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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: Eyler, Lisa T. | Elman, Jeremy A. | Hatton, Sean N. | Gough, Sarah | Mischel, Anna K. | Hagler, Donald J. | Franz, Carol E. | Docherty, Anna | Fennema-Notestine, Christine | Gillespie, Nathan | Gustavson, Daniel | Lyons, Michael J. | Neale, Michael C. | Panizzon, Matthew S. | Dale, Anders M. | Kremen, William S.
Article Type: Research Article
Abstract: Background: Large-scale brain networks such as the default mode network (DMN) are often disrupted in Alzheimer’s disease (AD). Numerous studies have examined DMN functional connectivity in those with mild cognitive impairment (MCI), a presumed AD precursor, to discover a biomarker of AD risk. Prior reviews were qualitative or limited in scope or approach. Objective: We aimed to systematically and quantitatively review DMN resting state fMRI studies comparing MCI and healthy comparison (HC) groups. Methods: PubMed was searched for relevant articles. Study characteristics were abstracted and the number of studies showing no group difference or hyper- versus …hypo-connnectivity in MCI was tallied. A voxel-wise (ES-SDM) meta-analysis was conducted to identify regional group differences. Results: Qualitatively, our review of 57 MCI versus HC comparisons suggests substantial inconsistency; 9 showed no group difference, 8 showed MCI > HC and 22 showed HC > MCI across the brain, and 18 showed regionally-mixed directions of effect. The meta-analysis of 31 studies revealed areas of significant hypo- and hyper-connectivity in MCI, including hypoconnectivity in the posterior cingulate cortex/precuneus (z = –3.1, p < 0.0001). Very few individual studies, however, showed patterns resembling the meta-analytic results. Methodological differences did not appear to explain inconsistencies. Conclusions: The pattern of altered resting DMN function or connectivity in MCI is complex and variable across studies. To date, no index of DMN connectivity qualifies as a useful biomarker of MCI or risk for AD. Refinements to MCI diagnosis, including other biological markers, or longitudinal studies of progression to AD, might identify DMN alterations predictive of AD risk. Show more
Keywords: Alzheimer’s disease, default mode network, functional connectivity, mild cognitive impairment, posterior cingulate cortex, resting state functional magnetic resonance imaging
DOI: 10.3233/JAD-180847
Citation: Journal of Alzheimer's Disease, vol. 70, no. 1, pp. 107-120, 2019
Authors: Wu, Yahui | Zhao, Yuhua | Xu, Tong | You, LiWen | Zhang, Hao | Liu, Fang
Article Type: Research Article
Abstract: Recent studies suggest that severity of asthma can be modulated by neuropsychiatric conditions, while the underlying mechanisms are not clear. Here, we used ovalbumin (OVA) to induce asthma in APP/PS1 mice, a mouse model of Alzheimer’s disease (AD), or in their wildtype control C57BL/6J mice. We found that all hallmarks of asthma by OVA were significantly attenuated in APP/PS1 mice, compared to age- and gender-matched C57BL/6J mice. Interestingly, significantly higher number of regulatory T cells (Treg) was detected in the APP/PS1 mouse lung, compared to those in the C57BL/6J mouse lung. Since Foxp3 is crucial for differentiation of naive T …cells into Treg and is the most important marker for Treg, we examined the Foxp3 levels in the T cells from the lung of these mice. We found that the Foxp3 levels in the APP/PS1 mouse lung were significantly higher than those in the C57BL/6J mouse lung, likely resulting from reduced Foxp3 promoter methylation. Thus, our study suggests that AD may affect severity of asthma through methylation control of Foxp3 promoter in T cells. Show more
Keywords: Alzheimer’s disease, asthma, Foxp3, regulatory T cells (Treg cells)
DOI: 10.3233/JAD-190315
Citation: Journal of Alzheimer's Disease, vol. 70, no. 1, pp. 121-129, 2019
Authors: Rafii, Michael S. | Donohue, Michael C. | Matthews, Dawn C. | Muranevici, Gabriela | Ness, Seth | O’Bryant, Sid E. | Rissman, Robert A.
