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Sets of serum exosomal microRNAs as candidate diagnostic biomarkers for Kawasaki disease

机译:血清外泌体microRNA组作为川崎病的候选诊断生物标志物

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摘要

Although Kawasaki disease is the main cause of acquired heart disease in children, no diagnostic biomarkers are available. We aimed to identify candidate biomarkers for diagnosing Kawasaki disease using serum exosomal microRNAs (miRNAs). Using frozen serum samples from a biobank, high-throughput microarray technologies, two-stage real-time quantitative PCR, and a self-referencing strategy for data normalization, we narrowed down the list of biomarker candidates to a set of 4 miRNAs. We further validated the diagnostic capabilities of the identified miRNAs (namely, CT(miR-1246)-CT(miR-4436b-5p) and CT(miR-197-3p)-CT(miR-671-5p)) in 79 samples from two hospitals. We found that this 4-miRNA set could distinguish KD patients from other febrile patients as well as from healthy individuals in a single pass, with a minimal rate of false positives and negatives. We thus propose, for the first time, that serum exosomal miRNAs represent candidate diagnostic biomarkers for Kawasaki disease. Additionally, we describe an effective strategy of screening for biomarkers of complex diseases even when little mechanistic knowledge is available.
机译:尽管川崎病是儿童后天性心脏病的主要原因,但尚无诊断性生物标志物。我们旨在鉴定使用血清外泌体微小RNA(miRNA)诊断川崎病的候选生物标志物。使用来自生物库的冷冻血清样品,高通量微阵列技术,两阶段实时定量PCR以及数据标准化的自参考策略,我们将候选生物标志物的范围缩小到了一组4个miRNA。我们进一步验证了已鉴定的miRNA(即CT(miR-1246)-CT(miR-4436b-5p)和CT(miR-197-3p)-CT(miR-671-5p))的诊断能力来自两家医院。我们发现,这种4-miRNA集可以一次将KD患者与其他高热患者以及健康个体区分开,且假阳性和阴性的发生率极低。因此,我们首次提出血清外泌体miRNA代表了川崎病的候选诊断生物标志物。此外,我们描述了一种即使复杂的机制知识不多的情况下,也可用于筛选复杂疾病生物标志物的有效策略。

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