Title of article :
Assessment of Genetic Aspects of Non-alcoholic Fatty Liver and Premature Cardiovascular Events
Author/Authors :
Saki, Sara Tehran University of Medical Sciences, Tehran, Iran , Saki, Nader Hoveizeh Cohort Study - Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran , Poustchi, Hossein Digestive Disease Research Institute - Tehran University of Medical Sciences, Tehran, Iran , Malekzadeh, Reza Digestive Disease Research Institute - Tehran University of Medical Sciences, Tehran, Iran
Abstract :
Recent evidence has demonstrated a strong interplay and multifaceted relationship
between non-alcoholic fatty liver disease (NAFLD) and cardiovascular disease (CVD).
CVD is the major cause of death in patients with NAFLD. NAFLD also has strong associations
with diabetes and metabolic syndrome. In this comprehensive review, we aimed to overview
the primary environmental and genetic risk factors of NAFLD, and CVD and also focus
on the genetic aspects of these two disorders.
NAFLD and CVD are both heterogeneous diseases with common genetic and
molecular pathways. We have searched for the latest published articles regarding this
matter and tried to provide an overview of recent insights into the genetic aspects of
NAFLD and CVD.
The common genetic and molecular pathways involved in NAFLD and CVD are insulin
resistance (IR), subclinical inflammation, oxidative stress, and atherogenic dyslipidemia.
According to an investigation, the exact associations between genomic characteristics
of NAFLD and CVD and casual relationships are not fully determined. Different
gene polymorphisms have been identified as the genetic components of the NAFLDCVD
association. Some of the most documented ones of these gene polymorphisms are
patatin-like phospholipase domain-containing protein 3 (PNPLA3), transmembrane 6
superfamily member 2 (TM6SF2), hydroxysteroid 17-beta dehydrogenase 13 (HSD17B13),
adiponectin-encoding gene (ADIPOQ), apolipoprotein C3 (APOC3), peroxisome
proliferator-activated receptors (PPAR), leptin receptor (LEPR), sterol regulatory
element-binding proteins (SREBP), tumor necrosis factor-alpha (TNF-α), microsomal
triglyceride transfer protein (MTTP), manganese superoxide dismutase (MnSOD),
membrane-bound O-acyltransferase domain-containing 7 (MBOAT7), and mutation in
DYRK1B that substitutes cysteine for arginine at position 102 in kinase-like domain.
Further cohort studies with a significant sample size using advanced genomic
assessments and next-generation sequencing techniques are needed to shed more light
on genetic associations between NAFLD and CVD.
Keywords :
Non-alcoholic fatty liver disease , Cardiovascular disease , Gene polymorphism , Genetic aspect
Journal title :
Middle East Journal of Digestive Diseases(MEJDD)