Background: Apathy (loss of motivation or goal-directed behaviour) and depression each confer risk for dementia, cardiovascular disease and mortality in older adults. Mechanisms for this are not yet understood, and may involve systemic inflammation. However, this has received little attention, particularly in older adults where depression may present differently. Symptoms of apathy, fatigue, and physical symptoms are more common in late-life depression. This research aims to investigate whether apathy, depression and fatigue are differentially associated with inflammatory biomarkers in older adults.
Method: 1,037 community-dwelling older adults without dementia (aged 70-90, 55% women) completed self-report assessments including measures of apathy and depression from the Geriatric Depression Scale, and fatigue from Assessment of Quality of Life-6D. Inflammatory biomarkers from early morning fasting blood collection included C-reactive protein (CRP) and interleukin-6. Logistic regressions examined associations between levels of biomarkers and apathy, depression and fatigue separately. Analyses were initially unadjusted, then adjusted for baseline age, sex, education, global cognition (MMSE), health conditions, medications and BMI.
Result: Interleukin-6 was associated with apathy, depression and fatigue in unadjusted models (odds ratio [OR] per natural log unit increase in IL-6: 1.73, 95% confidence interval [CI] 1.38-2.22; OR 1.56, 95% CI 1.12-2.15; OR 1.72, 95% CI 1.14-2.59 respectively). The association with apathy remained significant after adjustment for other symptoms, socio-demographics, cognition and health-related covariates, but findings for depression and fatigue were attenuated. CRP was associated with apathy and fatigue (OR 1.10, 95% CI 1.00-1.21; OR 1.34, 95% CI 1.11-1.60 respectively) although the former was attenuated by adjustment for covariates. Previous associations between CRP and depression were not replicated.
Conclusion: In older persons, apathy and fatigue were differentially linked with inflammatory biomarkers, whereas previous associations between inflammation and depression were not replicated. Findings confirm the importance of fatigue, and provide novel insight into apathy, as prevalent and impairing symptoms which map to peripheral inflammation in older adults. Inflammation may at least partially underly the complex associations between apathy, depression and poorer health outcomes including dementia.
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http://dx.doi.org/10.1002/alz.093242 | DOI Listing |
Alzheimers Dement
December 2024
G. H. Sergievsky Center, Vagelos College of Physicians and Surgeons, Columbia University, New York, NY, USA.
Background: Neuropsychiatric Symptoms (NPS) (e.g., aggression, psychosis, anxiety, apathy, depression, agitation, sleep disturbances, repetitive behaviors) occur in 85% of AD patients, and are associated with accelerated decline, out-of-home placement, increased costs, and greatly increased suffering of patients and families.
View Article and Find Full Text PDFAlzheimers Dement
December 2024
G. H. Sergievsky Center, Vagelos College of Physicians and Surgeons, Columbia University, New York, NY, USA.
Background: Neuropsychiatric Symptoms (NPS) including aggression, psychosis, anxiety, apathy and depression are highly prevalent in Alzheimer's Disease patients and are associated with accelerated decline and a detrimental impact on suffering and quality of life of both patients and caregivers. There are no effective pharmaceutical interventions targeting these symptoms, making a better understanding of the etiologic mechanisms underlying NPS in AD critical to develop improved treatments.
Method: To facilitate identification of genetic loci and mechanistic pathways underlying NPS in AD, we have initiated an effort (NIH: U01AG079850) to collate and harmonize all available NPS data in over 70 cohorts (>80,000 samples) of diverse ancestries with whole-genome sequencing data from the Alzheimer's Disease Sequencing Project (ADSP), and analyze these data to identify genetic loci and mechanistic pathways associated with NPS in AD.
Background: Approximately 85% of individuals living with MCI or ADRD experience one or more neuropsychiatric symptoms (NPS), referred to as ADRD-NPS. They include depression, anxiety, irritability, apathy, agitation, delusions, hallucinations, and sleep disturbances. ADRD-NPS are associated with greater functional impairment, higher caregiver burden, and earlier institutionalization.
View Article and Find Full Text PDFBackground: Despite the clinical importance and significant social burden of neuropsychiatric symptoms (NPS) in dementia, the underlying neurobiological mechanism remains poorly understood. Recently, neuroimaging-derived brain-age estimation by machine-learning analysis has shown promise as an individual-level biomarker. We investigated the relationship between NPS and brain-age in amnestic mild cognitive impairment (MCI) and early dementia.
View Article and Find Full Text PDFFuture clinical trials targeting Alzheimer's disease (AD) on new disease modifying drugs necessitate a paradigm shift towards early identification of individuals at risk. Emerging evidence indicates that subtle alterations in language and speech characteristics may manifest concurrently with the progression of neurodegenerative disorders like AD. These changes manifest as discernible variations, assessable through semantic nuances, word choices, sentiment, grammar usage (linguistic features), and phonetic/acoustic traits (paralinguistic features).
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