Publications by authors named "Charlotte L Allan"

Background: Trajectories of depressive symptoms over the lifespan vary between people, but it is unclear whether these differences exhibit distinct characteristics in brain structure and function.

Methods: In order to compare indices of white matter microstructure and cognitive characteristics of groups with different trajectories of depressive symptoms, we examined 774 participants of the Whitehall II Imaging Sub-study, who had completed the depressive subscale of the General Health Questionnaire up to nine times over 25 years. Twenty-seven years after the first examination, participants underwent magnetic resonance imaging to characterize white matter hyperintensities (WMH) and microstructure and completed neuropsychological tests to assess cognition.

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Depression is a common comorbidity in dementia. Randomised controlled studies of antidepressants do not show a significant improvement in depressive symptoms in patients with comorbid dementia and are known to lead to an increase in side effects. However, there are relatively few studies of depression in dementia, and drawing firm conclusions about the use of antidepressants is limited by the amount of data available.

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Objective: To investigate the relationship between visual hallucinations in Parkinson disease (PD) and levels of γ-aminobutyric acid (GABA) in the primary visual cortex.

Methods: We utilized magnetic resonance spectroscopy to investigate occipital GABA levels in 36 participants with PD, 19 with and 17 without complex visual hallucinations, together with 20 healthy controls without hallucinations. In addition, we acquired T1-weighted MRI, whole-brain fMRI during a visual task, and diffusion tensor imaging.

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Dementia is a chronic, progressive disease that is now much more widely recognised and treated. Patients with dementia may require palliative care when they reach the end stage of their illness, or they may have mild-moderate cognitive symptoms comorbid with a life-limiting illness. The variety of presentations necessitates a highly individual approach to care planning, and patients should be encouraged to set their own goals and contribute to advanced care planning where possible.

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There has been a rapid rise in the number of people diagnosed with dementia in England from 232,000 in 2008 to 850,000 in 2014. Currently, it is estimated that the prevalence of mild cognitive impairment in adults aged 65 and over is 10-20%. It is likely that this figure will increase in line with trends in dementia diagnosis.

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Depression and dementia are both common conditions in older people, and they frequently occur together. Late life depression affects about 3.0-4.

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  • UCP2 is a mitochondrial protein that uncouples electron transport from ATP production and its gene variants can influence longevity and health in humans.
  • This study examined the relationship between UCP2 gene polymorphisms and the risk of neurodegenerative or mental health disorders, as well as brain structure and function, using neuroimaging data from 536 older adults.
  • Results showed no significant associations for neurodegenerative disorders or brain measures, but certain UCP2 variants were linked to a higher likelihood of mood disorders in men, suggesting a potential but subtle impact of UCP2 on mental health rather than brain structure.
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  • Sleep disturbances and declines in white matter microstructure are common in older adults and are linked to psychiatric and neurological issues, but few studies have explored the connection between sleep quality and brain microstructure directly.
  • A study using diffusion tensor imaging involved 448 participants aged 60-82 and found that poor sleep quality correlated with changes in white matter microstructure, specifically reduced global fractional anisotropy and increased diffusivity, particularly in frontal-subcortical areas.
  • The findings suggest a link between current sleep quality and white matter changes, but small effect sizes indicate that poor sleep may not be a strong modifiable factor for improving brain health in aging.
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 To investigate whether moderate alcohol consumption has a favourable or adverse association or no association with brain structure and function. Observational cohort study with weekly alcohol intake and cognitive performance measured repeatedly over 30 years (1985-2015). Multimodal magnetic resonance imaging (MRI) was performed at study endpoint (2012-15).

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Mild cognitive impairment (MCI) is a term used to describe cognitive impairment in one or more cognitive domains that is greater than any expected age-related changes, but not of the magnitude to warrant a diagnosis of dementia. This review considers how early cognitive decline is diagnosed, focusing on the use of neuropsychological tests and neuroimaging, as well as the differential diagnosis. Potential treatments, including secondary prevention, post-diagnostic support and self-help are discussed.

