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LURIC

Publikation · PMID 32606866

Intronic Variants in OCT1 are Associated with All-Cause and Cardiovascular Mortality in Metformin Users with Type 2 Diabetes

Schweighofer N, Genser B, Maerz W, Kleber ME, Trummer O, Pieber TR, Obermayer-Pietsch B

Genotypes of 27 intronic OCT1 SNPs were investigated in the LURIC cohort (n = 3316) for association with all-cause and cardiovascular mortality. Multivariate Cox regression adjusted for cardiovascular risk factors identified 4 SNPs significantly associated with both outcomes in the 73 participants with type 2 diabetes on metformin. The results suggest that OCT1 genotype may stratify cardiovascular mortality risk in metformin-treated patients.

Diabetes, Metabolic Syndrome and Obesity, 18. Juni 2020 | PMID 32606866

Zeitschrift
Diabetes, Metabolic Syndrome and Obesity
DOI
10.2147/DMSO.S235663
PMID
32606866
Quelle
https://pubmed.ncbi.nlm.nih.gov/32606866/
Zitationen
3 Relative Zitationsrate 0.21 (1,0 = Durchschnitt des Fachgebiets) · NIH iCite, Stand 16.08.2026