Proteomics data in vitiligo: a scoping review

Danique Berrevoet, Filip Van Nieuwerburgh, Dieter Deforce, Reinhart Speeckaert
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Abstract

An unbiased screening of which proteins are deregulated in vitiligo using proteomics can offer an enormous value. It could not only reveal robust biomarkers for detecting disease activity but can also identify which patients are most likely to respond to treatments. We performed a scoping review searching for all articles using proteomics in vitiligo. Eight manuscripts could be identified. Unfortunately, very limited overlap was found in the differentially expressed proteins between studies (15 out of 272; 5,51%) with variable degrees of the type of proteins and a substantial variety in the prevalence of acute phase proteins (range: 6-65%). Proteomics research has therefore brought little corroborating evidence on which proteins are differentially regulated between vitiligo patients and healthy controls or between active and stable vitiligo patients. While a limited patient size is an obvious weakness for several studies, an incomplete description of patient characteristics is an unfortunate and avoidable shortcoming. Additionally, the variations in the used methodology and analyses may further contribute to the overall observed variability. Nonetheless, more recent studies investigating the response to treatment seem to be more robust, as more differentially expressed proteins that have previously been confirmed to be involved in vitiligo were found. The further inclusion of proteomics analyses in clinical trials is recommended to increase insights into the pathogenic mechanisms in vitiligo and identify reliable biomarkers or promising drug targets. A harmonization in the study design, reporting and proteomics methodology could vastly improve the value of vitiligo proteomics research.
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白癜风的蛋白质组学数据:范围综述
利用蛋白质组学对白癜风患者体内哪些蛋白质发生了失调进行无偏见的筛查具有巨大的价值。它不仅能揭示检测疾病活动的可靠生物标志物,还能确定哪些患者最有可能对治疗产生反应。我们对所有使用蛋白质组学研究白癜风的文章进行了范围界定。共找到 8 篇手稿。遗憾的是,我们发现不同研究之间差异表达蛋白质的重叠非常有限(272 篇中有 15 篇,占 5.51%),蛋白质的类型各不相同,急性期蛋白质的比例也有很大差异(范围:6-65%)。因此,蛋白质组学研究几乎没有提供确凿证据,证明哪些蛋白质在白癜风患者和健康对照组之间或在活动期和稳定期白癜风患者之间受到不同程度的调控。虽然患者人数有限是几项研究的明显弱点,但对患者特征描述不完整也是一个令人遗憾且可以避免的缺陷。此外,所用方法和分析的不同也可能进一步导致观察到的总体差异。尽管如此,最近对治疗反应的调查研究似乎更加可靠,因为发现了更多以前已证实与白癜风有关的差异表达蛋白。建议在临床试验中进一步纳入蛋白质组学分析,以加深对白癜风发病机制的了解,并确定可靠的生物标志物或有前景的药物靶点。统一研究设计、报告和蛋白质组学方法可大大提高白癜风蛋白质组学研究的价值。
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