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白癜风近期研究的简要综述。

Concise review of recent studies in vitiligo.

作者信息

Allam Mohamed, Riad Hassan

机构信息

Dermatology Department, Hamad Medical Corporation, Doha, Qatar.

Dermatology Department, Rumailah Hospital, Hamad Medical Corporation, Doha, Qatar.

出版信息

Qatar Med J. 2013 Dec 23;2013(2):1-19. doi: 10.5339/qmj.2013.10. eCollection 2013.

DOI:10.5339/qmj.2013.10
PMID:25003059
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4080492/
Abstract

Vitiligo is an acquired pigmentry disorder of the skin and mucous membranes which manifests as white macules and patches due to selective loss of melanocytes. Etiological hypotheses of vitiligo include genetic, immunological, neurohormonal, cytotoxic, biochemical, oxidative stress and newer theories of melanocytorrhagy and decreased melanocytes survival. There are several types of vitiligo which are usually diagnosed clinically and by using a Wood's lamp; also vitiligo may be associated with autoimmune diseases, audiological and ophthalmological findings or it can be a part of polyendocrinopathy syndromes. Several interventions are available for the treatment for vitiligo to stop disease progression and/or to attain repigmentation or even depigmentation. In this article, we will present an overall view of current standing of vitiligo research work especially in the etiological factors most notably the genetic components, also, types and associations and various and newer treatment modalities.

摘要

白癜风是一种获得性皮肤和黏膜色素沉着紊乱疾病,由于黑素细胞选择性缺失而表现为白色斑疹和斑块。白癜风的病因假说包括遗传、免疫、神经激素、细胞毒性、生化、氧化应激以及黑素细胞外渗和黑素细胞存活率降低等新理论。白癜风有几种类型,通常通过临床诊断和伍德灯检查来诊断;此外,白癜风可能与自身免疫性疾病、听力学和眼科检查结果相关,或者可能是多内分泌病综合征的一部分。有几种干预措施可用于白癜风的治疗,以阻止疾病进展和/或实现色素再生甚至色素脱失。在本文中,我们将全面介绍白癜风研究工作的现状,特别是病因因素,最显著的是遗传成分,以及类型、关联和各种新的治疗方式。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebe6/4080492/3c4d24ecb8e2/qmj-2013-010-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebe6/4080492/3c4d24ecb8e2/qmj-2013-010-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebe6/4080492/3c4d24ecb8e2/qmj-2013-010-g001.jpg

