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Association of OPRK1 rs963549 and rs997917 polymorphisms with opioid use disorder and the related phenotypes      
Yazarlar
Doç. Dr. Selin ÖZKAN KOTİLOĞLU Doç. Dr. Selin ÖZKAN KOTİLOĞLU
Kırşehir Ahi Evran Üniversitesi, Türkiye
Dilek Akyüzlü
Ankara Üniversitesi, Türkiye
Şafak Yalçın Şahiner
Ankara Üniversitesi, Türkiye
Nagihan Ayaz
Özet
Aim: To evaluate the association between OPRK1 rs963549 and rs997917 and opioid use disorder (OUD) and related phenotypes.Methods: A sample of 208 individuals with (n = 100) and without (n = 108) OUD were enrolled. OPRK1 rs963549 and rs997917 were analyzed by PCR-RFLP. Craving, opioid withdrawal and the intensity of depressive and anxiety symptoms were measured by the appropriate scales.Results: OPRK1 rs963549 variation showed a trend of association with decreased opioid withdrawal. No significant associations were found between OPRK1 rs963549 and rs997917 polymorphisms and craving, depression or anxiety symptoms. Neither single OPRK1 SNPs nor OPRK1 haplotypes were associated with OUD.Conclusion: Our results could be useful for treatment failures of individuals who experience greater opioid withdrawal due to their OPRK1 rs963549 genotypes.
Anahtar Kelimeler
individual differences | opioid use disorder | opioid withdrawal | OPRK1 gene | kappa-opioid receptor
Makale Türü Özgün Makale
Makale Alt Türü SSCI, AHCI, SCI, SCI-Exp dergilerinde yayımlanan tam makale
Dergi Adı PHARMACOGENOMICS
Dergi ISSN 1462-2416
Dergi Tarandığı Indeksler SCI-Expanded
Dergi Grubu Q3
Makale Dili İngilizce
Basım Tarihi 03-2023
Cilt No 24
Sayı 6
Sayfalar 325 / 334
Doi Numarası 10.2217/pgs-2023-0037
Makale Linki http://dx.doi.org/10.2217/pgs-2023-0037