CENTOGENE AG, Am Strande 7, 18055 Rostock, Germany.
Pediatric Department, University Hospital 'Mother Teresa', 1000 Tirana, Albania.
Int J Mol Sci. 2020 Jun 27;21(13):4577. doi: 10.3390/ijms21134577.
Gaucher disease (GD) is a lysosomal storage disorder that responds well to enzyme replacement therapy (ERT). Certain laboratory parameters, including blood concentration of glucosylsphingosine (Lyso-Gb1), the lyso-derivate of the common glycolipid glucocerebroside, correlate with clinical improvement and are therefore considered candidate-monitoring biomarkers. Whether they can indicate a reduction or loss of treatment efficiency, however, has not been systematically addressed for obvious reasons. We established and validated measurement of Lyso-Gb1 from dried blood spots (DBSs) by mass spectrometry. We then characterized the assay's longitudinal performance in 19 stably ERT-treated GD patients by dense monitoring over a 3-year period. The observed level of fluctuation was accounted for in the subsequent development of a unifying data normalization concept. The resulting approach was eventually applied to data from Lyso-Gb1 measurements after an involuntary treatment break for all 19 patients. It enabled separation of the "under treatment" versus "not under treatment" conditions with high sensitivity and specificity. We conclude that Lyso-Gb1 determination from DBSs indicates treatment issues already at an early stage before clinical consequences arise. In addition to its previously shown diagnostic utility, Lyso-Gb1 thereby qualifies as a monitoring biomarker in GD patients.
戈谢病(GD)是一种溶酶体贮积症,对酶替代疗法(ERT)反应良好。某些实验室参数,包括葡萄糖神经酰胺的溶酶体衍生物(Lyso-Gb1)的血液浓度,与临床改善相关,因此被认为是候选监测生物标志物。然而,由于显而易见的原因,它们是否能够表明治疗效率的降低或丧失尚未得到系统解决。我们通过质谱法建立并验证了从干血斑(DBS)中测量 Lyso-Gb1 的方法。然后,我们通过在 3 年内进行密集监测,对 19 名稳定接受 ERT 治疗的 GD 患者的纵向性能进行了特征描述。在随后的统一数据归一化概念的发展中,考虑了观察到的波动水平。最终,该方法应用于所有 19 名患者因非自愿治疗中断后的 Lyso-Gb1 测量数据。它能够以高灵敏度和特异性区分“在治疗下”与“不在治疗下”的情况。我们得出结论,从 DBS 中测定 Lyso-Gb1 可以在出现临床后果之前的早期阶段表明治疗问题。除了之前显示的诊断效用外,Lyso-Gb1 因此有资格成为 GD 患者的监测生物标志物。