- Research note
- Open Access
Glutathione S-transferase M1 and T1 genes deletion polymorphisms and blood pressure control among treated essential hypertensive patients in Burkina Faso
BMC Research Notes volume 14, Article number: 244 (2021)
Glutathione S-transferases have been associated with experimental resistance to some drugs. The present study investigated the factors associated with blood pressure control in patients with essential hypertension, especially the role of GSTT1 and GSTM1 genes polymorphisms. This cross-sectional study in Burkina Faso consisted of 200 patients with essential hypertension and under treatment.
In the present study, 57.5% (115/200) of patients had their hypertension under control. No statistically significant difference was found between controlled and uncontrolled groups for anthropometric and biochemical parameters as well as for GSTT1 or GSTM1 gene polymorphisms (all p > 0.05). Current alcohol consumption (OR = 3.04; CI 1.88–6.13; p < 0.001), Physical inactivity (OR = 3.07; CI 1.71–5.49; p < 0.001), severe hypertension before any treatment (Grade III [OR = 3.79; CI 2.00–7.17; p < 0.001]) and heart damage (OR = 3, 14; CI 1.59–6.02; p < 0.001) were statistically more frequent in uncontrolled essential hypertensive patients than controlled hypertensive patients.
Normalization of blood pressure (BP) in hypertensive patients significantly decreases the risk of stroke, heart diseases and improves patients' quality of life .
However, the achievement rates of the BP target values (Systolic Blood Pressure [SBP] < 140 mmHg and Diastolic Blood Pressure [DBP] < 90 mmHg) remain low in treated patients, estimated at 37.1% worldwide in 2010 and less than 10% in Sub-Saharan Africa in 2013 [2, 3]. Black people are the more susceptible subgroup to hypertension and its complications , and are more exposed to uncontrolled hypertension or use of multiple drugs to control their BP . It therefore becomes crucial to better understand factors that affect BP control in order to minimize their effects. Many studies have looked for factors associated with hypertension control but the contribution of genetic factors is less studied. Glutathione S-transferase (GST) plays a crucial role in the detoxification mechanisms of drugs and xenobiotics . Studies in both humans and animals have shown that polymorphisms which affect the expression of certain enzymes in the GST family also affect the effectiveness of certain drugs [7,8,9,10]. These results suggest that GST could affect the bioavailability of certain drugs which acts as GST enzyme substrate. To date, no study to our knowledge has evaluated the link between GST gene polymorphisms and response to antihypertensive drugs, although Glutathione S-transferases Mu1 deletion has been associated with resistant hypertension . We previously investigated the link between Glutathione S-transferases Mu1 (GSTM1) and theta 1 (GSTT1) variants and the risk of developing essential hypertension and found that GSTT1-null genotype was associated with the risk of developing hypertension in Burkina Faso . In the present study, we want to specifically determine the implication of GSTM1/GSTT1 deletion polymorphisms in BP control among the followed hypertensive patients in the same population. We hypothesis that the GSTM1/GSTT1 active variants with normal detoxification activity, could reduce the bioavailability of antihypertensive drugs and by doing so, GSTM1/GSTT1 deletion polymorphisms, in addition to their association with the risk of developing essential hypertension, could modulate the response to antihypertensive treatments, therefore the control of BP. Hence, we aim to determine the factors associated with BP control among hypertensive patients in Burkina Faso, especially identify the contribution of GSTM1 / GSTT1 deletion polymorphisms.
We conducted a cross-sectional study from July 15, 2017 to March 27, 2018, including 200 essential hypertensive patients followed in the cardiology department of Saint Camille Hospital of Ouagadougou (HOSCO), University Hospital Center Yalgado Ouédraogo (CHUYO) and the Medical Center of General Aboubacar Sangoulé Lamizana military Camp).
The study population consisted of subjects under antihypertensive treatments regardless of gender or social characteristics, aged from 18 to 70 years old.
Patients with secondary hypertension or no antihypertensive treatment, pregnant women and subjects not descendants from Burkina Faso were not included in this study.
Controlled blood pressure was defined as an average of SBP < 140 mmHg and DBP < 90 mmHg for all patients  during the last two consecutive medical visits under treatment.
Samples and data collection
A standardized questionnaire was used to collect socio-demographic, lifestyle, clinical and biological data (see questionnaire in Additional file 3).
BP was measured using an electronic cuffed sphygmomanometer by cardiologist as described previously .
