The correlation between cardiac and skeletal muscle pathology in animal models of idiopathic inflammatory myopathies.

Q3 Medicine Acta Myologica Pub Date : 2020-12-01 DOI:10.36185/2532-1900-035
Francesco Prisco, Serenella Papparella, Orlando Paciello
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引用次数: 10

Abstract

Idiopathic inflammatory myopathies (IIMs) represent a heterogeneous group of disorders in which skeletal muscle is inappropriately targeted by the immune system. IIMs are characterized by inflammation of muscle and varying degrees of muscle dysfunction. Extra-muscular manifestations may involve heart, skin, joints, lungs, and gastrointestinal tract. Cardiovascular involvement is a feared event because is one of the leading causes of mortality in IIM patients. As the myocardium shares many features with the skeletal muscle, it is supposed that it can be affected by the same inflammatory processes, which take place during the different forms of IIMs. However, the full extent of this link and the mechanisms behind it are still not fully understood. Animal models have greatly improved our understanding of IIM pathomechanisms and have proven to be a useful tool for discovering therapeutic drug targets. Here we report the evidence of heart muscle involvement in different animal models of spontaneous IIMs, assuming a common autoimmune mechanism and presenting them as study models for human pathology.

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特发性炎性肌病动物模型中心脏和骨骼肌病理的相关性。
特发性炎症性肌病(IIMs)代表了一组异质性疾病,其中骨骼肌被免疫系统不适当地靶向。IIMs的特点是肌肉炎症和不同程度的肌肉功能障碍。肌肉外表现可累及心脏、皮肤、关节、肺和胃肠道。心血管疾病是一种令人恐惧的事件,因为它是IIM患者死亡的主要原因之一。由于心肌与骨骼肌有许多共同的特征,因此我们认为它可能受到相同的炎症过程的影响,这些炎症过程发生在不同形式的iim中。然而,这种联系的全部程度及其背后的机制仍未完全了解。动物模型极大地提高了我们对IIM病理机制的理解,并已被证明是发现治疗药物靶点的有用工具。在这里,我们报告了自发性IIMs的不同动物模型中心肌参与的证据,假设一个共同的自身免疫机制,并将它们作为人类病理学的研究模型。
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来源期刊
Acta Myologica
Acta Myologica Medicine-Cardiology and Cardiovascular Medicine
CiteScore
3.70
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0.00%
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0
期刊最新文献
PROCEEDINGS OF THE XXIII CONGRESS OF THE ITALIAN ASSOCIATION OF MYOLOGY: PadovaJune 8-10, 2023. Year 2023: a new look for Acta Myologica. Experience with telemedicine in neuromuscular clinic during COVID-19 pandemic. VCP-related myopathy: a case series and a review of literature. Xp21 contiguous gene deletion syndrome presenting as Duchenne muscular dystrophy and glycerol kinase deficiency associated with intellectual disability: case report and review literature.
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