Searching for just a few words should be enough to get started. If you need to make more complex queries, use the tips below to guide you.
Purchase individual online access for 1 year to this journal.
Price: EUR 595.00Impact Factor 2024: 3.4
The Journal of Alzheimer’s Disease is an international multidisciplinary journal to facilitate progress in understanding the etiology, pathogenesis, epidemiology, genetics, behavior, treatment and psychology of Alzheimer’s disease.
The journal publishes research reports, reviews, short communications, book reviews, and letters-to-the-editor. The journal is dedicated to providing an open forum for original research that will expedite our fundamental understanding of Alzheimer’s disease.
Authors: Grande, Giulia | Wu, Jing | Ljungman, Petter L.S. | Stafoggia, Massimo | Bellander, Tom | Rizzuto, Debora
Article Type: Research Article
Abstract: Background: A growing but contrasting evidence relates air pollution to cognitive decline. The role of cerebrovascular diseases in amplifying this risk is unclear. Objectives: 1) Investigate the association between long-term exposure to air pollution and cognitive decline; 2) Test whether cerebrovascular diseases amplify this association. Methods: We examined 2,253 participants of the Swedish National study on Aging and Care in Kungsholmen (SNAC-K). One major air pollutant (particulate matter ≤2.5μm, PM2.5 ) was assessed yearly from 1990, using dispersion models for outdoor levels at residential addresses. The speed of cognitive decline (Mini-Mental State Examination, MMSE) was estimated …as the rate of MMSE decline (linear mixed models) and further dichotomized into the upper (25%fastest cognitive decline), versus the three lower quartiles. The cognitive scores were used to calculate the odds of fast cognitive decline per levels of PM2.5 using regression models and considering linear and restricted cubic splines of 10 years exposure before the baseline. The potential modifier effect of cerebrovascular diseases was tested by adding an interaction term in the model. Results: We observed an inverted U-shape relationship between PM2.5 and cognitive decline. The multi-adjusted piecewise regression model showed an increased OR of fast cognitive decline of 81%(95%CI = 1.2–3.2) per interquartile range difference up to mean PM2.5 level (8.6μg/m3 ) for individuals older than 80. Above such level we observed no further risk increase (OR = 0.89;95%CI = 0.74–1.06). The presence of cerebrovascular diseases further increased such risk by 6%. Conclusion: Low to mean PM2.5 levels were associated with higher risk of accelerated cognitive decline. Cerebrovascular diseases further amplified such risk. Show more
Keywords: Air pollution, cerebrovascular diseases, cognitive decline, particulate matter, population-based study
DOI: 10.3233/JAD-200852
Citation: Journal of Alzheimer's Disease, vol. 80, no. 2, pp. 591-599, 2021
Authors: Rostamzadeh, Ayda | Schwegler, Carolin | Gil-Navarro, Silvia | Rosende-Roca, Maitée | Romotzky, Vanessa | Ortega, Gemma | Canabate, Pilar | Moreno, Mariola | Schmitz-Luhn, Björn | Boada, Mercè | Jessen, Frank | Woopen, Christiane
Article Type: Research Article
Abstract: Background: Today, a growing number of individuals with mild cognitive impairment (MCI) wish to assess their risk of developing Alzheimer’s disease (AD) dementia. The expectations as well as the effects on quality of life (QoL) in MCI patients and their close others through biomarker-based dementia risk estimation are not well studied. Objective: The PreDADQoL project aims at providing empirical data on effects of such prediction on QoL and at developing an ethical and legal framework of biomarker-based dementia risk estimation in MCI. Methods: In the empirical study, 100 MCI-patients and their close others will be recruited …from two sites (Germany and Spain). They receive standardized counselling on cerebrospinal fluid (CSF) biomarker-based prediction of AD dementia and a risk disclosure based on their AD biomarker status. A mixed methods approach will be applied to assess outcomes. Results: The pilot-study yielded a specification of the research topics and newly developed questionnaires for the main assessment. Within this binational quantitative and qualitative study, data on attitudes and expectations toward AD risk prediction, QoL, risk communication, coping strategies, mental health, lifestyle changes, and healthcare resource utilization will be obtained. Together with the normative part of the project, an empirically informed ethical and legal framework for biomarker-based dementia risk estimation will be developed. Conclusion: The empirical research of the PreDADQoL study together with the ethical and legal considerations and implications will help to improve the process of counselling and risk disclosure and thereby positively affect QoL and health of MCI-patients and their close others in the context of biomarker-based dementia risk estimation. Show more
Keywords: Alzheimer’s disease, biomarker, caregiver, dementia, disclosure, ethics, mild cognitive impairment, quality of life, risk
DOI: 10.3233/JAD-200484
Citation: Journal of Alzheimer's Disease, vol. 80, no. 2, pp. 601-617, 2021
Authors: Grothe, Jessica | Schomerus, Georg | Dietzel, Jens | Riedel-Heller, Steffi | Röhr, Susanne
Article Type: Research Article
Abstract: Background: Social functioning is an important parameter for the early detection and diagnosis of dementia, as well as the description of its course and the assessment of intervention effects. Therefore, valid and reliable instruments to measure social functioning in individuals with dementia are needed. Objective: We aimed to provide an overview of such instruments including information on feasibility and psychometric properties. Methods: The review is informed by the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. Relevant literature was identified using a pre-specified search string in the databases MEDLINE, PsycINFO, and Web of Science. …Information on the characteristics, feasibility, and psychometric properties of the identified instruments were extracted, summarized, and discussed. Results: Out of 5,307 articles, 8 were selected to be included in the study, describing a total of three instruments for measuring social functioning in individuals with dementia: the Nurses’ Observation Scale for Geriatric Patients (NOSGER; dimension “social behavior”), the Socioemotional Dysfunction Scale (SDS), and the Social Functioning in Dementia Scale (SF-DEM). The validity of all the three instruments was overall acceptable. Reliability was high for the NOSGER scale “social behavior” and the SF-DEM. Information on the usability of the instruments tended to be scarce. Conclusion: There are a few valid and reliable instruments to assess social functioning in individuals with dementia. Further considerations could comprise their feasibility with regard to measuring changes in social functioning over time, in additional target groups, e.g., different types and stages of dementia, and adaptions to different languages and cultural backgrounds. Show more
Keywords: Assessment, dementia, instrument, measurement, psychometric properties, reliability, social functioning, systematic review, validity
DOI: 10.3233/JAD-200762
Citation: Journal of Alzheimer's Disease, vol. 80, no. 2, pp. 619-637, 2021
Authors: Futamura, Akinori | Hieda, Sotaro | Mori, Yukiko | Kasuga, Kensaku | Sugimoto, Azusa | Kasai, Hideyo | Kuroda, Takeshi | Yano, Satoshi | Tsuji, Mayumi | Ikeuchi, Takeshi | Irie, Kazuhiro | Ono, Kenjiro
Article Type: Research Article
