Association of GSTM1 and GSTT1 gene polymorphisms with COVID‐19 susceptibility and its outcome

Abstract

Coronavirus disease 2019 (COVID‐19) caused by severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) infection has become a global health issue and develops into a broad range of illnesses from asymptomatic to fatal respiratory diseases. SARS‐CoV‐2 infection is associated with oxidative stress that triggers cytokine production, inflammation, and other pathophysiological processes. Glutathione‐S‐transferase (GST) is an important enzyme that catalyzes the conjugation of glutathione (GSH) with electrophiles to protect the cell from oxidative damage and participates in the antioxidant defense mechanism in the lungs. Thus, in this study, we investigated the role of GSTM1 and GSTT1 gene polymorphism with COVID‐19 susceptibility, as well as its outcome. The study included 269 RT‐PCR confirmed COVID‐19 patients with mild (n = 149) and severe (n = 120) conditions. All subjects were genotyped for GSTM1 and GSTT1 by multiplex polymerase chain reaction (mPCR) followed by statistical analysis. The frequency of GSTM1^−/−, GSTT1^−/− and GSTM1^−/−/GSTT1^−/− was higher in severe COVID‐19 patients as compared to mild patients but we did not observe a significant association. In the Cox hazard model, death was significantly 2.28‐fold higher in patients with the GSTT1^−/− genotype (p = 0.047). In combination, patients having GSTM1^+/+ and GSTT1^−/− genotypes showed a poor survival rate (p = 0.02). Our results suggested that COVID‐19 patients with the GSTT1^−/− genotype showed higher mortality.

1. INTRODUCTION

Coronavirus disease 2019 (COVID‐19), caused by severe acute respiratory syndrome coronavirus 2 (SARS‐COV‐2) has recently emerged as a new challenge for the medical sciences. It has been considered a pandemic by the World Health Organization (WHO) from March 11, 2020, onwards. ¹ The pathogenesis of COVID‐19 and its cause of severity are still poorly understood. SARS‐CoV‐2 is associated with oxidative stress (OS) that triggers cytokine production, inflammation, and other pathophysiological activities. ² OS is defined as the disturbance of the antioxidant and prooxidant balance in a biological system. ³ During OS, highly reactive oxygen/nitrogen species (RONS) are produced such as hydroxyl, superoxide anion, nitric oxide, and nitrosyl anion, which target various cells and damage DNA, proteins, and lipids, leading to the pathogenesis of respiratory viral infections including SARS‐CoV‐2 infections.3, 4, 5 Delgado‐Roche and Mesta, ⁵ suggested that OS coupled with innate immunity affects the onset of severe lung injury in COVID‐19 patients and stimulates transcription factors, such as NF‐kB, resulting in an exacerbated pro‐inflammatory host response. However, the COVID‐19 patients with pre‐existing conditions such as diabetes, hypertension, and pulmonary, cardiac, and kidney diseases are at a higher risk of developing a severe infection.6, 7, 8, 9

Glutathione S‐transferases (GSTs) are a superfamily of multifunctional isoenzymes that catalyzes glutathione conjugation with electrophilic compounds, resulting in the cellular detoxification of several endogenous and exogenous compounds. ¹⁰ GSTs play an important role in the detoxification of different carcinogens, drugs, and against various types of cellular oxidative damage. ¹¹ The GST enzyme contributes to different interindividual activity in response to clearance of oxidative stress products. ¹² In mammalian tissue, eight distinct classes of the cytosolic GST enzymes have been recognized such as alpha (α)‐GSTA, mu (μ)‐GSTM, pi (π)‐GSTP, omega (ω)‐GSTO, theta (θ)‐GSTT, sigma (σ)‐GSTS, kappa (κ)‐GSTK), and zeta (ζ)‐GSTZ. ¹³ The μ (GSTM1: MIM: 600436) and θ (GSTT1: MIM: 138350) members are the most common variant of GST genes, which are located on chromosome 1p13.3 and 22q11.23, respectively.14, 15 The homozygous deletion (null genotype) of the GSTM1 (GSTM1 ^−/− ) and GSTT1 (GSTT1 ^−/−) genes are associated with the loss of enzyme activity and increase the risk of several oxidative stress associated multifactorial diseases including cardiovascular and respiratory diseases.16, 17, 18, 19, 20

Thus, in this study, we investigated the association of GSTM1 and/or GSTT1 polymorphisms with COVID‐19 susceptibility as well as its outcome in the North Indian population.

