Recent studies have reported that pro‐inflammatory mediators and cytokines related to innate immune responses and insulin resistance related factors, which induce sebaceous lipogenesis, sebocyte, and keratinocyte proliferation via milk consumption and hyperglycemic diets, are important roles in the pathogenesis of acne vulgaris. However, current level of evidence is poor to sufficiently explain the pathophysiology of acne vulgaris. Therefore, this study was designed to find out the molecular biological and metabolism bio‐marker between healthy population and patients with acne vulgaris. The study will consist of 40 healthy subjects and 60 patients with acne vulgaris. The molecular biological biomarker will be analyzed with the use of several cytokines (IL‐1α, IL‐1β, IL‐12 β, IL‐15, IL‐6 and TNF α) and chemokines (MCP‐1 and IL‐8) examinined by ELISA, real‐time PCR, or Western blot assay, whereas the metabolism biomarker will be assessed with steroidal hormones (DHEA, androstenedione, testosterone, DHT, estrone, and estradiol), saturated / trans‐fats (palmitic acid, elaidic acid, etc.) and untargeted markers related to TCA cycle by using the LC‐MS. We will examine skin sebum, skin surface temperature and skin viscosity elasticity in constant temperature and humidity room at Korean Medicine Clinical Trial Center, Kyung Hee University Korean Medicine Hospital (Seoul, Republic of Korea). In addition, we will collect the information including their diet pattern, menstruation (only female), medication history, smoking, and sleep pattern from subjects through a questionnaire.Support or Funding InformationThis study was supported by a grant from the Traditional Korean Medicine R&D Project, Ministry of Health & Welfare, Republic of Korea. (HI16C0801)
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