Journal of Alzheimer's Disease - Volume 48, issue 3

Authors: Hu, Shunze | Wang, Huan | Chen, Kun | Cheng, Peng | Gao, Shutao | Liu, Jian | Li, Xiao | Sun, Xuying

Article Type: Research Article

Abstract: MicroRNAs (miRNAs) are small (∼22-nucleotide [nt]) noncoding RNAs that regulate biological processes at the post-transcriptional level. Dysregulation of specific miRNAs leads to impaired synaptic plasticity resulting in Alzheimer’s disease (AD). Amyloid-β (Aβ) accumulation is the most important pathogenic factor for AD development. Therefore, focusing on Aβ-targeted miRNAs may have therapeutic implications for AD. We found that miR-34c, a miRNA that was previously reported to be upregulated in a transgenic AD model and patients, was significantly increased in hippocampal neurons exposed to Aβ. Western blots and luciferase assay confirmed that increased miR-34c was closely related to VAMP2 reduction. Furthermore, miR-34c blockade …upregulated VAMP2 expression and rescued synaptic failure as well as learning and memory deficits caused by Aβ. The Aβ-miR-34c-VAMP2 pathway mediates the sustained VAMP2 reduction in AD patients and provides a novel underlying epigenetic mechanism for attenuation of Aβ toxicity in AD. Show more

Keywords: Alzheimer’s disease, amyloid-β, miR-34c, VAMP2

DOI: 10.3233/JAD-150432

Citation: Journal of Alzheimer's Disease, vol. 48, no. 3, pp. 673-686, 2015

Authors: Meier, Shelby | Bell, Michelle | Lyons, Danielle N. | Ingram, Alexandria | Chen, Jing | Gensel, John C. | Zhu, Haining | Nelson, Peter T. | Abisambra, Jose F.

Article Type: Research Article

Abstract: Alzheimer’s disease (AD) is a progressive neurodegenerative disorder that is pathologically characterized by the formation of extracellular amyloid plaques and intraneuronal tau tangles. We recently identified that tau associates with proteins known to participate in endoplasmic reticulum (ER)-associated degradation (ERAD); consequently, ERAD becomes dysfunctional and causes neurotoxicity. We hypothesized that tau associates with other ER proteins, and that this association could also lead to cellular dysfunction in AD. Portions of human AD and non-demented age matched control brains were fractionated to obtain microsomes, from which tau was co-immunoprecipitated. Samples from both conditions containing tau and its associated proteins were analyzed …by mass spectrometry. In total, we identified 91 ER proteins that co-immunoprecipitated with tau; 15.4% were common between AD and control brains, and 42.9% only in the AD samples. The remainder, 41.8% of the proteins, was only seen in the control brain samples. We identified a variety of previously unreported interactions between tau and ER proteins. These proteins participate in over sixteen functional categories, the most abundant being involved in RNA translation. We then determined that association of tau with these ER proteins was different between the AD and control samples. We found that tau associated equally with the ribosomal protein L28 but more robustly with the ribosomal protein P0. These data suggest that the differential association between tau and ER proteins in disease could reveal the pathogenic processes by which tau induces cellular dysfunction. Show more

Keywords: Alzheimer’s disease, co-immunoprecipitation, endoplasmic reticulum, mass spectrometry, microsome, ribosome, tau, tauopathies

DOI: 10.3233/JAD-150298

Citation: Journal of Alzheimer's Disease, vol. 48, no. 3, pp. 687-702, 2015

Authors: Guido, Davide | Morandi, Gabriella | Palluzzi, Fernando | Borroni, Barbara

