Association of OPRK1 rs963549 and rs997917 polymorphisms with opioid use disorder and the related phenotypes
     
Yazarlar (4)
Doç. Dr. Selin ÖZKAN KOTİLOĞLU Kırşehir Ahi Evran Üniversitesi, Türkiye
Dilek Akyüzlü Ankara Üniversitesi, Türkiye
Şafak Yalçın Şahiner Ankara Üniversitesi, Türkiye
Nagihan Ayaz
City Hospital Ankara, Türkiye
Makale Türü Özgün Makale (SSCI, AHCI, SCI, SCI-Exp dergilerinde yayınlanan tam makale)
Dergi Adı PHARMACOGENOMICS (Q3)
Dergi ISSN 1462-2416 Wos Dergi Scopus Dergi
Dergi Tarandığı Indeksler SCI-Expanded
Makale Dili İngilizce Basım Tarihi 03-2023
Cilt / Sayı / Sayfa 24 / 6 / 325–334 DOI 10.2217/pgs-2023-0037
Makale Linki http://dx.doi.org/10.2217/pgs-2023-0037
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