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Glutathione S-transferase M1 and T1 genes deletion polymorphisms and risk of developing essential hypertension: a case-control study in Burkina Faso population (West Africa)

Authors :
Herman Karim Sombié
Abel Pegdwendé Sorgho
Jonas Koudougou Kologo
Abdoul Karim Ouattara
Sakinata Yaméogo
Albert Théophane Yonli
Florencia Wendkuuni Djigma
Daméhan Tchelougou
Dogfounianalo Somda
Isabelle Touwendpoulimdé Kiendrébéogo
Prosper Bado
Bolni Marius Nagalo
Youssoufou Nagabila
Enagnon Tiémoko Herman Donald Adoko
Patrice Zabsonré
Hassanata Millogo
Jacques Simporé
Source :
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-10 (2020)
Publication Year :
2020
Publisher :
BMC, 2020.

Abstract

Abstract Background Glutathione S-transferases play a key role in the detoxification of persistent oxidative stress products which are one of several risks factors that may be associated with many types of disease processes such as cancer, diabetes, and hypertension. In the present study, we characterize the null genotypes of GSTM1 and GSTT1 in order to investigate the association between them and the risk of developing essential hypertension. Methods We conducted a case-control study in Burkina Faso, including 245 subjects with essential hypertension as case and 269 control subjects with normal blood pressure. Presence of the GSTT1 and GSTM1 was determined using conventional multiplex polymerase chain reaction followed by gel electrophoresis analysis. Biochemical parameters were measured using chemistry analyzer CYANExpert 130. Results Chi-squared test shows that GSTT1-null (OR = 1.82; p = 0.001) and GSTM1-active/GSTT1-null genotypes (OR = 2.33; p 0.05). Multinomial logistic regression revealed that age ≥ 50 years, central obesity, family history of hypertension, obesity, alcohol intake and GSTT1 deletion were in decreasing order independent risk factors for essential hypertension. Analysis by gender, BMI and alcohol showed that association of GSTT1-null with risk of essential hypertension seems to be significant when BMI

Details

Language :
English
ISSN :
14712350
Volume :
21
Issue :
1
Database :
Directory of Open Access Journals
Journal :
BMC Medical Genetics
Publication Type :
Academic Journal
Accession number :
edsdoj.6cd6f33022e245bfb262478a397fe91e
Document Type :
article
Full Text :
https://doi.org/10.1186/s12881-020-0990-9