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Potential role of FKBP5 single-nucleotide polymorphisms in functional seizures.

Ali Akbar Asadi-PooyaLeila SimaniMarjan AsadollahiFatemeh Sadat RashidiEhsan AhmadipourAfagh AlaviMehrdad RoozbehNayyereh AkbariNegar Firouzabadi
Published in: Epilepsia open (2023)
Patients with FS and those with MDD had significantly different genotypes in both rs9470080 and rs1360780 SNPs compared with those in healthy controls. However, it seems that FKBP5 polymorphisms were not associated with FS in the absence of depression. Further genetic investigations of patients with FS may increase our understanding of the neurobiological underpinnings of this condition, but such studies should be large enough and very well designed; they should include a comparison group with depression in addition to a healthy control group.
Keyphrases
  • depressive symptoms
  • genome wide
  • sleep quality
  • dna methylation
  • physical activity
  • genome wide association