Body mass index (BMI) was used to classify patients as obese (≥ 30 kg/m2), overweight (25–30 kg/m2), normal weight (20–25 kg/m2) and underweight (≤ 20 kg/m2). We determined waist circumference (WC) and abdominal obesity in men was determined when WC ˃ 102 cm and in women when WC > 88 cm . Family history of hypertension was determined in participants with at least one close family member being hypertensive before the age of 60 years.
Alcohol consumption corresponds to any consumption during the last 30 days preceding the survey as mentioned in the report of the STEPS survey in Burkina Faso in 2013 . We distinguished 3 types of alcohol drinkers: heavy drinkers (more than 6 drinks on any day for men or more than 4 drinks on any day for women), intermediate drinkers (between 3 and 6 drinks on any day for men or between 2 and 4 drinks on any day for women) and moderate or occasional drinkers (2 drinks or less in a day for men and 1 drink or less in a day for women).
From each patient, venous blood sample was taken in EDTA tube and anticoagulant-free tube. Sera were directly used for biochemical analysis using CYANExpert 130 analyzer, and blood pellet were stored at -20 °C until DNA extraction.
DNA extraction and genotyping
The salting out method as described by Miller and al. in 1988 was used to isolate genomic DNA from peripheral white blood cells .
Genotyping of the GSTM1 and GSTT1 genes has been previously described . Briefly we performed multiplex PCR with the GeneAmp PCR system 9700 (Applied Biosystem, USA) in a reaction volume of 25µL including 10µL of Master Mix AmpliTaq Gold® (Applied Biosystems, USA), 7µL of nuclease-free water, 5µL of DNA and 1µL of each primer pairs for each gene (β-globin, GSTM1, GSTT1). After amplification, PCR products were migrated on ethidium bromide-stained 3% agarose gel during 45 mn, bands were visualized under UV light at 312 nm using the Geneflash revelation device (Additional file 1) and the generated data were interpreted as previously described .
We used Statistical Package for Social Sciences (20.0) and Epi Info (6.0) for data analyses. To determine sample size, we have taken into account following values: 95% of two-sided confidence level, 80% of power, odds ratio more than 2.2, ratio of controlled BP to uncontrolled BP 1.1, the proportion of controlled BP patients group having GSTM1-null and GSTT1-null about 50%. We expressed quantitative variables and frequencies as mean ± standard deviation and percentage respectively and comparisons between groups were done with t-test and chi-squared test respectively. Difference was considered as statistically significant when p < 0.05.
Characteristics of the study population
The Table 1 presents the general characteristics of the study population. The BP levels of participants under treatment allowed us to classify them into patients with controlled and uncontrolled hypertension. We showed that 115 (57.5%) had their BP under control.
Regarding the socio-demographic and biochemical data, there was no significant difference between the controlled and the uncontrolled group (all p > 0.05).
Of the 200 patients under antihypertensive treatments, 99 patients were under monotherapy, 65 patients under bitherapy and 36 patients under Tritherapy (data not shown). Additional file 2.
Influence of genetic variants of GSTM1 and GSTT1 on the control of blood pressure and essential hypertension
The Table 2 presents and compares the frequencies of GSTM1 and GSTT1 variants between the controlled and uncontrolled SBP groups, between the controlled and uncontrolled DBP groups and between the controlled and uncontrolled hypertension group. We did not find any significant difference between those groups (p > 0.05). Stratified Analysis by age and sex also showed no association (Additional file 3).
Research of non-genetic factors associated with the control of essential hypertension
The Table 3 presents and compares the frequencies of non-genetic factors that have been associated with hypertension control in previous studies. Our results showed that current alcohol consumption (OR = 3.04; CI 1.88–6.13; p < 0.001), physical inactivity (OR = 3.07; CI 1.71–5.49; p < 0.001), severe hypertension before any treatment (Grade III [OR = 3.79; CI 2.00–7.17; p < 0.001]) and heart damages, including left ventricular hypertrophy, left ventricular relaxation anomalies, left atrial hypertrophy and mitral insufficiency (OR = 3, 14; CI 1.59–6.02; p < 0.001) were more frequent in uncontrolled group than controlled group and differences were significant. Age and sex-stratified analysis showed that this association is specific to women and elderly subjects for current alcohol use, specific to men and elderly subjects for cardiac damages and specific to women for diabetes mellitus (Additional file 4).
