CRLR基因单核苷酸多态性与原发性前房角关闭人群的关联研究
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江苏省卫生厅科技项目(No.H201424)


Association of the single nucleotide polymorphisms in the calcitonin receptor-like receptor gene with primary angle closure in a Han Chinese population
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Science and Technology Project of Department of Public Health in Jiangsu(No.H201424)

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    摘要:

    目的:探讨降钙素受体样受体(calcitonin receptor-like receptor,CRLR)基因单核苷酸多态性(single nucleotide polymorpnism,SNP)与汉族原发性前房角关闭人群的关联性。

    方法:以流行病学人群为研究对象,采用病例对照设计。收集江苏省阜宁县流行病学调查中筛查出的原发性前房角关闭(primary angle closure,PAC)患者232例,正常对照306例。血样经DNA提取后采用TaqMan-MGB荧光探针法检测CRLR基因的rs1157699(C/T)位点SNP基因型,比较两组等位基因及基因型频率的分布。

    结果:病例组的基因型分布(CC 67.4%,CT 30.0%,TT 2.6%),对照组的基因型分布(CC 71.3%,CT 27.0%,TT 1.7%),两组之间差异无统计学意义(P>0.05)。

    结论:中国汉族人群的CRLR rs1157699位点SNP与原发性前房角关闭无相关性。

    Abstract:

    AIM: To study the association of the single nucleotide polymorphism(SNP)rs1157699 in the calcitonin receptor-like receptor(CRLR)gene with primary angle closure(PAC)in a Han Chinese population.

    METHODS: All samples, involved 232 PAC cases and 306 controls, were obtained from an epidemiologic survey conducted in Funing, Jiangsu Province, China. Genotyping were carried out by TaqMan-MGB probe using the real time quantitative polymerase chain reaction system to study the relationship between SNP of rs1157699 in CRLR gene and PAC.

    RESULTS: The prevalence of CRLRrs1157699 genotype was 67.4%, 30.0%, 2.6% for CC, CT, TT in cases, and 71.3%, 27.0%, 1.7% in controls respectively. There was no difference between the two groups in the distribution of genotype and allele frequencies of rs1157699(P>0.05).

    CONCLUSION: Our results do not support a significant role for rs1157699 in CRLR with PAC.

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秦柏,石海红,朱蓉嵘,等. CRLR基因单核苷酸多态性与原发性前房角关闭人群的关联研究.国际眼科杂志, 2016,16(8):1570-1572.

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  • 收稿日期:2016-04-25
  • 最后修改日期:2016-07-04
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  • 在线发布日期: 2016-07-26
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