Melatonin receptor gene polymorphisms as a risk factor in patients with diabetic peripheral neuropathy


OCAK Ö., SILAN F., ŞAHİN E. M.

DIABETES-METABOLISM RESEARCH AND REVIEWS, cilt.38, sa.8, 2022 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 38 Sayı: 8
  • Basım Tarihi: 2022
  • Doi Numarası: 10.1002/dmrr.3573
  • Dergi Adı: DIABETES-METABOLISM RESEARCH AND REVIEWS
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, BIOSIS, CAB Abstracts, CINAHL, EMBASE, MEDLINE, Veterinary Science Database
  • Anahtar Kelimeler: diabetic peripheral neuropathy, genetics, inflammation, melatonin gene polymorphism, OXIDATIVE STRESS, MTNR1B, CELL, REDUCTION, DAMAGE
  • Çanakkale Onsekiz Mart Üniversitesi Adresli: Evet

Özet

Aims Oxidative stress plays an important role in the pathogenesis of diabetic peripheral neuropathy (DPN). Melatonin is one of the most powerful endogenous antioxidants and has anti-inflammatory properties. We investigated how the gene polymorphism of melatonin differs in patients with DPN compared to an healthy control group. Materials and Methods A total of 54 diabetic peripheral neuropathy patients who applied to the Neurology outpatient clinic between 2020 and 2021, and 53 healthy controls comparable with the patient group in terms of age and gender were included in the study. Electromyography was performed and the melatonin gene polymorphism was analysed using the pyrosequencing method. Results Melatonin gene variants rs2119882, rs13140012, and rs10830963 were analysed in patients and controls. The rs2119882 (G allele) has a protective role, and rs13140012 polymorphism has a related 5-fold higher risk of DPN in the recessive model. Conclusions Melatonin gene polymorphisms have been shown to be associated with DPN. This is the first and only study investigating the relationship between melatonin gene polymorphisms and DPN. Ethnicity is very important in genetic studies, and it will give us more information on the role of melatonin gene variants in larger study groups of diabetic patients of other ethnic origin.