<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Skov-Jeppesen K</submitter><funding>AP Møller Fonden</funding><funding>NIDDK NIH HHS</funding><funding>Foundation for the National Institutes of Health</funding><funding>Novo Nordisk Foundation Center for Basic Metabolic Research</funding><funding>Novo Nordisk Fonden</funding><pagination>1448-1458</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8338760</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>36(8)</volume><pubmed_abstract>Glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide-2 (GLP-2) are gut hormones secreted postprandially. In healthy humans, both hormones decrease bone resorption accompanied by a rapid reduction in parathyroid hormone (PTH). The aim of this study was to investigate whether the changes in bone turnover after meal intake and after GIP- and GLP-2 injections, respectively, are mediated via a reduction in PTH secretion. This was tested in female patients with hypoparathyroidism given a standardized liquid mixed-meal test (n = 7) followed by a peptide injection test (n = 4) using a randomized crossover design. We observed that the meal- and GIP- but not the GLP-2-induced changes in bone turnover markers were preserved in the patients with hypoparathyroidism. To understan</pubmed_abstract><journal>Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research</journal><pubmed_title>The Antiresorptive Effect of GIP, But Not GLP-2, Is Preserved in Patients With Hypoparathyroidism-A Randomized Crossover Study.</pubmed_title><pmcid>PMC8338760</pmcid><funding_grant_id>1R01DK088188‐01</funding_grant_id><funding_grant_id>NNF18OC0052699</funding_grant_id><funding_grant_id>R01 DK088188</funding_grant_id><funding_grant_id>NNF19OC0055047</funding_grant_id><funding_grant_id>NNF18CC0034900</funding_grant_id><funding_grant_id>1R01DK088188-01</funding_grant_id><pubmed_authors>Hansen MS</pubmed_authors><pubmed_authors>Jafari A</pubmed_authors><pubmed_authors>Holst JJ</pubmed_authors><pubmed_authors>Hartmann B</pubmed_authors><pubmed_authors>Oeke J</pubmed_authors><pubmed_authors>Hepp N</pubmed_authors><pubmed_authors>Olson JA</pubmed_authors><pubmed_authors>Balenga N</pubmed_authors><pubmed_authors>Svane MS</pubmed_authors><pubmed_authors>Madsbad S</pubmed_authors><pubmed_authors>Rosenkilde MM</pubmed_authors><pubmed_authors>Skov-Jeppesen K</pubmed_authors><pubmed_authors>Kassem M</pubmed_authors><pubmed_authors>Frost M</pubmed_authors><pubmed_authors>Beck Jensen JE</pubmed_authors></additional><is_claimable>false</is_claimable><name>The Antiresorptive Effect of GIP, But Not GLP-2, Is Preserved in Patients With Hypoparathyroidism-A Randomized Crossover Study.</name><description>Glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide-2 (GLP-2) are gut hormones secreted postprandially. In healthy humans, both hormones decrease bone resorption accompanied by a rapid reduction in parathyroid hormone (PTH). The aim of this study was to investigate whether the changes in bone turnover after meal intake and after GIP- and GLP-2 injections, respectively, are mediated via a reduction in PTH secretion. This was tested in female patients with hypoparathyroidism given a standardized liquid mixed-meal test (n = 7) followed by a peptide injection test (n = 4) using a randomized crossover design. We observed that the meal- and GIP- but not the GLP-2-induced changes in bone turnover markers were preserved in the patients with hypoparathyroidism. To understan</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Aug</publication><modification>2026-05-07T21:27:23.945Z</modification><creation>2022-02-11T11:27:55.565Z</creation></dates><accession>S-EPMC8338760</accession><cross_references><pubmed>33852173</pubmed><doi>10.1002/jbmr.4308</doi></cross_references></HashMap>