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首页> 外文期刊>Journal of genetics >Genetics of ulcerative colitis: putting into perspective the incremental gains from Indian studies
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Genetics of ulcerative colitis: putting into perspective the incremental gains from Indian studies

机译:溃疡性结肠炎的遗传学:透视印度研究的增量收益

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Ulcerative colitis (UC), one of the two clinical subtypes of inflammatory bowel disease is perceived as a potential sleeping giant' in the Indian subcontinent. Clinical manifestation is overall believed to be the same across ethnic groups but overwhelming genetics from large European and fewer non-European studies have revealed shared as well as unique disease susceptibly signatures between them, pointing to population specific differences at genomic and environmental levels. A systematic recount of the four major eras in UC genetics spanning earliest linkage analysis, cherry picked candidate gene association studies, unbiased genomewide association studies, their logical extension in trans-ethnic setting (Immunochip study), lastly whole exome sequencing efforts for rare variant burden; and lessons learnt thereof in context of genetically distinct Indian population was attempted in this review. Genetic heterogeneity manifesting at allelic/locus level across these approaches has been the consistent finding through the range of pan India studies. On the other hand, these salient findings also highlight the limitations of even the best of these genetic leads for prognostic/clinical application. The imminent need, therefore, for the UC research community to adopt newer approaches/tools with improved study design to (i) gain better insight into genetic/mechanistic basis of disease; (ii) identify biomarkers of immediate translational value; and (iii) develop new/alternate therapeutic options is emphasized at the end.
机译:溃疡性结肠炎(UC),炎症性肠疾病的两种临床亚型之一被认为是印度次大陆的潜在睡眠巨头。临床表现在族裔群体中,族裔群体相同,而且大量欧洲和更少的非欧洲研究的遗传揭示了分担,以及在它们之间存在的独特疾病,指向基因组和环境水平的人口特定差异。系统叙述了UC遗传学中的四个主要时代,涵盖了最早的联系分析,樱桃采摘候选基因关联研究,无偏见的基因组关联研究,它们在跨越民族环境中的逻辑延伸(免疫噬成像),最后全面的稀有变体负荷努力;在本综述中尝试了在转基因鲜明的印度人群的背景下学到的经验教训。这些方法的等位基因/基因座水平在等位基因/基因座级别的遗传异质性一直是泛印度研究范围一致的发现。另一方面,这些突出的结果还突出了甚至最佳这些遗传铅的局限性,用于预后/临床应用。因此,迫在眉睫的需求对于UC研究界采用新的方法/工具,改进的研究设计至(i)获得更好地了解疾病的遗传/机械基础; (ii)识别立即翻译价值的生物标志物; (iii)在最后强调了新的/备用治疗选择。

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