Judith Haschka, Zora Messner, Julia Feurstein, Benjamin Hadzimuratovic, Jochen Zwerina, Andreas B Diendorfer, Marianne Pultar, Matthias Hackl, Martin Kuzma, Juraj Payer, Heinrich Resch, Roland Kocijan
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引用次数: 0
Abstract
Introduction: Adult hypophosphatasia (HPP) patients present with diffuse heterogenous symptoms often mimicking rheumatological diseases or osteoporosis and therefore accompanied by delayed diagnosis. The aim of this study was to identify circulating microRNAs (miRNAs) in adult HPP patients and to identify potential associations with clinical patients' characteristics.
Methods: We utilized untargeted miRNA biomarker discovery by small RNA-sequencing to investigate cell-free miRNA profiles in 24 adult HPP patients (pathogenic variant of the ALPL gene, HPP-related clinical symptoms, and repeatedly low alkaline phosphatase) and 24 healthy controls (CTRL).
Results: Patients and CTRL were comparable in age (47.9 ± 14.2 vs 45.9 ± 8.8 years, P = .980) and sex (55.5% vs 47.8% females, P = 1.000). In total, 91% of patients reported musculoskeletal pain, 41% diffuse neurological symptoms, and 64% history of fractures. In total, 84 miRNAs were significantly differently expressed between HPP and CTRL in next-generation sequencing analysis (P < .05). Of these, 14 miRNAs were selected (selection criteria: P < .05, tissue specificity index >0.7, log2 fold change >+0.8 or <-0.8) for validation using RT-qualitative PCR, which verified 6 of 14 selected miRNAs (P < .05; miR-122-3p, miR-140-5p, miR-143-3p, miR-155-5p, miR-451a, miR-92a-3p). Target prediction and enrichment analysis identified associations with the musculoskeletal system and the central nervous system. In total, 37 miRNAs correlated with alkaline phosphatase levels, but only 3 miRNAs with pyridoxal-5'-phosphate.
Conclusion: These findings highlight a profound involvement of multiple organ systems and the potential of miRNAs as biomarkers for the effect of HPP on various systems.
成人磷酸酶减少症(HPP)患者表现为弥漫性异质症状,通常与风湿病或骨质疏松症相似,因此伴有延迟诊断。本研究的目的是确定成年HPP患者的循环mirna,并确定其与临床患者特征的潜在关联。方法:利用小rna测序技术发现非靶向miRNA生物标志物,研究24例成人HPP患者(ALPL基因致病性变异、HPP相关临床症状和反复低ALP)和24例健康对照(CTRL)的无细胞miRNA谱。结果:两组患者年龄(47.9±14.2比45.9±8.8,p=0.980)、性别(55.5%比47.8%,p=1.000)具有可比性。总的来说,91%的患者报告了肌肉骨骼疼痛,41%的患者报告了弥漫性神经症状,64%的患者报告了骨折史。在下一代测序(NGS)分析中,总共有84个mirna在HPP和CTRL之间表达显著不同(p0.7, log2 FC >+0.8或< -0.8),用于RT-qPCR验证,验证了14个选定mirna中的6个(p结论:这些发现突出了HPP对多器官系统的深远影响,以及mirna作为HPP对各种系统影响的生物标志物的潜力。
期刊介绍:
The Journal of Clinical Endocrinology & Metabolism is the world"s leading peer-reviewed journal for endocrine clinical research and cutting edge clinical practice reviews. Each issue provides the latest in-depth coverage of new developments enhancing our understanding, diagnosis and treatment of endocrine and metabolic disorders. Regular features of special interest to endocrine consultants include clinical trials, clinical reviews, clinical practice guidelines, case seminars, and controversies in clinical endocrinology, as well as original reports of the most important advances in patient-oriented endocrine and metabolic research. According to the latest Thomson Reuters Journal Citation Report, JCE&M articles were cited 64,185 times in 2008.