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ENPP1-Fc prevents mortality and vascular calcifications in rodent model of generalized arterial calcification of infancy

机译:ENPP1-FC在婴儿期的广义动脉钙化啮齿动物模型中阻止死亡率和血管钙化

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Diseases of ectopic calcification of the vascular wall range from lethal orphan diseases such as generalized arterial calcification of infancy (GACI), to common diseases such as hardening of the arteries associated with aging and calciphylaxis of chronic kidney disease (CKD). GACI is a lethal orphan disease in which infants calcify the internal elastic lamina of their medium and large arteries and expire of cardiac failure as neonates, while calciphylaxis of CKD is a ubiquitous vascular calcification in patients with renal failure. Both disorders are characterized by vascular Monckeburg's sclerosis accompanied by decreased concentrations of plasma inorganic pyrophosphate (PPi). Here we demonstrate that subcutaneous administration of an ENPP1-Fc fusion protein prevents the mortality, vascular calcifications and sequela of disease in animal models of GACI, and is accompanied by a complete clinical and biomarker response. Our findings have implications for the treatment of rare and common diseases of ectopic vascular calcification.
机译:血管壁异位钙化的疾病范围从致命孤儿疾病如婴儿期(GACI)的广义动脉钙化,常见疾病,例如与慢性肾脏疾病(CKD)的衰老和钙肝相关的动脉硬化。 Gaci是一种致死的孤儿疾病,其中婴儿钙化其培养基和大动脉的内部弹性薄片,并作为新生儿的心脏衰竭过期,而CKD的钙糊涂是肾衰竭患者患有普遍无处不在的血管钙化。这两种疾病的特征在于血管蒙古堡的硬化症,伴有血浆无机焦磷酸浓度降低(PPI)。在这里,我们证明皮下施用ENPP1-FC融合蛋白可防止GACI动物模型中的死亡率,血管钙化和疾病后遗症,并伴有完整的临床和生物标志物反应。我们的研究结果对治疗异位血管钙化的罕见和常见疾病有影响。

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