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Endocrine Abstracts (2017) 49 GP107 | DOI: 10.1530/endoabs.49.GP107

Diabetes therapy & complications 2

Specific Oct1 gene variants are associated with changes in the risk of cardiovascular death in metformin users

Natascha Schweighofer1,7, Bernd Genser2,3, Winfried März4,5, Marcus E Kleber6, Thomas R Pieber1,7 & Barbara Obermayer-Pietsch1,7


1Division of Endocrinology and Diabetology, Department of Internal Medicine, Medical University Graz, Graz, Austria; 2BG Statistical Consulting, Vienna, Austria; 3Institute of Public Health, Social and Preventive Medicine, Medical Faculty of Mannheim, University of Heidelberg, Mannheim, Germany; 4Clinical Institute of Medical and Chemical Laboratory Diagnostics, Medical University Graz, Graz, Austria; 5Synlab Center of Laboratory Diagnostics, Heidelberg, Germany; 6Vth Department of Medicine (Nephrology, Hypertensiology, Endocrinology, Diabetology, Rheumatology), Medical Faculty Mannheim, Heidelberg University and Competence Cluster of Nutrition and Cardiovascul, Heidelberg/Halle-Jena-Leipzig, Germany; 7CBmed GmbH, Center for Biomarker Research in Medicine, Graz, Austria.

Aim: Increased cardiovascular incidents and a high risk for microvascular complications are associated with type 2 diabetes. Worldwide, metformin is the most commonly prescribed antidiabetic drug. Polymorphisms in the Oct1 gene can alter the function or activity of organic cation transporter 1 (Oct1), thus changing metformin efficacy (Oct1 acting as its main transporter) as well as influencing the actions of Oct1 physiological substrates. In the past, polymorphisms in Oct1 were associated with cardiovascular risk factors, thus they might contribute to cardiovascular risk development.

We investigated, whether the Oct1 polymorphism rs3777392 is associated with increased risk for cardiovascular death in a cohort of patients with and without type 2 diabetes (T2DM) on various therapies.

Methods: Data from the LURIC study (n=3316), a prospective cohort study of Caucasians scheduled for coronary angiography were analysed. We identified 1820 non-diabetics, 1220 T2DM patients, including 73 metformin users (Met), 154 sulfonylurea users (SF) and 967 T2DM individuals without medication. Cardiovascular mortality was assessed in all groups according to Oct1 rs3777392 genotypes using Cox proportional hazard models and associations with cardiovascular biomarkers were investigated.

Results: Cardiovascular mortality risk for each minor allele copy was HR 2.08 (95% CI: 1.01, 4.28) only in metformin users. Variants of rs3777392 were associated with BMI, baseline insulin values and triglyceride levels in all T2DM patients (P=0.016, P=0.048 and P=0.007, respectively), patients without medication (P=0.006, P=0.041, P=0.008, respectively) and non-diabetics (P=0.021, P=0.074, P=0.125, respectively) but not in the Met and SF groups.

Conclusion: In our study, the minor allele of rs3777392 in the Oct1 gene was associated with an increased cardiovascular mortality risk in T2DM patients on metformin therapy, which might be due to loss of association with cardiovascular parameters. Besides very positive effects in the majority of metformin users, some individuals may profit from a pre-treatment genotyping and careful monitoring.

Volume 49

19th European Congress of Endocrinology

Lisbon, Portugal
20 May 2017 - 23 May 2017

European Society of Endocrinology 

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