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中国人群渗出性年龄相关性黄斑变性中LOC387715和HTRA1基因的单核苷酸多态性及单倍型连锁分析

Analyses of single nucleotide polymorphisms and haplotype linkage of LOC387715 and the HTRA1 gene in exudative age-related macular degeneration in a Chinese cohort.

作者信息

Jiang Hua, Qu Yi, Dang Guangfu, Zhang Xiao, Yin Ningning, Zhang Ying, Bi Hongsheng, Pan Xuemei, Xu Xiaoyi, Zhou Fang, Dai Hong

机构信息

Department of Ophthalmology, Qilu Hospital of Shandong University, Jinan, China.

出版信息

Retina. 2009 Jul-Aug;29(7):974-9. doi: 10.1097/IAE.0b013e3181a3b90e.

Abstract

PURPOSE

To investigate the effect of single nucleotide polymorphisms (SNPs) and haplotypes in the genes encoding age-related maculopathy susceptibility 2 (LOC387715/ARMS2) and high-temperature requirement A-1 (HTRA1) in a case-control study in a Chinese cohort of individuals with exudative age-related macular degeneration (AMD).

METHODS

We genotyped 2 SNPs, namely, LOC387715 rs10490924 and HTRA1 rs11200638, in 159 exudative AMD patients and 140 age- and sex-matched control subjects. All the four possible haplotypes of these two SNPs were detected. Comparisons of the risk genotypes and risk or protective haplotypes across multiple populations were performed.

RESULTS

Allelic or genotype association tests yielded significant results at P < 0.001. We observed that homozygous risk genotypes (TT in rs10490924 and AA in rs11200638) were more strongly associated with AMD than the heterozygous genotypes (GT in rs10490924 and geographic atrophy in rs11200638) for both SNPs. Comparisons of the odds ratios for genotypes revealed that there is ethnic disparity in AMD prevalence, even within the Chinese population. The haplotype TA, comprising both the SNPs, was identified as an at-risk factor and was significantly associated with AMD, whereas the protective haplotype GG was significantly overrepresented in the controls (P < 0.001). The frequency of the TA haplotype was relatively higher in the Chinese population than in the white population in both groups, whereas the frequency of the GG haplotype was relatively lower in the Chinese controls than in the white and Japanese controls.

CONCLUSION

Both SNPs are significantly associated with exudative AMD in the Chinese cohort and seem to contribute equally to the disease status. A higher frequency of homozygous risk genotypes and risk haplotype and a lower frequency of protective haplotype in the Chinese may be the cause of higher prevalence of exudative AMD in the Chinese than in the whites.

摘要

目的

在一项针对中国渗出性年龄相关性黄斑变性(AMD)患者队列的病例对照研究中,调查编码年龄相关性黄斑病变易感性2(LOC387715/ARMS2)和高温需求蛋白A-1(HTRA1)的基因中的单核苷酸多态性(SNP)和单倍型的作用。

方法

我们对159例渗出性AMD患者和140例年龄及性别匹配的对照受试者进行了两个SNP的基因分型,即LOC387715 rs10490924和HTRA1 rs11200638。检测了这两个SNP的所有四种可能单倍型。对多个群体中的风险基因型以及风险或保护性单倍型进行了比较。

结果

等位基因或基因型关联测试在P < 0.001时得出显著结果。我们观察到,对于这两个SNP,纯合风险基因型(rs10490924中的TT和rs11200638中的AA)与AMD的关联比杂合基因型(rs10490924中的GT和rs11200638中的GA)更强。基因型优势比的比较表明,即使在中国人群中,AMD患病率也存在种族差异。包含这两个SNP的单倍型TA被确定为一个风险因素,并且与AMD显著相关,而保护性单倍型GG在对照组中显著过量存在(P < 0.001)。在两组中,中国人群中TA单倍型的频率相对高于白种人群,而中国对照组中GG单倍型的频率相对低于白种人和日本对照组。

结论

在中国队列中,这两个SNP均与渗出性AMD显著相关,并且似乎对疾病状态的贡献相同。中国人中纯合风险基因型和风险单倍型的频率较高,而保护性单倍型的频率较低,这可能是中国渗出性AMD患病率高于白种人的原因。

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