In this study, we investigate the factors associated with BP control in essential hypertensive patients from Burkina Faso. Our results showed that there was no significant difference between the controlled and the uncontrolled hypertension group by comparing the levels of biochemical parameters, suggesting that BP control is independent of blood glucose, cholesterol, triglycerides and creatinine levels in hypertensive patients.
There was also no significant difference between the control rates of patients under monotherapy and bitherapy or tritherapy, unlike some previous studies which have shown that monotherapy in Burkinabe  or multi-drug therapy in Brazilian  was associated with uncontrolled BP.
However, we found that alcohol consumption, physical inactivity, the high grade of initial hypertension before any medication and cardiac affections were associated with uncontrolled BP. The influence of alcohol consumption on antihypertensive therapy has long been studied. Stewart et al., in a multi-ethnic cohort (including 76% non-Hispanic white, 12% Hispanic, 8% African American, and 4% other ethnic groups), showed that the reduction of alcohol consumption increase the antihypertensive drugs response and that the management of alcohol consumption must be considered as a major component of antihypertensive therapy in alcoholics . Concerning physical exercise, many studies have consistently demonstrated its beneficial effects on hypertension. Diaz and Shimbo in a review, showed reductions in SBP and DBP up to 5–7 mmHg  and Pescatello in another review found that more frequent and long-term exercise leads to a more sustained reduction in BP, called exercise training response . It is believed that the reduction in BP with physical activity is due to the attenuation of peripheral vascular resistance, which may be due to neurohormonal and structural responses . Other mechanisms suggested in reducing BP through exercise include favorable changes in oxidative stress, inflammation, endothelial function, body mass, activity of the renin-angiotensin system, renal function, and insulin sensitivity .
Cardiac damages were found more in the uncontrolled group compared to the controlled group and this may be the cause or the effect of uncontrolled BP in essential hypertensive patients.
Our results also showed that there was no association between socio-demographic characteristics, residence areas and gender with BP control, unlike other studies which have shown that women had a higher control rate than men in African countries . Our results are similar to those reported in Tanzania by Maginga et al., who showed that age, gender, educational level, marital status, professional status and residency did not affect the control of hypertension . However, unlike our study which found no association between obesity and the control of essential hypertension, that of Maginga et al., showed that it was associated with a poor control rate in Tanzania.
Considering the genetic aspects, we investigated the influence of variants of the GSTM1 and GSTT1 genes on the control of essential hypertension. Genetic factors may influence the pharmacokinetics and pharmacodynamics (tissue or organ responsiveness) of drugs .
In our study, out of 99 patients, 96 used vasodilator drugs (Amlodipine, Nifedipine, Captopril, Ramipril, Enalapril) which reduced blood pressure by dilating or preventing constriction of the blood vessels . The remaining 3 patients were using Atenolol, a beta blocker which binds to the beta receptors for adrenaline and norepinephrine, blocking their actions and thus promoting a slowing of the heart rate and drop in blood pressure . In dual therapy, all patients used at least one vasodilator in addition to other classes of antihypertensive drugs such as beta blockers (14/65) and diuretics (39/65) which lower the blood pressure by increasing diuresis and thus reducing blood volume . In triple therapy in 36 patients, 35 used two vasodilators in addition to a diuretic (32/35) or a beta blocker (2/35) or a central antihypertensive (1/35). Only one out of the 36 patients used a vasodilator in addition to a diuretic and a beta blocker. Altogether, vasodilators were the most used therapy (72.40%), followed by diuretics (21.36%), beta-blockers (5.4%) and centrally acting antihypertensive (0.30%). In the literature, to our knowledge, no direct link has been shown between these antihypertensive drugs used and the GST genes; however, associations have been demonstrated with the efficacy of other drugs in other pathologies and conditions. So in cancer cells, Gate et al., demonstrated that GST often show high levels of expression when compared to normal cells  and this may contribute to increase detoxification of anticancer drugs . It have been also shown that GST Through their detoxification activity, might play an important role in the protection against the toxic effect of the antimicrobial agents which leads bacteria to become resistant to antibiotics . In Ghanaian HIV treated patients, homozygous deletion of GSTM1 and GSTT1 have been associated with CD4 + count rising above 