Li Min, Zhan Dan Dan, Fan Li Li, Wang Yu, Hu Xiao Han, Zhang Ming, Zhou Zhou
Department of Dermatology, Chinese People's Liberation Army Western Theater Command General Hospital, Chengdu, China.
J Cosmet Dermatol. 2025 Jan;24(1):e16763. doi: 10.1111/jocd.16763.
Acne is a common skin disorder that may be linked to metabolic dysfunction. However, the causal impact of blood metabolites on acne has not been thoroughly investigated.
We performed a metabolome-wide Mendelian randomization (MR) analysis on 486 blood metabolites and acne using a genome-wide association dataset. The study included preliminary inverse-variance weighted (IVW) analysis, multivariable MR analysis, linkage disequilibrium score (LDSC) analysis, and colocalization analysis, along with reverse MR to address potential reverse causation.
Our analysis identified 12 metabolites significantly associated with acne. LDSC analysis revealed a genetic correlation between nonanoylcarnitine and acne. Colocalization analysis confirmed shared genetic variants, and metabolic pathway analysis implicated the arginine biosynthesis pathway and the selenocompound metabolism pathway in the development of acne.
This study offers a comprehensive understanding of the causal relationships between plasma metabolites and acne. The findings provide insights into potential biomarkers and therapeutic targets for acne treatment, underscoring the need for further research.
痤疮是一种常见的皮肤疾病,可能与代谢功能障碍有关。然而,血液代谢物对痤疮的因果影响尚未得到充分研究。
我们使用全基因组关联数据集对486种血液代谢物和痤疮进行了全代谢组孟德尔随机化(MR)分析。该研究包括初步的逆方差加权(IVW)分析、多变量MR分析、连锁不平衡评分(LDSC)分析和共定位分析,以及反向MR以解决潜在的反向因果关系。
我们的分析确定了12种与痤疮显著相关的代谢物。LDSC分析揭示了壬酰肉碱与痤疮之间的遗传相关性。共定位分析证实了共享的遗传变异,代谢途径分析表明精氨酸生物合成途径和硒化合物代谢途径与痤疮的发生有关。
本研究全面了解了血浆代谢物与痤疮之间的因果关系。这些发现为痤疮治疗的潜在生物标志物和治疗靶点提供了见解,强调了进一步研究的必要性。