Ong Michael M, Zhou Maggie H, Singal Amit, Lipner Shari R
MD Program, Weill Cornell Medical College, New York, NY, USA.
Columbia University Vagelos College of Physicians and Surgeons, New York, NY, USA.
Skin Appendage Disord. 2025 Jun 4. doi: 10.1159/000546799.
Central centrifugal cicatricial alopecia (CCCA) is a primary scarring alopecia with unclear etiology. Emerging evidence suggests an association with metabolic dysregulation, including altered protein levels in affected scalp tissue and increased insulin resistance. This study investigated potential associations between CCCA and metabolic dysfunction using a large, multicenter database.
Using the TriNetX database, we analyzed 2,482 black women with CCCA and 2,482 propensity score-matched controls with other primary scarring alopecias (2004-2024). Metabolic disorders and laboratory values were compared (Benjamini-Hochberg-adjusted < 0.0042).
CCCA patients showed no differences in incidence of type 2 diabetes (19.7% vs. 19.5%, = 0.591), prediabetes (17.8% vs. 21.0%, = 0.265), obesity (30.9% vs. 38.5%, = 0.054), or metabolic syndrome (1.4% vs. 1.2%, = 0.404) compared to controls. CCCA patients had lower hypertension incidence (39.7% vs. 49.5%, < 0.0001), higher HDL (58.0 vs. 55.5 mg/dL, = 0.0016), and lower triglyceride (96.4 vs. 106.3 mg/dL, = 0.0001) values.
We found that CCCA was not associated with most metabolic disorders. Thus, metabolic screening in CCCA patients should be individualized based on history and review of systems. Future research exploring genetic, inflammatory, and autoimmune pathways in CCCA pathogenesis is needed.
中心离心性瘢痕性秃发(CCCA)是一种病因不明的原发性瘢痕性秃发。新出现的证据表明其与代谢失调有关,包括受累头皮组织中蛋白质水平的改变和胰岛素抵抗增加。本研究使用一个大型多中心数据库调查了CCCA与代谢功能障碍之间的潜在关联。
我们使用TriNetX数据库分析了2482名患有CCCA的黑人女性和2482名倾向得分匹配的其他原发性瘢痕性秃发对照者(2004 - 2024年)。比较了代谢紊乱和实验室值(经Benjamini - Hochberg校正<0.0042)。
与对照组相比,CCCA患者在2型糖尿病发病率(19.7%对19.5%,P = 0.591)、糖尿病前期(17.8%对21.0%,P = 0.265)、肥胖(30.9%对38.5%,P = 0.054)或代谢综合征(1.4%对1.2%,P = 0.404)方面无差异。CCCA患者的高血压发病率较低(39.7%对49.5%,P<0.0001),高密度脂蛋白较高(58.0对55.5mg/dL,P = 0.0016),甘油三酯较低(96.4对106.3mg/dL,P = 0.0001)。
我们发现CCCA与大多数代谢紊乱无关。因此,CCCA患者的代谢筛查应根据病史和系统回顾进行个体化。未来需要研究探索CCCA发病机制中的遗传、炎症和自身免疫途径。