2. MATERIALS AND METHODS

2.1. Sample collection and experimental design

This study was approved by the Ethics Committee of the Era University, India. We recruited 269 RT‐PCR confirmed COVID‐19 patients, enrolled in Eras Lucknow Medical College and Hospital (ELMC&H), Era University, Lucknow from August 2020 to September 2020, and all patients were followed up for 1 month from the date of admission. Informed consent from all participants was obtained in accordance with the ethical standards of Era University, India. All demographic and clinical data of patients were collected as per a self‐administered questionnaire and other clinical data was collected from hospital records with the help of an expert clinician. All patients with inclusion criteria (COVID‐19 patients confirmed by RT‐PCR of more than 20 years) and no exclusion criteria (Pregnant patients, patients with known malignant disease) were selected.

Patients were categorized into two groups, mild and severe as per the criteria of the Indian Council of Medical Research (ICMR), New Delhi, India. Patients with a respiratory rate less than 24 per min and SpO₂ > 94% on room air were considered as mild patients while patients with a respiratory rate more than 30 per min and SpO₂ < 90% on room air with pneumonia were categorized into severe patients.21, 22 2 ml of the blood sample from all patients were collected in ethylene diamine tetraacetic acid (EDTA) vials and stored at −20°C until further use.

2.2. Genotyping

Genomic DNA was extracted from peripheral blood samples by using a Commercially Available Kit (Macherey‐Nagel) and the quality/quantity of DNA was assessed by using a spectrophotometer and gel electrophoresis checked on 1% agarose gel and quantified in a biophotometer (Eppendorf). GSTM1 and GSTT1 null genotypes were detected by using multiplex polymerase chain reaction (mPCR) using specific primers: F‐5′GAACTCCCTGAAAAGCTAAAGC‐3′ and R‐5′GTTGGGCTCAAATATACGGTGG‐3′; F‐5′TCCTTACTGGTCCTCACATCTC‐3′ and R‐5′TCACCGGATCATGGCCAGCA‐3′ respectively and for positive control, angiotensin II receptor type 1 (AGTR1) gene primers were used: F‐5′GCCAAATCCCACTCAAACCTTTCAACAA‐3′ and R‐5′AAGCAGGCTAGGGAGATTGC ATTTCTGT‐3′.

PCR was performed in a 25 µl reaction mixture of 150–200 ng genomic DNA, 5 pmol of each primer, 2× master mix (Takara), and 0.5 U of Taq DNA polymerase (G‐Biosciences) per tube using a gradient Master Cycler (Bio‐Rad). The PCR products were visualized by 2.5% agarose gels in a Gel Documentation System (EZ, Bio‐Rad). The null genotypes of both genes (GSTM1 and GSTT1) were determined by the absence of gene products. The AGTR1 gene was co‐amplified and used as a positive control (Figure 1).

Figure 1.

Agarose gel showing multiplex PCR products of different genotypes of GSTM1 (230 bp) and GSTT1 (458 bp). Lane 1: 100 bp ladder; Lane 2: GSTM1^–/–/GSTT1^+/+; Lane 3: GSTM1^+/+/GSTT1^–/–; Lane 4: Non template control; Lane 5: GSTM1^+/+/GSTT1^+/+; Lane 6: GSTM1^–/–/GSTT1^–/–. AGTR1 gene (421 bp) was used as a positive control. PCR, polymerase chain reaction

2.3. Statistical analysis

Demographic and clinical data were compared with genotypes using χ2 analysis and Fisher's exact test. Allele and genotype frequencies in mild and severe cases were compared using a 2 × 2 contingency table by Fisher's exact test. The odds ratio (OR) at 95% confidence interval (CI) was used to determine the strength of association. All p values were considered statistically significant if p < 0.05. Genotype effects GSTM1 and GSTT1 on overall survival were evaluated by the Kaplan–Meier function and the Cox proportional hazards model. The differences in overall survival and genotypes were compared using the log‐rank test. Hazard ratios (HRs) were estimated using a multivariate Cox hazards model/Cox regression analysis with adjustment for age, sex, hypertension, and diabetes.

3. RESULTS

3.1. Clinical characteristics of patients

The mean age of patients was 52.7 years. A total of 269 COVID‐19 patients were enrolled in this study. Out of 269, 149 patients (47.2%) were showing mild symptoms and 120 patients (38.0%) were showing severe symptoms. A total of 32 deaths (10%) were observed from 120 severe patients.

3.2. Genotyping

The distribution of GSTM1 and GSTT1 genotypes in mild and severe patients is shown in Table 1. The frequency of GSTM1 ^−/− and GSTT1 ^−/− (null genotypes) was higher among severe patients than in mild (13.3% vs. 10.7%; 14.2% vs. 10.7%, respectively) that showed the corresponding marginal increased risk of severity with null genotypes (Table 1). Individuals with a combination of two null genotypes (GSTM1 ^−/−/GSTT1 ^−/−) showed a 3.91‐folds higher risk of severity due to COVID‐19 infection when adjusted with age, sex, hypertension, and diabetes (Table 1). However, GSTM1/GSTT1 polymorphism was not shown to have a significant association with the severity of the COVID‐19 (p > 0.05, Table 1). We have also shown the distribution of GSTM1 and GSTT1 genotypes with demographic and clinical data in COVID‐19 severe patients. But none of the demographic and clinical parameters showed a significant association with GSTM1/GSTT1 polymorphism (p > 0.05, Table 2).