Abstract: Background: Toxic amyloid-β protein (Aβ) conformers play an important role in the progression of Alzheimer’s disease (AD). The ratio of toxic conformer to total Aβ42 in cerebrospinal fluid (CSF) was significantly high in AD and mild cognitive impairment (MCI) due to AD using an enzyme-linked immunosorbent assay kit with a 24B3 antibody. Objective: We compared the toxic Aβ42 , conformer at different stages of AD to identify its contribution to AD pathogenesis. Methods: We compared 5 patients with preclinical AD, 11 patients with MCI due to AD, 21 patients with AD, and 5 healthy controls …to measure CSF levels of total Aβ42 , total tau, tau phosphorylated at threonine 181 (p-tau), and toxic Aβ conformers. All were classified using the Clinical Dementia Rating. Cognitive function was assessed using the Japanese version of the Mini-Mental State Examination (MMSE-J). Results: Toxic Aβ conformer level was insignificant between groups, but its ratio to Aβ42 was significantly higher in AD than in preclinical AD (p < 0.05). Toxic Aβ42 conformer correlated positively with p-tau (r = 0.67, p < 0.01) and p-tau correlated negatively with MMSE-J (r = –0.38, p < 0.05). Conclusion: Toxic Aβ conformer triggers tau accumulation leading to neuronal impairment in AD pathogenesis. Show more
Keywords: Alzheimer’s disease, amyloid-β protein, cerebrospinal fluid, preclinical Alzheimer’s disease, tau protein, toxic conformer
DOI: 10.3233/JAD-201407
Citation: Journal of Alzheimer's Disease, vol. 80, no. 2, pp. 639-646, 2021
Authors: Yang, Dalin | Hong, Keum-Shik
Article Type: Research Article
Abstract: Background: Mild cognitive impairment (MCI) is considered a prodromal stage of Alzheimer’s disease. Early diagnosis of MCI can allow for treatment to improve cognitive function and reduce modifiable risk factors. Objective: This study aims to investigate the feasibility of individual MCI detection from healthy control (HC) using a minimum duration of resting-state functional near-infrared spectroscopy (fNIRS) signals. Methods: In this study, nine different measurement durations (i.e., 30, 60, 90, 120, 150, 180, 210, 240, and 270 s) were evaluated for MCI detection via the graph theory analysis and traditional machine learning approach, such as linear discriminant analysis, …support vector machine, and K-nearest neighbor algorithms. Moreover, feature representation- and classification-based transfer learning (TL) methods were applied to identify MCI from HC through the input of connectivity maps with 30 and 90 s duration. Results: There was no significant difference among the nine various time windows in the machine learning and graph theory analysis. The feature representation-based TL showed improved accuracy in both 30 and 90 s cases (i.e., 30 s: 81.27% and 90 s: 76.73%). Notably, the classification-based TL method achieved the highest accuracy of 95.81% using the pre-trained convolutional neural network (CNN) model with the 30 s interval functional connectivity map input. Conclusion: The results indicate that a 30 s measurement of the resting-state with fNIRS could be used to detect MCI. Moreover, the combination of neuroimaging (e.g., functional connectivity maps) and deep learning methods (e.g., CNN and TL) can be considered as novel biomarkers for clinical computer-assisted MCI diagnosis. Show more
Keywords: Alzheimer’s disease, convolutional neural network, functional connectivity, functional near-infrared spectroscopy, mild cognitive impairment, resting state, transfer learning
DOI: 10.3233/JAD-201163
Citation: Journal of Alzheimer's Disease, vol. 80, no. 2, pp. 647-663, 2021
Authors: Shen, Ling-Xiao | Yang, Yu-Xiang | Kuo, Kevin | Li, Hong-Qi | Chen, Shi-Dong | Chen, Ke-Liang | Dong, Qiang | Tan, Lan | Yu, Jin-Tai
Article Type: Research Article
Abstract: Background: Social isolation and social interaction have been suggested to be associated with Alzheimer’s disease. However, the causality cannot be unambiguously assessed as traditional epidemiological methods are easily subject to unmeasured confounders and potential bias. Objective: To examine bidirectional relationships between social isolation, social interaction, and Alzheimer’s disease using Mendelian randomization method for assessing potential causal inference. Methods: This bidirectional two-sample Mendelian randomization study used independent genetic variants associated with social isolation and social interaction (n = 302,567–487,647), and Alzheimer’s disease (n = 455,258). MR analyses were performed using the inverse-variance-weighted (IVW) as the main MR analytical method …to estimate the causal effect. For sensitivity analyses, we applied weighted median, MR Egger to further assess the credibility of the causal effect. Results: Of the five types of social engagement examined in our study, only one showed evidence of an association with the risk of Alzheimer’s disease. Attendance at a gym or sports club (IVW OR per SD change: 0.670; 95% CI: 0.463–0.970; p = 0.034) was inversely associated with the risk of Alzheimer’s disease. We also found that AD may reduce the attendance at religious group (IVW OR per SD change: 1.017; 95% CI: 1.005–1.030; p = 0.004). Conclusion: This study suggests that regular attendance at a gym or sports club is causally associated with reduced risk of Alzheimer’s disease. Further studies are warranted to elucidate potential mechanisms. Show more
Keywords: Alzheimer’s disease, causal relations, social interaction, social isolation, Mendelian randomization
DOI: 10.3233/JAD-201442
Citation: Journal of Alzheimer's Disease, vol. 80, no. 2, pp. 665-672, 2021
Authors: Wang, Jin | Guo, Xiaojuan | Lu, Wenhui | Liu, Jie | Zhang, Hong | Quan, Qingyun | Su, Hang | Ma, Li | Gao, Fan | Qu, Qiumin
Article Type: Research Article
Abstract: Background: Vascular factors and mitochondria dysfunction contribute to the pathogenesis of Alzheimer’s disease (AD). DL-3-n-butylphthalide (NBP) has an effect in protecting mitochondria and improving microcirculation. Objective: The aim was to investigate the effect of donepezil combined NBP therapy in patients with mild-moderate AD. Methods: It was a prospective cohort study. 92 mild-moderate AD patients were classified into the donepezil alone group (n = 43) or the donepezil combined NBP group (n = 49) for 48 weeks. All patients were evaluated with Alzheimer’s Disease Assessment Scale-Cognitive subscale (ADAS-cog), Clinician’s Interview-Based Impression of Change plus caregiver input (CIBIC-plus), Alzheimer’s Disease …Cooperative Study-Activities of Daily Living (ADCS-ADL), and Neuropsychiatric Inventory (NPI) every 12 weeks. All patients were monitored for adverse events (AEs). The efficacy was analyzed using multivariate logistic regression analysis. Results: The multivariate logistic regression analysis showed that the changes of ADAS-cog score (OR = 2.778, 95% CI: [1.087, 7. 100], p = 0.033) and ADCS-ADL score (OR = 2.733, 95% CI: [1.002, 7.459], p = 0.049) had significant difference between donepezil alone group and donepezil combined NBP group, while the changes of NPI (OR = 1.145, 95% CI: [0.463, 2.829], p = 0.769), MMSE (OR = 1.563, 95% CI: [0.615, 3.971], p = 0.348) and CIBIC-plus (OR = 2.593, 95% CI: [0.696, 9.685], p = 0.156) had no significant difference. The occurrence of AEs was similar in the two groups. Conclusion: Over the 48-week treatment period, donepezil combined NBP group had slower cognitive decline and better activities of daily living in patients with mild to moderate AD. These indicated that the multi-target therapeutic effect of NBP may be a new choice for AD treatment. Show more
Keywords: Alzheimer’s disease, clinical trial, DL–3-n-butylphthalide, drug treatment, prospective cohort study
DOI: 10.3233/JAD-201381
Citation: Journal of Alzheimer's Disease, vol. 80, no. 2, pp. 673-681, 2021
Authors: Buciuc, Marina | Tosakulwong, Nirubol | Machulda, Mary M. | Whitwell, Jennifer L. | Weigand, Stephen D. | Murray, Melissa E. | Reichard, R. Ross | Parisi, Joseph E. | Dickson, Dennis W. | Boeve, Bradley F. | Knopman, David S. | Petersen, Ronald C. | Josephs, Keith A.
