Page 58 - The prevalence of the Val66Met polymorphism in musicians: Possible evidence for compensatory neuroplasticity from a pilot study
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S. Si et al.                                                                          NeuroImage 213 (2020) 116681
         Table 3                                              only one of each of them was included in single variants   parenting style
         Characteristics of the genotyped single-nucleotide polymorphisms (SNPs) of  analysis. rs1800497, rs6276, rs6277, rs2283265, rs1076560 and
         COMT.                                                rs4938019 were excluded. For COMT, strong LDs were observed for
                                                                                2
                                                                                                      2
          SNP     Position  Location  Allele (minor/  MAF  HWE p  rs6269 and rs4646312 (r ¼.92), rs4818 and rs4646312 (r ¼.92), rs4818
                                                                        2
                                                                                             2
                                 major)        (%)            and rs6269 (r ¼.92), rs4633 and rs4680 (r ¼.92). Hence, rs4646312,
          rs737865  18310121  Intron 1  C/T    29.7   .907    rs4818 and rs4680 were excluded. Finally, 9 SNPs of DRD2 (rs6278,
          rs174675  18314051  Intron 1  T/C    39.3   .612    rs6279, rs7122246, rs4648317, rs1799978, rs1799732, rs4245148,
          rs5993882  18317533  Intron 1  G/T   12.1   1       rs4648319, rs4436578) and 9 SNPs of COMT (rs6269, rs4633, rs737865,
          rs5993883  18317638  Intron 1  G/T   41.3   .690    rs174675, rs5993882, rs5993883, rs6267, rs769224, rs174697) were
          rs4646312  18328337  Intron 1  C/T   37.6   .217
          rs6269  18329952  Exon 3  G/A        37.9   .182    selected to conduct single variants   parenting style analysis.
          rs4633  18330235  Exon 3  T/C        26.2   .104       To minimize the likelihood of a Type I error, we adjusted our alpha
          rs6267  18330263  Exon 3  T/G        7.5    .721    based on the number of genetic polymorphisms we planned to examine in
          rs4818  18331207  Exon 4  G/C        37.2   .254    a gene. Given that we are investigating nine polymorphisms in each gene,
          rs4680  18331271  Exon 4  A/G        26.6   .048*   we used a conservative Bonferroni adjusted alpha of .006 (a ¼ .05/9) to
          rs769224  18331804  Exon 5  A/G      6.9    .710
          rs174697  18333832  Intron 5  A/G    32.9   .021*   determine statistical significance.
                                                                 The significant results for each model testing the individual variant
         Note:*p<.05; MAF ¼ minor allele frequency; HWE ¼ Hardy-Weinberg equilib-  parenting style interactions for the prediction of fluency, originality and
         rium; UTR ¼ untranslated region.
         a                                      0       0     flexibility are shown in supplementary materials (Supplementary Table 3
         SNPs are listed down the column in sequential order from the 5 end to the 3 end
         of the sense strand of COMT.                         and Table 4). While neither single polymorphism nor parenting style was
         b Physical position is based on NCBI Genome Build 36.3.  independently significant in the model including rs5993882 and
                                                              rs5993883, the two-way interaction term of mother authoritativeness
         SNPs were excluded in single variants   parenting style analysis because  and COMT genotype, controlling for participant gender and intelligence,
                                                              was significant in predicting creativity (fluency: β ¼ 0.14, p ¼ 0.002;
         of their strong LDs with other SNPs. For DRD2, strong LDs were observed
                                                2
                            2
         for rs6278 and rs1800497 (r ¼.97), rs6276 and rs6279 (r ¼.99), rs6277  flexibility: β ¼ 0.14, p ¼ 0.004). However, none of the models including
                    2
                                              2
         and rs7122246 (r ¼.91), rs2283265 and rs1076560 (r ¼.97), rs1076560  other polymorphisms in DRD2 and COMT passed the Bonferroni adjusted
                   2
                                              2
         and rs6278 (r ¼.90), rs4938019 and rs4648317 (r ¼.92). Therefore,  threshold (p < 0.006) for statistical significance though there were seven











































                                Fig. 1. Linkage disequilibrium (LD) pattern of the 15 DRD2 SNPs analyzed in this study.

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