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Association of single nucleotide polymorphisms in micro RNA RNA s with susceptibility to hepatitis B virus infection and HBV HBV ‐related liver complications: A study in a Saudi Arabian population

机译:微核苷酸多态性与乙型肝炎病毒感染易感性的单核苷酸多态性与HBV HBV -Reled肝脏并发症中的敏感性:沙特阿拉伯人口的研究

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摘要

Summary The aim of this study was to evaluate the association of 10 SNP s in different micro RNA s (mi RNA s) with susceptibility to hepatitis B virus ( HBV ) infection, HBV clearance, persistence of chronic HBV infection, and progression to liver cirrhosis and hepatocellular carcinoma ( HCC ). Patients were categorized into the following groups: inactive HBV carrier, active HBV carrier, HBV ‐cleared subject and cirrhosis+ HCC . Samples were analysed for 10 SNP s in micro RNA s using either PCR ‐based genotyping or the TaqMan assay. We found that rs1358379 was associated with susceptibility to HBV infection, HBV clearance, persistent chronic HBV infection and liver cirrhosis+ HCC . In addition, we found that rs2292832 and rs11614913 were associated with risk of HBV infection, viral clearance and cirrhosis+ HCC , whereas rs2910164 was associated with proneness to HBV infection, and ability to clear the virus. There was evidence of associations between rs6505162 and HBV clearance and the development of liver disease, whereas a single association was found between rs2289030 and HBV clearance. Similarly, rs7372209 and rs4919510 were specifically associated with the development of HBV ‐induced liver complications. SNP s in mi RNA s affect the susceptibility, clearance and progression of HBV infection in Saudi Arabian patients. We found, using Gene Ontology or pathway analyses, that these genes may contribute to the pathophysiology of HBV infection and related liver complications. However, differences in the association of examined SNP s with various clinical stages indicate variations in the respective functional roles of these polymorphisms and their mi RNA s, and thus, further investigation to fully explore their therapeutic potential is warranted.
机译:发明内容本研究的目的是评估10个SNP S在不同的微RNA S(MI RNA S)的关联,易感性对乙型肝炎病毒(HBV)感染,HBV间隙,慢性HBV感染持续性以及对肝硬化的进展和肝细胞癌(HCC)。患者被分类为以下组:无活性HBV载体,活性HBV载体,HBV型对象和肝硬化+ HCC。使用PCR基因分型或Taqman测定法分析样品在微RNA中分析10 snP s。我们发现RS1358379与HBV感染,HBV间隙,持续慢性HBV感染和肝硬化+ HCC有关。此外,我们发现RS2292832和RS11614913与HBV感染,病毒间隙和肝硬化+ HCC的风险有关,而RS2910164与HBV感染的尺寸相关,以及清除病毒的能力。有证据表明RS6505162和HBV间隙之间的关联以及肝病的发展,而单一的关联是在RS2289030和HBV间隙之间发现的。同样,RS7372209和RS4919510与HBV诱导的肝脏并发症的发展有关。 MI RNA的SNP S影响沙特阿拉伯患者HBV感染的易感性,清除和进展。我们发现,使用基因本体或途径分析,这些基因可能有助于HBV感染和相关肝脏并发症的病理生理学。然而,具有各种临床阶段的检查的SNP S关联的差异表示这些多态性和其Mi RNA S的各个功能作用的变化,因此需要进一步调查它们的治疗潜力。

著录项

  • 来源
    《Journal of viral hepatitis.》 |2017年第12期|共11页
  • 作者单位

    Department of Infection and ImmunityKing Faisal Specialist Hospital &

    Research CenterRiyadh Saudi;

    Department of Infection and ImmunityKing Faisal Specialist Hospital &

    Research CenterRiyadh Saudi;

    Department of Infection and ImmunityKing Faisal Specialist Hospital &

    Research CenterRiyadh Saudi;

    Biomarkers Research ProgramKing Saud UniversityRiyadh Saudi Arabia;

    Gastroenterology SectionKing Saud UniversityRiyadh Saudi Arabia;

    Liver Disease Research CenterKing Saud UniversityRiyadh Saudi Arabia;

    Department of MedicineKing Faisal Specialist Hospital &

    Research CenterRiyadh Saudi Arabia;

    Department of MedicineKing Faisal Specialist Hospital &

    Research CenterRiyadh Saudi Arabia;

    Department of Gastroenterology &

    HepatologyPrince Sultan Military Medical CityRiyadh Saudi Arabia;

    Gastroenterology SectionKing Saud UniversityRiyadh Saudi Arabia;

    Gastroenterology SectionKing Saud UniversityRiyadh Saudi Arabia;

    Department of Infection and ImmunityKing Faisal Specialist Hospital &

    Research CenterRiyadh Saudi;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 传染病;
  • 关键词

    carcinoma; hepatitis B; hepatocellular; micro RNA; polymorphism;

    机译:癌;乙型肝炎;肝细胞;微RNA;多态性;

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