Table 1.

Genotype frequencies of GSTM1 and GSTT1 and their association with severity of COVID‐19

Genes	Mild, n (%)	Severe, n (%)	Unadjusted OR (95% CI)	p	Adjusteda OR (95% CI)	p
GSTM1	149	120
M1+/+	133 (89.3)	104 (86.7)	1.0 (Ref.)		1.0 (Ref.)
M1−/−	16 (10.7)	16 (13.3)	1.28 (0.611–2.677)	0.514	1.47 (0.638–3.384)	0.367
GSTT1
T1+/+	133 (89.3)	103 (85.8)	1.0 (Ref.)		1.0 (Ref.)
T1−/−	16 (10.7)	17 (14.2)	1.37 (0.661–2.846)	0.396	1.33 (0.574–3.059)	0.51
GSTM1/GSTT1
M1+/+/T1+/+	120 (80.6)	90 (75.0)	1.0 (Ref.)		1.0 (Ref.)
M1+/+/T1−/−	13 (8.7)	14 (11.7)	1.44 (0.643–3.205)	0.377	1.08 (0.436–2.694)	0.863
M1−/−/T1+/+	13 (8.7)	13 (10.8)	1.33 (0.590–3.015)	0.49	1.22 (0.493–3.009)	0.67
M1−/−/T1−/−	3 (2.0)	3 (2.5)	1.33 (0.263–6.761)	0.728	3.91 (0.587–26.062)	0.159

Note: n, number; %, percentage; Significance association (p < 0.05); CI, confidence interval; OR, odds ratio; 1.0 (Reference); (+/+), present; (−/−), null.

^a Adjusted for age, sex, hypertension, and diabetes.

Table 2.

Distribution of GSTM1 and GSTT1 genotypes with demographic and clinical data in COVID‐19 severe patients

	GSTM1			GSTT1
Patients	M1+/+, n (%)	M1−/−, n (%)	p	T1+/+, n (%)	T1−/−, n (%)	p
Age
≤45	11 (78.6)	93 (87.7)	0.343	12 (85.7)	91 (85.8)	0.989
≥46	3 (21.4)	13 (12.3)	2 (14.3)	15 (14.2)
Gender
Male	63 (86.3)	41 (87.2)	0.883	60 (82.2)	43 (91.5)	0.154
Female	10 (13.7)	6 (12.8)	13 (17.8)	4 (8.5)
Diabetes
No	74 (86.0)	30 (88.2)	0.751	76 (88.4)	27 (79.4)	0.205
Yes	12 (14.0)	4 (11.8)	10 (11.6)	7 (20.6)
Hypertension
No	85 (85.0)	19 (95.0)	0.23	87 (87.0)	16 (80.0)	0.412
Yes	15 (15.0)	1 (5.0)	13 (13.0)	4 (20.0)

Note: n, number; %, percentage; Significant association (p < 0.05); (+/+), Present; (−/−), null.

3.3. Survival of patients

The follow‐up duration for all patients was 1 month. During the study period, 11.9% of patients succumbed to death. The median survival had not been reached and the overall mean survival time was 27.79 days. The association of GSTM1 and GSTT1 genotypes with overall survival were analyzed by Cox proportional hazards model, adjusted for age, sex, hypertension, and diabetes are shown in Table 3. There was a significant increase in the hazard of death to 2.28 among patients with GSTT1^−/− when compared with patients having the GSTT1^+/+ genotype (95% CI = 1.013–5.141; p = 0.047). However, there was no significant association with GSTM1 genotypes (p = 0.853). In the combined effect of GSTM1 and GSTT1, individuals with GSTM1^+/+ and GSTT1^−/−genotypes showed a significantly 2.72‐folds higher risk of death due to COVID‐19 (95% CI = 1.172–6.295; p = 0.02). The Kaplan–Meier function for survival in cases with GSTM1 and GSTT1 genotypes is shown in Figure 2. In the Kaplan–Meier curve, GSTT1^−/− was associated with poor overall survival (log‐rank, p = 0.020, Figure 1B). In addition, the combined effect showed that both genes have an impact on survival. Patients with GSTM1^+/+/GSTT1^−/− genotype showed significantly poor overall survival as compared to patients having GSTM1^+/+/GSTT1^+/+ genotypes (log‐rank, p = 0.015, Figure 1C).

Table 3.

