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Genetic variants on chromosome 19 (rs439401 and rs4420638) are associated with obesity and high blood pressure in the Algerian population

https://doi.org/10.18699/VJ19.532

Abstract

Metabolic syndrome (MetS) represents a combination of at least three primary metabolic abnormalities from among obesity, hyperglycemia, dyslipidemia, and high blood pressure, once combined, they increase significantly the cardiovascular risk. The APOE gene is considered as a genetic risk factor for cardiovascular diseases, it has been linked to MetS or its traits in several populations. Our study aimed to analyze the association of three APOE gene polymorphisms with MetS risk and its components in a general population sample, and to highlight the potential influence of these polymorphisms on individual susceptibility to MetS. We performed this work using a population-based, cross-sectional study of a representative sample of 787 individuals (378 men and 409 women, aged between 30 and 64 years) recruited in the city of Oran, Algeria (the ISOR Study); the subjects were genotyped for four polymorphisms, rs7412, rs429358, rs4420638 and rs439401, located in the APOE gene, using the KASPar technology. rs439401 showed a significant association with hypertension (HBP). The T allele confers a high risk of hypertension with an odds ratio (OR) of 1.46 (95 % CI [1.12–1.9], = 0.006). rs4420638 was significantly associated with obesity in the general population. The G allele provides protection against obesity, the resulting OR is 0.48 (95 % CI [0.29–0.81], = 0.004). Although APOE variants were not associated with the risk of MetS, the APOE polymorphism alleles were associated with some of the metabolic parameters in Algerian subjects. The relation of APOE rs439401 alleles with a HBP is likely to be indicative of a state of stress of the population.

About the Authors

H. Boulenouar
Université Aboubekr Belkaid; Université des Sciences et de la Technologie d’Oran Mohamed Boudiaf
Algeria

Département de Médecine and Laboratoire de Recherche CancerLab No. 30, Faculté de Médecine “Dr Benzerdjeb Benaouda”, Université Aboubekr Belkaid; Laboratoire de Génétique Moléculaire et Cellulaire, Université des Sciences et de la Technologie d’Oran 




S. Mediene Benchekor
Université des Sciences et de la Technologie d’Oran Mohamed Boudiaf; Université Oran 1 Ahmed Ben Bella
Algeria

Laboratoire de Génétique Moléculaire et Cellulaire, Université des Sciences et de la Technologie; 

Département de Biotechnologie, Faculté des Sciences de la Nature et de la Vie, Université Oran



H. Ouhaibi Djellouli
Université des Sciences et de la Technologie d’Oran Mohamed Boudiaf
Russian Federation
Laboratoire de Génétique Moléculaire et Cellulaire


S. Larjam Hetraf
Université des Sciences et de la Technologie d’Oran Mohamed Boudiaf
Algeria
Laboratoire de Génétique Moléculaire et Cellulaire


L. Houti
Université d’Oran 1
Algeria
Faculté de Médecine, LABoratoire des Systèmes d’Information en Santé


I. Hammani-Medjaoui
Caisse Nationale des Assurances Sociales des travailleurs salariés
Algeria
Clinique Spécialisée en Orthopédie et Rééducation des Victimes des Accidents de Travail


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