Recent studies on non-invasive biomarkers useful in biliary atresia - a literature review.

IF 1.4 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Anna Lew-Tusk, Marta Pęksa, Teresa Stachowicz-Stencel
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引用次数: 0

Abstract

The aim of this review is to specify new potential reliable and non-invasive methods for the diagnosis of biliary atresia (BA) that could shorten the way to diagnose BA, and finally the surgical treatment. Apart from the biomarkers that have been proven helpful and are used nowadays in neonatal wards, there are several new potential biomarkers that researchers have found to be helpful in the diagnosis of biliary atresia. Circulating microRNAs, matrix metalloproteinase-7, stool proteins, interleukin-33, Th17-associated cytokines, urinary metabolomics, anti-smooth muscle antibodies, heat shock proteins 90 and positive biliary epithelial cells CD56 are among those presented in this summary. These markers may play a new significant role in BA diagnosis. The described methods include Nomogram, Circulating microRNAs (miRNAs), Matrix metalloproteinase-7 (MMP-7), Stool proteins, Interleukin-33 (IL-33), Th17-associated cytokines, Alpha-aminoadipic acid and N-acetyl-d-mannosamine in urine, Anti-smooth muscle antibodies (ASMA), Heat shock proteins 90 (HSP90), Positive biliary epithelial cells CD56.

近年来对胆道闭锁有用的非侵入性生物标志物的研究——文献综述。
这篇综述的目的是为胆道闭锁(BA)的诊断指明新的、潜在的、可靠的、非侵入性的方法,这些方法可以缩短BA的诊断方法,并最终缩短手术治疗。除了已被证明有帮助并在新生儿病房中使用的生物标志物外,研究人员还发现了一些新的潜在生物标志物有助于诊断胆道闭锁。循环微小RNA、基质金属蛋白酶-7、粪便蛋白、白细胞介素33、Th17相关细胞因子、尿液代谢组学、抗平滑肌抗体、热休克蛋白90和阳性胆管上皮细胞CD56都在本综述中介绍。这些标志物可能在BA诊断中发挥新的重要作用。所述方法包括诺模图、循环微小RNA(miRNA)、基质金属蛋白酶-7(MMP-7)、大便蛋白、白细胞介素-33(IL-33)、Th17相关细胞因子、尿中的α-氨基己二酸和N-乙酰-d-甘露糖胺、抗平滑肌抗体(ASMA)、热休克蛋白90(HSP90)、阳性胆管上皮细胞CD56。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Acta biochimica Polonica
Acta biochimica Polonica 生物-生化与分子生物学
CiteScore
2.40
自引率
0.00%
发文量
99
审稿时长
4-8 weeks
期刊介绍: Acta Biochimica Polonica is a journal covering enzymology and metabolism, membranes and bioenergetics, gene structure and expression, protein, nucleic acid and carbohydrate structure and metabolism.
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