Associations between GSTM1 and GSTT1 genetic polymorphisms and survival of COVID‐19 patients

Genotypes	No. of cases, n (%)	Deaths, n (%)	HRa (95% CI)	p
GSTM1
M1+/+	209 (88.2)	28 (87.5)	1.0 (Ref.)
M1−/−	28 (11.8)	4 (12.5)	1.11 (0.386–3.165)	0.853
GSTT1
T1+/+	212 (89.5)	24 (75.0)	1.0 (Ref.)
T1−/−	25 (10.5)	8 (25.0)	2.28 (1.013–5.141)	0.047
GSTM1/GSTT1
M1+/+/T1+/+	190 (80.2)	20 (62.5)	1.0 (Ref.)
M1+/+/T1−/−	19 (8.0)	8 (25.0)	2.72 (1.172–6.295)	0.02
M1−/−/T1+/+	22 (9.3)	4 (12.5)	1.52 (0.515–4.468)	0.449
M1−/−/T1−/−	6 (2.5)	0

Note: n, number; %, percentage; Significant association (p < 0.05); CI, confidence interval; HR, hazard ratio; 1.0 (Reference); (+/+), present; (−/−), Null.

^a Adjusted for age, sex, hypertension, and diabetes.

Figure 2.

Kaplan–Meier estimates of 30‐day survival of the 269 COVID‐19 patients, by GSTM1 (A) and GSTT1 (B) genotypes, in combination (C). Survival difference by log‐rank test

4. DISCUSSION

GST‐mediated GSH conjugations have been well recognized for the detoxification of several exogenous xenobiotics and/or their Phase I metabolites.17, 23 However, the null genotype of the GSTM1 and GSTT1 genes raise the risk of several oxidative stress‐associated multifactorial diseases, including COVID19.18, 24, 25 GST polymorphisms are associated with a higher risk of oxidative stress, which may play an important role in susceptibility to infection with SARS‐CoV‐2 and/or its outcome. ²⁵ SARS‐CoV‐2 induced reactive oxygen species (ROS) production disturbs the antioxidant defense system that triggers a pro‐inflammatory environment and severe tissue damage, contributing to the fatal outcomes of COVID‐19 patients. ²⁶ However, the mechanisms of virus‐induced OS and its subsequent effects in cells, tissue, and the organism are not well known. There are indeed many contradictory data on antioxidants and the role of ROS in viral replication. ²⁷ Melatonin treated animals showed significantly enhanced activity of the GST enzyme that may reduce COVID‐19 infection‐associated OS.28, 29

The current study found that COVID‐19 patients with GSTT1^−/− have a higher risk of mortality and lower overall survival. These findings support the theory that oxidative stress is more prevalent in patients with low or no GST activity. Saadat ²⁵  reported that individuals with GSTT1^−/− had a higher risk of COVID‐19 infection as compared to an individual with GSTT1^+/+, however, the population with a low prevalence of GSTT1^−/− genotype showed the higher numbers of COVID‐19 cases and deaths in East‐Asian countries. Another study reported that individual with GSTT1^−/− alone or in combination with GSTM1^−/− genotype had an excess decrease in forced expiratory volume in the first second (FEV₁) in men, regardless of the smoking status. ³⁰ Ding et al. ³¹ reported that individual with GSTT1^−/− and/or GSTM1^−/− had a higher risk for the development of pulmonary fibrosis in chronic obstructive pulmonary disease which is also one of the most important complications of COVID‐19 and characterized by long‐term breathing problems. The main observations of the present study are that GSTT1^−/− was positively associated with COVID‐19 mortality in our population but does not have a correlation with the prevalence of COVID‐19. The present findings suggest that the GSTT1^−/− could have a clinical impact on the COVID‐19 treatment and help to identify the individuals who are at high risk of COVID‐19 severity in the North Indian population. However, the present study is preliminary with limited sample size. Thus, further experiments are currently ongoing in our laboratory to identify the role of GSTT1 polymorphisms for the cause‐effect on COVID‐19 severity in a larger patient population.

CONFLICT OF INTERESTS

The authors declare that there are no conflict of interests.

AUTHOR CONTRIBUTIONS

Farzana Mahdi, Mohammad Abbas, Faizan H. Khan, and Sushma Verma conceived and designed the experiments. Shrikant Verma and Mohammad Abbas carried out the practicability study. Shrikant Verma and Ale Eba performed the experiments. Mohammad Abbas, Sahabjada Siddiqui, Zeba Siddiqi, Syed T. Raza analyzed the data, and Mohammad Abbas, Faizan H. Khan, and Sushma Verma wrote the paper.

Abbas M, Verma S, Verma S, et al. Association of GSTM1 and GSTT1 gene polymorphisms with COVID‐19 susceptibility and its outcome. J Med Virol. 2021;93:5446–5451. 10.1002/jmv.27076