350 cells/mm3 suggesting that patients with homozygous deletion have slower disease progression and better drug response . Among GST genes, GSTM1 and GSTT1 are the most investigated in studies exploring genetic and drug response and they have been described as polymorphic in humans . The most common polymorphisms of the loci of the GSTM1 and GSTT1 genes consist in the complete deletion of these genes (GSTM1-null and GSTT1-null) . The GSTM1-null variant represents the complete or partial deletion of the GSTM1 gene and results in loss of function for GSTM1 enzyme. The GSTM1 locus has been mapped on chromosome 1p13.3 (GRCh38/hg38). Three different alleles have been identified in the same locus, including gene deletion, and two other mutations (GSTM1a and GSTM1b) that differ by C to G substitution at base position 534 . Similarly, a deletion polymorphism in GSTT1 leads to lack of enzyme activity. The human GSTT1 locus has been mapped on chromosome 22q11.23 (GRCh38/hg38). Regarding GSTT1, the null allele results from the homologous recombination of the left and right repeats of 403 bp, which results in a deletion of 54, 251 bps containing the entire GSTT1 gene. Whether it is GSTM1 or GSTT1, three distinct phenotypes can thus be observed in the population namely the “nonconjugators: 0/0”, the “low conjugators: 1/0” and “high conjugators: 1/1” . The “nonconjugators” (homozygous deletion or null genotype) who lost GSTM1 or GSTT1 gene entirely, no longer have the capacity to conjugate the glutathione to the specific substrate, hence their accumulation in the organism. The “low conjugators” (heterozygotes) which have half-conserved the GSTM1 or GSTT1 gene have a reduced capacity for conjugation of the glutathione and “high conjugators” (without deletion) which have retained the gene in its entirety have a high conjugation activity and therefore elimination of substrates specific to the gene. The frequencies of GSTM null and GSTT1 null varies widely in different populations. Previous studies in Burkina Faso reported that approximately 28.75%–31.23% and 30%–55.76% of the population have the null variant of GSTM1 and GSTT1 respectively [12, 38], which fell into the range of allele frequency values registered in west African Nigeria (0.3 for GSTM1 null allele; 0.37 for GSTT1 null allele)  and other Black African populations . GSTM1 and GSTT1 play a key role in the metabolism of certain drugs and xenobiotic through their participation in the second phase of xenobiotic metabolism. They facilitate the excretion of electrophilic compounds from cells by conjugating them to hydrophilic compounds with reduced glutathione [41, 42]. Thus the “conjugators” and “high conjugators” with their capacity of elimination could be subject to a decrease in the bioavailability of drugs which are substrates of GSTM1 or GSTT1, therefore a decrease in the response to these drugs, hence the absence or decrease in BP control in those subjects. However our results showed that neither GSTM1 nor GSTT1 was associated with BP control. This at first sight indicates an absence of association between the active variants of these two genes and the low availability and efficacy of antihypertensive drugs. Some studies estimate that other members of the GST enzyme family must have compensated for the absence of a functional enzyme in the null genotype subjects [43, 44], which leads to the same level of activity of GST enzymes both in the GSTM1/GSTT1 null and active genotypes.
In this study, we have not detected any apparent link between GSTM1 and GSTT1 deletion polymorphisms and systolic or diastolic BP control. The patient’s lifestyle seems to be more determining in BP control under treatment than studied genetic factors. Especially alcohol consumption and physical inactivity are associated with a poor control or uncontrolled BP. In addition, given the fact that advanced disease stage, with or without cardiac complications, is also linked to an uncontrolled BP, early diagnosis should be therefore encouraged for effective management and for better therapeutic responses.
Our study could have certain limitations, in particular the size of the study population and the lack of information on adherence to antihypertensive therapy. These observations could be taken into account in future studies.
Availability of data and materials
The dataset generated in this study is available from NCBI Nucleotide under the accession number LC517160.1.
Body mass index
Pietro Annigoni Biomolecular Research Center
Diastolic blood pressure
- GSTM1 :
S-transferases Mu 1
- GSTT1 :
Glutathione S-transferases Theta 1
High-density lipoprotein cholesterol
Laboratory of molecular biology and genetics
Low-density lipoprotein cholesterol
Polymerase chain reaction
Reactive Oxygen Species
Systolic blood pressure
Statistical Package for the Social Sciences
Park JY, Kim KA, Lee GS, Park PW, Kim SL, Lee YS, Lee YW, Shin EK. Randomized, open-label, two-period crossover comparison of the pharmacokinetic and pharmacodynamic properties of two amlodipine formulations in healthy adult male Korean subjects. Clin Ther. 2004;26(5):715–23.
