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Large well-designed studies are needed to fully describe the association between this polymorphism and RPL.
We also analyzed the possible interaction between this polymorphism and caffeine intake.
However, a meta-analysis showed no significant associations between this polymorphism and obesity in all genetic comparison models.
The aim of this study was to investigate the association between this polymorphism and the risk of myocardial infarction (MI) in the Tunisian population.
Both studies found no association between this polymorphism and migraine or its clinical subtypes [88, 89].
We examined the relationship between this polymorphism and antidepressant remission rates in an elderly sample with MDD, while also testing for mediation effects of social support and hyperintensities.
No association between this polymorphism and treatment response was recorded.
No genetic association was found between this polymorphism and the progression of NPC.
Evidence of an association between this polymorphism and breast cancer risk has been inconclusive [13] [16].
We have limited power to detect, however, more moderate (OR<1.26) associations between this polymorphism and breast cancer risk.
Recently, Setiawan et al. did not observe an association between this polymorphism and breast cancer risk among African-American populations in California (1456 cases and 978 controls) [13].
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