press release
Published: 02 October 2024

Dementia diagnostic markers change with time of day

The time of day when blood is taken can affect the results of tests for diagnosing dementia, according to new research led by the University of Surrey.  

Researchers found that the biomarkers used to diagnose Alzheimer's, including a promising marker for early diagnosis of the condition, varied significantly depending on the time of day. Biomarker levels were at their lowest in the morning when participants woke and highest in the evening.  

The p-tau217 biomarker, which could help with early diagnosis of dementia, showed big differences depending on the time of day. Researchers discovered that the variation between morning and evening levels was similar to the changes seen in people whose mild memory problems get worse over a year. 

The study looked at 38 participants living with mild Alzheimer's, their caregivers and health controls while they were residents at the Surrey Sleep Research Centre, which is part of the UK Dementia Research Institute’s (UK DRI) Care Research & Technology Centre. 

Instead of taking one blood sample, as is the case in the majority of clinical practices, the participants had their blood taken every three hours for 24 hours.  

Four out of five measured biomarkers (p-tau217, Aβ40, Aβ42, and NfL) showed levels of fluctuation throughout the day. Only GFAP did not show a statistically significant variation. 

Currently, it is not known what is driving these time-of-day differences.  It may relate to sleep and sleep-related reduction in the production or clearance of these markers from the brain to the circulation, meals, posture, activity, or circadian mechanisms. Nevertheless, the findings imply that the time of day of sample collection is relevant in the implementation and interpretation of plasma biomarkers in dementia research and care. Overall, these findings indicate that the time of sampling should be standardised or at least recorded.   

The study has been published in Translational Psychiatry

 

Note to editors 

 

  • The study was conducted at the University of Surrey by researchers funded by the UK Dementia Research Institute's (UK DRI) Care Research and Technology Centre based at Imperial College London and the University of Surrey and in close collaboration with the UK DRI’s Biomarker Factory at UCL.   

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