Article Type: Research Article

Abstract: In this paper, we reconstructed the medical history of frontotemporal dementia (FTD) by reviewing the literature and analyzing papers with the highest impact through citation index. Several research studies and groups involved in FTD have been reviewed. An increasing amount of knowledge has been made available in the last 20 years through a large number of publications, leading to a better definition of the genetic and clinical bases of the disease. A total of 1,436 references (articles and reviews), published in 395 journals, were retrieved through the Scopus database. The two highest publication peaks (i.e., largest number of publications) were …found in 2000 and 2008. The most cited papers considering both total citation number and the number of citations within the first two years after publication refer to: (i) the genetic bases of FTD, (ii) the clinical criteria that progressively refined the different FTD phenotypes, and (iii) FTD epidemiology. Advanced neuroimaging techniques, genotype-phenotype heterogeneity, and animal models gave us a broader understanding of various aspects of the disorder. These findings confirm the great interest in FTD research. The analysis of the literature might help in guiding future goals in the field. Show more

Keywords: Bibliometric analysis, citations analysis, frontotemporal dementia, frontotemporal lobar degeneration

DOI: 10.3233/JAD-150275

Citation: Journal of Alzheimer's Disease, vol. 48, no. 3, pp. 703-709, 2015

Authors: Duits, Flora H. | Hernandez-Guillamon, Mar | Montaner, Joan | Goos, Jereon D.C. | Montañola, Alex | Wattjes, Mike P. | Barkhof, Frederik | Scheltens, Philip | Teunissen, Charlotte E. | van der Flier, Wiesje M.

Article Type: Research Article

Abstract: Matrix metalloproteinases (MMPs) are a family of enzymes able to degrade components of the extracellular matrix, which is important for normal blood-brain barrier function. Their function is regulated by tissue inhibitors of matrix metalloproteinases (TIMPs). We investigated whether MMPs and TIMPs in cerebrospinal fluid (CSF) and plasma were altered in Alzheimer’s disease (AD) and vascular dementia (VaD), and whether this effect was modified by presence of cerebral micro-bleeds in AD patients. In addition, we assessed associations of MMPs and TIMPs with CSF amyloid-β1 - 42 (Aβ42 ), tau, and tau phosphorylated at threonine-181 (p-tau). We measured MMP2, MMP9, and MMP10, and …TIMP1 and TIMP2 in CSF and plasma of 52 AD patients, 26 matched controls, and 24 VaD patients. AD patients showed higher plasma MMP2 levels compared to VaD patients (p  <  0.05), and higher CSF MMP10 levels compared to controls (p  <  0.05). Microbleeds in AD were associated with lower CSF TIMP1, TIMP2 and MMP9 in a dose-response relation. In addition, CSF MMP2 was associated with p-tau (St.B 0.23, p  <  0.05), and CSF MMP10 with tau (St.B 0.38, p  <  0.001) and p-tau (St.B 0.40, p  <  0.001). Our findings suggest involvement of MMP2 and MMP10 in AD pathology. Lower levels of TIMPs in AD patients with microbleeds suggest less MMP inhibition in patients with concurrent cerebral microbleeds, which may hypothetically lead to a more vulnerable blood-brain barrier in these patients. Show more

Keywords: Alzheimer’s disease, cerebral amyloid angiopathy, cerebrospinal fluid, matrix metalloproteinases, microbleeds, tissue inhibitors of matrix metalloproteinases

DOI: 10.3233/JAD-143186

Citation: Journal of Alzheimer's Disease, vol. 48, no. 3, pp. 711-720, 2015

Authors: Soto-Gordoa, Myriam | Arrospide, Arantzazu | Moreno-Izco, Fermín | Martínez-Lage, Pablo | Castilla, Iván | Mar, Javier

