Publications by authors named "Meryl Butters"

Introduction: We examined whether the Performance Assessment of Self-Care Skills (PASS) and Everyday Cognition Scale-12 (ECog-12) dichotomized cognitive groups in a sample of predominantly Black adults.

Methods: Two hundred forty-six community-dwelling adults (95% Black, age 50+) completed cognitive testing, the PASS, and the ECog. Cognitive groups (probable vs unlikely cognitive impairment) were determined by performance on the Modified Mini-Mental State Examination.

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This commentary focuses on the clinical utility of plasma amyloid-β (Aβ) 42/40 to detect semantic intrusion errors in amnestic mild cognitive impairment, as investigated Curiel Cid et al. in a recent issue of the . This commentary highlights the importance of testing the sensitivity of plasma Aβ to clinical symptoms in the quest to develop a comprehensive definition of AD that incorporates both biological precursors and clinical consequences.

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This study was conducted to clarify patterns of cortico-limbic volume abnormalities in late life depression (LLD) relative to non-depressed (ND) adults matched for amyloid β (Aβ) deposition and to evaluate the relationship of volume abnormalities with cognitive performance. Participants included 116 LLD and 226 ND. Classification accuracy of LLD status was estimated using area under the receiver operator characteristic curve.

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  • The study investigated how 6 months of intermittent exercise affects cognitive function in older adults, comparing low-intensity movement (LIM) and moderate-intensity aerobic exercise (AE).
  • Results showed that LIM improved learning and memory, while AE enhanced executive functioning, indicating different cognitive benefits from each type of exercise.
  • Neuroimaging revealed that changes in brain structure and certain inflammatory markers correlated with cognitive improvements, underlining the distinct advantages of both LIM and AE in older populations.
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  • Older adults with major depressive disorder (MDD) or mild cognitive impairment (MCI) are at increased risk for cognitive decline, making effective interventions crucial.
  • This study aimed to evaluate the effectiveness of combining cognitive remediation (CR) and transcranial direct current stimulation (tDCS) on cognitive decline in older adults with remitted MDD (rMDD) and/or MCI.
  • Results indicated that this intervention slowed cognitive decline over time but did not lead to immediate improvements in cognition after 2 months.
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  • Major depressive disorder in older adults (late-life depression) often leads to cognitive impairment, particularly in executive function, which may contribute to treatment resistance.
  • This study analyzed baseline cognitive data from 369 older participants in a clinical trial to understand the relationship between cognitive deficits and the effectiveness of pharmacotherapy for treatment-resistant late-life depression.
  • The findings revealed that participants exhibited significant challenges in inhibitory control and processing speed, with deficits in set shifting specifically predicting poorer response to treatment, indicating a need for tailored therapeutic approaches.
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  • Researchers aimed to identify clusters of severe maternal morbidity (SMM) using data from over 97,000 deliveries between 2008 and 2017 in Pennsylvania, applying a data-driven clustering technique.
  • They found four main SMM clusters: Hemorrhage, Critical Care, Vascular, and Shock, each characterized by specific conditions and risk factors.
  • The study revealed that all clusters had a high risk of maternal death and neonates in the Shock cluster faced the highest odds of adverse outcomes, emphasizing the role of comorbidities and social determinants in maternal health risks.*
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  • Late-life depression (LLD) might be linked to changes in brain structure and aging, but this study looked to see if brain age could help predict if someone with LLD would relapse.
  • Researchers studied 102 people with LLD and 43 healthy individuals over two years to see how their brain age compared and if it related to relapsing.
  • The results showed that brain age wasn’t different between healthy people and those with LLD, and it didn’t predict whether someone would relapse, which was unexpected based on previous studies.
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Objective: Anxiety is a common comorbid feature of late-life depression (LLD) and is associated with poorer global cognitive functioning independent of depression severity. However, little is known about whether comorbid anxiety is associated with a domain-specific pattern of cognitive dysfunction. We therefore examined group differences (LLD with and without comorbid anxiety) in cognitive functioning performance across multiple domains.

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Worry is a transdiagnostic symptom common to many neurocognitive disorders of aging, including early stages of Alzheimer's disease and related dementias (ADRD). Severe worry is associated with amyloid burden in cognitively intact older adults, yet the mechanisms underlying this association are not well understood. We hypothesize that this relationship involves altered brain and cardiovascular reactivity to acute stressors, a brain-body phenotype that also increases risk for cardiovascular disease.

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Background: The combination of exposure to multiple stressors and psychological distress may contribute to the disproportionate burden of dementia risk among Black Americans. This study estimates the effect of an index of stress and psychological distress (ie, "stress burden") on cognitive function and clinically adjudicated cognitive outcomes among older Black American adults, and examines sleep as a mediator.

Methods: The sample included 204 Black adults (79% female; mean age = 64 years) from Pittsburgh, PA, USA.