Article Type: Research Article
Abstract: Background: Transactive response DNA-binding protein of 43 kDa (TDP-43) is associated with memory impairment and overall cognitive decline. It is unclear how TDP-43 contributes to the rate of clinical decline. Objective: To determine whether cross-sectional and longitudinal cognitive and functional decline are associated with anatomical distribution of TDP-43 in the brain. Methods: Longitudinal clinical-neuropathologic autopsy cohort study of 385 initially cognitively normal/mildly impaired older adults prospectively followed until death. We investigated how TDP-43, amyloid-β (Aβ), tau neurofibrillary tangles (NFT), Lewy body disease (LBD), age, sex, and genetics are associated with clinical scores and rates of their longitudinal …decline. Results: Of 385 participants, 260 (68%) had no TDP-43, 32 (8%) had TDP-43 limited to amygdala, and 93 (24%) had TDP-43 in the hippocampus and beyond. Higher TDP-43 and Braak NFT stages independently were associated with faster decline in global cognition, functional performance measured by Clinical Dementia Rating scale, and naming and episodic memory, whereas older age was associated with slower rate of cognitive, psychiatric, and functional decline. Cross-sectionally the following associations were found: higher TDP-43 and Braak NFT - worse performance; higher Aβ burden - worse global cognition, more behavioral changes, the latter also with higher LBD; older age - worse naming, lower frequency of behavioral changes; female sex - more impaired naming and better preserved episodic memory. There were no genetic associations. Conclusion: The association of TDP-43 distribution with decline in cognitive and functional performance suggests that TDP-43 is playing a role in the clinical progression to dementia. Further characterization of clinical features associated with TDP-43 can facilitate establishment of antemortem diagnosis. Show more
Keywords: Alzheimer’s disease, clinical decline, dementia, neuropsychology, TDP-43 proteinopathy
DOI: 10.3233/JAD-201166
Citation: Journal of Alzheimer's Disease, vol. 80, no. 2, pp. 683-693, 2021
Authors: Yuan, Li | Zhang, Jun | Guo, Jun-Hong | Holscher, Christian | Yang, Jun-Ting | Wu, Mei-Na | Wang, Zhao-Jun | Cai, Hong-Yan | Han, Ling-Na | Shi, Hui | Han, Yu-Fei | Qi, Jin-Shun
Article Type: Research Article
Abstract: Background: Alzheimer’s disease (AD) is a neurodegenerative disease characterized by progressive decline in cognitive function. Type 2 diabetes mellitus (T2DM) is an important risk factor for AD. Glucose-dependent insulinotropic polypeptide (GIP) has been identified to be effective in T2DM treatment and neuroprotection. Objective: The present study investigated the neuroprotective effects and possible mechanisms of DAla2GIP-Glu-PAL, a novel long-lasting GIP analogue, in APP/PS1 AD mice. Methods: Multiple behavioral tests were performed to examine the cognitive function of mice. In vivo hippocampus late-phase long-term potentiation (L-LTP) was recorded to reflect synaptic plasticity. Immunohistochemistry and immunofluorescence were used …to examine the Aβ plaques and neuroinflammation in the brain. IL-1β, TNF-α , and cAMP/PKA/CREB signal molecules were also detected by ELISA or western blotting. Results: DAla2GIP-Glu-PAL increased recognition index (RI) of APP/PS1 mice in novel object recognition test, elevated spontaneous alternation percentage of APP/PS1 mice in Y maze test, and increased target quadrant swimming time of APP/PS1 mice in Morris water maze test. DAla2GIP-Glu-PAL treatment enhanced in vivo L-LTP of APP/PS1 mice. DAla2GIP-Glu-PAL significantly reduced Aβ deposition, inhibited astrocyte and microglia proliferation, and weakened IL-1β and TNF-α secretion. DAla2GIP-Glu-PAL also upregulated cAMP/PKA/CREB signal transduction and inhibited NF-κ B activation in the hippocampus of APP/PS1 mice. Conclusion: DAla2GIP-Glu-PAL can improve cognitive behavior, synaptic plasticity, and central pathological damage in APP/PS1 mice, which might be associated with the inhibition of neuroinflammation, as well as upregulation of cAMP-/PKA/CREB signaling pathway. This study suggests a potential benefit of DAla2GIP-Glu-PAL in the treatment of AD. Show more
Keywords: Amyloid-β, cognitive behaviors, DAla2GIP-Glu-PAL, long-term synaptic plasticity, neuroinflammation
DOI: 10.3233/JAD-201262
Citation: Journal of Alzheimer's Disease, vol. 80, no. 2, pp. 695-713, 2021
Authors: Ma, Da | Yee, Evangeline | Stocks, Jane K. | Jenkins, Lisanne M. | Popuri, Karteek | Chausse, Guillaume | Wang, Lei | Probst, Stephan | Beg, Mirza Faisal
Article Type: Research Article
Abstract: Background: Advanced machine learning methods can aid in the identification of dementia risk using neuroimaging-derived features including FDG-PET. However, to enable the translation of these methods and test their usefulness in clinical practice, it is crucial to conduct independent validation on real clinical samples, which has yet to be properly delineated in the current literature. Objective: In this paper, we present our efforts to enable such clinical translational through the evaluation and comparison of two machine-learning methods for discrimination between dementia of Alzheimer’s type (DAT) and Non-DAT controls. Methods: FDG-PET-based dementia scores were generated on an …independent clinical sample whose clinical diagnosis was blinded to the algorithm designers. A feature-engineered approach (multi-kernel probability classifier) and a non-feature-engineered approach (3D convolutional neural network) were analyzed. Both classifiers were pre-trained on cognitively normal subjects as well as subjects with DAT. These two methods provided a probabilistic dementia score for this previously unseen clinical data. Performance of the algorithms were compared against ground-truth dementia rating assessed by experienced nuclear physicians. Results: Blinded clinical evaluation on both classifiers showed good separation between the cognitively normal subjects and the patients diagnosed with DAT. The non-feature-engineered dementia score showed higher sensitivity among subjects whose diagnosis was in agreement between the machine-learning models, while the feature-engineered approach showed higher specificity in non-consensus cases. Conclusion: In this study, we demonstrated blinded evaluation using data from an independent clinical sample for assessing the performance in DAT classification models in a clinical setting. Our results showed good generalizability for two machine-learning approaches, marking an important step for the translation of pre-trained machine-learning models into clinical practice. Show more
