Laboratory of Cutaneous Physiopathology and Integrated Center of Metabolomics Research, San Gallicano Dermatological Institute, IRCCS, 00144 Rome, Italy.
Microbiology and Virology, San Gallicano Dermatological Institute, IRCCS, 00144 Rome, Italy.
Int J Mol Sci. 2024 Sep 23;25(18):10201. doi: 10.3390/ijms251810201.
While vitiligo is primarily caused by melanocyte deficiency or dysfunction, recent studies have revealed a notable prevalence of metabolic syndrome (MetS) among patients with vitiligo. This suggests shared pathogenic features between the two conditions. Individuals with vitiligo often exhibit variations in triglyceride levels, cholesterol, and blood pressure, which are also affected in MetS. Given the similarities in their underlying mechanisms, genetic factors, pro-inflammatory signalling pathways, and increased oxidative stress, this study aims to highlight the common traits between vitiligo and metabolic systemic disorders. Serum analyses confirmed increased low-density lipoprotein (LDL) levels in patients with vitiligo, compared to physiological values. In addition, we reported significant decreases in folate and vitamin D (Vit D) levels. Oxidative stress is one of the underlying causes of the development of metabolic syndromes and is related to the advancement of skin diseases. This study found high levels of inflammatory cytokines, such as interleukin-6 (IL-6) and chemokine 10 (CXCL10), which are markers of inflammation and disease progression. The accumulation of insulin growth factor binding proteins 5 (IGFBP5) and advanced glycation end products (AGEs) entailed in atherosclerosis and diabetes onset, respectively, were also disclosed in vitiligo. In addition, the blood-associated activity of the antioxidant enzymes catalase (Cat) and superoxide dismutase (SOD) was impaired. Moreover, the plasma fatty acid (FAs) profile analysis showed an alteration in composition and specific estimated activities of FAs biosynthetic enzymes resembling MetS development, resulting in an imbalance towards pro-inflammatory n6-series FAs. These results revealed a systemic metabolic alteration in vitiligo patients that could be considered a new target for developing a more effective therapeutic approach.
虽然白癜风主要是由于黑素细胞缺乏或功能障碍引起的,但最近的研究表明,白癜风患者中代谢综合征(MetS)的患病率显著升高。这表明这两种疾病存在共同的发病特征。白癜风患者常表现出血甘油三酯水平、胆固醇和血压的变化,而代谢综合征也会受到影响。鉴于它们在潜在机制、遗传因素、促炎信号通路和氧化应激增加方面的相似性,本研究旨在强调白癜风和代谢性全身性疾病之间的共同特征。血清分析证实,白癜风患者的低密度脂蛋白(LDL)水平升高,超过了生理值。此外,我们还报告叶酸和维生素 D(Vit D)水平显著降低。氧化应激是代谢综合征发展的潜在原因之一,与皮肤疾病的进展有关。本研究发现,炎症细胞因子如白细胞介素-6(IL-6)和趋化因子 10(CXCL10)的水平升高,这些都是炎症和疾病进展的标志物。在白癜风中还发现了胰岛素生长因子结合蛋白 5(IGFBP5)和晚期糖基化终产物(AGEs)的积累,分别与动脉粥样硬化和糖尿病的发生有关。此外,抗氧化酶过氧化氢酶(Cat)和超氧化物歧化酶(SOD)的血液相关活性受损。此外,血浆脂肪酸(FAs)谱分析显示,组成和特定估计的 FA 生物合成酶的活性发生改变,类似于 MetS 的发展,导致促炎 n6 系列 FA 的不平衡。这些结果揭示了白癜风患者的系统性代谢改变,这可能被认为是开发更有效的治疗方法的新目标。