Lack of association between the 389C>T polymorphism (rs769217) in the catalase (CAT) gene and the risk of vitiligo: An update by meta-analysis

Australasian Journal of Dermatology

Volumn 56, Issue 3, 2015, Pages 180-185

  He, Jie ^a   Li, Xiaoyan ^a   Li, Yunhui ^a   Ren, Bocheng ^a   Sun, Jian ^a   Zhang, Wei ^a   Li, Wancheng ^a  

^a CHENGDU MEDICAL COLLEGE   (China)

Author keywords

catalase; meta analysis; polymorphism; risk; vitiligo

Indexed keywords

CATALASE;

ALLELE; ARTICLE; ASIAN; CASE CONTROL STUDY; CAT GENE; CAUCASIAN; CODON; DISEASE ASSOCIATION; DISEASE SURVEILLANCE; ETHNIC DIFFERENCE; GENE INTERACTION; GENETIC ASSOCIATION; GENETIC POLYMORPHISM; GENETIC SUSCEPTIBILITY; GENOTYPE; HUMAN; RISK FACTOR; SYSTEMATIC REVIEW; VITILIGO; GENETICS; META ANALYSIS; SINGLE NUCLEOTIDE POLYMORPHISM;

CASE-CONTROL STUDIES; CATALASE; HUMANS; POLYMORPHISM, SINGLE NUCLEOTIDE; VITILIGO;

EID: 84937442174     PISSN: 00048380     EISSN: 14400960     Source Type: Journal    
DOI: 10.1111/ajd.12204     Document Type: Article

References (17)

1. Colucci R, Lotti T, Moretti S,. Vitiligo: an update on current pharmacotherapy and future directions. Expert Opin. Pharmacother. 2012; 13: 1885-1899.
2. Sravani PV, Babu NK, Gopal KV, et al. Determination of oxidative stress in vitiligo by measuring superoxide dismutase and catalase levels in vitiliginous and non-vitiliginous skin. Indian J. Dermatol. Venereol. Leprol. 2009; 75: 268-271.
3. Liu L, Li C, Gao J, et al. Promoter variant in the catalase gene is associated with vitiligo in Chinese people. J. Invest. Dermatol. 2010; 130: 2647-2653.
4. Malhotra N, Dytoc M,. The pathogenesis of vitiligo. J. Cutan. Med. Surg. 2013; 17: 153-172.
5. Yesilova Y, Turan E, Ucmak D, et al. Reduced serum paraoxonase-1 levels in vitiligo: further evidence of oxidative stress. Redox Rep. 2012; 17: 214-218.
6. Yildirim M, Baysal V, Inaloz HS, et al. The role of oxidants and antioxidants in generalized vitiligo at tissue level. J. Eur. Acad. Dermatol. Venereol. 2004; 18: 683-686.
7. Schallreuter KU, Salem MA, Gibbons NC, et al. Blunted epidermal L-tryptophan metabolism in vitiligo affects immune response and ROS scavenging by Fenton chemistry, part 1: epidermal H2O2/ONOO(-)-mediated stress abrogates tryptophan hydroxylase and dopa decarboxylase activities, leading to low serotonin and melatonin levels. FASEB J. 2012; 26: 2457-2470.
8. Bulut H, Pehlivan M, Alper S, et al. Lack of association between catalase gene polymorphism (T/C exon 9) and susceptibility to vitiligo in a Turkish population. Genet. Mol. Res. 2011; 10: 4126-4132.
9. Goth L, Rass P, Pay A,. Catalase enzyme mutations and their association with diseases. Mol. Diagn. 2004; 8: 141-149.
10. Akbas H, Dertlioglu SB, Dilmec F, et al. No association between catalase (CAT) gene polymorphisms and susceptibility to vitiligo in a Turkish population. Clin. Ter. 2013; 164: e173-177.
11. Casp CB, She JX, McCormack WT,. Genetic association of the catalase gene (CAT) with vitiligo susceptibility. Pigment Cell Res. 2002; 15: 62-66.
12. Em S, Laddha NC, Chatterjee S, et al. Association of catalase T/C exon 9 and glutathione peroxidase codon 200 polymorphisms in relation to their activities and oxidative stress with vitiligo susceptibility in Gujarat population. Pigment Cell Res. 2007; 20: 405-407.
13. Lv YJ, Liao WJ, Luan Q, et al. The polymorphism of catalase T/C codon 389 in exon 9 and vitiligo susceptibility: a meta-analysis. J. Eur. Acad. Dermatol. Venereol. 2011; 25: 955-958.
14. Park HH, Ha E, Uhm YK, et al. Association study between catalase gene polymorphisms and the susceptibility to vitiligo in Korean population. Exp. Dermatol. 2006; 15: 377-380.
15. Gavalas NG, Akhtar S, Gawkrodger DJ, et al. Analysis of allelic variants in the catalase gene in patients with the skin depigmenting disorder vitiligo. Biochem. Biophys. Res. Commun. 2006; 345: 1586-1591.
16. Birlea SA, Jin Y, Bennett DC, et al. Comprehensive association analysis of candidate genes for generalized vitiligo supports XBP1, FOXP3, and TSLP. J. Invest. Dermatol. 2011; 131: 371-381.
17. Jin Y, Birlea SA, Fain PR, et al. Genome-wide association analyses identify 13 new susceptibility loci for generalized vitiligo. Nat. Genet. 2012; 44: 676-680.