Article Type: Research Article
Abstract: Background: Adults with Down syndrome (DS) are at very high risk for Alzheimer’s disease (AD). Neurofilament light (NF-L) has emerged as a potential blood-based biomarker of neurodegeneration due to AD. Objective: To understand the relationship between plasma NF-L with age, brain amyloid, and tau pathology, neurodegeneration as well as cognitive and functional performance. Methods: We analyzed imaging data as well as cognitive measures in relation to plasma NF-L in adults with DS, ages 30 to 60 who were enrolled in the Down Syndrome Biomarker Initiative. Results: We found significant correlations between NF-L plasma concentrations …and amyloid pathology (r = 0.73, p = 0.007, pa = 0.041) and significant inverse correlations with regional glucose metabolism in 5 of 6 regions examined, which were Anterior cingulate (r = –0.55, p = 0.067, pa = 0.067), Posterior cingulate r = –0.90, p < 0.001, pa < 0.001), Lateral Temporal (r = –0.78, p = 0.004, pa = 0.012), Frontal cortex (r = –0.90, p < 0.001, p pa < 0.001), Parietal cortex (r = –0.82, p = 0.002, pa = 0.008), Precuneus (r = –0.73, pa = 0.010, pa = 0.020), and with hippocampal volume (r = –0.52, p = 0.084, pa = 0.084); and an inverse correlation with direct measures of cognition: CAMCOG (r = –0.66 p = 0.022, pa = 0.066) and positive correlation with CANTAB Paired Associates Learning (PAL) error rate (r = 0.68, p = 0.015, pa = 0.060). Finally, we found inverse relationships with informant-based functional measures (r = –0.57, p = 0.059, pa = 0.084) and OMQ-PF (r = –0.74, p = 0.008, pa = 0.041). Conclusion: Plasma NF-L is associated with progressive neurodegeneration as well as with declines in cognitive and functional measures in adults with DS. Show more
Keywords: Alzheimer’s disease, amyloid, biomarkers, blood, Down syndrome, neurofilament light, plasma, tau
DOI: 10.3233/JAD-190322
Citation: Journal of Alzheimer's Disease, vol. 70, no. 1, pp. 131-138, 2019
Authors: Cavendish, John Z. | Sarkar, Saumyendra N. | Colantonio, Mark A. | Quintana, Dominic D. | Ahmed, Nadia | White, Brishti A. | Engler-Chiurazzi, Elizabeth B. | Simpkins, James W.
Article Type: Research Article
Abstract: Mitochondrial dysfunction is often found in Alzheimer’s disease (AD) patients and animal models. Clinical severity of AD is linked to early deficiencies in cognitive function and brain metabolism, indicating that pathological changes may begin early in life. Previous studies showed decreased mitochondrial function in primary hippocampal neurons from triple-transgenic Alzheimer’s disease (3xTg-AD) mice and mitochondrial movement and structure deficits in primary neurons exposed to amyloid-β oligomers. The present study characterized mitochondrial movement, number, and structure in 3xTg-AD primary cortical neurons and non-transgenic (nonTg) controls. We found a significant reduction in mitochondrial number and movement in 3xTg-AD primary cortical neurons with …modest structural changes. Additionally, application of the sigma-1 receptor agonist, (+)SKF-10,047, markedly increased mitochondrial movement in both 3xTg-AD and nonTg primary cortical cultures after one hour of treatment. (+)SKF-10,047 also led to a trend of increased mitochondrial number in 3xTg-AD cultures. Embryonic mitochondrial movement and number deficits could be among the key steps in the early pathogenesis of AD that compromise cognitive or metabolic reserve, and amelioration of these deficits could be a promising area for further preclinical and clinical study. Show more
Keywords: Alzheimer’s disease, mitochondrial dynamics, mitochondrial size, sigma receptors
DOI: 10.3233/JAD-190143
Citation: Journal of Alzheimer's Disease, vol. 70, no. 1, pp. 139-151, 2019