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本文引用的文献

1
Evaluation of Five Different Regimes For the Treatment of Vitiligo.五种不同白癜风治疗方案的评估
Indian J Dermatol Venereol Leprol. 1989 Jan-Feb;55(1):18-21.
2
Guidelines for the management of vitiligo: the European Dermatology Forum consensus.白癜风管理指南:欧洲皮肤病学会共识。
Br J Dermatol. 2013 Jan;168(1):5-19. doi: 10.1111/j.1365-2133.2012.11197.x. Epub 2012 Nov 2.
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Global activation of CD8+ cytotoxic T lymphocytes correlates with an impairment in regulatory T cells in patients with generalized vitiligo.
银纳米粒子和(甘草)根提取物作为水凝胶改性剂,设计为创新敷料。
Int J Mol Sci. 2022 Dec 22;24(1):217. doi: 10.3390/ijms24010217.
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Discovery of Pinostrobin as a Melanogenic Agent in cAMP/PKA and p38 MAPK Signaling Pathway.发现 Pinostrobin 是 cAMP/PKA 和 p38 MAPK 信号通路中的黑色素生成剂。
Nutrients. 2022 Sep 9;14(18):3713. doi: 10.3390/nu14183713.
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Fractional Carbon Dioxide Laser versus Fractional Carbon Dioxide Laser with Autologous Intralesional Platelet-rich Plasma in the Treatment of Stable, Non-segmental Vitiligo: A Randomized Comparative Study.分次二氧化碳激光与分次二氧化碳激光联合自体病灶内富血小板血浆治疗稳定型非节段性白癜风的随机对照研究
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Morin Induces Melanogenesis via Activation of MAPK Signaling Pathways in B16F10 Mouse Melanoma Cells.莫林通过激活 B16F10 小鼠黑素瘤细胞中的 MAPK 信号通路诱导黑色素生成。
Molecules. 2021 Apr 8;26(8):2150. doi: 10.3390/molecules26082150.
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Novel immunological and genetic factors associated with vitiligo: A review.与白癜风相关的新型免疫和遗传因素:综述
Exp Ther Med. 2021 Apr;21(4):312. doi: 10.3892/etm.2021.9743. Epub 2021 Feb 1.
8
Associations of Angiotensin-Converting Enzyme Gene Insertion/Deletion (ACE Gene I/D) Polymorphism With Vitiligo: An Updated Systematic Review and Meta-Analysis.血管紧张素转换酶基因插入/缺失(ACE基因I/D)多态性与白癜风的关联:一项更新的系统评价和荟萃分析
Cureus. 2020 May 10;12(5):e8046. doi: 10.7759/cureus.8046.
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Evaluation of skin expression profiles of patients with vitiligo treated with narrow-band UVB therapy by targeted RNA-seq.通过靶向RNA测序评估窄谱中波紫外线治疗的白癜风患者的皮肤表达谱。
An Bras Dermatol. 2018 Nov/Dec;93(6):843-851. doi: 10.1590/abd1806-4841.20187589.
10
Vitamin D receptor gene polymorphism, serum 25-hydroxyvitamin D levels, and risk of vitiligo: A meta-analysis.维生素D受体基因多态性、血清25-羟基维生素D水平与白癜风风险:一项荟萃分析。
Medicine (Baltimore). 2018 Jul;97(29):e11506. doi: 10.1097/MD.0000000000011506.
全身性白癜风患者的 CD8+ 细胞毒性 T 淋巴细胞的整体激活与调节性 T 细胞的损伤有关。
PLoS One. 2012;7(5):e37513. doi: 10.1371/journal.pone.0037513. Epub 2012 May 23.
4
Systemic analyses of immunophenotypes of peripheral T cells in non-segmental vitiligo: implication of defective natural killer T cells.非节段性白癜风外周 T 细胞免疫表型的系统分析:自然杀伤 T 细胞缺陷的意义。
Pigment Cell Melanoma Res. 2012 Sep;25(5):602-11. doi: 10.1111/j.1755-148X.2012.01019.x. Epub 2012 Jul 12.
5
Revised classification/nomenclature of vitiligo and related issues: the Vitiligo Global Issues Consensus Conference.白癜风的修订分类/命名法及相关问题:白癜风全球问题共识会议。
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A single nucleotide polymorphism rs9468925 of MHC region is associated with clinical features of generalized vitiligo in Chinese Han population.MHC 区域的单核苷酸多态性 rs9468925 与中国汉族人群泛发性白癜风的临床特征相关。
J Eur Acad Dermatol Venereol. 2012 Sep;26(9):1137-41. doi: 10.1111/j.1468-3083.2011.04259.x. Epub 2011 Sep 26.
8
Vitiligo: a comprehensive overview Part I. Introduction, epidemiology, quality of life, diagnosis, differential diagnosis, associations, histopathology, etiology, and work-up.白癜风:全面概述 第一部分。引言、流行病学、生活质量、诊断、鉴别诊断、关联、组织病理学、病因学和检查。
J Am Acad Dermatol. 2011 Sep;65(3):473-491. doi: 10.1016/j.jaad.2010.11.061.
9
Immunopathogenesis of vitiligo.白癜风的免疫发病机制。
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10
Comprehensive association analysis of candidate genes for generalized vitiligo supports XBP1, FOXP3, and TSLP.候选基因在泛发性白癜风中的综合关联分析支持 XBP1、FOXP3 和 TSLP。
J Invest Dermatol. 2011 Feb;131(2):371-81. doi: 10.1038/jid.2010.337. Epub 2010 Nov 18.