Article Type: Research Article

Abstract: Risk and protective factors such as obesity, hypercholesterolemia, physical activity, and hypertension can play a role in the development of dementia. Our objective was to measure the effect of modification of risk and protective factors on the prevalence and economic burden of dementia in the aging Spanish population during 2010–2050. A discrete event simulation model including risk and protective factors according to CAIDE (Cardiovascular Risk Factors, Aging and Incidence of Dementia) Risk Score was built to represent the natural history of dementia. Prevalence of dementia was calculated from 2010 to 2050 according to different scenarios of risk factor prevalence to …assess the annual social and health care costs of dementia. The model also supplied hazard ratios for dementia. Aging will increase between 49% and 16% each decade in the number of subjects with dementia. The number of working-age individuals per person with dementia will decrease to a quarter by 2050. An intervention leading to a 20% change in risk and protective factors would reduce dementia by 9% , prevent over 100,000 cases, and save nearly 4,900 million euros in 2050. Switching individuals from a group with a specific risk factor to one without it nearly halved the risk of the development of dementia. Dementia prevalence will grow unmanageable if effective prevention strategies are not developed. Interventions aiming to reduce modifiable risk factor prevalence represent valid and effective alternatives to reduce dementia burden. However, further research is needed to identify causal relationships between dementia and risk factors. Show more

Keywords: Alzheimer’s disease, dementia, hypercholesterolemia, hypertension, obesity, primary prevention, projections, physical activity, risk factors

DOI: 10.3233/JAD-150233

Citation: Journal of Alzheimer's Disease, vol. 48, no. 3, pp. 721-730, 2015

Authors: Hong, Hyun-Seok | Maezawa, Izumi | Petrlova, Jitka | Zhao, Xiao-Yan | C. Voss, John | Jin, Lee-Way

Article Type: Research Article

Abstract: Amyloid-β (Aβ) protein causes neurotoxicity and its abnormal aggregation into amyloid is a pathological hallmark of Alzheimer’s disease (AD). Cellular proteins able to interact with Aβ or its precursor, AβPP (amyloid-β protein precursor), may regulate Aβ production and neurotoxicity. We identified a brain-enriched type I transmembrane protein, tomoregulin (TR), that directly binds Aβ and Aβ oligomers (AβO). TR co-immunoprecipitated with Aβ and AβO in cultured cells and co-localized with amyloid plaques and intraneuronal Aβ in the 5xFAD AD mouse model. TR was also enriched in astrocytic processes reactive to amyloid plaques. Surface plasmon resonance spectroscopy studies showed that the extracellular …domain of TR binds to AβO with a high affinity (KD  = 76.8 nM). Electron paramagnetic resonance spectroscopy also demonstrated a physical interaction between spin-labeled Aβ and the TR extracellular domain in solution. Furthermore, TR also interacted with AβPP and enhanced its cleavage by α -secretase. Both cellular expression of TR and application of recombinant TR extracellular domain protected N2a neurons from AβO-induced neuronal death. These data provide first evidence that neuronal and astrocytic expression of TR is intimately related to Aβ metabolism and toxicity, and could be neuroprotective through its direct interaction with Aβ and AβPP. Show more

Keywords: Alzheimer’s disease, amyloid, binding, neuroprotection, neurotoxicity, tomoregulin

DOI: 10.3233/JAD-150318

Citation: Journal of Alzheimer's Disease, vol. 48, no. 3, pp. 731-743, 2015

Authors: Foraker, Jessica | Millard, Steven P. | Leong, Lesley | Thomson, Zachary | Chen, Sunny | Keene, C. Dirk | Bekris, Lynn M. | Yu, Chang-En

