Whole Exome Sequencing and Whole Genome Sequencing for Investigation of the Genetic Basis of Obesity: A Rapid Review

被引:0
|
作者
Dehghan, Roghayeh [1 ]
Salehi, Mansoor [2 ]
机构
[1] Isfahan Univ Med Sci, Sch Med, Dept Genet & Mol Biol, Esfahan, Iran
[2] Isfahan Univ Med Sci, Res Inst Primordial Prevent Noncommunicable Dis, Pediat Inherited Dis Res Ctr,Dept Genet & Mol Biol, Child Growth & Dev Res Ctr,Sch Med, Esfahan, Iran
关键词
Genetic Research; Obesity; Whole Exome Sequencing; Whole Genome Sequencing; SUSCEPTIBILITY GENE; CHILDHOOD OBESITY; CANDIDATE GENES; RARE VARIANTS; ARCHITECTURE; POPULATION; MUTATIONS; INSIGHTS; DISEASE;
D O I
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中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: In recent decades, the prevalence of obesity has reached a global epidemic level. This study was done to assess the whole exome sequencing and whole genome sequencing methods used to investigate the genetic basis of obesity. Materials and Methods: Different studies on Pubmed, Scopuis, Google Scholar and other data bases were extracted and their findings were analyzed. Results: Childhood obesity has risen to alarming levels as World Health Organization (WHO) estimates that there were 38.2 million children under the age of 5 years with overweight or obesity in 2019. It has been shown that genetic factors also play a key role in the risk of obesity, and strong evidence suggests that BMI is highly heritable. However, in both adults and children, a major part of the genetic aetiology of obesity is still unknown. Recent advances and increasing affordability of whole exome sequencing (WES) and/or whole genome sequencing (WGS) have provided a rapid and comprehensive method for identifying the novel genes in obesity, particularly in children with severe early-onset obesity. Conclusion: This rapid review aimed to review a variety of literature reporting novel candidate genes for non-syndromic obesity identified through applying WES and WGS techniques in humans.
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页码:1492 / 1497
页数:6
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