Elsevier

Sleep Medicine

Volume 38, October 2017, Pages 85-91
Sleep Medicine

Original Article
Sleep and cognitive performance: cross-sectional associations in the UK Biobank

https://doi.org/10.1016/j.sleep.2017.07.001Get rights and content

Highlights

  • How different aspects of sleep health relate to cognition is unclear.

  • We examined sleep and cognitive performance in ∼500,000 adults aged 40–69 years.

  • Unexpectedly, frequent insomnia symptoms were independently associated with better cognitive performance.

  • Sleep medication and long and short sleep durations were linked to cognitive impairment.

  • Morningness was linked to impairment, while eveningness showed superior performance.

Abstract

Objective

The relationship between insomnia symptoms and cognitive performance is unclear, particularly at the population level. We conducted the largest examination of this association to date through analysis of the UK Biobank, a large population-based sample of adults aged 40–69 years. We also sought to determine associations between cognitive performance and self-reported chronotype, sleep medication use and sleep duration.

Methods

This cross-sectional, population-based study involved 477,529 participants, comprising 133,314 patients with frequent insomnia symptoms (age: 57.4 ± 7.7 years; 62.1% female) and 344,215 controls without insomnia symptoms (age: 56.1 ± 8.2 years; 52.0% female). Cognitive performance was assessed by a touchscreen test battery probing reasoning, basic reaction time, numeric memory, visual memory, and prospective memory. Adjusted models included relevant demographic, clinical, and sleep variables.

Results

Frequent insomnia symptoms were associated with cognitive impairment in unadjusted models; however, these effects were reversed after full adjustment, leaving those with frequent insomnia symptoms showing statistically better cognitive performance over those without. Relative to intermediate chronotype, evening chronotype was associated with superior task performance, while morning chronotype was associated with the poorest performance. Sleep medication use and both long (>9 h) and short (<7 h) sleep durations were associated with impaired performance.

Conclusions

Our results suggest that after adjustment for potential confounding variables, frequent insomnia symptoms may be associated with a small statistical advantage, which is unlikely to be clinically meaningful, on simple neurocognitive tasks. Further work is required to examine the mechanistic underpinnings of an apparent evening chronotype advantage in cognitive performance and the impairment associated with morning chronotype, sleep medication use, and sleep duration extremes.

Introduction

Insomnia is defined as persistent difficulties with sleep initiation and/or maintenance, resulting in significant impairment to daytime functioning. At the symptom level, insomnia affects up to one-third of the adult population, while persistent insomnia affects approximately 10–12% and is associated with increased risk for cardiovascular disease, depression, and early mortality [1], [2]. Both daytime functioning and quality of life are known to be severely affected in those with insomnia and often drive treatment seeking [3], [4], [5]. More specifically, previous work shows that the most commonly cited areas of daytime dysfunction are problems with fatigue, work performance, cognitive performance, and emotion regulation [6]. Insomnia has also been associated with a range of serious and non-serious sleep-related accidents [7].

While experimental sleep loss engenders reliable cognitive impairment, particularly for vigilance, complex attention, and working memory [8], there has been comparatively little work on insomnia. In general, the field has been characterised by mixed findings, with some studies showing impairment and others failing to observe differences from controls [9]. Nevertheless, meta-analytic data suggest that patients exhibit reliable impairments in tasks probing episodic memory, working memory, and problem solving, with small-to-medium effect sizes [10]. Recent, well-controlled studies have found evidence of insomnia-related impairments in switching of attention and working memory [11], and sustained attention and episodic memory [12]. However, there continues to be conflicting findings in the insomnia literature [13], [14], [15], and studies generally recruit small samples of patients with ‘primary insomnia’, who are otherwise healthy.

Larger epidemiology-based studies of insomnia symptoms and cognitive performance similarly display mixed results: showing evidence of impairment [16], no evidence of impairment [17] or impairment only for specific insomnia sub-groups [15], [18]. To our knowledge, no study has investigated insomnia symptoms and cognitive performance in a large population-based sample of middle-aged adults, with a standardised test battery, while simultaneously appraising the effects of other important sleep variables, including chronotype, sleep duration, and sleep medication.

The present study aimed to conduct the largest investigation of insomnia symptoms and cognitive performance to date through analysis of UK Biobank data. The UK Biobank is a large population-based study of >500000 adults aged between 40 and 69 years, providing a unique opportunity to assess associations in groups of poor and good sleepers and to adequately control for the influence of several potential confounding variables. We hypothesised that insomnia would be independently associated with impairments in all measures of cognition (reasoning, basic reaction time, numeric memory, visual memory, and prospective memory) after controlling for potential confounding variables. As a secondary aim, we examined associations between cognitive performance and chronotype, sleep medication use and self-reported sleep duration.

Section snippets

Participants

Details of the UK Biobank are available elsewhere [19]. In brief, adults aged 40–69 years who were registered with the UK National Health Service and living within 25 miles of a study assessment centre were invited to participate. Approximately nine million invitations led to a final sample of 501,718 participants. For the purposes of the present study, participants were excluded if they self-reported a neurological condition (eg, neurodegenerative disease, stroke, head injury or epilepsy;

Sample description

Sociodemographic data for the sample are presented in Table 1. Those with frequent insomnia symptoms were older and more likely to be female, reported shorter sleep duration, were more likely to report using sleep medication, were less likely to hold a university or college degree, were from a lower socioeconomic background, had a higher BMI, were more likely to report hypertension, use of antihypertensive medication or cardiovascular disease, were more likely to report recent depressive

Discussion

The principal aim of the present study was to examine cross-sectional associations between insomnia symptoms and cognitive performance in a large population-based sample. We also sought to assess relationships between cognitive performance and sleep duration, chronotype and sleep medication use. Prevalence, demographic and comorbidity profiles of those with insomnia symptoms were consistent with those in previous epidemiological investigations [1]. Unadjusted analyses revealed that those with

Disclosure

AIL receives a salary from Big Health Ltd. CAE is a shareholder and co-founder of Big Health Ltd. MKR has received research support from GSK and Novo Nordisk, acted as a consultant for GSK, Roche and Cell Catapult, and is a stockholder in GSK. RS has received salary from and is a stockholder in Astrazeneca and Surface Oncology. SDK has previously acted as a consultant for Big Health Ltd. All remaining authors declare no potential conflicts of interest.

Acknowledgement

This research has been conducted using the UK Biobank Resource.

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