Keywords: Alzheimer’s disease, blinded clinical evaluation, dementia of Alzheimer’s type, FDG-PET, feature-engineered classification, non-feature-engineered classification
DOI: 10.3233/JAD-201591
Citation: Journal of Alzheimer's Disease, vol. 80, no. 2, pp. 715-726, 2021
Authors: Lee, Seunghyun | Choi, Joon Yul | Lee, Wanhyung
Article Type: Research Article
Abstract: Background: Recent studies have shown that long working hours can have adverse consequences on health and possibly trigger biological processes that mediate the relationship between long working hours and cognitive decline. Objective: To investigate whether long working hours and the overall duration such exposure is associated with a decline in cognitive function. Methods: Data obtained during the Korean Longitudinal Study on Aging (n = 2,518) during the period 2006–2018 were used to explore the relationship between long working hours and cognitive decline. Korean version of the Mini-Mental State Examination (K-MMSE) scores were used to evaluate cognitive function. …Cox proportional hazard regression models were used to calculate hazard ratios (HRs) and 95% confidence intervals (CIs), which were used to evaluate declines in K-MMSE scores over the 12-year study period. Results: Overall HR (95% CI) for a decline in cognitive function in long working hours group was 1.13 (0.73–1.17). When categorized by sex, women with long working hours had an HR (95% CI) of 1.50 (1.05–2.22), K-MMSE scores decreased significantly after working long hours for 5 years (p < 0.01). Conclusion: The study furthers understanding of the effects of long working hours on cognitive decline among female workers. Further research is required to determine the effects of long working hours on cognitive functions. Show more
Keywords: Alzheimer’s disease, cognitive screening test, cohort study, dementia, epidemiology, KLoSA, long working hours, workers
DOI: 10.3233/JAD-201404
Citation: Journal of Alzheimer's Disease, vol. 80, no. 2, pp. 727-734, 2021
Authors: Sood, Ajay | Pavlik, Valory | Darby, Eveleen | Chan, Wenyaw | Doody, Rachelle
Article Type: Research Article
Abstract: Background: Cognitive profiles characterized by primarily language or visuospatial deficits have been documented in individuals meeting diagnostic criteria for probable Alzheimer’s disease (AD), but their association with progression rate or overall survival is not well described. Objective: To compare time from diagnosis to severe disease stage and death in probable AD patients classified into three groups based on neuropsychological test performance: marked verbal impairment (Verb-PI) with relatively preserved visuospatial function, marked visuospatial impairment with preserved verbal function (Vis-PI), and balanced verbal and visuospatial impairments (Bal-PI). Methods: This prospective cohort study included 540 probable AD patients attending …an academic memory clinic who were enrolled from 1995–2013 and followed annually. Eligible individuals had a Mini-Mental State Exam (MMSE) score ≥10 at baseline, and at least one annual follow up visit. We used Cox proportional hazards modeling to analyze the association of cognitive profiles with time to decline in MMSE and CDR Global Score. Results: Sixty-one (11.3%) individuals had a Verb-PI profile, 86 (16%) had a Vis-PI profile, and 393 (72.8%) a Bal-PI profile. MMSE decline to <10 was faster in Verb-PI than Vis-PI (HR 2.004, 95%CI, 1.062–3.780; p = 0.032). Progression to CDR-GS = 3 was faster in Verb-PI individuals compared to Bal-PI (HR 1.604, 95%CI, 1.022–2.515; p = 0.040) or Vis-PI (HR 2.388, 95%CI, 1.330–4.288; p = 0.004) individuals. Baseline cognitive profile did not affect mortality. Conclusion: A recognition of different AD profiles may help to personalize care by providing a better understanding of pathogenesis and expected progression. Show more
Keywords: Alzheimer’s disease variants, cognitive subtypes, disease progression, survival
DOI: 10.3233/JAD-201124
Citation: Journal of Alzheimer's Disease, vol. 80, no. 2, pp. 735-747, 2021
Authors: Lladó, Albert | Froelich, Lutz | Khandker, Rezaul K. | Roset, Montserrat | Black, Christopher M. | Lara, Nuria | Chekani, Farid | Ambegaonkar, Baishali M.
Article Type: Research Article
Abstract: Background: There exists considerable variation in disease progression rates among patients with Alzheimer’s disease (AD). Objective: The primary objective of this observational study is to assess the progression of AD by characterizing cognitive, functional, and behavioral changes during the follow-up period between 6 and 24 months. Methods: A longitudinal prospective study with community-dwelling patients with an established clinical diagnosis of AD of mild to moderate severity was conducted in Germany, Spain and the UK. A sample of 616 patients from 69 sites was included. Results: Patients had a mean of 1.9 years (SD = 1.9) since …AD diagnosis at study inclusion. Cognitive symptoms were reported to have first occurred a mean of 1.1 years (SD = 1.7) prior to AD diagnosis and 1.4 (SD = 1.8) years prior to AD treatment. Patients initially diagnosed with mild and moderate AD spent a median (95%CI) of 3.7 (2.8; 4.4) and 11.1 (6.1, ‘not reached’) years until progression to moderate and severe AD, respectively, according to the Mini-Mental State Examination (MMSE) scores. A mixed model developed for cognitive, functional, and neuropsychiatric scores, obtained from study patients at baseline and during follow-up period, showed progressive deterioration of AD patients over time. Conclusion: The study showed a deterioration of cognitive, functional, and neuropsychiatric functions during the follow-up period. Cognitive deterioration was slightly faster in patients with moderate AD compared to mild AD. The duration of moderate AD can be overestimated due to the use of retrospective data, lack of availability of MMSE scores in clinical charts and exclusion of patients at time of institutionalization. Show more
Keywords: Alzheimer’s disease, dementia, disease progression, real-world
DOI: 10.3233/JAD-201172
Citation: Journal of Alzheimer's Disease, vol. 80, no. 2, pp. 749-759, 2021
Authors: Sahu, Bijayani | Mackos, Amy R. | Floden, Angela M. | Wold, Loren E. | Combs, Colin K.
