Department of Dermatology and Cutaneous Biology, Jefferson Medical College, Jefferson Institute of Molecular Medicine, Thomas Jefferson University, Philadelphia, USA.
J Dtsch Dermatol Ges. 2011 Aug;9(8):586-93. doi: 10.1111/j.1610-0387.2011.07658.x. Epub 2011 Mar 16.
Pseudoxanthoma elasticum (PXE) is a heritable multi-system disorder manifesting with characteristic cutaneous lesions, associated with ocular findings and cardiovascular involvement. The skin lesions, yellowish papules which coalesce into plaques of inelastic and leathery skin, demonstrate by histopathologic and ultrastructural examinations ectopic mineralization of dermal connective tissues, primarily the elastic structures. PXE is inherited in an autosomal recessive fashion due to mutations in the ABCC6 gene. Significant insights into the pathogenesis of PXE have been recently obtained from observations on the Abcc6(-/-) knockout mouse which mimics the genetic, histopathologic and ultrastructural features of PXE. This mouse model has provided a platform to test various treatment modalities to counteract the mineralization phenotypes. One of the intriguing findings emanating from these studies is that supplementation of the mouse diet with magnesium, at levels that are ∼5-fold higher than those in control diet, completely inhibits the development of tissue mineralization. These and related observations suggest that changes in the diet might counteract the progression of PXE and improve the quality of life of patients with this, currently intractable, disease.
弹性假黄瘤(PXE)是一种遗传性多系统疾病,表现为特征性皮肤损伤,伴有眼部表现和心血管受累。皮肤损伤为黄色丘疹,融合成无弹性和皮革样皮肤的斑块,组织病理学和超微结构检查显示真皮结缔组织的异位矿化,主要是弹性结构。由于 ABCC6 基因突变,PXE 以常染色体隐性遗传方式遗传。最近,通过对模仿 PXE 遗传、组织病理学和超微结构特征的 Abcc6(-/-) 基因敲除小鼠的观察,我们对 PXE 的发病机制有了更深入的了解。该小鼠模型为测试各种治疗方法以对抗矿化表型提供了一个平台。这些研究中一个有趣的发现是,在小鼠饮食中补充镁,其水平比对照饮食高约 5 倍,可完全抑制组织矿化的发展。这些和相关的观察结果表明,饮食的改变可能会阻止 PXE 的进展,提高患有这种目前难以治愈疾病的患者的生活质量。