Open Access Peer-Reviewed
Artigo Original

TXNRD2 (rs35934224) CT genotype as possible protective marker for primary open-angle glaucoma in a Brazilian population

Genótipo CT do TXNRD2 (rs35934224) como um possível marcador de proteção para glaucoma primário de ângulo aberto em uma população brasileira

Artur Lins Tenório1; Rodrigo Pessoa Cavalcanti Lira1; Rodrigo Feliciano do Carmo2; Roberto Pedrosa Galvão Filho3; Pedro Teixeira Falcão Neto3; Rinalva Tenório Vaz4; Raul Emidio de Lima5; André Lins Tenório6; Luydson Richardson Vasconcelos5

DOI: 10.5935/0004-2749.20220019

ABSTRACT

Purpose: To investigate the association of the single-nucleotide polymorphism rs35934224 in the TXNRD2 gene with primary open-angle glaucoma in a Brazilian population.
Methods: This was a cross-sectional study conducted to verify the association between the rs35934224 TXNRD2 (thioredoxin reductase 2) and primary open-angle glaucoma in a population from the Northeast region of Brazil. A total of 184 individuals were enrolled, including 94 with primary open-angle glaucoma (45 men and 49 women) and 94 controls (40 men and 54 women) from the Recife Eye Institute.
Results: The mean age was 68.85 years for the patients with glaucoma and 68.55 years for the controls. Genomic DNA was isolated using commercially available kits, and single-nucleotide polymorphism was detected with real-time polymerase chain reaction using TaqMan probes. The studied population was in Hardy-Weinberg equilibrium. The CT genotype was associated with protection against primary open-angle glaucoma (p=0.022).
Conclusion: Our data suggest an association between TXNRD2 gene polymorphism (rs35934224) with primary open-angle glaucoma in an admixed Brazilian population. This is the first study to investigate this single-nucleotide polymorphism in Latin American individuals with primary open-angle glaucoma.

Keywords: Polymorphism, Thioredoxin reductase; Glaucoma, open-angle

RESUMO

Objetivo: Investigar a associação do Polimorfismo de nucleotídeo único rs35934224 no gene TXNRD2 com o glaucoma primário de ângulo aberto em uma população brasileira.
Métodos: Tratou-se de um estudo transversal para verificar a associação entre o rs35934224 do TXNRD2 (tioredoxina redutase 2) e o glaucoma primário de ângulo aberto em uma população da região nordeste do Brasil. Foram incluídos 184 indivíduos: 94 casos com glaucoma primário de ângulo aberto (45 homens e 49 mulheres) e 94 controles (40 homens e 54 mulheres) do Instituto de Olhos de Recife.
Resultados: A idade média foi de 68,85 anos para os pacientes com glaucoma e 68,55 anos para os controles. O DNA genômico foi isolado usando kits comerciais disponíveis e a detecção do polimorfismo de nucleotídeo único foi realizada por PCR em tempo real usando sondas TaqMan. A população estudada estava em equilíbrio de Hardy-Weinberg. O genótipo CT foi associado à proteção ao glaucoma primário de ângulo aberto (p=0,022).
Conclusão: Nossos dados sugerem uma associação entre o polimorfismo do gene TXNRD2 (rs35934224) e o glaucoma primário de ângulo aberto em uma população brasileira. Este é o primeiro estudo a investigar esse polimorfismo de nucleotídeo único em indivíduos com glaucoma primário de ângulo aberto latino-americanos.

Descritores: Polimorfismo; Tiorredoxina redutase; Glaucoma de ângulo aberto

INTRODUCTION

Primary open-angle glaucoma (POAG) is characterized by loss of retinal ganglion cells, optic nerve damage, and consequently, irreversible loss of the visual field(1). An estimated 35-58 million people are affected by POAG worldwide, and this number is expected to increase up to 53 to 65.5 million by 2020 owing to the aging world population(2-3).

Although many mechanisms have been proposed, the pathophysiology of POAG and the factors that contribute to the worsening of the disease still remains obscure(4). Recent advances in genomic technologies and genome-wide association studies (GWAS) have greatly accelerated the discovery and understanding of genes and genomic regions associated with POAG and influence the quantitative endophenotype traits related to POAG pathogenesis(5). However, most studies have been conducted in European and Asian populations. Data regarding the influence of these genes in other populations are lacking.