Authors: Wharton, Whitney | Zhao, Liping | Steenland, Kyle | Goldstein, Felicia C. | Schneider, Julie A. | Barnes, Lisa L. | Gearing, Marla | Yasar, Sevil
Article Type: Research Article
Abstract: Background: Individuals taking renin angiotensin system (RAS) acting antihypertensives exhibit slower cognitive decline and are less likely to progress from mild cognitive impairment (MCI) to Alzheimer’s disease (AD), but the mechanism remains unclear. Objective: We tested the hypothesis that individuals taking RAS acting antihypertensives exhibit less AD-related neuropathology and slower disease progression than individuals taking non-RAS acting antihypertensives. Method: Participants included 83 individuals with MCI who were taking an antihypertensive at baseline, had at least two follow-up visits, and had postmortem neuropathological data. Participants were old (M = 83.1 years), 32% male, well educated (M = 15.7 years), …and 9.2% Black. Results: RAS medication users (N = 38) were less likely to progress to AD than non-RAS users (N = 45). RAS users exhibited fewer neurofibrillary tangles than non-RAS users in the hippocampal CA1 region (p < 0.01), entorhinal cortex (p = 0.03), and the angular gyrus, inferior temporal, mid-frontal cortex, and superior frontal (p = 0.01). Conclusion: Prevention or clearance of neurofibrillary tangles represents a mechanism by which RAS medications may slow disease progression. Show more
Keywords: Alzheimer’s disease, blood pressure, hypertension, mild cognitive impairment, neuropathology, prevention, renin angiotensin system, tau
DOI: 10.3233/JAD-190011
Citation: Journal of Alzheimer's Disease, vol. 70, no. 1, pp. 153-161, 2019
Authors: Samudra, Niyatee | Motes, Michael | Lu, Hanzhang | Sheng, Min | Diaz-Arrastia, Ramon | Devous, Michael | Hart, John | Womack, Kyle B.
Article Type: Research Article
Abstract: Alzheimer’s disease (AD) is the most common cause of neurodegenerative cognitive impairment, defined by abnormal accumulations of amyloid-β and tau. Approaches directly targeting these proteins have not resulted in a disease modifying therapy. Neurovascular unit dysfunction is a feature of AD offering an alternative target for intervention. Sildenafil, a phosphodiesterase 5 (PDE5) inhibitor, improves cognitive functioning in mouse models of AD. Recent work in AD patients has demonstrated increased cerebral blood flow, as well as brain oxygen utilization after a single dose of sildenafil. Its effect on nitric oxide-cGMP signaling may have downstream effects on neuroplasticity, amyloid-β processing, and improved …neurovascular unit function. Fractional amplitude of low frequency fluctuations (fALFF) assesses spontaneous neural activity via resting state fMRI BOLD signal (0.01–0.08 or 0.10 Hz). In AD, other assessments have revealed increased fALFF in hippocampi and parahippocampal gyri. Here, we examined the effects of a single dose of sildenafil on fALFF in a cohort of 10 AD patients. We found a decrease (p < 0.03, α = 0.05) in fALFF an hour after sildenafil administration in the right hippocampus. Additionally, cerebral vascular reactivity in response to carbon dioxide inhalation, a measure of neural vascular reserve previously collected on most of these participants, was not significantly correlated with this decrease, implying that change in fALFF may not have been solely due to altered vascular reactivity to CO2 . We demonstrate that in patients with AD, hippocampal fALFF decreases in response to sildenafil, suggesting a normalization. These findings support further investigation into the effects of sildenafil in AD. Show more
Keywords: Alzheimer’s disease, cognitive impairment, fractional amplitude of low frequency fluctuations, functional magnetic resonance imaging, sildenafil.
