MEFV gene pathogenic variants: a risk factor for dysmenorrhea in the Turkish population


Nacar M. C., Yiğit S., Ozsoy A. Z., Demirturk F., Nursal A. F., Karakus N.

NUCLEOSIDES NUCLEOTIDES & NUCLEIC ACIDS, vol.43, no.7, pp.643-654, 2024 (SCI-Expanded) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 43 Issue: 7
  • Publication Date: 2024
  • Doi Number: 10.1080/15257770.2023.2293074
  • Journal Name: NUCLEOSIDES NUCLEOTIDES & NUCLEIC ACIDS
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, BIOSIS, Chemical Abstracts Core, Chimica, MEDLINE
  • Page Numbers: pp.643-654
  • Keywords: Mediterranean fever gene, variant
  • Ondokuz Mayıs University Affiliated: Yes

Abstract

Background/Aim: The Mediterranean fever (MEFV) gene codes for protein pyrin, which is among the modulators of inflammasome activity in innate immune cells. It was suggested that there is a relation between MEFV variations and inflammatory diseases. The aim of this study was to investigate MEFV gene variations in the patients with primary dysmenorrhea.Methods: The prevalence of common MEFV gene variations (M694V, M680I, V726A, E148Q and R202Q) was investigated in 145 young women with primary dysmenorrhea and 135 unrelated healthy controls. MEFV gene variations were genotyped using PCR-based RFLP assay.Results: Number of childbirth and marriage were significantly lower in the study group than the controls, respectvely (p < 0.001, p = 0.001). Family history was statistically higher in the patient group (p < 0.001). In total, MEFV genotype and allele frequencies were significantly higher in patients than controls, respectively (p = 0.008 and p = 0.005, respectively). It was found that MEFV gene E148Q allele was more common in patient group (p = 0.039). MEFV R202Q A allele was higher in the patients than the controls (p = 0.045). A significant association was observed when the patients were compared with the controls according to R202Q variant AA versus GG+GA genotypes (p=0.020).Conclusion: Our findings suggest that MEFV variations may be a risk factor for patients with dysmenorrhea in a Turkish cohort.