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接受酶替代疗法治疗的戈谢病患者的微小RNA表达

MiRNA Expression in Patients with Gaucher Disease Treated with Enzyme Replacement Therapy.

作者信息

Pawliński Łukasz, Polus Anna, Tobór Ewa, Sordyl Maria, Kopka Marianna, Solnica Bogdan, Kieć-Wilk Beata

机构信息

Clinical Department of Metabolic Diseases and Diabetology, University Hospital in Krakow, 30-688 Kraków, Poland.

European Reference Network for Hereditary Metabolic Disorders (MetabERN), 31-501 Kraków, Poland.

出版信息

Life (Basel). 2020 Dec 22;11(1):2. doi: 10.3390/life11010002.

Abstract

AIMS

The aim of the work was to establish potential biomarkers or drug targets by analysing changes in miRNA concentration among patients with Gaucher disease (GD) compared to in healthy subjects.

METHODS

This study was an observational, cross-sectional analysis of 30 adult participants: 10 controls and 20 adults with GD type 1. Patients with GD type 1 were treated with enzyme replacement therapy (ERT) for at least two years. The control group was composed of healthy volunteers, unrelated to the patients, adjusted with age, sex and body mass index (BMI). The miRNA alteration between these groups was examined. After obtaining preliminary results on a group of six GD patients by the high-output method (TaqMan low-density array (TLDA)), potential miRNAs were selected for confirming the results by using the qRT-PCR method. With Diane Tools, we analysed miRNAs of which differential expression is most significant and their potential role in GD pathophysiology. We also determined the essential pathways these miRNAs are involved in.

RESULTS

266 dysregulated miRNAs were found among 753 tested. Seventy-eight miRNAs were downregulated, and 188 were upregulated. Thirty miRNAs were significantly altered; all of them were upregulated. The analysis of pathways regulated by the selected miRNAs showed an effect on bone development, inflammation or regulation of axonal transmission in association with Parkinson's disease.

CONCLUSIONS

We revealed few miRNAs, like miR-26-5p, which are highly altered and fit the GD pathophysiological model, might be considered as novel biomarkers of disease progression but need further evaluation.

摘要

目的

本研究旨在通过分析戈谢病(GD)患者与健康受试者之间miRNA浓度的变化,确定潜在的生物标志物或药物靶点。

方法

本研究是一项对30名成年参与者的观察性横断面分析,其中包括10名对照者和20名1型GD成年患者。1型GD患者接受酶替代疗法(ERT)治疗至少两年。对照组由与患者无关的健康志愿者组成,并根据年龄、性别和体重指数(BMI)进行匹配。检测了两组之间的miRNA变化。通过高产量方法(TaqMan低密度阵列(TLDA))在一组6名GD患者中获得初步结果后,选择潜在的miRNA,使用qRT-PCR方法确认结果。利用Diane Tools,我们分析了差异表达最显著的miRNA及其在GD病理生理学中的潜在作用。我们还确定了这些miRNA所涉及的关键途径。

结果

在753个检测的miRNA中发现了266个失调的miRNA。78个miRNA下调,188个上调。30个miRNA有显著变化,均为上调。对所选miRNA调控的途径分析显示,其对骨发育、炎症或与帕金森病相关的轴突传递调节有影响。

结论

我们发现少数miRNA,如miR-26-5p,高度改变且符合GD病理生理模型,可能被视为疾病进展的新型生物标志物,但需要进一步评估。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a98/7822051/28973819500e/life-11-00002-g0A1.jpg

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