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Primary Angle Closure Glaucoma-associated Genetic Polymorphisms in Northeast Iran.
Yousefian, Ali; Shokoohi-Rad, Saeed; Abbaszadegan, Mohammad Reza; Rad, Dorsa Morshedi; Zargari, Selma; Milanizadeh, Saman; Morovatdar, Negar; Daneshvar, Ramin.
Afiliação
  • Yousefian A; Eye Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.
  • Shokoohi-Rad S; Eye Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.
  • Abbaszadegan MR; Medical Genetics Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.
  • Rad DM; Immunology Research Center, Avicenna Research Institute, Mashhad University of Medical Sciences, Mashhad, Iran.
  • Zargari S; Medical Genetics Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.
  • Milanizadeh S; Medical Genetics Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.
  • Morovatdar N; Clinical Research Unit, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
  • Daneshvar R; Eye Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.
J Ophthalmic Vis Res ; 15(1): 45-52, 2020.
Article em En | MEDLINE | ID: mdl-32095208
PURPOSE: To evaluate the association of five different polymorphisms from a genome-wide-associated study with susceptibility to glaucoma in the northeast Iranian population. METHODS: Hundred and thirty patients with primary angle closure glaucoma (PACG) and 130 healthy controls were genotyped for the polymorphic regions with the aid of tetra-amplification refractory mutation system-polymerase chain reaction. The association of these variants with the disease susceptibility was measured statistically with the logistic regression method. RESULTS: Hundred and thirty patients with PACG (53 males, 77 females) with a mean age of 64.5 ± 6.2 years and 130 healthy control subjects (51 males, 79 females) with a mean age of 64.0 ± 5.7 years were selected for evaluation. There was a significant association between rs3816415 (P = 0.005), rs736893 (P < 0.001), rs7494379 (P < 0.001), and rs1258267 (P = 0.02) with PACG susceptibility. This association could not be shown for rs3739821. CONCLUSION: It was revealed that studied variants in GLIS3, EPDR1, FERMT2, and CHAT genes can contribute to the incidence of PACG. Additional studies in other populations are needed to evaluate DPM2-FAM102A.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Ano de publicação: 2020 Tipo de documento: Article