Association of Nicotinamide-N-Methyltransferase Gene rs694539 Variant with Epilepsy

Sazci G., Sazci B., SAZCI A., Idrisoglu H. A.

MOLECULAR NEUROBIOLOGY, cilt.53, sa.6, ss.4197-4200, 2016 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 53 Sayı: 6
  • Basım Tarihi: 2016
  • Doi Numarası: 10.1007/s12035-015-9364-2
  • Dergi Adı: MOLECULAR NEUROBIOLOGY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.4197-4200
  • İstanbul Üniversitesi Adresli: Hayır

Özet

Here, we report the association of the rs694539 variant of nicotinamide-N-methyltransferase gene with epilepsy in a case-control study of 215 patients with epilepsy and 239 healthy controls (chi (2) = 11.641, P = 0.003). The individuals with the GG genotype revealed protection against epilepsy (chi (2) = 5.866, P = 0.015, OR = 0.623, 95 % CI = 0.425-0.915), whereas the individuals with the AA genotype showed statistically significant increased risk for epilepsy (chi (2) = 8.676, P = 0.003, OR = 5.479, 95 % CI = 1.553-19.337). In addition, the G allele was protective against epilepsy (chi (2) = 8.676, P = 0.003, OR = 0.183, 95 % CI = 0.052-0.644); on the contrary, the A allele was a genetic risk factor for epilepsy (chi (2) = 5.866, P = 0.015, OR = 1.604, 95 % CI = 1.093-2.354). Stratification analysis revealed that the association was statistically significant in male patients with epilepsy (chi (2) = 6.682, P = 0.035). However, the statistical power was only 0.33 in female patients with epilepsy (chi (2) = 5.275, P = 0.072). This finding, for the first time, suggests the involvement of the NNMT gene rs694539 variant in the etiology of epilepsy.