Article Type: Research Article
Abstract: Background: Alzheimer’s disease (AD) is a progressive neurodegenerative disorder characterized by the accumulation of amyloid-β (Aβ) plaques, neuroinflammation, and neuronal death. There are several well-established genetic and environmental factors hypothesized to contribute to AD progression including air pollution. However, the molecular mechanisms by which air pollution exacerbates AD are unclear. Objective: This study explored the effects of particulate matter exposure on AD-related brain changes using the APP/PS1 transgenic model of disease. Methods: Male C57BL/6;C3H wild type and APP/PS1 mice were exposed to either filtered air (FA) or particulate matter sized under 2.5μm (PM2.5 ) for 6 h/day, …5 days/week for 3 months and brains were collected. Immunohistochemistry for Aβ, GFAP, Iba1, and CD68 and western blot analysis for PS1, BACE, APP, GFAP, and Iba1 were performed. Aβ ELISAs and cytokine arrays were performed on frozen hippocampal and cortical lysates, respectively. Results: The Aβ plaque load was significantly increased in the hippocampus of PM2.5 -exposed APP/PS1 mice compared to their respective FA controls. Additionally, in the PM2.5 -exposed APP/PS1 group, increased astrocytosis and microgliosis were observed as indicated by elevated GFAP, Iba1, and CD68 immunoreactivities. PM2.5 exposure also led to an elevation in the levels of PS1 and BACE in APP/PS1 mice. The cytokines TNF-α, IL-6, IL-1β, IFN-γ , and MIP-3α were also elevated in the cortices of PM2.5 -exposed APP/PS1 mice compared to FA controls. Conclusion: Our data suggest that chronic particulate matter exposure exacerbates AD by increasing Aβ plaque load, gliosis, and the brain inflammatory status. Show more
Keywords: Alzheimer’s disease, amyloid-β plaques, neuroinflammation, particulate matter
DOI: 10.3233/JAD-200919
Citation: Journal of Alzheimer's Disease, vol. 80, no. 2, pp. 761-774, 2021
Authors: Shoup, Timothy M. | Griciuc, Ana | Normandin, Marc D. | Quinti, Luisa | Walsh, Lindsay V. | Dhaynaut, Maeva | Moon, Sung-Hyun | Guehl, Nicolas J. | Brugarolas, Pedro | Elmaleh, David R. | Fakhri, Georges El | Tanzi, Rudolph E.
Article Type: Research Article
Abstract: Background: Cromolyn is an anti-neuroinflammatory modulator with a multifactorial mechanism of action that has been shown to inhibit amyloid-β (Aβ) aggregation and enhance microglial uptake and clearance of Aβ. Objective: We report the effects of fluoro-cromolyn derivatives on microglial cell toxicity and microglial clearance of Aβ42 . Methods: Microglial cell toxicity for cromolyn derivatives were determined in naive BV2 microglial cells. Microglial clearance assays were performed with Aβ42 in naive BV2 microglial cell line and single cell clone BV2 line expressing CD33WT . PET imaging was performed for three F-18 analogs in a rhesus …macaque. Results: All compounds but derivative 8 exhibited low microglial cell toxicity. Cromolyn 1 and derivatives 2 , 4 , and 7 displayed an increased uptake on Aβ42 in naïve BV2 microglial cells. Derivative 4 increased Aβ42 uptake in a dose-dependent manner and at 75μM resulted in a one-fold increase in Aβ42 uptake in BV2-CD33WT . PET imaging for three [18 F]cromolyn analogs revealed the order of brain tracer penetration to be 4a > 10 > 2a . Tracer 4a exhibited enhanced uptake in areas of high perfusion (putamen, grey matter, and cerebellum) and lower signal in areas of lower perfusion (caudate, thalamus, and white matter). Conclusion: Substantial uptake of Aβ42 in both naïve BV2 and BV2-CD33WT cells observed with 4 indicate conversion of microglial cells from a pro-inflammatory to an activation state favoring Aβ phagocytosis/clearance. These findings suggest that a fluoro-cromolyn analog could reduce fibril-prone Aβ42 in vivo and thereby serve as a therapeutic for the treatment and prevention of AD. Show more
Keywords: Aβ phagocytosis, Alzheimer’s disease therapy, amyloid, microglial, PET imaging
DOI: 10.3233/JAD-201419
Citation: Journal of Alzheimer's Disease, vol. 80, no. 2, pp. 775-786, 2021
Authors: Wang, Yi-Zhen | Meng, Lei | Zhuang, Qi-Shuai | Shen, Liang
Article Type: Research Article
Abstract: Background: In recent years, the efficacy of type 2 diabetes mellitus (T2DM) drugs in the treatment of Alzheimer’s disease (AD) has attracted extensive interest owing to the close associations between the two diseases. Objective: Here, we screened traditional Chinese medicine (TCM) and multi-target ingredients that may have potential therapeutic effects on both T2DM and AD from T2DM prescriptions. Methods: Network pharmacology and molecular docking were used. Results: Firstly, the top 10 frequently used herbs and corresponding 275 active ingredients were identified from 263 T2DM-related TCM prescriptions. Secondly, through the comparative analysis of 208 potential …targets of ingredients, 1,740 T2DM-related targets, and 2,060 AD-related targets, 61 common targets were identified to be shared. Thirdly, by constructing pharmacological network, 26 key targets and 154 representative ingredients were identified. Further enrichment analysis showed that common targets were involved in regulating multiple pathways related to T2DM and AD, while network analysis also found that the combination of Danshen (Radix Salviae )-Gancao (Licorice )-Shanyao (Rhizoma Dioscoreae ) contained the vast majority of the representative ingredients and might be potential for the cotreatment of the two diseases. Fourthly, MAPK1, PPARG, GSK3B, BACE1, and NR3C1 were selected as potential targets for virtual screening of multi-target ingredients. Further docking studies showed that multiple natural compounds, including salvianolic acid J, gancaonin H, gadelaidic acid, icos-5-enoic acid, and sigmoidin-B, exhibited high binding affinities with the five targets. Conclusion: To summarize, the present study provides a potential TCM combination that might possess the potential advantage of cotreatment of AD and T2DM. Show more
Keywords: Alzheimer’s disease, network pharmacology, traditional Chinese medicines, type 2 diabetes mellitus
DOI: 10.3233/JAD-201336
Citation: Journal of Alzheimer's Disease, vol. 80, no. 2, pp. 787-797, 2021
Authors: Di Lorito, Claudio | Bosco, Alessandro | Godfrey, Maureen | Dunlop, Marianne | Lock, Juliette | Pollock, Kristian | Harwood, Rowan H. | van der Wardt, Veronika
Article Type: Research Article