Article Type: Research Article

Abstract: The ɛ 4 allele of the human apolipoprotein E gene (APOE ) is a well-proven genetic risk factor for the late onset form of Alzheimer’s disease (AD). However, the biological mechanisms through which the ɛ 4 allele contributes to disease pathophysiology are incompletely understood. The three common alleles of APOE , ɛ 2, ɛ 3 and ɛ 4, are defined by two single nucleotide polymorphisms (SNPs) that reside in the coding region of exon 4, which overlaps with a well-defined CpG island (CGI). Both SNPs change not only the protein codon but also the quantity of CpG dinucleotides, primary sites …for DNA methylation. Thus, we hypothesize that the presence of an ɛ 4 allele changes the DNA methylation landscape of the APOE CGI and that such epigenetic alteration contributes to AD susceptibility. To explore the relationship between APOE genotype, AD risk, and DNA methylation of the APOE CGI, we applied bisulfite pyrosequencing and evaluated methylation profiles of postmortem brain from 15 AD and 10 control subjects. We observed a tissue-specific decrease in DNA methylation with AD and identified two AD-specific differentially methylated regions (DMRs), which were also associated with APOE genotype. We further demonstrated that one DMR was completely un-methylated in a sub-population of genomes, possibly due to a subset of brain cells carrying deviated APOE methylation profiles. These data suggest that the APOE CGI is differentially methylated in AD brain in a tissue- and APOE -genotype-specific manner. Such epigenetic alteration might contribute to neural cell dysfunction in AD brain. Show more

Keywords: Alzheimer’s disease, apolipoprotein E, CGI, CpG island, DMR, DNA methylation, epigenetics, pyrosequencing

DOI: 10.3233/JAD-143060

Citation: Journal of Alzheimer's Disease, vol. 48, no. 3, pp. 745-755, 2015

Authors: Matsuzono, Kosuke | Sato, Kota | Kono, Syoichiro | Hishikawa, Nozomi | Ohta, Yasuyuki | Yamashita, Toru | Deguchi, Kentaro | Nakano, Yumiko | Abe, Koji

Article Type: Research Article

Abstract: Background/Objective: Alzheimer’s disease (AD) is one of the most important diseases in an aging society, but the clinical effects of rivastigmine have not been fully examined in real world domestic clinics. Methods: We performed the “Okayama Rivastigmine Study (ORS)” to retrospectively analyze the clinical effects of rivastigmine (n  = 75) or donepezil (n  = 71) on AD patients with seven dementia assessment batteries at the baseline, 3, 6, and 12 months. In addition, we divided the rivastigmine group into two subgroups at the baseline: the mild behavioral and psychological symptoms of dementia (BPSD) group (Abe’s BPSD score …(ABS) <6) and the severe BPSD group (6≤ABS). In these two subgroups, baseline scores and changes were also retrospectively analyzed until 12 months. Results: Rivastigmine significantly improved the Mini-Mental State Examination score at 3 months (* p  <  0.05 versus baseline) and at 6 months (* p  <  0.05), the Frontal Assessment Battery (FAB) at 6 months (* p  <  0.05), and ABS at 3 months (** p  <  0.01) while donepezil only stabilized the three cognitive scores. On the other hand, the Geriatric Depression Scale and the Apathy Scale were stable until 12 months in both groups. Baseline BPSD severity-dependent analysis showed a small improvement of FAB at 6 months in the mild BPSD subgroup (* p  <  0.05) and a great improvement of ABS at 3 months in the severe BPSD subgroup (** p  <  0.01) in the rivastigmine group. Conclusions: Our present study showed that rivastigmine improved both cognitive and affective functions at 3 and 6 months, and suggested an advantage at 3 and 6 months compared to donepezil in real world dementia clinics. Show more

Keywords: Affective function, Alzheimer’s disease, cognitive function, donepezil, rivastigmine

DOI: 10.3233/JAD-150518

Citation: Journal of Alzheimer's Disease, vol. 48, no. 3, pp. 757-763, 2015

Authors: Pertl, Marie-Theres | Benke, Thomas | Zamarian, Laura | Delazer, Margarete