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Studies have confirmed that anxiety, especially worry and rumination, are associated with increased risk for cognitive decline, including Alzheimer's disease and related dementias (ADRD). Hippocampal atrophy is a hallmark of ADRD. We investigated the association between hippocampus and its subfield volumes and late-life global anxiety, worry, and rumination, and emotion regulation strategies.

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  • The REMBRANDT study looks at late-life depression, which can cause problems like forgetting things and being sad again after feeling better.
  • Researchers will enroll 300 older people who either have been treated for depression or have no mental health issues, and observe them for two years.
  • The study aims to figure out what causes depression to come back and how it affects thinking abilities, so they can find ways to help people stay well.
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Objectives: To identify data-driven cognitive profiles in older adults with remitted major depressive disorder (rMDD) with or without mild cognitive impairment (MCI) and examine how the profiles differ regarding demographic, clinical, and neuroimaging measures.

Design: Secondary cross-sectional analysis using latent profile analysis.

Setting: Multisite clinical trial in Toronto, Canada.

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  • Previous studies indicated notable sex-specific differences in major depressive disorder (MDD), but limited research has been done on older adults, particularly regarding late-life depression (LLD).
  • This study analyzed biological differences in a substantial group of older adults (ages 60-85) by measuring 344 plasma proteins in 430 individuals with LLD and 140 healthy comparisons, revealing unique protein expressions for each sex.
  • Results showed that while females had proteins mostly linked to immune control, males demonstrated dysregulation across various biological pathways, highlighting the need for sex-specific treatment approaches for LLD.
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  • Late-life depression (LLD) is common in older adults and often occurs alongside neurodegenerative diseases, with anxiety being a significant factor influencing LLD variation.
  • A study involving 121 participants (ages 65-91) assessed the connection between anxiety severity and various neurodegenerative factors such as brain volume, cognitive dysfunction, and functional ability.
  • Results indicated that higher anxiety was linked to reduced orbitofrontal cortex volume and greater cognitive dysfunction, highlighting cognitive issues as a crucial factor in understanding anxiety within LLD, which may inform treatment strategies.
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Hoarding disorder (HD) is a debilitating neuropsychiatric condition that affects 2%-6% of the population and increases in incidence with age. Major depressive disorder (MDD) co-occurs with HD in approximately 50% of cases and leads to increased functional impairment and disability. However, only one study to date has examined the rate and trajectory of hoarding symptoms in older individuals with a lifetime history of MDD, including those with current active depression (late-life depression; LLD).

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Objective: Previous findings suggest that time setting errors (TSEs) in the Clock Drawing Test (CDT) may be related mainly to impairments in semantic and executive function. Recent attempts to dissociate the classic stimulus-bound error (setting the time to "10 11" instead of "10 11") from other TSEs, did not support hypotheses regarding this error being primarily executive in nature or different from other time setting errors in terms of neurocognitive correlates. This study aimed to further investigate the cognitive correlates of stimulus-bound errors and other TSEs, in order to trace possible underlying cognitive deficits.

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Objectives: We examined within-individual changes in self-reported sleep health as community-dwelling older adults age as well as potential differences in these changes by self-reported sex and racial identity.

Methods: Participants were from the United States and enrolled in the Rush Memory and Aging Project, Minority Aging Research Study, or Religious Orders Study (N = 3539, 20% Black, 75% female, mean 78years [range 65-103]), and they received annual, in-person clinical evaluations (median 5 visits [range 1-27]). A sleep health composite score measured the number of poor sleep characteristics among satisfaction, daytime sleepiness, efficiency, and duration.

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Objective: We investigated the relationship between anxiety phenotypes (global anxiety, worry, and rumination) and white matter hyperintensities (WMH), with special consideration for the roles of age and executive function (EF). Our hypotheses were 1) anxiety phenotypes would be associated with WMH and 2) EF would moderate this relationship.

Design: Cross-sectional.

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Introduction: Amyloid PET scans provide individuals with mild cognitive impairment (MCI) information about their risk of progressing to Alzheimer's dementia (AD). Given the wide-ranging implications of this information, best practice guidelines are needed to support researchers and clinicians disclosing these high-stakes test results. To inform the development of such guidelines, this analysis aims to describe questions and concerns raised during the disclosure of amyloid PET results in the context of MCI.

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Background: Psychomotor disturbance is common in psychotic depression and is associated with relapse. In this analysis, we examined whether white matter microstructure is associated with relapse probability in psychotic depression and, if so, whether white matter microstructure accounts for the association between psychomotor disturbance and relapse.

Methods: We used tractography to characterize diffusion-weighted MRI data in 80 participants enrolled in a randomized clinical trial that compared efficacy and tolerability of sertraline plus olanzapine with sertraline plus placebo in the continuation treatment of remitted psychotic depression.

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