TXNRD2 is on chromosome 22q11.21 and consists of 18 exons of relatively small size, with intron sizes ranging from 200 and 10,000 bp(6,7). In addition, TXNRD2 codes for thioredoxin reductase 2, a mitochondrial protein necessary for reducing the damage of reactive oxygen species (ROS) generated by oxidative phosphorylation and other mitochondrial functions(8,9).

The importance of studying the single-nucleotide polymorphism (SNP) in the thioredoxin reductase 2 (TXNRD2) gene (rs35934224) is due the strong association found between this SNP and POAG in a recent GWAS(6). In this study, Bailey et al. found a significant association of the T variant with POAG in European, Asian, and Oceanian populations, showing the protection of the T allele in relation to POAG (p=4.05 × 10-11)(6). In addition to POAG, the genetic variation in TXNRD2 was found to be associated with diabetic retinopathy(10), prostate cancer(11,12), gastric cancer(13), and colon and rectal cancers(14).

Whether this genetic protective factor is also found in more mixed-race Latin American populations is not yet known. Northeastern Brazil has a highly miscegenated population. Therefore, the aim of this study was to investigate the association of the SNP rs35934224 in the TXNRD2 gene with POAG in this population.

 

METHODS

Study population

For the present study, individuals from Northeast Brazil who attended the Fundação Ação Visual/IOR in the city of Recife, Pernambuco, were recruited. The participants underwent a comprehensive ophthalmologic examination, which included a medical history review and slit-lamp biomicroscopy, gonioscopy, dilated fundoscopy examinations (90-dioptre lens; Volk Optical Inc., Mentor, OH, USA). Intraocular pressure (IOP) was assessed using a Goldmann applanation tonometer (Haag Streit AG, Bern, Switzerland). The standard automated perimetry was performed using the 24-2 Swedish Interactive Thresholding Algorithm (SITA) FAST of the Humphrey Field Analyzer II (Carl Zeiss Meditec, Inc., Dublin, CA, USA), and the peripapillary retinal nerve fiber layer (RNFL) thickness was measured on spectral-domain (SD) optical coherence tomography (OCT; Heidelberg Engineering, Heidelberg, Germany) to assess visual field defects or quantify glaucomatous damage in glaucoma patients, respectively.

A total of 94 individuals with POAG were included in the present study. POAG was diagnosed if glaucoma optic neuropathy (GON) and defects in the visual field or retinal nerve fiber layer thickness, regardless of the IOP in one or both eyes, were found, on the basis of the following three criteria: (1) morphological changes in the optic nerve head characteristic of GON, with a cutoff cup-to-disk ratio of 0.7 to distinguish GON from healthy eyes or an asymmetry ≥0.2 between eyes, and the presence of localized defects in the RNFL and/or neuroretinal rim area; (2) at least two OCT images showing progressive retinal nerve fiber layer thinning or visual field defects corresponding to the RNFL thinning in the standard automated perimetry, considering glaucomatous visual field defects with a pattern standard deviation outside the 95% normal limits or a glaucoma hemifield test result >99% (Humphrey Swedish Interactive 24-2 SITA-FAST protocol); and (3) open and normally appearing angle of the anterior chamber in gonioscopy.

POAG was diagnosed in the patients before enrollment in the study. Patients who were using eye drops other than hypotensive medications after any ocular surgery and had <6 months of treatment with any glucocorticosteroid or immunosuppressive drugs were excluded from the study.

The control group consisted of 94 individuals without glaucomatous optic nerve neuropathy, with a cup-to-disk ratio of up to 0.5 and an IOP <18 mmHg. None of the healthy controls had evidence of any ocular diseases or autoimmune/autoinflammatory and systemic disorders matched by geographical region. Furthermore, patients with a familial history of glaucoma or blindness were excluded.

Written informed consent was obtained from all the participants, and the ethics committee for research of the University of Pernambuco, under protocol No. 56467316.8.0000.5207, approved all the methods used. All the study methods were performed in accordance with the provisions of the Declaration of Helsinki and Good Clinical Practice guidelines.

