ADAM33基因位點(diǎn)多態(tài)性與慢性阻塞性肺疾病的相關(guān)性研究
本文選題:慢性阻塞性肺疾病 + 聚合酶鏈?zhǔn)椒磻?yīng)。 參考:《山西醫(yī)科大學(xué)》2013年碩士論文
【摘要】:目的探討解整合素-金屬蛋白酶33(ADAM33)基因單核苷酸多態(tài)性(SNPs)與山西漢族人群慢性阻塞性肺疾病(COPD)發(fā)病的相關(guān)性。 方法對(duì)100例健康者(對(duì)照組)、103例COPD患者(病例組),利用聚合酶鏈?zhǔn)椒磻?yīng)(PCR)以及DNA測(cè)序的方法,對(duì)ADAM33基因的BC+1和F+1位點(diǎn)多態(tài)性與COPD及肺功能的關(guān)系進(jìn)行統(tǒng)計(jì)學(xué)分析。 結(jié)果ADAM33基因BC+1位點(diǎn)3種基因型AA.AG.GG在對(duì)照組中分布為17.0%、56.0%、27.0%,在病例組中分布為15.5%、45.6%、38.8%,差異無(wú)統(tǒng)計(jì)學(xué)意義(x2=3.296,P0.05),其等位基因A和G的頻率在對(duì)照組分別為45.5%、55.0%,病例組中分別為38.3%、61.7%,差異無(wú)統(tǒng)計(jì)學(xué)意義(x2=1.847,P0.05)。 ADAM33基因F+1位點(diǎn)3種基因型AA、AG、GG在對(duì)照組中分布為7.0%、51.0%、42.0%,在病例組中分布為20.4%、38.8%和40.8%,差異有統(tǒng)計(jì)學(xué)意義(x2=8.287,P0.05),其等位基因A和G的頻率在對(duì)照組分別為32.5%、67.5%,在病例組中分別為39.8%、60.2%,差異無(wú)統(tǒng)計(jì)學(xué)意義(x2=2.345,P0.05)。 ADAM33基因的F+1位點(diǎn)多態(tài)性與肺功能的關(guān)系:該位點(diǎn)3種基因型間FEV1/FVC(%)比較,差異有統(tǒng)計(jì)學(xué)意義(F=2.837,P0.05);但是與FEV1預(yù)計(jì)值(%)比較,差異無(wú)統(tǒng)計(jì)學(xué)意義(F=0.396,P0.05)。 結(jié)論BC+1位點(diǎn)與該人群COPD的發(fā)病關(guān)系不明顯;但是F+1位點(diǎn)對(duì)山西漢族人群COPD發(fā)病有一定的影響;F+1位點(diǎn)的多態(tài)性可能與肺功能有關(guān)指標(biāo)的下降有關(guān)聯(lián)。
[Abstract]:Objective To investigate the association between single nucleotide polymorphism ( SNPs ) of integrin - metal proteinase 33 ( SNPs ) and chronic obstructive pulmonary disease ( COPD ) in Shanxi Han population .
Methods 100 healthy subjects ( control group ) , 103 patients with COPD ( case group ) , polymerase chain reaction ( PCR ) and DNA sequencing were used to analyze the relationship between the polymorphism of BC + 1 and F + 1 sites in patients with COPD and lung function .
Results The three genotypes AA , AG and GG in the BC + 1 locus were 17.0 % , 56.0 % and 27.0 % in the control group , 15.5 % , 45.6 % and 38.8 % in the case group respectively . The frequencies of the alleles A and G were 45.3 % and 61.7 % in the control group , respectively , and the difference was not statistically significant ( x2 = 1.847 , P0.05 ) .
The frequencies of the alleles A and G of the three genotypes AA , AG and GG were 7.0 % , 51.0 % and 42.0 % in the control group . The frequencies of the alleles A and G were 32.5 % , 67.2 % in the control group and 39.8 % and 60.2 % respectively in the case group ( x2 = 2.345 , P0.05 ) .
The relationship between the polymorphism of the F + 1 locus and the lung function was found between the three genotypes : FEV1 / FVC ( % ) in the three genotypes ( F = 2.837 , P0.05 ) .
However , the difference was not statistically significant compared to predicted FEV1 ( % ) ( F = 0.396 , P0.05 ) .
Conclusion The BC + 1 locus is not related to the pathogenesis of COPD .
However , the F + 1 locus had some effects on COPD in the Han population in Shanxi Province .
The F + 1 site polymorphism may be associated with a decrease in lung function - related indicators .
【學(xué)位授予單位】:山西醫(yī)科大學(xué)
【學(xué)位級(jí)別】:碩士
【學(xué)位授予年份】:2013
【分類號(hào)】:R563.9
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