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Mitochondrial DNA D-loop sequencing reveals obesity variants in an Arab population.
Eaaswarkhanth, Muthukrishnan; Melhem, Motasem; Sharma, Prem; Nizam, Rasheeba; Al Madhoun, Ashraf; Chaubey, Gyaneshwer; Alsmadi, Osama; AlOzairi, Ebaa; Al-Mulla, Fahd.
Afiliação
  • Eaaswarkhanth M; Genetics and Bioinformatics Department, Dasman Diabetes Institute, Dasman, 15462, Kuwait.
  • Melhem M; Genetics and Bioinformatics Department, Dasman Diabetes Institute, Dasman, 15462, Kuwait.
  • Sharma P; Genetics and Bioinformatics Department, Dasman Diabetes Institute, Dasman, 15462, Kuwait.
  • Nizam R; Genetics and Bioinformatics Department, Dasman Diabetes Institute, Dasman, 15462, Kuwait.
  • Al Madhoun A; Genetics and Bioinformatics Department, Dasman Diabetes Institute, Dasman, 15462, Kuwait.
  • Chaubey G; Cytogenetics Laboratory, Department of Zoology, Banaras Hindu University, Varanasi, India.
  • Alsmadi O; Department of Cell Therapy & Applied Genomics, King Hussein Cancer Center, Amman, Jordan.
  • AlOzairi E; Genetics and Bioinformatics Department, Dasman Diabetes Institute, Dasman, 15462, Kuwait.
  • Al-Mulla F; Genetics and Bioinformatics Department, Dasman Diabetes Institute, Dasman, 15462, Kuwait.
Appl Clin Genet ; 12: 63-70, 2019.
Article em En | MEDLINE | ID: mdl-31213875
Background: The association of mitochondrial DNA (mtDNA) variations with obesity has been investigated in diverse populations across the world. However, such obesity-associated mtDNA examinations are rarely conducted in Arab populations. Materials and methods: We re-sequenced mtDNA displacement loop (D-loop) region of 395 Arab individuals of Kuwait. We categorized the individuals based on their BMI scores as obese (n=232; BMI ≥30 kg/m2), overweight (n=110; BMI ≥25 kg/m2 and <30 kg/m2), and lean (n=53; BMI <25 kg/m2). We performed all the statistical tests by combining obese and overweight individuals in one group. Association analyses were conducted applying Fisher's exact test and logistic regression model. Results: We identified that the mtDNA variations m.73A>G, and m.523delAC were positively correlated with obesity, while m.310T>C, and m.16318A>T were negatively associated. All these variants, except m.16318A>T, remain statistically significant after adjusting for age and gender. We found that the variant m.73A>G increases the likelihood of being obese by 6-fold, whereas haplogroup H decreases the probability of being obese in Arab individuals of Kuwait. Haplotype analysis revealed that a haplotype, A263G-C309CT-T310C, defining the H2a clade of H haplogroup, reduces the probability of being obese. Conclusion: Our study reports, for the first time, the obesity-related mtDNA variants in Arabs of Kuwait. Based on the mtDNA D-loop region variations, we detected particular variants and haplogroup that are related with increased and decreased probability of being obese in the Kuwait Arab population.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Appl Clin Genet Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Kuait

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Appl Clin Genet Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Kuait