From the MRC Unit for Lifelong Health and Ageing at UCL (A.T., M.R., D.D.) and Department of Epidemiology and Public Health (A.S.-M.), University College London, UK; Epidemiology of Ageing & Neurodegenerative Diseases (A.S.-M.), INSERM, U1153, Hotel Dieu, Paris, France; Neuroepidemiology and Ageing Research Unit (C.U.-M.), School of Public Health, Faculty of Medicine, The Imperial College of Science, Technology and Medicine, London; and Translational Health Sciences (C.U.-M.), Bristol Medical School, University of Bristol, UK.
Neurology. 2020 Jan 14;94(2):e133-e141. doi: 10.1212/WNL.0000000000008729. Epub 2019 Dec 12.
To determine whether hypothalamus-pituitary-adrenal axis (HPAA) dysfunction is prospectively associated with global cognitive impairment in later life.
This cross-cohort study integrates 2 large longitudinal datasets, Whitehall II and the National Survey for Health and Development (NSHD), on data collected in the Whitehall II study between 2002-2004, 2007-2009, and 2012-2013; and for NSHD between 2006-2010 and in 2015. Serial salivary cortisol samples were collected multiple times within a 24-hour period at mean ages 61.2 and 65.9 years in Whitehall II and at age 60-64 years from NSHD participants. Cortisol profile is defined using cortisol awakening response and am:pm ratio. Cognitive function was measured using the Mini-Mental State Examination in Whitehall II and Addenbrooke's Cognitive Examination, third version, in NSHD, harmonized into a 30-point score. Models were adjusted for age, sex, diagnoses of hypertension and diabetes, body mass index (BMI), educational attainment, and interval between HPAA and cognitive assessments.
In fully adjusted models, increased am:pm cortisol ratio was prospectively associated with better later-life cognitive function years later (0.02 fewer errors per SD increase in am:pm cortisol ratio, < 0.01) and verbal fluency (0.03 SD increase in verbal fluency per SD increase in am:pm ratio, < 0.01). Increasing age, lower educational attainment, diagnosis of hypertension, diagnosis of diabetes, and increased BMI were associated with worse cognitive function and poorer verbal fluency. There were no associations between depression and later-life cognition or reverse associations between cognition and later-life cortisol profiles.
Loss of diurnal HPAA variation is evident in individuals subsequently experiencing more cognitive impairment. It may serve as an early preclinical marker of cognitive decline.
确定下丘脑-垂体-肾上腺轴(HPAA)功能障碍是否与晚年的整体认知障碍存在前瞻性关联。
本交叉队列研究整合了两个大型纵向数据集,即白厅二世和国家健康与发展调查(NSHD),数据来自于白厅二世研究在 2002-2004 年、2007-2009 年和 2012-2013 年期间的收集,以及 NSHD 在 2006-2010 年和 2015 年期间的收集。在白厅二世研究中,在参与者的平均年龄为 61.2 岁和 65.9 岁时的 24 小时内多次采集唾液皮质醇样本;在 NSHD 参与者中,在 60-64 岁时采集样本。皮质醇谱通过皮质醇觉醒反应和 am:pm 比值来定义。在白厅二世研究中使用简易精神状态检查,在 NSHD 中使用 Addenbrooke 的认知测验,第三版,将认知功能测量结果统一为 30 分。模型调整了年龄、性别、高血压和糖尿病诊断、体重指数(BMI)、教育程度以及 HPAA 和认知评估之间的间隔。
在完全调整的模型中,am:pm 皮质醇比值的增加与以后的晚年认知功能较好相关(am:pm 皮质醇比值每增加一个标准差,错误减少 0.02, < 0.01)和语言流畅性(am:pm 比值每增加一个标准差,语言流畅性增加 0.03 个标准差, < 0.01)。年龄增长、教育程度较低、高血压诊断、糖尿病诊断和 BMI 增加与认知功能较差和语言流畅性较差相关。抑郁与晚年认知之间没有关联,认知与晚年皮质醇谱之间也没有反向关联。
在随后经历更多认知障碍的个体中,明显存在昼夜 HPAA 变化的丧失。它可能是认知能力下降的早期临床前标志物。