Publication:
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-pena, Jose D.
dc.contributor.authorde la Cruz-ares, Silvia
dc.contributor.authorRangel-zuniga, 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.authorAlcala-diaz, Juan F.
dc.contributor.authorLopez-miranda, Jose
dc.contributor.authoraffiliationUniv Cordoba, Maimonides Biomed Res Inst Cordoba IMIBIC, Dept Internal Med, Lipids & Atherosclerosis Unit,Reina Sofia Univ Ho, Cordoba, SpainInst Salud Carlos III, CIBER Fisiopatol Obesidad & Nutr CIBEROBN, Cordoba, SpainMaimonides Inst Biomed Res Cordoba IMIBIC, Cordoba, SpainUniv Cordoba, Dept Cell Biol Physiol & Immunol, Cordoba, SpainTufts Univ, JM US Dept Agr Human Nutr Res Ctr Aging, Nutr & Genom Lab, Boston, MA 02111 USACNIC, IMDEA Alimentac, Madrid, Spain
dc.contributor.funderFundacion Patrimonio Comunal Olivarero
dc.contributor.funderJunta de Andalucia (Consejeria de Salud, Consejeria de Agricultura y Pesca, Consejeria de Innovacion, Ciencia y Empresa)
dc.contributor.funderDiputaciones de Jaen y Cordoba, Centro de Excelencia en Investigacion sobre Aceite de Oliva y Salud
dc.contributor.funderMinisterio de Medio Ambiente, Medio Rural y Marino, Gobierno de Espana
dc.contributor.funderMinisterio de Economia y Competitividad
dc.contributor.funderInstituto de Salud Carlos III (ISCIII) of Spain
dc.contributor.funderDirectorate General for Assessment and Promotion of Research
dc.contributor.funderEU's European Regional Development Fund (FEDER)
dc.contributor.funderUniversidad de Cordoba/CBUA
dc.contributor.funderISCIII postdoctoral research contract
dc.contributor.funderCIBEROBN postdoctoral research contract
dc.contributor.funderJunta de Andalucia (Consejeria de Salud, Consejeria de Agri cultura y Pesca, Consejeria de Innovacion, Ciencia y Empresa)
dc.contributor.funderDiputaciones de Jaen y Cordoba, Centro de Excelencia en Investigacion sobre Aceite de Oliva y Salud
dc.contributor.funderMinisterio de Medio Ambiente, Medio Rural y Marino, Gobierno de España
dc.contributor.funderISCIII
dc.date.accessioned2023-02-12T02:21:11Z
dc.date.available2023-02-12T02:21:11Z
dc.date.issued2021-07-14
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.description.sponsorshipThe CORDIOPREV study is supported by the Fundacion Patrimonio Comunal Olivarero, by Junta de Andalucia (Consejeria de Salud, Consejeria de Agricultura y Pesca, Consejeria de Innovacion, Ciencia y Empresa CVI-7450 to J. L-M), Diputaciones de Jaen y Cordoba, Centro de Excelencia en Investigacion sobre Aceite de Oliva y Salud and Ministerio de Medio Ambiente, Medio Rural y Marino, Gobierno de España. The CORDIOPREV study has also received research grants from the Ministerio de Economia y Competitividad (AGL2012/39615 and AGL2015-67896-P to J. L-M, FIS PI10/01041 to P. P-M, FIS PI13/00023 to J. D-L), integrated into the framework of the National Plan for Scientific Research, Techno logical Development and Innovation 2013-2016, co financed by the Instituto de Salud Carlos III (ISCIII) of Spain, the Directorate General for Assessment and Pro motion of Research and the EU’s European Regional Development Fund (FEDER). The CIBEROBN is an initiative of the ISCIII. Funding for open access charge: Universidad de C ordoba/CBUA. Irene Roncero-Ramos is supported by an ISCIII postdoctoral research contract (Programa Sara Borrell CD16/00047). Francisco M Gutierrez-Mariscal is supported by a CIBEROBN postdoctoral research contract. The contents of this paper are not intended for any commercial use
dc.description.versionSi
dc.identifier.citationRoncero-Ramos I, Gutierrez-Mariscal FM, Gomez-Delgado F, Villasanta-Gonzalez A, Torres-Peña JD, Cruz-Ares S, et al. Beta cell functionality and hepatic insulin resistance are major contributors to type 2 diabetes remission and starting pharmacological therapy: from CORDIOPREV randomized controlled trial. Transl Res. 2021 Dec;238:12-24
dc.identifier.doi10.1016/j.trsl.2021.07.001
dc.identifier.essn1878-1810
dc.identifier.issn1931-5244
dc.identifier.unpaywallURLhttp://www.translationalres.com/article/S1931524421001584/pdf
dc.identifier.urihttp://hdl.handle.net/10668/18890
dc.identifier.wosID716448300002
dc.journal.titleTranslational research
dc.journal.titleabbreviationTransl. res.
dc.language.isoen
dc.organizationInstituto Maimónides de Investigación Biomédica de Córdoba-IMIBIC
dc.page.number12-24
dc.provenanceRealizada la curación de contenido 08/08/2024
dc.publisherElsevier
dc.relation.projectIDCVI-7450
dc.relation.projectIDAGL2012/39615
dc.relation.projectIDAGL2015-67896-P
dc.relation.projectIDPI10/01041
dc.relation.publisherversionhttps://linkinghub.elsevier.com/retrieve/pii/S1931-5244(21)00158-4
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectGlucose-production
dc.subjectCardiovascular-disease
dc.subjectFat accumulation
dc.subjectGlycemic control
dc.subject.decsSecreciones corporales
dc.subject.decsSensibilidad y especificidad
dc.subject.decsPérdida de peso
dc.subject.meshWeight-loss
dc.subject.meshSensitivity
dc.subject.meshPathophysiology
dc.subject.meshDysfunction
dc.subject.meshTolerance
dc.subject.meshSecretion
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
dc.wostypeArticle
dspace.entity.typePublication

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