Article Type: Research Article

Abstract: Making advantageous decisions is important in everyday life. This study aimed at assessing how patients with mild cognitive impairment (MCI) make decisions under risk. Additionally, it investigated the relationship between decision making, ratio processing, basic numerical abilities, and executive functions. Patients with MCI (n  = 22) were compared with healthy controls (n  = 29) on a complex task of decision making under risk (Game of Dice Task-Double, GDT-D), on two tasks evaluating basic decision making under risk, on a task of ratio processing, and on several neuropsychological background tests. Patients performed significantly lower than controls on the GDT-D and on ratio processing, …whereas groups performed comparably on basic decision tasks. Specifically, in the GDT-D, patients obtained lower net scores and lower mean expected values, which indicate a less advantageous performance relative to that of controls. Performance on the GDT-D correlated significantly with performance in basic decision tasks, ratio processing, and executive-function measures when the analysis was performed on the whole sample. Patients with MCI make sub-optimal decisions in complex risk situations, whereas they perform at the same level as healthy adults in simple decision situations. Ratio processing and executive functions have an impact on the decision-making performance of both patients and healthy older adults. In order to facilitate advantageous decisions in complex everyday situations, information should be presented in an easily comprehensible form and cognitive training programs for patients with MCI should focus—among other abilities—on executive functions and ratio processing. Show more

Keywords: Aging, decision making, dementia, ratio processing

DOI: 10.3233/JAD-150291

Citation: Journal of Alzheimer's Disease, vol. 48, no. 3, pp. 765-779, 2015

Authors: Zhang, Sisi | Chen, Yaojing | Liu, Zhen | Zhang, Junying | Li, Xin | Cui, Ruixue | Zhang, Zhanjun

Article Type: Research Article

Abstract: The apolipoprotein E (APOE ) ɛ 4 allele is the strongest genetic risk factor for Alzheimer’s disease (AD). This study aimed to investigate abnormality of white matter integrity and its relationship to cognitive impairments in Chinese non-demented elderly with and without the ɛ 4 allele. We assessed cognitive differences using a series of neuropsychological tests and assessed white matter integrity using tract-based spatial statistics to measure mean diffusivity and fractional anisotropy. We determined that there were no statistically significant group differences in any neuropsychological measures. However, APOE ɛ 4 carriers without cognitive decline exhibited widespread disruption of the white …matter tracts in several areas, including the cingulum, fornix, corpus callosum, and corona radiate. Furthermore, a correlation analysis in ɛ 4 carriers indicated that disruption of the right fornix stria terminalis and the genu of the corpus callosum were positively associated with cognitive impairment, including memory, executive function, spatial processing, attention, and language. The present study reveals the deleterious effects of the ɛ 4 allele on white matter, and this damage may potentially serve as a biomarker in preclinical investigations. Our promising results encourage further investigation using a multidimensional longitudinal approach with larger samples. Show more

Keywords: Alzheimer’s disease, APOE ɛ4 allele, cognition, diffusion tensor imaging, tract-based spatial statistics, white matter

DOI: 10.3233/JAD-150357

Citation: Journal of Alzheimer's Disease, vol. 48, no. 3, pp. 781-791, 2015

Authors: Di Stefano, Francesca | Epelbaum, Stephane | Coley, Nicola | Cantet, Christelle | Ousset, Pierre-Jean | Hampel, Harald | Bakardjian, Hovagim | Lista, Simone | Vellas, Bruno | Dubois, Bruno | Andrieu, Sandrine | for the GuidAge study group

Article Type: Research Article

Abstract: In therapeutic trials, it is crucial to identify Alzheimer’s disease (AD) at its prodromal stage. We assessed the accuracy of the free and cued selective reminding test (FCSRT) compared to other cognitive tests to predict AD dementia in subjects with subjective cognitive decline or mild cognitive impairment. Subjects from the placebo group of the GuidAge trial over 70 years old and without clinical signs of dementia at baseline who completed the 5-year follow-up free of dementia (n  = 840) or developed AD dementia (n  = 73) were included in our study. Among all the tests, the sum of the 3 free recall …of the FCSRT (FCSRT-FR) and the sum of free and cued recall (FCSRT-TR) yielded the best results to predict AD dementia occurrence (all p values <0.05 for comparison of FCSRT-FR ROC and MMSE, CDRsb, and CVF ROCs). FCSRT-FR had an area under the ROC curve of 0.799 (95% CI 0.738–0.85) and the optimal cut-off was 20 (se 68.06% , sp 81.43% , PPV 23.90% , NPV 96,75%). Concerning FCSRT-TR, the AUC was 0.776 and the optimal cut-off was 42 (se 62.5% , sp 82.26% , PPV 23.20% and NPV 96.24%). This study sets the framework for implementing the FCSRT in clinical and therapeutic trials for efficient subject selection. Show more

