Abstract

BackgroundIt is well-established that what is good for the heart is good for the brain. Vascular factors such as hypertension, diabetes, and high cholesterol, and genetic factors such as the apolipoprotein E4 allele increase the risk of developing both cardiovascular disease and dementia. However, the mechanisms underlying the heart–brain association remain unclear. Recent evidence suggests that impairments in vascular phenotypes and cerebrovascular reactivity (CVR) may play an important role in cognitive decline. The Heart and Brain Study combines state-of-the-art vascular ultrasound, cerebrovascular magnetic resonance imaging (MRI) and cognitive testing in participants of the long-running Whitehall II Imaging cohort to examine these processes together. This paper describes the study protocol, data pre-processing and overarching objectives.Methods and DesignThe 775 participants of the Whitehall II Imaging cohort, aged 65 years or older in 2019, have received clinical and vascular risk assessments at 5-year-intervals since 1985, as well as a 3T brain MRI scan and neuropsychological tests between 2012 and 2016 (Whitehall II Wave MRI-1). Approximately 25% of this cohort are selected for the Heart and Brain Study, which involves a single testing session at the University of Oxford (Wave MRI-2). Between 2019 and 2023, participants will undergo ultrasound scans of the ascending aorta and common carotid arteries, measures of central and peripheral blood pressure, and 3T MRI scans to measure CVR in response to 5% carbon dioxide in air, vessel-selective cerebral blood flow (CBF), and cerebrovascular lesions. The structural and diffusion MRI scans and neuropsychological battery conducted at Wave MRI-1 will also be repeated. Using this extensive life-course data, the Heart and Brain Study will examine how 30-year trajectories of vascular risk throughout midlife (40–70 years) affect vascular phenotypes, cerebrovascular health, longitudinal brain atrophy and cognitive decline at older ages.DiscussionThe study will generate one of the most comprehensive datasets to examine the longitudinal determinants of the heart–brain association. It will evaluate novel physiological processes in order to describe the optimal window for managing vascular risk in order to delay cognitive decline. Ultimately, the Heart and Brain Study will inform strategies to identify at-risk individuals for targeted interventions to prevent or delay dementia.

Highlights

  • The majority of dementia patients have cardiovascular comorbidities, and dementia and cardiovascular diseases share many risk factors (Poblador-Plou et al, 2014)

  • We created manually segmented white matter hyperintensities (WMHs) masks for 12 participants of the Heart and Brain Study, who had a range of WMH loads at Waves magnetic resonance imaging (MRI)-1 and MRI-2

  • We measured the volumetric agreement between the total WMH volume obtained from BIANCA and manual segmentations using the intra class correlation coefficient (ICC; two-way mixed model with absolute agreement definition)

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Summary

Introduction

The majority of dementia patients have cardiovascular comorbidities, and dementia and cardiovascular diseases share many risk factors (Poblador-Plou et al, 2014). Vascular risk is potentially treatable, and managing it alongside other modifiable lifestyle factors could prevent an estimated 40% of dementia cases (Livingston et al, 2020) Prevention on this scale would substantially improve quality of life for a society which in the 50 years is predicted to see a near tripling in the prevalence of dementia (Patterson, 2018). The Heart and Brain Study combines detailed vascular phenotyping and state-of-the-art magnetic resonance imaging (MRI) of the brain in a longitudinal prospective ageing cohort to investigate these questions with three overarching objectives. It is well-established that what is good for the heart is good for the brain. This paper describes the study protocol, data pre-processing and overarching objectives

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