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弹性假黄瘤

Pseudoxanthoma elasticum.

作者信息

Germain Dominique P

机构信息

Division of Medical Genetics, University of Versailles - Saint Quentin en Yvelines, Paris-Saclay University, 2 avenue de la source de la Bièvre, F-78180, Montigny, France.

出版信息

Orphanet J Rare Dis. 2017 May 10;12(1):85. doi: 10.1186/s13023-017-0639-8.

Abstract

Pseudoxanthoma elasticum (PXE) is a genetic metabolic disease with autosomal recessive inheritance caused by mutations in the ABCC6 gene. The lack of functional ABCC6 protein leads to ectopic mineralization that is most apparent in the elastic tissues of the skin, eyes and blood vessels. The clinical prevalence of PXE has been estimated at between 1 per 100,000 and 1 per 25,000, with slight female predominance. The first clinical sign of PXE is almost always small yellow papules on the nape and sides of the neck and in flexural areas. The papules coalesce, and the skin becomes loose and wrinkled. The mid-dermal elastic fibers are short, fragmented, clumped and calcified. Dystrophic calcification of Bruch's membrane, revealed by angioid streaks, may trigger choroidal neovascularization and, ultimately, loss of central vision and blindness in late-stage disease. Lesions in small and medium-sized artery walls may result in intermittent claudication and peripheral artery disease. Cardiac complications (myocardial infarction, angina pectoris) are thought to be relatively rare but merit thorough investigation. Ischemic strokes have been reported. PXE is a metabolic disease in which circulating levels of an anti-mineralization factor are low. There is good evidence to suggest that the factor is inorganic pyrophosphate (PPi), and that the circulating low levels of PPi and decreased PPi/Pi ratio result from the lack of ATP release by hepatocytes harboring the mutant ABCC6 protein. However, the substrate(s) bound, transported or modulated by the ABCC6 protein remain unknown. More than 300 sequence variants of the ABCC6 gene have been identified. There is no cure for PXE; the main symptomatic treatments are vascular endothelial growth factor inhibitor therapy (for ophthalmic manifestations), lifestyle, lipid-lowering and dietary measures (for reducing vascular risk factors), and vascular surgery (for severe cardiovascular manifestations). Future treatment options may include gene therapy/editing and pharmacologic chaperone therapy.

摘要

弹性假黄瘤(PXE)是一种常染色体隐性遗传的基因代谢疾病,由ABCC6基因突变引起。功能性ABCC6蛋白的缺乏会导致异位矿化,这在皮肤、眼睛和血管的弹性组织中最为明显。据估计,PXE的临床患病率在每10万人中有1例至每2.5万人中有1例之间,女性略占优势。PXE的首个临床症状几乎总是出现在颈部后和两侧以及屈侧部位的小黄丘疹。丘疹融合,皮肤变得松弛且起皱。真皮中层的弹性纤维变短、断裂、聚集并钙化。血管样条纹显示的布鲁赫膜营养不良性钙化可能引发脉络膜新生血管,最终导致晚期疾病的中心视力丧失和失明。中小动脉壁的病变可能导致间歇性跛行和外周动脉疾病。心脏并发症(心肌梗死、心绞痛)被认为相对罕见,但值得深入研究。已有缺血性中风的报道。PXE是一种代谢疾病,其中抗矿化因子的循环水平较低。有充分证据表明该因子是无机焦磷酸(PPi),并且循环中PPi水平低和PPi/Pi比值降低是由于携带突变ABCC6蛋白的肝细胞缺乏ATP释放所致。然而,ABCC6蛋白结合、转运或调节的底物仍然未知。已鉴定出ABCC6基因的300多个序列变体。PXE无法治愈;主要的对症治疗方法是血管内皮生长因子抑制剂治疗(用于眼部表现)、生活方式、降脂和饮食措施(用于降低血管危险因素)以及血管手术(用于严重的心血管表现)。未来的治疗选择可能包括基因治疗/编辑和药物伴侣疗法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0a24/5424392/1234647fcb1d/13023_2017_639_Fig1_HTML.jpg

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