Chinese Journal of Tissue Engineering Research ›› 2019, Vol. 23 ›› Issue (19): 2980-2985.doi: 10.3969/j.issn.2095-4344.1243
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Liu Yang, Yang Qinghua, Guan Yewen, Wang Jiaqi, Jiang Hua
Received:
2019-02-19
Online:
2019-07-08
Published:
2019-07-08
Contact:
Jiang Hua, MD, Associate chief physician, Master’s supervisor, Department of Spinal Surgery, the First Affiliated Hospital of Guangxi Medical University, Nanning 530021, Guangxi Zhuang Autonomous Region, China
About author:
Liu Yang, Master candidate, Department of Spinal Surgery, the First Affiliated Hospital of Guangxi Medical University, Nanning 530021, Guangxi Zhuang Autonomous Region, China
Supported by:
the National Natural Science Foundation of China, No. 81460353 and 81860406 (both to JH); the Natural Science Foundation of Guangxi Zhuang Autonomous Region, No. 2015GXNSFBA139167 (to JH)
CLC Number:
Liu Yang, Yang Qinghua, Guan Yewen, Wang Jiaqi, Jiang Hua. Association between single nucleotide polymorphism (8q24.21) and lumbar degeneration disease in 800 cases from Guangxi Zhuang Autonomous Region [J]. Chinese Journal of Tissue Engineering Research, 2019, 23(19): 2980-2985.
2.2 8q24.21区域rs7816342、rs4130415位点的检测结果 ABI7500型实时荧光定量PCR系统测得的SNP结果显示,rs7816342位点的基因型有3种,分别是AA、AG、GG;rs4130415位点的基因型有3种,分别是TT、TC、CC。 2.3 Hardy-Weinberg平衡定律检测 经χ2检验,病例组和对照组的研究对象在该群体均存在Hardy-Weinberg平衡(P > 0.05)。 2.4 8q24.21区域rs7816342、rs4130415位点与腰椎退行性疾病的相关性关系 2.4.1 rs7816342位点在病例组及对照组中的各等位基因、基因型频率 见表4,A和G等位基因频率在病例组分别为75.0%和25.0%,在对照组分别占75.0%和25.0%,2组间等位基因频率分布差异无显著性意义(χ2=0.00,P=0.999,OR=1.000,95%CI:0.787-1.271),2组间的基因型频率分布差异无显著性意义(χ2=1.986,P=0.370)。 在亚组分析中,腰椎间盘突出组(亚组1)的A和G等位基因频率在腰椎退行性疾病中分别为75.7%、24.3%,在对照组中分别占75.0%、25.0%,2组间等位基因频率分布差异无显著性意义(χ2=0.085,P=0.771,OR=0.961,95%CI=0.737-1.254),2组间的基因型频率分布差异无显著性意义(χ2=0.426,P=0.808)。 腰椎滑脱组(亚组2)组的A和G等位基因频率在腰椎退行性疾病中分别为80.2%、19.8%,在对照组中分别占75.0%、25.0%,2组间等位基因频率分布差异无显著性意义(χ2=1.145,P=0.285,OR=0.739,95%CI=0.424- 1.288),2组间的基因型频率分布差异无显著性意义(χ2= 1.182,P=0.554)。"
腰椎管狭窄组(亚组3)和对照组的A和G等位基因频率在腰椎退行性疾病中分别为:47.6%、52.4%,在对照组中分别占75.0%、25.0%,2组间等位基因分布差异无显著性意义(χ2=2.702,P=0.100,OR=1.438,95%CI= 0.931-2.222),2 组间的基因型频率分布差异有显著性意义(χ2=9.515,P=0.008)。 2.4.2 rs4130415位点在病例组及对照组中的各等位基因、基因型频率 见表5,T和C等位基因频率在病例组中分别为78.6%、21.4%,在对照组中分别占77.6%、22.3%,2组间等位基因频率分布差异无显著性意义(χ2=0.235,P=0.628,OR=0.941,95%CI=0.782-1.207),2组间的基因型频率分布差异无显著性意义(χ2=0.807,P=0.668)。"
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