Plasma endocannabinoids as potential biomarkers of type 2 diabetes mellitus in elderly patients with mild cognitive impairment

dc.centroFacultad de Medicinaes_ES
dc.contributor.authorLópez-Gambero, Antonio J.
dc.contributor.authorReyes, José Antonio
dc.contributor.authorFernández-Arjona, María del Mar
dc.contributor.authorRubio-Lamia, Leticia Olga
dc.contributor.authorRivera-González, Patricia
dc.contributor.authorSerrano-Castro, Pedro Jesús
dc.contributor.authorRodriguez-de-Fonseca, Fernando
dc.contributor.authorSuárez-Pérez, Juan
dc.date.accessioned2022-11-28T13:01:26Z
dc.date.available2022-11-28T13:01:26Z
dc.date.created2022
dc.date.issued2022
dc.departamentoSalud Pública y Psiquiatría
dc.descriptionBackground: Besides their role in the nervous system and the development of cognitive impairment in elderly patients, compelling evidence suggests that endocannabinoids (ECBs) are related to motivational responses in obesity and the development of insulin resistance and diabetes. Few studies indicate that ECBs modulate insulin secretion via cannabinoid receptors (CBs) in the human pancreas and alter glucose metabolism. Objectives: The present cross-sectional study aims to evaluate the association between plasma ECBs and the incidence of type 2 diabetes mellitus (T2DM) in a cohort of elderly patients with mild cognitive impairment (MCI). We also aimed to identify possible associations between brain metabolism as determined by PET-18FDG in T2DM patients and plasma levels of ECBs and diabetes-related metabolites. The sample included age and gender-matched MCI patients without (non-T2DM, n = 113) and with T2DM diagnostic (n = 49). Results: T2DM patients presented higher levels of acyl glycerols 2-AG and 2-OG, whereas DHEA was significantly decreased as compared to non-T2DM patients. Moreover, 2-AG and 2-OG were significantly associated with the triglyceride/glucose (TyG) index, a surrogate marker of insulin-resistance. 2-AG and 2-OG plasma levels were significantly associated with cognitive decline determined by MMSE and BLESSED tests, specifically in non-T2DM patients, but not in T2DM patients. T2DM patients showed hypermetabolism specifically in the hippocampus, parahippocampus and amygdala, brain regions associated with control of memory, decision-making, and social cognition. We performed binary logistic regression with stepwise selection of variables including ECBs, GLP-1, C-Peptide, insulin, glucagon, leptin, glucose, triglycerides, and cholesterol molecules in order to create a predictive model of T2DM in elderly patients with MCI. We selected glucose (standardized β: 2.215), 2-OG (standardized β: 0.519), and LDL (standardized β: -0.649), with a positive predictive power of T2DM diagnosis of 89.74%, and an AUC of 0.87 in the ROC curve. We created a surrogate marker of T2DM in elderly patients consisting of variables selected (ECB-T2DM index: (Ln(4*glucose + 2-OG)/Ln(LDL)), which was significantly associated with glucose metabolism in hippocampus, parahippocampus and amygdala. Conclusions: Plasma 2-OG is a promising biomarker of T2DM in elderly patients with MCI and is associated with altered brain metabolism.es_ES
dc.description.abstractBackground: Besides their role in the nervous system and the development of cognitive impairment in elderly patients, compelling evidence suggests that endocannabinoids (ECBs) are related to motivational responses in obesity and the development of insulin resistance and diabetes. Few studies indicate that ECBs modulate insulin secretion via cannabinoid receptors (CBs) in the human pancreas and alter glucose metabolism. Objectives: The present cross-sectional study aims to evaluate the association between plasma ECBs and the incidence of type 2 diabetes mellitus (T2DM) in a cohort of elderly patients with mild cognitive impairment (MCI). We also aimed to identify possible associations between brain metabolism as determined by PET-18FDG in T2DM patients and plasma levels of ECBs and diabetes-related metabolites. The sample included age and gender-matched MCI patients without (non-T2DM, n = 113) and with T2DM diagnostic (n = 49). Results: T2DM patients presented higher levels of acyl glycerols 2-AG and 2-OG, whereas DHEA was significantly decreased as compared to non-T2DM patients. Moreover, 2-AG and 2-OG were significantly associated with the triglyceride/glucose (TyG) index, a surrogate marker of insulin-resistance. 2-AG and 2-OG plasma levels were significantly associated with cognitive decline determined by MMSE and BLESSED tests, specifically in non-T2DM patients, but not in T2DM patients. T2DM patients showed hypermetabolism specifically in the hippocampus, parahippocampus and amygdala, brain regions associated with control of memory, decision-making, and social cognition. We performed binary logistic regression with stepwise selection of variables including ECBs, GLP-1, C-Peptide, insulin, glucagon, leptin, glucose, triglycerides, and cholesterol molecules in order to create a predictive model of T2DM in elderly patients with MCI. We selected glucose (standardized β: 2.215), 2-OG (standardized β: 0.519), and LDL (standardized β: -0.649)...es_ES
dc.description.sponsorshipUniversidad de Málaga. Campus de Excelencia Internacional Andalucía Tech.es_ES
dc.identifier.urihttps://hdl.handle.net/10630/25522
dc.language.isospaes_ES
dc.publisherSociedad Española de Investigación sobre Cannabinoides (SEIC)es_ES
dc.relation.eventdate24-11-2022es_ES
dc.relation.eventplacePamplonaes_ES
dc.relation.eventtitleSociedad Española de Investigación sobre Cannabinoideses_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.accessRightsopen accesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectMedicina - Investigaciónes_ES
dc.subject.otherEndocannabinoides_ES
dc.subject.otherBiomarkerses_ES
dc.subject.otherDiabetes mellituses_ES
dc.subject.otherMild cognitive impairmentes_ES
dc.titlePlasma endocannabinoids as potential biomarkers of type 2 diabetes mellitus in elderly patients with mild cognitive impairmentes_ES
dc.typeconference outputes_ES
dspace.entity.typePublication
relation.isAuthorOfPublicationc156c6fa-f848-4824-a568-59b2cf8b40a8
relation.isAuthorOfPublicationfb22bc1a-a852-4269-bf93-379dd514c366
relation.isAuthorOfPublication0066068d-e487-482c-84c7-832a82b3b544
relation.isAuthorOfPublication.latestForDiscoveryc156c6fa-f848-4824-a568-59b2cf8b40a8

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