Ataklte F, Erqou S, Kaptoge S, Taye B, Echouffo-Tcheugui JB, Kengne AP. Burden of undiagnosed hypertension in sub-saharan Africa: a systematic review and meta-analysis. Hypertension. 2015;65(2):291–8.
Mills KT, Bundy JD, Kelly TN, Reed JE, Kearney PM, Reynolds K, Chen J, He J. Global disparities of hypertension prevalence and control: a systematic analysis of population-based studies from 90 countries. Circulation. 2016;134(6):441–50.
Gu Q, Burt VL, Dillon CF, Yoon S. Trends in antihypertensive medication use and blood pressure control among United States adults with hypertension: the National Health And Nutrition Examination Survey, 2001 to 2010. Circulation. 2012;126(17):2105–14.
Hajjar I, Kotchen TA. Trends in prevalence, awareness, treatment, and control of hypertension in the United States, 1988–2000. JAMA. 2003;290(2):199–206.
Hayes JD, Flanagan JU, Jowsey IR. Glutathione transferases. Annu Rev Pharmacol Toxicol. 2005;45:51–88.
Zhang Y, Yang L, Li R, Zhang L, Zhang MR, Xiao ZJ. The effects of glutathione S-transferase (GSTT1 and GSTM1) genes polymorphisms on treatment efficacy and prognosis of acute myeloid leukemia. Zhonghua Nei Ke Za Zhi. 2006;45(3):213–6.
Barahmani N, Carpentieri S, Li X-N, Wang T, Cao Y, Howe L, Kilburn L, Chintagumpala M, Lau C, Okcu MF. Glutathione S-transferase M1 and T1 polymorphisms may predict adverse effects after therapy in children with medulloblastoma. Neuro Oncol. 2009;11(3):292–300.
Kang HW, Song PH, Ha Y-S, Kim WT, Kim Y-J, Yun S-J, Lee S-C, Choi YH, Moon S-K, Kim W-J. Glutathione S-transferase M1 and T1 polymorphisms: susceptibility and outcomes in muscle invasive bladder cancer patients. Eur J Cancer. 2013;49(14):3010–9.
Ye H, Shao M, Shi X, Wu L, Xu B, Qu Q, Qu J. Predictive assessment in pharmacogenetics of Glutathione S-transferases genes on efficacy of platinum-based chemotherapy in non-small cell lung cancer patients. Sci Rep. 2017;7(1):2670.
Cruz-Gonzalez I, Corral E, Sanchez-Ledesma M, Sanchez-Rodriguez A, Martin-Luengo C, Gonzalez-Sarmiento R. An association between resistant hypertension and the null GSTM1 genotype. J Hum Hypertens. 2009;23(8):556–8.
Sombié HK, Sorgho AP, Kologo JK, Ouattara AK, Yaméogo S, Yonli AT, Djigma FW, Tchelougou D, Somda D, Kiendrébéogo IT, et al. 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). BMC Med Genet. 2020;21(1):55.
Kjeldsen S, Feldman RD, Lisheng L, Mourad JJ, Chiang CE, Zhang W, Wu Z, Li W, Williams B. Updated national and international hypertension guidelines: a review of current recommendations. Drugs. 2014;74(17):2033–51.
Sombié HK, Sorgho AP, Kologo JK, OUATTARA AK, Yaméogo S, Yonli AT, Djigma FW, Tchelougou D, Somda D, Kiendrébéogo IT et al: 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). BMC Med Genetics 2020(In press).
Zhang C, Rexrode KM, van Dam RM, Li TY, Hu FB. Abdominal obesity and the risk of all-cause, cardiovascular, and cancer mortality: sixteen years of follow-up in US women. Circulation. 2008;117(13):1658–67.
santé. Mdl: Rapport de l'enquête nationale sur la prévalence des principaux facteurs de risque communs aux maladies non transmissibles au Burkina Faso. Enquête STEPS 2013 Burkina Faso. https://www.who.int/chp/steps/BurkinaFaso_2013_STEPS_FactSheet.pdf?ua=1. 2014.
Miller SA, Dykes DD, Polesky HF. A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res. 1988;16(3):1215.
Yameogo NV, Kagambega LJ, Millogo RC, Kologo KJ, Yameogo AA, Mandi GD, Ilboudo E, Toguyeni BJ, Samadoulougou AK, Zabsonre P. Factors associated with poor blood pressure control in hypertensive black Africans: cross-sectional study of 456 hypertensive patients from Burkina Faso. Ann Cardiol Angeiol (Paris). 2013;62(1):38–42.
