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非线性光学显微镜是一种分析弹性假黄瘤皮肤改变的新工具。

Nonlinear optical microscopy is a novel tool for the analysis of cutaneous alterations in pseudoxanthoma elasticum.

机构信息

Department of Dermatology, Venereology and Dermatooncology, Semmelweis University, 41 Mária Street, Budapest, H-1085, Hungary.

Wigner RCP, Institute for Solid State Physics and Optics, Hungarian Academy of Sciences, Budapest, Hungary.

出版信息

Lasers Med Sci. 2020 Oct;35(8):1821-1830. doi: 10.1007/s10103-020-03027-w. Epub 2020 May 6.

DOI:10.1007/s10103-020-03027-w
PMID:32372237
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7505829/
Abstract

Pseudoxanthoma elasticum (PXE, OMIM 264800) is a rare autosomal recessive disorder with ectopic mineralization and fragmentation of elastin fibers. It is caused by mutations of the ABCC6 gene that leads to decreased serum levels of inorganic pyrophosphate (PPi) anti-mineralization factor. The occurrence of severe complications among PXE patients highlights the importance of early diagnosis so that prompt multidisciplinary care can be provided to patients. We aimed to examine dermal connective tissue with nonlinear optical (NLO) techniques, as collagen emits second-harmonic generation (SHG) signal, while elastin can be excited by two-photon excitation fluorescence (TPF). We performed molecular genetic analysis, ophthalmological and cardiovascular assessment, plasma PPi measurement, conventional histopathological examination, and ex vivo SHG and TPF imaging in five patients with PXE and five age- and gender-matched healthy controls. Pathological mutations including one new variant were found in the ABCC6 gene in all PXE patients and their plasma PPi level was significantly lower compared with controls. Degradation and mineralization of elastin fibers and extensive calcium deposition in the mid-dermis was visualized and quantified together with the alterations of the collagen structure in PXE. Our data suggests that NLO provides high-resolution imaging of the specific histopathological features of PXE-affected skin. In vivo NLO may be a promising tool in the assessment of PXE, promoting early diagnosis and follow-up.

摘要

弹性假黄瘤(PXE,OMIM 264800)是一种罕见的常染色体隐性遗传病,其特征为弹性纤维的异位矿化和碎裂。该病由 ABCC6 基因突变引起,导致血清中无机焦磷酸盐(PPi)抗矿化因子水平降低。PXE 患者发生严重并发症,突出了早期诊断的重要性,以便及时为患者提供多学科治疗。我们旨在使用非线性光学(NLO)技术检查皮肤结缔组织,因为胶原会发出二次谐波产生(SHG)信号,而弹性蛋白可以通过双光子激发荧光(TPF)激发。我们对 5 名 PXE 患者和 5 名年龄和性别匹配的健康对照者进行了分子遗传学分析、眼科和心血管评估、血浆 PPi 测量、常规组织病理学检查以及离体 SHG 和 TPF 成像。在所有 PXE 患者中均发现 ABCC6 基因存在病理性突变,包括一种新变异,且其血浆 PPi 水平明显低于对照组。PXE 患者的中真皮弹性纤维降解和矿化以及钙沉积广泛,胶原结构改变也可通过 NLO 成像进行可视化和定量分析。我们的数据表明 NLO 可提供 PXE 皮肤特定组织病理学特征的高分辨率成像。体内 NLO 可能成为 PXE 评估的一种有前途的工具,有助于早期诊断和随访。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94d2/7505829/b94d204e05ea/10103_2020_3027_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94d2/7505829/c18dfba48114/10103_2020_3027_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94d2/7505829/099c2b8addab/10103_2020_3027_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94d2/7505829/7c81c4911dc5/10103_2020_3027_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94d2/7505829/b94d204e05ea/10103_2020_3027_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94d2/7505829/c18dfba48114/10103_2020_3027_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94d2/7505829/099c2b8addab/10103_2020_3027_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94d2/7505829/7c81c4911dc5/10103_2020_3027_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94d2/7505829/b94d204e05ea/10103_2020_3027_Fig4_HTML.jpg

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