Dermatology Unit, Federal Medical Centre, Keffi, Nasarawa, Nigeria.
Laboratory of Cutaneous Physiopathology, San Gallicano Dermatological Institute-IRCCS, Rome, Italy.
Sci Rep. 2021 Aug 16;11(1):16591. doi: 10.1038/s41598-021-96043-x.
Lipidomics is advantageous in the study of sebum perturbations occurring in acne. An extended evaluation of the sebum lipid profiles in acne-prone sebaceous areas is lacking in dark skin. Yet, there is a void space in understanding how the building blocks of sebum lipids, i.e. individual fatty acids (FAs), are intertwined with acne-prone skin. We aimed to determine the sebum lipidome in facial areas of adolescents with and without acne in Nigeria. A cross-sectional analytical study was conducted in 60 adolescents/young adults divided in 30 acne patients (15F, 15M) and 30 age and sex-matched controls. Sebum samples obtained from foreheads and cheeks were analysed separately by gas chromatography-mass spectrometry (GCMS) and thin layer chromatography (HPTLC). Distributions of sebum components were investigated with multivariate ANOVA-simultaneous component analysis (ASCA). Sebum incretion in acne was paralleled by significantly higher abundance of triglycerides, wax esters, and squalene together with monounsaturated FAs (MUFAs), and straight chain saturated FAs (SFAs), especially those with odd-carbon chain, i.e. C13:0, C15:0, and C17:0. Profiling weight/weight percentage of individual components revealed that, in acne, the free FAs (FFAs) array was shifted towards higher relative abundance of the SFAs C15:0, C16:0, and C17:0 and lower percentage of the anteiso-branched FFAs with 12, 14, 16, and 18 carbons. In acne patients, MUFAs and PUFAs were quantitatively increased and decreased on foreheads and cheeks, respectively. Relative abundance of fatty alcohols was decreased in acne independent on the site. The results indicated that acne associates with site-specific derangement of the pathways regulating the balance among odd straight-chain and branched-chain SFAs, MUFAs, which included sapienate (C16:1n-10), PUFAs, and squalene.
脂质组学在研究痤疮中皮脂的变化方面具有优势。在深色皮肤中,对痤疮皮脂腺区域皮脂脂质谱的扩展评估是缺乏的。然而,对于皮脂脂质的组成部分,即单个脂肪酸(FAs),如何与易患痤疮的皮肤交织在一起,我们的理解还存在空白。我们旨在确定尼日利亚青少年痤疮患者和非痤疮患者面部皮脂的脂质组学。在 60 名青少年/年轻人中进行了一项横断面分析研究,他们分为 30 名痤疮患者(15 名女性,15 名男性)和 30 名年龄和性别匹配的对照组。通过气相色谱-质谱法(GCMS)和薄层色谱(HPTLC)分别分析来自前额和脸颊的皮脂样本。使用多元方差分析-同时成分分析(ASCA)研究皮脂成分的分布。痤疮中的皮脂分泌增加伴随着甘油三酯、蜡酯和角鲨烯以及单不饱和脂肪酸(MUFAs)和直链饱和脂肪酸(SFAs)的含量显著增加,特别是那些具有奇数碳链的脂肪酸,即 C13:0、C15:0 和 C17:0。对个体成分的重量/重量百分比进行分析表明,在痤疮中,游离脂肪酸(FFAs)的排列向更高的相对丰度的 SFAs C15:0、C16:0 和 C17:0 和较低的 12、14、16 和 18 个碳原子的支链 FFAs 百分比转变。在痤疮患者中,MUFAs 和 PUFAs 在额头上和脸颊上分别定量增加和减少。脂肪酸醇的相对丰度在痤疮中减少,与部位无关。研究结果表明,痤疮与调节奇数直链和支链 SFAs、MUFAs 之间平衡的途径的特定部位失调有关,其中包括sapienate(C16:1n-10)、PUFAs 和角鲨烯。