DOI: 10.3233/JAD-190128
Citation: Journal of Alzheimer's Disease, vol. 70, no. 1, pp. 163-170, 2019
Authors: Jones, Marggie | McDermott, Barry | Oliveira, Bárbara Luz | O’Brien, Aoife | Coogan, Declan | Lang, Mark | Moriarty, Niamh | Dowd, Eilis | Quinlan, Leo | Mc Ginley, Brian | Dunne, Eoghan | Newell, David | Porter, Emily | Elahi, Muhammad Adnan | O’ Halloran, Martin | Shahzad, Atif
Article Type: Research Article
Abstract: Background: It is known that proteins associated with Alzheimer’s disease (AD) pathogenesis are significantly reduced by 40 Hz entrainment in mice. If this were to translate to humans, verifying that such a light stimulus can induce a 40 Hz entrainment response in humans and harnessing insights from these case studies could be one step in the development of a multisensory device to prevent and treat AD. Objective: Verify the inducement of a 40 Hz response in the human brain by a 40 Hz light stimulus and obtain insights that could potentially aid in the development of a multisensory device for the prevention …and treatment of AD. Methods: Electroencephalographic brain activity was recorded simultaneously with application of stimulus at different frequencies and intensities. Power spectral densities were analyzed. Results: Entrainment to visual stimuli occurred with the largest response at 40 Hz. The high intensity 40 Hz stimulus caused widespread entrainment. The number of electrodes demonstrating entrainment increased with increasing light intensity. Largest amplitudes for the high intensity 40 Hz stimulus were consistently found at the primary visual cortex. There was a harmonic effect at double the frequency for the 40 Hz stimulus. An eyes-open protocol caused more entrainment than an eyes-closed protocol. Conclusion: It was possible to induce widespread entrainment using a 40 Hz light stimulus in this sample cohort. Insights gleaned from these case studies could potentially aid in the development of a multisensory medical device to prevent and treat AD. Show more
Keywords: 40 Hz, Alzheimer’s disease, gamma band, human study, light stimulus
DOI: 10.3233/JAD-190299
Citation: Journal of Alzheimer's Disease, vol. 70, no. 1, pp. 171-185, 2019
Authors: McClure, Richard | Redha, Rey | Vinson, Paige | Pham, Wellington
Article Type: Research Article
Abstract: A robust fluorescent readout assay using topologically-sensitive dyes improves the screening of novel amyloid-binding molecules. One of the key components that make this assay more realistic is the use of endogenous amyloid obtained from 5XFAD mouse brains. The assay conditions were optimized for high throughput screening operation with Z -prime values >0.6. Using a combination of library of 3,500 compounds including known drugs, natural-derived molecules and random organic molecules, 8 unique molecules were identified as potential amyloid-binding agents.
Keywords: Alzheimer’s disease, amyloid, high throughput screening
DOI: 10.3233/JAD-190316
Citation: Journal of Alzheimer's Disease, vol. 70, no. 1, pp. 187-197, 2019
Authors: Royall, Donald R. | Palmer, Raymond F.
Article Type: Research Article
Abstract: Background: The latent variable “δ ” (for “dementia) is a transdiagnostic measure of dementia severity. δ can be reified and applied to individuals as a composite “d-score”. Like Spearman’s general intelligence factor “g ”, δ can be constructed from almost any cognitive battery. So many are available that we must further distinguish each composite as a δ “homolog”. Fourteen have been validated. All are strongly associated with dementia severity and potentially with mild cognitive impairment (MCI) conversion. Objectives: To assess δ ’s impact on MCI conversion risk. Methods: A new δ homolog …(dDx) was constructed in 1,230 Mexican-American (MA) and 2,215 non-Hispanic White (NHW) participants in the Texas Alzheimer’s Research and Care Consortium (TARCC). 1,445 normal controls (NC) and 723 MCI were followed annually for up to 6 years. Results: Each SD decrease in the dDx score increased the risk of conversion sixteen-fold [OR = 16.39 (CI: 5.0–52.6)]. Cases below the optimal diagnostic threshold for Alzheimer’s disease (AD) versus NC were labeled as having a functionally salient cognitive impairment (FSCI). Such cases were at a 73-fold increase risk of a diagnosis of AD [OR = 73.19 (95% CI: 58.3–92.0)]. However, 25.6% of MCI cases were also FSCI(+). They accounted disproportionately for prospective conversions. Age <80 years, the absence of an ɛ 4 allele, <12 years of education, and MA ethnicity independently increased the risk of diagnosing FSCI as MCI. Conclusion: A sizable minority of MCI cases may be misdiagnosed and they account disproportionately for AD conversions. Show more
Keywords: Aging, cognition, dementia, δ , functional status, g , intelligence, mild cognitive impairment
DOI: 10.3233/JAD-190266
Citation: Journal of Alzheimer's Disease, vol. 70, no. 1, pp. 199-210, 2019
Authors: Tort-Merino, Adrià | Olives, Jaume | León, María | Peñaloza, Claudia | Valech, Natalia | Santos-Santos, Miguel A. | Càmara, Estela | Grönholm-Nyman, Petra | Martínez-Lage, Pablo | Fortea, Juan | Molinuevo, José L. | Sánchez-Valle, Raquel | Laine, Matti | Rodríguez-Fornells, Antoni | Rami, Lorena
Article Type: Research Article