Barreto MDS, Matsuda LM, Marcon SS. Fatores associados ao inadequado controle pressórico em pacientes da atenção primária. Escola Anna Nery. 2016;20:114–20.
Stewart SH, Latham PK, Miller PM, Randall P, Anton RF. Blood pressure reduction during treatment for alcohol dependence: results from the Combining Medications and Behavioral Interventions for Alcoholism (COMBINE) study. Addiction. 2008;103(10):1622–8.
Diaz KM, Shimbo D. Physical activity and the prevention of hypertension. Curr Hypertens Rep. 2013;15(6):659–68.
Pescatello LS. Exercise and hypertension: recent advances in exercise prescription. Curr Hypertens Rep. 2005;7(4):281–6.
Hamer M. The anti-hypertensive effects of exercise. Sports Med. 2006;36:109.
Kayima J, Wanyenze RK, Katamba A, Leontsini E, Nuwaha F. Hypertension awareness, treatment and control in Africa: a systematic review. BMC Cardiovasc Disord. 2013;13:54.
Maginga J, Guerrero M, Koh E, Holm Hansen C, Shedafa R, Kalokola F, Smart LR, Peck RN. Hypertension control and its correlates among adults attending a hypertension clinic in Tanzania. J Clin Hypertens (Greenwich). 2016;18(3):207–16.
Roden DM, George AL Jr. The genetic basis of variability in drug responses. Nat Rev Drug Discov. 2002;1(1):37–44.
Hariri L, JP. Vasodilators (Updated 2021 Feb 13). In: StatPearls. Treasure Island (FL): StatPearls Publishing; 2021. https://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/books/NBK554423/.
Farzam K, AJ. (Updated 2021 Mar 12). In: StatPearls. Treasure Island (FL): StatPearls Publishing; 2021. https://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/books/NBK532906/.
Huxel C, Raja A, MD. O-L. Loop Diuretics. (Updated 2021 Mar 16). In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2021. https://0-www-ncbi-nlm-nih-gov.brum.beds.ac.uk/books/NBK546656/.
Gate L, Tew KD. Glutathione S-transferases as emerging therapeutic targets. Expert Opin Ther Targets. 2001;5(4):477–89.
Sau A, Pellizzari Tregno F, Valentino F, Federici G, Caccuri AM. Glutathione transferases and development of new principles to overcome drug resistance. Arch Biochem Biophys. 2010;500(2):116–22.
Pugazhendhi A, Dhanarani S, Shankar C, Prakash P, Ranganathan K, Saratale RG, Thamaraiselvi K. Electrophoretic pattern of glutathione S-transferase (GST) in antibiotic resistance Gram-positive bacteria from poultry litter. Microb Pathog. 2017;110:285–90.
Kuleape JA, Tagoe EA, Puplampu P, Bonney EY, Quaye O. Homozygous deletion of both GSTM1 and GSTT1 genes is associated with higher CD4+ T cell counts in Ghanaian HIV patients. PloS one. 2018;13(5):e0195954.
Ebeshi BU, Bolaji OO, Masimirembwa CM. Glutathione-S-transferase (M1 and T1) polymorphisms in Nigerian populations. J Med Genet Genomics. 2011;3(4):56–60.
Palma-Cano LE, Córdova EJ, Orozco L, Martínez-Hernández A, Cid M, Leal-Berumen I, Licón-Trillo A, Lechuga-Valles R, González-Ponce M, González-Rodríguez E, et al. GSTT1 and GSTM1 null variants in Mestizo and Amerindian populations from northwestern Mexico and a literature review. Genet Mol Biol. 2017;40(4):727–35.
Rebbeck TR. Molecular epidemiology of the human glutathione S-transferase genotypes GSTM1 and GSTT1 in cancer susceptibility. Cancer Epidemiol Biomark Prevention. 1997;6:733–43.
Pemble S, Schroeder KR, Spencer SR, Meyer DJ, Hallier E, Bolt HM, Ketterer B, Taylor JB. Human glutathione S-transferase theta (GSTT1): cDNA cloning and the characterization of a genetic polymorphism. Biochem J. 1994;300(1):271–6.
