Department of Biomedical and Clinical Sciences, Division of Clinical Chemistry and Pharmacology, Linköping University, Linköping, Sweden.
Department of Neurology, Faculty of Medicine and Health, Örebro University, Örebro, Sweden.
Sci Rep. 2023 Sep 25;13(1):16015. doi: 10.1038/s41598-023-41672-7.
Testosterone is thought to be incorporated in growing hair strands so that specific hair segments reflect average free hormone concentrations from the corresponding time period. However, the exact mechanisms of hormone integration in scalp hair have not yet been established and it is not known how testosterone is stored in the hair segments over time. The aim of this study was to investigate the stability of testosterone concentrations in hair as it grows and to determine if segmental hair analysis can be used as a retrospective testosterone diary. Thirty men and 40 women provided two hair samples and 16 saliva samples during a period of three months. Hair growth between the two samplings was measured. Hair samples were cut into 10 mm segments resulting in three segments from the first sampling and six segments from the second sampling. Hair samples were pulverised and extracted with methanol. Hair testosterone concentrations were analysed using an in-house radioimmunoassay. Salivary testosterone was analysed using a commercial enzyme-linked immunosorbent assay (Demeditec). The results demonstrated that there is a degree of segmental hormone conservation over time (rho = 0.405-0.461, p < 0.001, n = 66-67), but also highlighted three potential confounders. Firstly, testosterone concentrations were higher in distal hair segments (mean concentration ratio most distal by most scalp-near was 1.55, SD 0.70), which may be due to continuous hormone integration from sebum and changes in hair matrix composition. Secondly, more frequent hair washing stunted the increase in testosterone concentrations in distal segments (rho = -0.404, p = < 0.001, n = 66). And lastly, intra- and inter- individual variability in hair growth rate influenced the temporal resolution along the hair, although mean growth rate was indeed 30.0 mm for three months. In a multiple regression model the biological sex, natural hair colour, and relationship status were significant explanatory variables to hair testosterone concentrations. The current results indicate that repeated hair sampling near the hair roots during a study may be preferable to analysing concentration changes between proximal and distal segments within the same hair sample. Also, hair testosterone analysis needs to be adjusted for sex and the natural hair colour.
睾酮被认为是在生长中的头发丝中被结合,因此特定的头发段反映了相应时间段内的游离激素的平均浓度。然而,激素在头皮头发中的整合的确切机制尚未建立,也不知道睾酮随着时间的推移是如何储存在头发段中的。本研究的目的是研究睾酮在头发生长过程中的浓度稳定性,并确定分段头发分析是否可作为回顾性睾酮日记。30 名男性和 40 名女性在三个月期间提供了两份头发样本和 16 份唾液样本。测量两次采样之间的头发生长。将头发样本切成 10mm 的段,从第一次采样中得到 3 段,从第二次采样中得到 6 段。将头发样本粉碎并用甲醇提取。使用内部放射免疫分析法分析头发中的睾酮浓度。使用商业酶联免疫吸附测定法(Demeditec)分析唾液中的睾酮。结果表明,随着时间的推移,存在一定程度的激素片段保存(rho=0.405-0.461,p<0.001,n=66-67),但也突出了三个潜在的混杂因素。首先,远端头发段中的睾酮浓度较高(最远端与最接近头皮的平均浓度比为 1.55,SD 0.70),这可能是由于皮脂的持续激素整合和毛基质成分的变化。其次,更频繁的洗发会阻碍远端段睾酮浓度的增加(rho=-0.404,p<0.001,n=66)。最后,头发生长速度的个体内和个体间变异性影响了头发上的时间分辨率,尽管三个月的平均生长速度确实为 30.0mm。在多元回归模型中,生物学性别、自然发色和关系状况是头发睾酮浓度的显著解释变量。目前的结果表明,在研究期间在靠近发根的地方重复进行头发采样可能比分析同一头发样本中近端和远端段之间的浓度变化更好。此外,头发睾酮分析需要根据性别和自然发色进行调整。