Abstract: Background: Caring for someone with dementia is associated with negative and positive experiences. There is little evidence based on large datasets. Objective: To present data around the experience of caring for someone with dementia, to identify support (emotional and practical) needs, and inform future service provision. Methods: A mixed-methods study embedded in the Promoting Activity, Independence and Stability in Early Dementia (PrAISED) Randomized Controlled Trial. We administered questionnaires on strain, quality of life (QoL), and perceived health to 301 caregivers and assessment of cognitive performance, depression, anxiety, and disability in activities of daily living to 301 …participants with dementia. Data were analyzed through descriptive and modelling statistics. A subsample of 20 patient-caregiver dyads were qualitatively interviewed. Data around caregivers’ experience of providing care were extrapolated and analyzed through inductive thematic analysis. Results: There were significant negative associations between caregiver strain and QoL (p < 0.01) and between caregiver age and QoL (p < 0.01), and significant positive associations between caregiver strain and disability (p < 0.01), cognitive impairment (p < 0.01), depression (p < 0.05), and anxiety of the person with dementia (p < 0.05). Older caregivers reported a lack of support, reinforced by their reluctance to seek help. All caregivers reported contradictory emotions associated with caring and accumulation of strain over time. Conclusion: While there is recognition that it is essential to support caregivers, dedicated intervention programs, and support strategies to respond to the needs of older caregivers are still needed. Show more
Keywords: Caregiver, caregiver exhaustion, dementia, quality of life, randomized controlled trial
DOI: 10.3233/JAD-201257
Citation: Journal of Alzheimer's Disease, vol. 80, no. 2, pp. 799-811, 2021
Authors: Quint, Wim Hendricus | Matečko-Burmann, Irena | Schilcher, Irene | Löffler, Tina | Schöll, Michael | Burmann, Björn Marcus | Vogels, Thomas
Article Type: Research Article
Abstract: Background: Alzheimer’s disease (AD) and other tauopathies are neurodegenerative disorders characterized by cellular accumulation of aggregated tau protein. Tau pathology within these disorders is accompanied by chronic neuroinflammation, such as activation of the classical complement pathway by complement initiation factor C1q. Additionally, about half of the AD cases present with inclusions composed of aggregated alpha-synuclein called Lewy bodies. Lewy bodies in disorders such as Parkinson’s disease and Lewy body dementia also frequently occur together with tau pathology. Objective: Immunotherapy is currently the most promising treatment strategy for tauopathies. However, the presence of multiple pathological processes within tauopathies makes …it desirable to simultaneously target more than one disease pathway. Methods: Herein, we have developed three bispecific antibodies based on published antibody binding region sequences. One bispecific antibody binds to tau plus alpha-synuclein and two bispecific antibodies bind to tau plus C1q. Results: Affinity of the bispecific antibodies to their targets compared to their monospecific counterparts ranged from nearly identical to one order of magnitude lower. All bispecific antibodies retained binding to aggregated protein in patient-derived brain sections. The bispecific antibodies also retained their ability to inhibit aggregation of recombinant tau, regardless of whether the tau binding sites were in IgG or scFv format. Mono- and bispecific antibodies inhibited cellular seeding induced by AD-derived pathological tau with similar efficacy. Finally, both Tau-C1q bispecific antibodies completely inhibited the classical complement pathway. Conclusion: Bispecific antibodies that bind to multiple pathological targets may therefore present a promising approach to treat tauopathies and other neurodegenerative disorders. Show more
Keywords: Alpha-synuclein, Alzheimer’s disease, C1q, immunotherapy, synucleinopathies, tau, tauopathies
DOI: 10.3233/JAD-201334
Citation: Journal of Alzheimer's Disease, vol. 80, no. 2, pp. 813-829, 2021
Authors: Golriz Khatami, Sepehr | Domingo-Fernández, Daniel | Mubeen, Sarah | Hoyt, Charles Tapley | Robinson, Christine | Karki, Reagon | Iyappan, Anandhi | Kodamullil, Alpha Tom | Hofmann-Apitius, Martin
Article Type: Research Article
Abstract: Background: Neuroimaging markers provide quantitative insight into brain structure and function in neurodegenerative diseases, such as Alzheimer’s disease, where we lack mechanistic insights to explain pathophysiology. These mechanisms are often mediated by genes and genetic variations and are often studied through the lens of genome-wide association studies. Linking these two disparate layers (i.e., imaging and genetic variation) through causal relationships between biological entities involved in the disease’s etiology would pave the way to large-scale mechanistic reasoning and interpretation. Objective: We explore how genetic variants may lead to functional alterations of intermediate molecular traits, which can further impact neuroimaging …hallmarks over a series of biological processes across multiple scales. Methods: We present an approach in which knowledge pertaining to single nucleotide polymorphisms and imaging readouts is extracted from the literature, encoded in Biological Expression Language, and used in a novel workflow to assist in the functional interpretation of SNPs in a clinical context. Results: We demonstrate our approach in a case scenario which proposes KANSL1 as a candidate gene that accounts for the clinically reported correlation between the incidence of the genetic variants and hippocampal atrophy. We find that the workflow prioritizes multiple mechanisms reported in the literature through which KANSL1 may have an impact on hippocampal atrophy such as through the dysregulation of cell proliferation, synaptic plasticity, and metabolic processes. Conclusion: We have presented an approach that enables pinpointing relevant genetic variants as well as investigating their functional role in biological processes spanning across several, diverse biological scales. Show more
Keywords: Alzheimer’s disease, genetic variants, knowledge graph, neuroimaging, systems biology
DOI: 10.3233/JAD-201397
Citation: Journal of Alzheimer's Disease, vol. 80, no. 2, pp. 831-840, 2021
Authors: Tomoto, Tsubasa | Liu, Jie | Tseng, Benjamin Y. | Pasha, Evan P. | Cardim, Danilo | Tarumi, Takashi | Hynan, Linda S. | Munro Cullum, C. | Zhang, Rong
Article Type: Research Article