DNA extraction and genotyping

Genomic DNA was extracted from whole blood by using a QIAamp DNA Blood Kit (Qiagen Inc, Chatsworth, CA), following the manufacturer’s instructions. The extracted DNA was measured using Nanodrop spectrometry technology and stored at -20°C until further analysis.

A 7500 real-time PCR system (Applied Biosystems, Foster City, CA) was used to detect the SNP of the gene TXNRD2 (rs35934224) by using the TaqMan probe (Assay: C___2539086_10). The assays were performed with a TaqMan genotyping master mix (Applied Biosystems, Foster City, CA) in 96-well plates.

Statistical analyses

The statistical analysis of the data was performed using the SPSS version 22.0 statistical software package (SPSS, Inc., Chicago, IL, USA). Categorical variables were compared using the chi-square test, and the results are presented using odds ratios (ORs) with 95% confidence intervals (CIs). Sex and age variables were analyzed between the groups using the Student t test or Mann-Whitney U test for parametrically or non-parametrically distributed data as appropriate. The differences were considered statistically significant when the p value was <0.05.

 

RESULTS

The study population was in Hardy-Weinberg equilibrium. Table 1 describes the mean age and sex distributions between the cases and controls. The frequencies of the males and females and the mean ages were similar between the cases and the controls (p>0.05).

 

 

On the basis of the genotypes CC and CT/TT of TXNRD2 rs35934224, the glaucoma group was categorized according to baseline characteristics. The analysis between the groups did not show statistically significant differences (Table 2).

 

 

Table 3 summarizes the allelic and genotype frequencies of TXNRD2 rs35934224 in the individuals with POAG and controls. The patients in the glaucoma group presented a higher frequency of the CC genotype than the control group (72.3% vs. 59.5%). In the comparison of the CT/TT and CC genotypes, the combination CT/TT presented a higher frequency in the control group than in the case group; however, these results were not statistically significant (40.5% vs. 27.7%; p=0.032; OR=0.56, 95% CI = 0.30-1.03). When evaluating only the CT × CC genotype, CT was associated with protection against POAG (38.2% vs. 24.4%, p=0.022, OR=0.52, 95% CI=0.27-0.98). Allelic distribution was not significantly associated.

 

 

DISCUSSION

In the present study, we found a significant association between the CT genotype in the TXNRD2 gene (rs35934224) with protection to POAG in a Brazilian admixed population(15). On the other hand, we observed a higher frequency of the CC genotype in the POAG group than in the control group.

Oxidative stress and antioxidant systems are important in ocular tissue. Several studies have demonstrated a significant contribution of oxidative stress to the POAG pathogenesis(16-21). In addition, a recent meta-analysis demonstrated an overall increase in oxidative stress molecules in glaucoma, both in the serum and aqueous humor. On the other hand, the authors observed decreases in the levels of some antioxidant markers, which suggests that reduction in ROS could be neuroprotective(18). The mitochondrial thioredoxin reductase (TXNRD) had a central importance for mitochondrial scavenging of ROS(22). It is well established that antioxidant molecules could be implicated in the pathogenesis of glaucoma because oxidative stress might play a causal role in the disease(18,23,24). In addition, polymorphisms in molecules associated to antioxidant systems(25) have been reported in patients with POAG(11,26,27).

Herein, the CT genotype was associated with protection from POAG, while the CC genotype was more prevalent in the POAG group. Our results corroborate, at least in part, the association found in the GWAS study performed by Bailey et al.(6). In this study, they found a significant association between the rs35934224 allele T with protection from POAG (OR 0.77), besides demonstrating the TXNRD2 expression in retinal ganglion cells and the optic nerve head in normal human ocular tissue(6).

In addition, other SNPs in TXNRD2 have been associated with POAG in different populations. Bonnemaijer et al. showed the association of the rs16984299 in TXNRD2 with POAG in African populations(28). Moreover, another study observed a significant association between rs17534001 in the TXNRD2 gene and POAG in European populations(29).

