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使用多重反应监测串联质谱法在干血斑中进行肌营养不良蛋白定量作为杜氏肌营养不良症的诊断生物标志物:初步研究。

Dystrophin Protein Quantification as a Duchenne Muscular Dystrophy Diagnostic Biomarker in Dried Blood Spots Using Multiple Reaction Monitoring Tandem Mass Spectrometry: A Preliminary Study.

机构信息

Department of Medical Laboratory Sciences, Jordan University of Science and Technology, Irbid 22110, Jordan.

Clinical Biochemistry Unit, Pathology Department, College of Medicine, King Saud University, Riyadh 11461, Saudi Arabia.

出版信息

Molecules. 2022 Jun 7;27(12):3662. doi: 10.3390/molecules27123662.

Abstract

Duchenne muscular dystrophy (DMD) is an X-linked recessive disorder characterized by progressive muscle loss, leading to difficulties in movement. Mutations in the DMD gene that code for the protein dystrophin are responsible for the development of DMD disorder, where the synthesis of this protein is completely halted. Therefore, circulating dystrophin protein could be a promising biomarker of DMD disease. Current methods for diagnosing DMD have sensitivity, specificity, and reproducibility limitations. Herein, a quantitative liquid chromatography-tandem spectrometry (LC-MS/MS) technique in multiple reaction monitoring (MRM) mode was designed and validated for accurate dystrophin protein measurement in a dried blood spot (DBS). The method was successfully validated on the basis of international guidelines regarding calibration curves, precision, and accuracy. In addition, patients and healthy controls were used to test the amount of dystrophin protein circulating in DBS samples as a potential biomarker for DMD disorders. DMD patients were found to have considerably lower levels than controls. To the best of our knowledge, this is the first study to report dystrophin levels in DBS through LC-MS/MS as a diagnostic marker for DMD to the proposed MRM method, providing a highly specific and sensitive approach to dystrophin quantification in a DBS that can be applied in DMD screening.

摘要

杜氏肌营养不良症(DMD)是一种 X 连锁隐性遗传病,其特征是进行性肌肉丧失,导致运动困难。编码肌营养不良蛋白的 DMD 基因突变是导致 DMD 疾病发生的原因,这种蛋白质的合成完全停止。因此,循环肌营养不良蛋白可能是 DMD 疾病的有前途的生物标志物。目前用于诊断 DMD 的方法存在灵敏度、特异性和重现性的局限性。在此,设计并验证了一种基于多重反应监测 (MRM) 模式的定量液相色谱-串联质谱 (LC-MS/MS) 技术,用于准确测量干血斑 (DBS) 中的肌营养不良蛋白。该方法是根据国际校准曲线、精密度和准确度指南成功验证的。此外,还使用患者和健康对照来测试 DBS 样本中循环肌营养不良蛋白的含量,作为 DMD 疾病的潜在生物标志物。结果发现 DMD 患者的水平明显低于对照组。据我们所知,这是第一项通过 LC-MS/MS 报告 DBS 中肌营养不良蛋白水平作为 DMD 诊断标志物的研究,为 DMD 筛查提供了一种高度特异性和敏感的 DBS 肌营养不良蛋白定量方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6256/9231037/bca24bc35269/molecules-27-03662-g001.jpg

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