Thrombosis Related ABO, F5, MTHFR, and FGG Gene Polymorphisms in Morbidly Obese Patients

Kristina Kupcinskiene1, Martyna Murnikovaite2, Greta Varkalaite2

  • 1Department of Anesthesiology, Lithuanian University of Health Sciences, Eiveniu Str. 2, LT-50009 Kaunas, Lithuania.

Disease Markers
|December 22, 2016
PubMed

Insights

This study investigated thrombosis-related gene polymorphisms in morbidly obese patients. Key gene variants, including MTHFR, were not significantly associated with morbid obesity or related traits in European subjects.

Area of Science:

  • Genetics
  • Obesity Research
  • Thrombosis

Background:

  • Obesity is a significant risk factor for thrombotic complications.
  • Understanding the genetic predisposition to thrombosis in obesity is crucial for risk stratification and management.
  • Specific gene polymorphisms in ABO, F5, MTHFR, and FGG have been implicated in thrombotic events.

Purpose of the Study:

  • To determine the frequency of specific thrombosis-related gene polymorphisms (ABO, F5, MTHFR, FGG) in morbidly obese patients.
  • To compare the distribution of these gene polymorphisms between morbidly obese individuals and nonobese controls.
  • To assess the association of these polymorphisms with anthropometric measures like height and weight in the studied populations.

Main Methods:

  • Genotyping of single nucleotide polymorphisms (SNPs) in ABO (rs505922), F5 (rs6427196), MTHFR (rs1801133), and FGG (rs6536024) was performed using RT-PCR.
  • The study included 320 morbidly obese patients (BMI > 40 kg/m²) and 303 nonobese control individuals (BMI < 30 kg/m²).
  • All participants were of European descent.

Main Results:

  • No significant differences were observed in the overall distribution of genotypes and alleles for the studied SNPs between morbidly obese and nonobese groups.
  • A non-significant tendency was noted for the MTHFR rs1801133 TT genotype to be linked with morbid obesity (OR 1.84, P=0.129).
  • The distribution of height and weight means did not significantly differ among individuals carrying different genotypes of the investigated SNPs.

Conclusions:

  • The investigated gene polymorphisms (ABO C>T, F5 C>G, MTHFR C>T, FGG C>T) were not found to be associated with morbid obesity in the European cohort studied.
  • These specific genetic variations do not appear to be significant risk factors for height, weight, or morbid obesity in this population.
  • Further research may be needed to explore other genetic or environmental factors contributing to thrombosis risk in obese individuals.

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