van Keulen Britt J, Dolan Conor V, Andrew Ruth, Walker Brian R, Hulshoff Pol Hilleke E, Boomsma Dorret I, Rotteveel Joost, Finken Martijn J J
Emma Children's Hospital, Amsterdam UMC, Vrije Universiteit Amsterdam, Pediatric Endocrinology, Amsterdam, the Netherlands.
Department of Biological Psychology, Vrije Universiteit Amsterdam, Amsterdam, the Netherlands.
Twin Res Hum Genet. 2020 Feb;23(1):33-38. doi: 10.1017/thg.2020.6. Epub 2020 Mar 25.
Life-course experiences have been postulated to program hypothalamus-pituitary-adrenal (HPA) axis activity, suggesting that HPA axis activity is, at least partially, stable over time. Yet, there is paucity of data on the long-term stability of cortisol production and metabolism. We performed a prospective follow-up study in twins recruited from a nationwide register to estimate the stability of cortisol production and metabolism over time, and the contribution of genetic and environmental factors to this stability. In total, 218 healthy mono- and dizygotic twins were included. At the ages of 9, 12 and 17 years, morning urine samples were collected for assessment (by gas chromatography-tandem mass spectrometry) of cortisol metabolites, enabling the calculation of cortisol metabolite excretion rate and cortisol metabolism activity. Our results showed a low stability for both cortisol metabolite excretion rate (with correlations <.20) and cortisol metabolism activity indices (with correlations of .25 to .46 between 9 and 12 years, -.02 to .15 between 12 and 17 years and .09 to .28 between 9 and 17 years). Because of the low stability over time, genetic and environmental contributions to this stability were difficult to assess, although it seemed to be mostly determined by genetic factors. The low stability in both cortisol production and metabolism between ages 9 and 17 years reflects the dynamic nature of the HPA axis.
生命历程经历被假定为可对下丘脑 - 垂体 - 肾上腺(HPA)轴活动进行编程,这表明HPA轴活动至少在一定程度上随时间推移是稳定的。然而,关于皮质醇产生和代谢的长期稳定性的数据却很匮乏。我们对从全国登记册招募的双胞胎进行了一项前瞻性随访研究,以估计皮质醇产生和代谢随时间的稳定性,以及遗传和环境因素对这种稳定性的贡献。总共纳入了218名健康的单卵和双卵双胞胎。在9岁、12岁和17岁时,采集晨尿样本(通过气相色谱 - 串联质谱法)用于评估皮质醇代谢物,从而能够计算皮质醇代谢物排泄率和皮质醇代谢活性。我们的结果显示,皮质醇代谢物排泄率(相关性<0.20)和皮质醇代谢活性指数(9至12岁之间的相关性为0.25至0.46,12至17岁之间为 - 0.02至0.15,9至17岁之间为0.09至0.28)的稳定性都较低。由于随时间的稳定性较低,尽管似乎主要由遗传因素决定,但遗传和环境对这种稳定性的贡献难以评估。9至17岁之间皮质醇产生和代谢的低稳定性反映了HPA轴的动态性质。