A focused review of visible light therapies for vitiligo.

IF 2.5 4区 医学 Q2 DERMATOLOGY Photodermatology, photoimmunology & photomedicine Pub Date : 2024-01-01 Epub Date: 2023-12-11 DOI:10.1111/phpp.12939
Mitchell J Winkie, Goranit Sakunchotpanit, Carlos E Salazar, Nicole S Gunasekera, Elizabeth A Buzney, Vinod E Nambudiri
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Abstract

Background: Vitiligo can be challenging to treat and exhibit an unpredictable clinical course. Phototherapy in the form of visible light can achieve both repigmentation and depigmentation outcomes in vitiligo, with minimal associated adverse events. This review focuses on the mechanistic understandings and clinical outcomes of visible light-based treatments for vitiligo.

Methods: Articles were retrieved from PubMed starting from May 1965 until August 2023, yielding 496 unique articles. We conducted title, abstract, and full-text screening to identify articles describing the use of visible light (380-750 nm), either as part of combination therapy or as monotherapy, for repigmentation or depigmentation treatment in vitiligo.

Results: Twenty-seven articles met inclusion criteria, offering preclinical and clinical data regarding the utilization of helium-neon laser (red light) and blue light-emitting diodes (LEDs) as methods of repigmentation therapy in vitiligo. Preclinical and clinical data on the utilization of Q-switched ruby laser (694 nm) and frequency-doubled (FD) Nd:YAG laser (532 nm) for vitiligo depigmentation therapy were also identified.

Conclusion: While limited by small studies and a lack of standardized administration of phototherapy, the evidence for visible light's effectiveness in managing vitiligo is encouraging. Red light therapy using He-Ne lasers and blue light therapy via LEDs can stimulate repigmentation in patients with vitiligo with minimal adverse events. Q-switched ruby and FD Nd:YAG lasers provide viable, visible light depigmentation options, either alone or with topical agents. With limited clinical data, larger studies are needed to validate the efficacy of visible light therapy in treating vitiligo and to better understand its long-term outcomes.

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对可见光疗法治疗白癜风的重点回顾。
背景:白癜风的治疗具有挑战性,其临床过程难以预测。可见光形式的光疗可实现白癜风的色素再形成和色素脱失,且相关不良反应极少。本综述重点关注可见光治疗白癜风的机理认识和临床效果:从1965年5月至2023年8月的PubMed上检索文章,共获得496篇文章。我们对文章的标题、摘要和全文进行了筛选,以确定描述使用可见光(380-750 纳米)作为联合疗法的一部分或作为单一疗法治疗白癜风的文章:结果:27 篇文章符合纳入标准,提供了有关使用氦氖激光(红光)和蓝色发光二极管(LED)作为白癜风色素恢复疗法的临床前和临床数据。此外,还发现了利用Q开关红宝石激光(694 nm)和倍频(FD)Nd:YAG激光(532 nm)治疗白癜风色素脱失的临床前和临床数据:尽管受到小规模研究和缺乏标准化光疗方法的限制,但可见光治疗白癜风的有效性证据还是令人鼓舞的。使用氦氖激光器的红光疗法和 LED 的蓝光疗法可以刺激白癜风患者的色素再生,且不良反应极少。Q开关红宝石激光和FD Nd:YAG激光提供了可行的可见光脱色选择,可单独使用或与外用药物一起使用。由于临床数据有限,需要进行更大规模的研究,以验证可见光疗法治疗白癜风的疗效,并更好地了解其长期疗效。
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来源期刊
CiteScore
4.40
自引率
7.70%
发文量
85
审稿时长
6-12 weeks
期刊介绍: The journal is a forum for new information about the direct and distant effects of electromagnetic radiation (ultraviolet, visible and infrared) mediated through skin. The divisions of the editorial board reflect areas of specific interest: aging, carcinogenesis, immunology, instrumentation and optics, lasers, photodynamic therapy, photosensitivity, pigmentation and therapy. Photodermatology, Photoimmunology & Photomedicine includes original articles, reviews, communications and editorials. Original articles may include the investigation of experimental or pathological processes in humans or animals in vivo or the investigation of radiation effects in cells or tissues in vitro. Methodology need have no limitation; rather, it should be appropriate to the question addressed.
期刊最新文献
Subjective and objective assessment of color match of universal tinted sunscreens in Fitzpatrick skin phototypes I-VI. Immunofluorescence findings in a reactivating lichenoid photoallergic chronic dermatitis (actinic reticuloid). Sunscreens prescribed to patients with skin of color and/or with melasma: A survey of 221 dermatologists and dermatology residents in Spain. Phototherapy for the treatment of cutaneous graft-versus-host disease: A systematic review. KGF-2 ameliorates UVB-triggered skin photodamage in mice by attenuating DNA damage and inflammatory response and mitochondrial dysfunction.
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