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Validating Glycoprotein Non-Metastatic Melanoma B (gpNMB osteoactivin) a new biomarker of Gaucher Disease

机译:验证糖蛋白非转移性黑色素瘤B(gpNMB骨激活素)一种高雪氏病的新生物标记

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摘要

In the spleens of Gaucher disease mice and patients, there is a striking elevation of expression of glycoprotein non-Metastatic Melanoma B (gpNMB). We conducted a study in a large cohort of patients with Gaucher disease to assess the utility of serum levels of soluble fragment of gpNMB as a biomarker of disease activity. There was >15-fold elevation of gpNMB in sera of untreated patients with Gaucher disease. gpNMB levels correlated with overall disease severity as well as the severity of individual organ compartments: liver, spleen, bone and hematological disease. Imiglucerase enzyme replacement therapy resulted in significant reduction of gpNMB. Serum levels of gpNMB were highly correlated with accumulation of bioactive lipid substrate of Gaucher disease, glucosylsphingosine as well as established biomarkers, chitotriosidase and chemokine, CCL18. Our results suggest utility of gpNMB as a biomarker of Gaucher disease to monitor individual patients and cohorts of patients for disease progression or response to therapy. Investigation of gpNMB in Gaucher disease pathophysiology is likely to illuminate our understanding disease mechanisms.
机译:在高雪氏病小鼠和患者的脾脏中,糖蛋白非转移性黑色素瘤B(gpNMB)的表达显着升高。我们对一大批戈谢病患者进行了一项研究,以评估gpNMB可溶性片段的血清水平作为疾病活动性生物标志物的实用性。未经治疗的高雪氏病患者血清中gpNMB升高> 15倍。 gpNMB水平与总体疾病严重程度以及单个器官区隔的严重程度相关:肝脏,脾脏,骨骼和血液系统疾病。异葡糖苷酶替代疗法导致gpNMB明显减少。血清gpNMB水平与高雪氏病的生物活性脂质底物,葡萄糖基鞘氨醇以及已建立的生物标志物,壳三糖苷酶和趋化因子CCL18的积累高度相关。我们的结果表明,gpNMB作为高雪氏病的生物标志物的用途可用于监测个别患者和患者群的疾病进展或对治疗的反应。高雪氏病病理生理学中gpNMB的研究可能会阐明我们对疾病机制的理解。

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