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SHR Neuro Cancer Cardio Lipid Metab Microb

Schweighofer, N; Lerchbaum, E; Trummer, O; Schwetz, V; Pieber, T; Obermayer-Pietsch, B.
Metformin resistance alleles in polycystic ovary syndrome: pattern and association with glucose metabolism.
Pharmacogenomics. 2014; 15(3):305-317 Doi: 10.2217/pgs.13.223
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Leading authors Med Uni Graz
Schweighofer Natascha
Co-authors Med Uni Graz
Lerchbaum Elisabeth
Obermayer-Pietsch Barbara
Pieber Thomas
Theiler-Schwetz Verena
Trummer Olivia
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Abstract:
Insulin-sensitizer treatment with metformin is common in polycystic ovary syndrome (PCOS). OCT alleles were investigated in PCOS patients to identify genetic 'bad responders' and 'nonresponders' to metformin including their possible effects on glucose metabolism without treatment. We genotyped eight SNPs in OCT1, OCT2 and ATM genes in 676 women with PCOS and 90 control women, we also measured oral glucose tolerance tests prior to treatment. Nonfunctional alleles were present in 29.8% and low-functional alleles in 57.9% of our PCOS cohort. OCT variants were significantly associated with elevated baseline and glucose-induced C-peptide levels in PCOS. Metformin bad responders or nonresponders based on OCT genotypes might be relevant in clinical practice - their modulation of metformin pharmacokinetics and pharmacodynamics and metformin-independent glucose effects remain to be elucidated.
Find related publications in this database (using NLM MeSH Indexing)
Adult -
Ataxia Telangiectasia Mutated Proteins - genetics
C-Peptide - metabolism
Drug Resistance - genetics
Female -
Genetic Association Studies -
Glucose - metabolism
Glucose Tolerance Test -
Humans -
Insulin Resistance - genetics
Metformin - administration & dosage
Organic Cation Transport Proteins - genetics
Organic Cation Transporter 1 - genetics
Polycystic Ovary Syndrome - drug therapy Polycystic Ovary Syndrome - pathology
Polymorphism, Single Nucleotide -

Find related publications in this database (Keywords)
ATM
C-peptide
metformin resistance
organic cation transporters
polycystic ovary syndrome
SNPs
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