Keywords: Alzheimer’s disease, free and cued selective reminding test, IWG criteria, prodromal, subjective cognitive decline

DOI: 10.3233/JAD-150013

Citation: Journal of Alzheimer's Disease, vol. 48, no. 3, pp. 793-804, 2015

Authors: Eriksdotter, Maria | Vedin, Inger | Falahati, Farshad | Freund-Levi, Yvonne | Hjorth, Erik | Faxen-Irving, Gerd | Wahlund, Lars-Olof | Schultzberg, Marianne | Basun, Hans | Cederholm, Tommy | Palmblad, Jan

Article Type: Research Article

Abstract: Background: ω3 fatty acids (ω3 FAs) may slow the rate of decline in cognitive performance in mild forms of cognitive impairment and Alzheimer’s disease (AD). However, the relationship between changes of plasma ω3 FA levels and cognitive performance, as well as effects of gender, are poorly known. Objective: To study the effect of 6-month administration of DHA-rich ω3 FA supplementation on plasma FA profiles in patients with mild to moderate AD in relation to cognitive performance and gender. This investigation is part of the OmegAD Study. Methods: 174 AD patients (74 ± 9 years) were …randomized to a daily intake of 2.3 g ω3 FA or placebo for 6 months; subsequently all received the ω3 FA preparation for the next 6 months. Baseline as well as changes in plasma levels of the main ω3 FAs in 165 patients, while receiving ω3 FA supplementation for 6 months, were analyzed for association to cognitive performance (assessed by ADAS-cog and MMSE scores) as well as to gender. Results: Preservation of cognitive functioning, assessed by ADAS-cog or its sub-items (but not MMSE) scores, was significantly associated to increasing plasma ω3 FA levels over time. Thus, the higher ω3 FA plasma levels rose, the lower was the rate of cognitive deterioration. This effect was not related to gender; since although females displayed higher ω3 FA plasma levels than did males after 6 months of supplementation, this difference disappeared when adjusted for body weight. Conclusions: Since our study suggests dose-response relationships between plasma levels of ω3 FA and preservation of cognition, future ω3 FA trials in patients with mild AD should consider exploring graded (and body weight adjusted) doses of ω3 FA. Show more

Keywords: Alzheimer’s disease, cognition, DHA, EPA, gender, ω3 fatty acids, ClinicalTrials.gov identifier: NCT00211159

DOI: 10.3233/JAD-150102

Citation: Journal of Alzheimer's Disease, vol. 48, no. 3, pp. 805-812, 2015

Authors: Hilal, Saima | Amin, Shaik Muhammad | Venketasubramanian, Narayanaswamy | Niessen, Wiro J. | Vrooman, Henri | Wong, Tien Yin | Chen, Christopher | Ikram, Mohammad Kamran

