin A1c (HbA1c) and CGM-derived average glucose (AG), and explored CGM measures that distinguish cystic fibrosis-related diabetes (CFRD) from normal and abnormal glucose tolerance.&lt;h4>Methods&lt;/h4>This prospective observational study included 77 adults with CF who had CGM and HbA1c measured at 2 to 3 time points 3 months apart.&lt;h4>Results&lt;/h4>Thirty-one of the 77 participants met American Diabetes Association-recommended diagnostic criteria for CFRD by oral glucose tolerance testing and/or HbA1c. In all participan</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Mar</publication><modification>2025-04-19T22:47:01.61Z</modification><creation>2025-04-19T22:47:01.61Z</creation></dates><accession>S-EPMC8947309</accession><cross_references><pubmed>34850006</pubmed><doi>10.1210/clinem/dgab857</doi></cross_references></HashMap>