Show simple item record

dc.contributor.authorGalicia García, Unai
dc.contributor.authorJebari Benslaiman, Shifa
dc.contributor.authorLarrea Sebal, Asier
dc.contributor.authorBelloso Uribe, Kepa
dc.contributor.authorSiddiqi, Haziq
dc.contributor.authorOstolaza Echabe, Elena Amaya
dc.contributor.authorBenito Vicente, Asier
dc.contributor.authorMartín Plágaro, César Augusto
dc.date.accessioned2020-07-23T11:58:39Z
dc.date.available2020-07-23T11:58:39Z
dc.date.issued2020-07-02
dc.identifier.citationInternational Journal of Molecular Sciences 21(13) : (2020) // Article ID 4725es_ES
dc.identifier.issn1422-0067
dc.identifier.urihttp://hdl.handle.net/10810/45544
dc.description.abstractStatins are the gold-standard treatment for the prevention of primary and secondary cardiovascular disease, which is the leading cause of mortality worldwide. Despite the safety and relative tolerability of statins, observational studies, clinical trials and meta-analyses indicate an increased risk of developing new-onset type 2 diabetes mellitus (T2DM) after long-term statin treatment. It has been shown that statins can impair insulin sensitivity and secretion by pancreatic β-cells and increase insulin resistance in peripheral tissues. The mechanisms involved in these processes include, among others, impaired Ca2+ signaling in pancreatic β-cells, down-regulation of GLUT-4 in adipocytes and compromised insulin signaling. In addition, it has also been described that statins’ impact on epigenetics may also contribute to statin-induced T2DM via differential expression of microRNAs. This review focuses on the evidence and mechanisms by which statin therapy is associated with the development of T2DM. This review describes the multifactorial combination of effects that most likely contributes to the diabetogenic effects of statins. Clinically, these findings should encourage clinicians to consider diabetes monitoring in patients receiving statin therapy in order to ensure early diagnosis and appropriate management.es_ES
dc.description.sponsorshipThis work was supported by the Basque Government (Grupos Consolidados IT-1264-19). U.G.-G. was supported by Fundación Biofísica Bizkaia. A.B.-V. was supported by Programa de especialización de Personal Investigador Doctor en la UPV/EHU (2019) 2019–2020. S.J. and A.L.-S. were supported by a grant PIF (2017–2018) and (2019–2020), Gobierno Vasco, respectively. A.L.-S. was partially supported by Fundación Biofísica Bizkaia.es_ES
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/
dc.subjectstatines_ES
dc.subjecttype 2 diabetes mellituses_ES
dc.subjectclinical triales_ES
dc.subjectinsulin resistancees_ES
dc.subjectmicroRNAes_ES
dc.titleStatin Treatment-Induced Development of Type 2 Diabetes: From Clinical Evidence to Mechanistic Insightses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.date.updated2020-07-10T13:37:35Z
dc.rights.holder2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).es_ES
dc.relation.publisherversionhttps://www.mdpi.com/1422-0067/21/13/4725/htmes_ES
dc.identifier.doi10.3390/ijms21134725
dc.departamentoesBioquímica y biología molecular
dc.departamentoeuBiokimika eta biologia molekularra


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record

2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
Except where otherwise noted, this item's license is described as 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).