Biomarkers and clinical indicators of disease activity in vitiligo

Liesbeth Delbaere, Reinhart Speeckaert, Sandrine Herbelet, Arno Belpaire, Jolien Duponselle, Nanja van Geel
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Abstract

Background: The management of vitiligo is guided by the assessment of disease activity. However, this assessment is hampered by the absence of a highly feasible and reliable single marker to evaluate activity. Furthermore, the need for an objective, easy, preferably noninvasive marker is further stressed by the increased amount of research performed on new treatment strategies for vitiligo.

Objectives: In this review, the available research on clinical signs linked to disease activity, and biomarkers in tissues and blood are summarized.

Results: In the group of clinical signs, the Koebner phenomenon has the strongest evidence of an association with disease activity, while confetti-like depigmentation is gaining importance and seems to outweigh this role. For the tissue markers, the most evidence is available for histopathological findings, such as epidermal spongiosis with vacuolar degeneration in the basal cells and inflammatory infiltrate. Circulating biomarkers such as interleukin-1β (IL-1β), IL-17, interferon-γ, tumor growth factor-β, soluble cluster of differentiation 25, autoantibodies, and oxidative stress markers show the most promising results. Nevertheless, none of them are currently regarded as the gold standard.

Discussion: In conclusion, we encourage researchers to investigate various biomarkers and clinical signs in their trials in a standardized manner to get insight into their exact value, so they can be used to optimize treatment selection, gain insight into the disease, and predict future disease progression.

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白癜风疾病活动性的生物标志物和临床指标
背景:白癜风的治疗以疾病活动性评估为指导。然而,由于缺乏高度可行和可靠的单一标志物来评估活性,这种评估受到阻碍。此外,对白癜风新治疗策略的研究越来越多,进一步强调需要一种客观、简单、最好是非侵入性的标志物。目的:本文综述了与疾病活动相关的临床体征以及组织和血液中生物标志物的研究进展。结果:在临床症状组中,Koebner现象与疾病活动相关的证据最强,而五彩纸屑样色素沉着越来越重要,似乎超过了这一作用。对于组织标志物,最有力的证据是组织病理学发现,如表皮海绵状病伴基底细胞空泡变性和炎症浸润。循环生物标志物,如白细胞介素-1β (IL-1β)、IL-17、干扰素-γ、肿瘤生长因子-β、可溶性分化簇25、自身抗体和氧化应激标志物显示出最有希望的结果。然而,目前没有一个被认为是黄金标准。讨论:总之,我们鼓励研究人员在他们的试验中以标准化的方式调查各种生物标志物和临床体征,以了解它们的确切价值,从而可以用于优化治疗选择,深入了解疾病,并预测未来的疾病进展。
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