Abstract: Background: We investigated a sample of cognitively healthy subjects with normal Alzheimer’s disease (AD) cerebrospinal fluid (CSF) biomarker levels to identify the earliest variables related to longitudinal memory changes. Objective: Employing a new highly demanding learning and memory test (the Ancient Farming Equipment Test; AFE-T), we aimed to investigate whether a biomarker related to neurodegeneration (i.e., CSF tau) was associated with longitudinal memory decline. Methods: Thirty-two cognitively and biologically normal (CBN) subjects underwent MRI, neuropsychological assessment, and the AFE-T at baseline and 18 months later. To explore the relationship between cognitive performance and relevant factors, a …linear model was set up. For a secondary analysis that further explore the effect of tau, the subjects were divided into CBN-Tau↓ (tau < 228.64 pg/ml; n = 16) and CBN-Tau↑ (tau > 228.64 pg/ml; n = 16). We also performed voxel-based morphometry (VBM) to identify regions of grey matter volume that would predict both baseline and longitudinal cognitive performance. Results: Our main finding was an association between CSF tau and longitudinal memory decline measured with AFE-T (B = –0.17, p < 0.05; r = –0.414; p < 0.01), and further analyses showed different evolvement between subgroups, with an accelerated decline in individuals with higher tau (F(1,31) = 8.37; p < 0.01). VBM results suggested that AFE-T performance is related to grey matter volume in a medial temporal, middle frontal, and posterior cerebellar network at baseline, and that there are strategic brain areas driving the longitudinal cognitive changes. Conclusions: The present findings provide evidence for structural and biological markers linked to cognitive aging by highlighting the role of tau, a marker of neurodegeneration, which can be related with the earliest memory changes in healthy subjects. Show more
Keywords: Aging, biomarkers, cognition, early detection, memory decline, tau, voxel-based morphometry
DOI: 10.3233/JAD-190046
Citation: Journal of Alzheimer's Disease, vol. 70, no. 1, pp. 211-225, 2019
Authors: Blanken, Anna E. | Dutt, Shubir | Li, Yanrong | Nation, Daniel A. | for the Alzheimer’s Disease Neuroimaging Initiative
Article Type: Research Article
Abstract: Background: Clinical-pathological Alzheimer’s disease (AD) subtypes may help distill heterogeneity in patient presentation. To date, no studies have utilized neuropsychological and biological markers to identify preclinical subtypes with longitudinal stability. Objective: The objective of this study was to empirically derive AD endophenotypes using a combination of cognitive and biological markers. Methods: Hierarchical cluster analysis grouped dementia-free older adults using memory, executive and language abilities, and cerebrospinal fluid amyloid-β and phosphorylated tau. Brain volume differences, neuropsychological trajectory, and progression to dementia were compared, controlling for age, gender, education, and apolipoprotein E4 (ApoE4 ). Results: Subgroups …included asymptomatic-normal (n = 653) with unimpaired cognition and subthreshold biomarkers, typical AD (TAD; n = 191) showing marked memory decline, high ApoE4 rates and abnormal biomarkers, and atypical AD (AAD; n = 132) with widespread cognitive decline, intermediate biomarker levels, older age, less education and more white matter lesions. Cognitive profiles showed longitudinal stability with corresponding patterns of cortical atrophy, despite nearly identical rates of progression to AD dementia. Conclusion: Two clinical-pathological AD subtypes are identified with potential implications for preventative efforts. Show more
Keywords: Alzheimer’s disease, atypical AD, cluster analysis, heterogeneity, neuroimaging
DOI: 10.3233/JAD-190230
Citation: Journal of Alzheimer's Disease, vol. 70, no. 1, pp. 227-239, 2019
Authors: Vorobyov, Vasily | Bakharev, Boris | Medvinskaya, Natalia | Nesterova, Inna | Samokhin, Alexander | Deev, Alexander | Tatarnikova, Olga | Ustyugov, Aleksey A. | Sengpiel, Frank | Bobkova, Natalia
Article Type: Research Article
Abstract: Cognitive malfunction, synaptic dysfunction, and disconnections in neural networks are core deficits in Alzheimer’s disease (AD). 5xFAD mice, a transgenic model of AD, are characterized by an enhanced level of amyloid-β and abnormal neurotransmission. The dopaminergic (DA) system has been shown to be involved in amyloid-β transformations and neuronal plasticity; however, its role in functional network changes in familial AD still remains unclear. In 5xFAD and non-transgenic freely moving mice, electroencephalograms (EEGs) were simultaneously recorded from the secondary motor cortex (MC), superficial layers of the hippocampal CA1 area (HPC), substantia nigra (SN), and ventral tegmental area (VTA). EEGs and their …frequency spectra were analyzed before and after systemic injection of a DA receptor agonist, apomorphine (APO). In the baseline EEG from MC and HPC of 5xFAD mice, delta and alpha oscillations were enhanced and beta activity was attenuated, compared to control mice. In VTA and SN of 5xFAD mice, delta -theta activity was decreased and beta oscillations dominated. In control mice, APO suppressed delta activity in VTA to a higher extent than in MC, whereas in 5xFAD mice, this difference was eliminated due to attenuation of the delta suppression in VTA. APO increased beta activity in MC of mice from both groups while significant beta suppression was observed in VTA of 5xFAD mice. These mice were characterized by significant decrease of tyrosine hydroxylase immunopositive cells in both VTA and SN and of DA transporter in MC and hippocampal dentate gyrus. We suggest that the EEG modifications observed in 5xFAD mice are associated with alterations in dopaminergic transmission, resulting in adaptive changes in the cerebral networks in the course of familial AD development. Show more