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Early diagnosis of dementia allows people to access effective treatment and make advance decisions while they still have capacity. We aimed to encourage people to attend memory clinic, in order to boost rates of diagnosis. We created a patient information video about Oxford Health NHS Foundation Trust Memory Clinics, to inform and empower those awaiting assessment and to promote early diagnosis.

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Most people with mild dementia can continue to drive, but dementia is progressive and many patients and clinicians will be faced with questions about driving safety in the course of their illness. Determining when this happens is a complex decision, with risks of personal and public safety needing to be weighed against individual patient benefits of driving in terms of autonomy, independence and well-being. Decisions need to make reference to cognitive abilities, as well as other factors including physical comorbidity, vision, mobility, insight and history of driving errors and accidents.

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Background: Late-life sub-threshold depressive symptoms (i.e. depressive symptoms that do not meet the criteria for a diagnosis of major depressive disorder) are associated with impaired physical health and function, and increased risk of major depressive disorder.

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Background: The contribution of education and intelligence to resilience against age-related cognitive decline is not clear, particularly in the presence of 'normal for age' minor brain abnormalities.

Method: Participants (n = 208, mean age 69.2 years, s.

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Background: Hypertension is associated with an increased risk of dementia and depression with uncertain longitudinal associations with brain structure.

Aims: To examine lifetime blood pressure as a predictor of brain structure in old age.

Method: A total of 190 participants (mean age 69.

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  • The Whitehall II study examines factors influencing brain health and cognitive ageing by tracking British civil servants over time, utilizing unique longitudinal data.
  • A random sample of 800 participants underwent MRI scans, cognitive assessments, and biological sample collection to study brain function and immune health, with data collection spanning from 2012 to 2016.
  • The combination of advanced MRI technology and extensive historical data allows researchers to explore connections between brain changes, age-related diseases, and various social and health factors influencing cognitive resilience.
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Background: Inflammatory markers are raised in cross-sectional studies of depressed patients and may represent an important mediating factor for behaviour, neural plasticity and brain structure.

Methods: We undertook a systematic review of longitudinal studies, investigating whether raised inflammatory markers indicate an increased risk of subsequent depressive symptoms. We searched three databases (1970-2012) for longitudinal studies with repeat data on CRP or IL-6 levels and subsequent depressive symptoms.

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Autism affects 1.1% of the adult population. The spectrum of symptoms is wide; some individuals have above average intelligence and are fully independent, while others have limited independence because of a learning disability.

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GPs should consider a diagnosis of dementia when a patient presents with functional impairment in addition to at least two changes in cognitive function e.g. short-term memory, language, reasoning, spatial orientation, or personality change.

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Self-harm is best defined as 'any act of self-poisoning or self-injury carried out by an individual irrespective of motivation'. With a 10.5% lifetime risk, self-reported self-harm is common in the community.

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Background: Late-life depression is a common and heterogeneous illness, associated with structural abnormalities in both grey and white matter.

Aims: To examine the relationship between age at onset and magnetic resonance imaging (MRI) measures of grey and white matter to establish whether they support particular hypotheses regarding the anatomy and aetiology of network disruption in late-life depression.

Method: We studied 36 participants with late-life depression.

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Context: Disruption of frontal-subcortical and limbic networks is hypothesized to have a key role in late-life depression (LLD) and can be examined using magnetic resonance imaging (MRI) techniques. Gray matter can be examined using T1-weighted MRI, white matter using T2-weighted MRI and diffusion tensor imaging, and functional connectivity in resting-state networks using functional MRI. Although independent MRI studies have supported gray and white matter abnormalities in frontosubcortical and limbic networks and increased functional connectivity in the default-mode network in depression, no study has concurrently examined gray matter, white matter, and functional connectivity.

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