The role of TXNRD2 in the glaucoma pathogenesis has been evidenced through an experimental glaucoma model in which overexpression of thioredoxin 2, the substrate of thioredoxin reductase 2, increased retinal ganglion cell survival(29). Thus, reduction of ROS levels by TXNRD2 could prevent glaucoma. In addition, the SNP rs35934224 is located in an inter-exon region and is in linkage disequilibrium with other SNPs in regulatory regions such as the 3’-UTR and promoter regions; thus, this nucleotide change may affect the expression levels of the molecule.

In summary, our data suggest the association between the TXNRD2 gene polymorphism (rs35934224) and POAG in an admixed Brazilian population. However, our study has some limitations such as the small number of subjects enrolled and the lack of functional characterization of TXNRD2. However, we believe that the preliminary results reported herein open new perspectives for the evaluation of the gene in Latin American populations. Further cross-sectional studies with larger cohorts in different populations are necessary to elucidate the potential use of TXNRD2 in clinical practice.

 

REFERENCES

1. Weinreb RN, Aung T, Medeiros FA. The pathophysiology and treatment of glaucoma: a review. JAMA. 2014;311(18):1901-11.

2. Tham YC, Li X, Wong TY, Quigley HA, Aung T, Cheng CY. Global prevalence of glaucoma and projections of glaucoma burden through 2040: a systematic review and meta-analysis. Ophthalmology. 2014;121(11):2081-90.

3. Weinreb RN, Leung CK, Crowston JG, Medeiros FA, Friedman DS, Wiggs JL, et al. Primary open-angle glaucoma. Nat Rev Dis Primers. 2016;2(1):16067.

4. Nunes HF, Ananina G, Costa VP, Zanchin NI, de Vasconcellos JP, de Melo MB. Investigation of CAV1/CAV2 rs4236601 and CDKN2B-AS1 rs2157719 in primary open-angle glaucoma patients from Brazil. Ophthalmic Genet. 2018;39(2):194-9.

5. Abu-Amero K, Kondkar AA, Chalam KV. An updated review on the genetics of primary open angle glaucoma. Int J Mol Sci. 2015; 16(12):28886-911.

6. Bailey JN, Loomis SJ, Kang JH, Allingham RR, Gharahkhani P, Khor CC, et al.; ANZRAG Consortium. Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma. Nat Genet. 2016;48(2):189-94.

7. Miranda-Vizuete A, Damdimopoulos AE, Pedrajas JR, Gustafsson JA, Spyrou G. Human mitochondrial thioredoxin reductase cDNA cloning, expression and genomic organization. Eur J Biochem. 1999;261(2):405-12.

8. Chen Y, Cai J, Jones DP. Mitochondrial thioredoxin in regulation of oxidant-induced cell death. FEBS Lett. 2006;580(28-29):6596-602.

9. Wiggs JL, Pasquale LR. Genetics of glaucoma. Hum Mol Genet. 2017;26 R1:R21-7.

10. Ramus SM, Cilensek I, Petrovic MG, Soucek M, Kruzliak P, Petrovic D. Single nucleotide polymorphisms in the Trx2/TXNIP and TrxR2 genes of the mitochondrial thioredoxin antioxidant system and the risk of diabetic retinopathy in patients with Type 2 diabetes mellitus. J Diabetes Complications. 2016;30(2):192-8.

11. Méplan C, Rohrmann S, Steinbrecher A, Schomburg L, Jansen E, Linseisen J, et al. Polymorphisms in thioredoxin reductase and selenoprotein K genes and selenium status modulate risk of prostate cancer. PLoS One. 2012;7(11):e48709.

12. Xie W, Yang M, Chan J, Sun T, Mucci LA, Penney KL, et al. Association of genetic variations of selenoprotein genes, plasma selenium levels, and prostate cancer aggressiveness at diagnosis. Prostate. 2016;76(7):691-9.

13. Wang J, Sun T, Yang M, Lin DX, Tan W, Li KJ, et al. [Association of genetic polymorphisms in selenoprotein GPX1 and TXNRD2 with genetic susceptibility of gastric cancer]. Zhonghua Yu Fang Yi Xue Za Zhi. 2008;42(7):511-4. Chinese.

14. Slattery ML, Lundgreen A, Welbourn B, Corcoran C, Wolff RK. Genetic variation in selenoprotein genes, lifestyle, and risk of colon and rectal cancer. PLoS One. 2012;7(5):e37312.