Keywords: Dopamine transporter, electroencephalogram, frequency spectrum, hippocampus, secondary motor cortex, substantia nigra, ventral tegmental area
DOI: 10.3233/JAD-181246
Citation: Journal of Alzheimer's Disease, vol. 70, no. 1, pp. 241-256, 2019
Authors: Niedźwieńska, Agnieszka | Kvavilashvili, Lia
Article Type: Research Article
Abstract: Identifying people with amnestic mild cognitive impairment (aMCI), who are at increased risk of developing Alzheimer’s disease, is important for improving early disease management and care. Although self- or informant-reported memory problems constitute one of the diagnostic criteria of aMCI, there is currently little empirical knowledge about the frequency and nature of everyday memory failures in aMCI compared to age-matched healthy controls. Consequently, clinicians rely on their personal judgements when assessing the seriousness of reported memory failures. To address this gap in our knowledge, 32 aMCI participants and 38 healthy controls recorded their everyday memory failures as and when they …occurred during a 7-day period, in a portable diary-booklet, by filling in a short questionnaire on a diary page. Descriptions of memory failures were coded into several subcategories of retrospective memory, prospective memory, and absent-minded failures. Results showed that a total number of recorded failures was significantly higher in participants with aMCI than controls. This group difference was mainly due to aMCI participants recording a higher number of retrospective memory failures, while groups did not differ in the number of prospective memory and absent-minded failures. Additionally, while certain types of failures (i.e., forgetting appointments and well-learned procedures) were recorded by a proportion of aMCI patients, they were never reported in a control group. Overall compliance rates were high and did not differ across the groups, suggesting that a structured diary method is feasible to use with aMCI patients, and can provide useful information about everyday memory functioning in this population. Show more
Keywords: Alzheimer’s disease, dementia, diary, memory, mild cognitive impairment
DOI: 10.3233/JAD-190219
Citation: Journal of Alzheimer's Disease, vol. 70, no. 1, pp. 257-275, 2019
Authors: Bergeron, Michael F. | Landset, Sara | Tarpin-Bernard, Franck | Ashford, Curtis B. | Khoshgoftaar, Taghi M. | Ashford, J. Wesson
Article Type: Research Article
Abstract: Background: Memory dysfunction is characteristic of aging and often attributed to Alzheimer’s disease (AD). An easily administered tool for preliminary assessment of memory function and early AD detection would be integral in improving patient management. Objective: Our primary aim was to utilize machine learning in determining initial viable models to serve as complementary instruments in demonstrating efficacy of the MemTrax online Continuous Recognition Tasks (M-CRT) test for episodic-memory screening and assessing cognitive impairment. Methods: We used an existing dataset subset (n = 18,395) of demographic information, general health screening questions (addressing memory, sleep quality, medications, and medical …conditions affecting thinking), and test results from a convenience sample of adults who took the M-CRT test. M-CRT performance and participant features were used as independent attributes: true positive/negative, percent responses/correct, response time, age, sex, and recent alcohol consumption. For predictive modeling, we used demographic information and test scores to predict binary classification of the health-related questions (yes/no) and general health status (healthy/unhealthy), based on the screening questions. Results: ANOVA revealed significant differences among HealthQScore groups for response time true positive (p = 0.000) and true positive (p = 0.020), but none for true negative (p = 0.0551). Both % responses and % correct had significant differences (p = 0.026 and p = 0.037, respectively). Logistic regression was generally the top-performing learner with moderately robust prediction performance (AUC) for HealthQScore (0.648–0.680) and selected general health questions (0.713–0.769). Conclusion: Our novel application of supervised machine learning and predictive modeling helps to demonstrate and validate cross-sectional utility of MemTrax in assessing early-stage cognitive impairment and general screening for AD. Show more
Keywords: Aging, Alzheimer’s disease, dementia, mass screening
DOI: 10.3233/JAD-190165
Citation: Journal of Alzheimer's Disease, vol. 70, no. 1, pp. 277-286, 2019
Authors: Anastasio, Thomas J.