Kiendrebeogo IT, Zoure AA, Sorgho PA, Yonli AT, Djigma FW, Ouattara AK, Sombie HK, Tovo SF, Yelemkoure ET, Bambara AH, et al. Glutathione S-transferase M1 (GSTM1) and T1 (GSTT1) variants and breast cancer risk in Burkina Faso. Biomol Concepts. 2019;10(1):175–83.
Ebeshi BU, Bolaji O, Masimirembwa C: Glutathione-S-transferase (M1 and T1) polymorphisms in Nigerian populations. 2011.
Kasthurinaidu SP, Ramasamy T, Ayyavoo J, Dave DK, Adroja DA. GST M1–T1 null allele frequency patterns in geographically assorted human populations: a phylogenetic approach. PLoS ONE. 2015;10(4):e0118660–e0118660.
Orrenius S, Thor H, Jernström B. The influence of inducers on drug-metabolizing enzyme activity and on formation of reactive drug metabolites in the liver. Environ Chem Enzym Funct Hum Dis. 2008;76:25–39.
Jancova P, Anzenbacher P, Anzenbacherova E. Phase II drug metabolizing enzymes. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2010;154(2):103–16.
Gronau S, Koenig-Greger D, Jerg M, Riechelmann H. Gene polymorphisms in detoxification enzymes as susceptibility factor for head and neck cancer? Otolaryngology Head Neck Surg. 2003;128(5):674–80.
Konig-Greger D, Riechelmann H, Wittich U, Gronau S. Genotype and phenotype of glutathione-S-transferase in patients with head and neck carcinoma. Otolaryngology Head Neck Surg. 2004;130(6):718–25.
The authors wish to thank all participants in this study. A deep gratitude to all the staff of Saint Camille Hospital of Ouagadougou (HOSCO) and Biomolecular Research Center Pietro Annigoni (CERBA) for technical support.
This work was supported by West African Economic and Monetary Union (WAEMU) through the “Programmed’appui et de développement des centresd’excellencerégionaux” (PACERII) and “Centre national de l’Information, de l’OrientationScolaire et Professionnelle, et des Bourses”(CIOSPB) especially for researcher life stipend. Financial support for reagents and consumables was provided by Italian Episcopal Conference (CEI). The funding bodies played no role in the design of the study and collection, analysis, and interpretation of data and in writing the manuscript.
Ethics approval and consent to participate
The present study has been approved by the ethics committee of CERBA/LABIOGENE and the National Ethics Committee for Health Research of Burkina Faso.CERS20186065, 6 June 2018, retrospectively registered. Free and written consent was obtained from all participants of this study. The anonymity and confidentiality of the patients were respected as stated in the IRB (Institutional Review Board) protocol.
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The authors declare that they have no competing interests.
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GSTM1, GSTT1 and β-globin genes and corresponding bands in electrophoresis gel. This file shows corresponding bands of GSTM1, GSTT1 and β-globin genes in electrophoresis gel. The number 1 through 14 represents individual sample and M represents Molecular weight marker. The strategy to identify presence or absence of GSTM1or GSTT1was as followed: to validate a PCR product (corresponding to a sample), we must have a band corresponding to β-globin and presence or absence of GSTM1 or GSTT1 was indicated respectively by the presence or absence of bands corresponding for each gene.
Level of treatment and antihypertensive drugs used by patients. This file shows the proportion of antihypertensive drugs used by study participants.
Sex and age stratified analysis of association between GSTM1 and GSTT1 variants with essential hypertension control. This file shows a stratified analysis of the association between GSTM1 and GSTT1 gene variants with essential hypertension control in order to highlight the probable interactions.
Age and sex-stratified analysis of non-genetic factors affecting blood pressure control in patients with essential hypertensive. This file shows a stratified analysis by sex and age of non-genetic factors affecting blood pressure control in patients with essential hypertensive to highlight the probable interactions.
Data collection sheet. Information sheet and questionnaire. This file shows the fact sheets used to explain the study during the recruitment of the participants and the questionnaire which served for the data collection.
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Sombié, H.K., Tchelougou, D., Ouattara, A.K. et al. Glutathione S-transferase M1 and T1 genes deletion polymorphisms and blood pressure control among treated essential hypertensive patients in Burkina Faso. BMC Res Notes 14, 244 (2021). https://0-doi-org.brum.beds.ac.uk/10.1186/s13104-021-05658-w
- Blood pressure control
- Essential hypertension
- Burkina Faso