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      Statin Treatment-Induced Development of Type 2 Diabetes: From Clinical Evidence to Mechanistic Insights

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          Abstract

          Statins 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 Ca 2+ 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.

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          Most cited references130

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          2013 ACC/AHA Guideline on the Treatment of Blood Cholesterol to Reduce Atherosclerotic Cardiovascular Risk in Adults

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            MiR-33 contributes to the regulation of cholesterol homeostasis.

            Cholesterol metabolism is tightly regulated at the cellular level. Here we show that miR-33, an intronic microRNA (miRNA) located within the gene encoding sterol-regulatory element-binding factor-2 (SREBF-2), a transcriptional regulator of cholesterol synthesis, modulates the expression of genes involved in cellular cholesterol transport. In mouse and human cells, miR-33 inhibits the expression of the adenosine triphosphate-binding cassette (ABC) transporter, ABCA1, thereby attenuating cholesterol efflux to apolipoprotein A1. In mouse macrophages, miR-33 also targets ABCG1, reducing cholesterol efflux to nascent high-density lipoprotein (HDL). Lentiviral delivery of miR-33 to mice represses ABCA1 expression in the liver, reducing circulating HDL levels. Conversely, silencing of miR-33 in vivo increases hepatic expression of ABCA1 and plasma HDL levels. Thus, miR-33 appears to regulate both HDL biogenesis in the liver and cellular cholesterol efflux.
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              MicroRNA-33 and the SREBP host genes cooperate to control cholesterol homeostasis.

              Proper coordination of cholesterol biosynthesis and trafficking is essential to human health. The sterol regulatory element-binding proteins (SREBPs) are key transcription regulators of genes involved in cholesterol biosynthesis and uptake. We show here that microRNAs (miR-33a/b) embedded within introns of the SREBP genes target the adenosine triphosphate-binding cassette transporter A1 (ABCA1), an important regulator of high-density lipoprotein (HDL) synthesis and reverse cholesterol transport, for posttranscriptional repression. Antisense inhibition of miR-33 in mouse and human cell lines causes up-regulation of ABCA1 expression and increased cholesterol efflux, and injection of mice on a western-type diet with locked nucleic acid-antisense oligonucleotides results in elevated plasma HDL. Our findings indicate that miR-33 acts in concert with the SREBP host genes to control cholesterol homeostasis and suggest that miR-33 may represent a therapeutic target for ameliorating cardiometabolic diseases.
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                Author and article information

                Journal
                Int J Mol Sci
                Int J Mol Sci
                ijms
                International Journal of Molecular Sciences
                MDPI
                1422-0067
                02 July 2020
                July 2020
                : 21
                : 13
                : 4725
                Affiliations
                [1 ]Fundación Biofisika Bizkaia, Barrio Sarriena s/n, 48940 Leioa, Spain; ugalicia001@ 123456ehu.eus (U.G.-G.); Alarrea001@ 123456ehu.eus (A.L.-S.); ofbmaplc@ 123456ehu.es (H.O.); asier.benito@ 123456ehu.eus (A.B.-V.)
                [2 ]Biofisika Institute (UPV/EHU, CSIC), Barrio Sarriena s/n, 48940 Leioa, Spain; sjebari001@ 123456ikasle.ehu.eus
                [3 ]Department of Biochemistry and Molecular Biology, Universidad del País Vasco UPV/EHU, Apdo. 644, 48080 Bilbao, Spain
                [4 ]Center for Cooperative Research in Biomaterials (CIC biomaGUNE), Basque Research and Technology Alliance (BRTA), Paseo de Miramon 182, 20014 Donostia San Sebastián, Spain; kbelloso@ 123456cicbiomagune.es
                [5 ]Harvard Medical School, Harvard University, 25 Shattuck St, Boston, MA 02115, USA; Haziq_Siddiqi@ 123456hms.harvard.edu
                Author notes
                [* ]Correspondence: cesar.martin@ 123456ehu.eus ; Tel.: +34-94-601-8052
                Author information
                https://orcid.org/0000-0002-4502-4853
                https://orcid.org/0000-0002-4087-8729
                Article
                ijms-21-04725
                10.3390/ijms21134725
                7369709
                32630698
                a614f461-ed13-424e-8308-f27bee7af517
                © 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/).

                History
                : 09 June 2020
                : 30 June 2020
                Categories
                Review

                Molecular biology
                statin,type 2 diabetes mellitus,clinical trial,insulin resistance,microrna
                Molecular biology
                statin, type 2 diabetes mellitus, clinical trial, insulin resistance, microrna

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