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脑特异性 miRNAs 的生物信息学分析鉴定创伤性脑损伤血液生物标志物候选物。

Bioinformatic analysis of brain-specific miRNAs for identification of candidate traumatic brain injury blood biomarkers.

机构信息

Frances Payne Bolton School of Nursing, Case Western Reserve University , Cleveland, Ohio, USA.

出版信息

Brain Inj. 2020 Jun 6;34(7):965-974. doi: 10.1080/02699052.2020.1764102. Epub 2020 Jun 4.

DOI:10.1080/02699052.2020.1764102
PMID:32497449
Abstract

BACKGROUND

Detection of brain-specific miRNAs in the peripheral blood could serve as a surrogate marker of traumatic brain injury (TBI). Here, we systematically identified brain-enriched miRNAs, and tested their utility as TBI biomarkers in the acute phase of care.

METHODS

Publically available microarray data generated from 29 postmortem human tissues were used to rank 1,364 miRNAs in terms of their degree of brain-specific expression. Levels of the top six ranked miRNAs were then prospectively measured in serum samples collected from 10 Patients with TBI at hospital admission, as well as from 10 controls.

RESULTS

The top six miRNAs identified in our analysis (miR-124-3p, miR-219a-5p, miR-9-5p, miR-9-3p, miR-137, and miR-128-3p) were enriched 70 to 320-fold in brain relative to other tissues, and exhibited dramatically greater brain specificity compared to several miRNAs previously proposed as biomarkers. Furthermore, their levels were elevated in serum from patients with TBI compared to controls, and could collectively discriminate between groups with 90% sensitivity and 100% specificity. Interestingly, subsequent informatic pathway analysis revealed that their target transcripts were enriched for components of signaling pathways active in peripheral organs involved in common post-TBI complications.

CONCLUSIONS

The six candidate miRNAs identified in this preliminary study have promise as blood biomarkers of TBI, and could also be molecular contributors to systemic physiologic changes commonly observed post-injury.

摘要

背景

在外周血中检测到脑特异性 miRNA 可以作为创伤性脑损伤 (TBI) 的替代标志物。在这里,我们系统地鉴定了富含脑的 miRNA,并测试了它们在急性期护理中作为 TBI 生物标志物的效用。

方法

使用来自 29 个人体组织的公开微阵列数据,根据其脑特异性表达程度对 1364 个 miRNA 进行排序。然后在入院时从 10 名 TBI 患者和 10 名对照者的血清样本中前瞻性测量排名前六的 miRNA 的水平。

结果

我们分析中确定的前六种 miRNA(miR-124-3p、miR-219a-5p、miR-9-5p、miR-9-3p、miR-137 和 miR-128-3p)在脑内的富集倍数为 70 至 320 倍,与先前提出的几种 miRNA 相比,它们的脑特异性显著增强。此外,它们在 TBI 患者的血清中的水平高于对照组,并且可以共同以 90%的敏感性和 100%的特异性来区分两组。有趣的是,随后的信息途径分析表明,它们的靶转录物富集了与常见 TBI 后并发症相关的外周器官中信号通路的组成部分。

结论

这项初步研究中鉴定的六种候选 miRNA 具有作为 TBI 血液生物标志物的潜力,并且可能也是常见损伤后观察到的全身生理变化的分子贡献者。

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