Department of Dermatology, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.
Department of Dermatology, Anhui Public Health Clinical Center, Hefei, Anhui, China.
J Cosmet Dermatol. 2024 Sep;23(9):3038-3044. doi: 10.1111/jocd.16371. Epub 2024 May 13.
Male androgenetic alopecia (MAA) is a multifactorial disease, with patients presenting at a younger age, which is a risk factor for many metabolic diseases.
To explore the risk factors associated with early-onset of MAA and its metabolic characteristics.
Forty patients with MAA and 45 healthy controls were collected. The serum levels of fasting blood glucose (FBG), total cholesterol (TC), triglyceride (TG), high-density lipoprotein cholesterol (HDL-C), low-density lipoprotein cholesterol (LDL-C), total testosterone (TT), uric acid (UA), and 25-hydroxyvitamin D (25(OH)D) were measured. Meanwhile, lipid metabolites were detected by ultra-high-performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS).
37.50% MAA patients had metabolic syndrome, compared to 17.78% in control group (p < 0.05). The levels of HDL-C, UA, and 25(OH)D were decreased in patients with MAA compared to healthy controls (p < 0.05). However, there was no significant difference in the level of TT between the two groups. Additionally, there were no significant differences in the levels of HDL-C, UA, 25(OH)D, and TT among different grades of hair loss (p > 0.05). The lipid profile of early-onset MAA differed significantly from healthy controls. In early-onset MAA, the levels of ceramide (Cer) and sphingomyelin (SM) were significantly lower. Cer(d38:5) and TG(15:0/18:1/18:1) may be the biomarkers.
Low HDL-C, UA, and 25(OH)D may be the independent risk factors for early-onset MAA. Abnormal lipid metabolism was observed in early-onset MAA, wherein Cer and SM may serve as protective factors.
男性雄激素性脱发(MAA)是一种多因素疾病,患者发病年龄较早,这是许多代谢性疾病的危险因素。
探讨早发性 MAA 的相关危险因素及其代谢特征。
收集 40 例 MAA 患者和 45 例健康对照者。检测空腹血糖(FBG)、总胆固醇(TC)、甘油三酯(TG)、高密度脂蛋白胆固醇(HDL-C)、低密度脂蛋白胆固醇(LDL-C)、总睾酮(TT)、尿酸(UA)和 25-羟维生素 D(25(OH)D)水平。同时,采用超高效液相色谱-串联质谱法(UHPLC-MS/MS)检测脂类代谢物。
37.50%的 MAA 患者合并代谢综合征,高于对照组的 17.78%(p<0.05)。与健康对照组相比,MAA 患者的 HDL-C、UA 和 25(OH)D 水平降低(p<0.05)。但两组 TT 水平无显著差异。此外,不同脱发程度的患者之间 HDL-C、UA、25(OH)D 和 TT 水平无显著差异(p>0.05)。早发性 MAA 的血脂谱与健康对照组有显著差异。早发性 MAA 患者中,神经酰胺(Cer)和神经鞘磷脂(SM)水平显著降低。Cer(d38:5)和 TG(15:0/18:1/18:1)可能是生物标志物。
低 HDL-C、UA 和 25(OH)D 可能是早发性 MAA 的独立危险因素。早发性 MAA 存在异常的脂代谢,Cer 和 SM 可能是保护因素。