Article Type: Research Article
Abstract: Identification of drug combinations that could be effective in Alzheimer’s disease treatment is made difficult by the sheer number of possible combinations. This analysis identifies as potentially therapeutic those drug combinations that rank highest when their efficacy is determined jointly from two independent data sources. Estimates of the efficacy of the same drug combinations were derived from a clinical dataset on cognitively impaired elderly participants and from pre-clinical data, in the form of a computational model of neuroinflammation. Linear regression was used to show that the two sets of estimates were correlated, and to rule out confounds. The ten highest …ranking, jointly determined drug combinations most frequently consisted of COX2 inhibitors and aspirin, along with various antihypertensive medications. Ten combinations of from five to nine drugs, and the three-drug combination of a COX2 inhibitor, aspirin, and a calcium-channel blocker, are discussed as candidates for consideration in future pre-clinical and clinical studies. Show more
Keywords: Combination therapy, computational modeling, data mining, deep learning, machine learning, microglia, neural network, neuroinflammation, polypharmacy, research database
DOI: 10.3233/JAD-190144
Citation: Journal of Alzheimer's Disease, vol. 70, no. 1, pp. 287-302, 2019
Authors: Huang, Xi | Wang, Chenchen | Tian, Sai | Huang, Rong | Guo, Dan | Zhang, Haoqiang | Shi, Jijing | Wang, Shaohua
Article Type: Research Article
Abstract: Background: In addition to glucose metabolism, adipocytokine Nicotinamide phosphoribosyltransferase (Nampt) has been proposed as a multifunctional protein involved in insulin resistance. Insulin resistance always occurs before the onset of type 2 diabetes mellitus (T2DM) and damages the cognition of T2DM patients very early. Objective: We aimed to investigate the role and potential clinical value of Nampt in early cognitive decline of T2DM. Methods: A total of 195 Chinese T2DM patients were enrolled and divided into a mild cognition impairment (MCI) group and a healthy cognition group according to Montreal Cognitive Assessment (MoCA) score. Their cognitive function …was extensively assessed. The plasma level of Nampt was measured via enzyme-linked immunosorbent assay. Results: In the MCI group (n = 78, MoCA < 26), the plasma level of Nampt was significantly higher than the controls (p < 0.01). After adjusting for age, sex, and level of education, Nampt levels were negatively associated with most of the cognitive domains forecasting hypomnesia (all p < 0.007). Nevertheless, hierarchical regression analysis further revealed that Nampt was an independent risk factor of MCI in Chinese T2DM patients (all p < 0.05), including Logic Memory Test (β= –0.31, p < 0.01), Auditory Verbal Learning Test delayed recall (β= –0.26, p < 0.01), and so on, which represent memory function. Correlation analysis showed that Nampt related to insulin resistance (HOMA-IR), glycosylated hemoglobin (HbA1c), and lipid levels (all p < 0.05). Conclusions: We found that higher plasma level of Nampt presages memory dysfunction in MCI in Chinese T2DM patients. Further studies are necessary to confirm its scanning and prognosis prediction value of the disease clinically. Show more
Keywords: Adipocytokine, Alzheimer’s disease, hypomnesia, mild cognition impairment, nicotinamide phosphoribosyltransferase, type 2 diabetes
DOI: 10.3233/JAD-190269
Citation: Journal of Alzheimer's Disease, vol. 70, no. 1, pp. 303-314, 2019
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