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Association of HK2 and NCK2 with normal-tension glaucoma in a population from the Republic of Korea.
Jung, Seung-Hyun; Lee, Young Chun; Lee, Mee Yon; Shin, Hye-Young.
Afiliação
  • Jung SH; Cancer Evolution Research Center, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
  • Lee YC; Department of Ophthalmology, Uijeongbu St. Mary's Hospital, College of Medicine, The Catholic University of Korea, 271 Cheonbo-ro, Uijeongbu-si, Gyeonggi-do, 11765, Republic of Korea.
  • Lee MY; Department of Ophthalmology, Uijeongbu St. Mary's Hospital, College of Medicine, The Catholic University of Korea, 271 Cheonbo-ro, Uijeongbu-si, Gyeonggi-do, 11765, Republic of Korea.
  • Shin HY; Department of Ophthalmology, Uijeongbu St. Mary's Hospital, College of Medicine, The Catholic University of Korea, 271 Cheonbo-ro, Uijeongbu-si, Gyeonggi-do, 11765, Republic of Korea. antares78@empal.com.
Graefes Arch Clin Exp Ophthalmol ; 257(12): 2717-2721, 2019 Dec.
Article em En | MEDLINE | ID: mdl-31512042
ABSTRACT

BACKGROUND:

Previous studies have reported the association of HK2 and NCK2 genes with normal-tension glaucoma (NTG) in Japan, but there has been no follow-up study in other countries, so the relevance of these genes to NTG appears uncertain at present. Thus, we investigated the relationship between the HK2 and NCK2 genes and NTG in a Korean NTG cohort.

METHODS:

In total, 154 unrelated Korean patients with NTG and 101 normal Korean controls were recruited. Thus, a total of 255 participants were analyzed for NCK2 (rs2033008) and HK2 (rs678350) gene polymorphisms.

RESULTS:

The minor allele frequency (MAF) of rs678350 was significantly higher in NTG patients (MAF = 0.32) than in controls (MAF = 0.23) (OR, 1.586; 95% CI, 1.058 to 2.375; P = 0.028). This trend was more significant in the dominant model (OR, 1.908; 95% CI, 1.144 to 3.180; P = 0.015). When we performed logistic regression analysis to adjust for age, both the allelic and dominant models were still statistically significant. No significant difference was observed in rs2033008 allele or genotype frequencies between the NTG patients and control subjects.

CONCLUSIONS:

The current study suggested that HK2 gene polymorphism may contribute to the genetic susceptibility to NTG.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: DNA / Proteínas Oncogênicas / Predisposição Genética para Doença / Polimorfismo de Nucleotídeo Único / Proteínas Adaptadoras de Transdução de Sinal / Glaucoma de Baixa Tensão / Hexoquinase / Pressão Intraocular Tipo de estudo: Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged País/Região como assunto: Asia Idioma: En Revista: Graefes Arch Clin Exp Ophthalmol Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: DNA / Proteínas Oncogênicas / Predisposição Genética para Doença / Polimorfismo de Nucleotídeo Único / Proteínas Adaptadoras de Transdução de Sinal / Glaucoma de Baixa Tensão / Hexoquinase / Pressão Intraocular Tipo de estudo: Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged País/Região como assunto: Asia Idioma: En Revista: Graefes Arch Clin Exp Ophthalmol Ano de publicação: 2019 Tipo de documento: Article