Investigative ophthalmology & visual science · 2008
High myopia is not associated with the SNPs in the TGIF, lumican, TGFB1, and HGF genes.
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Wang Panfeng, Li Shiqiang, Xiao Xueshan, Jia Xiaoyun, Jiao Xiaodong, Guo Xiangming, Zhang Qingjiong
Аннотация
PURPOSE: Four single-nucleotide polymorphisms (SNPs) in the TGIF, lumican, TGFB1, and HGF genes have been declared to be associated with high myopia in Chinese living in southeast China, but none of them has been confirmed by additional studies. This study was conducted to verify the reported positive association results by analysis of subjects from the same region.
METHODS: DNA was prepared from venous leukocytes of 288 patients with high myopia and 208 control subjects. The four SNPs (rs2229336, rs3759223, rs1982073, and rs3735520) in the four genes were genotyped by restriction fragment length polymorphism (RFLP) analysis. The allele and genotype frequencies of these SNPs from patients and control subjects were compared by chi(2) test.
RESULTS: Polymorphism at rs2229336 was not detected in all 496 subjects. There were no statistically significant differences between patients and control subjects for the other three SNPs: rs3759223, rs1982073, and rs3735520.
CONCLUSIONS: The study does not support the association of high myopia with alleles of rs2229336 in TGIF, rs3759223 in lumican, rs1982073 in TGFB1, and rs3735520 in HGF. These results provide a view contrary to those in previous reports. Reasonable criteria as well as replication should be the first priority for genetic association studies to avoid excessive expansion of false-positive results, especially for high myopia.
METHODS: DNA was prepared from venous leukocytes of 288 patients with high myopia and 208 control subjects. The four SNPs (rs2229336, rs3759223, rs1982073, and rs3735520) in the four genes were genotyped by restriction fragment length polymorphism (RFLP) analysis. The allele and genotype frequencies of these SNPs from patients and control subjects were compared by chi(2) test.
RESULTS: Polymorphism at rs2229336 was not detected in all 496 subjects. There were no statistically significant differences between patients and control subjects for the other three SNPs: rs3759223, rs1982073, and rs3735520.
CONCLUSIONS: The study does not support the association of high myopia with alleles of rs2229336 in TGIF, rs3759223 in lumican, rs1982073 in TGFB1, and rs3735520 in HGF. These results provide a view contrary to those in previous reports. Reasonable criteria as well as replication should be the first priority for genetic association studies to avoid excessive expansion of false-positive results, especially for high myopia.
Предметные рубрики MeSH
AdultAllelesAsian PeopleChinaChondroitin Sulfate ProteoglycansDNA PrimersExtracellular Matrix ProteinsGene FrequencyGenotypeHepatocyte Growth FactorHomeodomain ProteinsHumansKeratan SulfateLumicanMyopia, DegenerativePolymorphism, Restriction Fragment LengthPolymorphism, Single NucleotideRepressor ProteinsTransforming Growth Factor betabetaIG-H3 Protein