<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Amarikwa L</submitter><funding>NEI NIH HHS</funding><funding>National Institute of Health</funding><pagination>858-864</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10211488</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>108(4)</volume><pubmed_abstract>&lt;h4>Context&lt;/h4>Graves orbitopathy (GO) or thyroid eye disease is a potentially sight-threatening and disfiguring autoimmune disease. Teprotumumab is a monoclonal antibody against the insulin-like growth factor-I receptor that was recently approved for GO treatment. Hyperglycemia is a recognized adverse event of teprotumumab, occurring in 10% of patients in 2 recent randomized controlled trials.&lt;h4>Objective&lt;/h4>Our study aimed to report the incidence, severity, management, and longitudinal glycemic changes in patients treated with teprotumumab in an academic practice cohort.&lt;h4>Methods&lt;/h4>This longitudinal, observational study included all consecutive patients treated with teprotumumab between March 2020 and May 2022 at 1 institution. Hemoglobin A1c (HbA1c) was measured every 3 months.&lt;h</pubmed_abstract><journal>The Journal of clinical endocrinology and metabolism</journal><pubmed_title>Teprotumumab-Related Hyperglycemia.</pubmed_title><pmcid>PMC10211488</pmcid><funding_grant_id>P30 EY026877</funding_grant_id><funding_grant_id>NIH P30 026877</funding_grant_id><pubmed_authors>Kim SH</pubmed_authors><pubmed_authors>Kossler AL</pubmed_authors><pubmed_authors>Dosiou C</pubmed_authors><pubmed_authors>Mohamed A</pubmed_authors><pubmed_authors>Amarikwa L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Teprotumumab-Related Hyperglycemia.</name><description>&lt;h4>Context&lt;/h4>Graves orbitopathy (GO) or thyroid eye disease is a potentially sight-threatening and disfiguring autoimmune disease. Teprotumumab is a monoclonal antibody against the insulin-like growth factor-I receptor that was recently approved for GO treatment. Hyperglycemia is a recognized adverse event of teprotumumab, occurring in 10% of patients in 2 recent randomized controlled trials.&lt;h4>Objective&lt;/h4>Our study aimed to report the incidence, severity, management, and longitudinal glycemic changes in patients treated with teprotumumab in an academic practice cohort.&lt;h4>Methods&lt;/h4>This longitudinal, observational study included all consecutive patients treated with teprotumumab between March 2020 and May 2022 at 1 institution. Hemoglobin A1c (HbA1c) was measured every 3 months.&lt;h</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Mar</publication><modification>2025-05-29T20:47:25.989Z</modification><creation>2025-05-29T20:47:25.989Z</creation></dates><accession>S-EPMC10211488</accession><cross_references><pubmed>36300333</pubmed><doi>10.1210/clinem/dgac627</doi></cross_references></HashMap>