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Study on the Relationship Between Respiratory Distress Syndrome and SP-A1 (rs1059057) Gene Polymorphism in Mongolian Very Premature Infants

机译:蒙古族地生早产儿呼吸窘迫综合征和SP-A1(RS1059057)基因多态性关系的研究

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Aim: To study the relationship between rs1059057 polymorphism of pulmonary surfactant protein A1 (SP-A1) and respiratory distress syndrome (RDS) in Mongolian very premature infants. Methods: Applying the strategy of case-control study, 120 Mongolian RDS very premature infants (58 males and 62 females) in the western part of Inner Mongolia were selected as the case group, and 120 subjects of non-RDS very premature infants (56 males and 64 females) with the same nationality, same sex and similar gestational age were used as the control group. The single nucleotide polymorphism (SNP) site rs1059057 of SP-A1 was genotyped using polymerase chain reaction-single strand conformational polymorphism (PCR-SSCP). Results: Two genotypes, A/G and A/A , were detected at the SP-A1 rs1059057 locus in the western part of Inner Mongolia. In the case group, the frequencies of two genotypes were 53 and 47%, and the frequencies of A allele and G allele were 73 and 27%, respectively. In the control group, the frequencies of the two genotypes were 42 and 58%, and the frequencies of A allele and G allele were 79 and 21%, respectively. There was no significant difference in the genotype frequency of SP-A1 (rs1059057) locus between the case group and the control group ( X 2 = 3.275, P 0.05), and no significant difference in allele frequency between the case group and the control group ( X 2 = 2.255, P 0.05). Conclusion: The genotypes and allele frequencies of SP-A1 (rs1059057) locus were not associated with the incidence of RDS in Mongolian very premature infants in western Inner Mongolia.
机译:目的:研究蒙古族地下婴幼儿肺表面活性剂蛋白A1(SP-A1)和呼吸窘迫综合征(RDS)rs1059057多态性的关系。方法:将案例控制研究策略应用于内蒙古西部的120件蒙古RDS非常过早的婴儿(58名男性和62名女性)作为案例组,120名非RDS非常早产儿科(56个使用相同的国籍,相同的性别和类似的孕龄的男性和64名女性被用作对照组。使用聚合酶链反应 - 单链构象多态性(PCR-SSCP),SP-A1的单核苷酸多态性(SNP)位点RS1059057基因分型。结果:在内蒙古西部的SP-A1 RS1059057轨迹处检测到两种基因型,A / G和A / A.在病例组中,两个基因型的频率为53和47%,等位基因和G等位基因的频率分别为73%和27%。在对照组中,两个基因型的频率为42和58%,等位基因和G等位基因的频率分别为79%和21%。 SP-A1(RS1059057)基因座在壳体组和对照组之间的基因型频率没有显着差异(x 2 = 3.275,p& 0.05),并且案例组之间的等位基因频率没有显着差异对照组(x 2 = 2.255,p& 0.05)。结论:SP-A1(RS1059057)基因型和等位基因频率与西蒙古西部蒙古族地下婴幼儿的RDS发生率无关。

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