Relationship of glutathione S-transferase M1 and T1 polymorphisms with the susceptibility of primary angle-closure glaucoma of Chinese Han population in Chongqing
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Relationship of glutathione S-transferase M1 and T1 polymorphisms with the susceptibility of primary angle-closure glaucoma of Chinese Han population in Chongqing
Journal of Army Medical UniversityVol. 35, Issue 13, Pages: 1410-1414(2013)
Chen Jin,Hou Shengping,Gao Xiaojin,Hu Bo,Li Pinghua.Relationship of glutathione S-transferase M1 and T1 polymorphisms with the susceptibility of primary angle-closure glaucoma of Chinese Han population in Chongqing[J].J Amry Med Univ (J Third Mil Med Univ),2013,35(13):1410-1414.
Chen Jin,Hou Shengping,Gao Xiaojin,Hu Bo,Li Pinghua.Relationship of glutathione S-transferase M1 and T1 polymorphisms with the susceptibility of primary angle-closure glaucoma of Chinese Han population in Chongqing[J].J Amry Med Univ (J Third Mil Med Univ),2013,35(13):1410-1414.DOI:
Relationship of glutathione S-transferase M1 and T1 polymorphisms with the susceptibility of primary angle-closure glaucoma of Chinese Han population in Chongqing
Objective To investigate the relationship of genetic polymorphisms of glutathione S-transferase M1 (GSTM1)
and glutathione S-transferase T1 (GSTT1) with the susceptibility of primary angle-closure glaucoma in Chinese Han population. Methods Blood samples were collected from 211 Han patients with primary angle-closure glaucoma (PACG) and 422 health volunteers (control)
and the 211 PACG patients were separated into an acute PACG (APACG) group and a chronic PACG (CPACG) group according to diagnostic criteria. Furthermore
multiple allele-specific polymerase chain reaction (multiplex PCR) was employed to detect the genetic polymorphisms of GSTT1 and GSTM1. Results The distribution frequencies of GSTT1-null genotype were 53.1% and 53.8% in the PACG group and control group
respectively
but no significant difference was found (Chi square=0.028 6
P
=0.866). Furthermore
the distribution frequencies of GSTT1-null genotype in the APACG group and CPACG group were 46.3% and 55.4%
respectively
which were not significantly different from that of the control group (
Chi
square=0.126 7
P
=0.722;
Chi
square=0.036 2
P
=0.849). The distribution frequencies of GSTM1-null genotype were 58.3% and 56.3% in the PACG group and control group
respectively
but no significant difference was found (
Chi
square=0.206 3
P
=0.650). The distribution frequencies of GSTM1 were 61.1% and 56.3% in the APACG group and CPACG group
respectively
but no significant difference was found as compared with the control group (
Chi
square=0.027 9
P
=0.867;
Chi
square=0.006 4
P
=0.936). Moreover
the combined analysis of GSTT1 and GSTM1 genotypes showed that no significant difference was found in comparison of the four genotypes of GSTT1 and GSTM1 between the PACG (APACG and CPACG) group and control group. Conclusi
on In Han population with PACG in Chongqing area of China
no relationship is found between the null genotypes of GSTT1 and GSTM1 and PACG susceptibility
and the correlation of genetic polymorphisms of GSTT1 and GSTM1 with the susceptibility and classification of PACG is not found.
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