15. Giolo SR, Soler JM, Greenway SC, Almeida MA, de Andrade M, Seidman JG, et al. Brazilian urban population genetic structure reveals a high degree of admixture. Eur J Hum Genet. 2012;20(1):111-6.

16. Abu-Amero KK, Kondkar AA, Mousa A, Osman EA, Al-Obeidan SA. Decreased total antioxidants in patients with primary open angle glaucoma. Curr Eye Res. 2013;38(9):959-64.

17. Bagnis A, Izzotti A, Centofanti M, Saccà SC. Aqueous humor oxidative stress proteomic levels in primary open angle glaucoma. Exp Eye Res. 2012;103:55-62.

18. Benoist d’Azy C, Pereira B, Chiambaretta F, Dutheil F. Oxidative and anti-oxidative stress markers in chronic glaucoma: a systematic review and meta-analysis. PLoS One. 2016;11(12):e0166915.

19. Ferreira SM, Lerner SF, Brunzini R, Evelson PA, Llesuy SF. Oxidative stress markers in aqueous humor of glaucoma patients. Am J Ophthalmol. 2004;137(1):62-9.

20. Majsterek I, Malinowska K, Stanczyk M, Kowalski M, Blaszczyk J, Kurowska AK, et al. Evaluation of oxidative stress markers in pathogenesis of primary open-angle glaucoma. Exp Mol Pathol. 2011;90(2):231-7.

21. Pinazo-Durán MD, Zanón-Moreno V, Gallego-Pinazo R, García-Medina JJ. Oxidative stress and mitochondrial failure in the pathogenesis of glaucoma neurodegeneration. Prog Brain Res. 2015;220:127-53.

22. Arnér ES, Holmgren A. Physiological functions of thioredoxin and thioredoxin reductase. Eur J Biochem. 2000;267(20):6102-9.

23. Chidlow G, Wood JP, Casson RJ. Investigations into hypoxia and oxidative stress at the optic nerve head in a rat model of glaucoma. Front Neurosci. 2017;11:478.

24. Tezel G. Oxidative stress in glaucomatous neurodegeneration: mechanisms and consequences. Prog Retin Eye Res. 2006; 25(5): 490-513.

25. Micheal S, Ayub H, Khan MI, Bakker B, Schoenmaker-Koller FE, Ali M, et al. Association of known common genetic variants with primary open angle, primary angle closure, and pseudoexfoliation glaucoma in Pakistani cohorts. Mol Vis. 2014;20:1471-9.

26. Abu-Amero KK, Morales J, Mohamed GH, Osman MN, Bosley TM. Glutathione S-transferase M1 and T1 polymorphisms in Arab glaucoma patients. Mol Vis. 2008;14:425-30.

27. Malinowska K, Kowalski M, Szaflik J, Szaflik JP, Majsterek I. The role of Cat -262C/T, GPX1 Pro198Leu and Sod1+35A/C gene polymorphisms in a development of primary open-angle glaucoma in a Polish population. Pol J Pathol. 2016;67(4):404-10.

28. Bonnemaijer PW, Iglesias AI, Nadkarni GN, Sanyiwa AJ, Hassan HG, Cook C, et al.; GIGA Study Group; Eyes of Africa Genetics Consortium; NEIGHBORHOOD Consortium. Genome-wide association study of primary open-angle glaucoma in continental and admixed African populations. Hum Genet. 2018;137(10):847-62.

29. Khawaja AP, Cooke Bailey JN, Wareham NJ, Scott RA, Simcoe M, Igo RP Jr, et al.; UK Biobank Eye and Vision Consortium; NEIGHBORHOOD Consortium. Genome-wide analyses identify 68 new loci associated with intraocular pressure and improve risk prediction for primary open-angle glaucoma. Nat Genet. 2018;50(6):778-82.

Submitted for publication: March 11, 2020.
Accepted for publication: September 28, 2020.

Approved by the following research ethics committee: Universidade de Pernambuco (CAAE: 91705218.4.0000.5207)

Funding: This study received no specific financial support

Disclosure of potential conflicts of interest: None of the authors have any potential conflicts of interest to disclose


Dimension

© 2022 - All rights reserved - Conselho Brasileiro de Oftalmologia