Abstract: Background: Central arterial stiffness and brain hypoperfusion are emerging risk factors of Alzheimer’s disease (AD). Aerobic exercise training (AET) may improve central arterial stiffness and brain perfusion. Objective: To investigate the effects of AET on central arterial stiffness and cerebral blood flow (CBF) in patients with amnestic mild cognitive impairment (MCI), a prodromal stage of AD. Methods: This is a proof-of-concept, randomized controlled trial that assigned 70 amnestic MCI patients into a 12-month program of moderate-to-vigorous AET or stretching-and-toning (SAT) intervention. Carotid β-stiffness index and CBF were measured by color-coded duplex ultrasonography and applanation tonometry. Total …CBF was measured as the sum of CBF from both the internal carotid and vertebral arteries, and divided by total brain tissue mass assessed with MRI to obtain normalized CBF (nCBF). Episodic memory and executive function were assessed using standard neuropsychological tests (CVLT-II and D-KEFS). Changes in cardiorespiratory fitness were measured by peak oxygen uptake (VO2peak ). Results: Total 48 patients (29 in SAT and 19 in AET) were completed one-year training. AET improved VO2peak , decreased carotid β-stiffness index and CBF pulsatility, and increased nCBF. Changes in VO2peak were associated positively with changes in nCBF (r = 0.388, p = 0.034) and negatively with carotid β-stiffness index (r = –0.418, p = 0.007) and CBF pulsatility (r = –0.400, p = 0.014). Decreases in carotid β-stiffness were associated with increases in cerebral perfusion (r = –0.494, p = 0.003). AET effects on cognitive performance were minimal compared with SAT. Conclusion: AET reduced central arterial stiffness and increased CBF which may precede its effects on neurocognitive function in patients with MCI. Show more
Keywords: Aerobic exercise, arterial stiffness, carotid artery, cerebral blood flow, cognitive function, mild cognitive impairment
DOI: 10.3233/JAD-201456
Citation: Journal of Alzheimer's Disease, vol. 80, no. 2, pp. 841-853, 2021
Authors: Brewster, Katharine K. | Hu, Mei-Chen | Wall, Melanie M. | Brown, Patrick J. | Zilcha-Mano, Sigal | Roose, Steven P. | Stein, Alexandra | Golub, Justin S. | Rutherford, Bret R.
Article Type: Research Article
Abstract: Background: Age-related hearing loss (HL) has been associated with dementia, though the neurocognitive profile of individuals with HL is poorly understood. Objective: To characterize the neurocognitive profile of HL. Methods: N = 8,529 participants from the National Alzheimer’s Coordinating Center ≥60 years and free of cognitive impairment who were characterized as Untreated-, Treated-, or No HL. Outcomes included executive function (Trail Making Test [TMT] Part B), episodic memory (Immediate/Delayed Recall), language fluency (Vegetables, Boston Naming Test), and conversion to dementia. Regression models were fit to examine associations between HL and neurocognitive performance at baseline. Cox proportional hazards models …examined the links between HL, neurocognitive scores, and development of dementia over follow-up. Results: At baseline, those with Untreated HL (versus No HL) had worse neurocognitive performance per standardized difference on executive function (TMT Part B [mean difference = 0.05 (95% CI 0.00, 0.10)]) and language fluency (Vegetables [mean difference = –0.07 (95% CI –0.14, –0.01)], Boston Naming Test [mean difference = –0.07 (95% CI –0.13, –0.01)]). No differences in these neurocognitive performance scores were demonstrated between Treated HL and No HL groups other than MMSE [mean difference = –0.06 (95% CI –0.12, 0.00)]. Through follow-up, executive dysfunction differed by hearing group (χ 2 (2) = 46.08, p < 0.0001) and was present among 39.12% in No HL, 44.85% in Untreated HL, and 49.40% in Treated HL. Worse performance across all cognitive domains predicted incident dementia. Conclusion: The observed association between Untreated HL and lower cognitive ability that improved when hearing aids were worn may reflect an inability to hear the test instructions. Future studies using cognitive assessments validated for use in HL are needed to evaluate the neuropsychological profile of HL and identify individuals at risk for dementia. Show more
Keywords: Alzheimer’s disease, cognitive dysfunction, dementia, hearing loss, neuropsychological tests
DOI: 10.3233/JAD-200908
Citation: Journal of Alzheimer's Disease, vol. 80, no. 2, pp. 855-864, 2021
Authors: Tam, Mallorie T. | Dosso, Jill A. | Robillard, Julie M.
Article Type: Research Article
Abstract: Background: The COVID-19 pandemic is impacting the physical and emotional health of older adults living with dementia and their care partners. Objective: Using a patient-centered approach, we explored the experiences and needs of people living with dementia and their care partners during the COVID-19 pandemic as part of an ongoing evaluation of dementia support services in British Columbia, Canada. Methods: A survey instrument was developed around the priorities identified in the context of the COVID-19 and Dementia Task Force convened by the Alzheimer Society of Canada. Results: A total of 417 surveys were analyzed. …Overall, respondents were able to access information that was helpful for maintaining their own health and managing a period of social distancing. Care partners reported a number of serious concerns, including the inability to visit the person that they care for in long-term or palliative care. Participants also reported that the pandemic increased their levels of stress overall and that they felt lonelier and more isolated than they did before the pandemic. The use of technology was reported as a way to connect socially with their loved ones, with the majority of participants connecting with others at least twice per week. Conclusion: Looking at the complex effects of a global pandemic through the experiences of people living with dementia and their care partners is vital to inform healthcare priorities to restore their quality of life and health and better prepare for the future. Show more
Keywords: Aged, Alzheimer’s disease, caregiver burnout, carers, COVID-19, dementia, health services for the aged, pandemic, social isolation
DOI: 10.3233/JAD-201114
Citation: Journal of Alzheimer's Disease, vol. 80, no. 2, pp. 865-875, 2021
Authors: Hirao, Kentaro | Yamashita, Fumio | Tsugawa, Akito | Haime, Rieko | Fukasawa, Raita | Sato, Tomohiko | Kanetaka, Hidekazu | Umahara, Takahiko | Sakurai, Hirofumi | Hanyu, Haruo | Shimizu, Soichiro
Article Type: Research Article
