Beta cell functionality and hepatic insulin resistance are major contributors to type 2 diabetes remission and starting pharmacological therapy: from CORDIOPREV randomized controlled trial.

dc.contributor.authorRoncero-Ramos, Irene
dc.contributor.authorGutierrez-Mariscal, Francisco M
dc.contributor.authorGomez-Delgado, Francisco
dc.contributor.authorVillasanta-Gonzalez, Alejandro
dc.contributor.authorTorres-Peña, Jose D
dc.contributor.authorCruz-Ares, Silvia De La
dc.contributor.authorRangel-Zuñiga, Oriol A
dc.contributor.authorLuque, Raul M
dc.contributor.authorOrdovas, Jose M
dc.contributor.authorDelgado-Lista, Javier
dc.contributor.authorPerez-Martinez, Pablo
dc.contributor.authorCamargo, Antonio
dc.contributor.authorAlcalá-Diaz, Juan F
dc.contributor.authorLopez-Miranda, Jose
dc.date.accessioned2025-01-07T12:19:17Z
dc.date.available2025-01-07T12:19:17Z
dc.date.issued2021-07-21
dc.description.abstractIn order to assess whether previous hepatic IR (Hepatic-IRfasting) and beta-cell functionality could modulate type 2 diabetes remission and the need for starting glucose-lowering treatment, newly-diagnosed type 2 diabetes participants who had never received glucose-lowering treatment (190 out of 1002) from the CORonary Diet Intervention with Olive oil and cardiovascular PREVention study (a prospective, randomized and controlled clinical trial), were randomized to consume a Mediterranean or a low-fat diet. Type 2 diabetes remission was defined according to the American Diabetes Association recommendation for levels of HbA1c, fasting plasma glucose and 2h plasma glucose after oral glucose tolerance test, and having maintained them for at least 2 consecutive years. Patients were classified according to the median of Hepatic-IRfasting and beta-cell functionality, measured as the disposition index (DI) at baseline. Cox proportional hazards regression determined the potential for Hepatic-IRfasting and DI indexes as predictors of diabetes remission and the probability of starting pharmacological treatment after a 5-year follow-up. Low-Hepatic-IRfasting or high-DI patients had a higher probability of diabetes remission than high-Hepatic-IRfasting or low-DI subjects (HR:1.79; 95% CI 1.06-3.05; and HR:2.66; 95% CI 1.60-4.43, respectively) after a dietary intervention with no pharmacological treatment and no weight loss. The combination of low-Hepatic-IRfasting and high-DI presented the highest probability of remission (HR:4.63; 95% CI 2.00-10.70). Among patients maintaining diabetes, those with high- Hepatic-IRfasting and low-DI showed the highest risk of starting glucose-lowering therapy (HR:3.24;95% CI 1.50-7.02). Newly-diagnosed type 2 diabetes patients with better beta-cell functionality and lower Hepatic-IRfasting had a higher probability of type 2 diabetes remission in a dietary intervention without pharmacological treatment or weight loss, whereas among patients not achieving remission, those with worse beta-cell functionality and higher Hepatic-IRfasting index had the highest risk of starting glucose-lowering treatment after 5 years of follow-up.
dc.identifier.doi10.1016/j.trsl.2021.07.001
dc.identifier.essn1878-1810
dc.identifier.pmid34298148
dc.identifier.unpaywallURLhttp://www.translationalres.com/article/S1931524421001584/pdf
dc.identifier.urihttps://hdl.handle.net/10668/24452
dc.journal.titleTranslational research : the journal of laboratory and clinical medicine
dc.journal.titleabbreviationTransl Res
dc.language.isoen
dc.organizationSAS - Hospital Universitario Regional de Málaga
dc.organizationInstituto de Investigación Biomédica de Málaga - Plataforma Bionand (IBIMA)
dc.page.number12-24
dc.pubmedtypeJournal Article
dc.pubmedtypeRandomized Controlled Trial
dc.pubmedtypeResearch Support, Non-U.S. Gov't
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectALT = alanine aminotransferase
dc.subjectAUC = area under curve
dc.subjectAdipo-IR = Adipose tissue insulin resistance index
dc.subjectBMI = body mass index
dc.subjectCHD = coronary heart disease
dc.subjectCORDIOPREV = CORonary Diet Intervention with Olive oil and cardiovascular PREVention
dc.subjectDBP = diastolic blood pressure
dc.subjectDI = disposition index
dc.subjectFFA = free fatty acids
dc.subjectHDL-c = high-density lipoprotein
dc.subjectHepatic-IR(fasting) = hepatic insulin resistance index derived from fasting values
dc.subjectIGI = insulinogenic index
dc.subjectIR = insulin resistance
dc.subjectISI = insulin sensitivity index
dc.subjectLDL-c = low-density lipoprotein
dc.subjectLF diet = low-fat diet
dc.subjectMISI = muscular insulin sensitivity index
dc.subjectMUFA = monounsaturated fatty acids
dc.subjectMed diet = Mediterranean diet
dc.subjectOGTT = oral glucose tolerance test
dc.subjectPUFA = polyunsaturated fatty acids
dc.subjectSBP = systolic blood pressure
dc.subjectT2DM = type 2 diabetes mellitus
dc.subjectTG = triglycerides
dc.subject.meshAlanine Transaminase
dc.subject.meshDiabetes Mellitus, Type 2
dc.subject.meshDiet, Mediterranean
dc.subject.meshFatty Acids
dc.subject.meshFemale
dc.subject.meshGlucose Tolerance Test
dc.subject.meshGlycated Hemoglobin
dc.subject.meshHumans
dc.subject.meshHypoglycemic Agents
dc.subject.meshInsulin Resistance
dc.subject.meshInsulin-Secreting Cells
dc.subject.meshLiver
dc.subject.meshMale
dc.subject.meshMiddle Aged
dc.titleBeta cell functionality and hepatic insulin resistance are major contributors to type 2 diabetes remission and starting pharmacological therapy: from CORDIOPREV randomized controlled trial.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number238

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