肌球蛋白重链9基因单核苷酸多态性与炎症性肠病的关联
Association of the myosin heavy chain 9 gene single nucleotide polymorphism with inflammatory bowel disease.
作者信息
Abd Al-Aliem Ahmed Ezz El-Arab, Badr Eman A E, El-Shayeb Elsayed Ibrahem, Taman Ahmed Megahed Ahmed, Gadallah Abd El-Naser Abd El-Atty
机构信息
Department of Internal Medicine, Faculty of Medicine, Menoufia University, Egypt.
Department of Medical Biochemistry and Molecular Biology, Faculty of Medicine, Menoufia University, Egypt.
出版信息
Biochem Biophys Rep. 2021 Sep 21;28:101113. doi: 10.1016/j.bbrep.2021.101113. eCollection 2021 Dec.
BACKGROUND
To date, the cause of inflammatory bowel disease (IBD) remains a mystery. A balance between cell proliferation and apoptosis maintains intestinal tissue homeostasis. Dissociation-induced myosin-actin contraction results in stem cell apoptosis. This study aiming to evaluate the influence of the myosin heavy chain 9 () gene single nucleotide polymorphisms (SNPs) on inflammatory bowel disease.
SUBJECTS
: The study carried on eighty patients with IBD and seventy controls. All participants subjected to history taking, thorough physical examination, colonoscopy and laboratory investigations. Genotyping performed for rs4821480 and rs3752462 by SNP assay real-time PCR methods.
RESULTS
On analyzing rs3752462 CT and TT genotypes were significantly more frequent in IBD patients as compared to controls with 4.6 fold increase in the risk of IBD. While on analyzing rs4821480, The TG and GG genotypes have significant increased distribution among the IBD patients as compared to the controls with 5.3 fold increase in the risk of IBD and higher prevalence of GG genotype in patients with low hemoglobin level and higher BMI.
CONCLUSION
The rs3752462 T allele and rs4821480 G allele of are associated with more susceptibility to IBD.
背景
迄今为止,炎症性肠病(IBD)的病因仍是个谜。细胞增殖与凋亡之间的平衡维持着肠道组织的稳态。解离诱导的肌动球蛋白收缩导致干细胞凋亡。本研究旨在评估肌球蛋白重链9()基因单核苷酸多态性(SNP)对炎症性肠病的影响。
研究对象
该研究纳入了80例IBD患者和70例对照。所有参与者均接受病史采集、全面体格检查、结肠镜检查和实验室检查。通过SNP分析实时PCR方法对rs4821480和rs3752462进行基因分型。
结果
分析rs3752462时,IBD患者中CT和TT基因型的频率显著高于对照组,IBD风险增加4.6倍。分析rs4821480时,与对照组相比,IBD患者中TG和GG基因型的分布显著增加,IBD风险增加5.3倍,且GG基因型在血红蛋白水平低和BMI较高的患者中患病率更高。
结论
的rs3752462 T等位基因和rs4821480 G等位基因与IBD易感性增加有关。
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