<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13</volume><submitter>Brandon R</submitter><funding>Maurice Wilkins Centre for Molecular Biodiscovery</funding><funding>Health Research Council of New Zealand</funding><pubmed_abstract>&lt;h4>Background&lt;/h4>Understanding which group of patients with type 2 diabetes will have the most glucose lowering response to certain medications (which target different aspects of glucose metabolism) is the first step in precision medicine.&lt;h4>Aims&lt;/h4>We hypothesized that people with type 2 diabetes who generally have high insulin resistance, such as people of Māori/Pacific ethnicity, and those with obesity and/or hypertriglyceridemia (OHTG), would have greater glucose-lowering by pioglitazone (an insulin sensitizer) versus vildagliptin (an insulin secretagogue).&lt;h4>Methods&lt;/h4>A randomised, open-label, two-period crossover trial was conducted in New Zealand. Adults with type 2 diabetes, HbA1c>58mmol/mol (>7.5%), received 16 weeks of either pioglitazone (30mg) or vildagliptin (50mg) dail</pubmed_abstract><journal>Frontiers in endocrinology</journal><pagination>1091421</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9869378</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Stratified glucose-lowering response to vildagliptin and pioglitazone by obesity and hypertriglyceridemia in a randomized crossover trial.</pubmed_title><pmcid>PMC9869378</pmcid><pubmed_authors>Merry T</pubmed_authors><pubmed_authors>Smallman K</pubmed_authors><pubmed_authors>Shepherd PR</pubmed_authors><pubmed_authors>Nehren N</pubmed_authors><pubmed_authors>Tweedie-Cullen R</pubmed_authors><pubmed_authors>Brandon R</pubmed_authors><pubmed_authors>King F</pubmed_authors><pubmed_authors>Paul R</pubmed_authors><pubmed_authors>Merriman TR</pubmed_authors><pubmed_authors>Jiang Y</pubmed_authors><pubmed_authors>Doran RJ</pubmed_authors><pubmed_authors>Orr-Walker B</pubmed_authors><pubmed_authors>Yeu RQ</pubmed_authors><pubmed_authors>Macaskill-Smith KA</pubmed_authors><pubmed_authors>Hindmarsh JH</pubmed_authors><pubmed_authors>Moffitt A</pubmed_authors><pubmed_authors>Doherty G</pubmed_authors><pubmed_authors>Clark P</pubmed_authors><pubmed_authors>Leask MP</pubmed_authors><pubmed_authors>Murphy R</pubmed_authors></additional><is_claimable>false</is_claimable><name>Stratified glucose-lowering response to vildagliptin and pioglitazone by obesity and hypertriglyceridemia in a randomized crossover trial.</name><description>&lt;h4>Background&lt;/h4>Understanding which group of patients with type 2 diabetes will have the most glucose lowering response to certain medications (which target different aspects of glucose metabolism) is the first step in precision medicine.&lt;h4>Aims&lt;/h4>We hypothesized that people with type 2 diabetes who generally have high insulin resistance, such as people of Māori/Pacific ethnicity, and those with obesity and/or hypertriglyceridemia (OHTG), would have greater glucose-lowering by pioglitazone (an insulin sensitizer) versus vildagliptin (an insulin secretagogue).&lt;h4>Methods&lt;/h4>A randomised, open-label, two-period crossover trial was conducted in New Zealand. Adults with type 2 diabetes, HbA1c>58mmol/mol (>7.5%), received 16 weeks of either pioglitazone (30mg) or vildagliptin (50mg) dail</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2026-05-28T03:41:12.85Z</modification><creation>2025-04-05T21:07:37.168Z</creation></dates><accession>S-EPMC9869378</accession><cross_references><pubmed>36699039</pubmed><doi>10.3389/fendo.2022.1091421</doi></cross_references></HashMap>