Abstract: Background: White matter hyperintensities (WMH) on MRI have been reported to increase the risk of conversion from mild cognitive impairment (MCI) to Alzheimer’s disease (AD). However, effects of the progression of WMH on the cognition of patients with MCI remains unclear to date. Objective: To investigate the association between WMH progression and cognitive decline in amnestic MCI patients. Methods: Thirty-eight subjects with amnestic MCI were analyzed prospectively every year for 2 years. Fourteen MCI subjects dropped out on the final visit, and therefore 24 subjects with MCI were analyzed for the entire duration. The volumes of …periventricular hyperintensities (PVH) and deep WMH (DWMH) were measured on T2 FLAIR using the 3D-slicer. The associations between PVH/DWMH progression and cognitive decline were investigated. Results: An increase in DWMH volume significantly correlated with changes in Mini-Mental State Examination and category verbal fluency scores, whereas an increase in PVH volume did not correlate with changes in any item. Conclusion: DWMH progression was closely associated with a decline in frontal lobe function and semantic memory, suggesting that WMH progression might affect some AD pathophysiologies in amnestic MCI patients. Show more
Keywords: Deep white matter hyperintensities, mild cognitive impairment, periventricular hyperintensities
DOI: 10.3233/JAD-201451
Citation: Journal of Alzheimer's Disease, vol. 80, no. 2, pp. 877-883, 2021
Authors: Daniele, Simona | Baldacci, Filippo | Piccarducci, Rebecca | Palermo, Giovanni | Giampietri, Linda | Manca, Maria Laura | Pietrobono, Deborah | Frosini, Daniela | Nicoletti, Valentina | Tognoni, Gloria | Giorgi, Filippo Sean | Lo Gerfo, Annalisa | Petrozzi, Lucia | Cavallini, Chiara | Franzoni, Ferdinando | Ceravolo, Roberto | Siciliano, Gabriele | Trincavelli, Maria Letizia | Martini, Claudia | Bonuccelli, Ubaldo
Article Type: Research Article
Abstract: Background: Red blood cells (RBCs) contain the majority of α -synuclein (α -syn) in blood, representing an interesting model for studying the peripheral pathological alterations proved in neurodegeneration. Objective: The current study aimed to investigate the diagnostic value of total α -syn, amyloid-β (Aβ1–42 ), tau, and their heteroaggregates in RBCs of Lewy body dementia (LBD) and Alzheimer’s disease (AD) patients compared to healthy controls (HC). Methods: By the use of enzyme-linked immunosorbent assays, RBCs concentrations of total α -syn, Aβ1–42 , tau, and their heteroaggregates (α -syn/Aβ1–42 and α -syn/tau) were measured in 27 …individuals with LBD (Parkinson’s disease dementia, n = 17; dementia with Lewy bodies, n = 10), 51 individuals with AD (AD dementia, n = 37; prodromal AD, n = 14), and HC (n = 60). Results: The total α -syn and tau concentrations as well as α -syn/tau heterodimers were significantly lower in the LBD group and the AD group compared with HC, whereas α -syn/Aβ1–42 concentrations were significantly lower in the AD dementia group only. RBC α -syn/tau heterodimers had a higher diagnostic accuracy for differentiating patients with LBD versus HC (AUROC = 0.80). Conclusion: RBC α -syn heteromers may be useful for differentiating between neurodegenerative dementias (LBD and AD) and HC. In particular, RBC α -syn/tau heterodimers have demonstrated good diagnostic accuracy for differentiating LBD from HC. However, they are not consistently different between LBD and AD. Our findings also suggest that α -syn, Aβ1–42 , and tau interact in vivo to promote the aggregation and accumulation of each other. Show more
Keywords: α-Synuclein, Alzheimer’s disease, amyloid-β , Lewy body dementia, red blood cells
DOI: 10.3233/JAD-201038
Citation: Journal of Alzheimer's Disease, vol. 80, no. 2, pp. 885-893, 2021
Authors: Phyo, Aung Zaw Zaw | Gonzalez-Chica, David A. | Stocks, Nigel P. | Storey, Elsdon | Woods, Robyn L. | Murray, Anne M. | Orchard, Suzanne G. | Shah, Raj C. | Gasevic, Danijela | Freak-Poli, Rosanne | Ryan, Joanne | on behalf of the ASPREE Investigator Group
Article Type: Research Article
Abstract: Background: Health-related quality of life (HRQoL) has been shown to predict adverse health outcome in the general population. Objective: We examined the cross-sectional association between HRQoL and cognitive performance at baseline. Next, we explored whether baseline HRQoL predicted 5-year incident cognitive decline and dementia and whether there were gender differences. Methods: 19,106 community-dwelling participants from the ASPirin in Reducing Events in the Elderly (ASPREE) trial, aged 65–98 years, free of major cognitive impairments, and completed the HRQoL 12-item short-form (SF-12) at baseline (2010–2014), were followed until June 2017. The physical (PCS) and mental component scores (MCS) …of SF-12 were calculated. The cognitive tests were assessed at baseline, year 1, 3, 5, and 7 or close-out visit. Cognitive decline was defined as > 1.5 SD drop from baseline on any of the cognitive tests. Dementia was adjudicated according to DSM-IV criteria. Linear and Cox proportional-hazards regressions were used to examine the cross-sectional and longitudinal associations respectively. Results: At baseline, higher PCS and MCS were associated with better cognition. Over a median 4.7-year follow-up, higher MCS was associated with a reduced risk of cognitive decline and dementia (12% and 15% respectively, per 10-unit increase) and a 10-unit higher PCS was associated with a 6% decreased risk of cognitive decline. PCS did not predict dementia incidence. Findings were not different by gender. Conclusion: Our study found that higher HRQoL, in particular MCS, predicted a reduced risk of cognitive decline and dementia over time in community-dwelling older people. Show more
Keywords: Cognition, cognitive dysfunction, dementia, health-related quality of life (HRQoL), quality of life
DOI: 10.3233/JAD-201349
Citation: Journal of Alzheimer's Disease, vol. 80, no. 2, pp. 895-904, 2021
Article Type: Correction
DOI: 10.3233/JAD-219002
Citation: Journal of Alzheimer's Disease, vol. 80, no. 2, pp. 905-905, 2021
IOS Press, Inc.
6751 Tepper Drive
Clifton, VA 20124
USA
Tel: +1 703 830 6300
Fax: +1 703 830 2300
sales@iospress.com
For editorial issues, like the status of your submitted paper or proposals, write to editorial@iospress.nl
IOS Press
Nieuwe Hemweg 6B
1013 BG Amsterdam
The Netherlands
Tel: +31 20 688 3355
Fax: +31 20 687 0091
info@iospress.nl
For editorial issues, permissions, book requests, submissions and proceedings, contact the Amsterdam office info@iospress.nl
Inspirees International (China Office)
Ciyunsi Beili 207(CapitaLand), Bld 1, 7-901
100025, Beijing
China
Free service line: 400 661 8717
Fax: +86 10 8446 7947
china@iospress.cn
For editorial issues, like the status of your submitted paper or proposals, write to editorial@iospress.nl
如果您在出版方面需要帮助或有任何建, 件至: editorial@iospress.nl