<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>15</volume><submitter>Arefanian H</submitter><pubmed_abstract>&lt;h4>Introduction&lt;/h4>Familial hypercholesterolemia, the highly prevalent form of dyslipidemia, is a well-known risk factor for premature heart disease and stroke worldwide. Statins, which inhibit 3-hydroxy 3-methylglutaryl coenzyme A (HMG-CoA) reductase, are the first-choice treatment for dyslipidemias, and have been effective in reducing the risk of stroke and myocardial infarction. However, emerging evidence indicates that statins may increase the incidence of new-onset type 2 diabetes by reducing β-cell mass and function. Notably, past &lt;i>in vitro&lt;/i> reports studying the effects of statins on β-cells were performed without including free fatty acids in the model. This factor should have been addressed since these agents are used to treat individuals with hyperlipidemia.&lt;h4>Methods&lt;/h4></pubmed_abstract><journal>Frontiers in endocrinology</journal><pagination>1383448</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11560436</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Comparative efficacy, toxicity, and insulin-suppressive effects of simvastatin and pravastatin in fatty acid-challenged mouse insulinoma MIN6 β-cell model.</pubmed_title><pmcid>PMC11560436</pmcid><pubmed_authors>Albeloushi S</pubmed_authors><pubmed_authors>Ahmad R</pubmed_authors><pubmed_authors>Qaddoumi M</pubmed_authors><pubmed_authors>Almansour N</pubmed_authors><pubmed_authors>Alzaid F</pubmed_authors><pubmed_authors>Bahman F</pubmed_authors><pubmed_authors>Al-Mulla F</pubmed_authors><pubmed_authors>Al Madhoun A</pubmed_authors><pubmed_authors>Williams MR</pubmed_authors><pubmed_authors>Arefanian H</pubmed_authors><pubmed_authors>Sindhu S</pubmed_authors><pubmed_authors>Al-Rashed F</pubmed_authors></additional><is_claimable>false</is_claimable><name>Comparative efficacy, toxicity, and insulin-suppressive effects of simvastatin and pravastatin in fatty acid-challenged mouse insulinoma MIN6 β-cell model.</name><description>&lt;h4>Introduction&lt;/h4>Familial hypercholesterolemia, the highly prevalent form of dyslipidemia, is a well-known risk factor for premature heart disease and stroke worldwide. Statins, which inhibit 3-hydroxy 3-methylglutaryl coenzyme A (HMG-CoA) reductase, are the first-choice treatment for dyslipidemias, and have been effective in reducing the risk of stroke and myocardial infarction. However, emerging evidence indicates that statins may increase the incidence of new-onset type 2 diabetes by reducing β-cell mass and function. Notably, past &lt;i>in vitro&lt;/i> reports studying the effects of statins on β-cells were performed without including free fatty acids in the model. This factor should have been addressed since these agents are used to treat individuals with hyperlipidemia.&lt;h4>Methods&lt;/h4></description><dates><release>2024-01-01T00:00:00Z</release><publication>2024</publication><modification>2026-07-16T20:19:02.764Z</modification><creation>2025-04-04T14:43:00.147Z</creation></dates><accession>S-EPMC11560436</accession><cross_references><pubmed>39544235</pubmed><doi>10.3389/fendo.2024.1383448</doi></cross_references></HashMap>