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作 者:袁文浩[1] 常立文[1] 李文斌[1] 刘伟[1] 赵玲霞[1] 徐洪涛[1] 潘睿[1]
机构地区:[1]华中科技大学同济医学院附属同济医院儿科,武汉430030
出 处:《中国实用儿科杂志》2012年第9期682-685,共4页Chinese Journal of Practical Pediatrics
基 金:国家自然科学基金资助项目(No.30872795;No.81170001);湖北省自然科学基金资助项目(No.2008CDB139);新教师基金资助项目(高等学校博士点专项科研基金;No.200804871058)
摘 要:目的探讨血管内皮生长因子(VEGF)基因多态性与支气管肺发育不良(BPD)相关性。方法选自2009-07-01—2012-02-01华中科技大学同济医学院附属同济医院收治的符合BPD诊断标准的患儿64例(BPD组)和同期住院的无肺部疾病患儿106例(对照组)。利用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法分析两组VEGF+405、-2578基因频率分布,酶联免疫吸附试验(ELISA)分析BPD组血浆VEGF浓度。结果 (1)VEGF+405G>C:BPD组中G的基因型频率和等位基因频率均高于对照组,差异有统计学意义(P<0.05);VEGF-2578C>A:BPD组中A的基因型频率和等位基因频率均高于对照组,差异有统计学意义(P<0.05)。(2)BPD组VEGF+405GG/GC血浆表达低于VEGF+405CC(P<0.05),VEGF-2578CC/CA血浆表达与VEGF-2578AA差异无统计学意义(P>0.05)。结论 VEGF+405、-2578基因多态性和BPD相关,推测其和BPD遗传易感性相关。VEGF+405多态性与VEGF血浆表达相关,血浆中VEGF减低可能是BPD发病机因素之一。Objective To investigate the association between single nueleotide polymorphism of vascular endothelial growth faetor(VEGF)and bronchopulmonary dysplasia(BPD). Methods A total of 64 BPD patients in BPD group and 106 patients without lung disease in control group from July 1,2009 to February 1,2012 were included in the study.Gen- otype of VEGF polymorphisms were performed by polymerase chain reaction and restriction fragment length po]ymorphism analysis (PCR-RFLP). Enzyme-linked immunosorbent assay (ELISA)was used to detect the expression level of VEGF in plasma in BPD group. Results ( 1 ) VEGF +405G 〉 C: compared with control group, the genotype and allele frequencies of G was higher in BPD group with statistical difference (P 〈 0.05). VEGF-2578C〉A: compared with con- trol group, the genotype and allele frequencies of A was higher in BPD group with statistical difference (P 〈 0.05 ). (2) In BPD group the level of VEGF+405 was lower in the patients with genotype GG(P 〈 0.05)compared with CC while there was no difference for VEGF-2578 with genotype CC and GG (P 〉 0.05).Conclusion Single nucleotide polymorphisms of VEGF+405 and VEGF-2578 could be associated with BPD, and VEGF+405 influences its protein expression, and the lower VEGF level in plasma could he one of the factors for BPD pathogenesis.
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