特发性矮小患儿胰岛素样生长因子受体基因单核苷酸多态性研究

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摘要目的：探讨胰岛素样生长因子-I受体（IGF-IR）基因单核苷酸多态性（SNP）与特发性矮小（ISS）的发病危险的相关性。方法：2008~2011年确诊为ISS患儿804例，正常对照组575例，用Snapshot法检测两组 IGF-IR基因相关位点SNP。结果：两组rs1976667基因型分布频率差异无统计学意义（P>0.05）；rs1976667 A等位基因分布频率较正常对照组高，差异有统计学意义（P<0.01)。结论：IGF-IR基因rs1976667位点等位基因A是ISS发病的危险因素。

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	黄慧
	杨玉
	王伟
	杨利
	谢理玲
	王莹
	卫海燕

Abstract：OBJECTIVE: To study the association between single nucleotide polymorphism (SNP) of insulin-like growth factor I receptor (IGF-IR) gene and idiopathic short stature (ISS). METHODS: A total of 804 children with ISS and 575 normal controls were recruited from 2008 to 2011. IGF-IR gene SNP was genotyped using the Snapshot Multiplex System. RESULTS: The distribution frequency of genotype rs1976667 showed no significant difference between the ISS and the control groups, while that of the allele A of rs1976667 was significantly higher in the ISS group than in the control group (P<0.01). CONCLUSIONS: The allele A at rs1976667 SNP of IGF-IR gene is a risk factor for ISS.

Key words： Idiopathic short stature Insulin-like growth factor receptor Single nucleotide polymorphism Child

PACS:

R725.8

引用本文:

黄慧,杨玉,王伟等. 特发性矮小患儿胰岛素样生长因子受体基因单核苷酸多态性研究[J]. 中国当代儿科杂志, 2011, 13(12): 955-958.

HUANG Hui,YANG Yu,WANG Wei et al. Association between single nucleotide polymorphism of insulin-like growth factor receptor gene and idiopathic short stature[J]. CJCP, 2011, 13(12): 955-958.

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http://www.zgddek.com/CN/ 或 http://www.zgddek.com/CN/Y2011/V13/I12/955

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