Comparative screening of FMF mutations in various communities of the Israeli society

Rajech Sharkia1, Muhammad Mahajnah, Abdelnaser Zalan

  • 1The Triangle Regional Research and Development Center, P. O. Box-2167, Kfar Qari'-30075, Israel. rajachsharkia@hotmail.com

Insights

Familial Mediterranean Fever (FMF) is an inherited inflammatory disorder. This study screened 1700 Israelis for common MEFV gene mutations, finding M694V, E148Q, and V726A were most prevalent across communities.

Area of Science:

  • Genetics
  • Molecular Biology
  • Population Health

Background:

  • Familial Mediterranean Fever (FMF) is an autosomal recessive autoinflammatory disease prevalent in Mediterranean populations.
  • Characterized by recurrent fevers and inflammation, FMF requires understanding its genetic basis for effective management.
  • Genetic heterogeneity of FMF necessitates population-specific mutation screening.

Purpose of the Study:

  • To investigate the spectrum and frequency of common MEFV gene mutations in diverse Israeli communities.
  • To identify characteristic FMF mutations within Jewish, Arab, and Druze populations.
  • To determine the prevalence of homozygous FMF mutations across these ethnic groups.

Main Methods:

  • Genetic screening of 1700 suspected FMF patients from various Israeli communities (Jews, Arabs, Druze).
  • Analysis focused on six common MEFV gene mutations: M680I, M694V, M694I, V726A, E148Q, and K695R.
  • Statistical analysis of mutation frequencies and distribution among different ethnic groups.

Main Results:

  • MEFV mutations were confirmed in 55% of suspected cases.
  • M694V, E148Q, and V726A were the most common mutations overall.
  • Distinct mutation profiles were observed: M694V in Jews, V726A in Arabs, and E148Q in Druze. K695R was characteristic in Jews, M680I in Arabs.
  • Homozygous mutations were found in 18% of cases, with M694V most prevalent in Jews and E148Q in Druze.

Conclusions:

  • The study provides a comprehensive overview of FMF mutation spectrum in Israeli society.
  • Understanding ethnic-specific mutation patterns is crucial for accurate FMF diagnosis and genetic counseling.
  • The high prevalence of E148Q across all groups highlights its significance in FMF pathogenesis.