Blood Coagulation Disorders Among the Iranian Population: a Systematic Review

Clinical Laboratory
|August 10, 2023
PubMed

Insights

Blood coagulation disorders, particularly Factor XIII (FXIII) deficiency, are prevalent in Iran. The c.562T>C mutation is the most frequent genetic cause identified in this population.

Area of Science:

  • Hematology
  • Genetics
  • Public Health

Background:

  • Blood coagulation disorders represent a significant cause of mortality, necessitating focused research.
  • Investigating the prevalence and genetic basis of these disorders in specific populations, like Iran, is crucial for understanding disease burden.

Approach:

  • A systematic review adhering to PRISMA guidelines was conducted, analyzing data from 1990 to 2019.
  • Searches encompassed major databases (Web of Science, PubMed, Scopus, etc.), including diverse study designs (cross-sectional, cohort, experimental, case-control) without language or gender restrictions.

Key Points:

  • Factor XIII (FXIII) deficiency is the most common coagulation disorder identified in Southern Iran (599/1,165 individuals).
  • The c.559T>C and c.562T>C mutations were the most frequent genetic variants associated with FXIII deficiency.
  • Factor V (FV) Leiden was the second most common disorder (396/1,165), with the c.1691G>A mutation being its most prevalent genetic cause.

Conclusions:

  • FXIII deficiency is the most critical coagulation disorder within the Iranian population.
  • The c.562T>C mutation is identified as the most common genetic mutation contributing to coagulation disorders in Iran.
Abstract

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