一项针对弗里德里希共济失调症患者的 RNA 序列研究发现,hsa-miR-148a-3p 是该疾病的一种潜在预后生物标志物。

IF 3.8 3区 医学 Q2 GENETICS & HEREDITY Human Genomics Pub Date : 2024-05-22 DOI:10.1186/s40246-024-00602-y
Chiara Vancheri, Andrea Quatrana, Elena Morini, Caterina Mariotti, Alessia Mongelli, Mario Fichera, Alessandra Rufini, Ivano Condò, Roberto Testi, Giuseppe Novelli, Florence Malisan, Francesca Amati
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引用次数: 0

摘要

弗里德里希共济失调症(FRDA)是一种危及生命的遗传性共济失调症,在白种人口中的发病率为1:50,000。最近,美国食品和药物管理局(FDA)批准了一种治疗 FRDA 的独特药物--抗氧化剂 Omaveloxolone。FRDA 是一种多系统神经退行性疾病;除了进行性神经退行性病变外,FRDA 还伴有肥厚型心肌病、糖尿病和肌肉骨骼畸形。心肌病是导致过早死亡的主要原因。FRDA 的发病年龄通常在 5 至 15 岁之间。鉴于临床特征的复杂性和异质性以及发病的多变性,确定能够评估疾病进展和监测治疗效果的生物标志物对于促进临床实践决策至关重要。我们对 FRDA 患者和健康捐献者的外周血单核细胞进行了 RNA 序列分析,确定了能够区分健康人和大多数 FRDA 患者的小非编码 RNA(sncRNA)特征。在差异表达的 sncRNAs 中,microRNAs 是一类小型非编码内源性 RNAs,可调节转录后靶基因的沉默。在 FRDA 血浆样本中,hsa-miR-148a-3p 明显上调。结合 hsa-miR-148a-3p 和 hsa-miR-223-3p(本研究小组先前已发现)的循环表达水平进行的接收者操作特征曲线(ROC)分析显示,曲线下面积(AUC)为 0.86(95%,置信区间为 0.77-0.95;p 值为 0.05)。
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An RNA-seq study in Friedreich ataxia patients identified hsa-miR-148a-3p as a putative prognostic biomarker of the disease.

Friedreich ataxia (FRDA) is a life-threatening hereditary ataxia; its incidence is 1:50,000 individuals in the Caucasian population. A unique therapeutic drug for FRDA, the antioxidant Omaveloxolone, has been recently approved by the US Food and Drug Administration (FDA). FRDA is a multi-systemic neurodegenerative disease; in addition to a progressive neurodegeneration, FRDA is characterized by hypertrophic cardiomyopathy, diabetes mellitus and musculoskeletal deformities. Cardiomyopathy is the predominant cause of premature death. The onset of FRDA typically occurs between the ages of 5 and 15. Given the complexity and heterogeneity of clinical features and the variability of their onset, the identification of biomarkers capable of assessing disease progression and monitoring the efficacy of treatments is essential to facilitate decision making in clinical practice. We conducted an RNA-seq analysis in peripheral blood mononuclear cells from FRDA patients and healthy donors, identifying a signature of small non-coding RNAs (sncRNAs) capable of distinguishing healthy individuals from the majority of FRDA patients. Among the differentially expressed sncRNAs, microRNAs are a class of small non-coding endogenous RNAs that regulate posttranscriptional silencing of target genes. In FRDA plasma samples, hsa-miR-148a-3p resulted significantly upregulated. The analysis of the Receiver Operating Characteristic (ROC) curve, combining the circulating expression levels of hsa-miR-148a-3p and hsa-miR-223-3p (previously identified by our group), revealed an Area Under the Curve (AUC) of 0.86 (95%, Confidence Interval 0.77-0.95; p-value < 0.0001). An in silico prediction analysis indicated that the IL6ST gene, an interesting marker of neuroinflammation in FRDA, is a common target gene of both miRNAs. Our findings support the evaluation of combined expression levels of different circulating miRNAs as potent epi-biomarkers in FRDA. Moreover, we found hsa-miR-148a-3p significantly over-expressed in Intermediate and Late-Onset Friedreich Ataxia patients' group (IOG and LOG, respectively) compared to healthy individuals, indicating it as a putative prognostic biomarker in this pathology.

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来源期刊
Human Genomics
Human Genomics GENETICS & HEREDITY-
CiteScore
6.00
自引率
2.20%
发文量
55
审稿时长
11 weeks
期刊介绍: Human Genomics is a peer-reviewed, open access, online journal that focuses on the application of genomic analysis in all aspects of human health and disease, as well as genomic analysis of drug efficacy and safety, and comparative genomics. Topics covered by the journal include, but are not limited to: pharmacogenomics, genome-wide association studies, genome-wide sequencing, exome sequencing, next-generation deep-sequencing, functional genomics, epigenomics, translational genomics, expression profiling, proteomics, bioinformatics, animal models, statistical genetics, genetic epidemiology, human population genetics and comparative genomics.
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