Key result
Polymorphisms in ADRB1 and UCP3 were nominally associated with serum insulin and insulin resistance (HOMA-IR) (p<0.05), but not with obesity status or BMI among Swedish women.
Case-Control (n=773)
Polymorphisms in ADRB1 and UCP3 may contribute to insulin resistance rather than obesity among Swedish women.
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Hypothesis-generating for ADRB1/UCP3 variants in insulin resistance among women; requires replication before any clinical consideration.
Background: The uncoupling proteins (UCPs) and β-adrenoceptors (ADRBs) are important for energy balance and may be involved in the pathogenesis of insulin resistance. Obesity is strongly hunted by insulin resistance and susceptibility genes for the two conditions could be separate or common. Variations within the UCPs and ADRBs genes may give important clues to their involvement in disease. Methods: A total of four single nucleotide polymorphisms (SNPs) in the genes UCP1, UCP2, UCP3, and ADRB1 were examined for association with obesity and insulin sensitivity (HOMAIR) in obese (n = 292) and healthy non-obese (n = 481) females. Results: None of the SNPs was associated with obesity status or body mass index. However, ADRB1 (rs1801253) was nominally associated with serum insulin (nominal p = 0.034) and HOMAIR (nominal p = 0.022). UCP3 (rs1800006) was in post-hoc analysis nominally associated with serum insulin and HOMAIR (nominal p = 0.013 and 0.048, respectively). UCP1 and UCP2 showed no association with insulin sensitivity. Conclusion: Polymorphisms in ADRB1 and UCP3 may contribute to insulin resistance rather than obesity among Swedish women.
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Mottagui‐Tabar et al. (2007) conducted a case-control in Obesity and insulin resistance (n=773). ADRB1 and UCP3 gene polymorphisms vs. Non-carriers / reference genotypes was evaluated on Obesity status, body mass index, and insulin sensitivity (HOMAIR) (p=0.022). Polymorphisms in ADRB1 and UCP3 were nominally associated with serum insulin and insulin resistance (HOMA-IR) (p<0.05), but not with obesity status or BMI among Swedish women.
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