Article Type: Research Article

Abstract: Background: Cortical atrophy is a key neuroimaging feature of dementia. However, the role of subcortical gray matter reduction in cognitive impairment has not been explored extensively. Objectives: We examined the risk factors of subcortical structures on neuroimaging and their association with cognitive impairment and dementia. Methods: Data from two studies were used: a subsample from the Epidemiology of Dementia in Singapore (EDIS) study of non-demented community-dwelling subjects (n  = 550) and a case-control study. Subjects underwent similar neuropsychological tests and brain MRI. Subcortical volumes of accumbens, amygdala, caudate, pallidum, putamen, thalamus, hippocampus, and brainstem were measured. …Cognitive impairment no dementia (CIND), dementia and its subtypes, vascular cognitive impairment (VCI), were defined using accepted criteria. Cognitive function was also expressed as both composite and domain-specific Z-scores. Results: In the EDIS study, age, female gender, Malay ethnicity, diabetes, lacunar-infarcts, and white matter lesions were the most important risk factors for subcortical atrophy. Moreover, smaller volumes of accumbens, amygdala, caudate, thalamus, and brainstem were significantly associated with lower cognitive composite Z-scores. With respect to clinical outcomes in the case-control study, structures such as the accumbens, caudate, putamen, and hippocampus were associated with both CIND and dementia. Smaller caudate and pallidum volumes were related to VCI whereas amygdalar atrophy was only associated with non-VCI. Furthermore, subcortical atrophy was related to both VCI and non-VCI. Conclusion: Subcortical gray matter atrophy is not only observed in dementia, but also in the preclinical stages of cognitive impairment. Furthermore, besides VCI, subcortical structures were also related to non-VCI. Show more

Keywords: Cognitive impairment, magnetic resonance imaging, risk factors, subcortical atrophy

DOI: 10.3233/JAD-150473

Citation: Journal of Alzheimer's Disease, vol. 48, no. 3, pp. 813-823, 2015

Authors: Diehl-Wiesenecker, Eva | von Arnim, Christine A.F. | Dupuis, Luc | Müller, Hans-Peter | Ludolph, Albert C. | Kassubek, Jan

Article Type: Research Article

Abstract: Background: Total and central adiposity have been associated with increased risk of Alzheimer’s disease (AD). Visceral and subcutaneous adipose tissues have different metabolic characteristics and could therefore be differentially associated with AD. Objective: To compare regional fat distribution determined by magnetic resonance imaging (MRI) in AD patients and healthy controls and investigate associations with stage of the disease and chemical markers. The investigation was performed in a prospective case-control study. Methods: We examined thirty patients with mild to moderate AD by whole-body MRI (1.5 T) and clinical questionnaires in comparison to thirty …cognitively healthy age- and gender-matched study participants. Volumes of total, subcutaneous, and visceral body fat tissue were determined by an unbiased automatic analysis algorithm. Levels of leptin, ghrelin, and adiponectin were determined in serum, amyloid-β (Aβ)1-42 and tau protein levels in cerebrospinal fluid (CSF). Results: Male AD patients displayed significantly more total fat tissue than male controls. This difference was not observed in women. We observed a trend toward higher volume of visceral fat tissue in all patients (p  = 0.13). Severity of disease was not associated with fat distribution in our study. Increased leptin levels correlated with lower CSF Aβ1-42 in female, but not in male, AD patients. Conclusions: Fat volume is increased in male, but not in female AD patients. Negative correlation of leptin levels and CSF Aβ1-42 in females might be one co-factor for the increased AD risk of females. Further studies are required to confirm this gender difference in fat volume during AD and evaluate its pathophysiological importance. Show more

Keywords: Leptin, magnetic resonance imaging, subcutaneous fat, visceral fat

DOI: 10.3233/JAD-150426

Citation: Journal of Alzheimer's Disease, vol. 48, no. 3, pp. 825-832, 2015

Authors: Price, Catherine C. | Tanner, Jared J. | Schmalfuss, Ilona M. | Brumback, Babette | Heilman, Kenneth M. | Libon, David J.

Article Type: Research Article

Abstract: Background: There is remarkable heterogeneity in clinical Alzheimer’s disease (AD) or vascular dementia (VaD). Objectives: 1) To statistically examine neuropsychological data to determine dementia subgroups for individuals clinically diagnosed with AD or VaD and then 2) examine group differences in specific gray/white matter regions of interest. Methods: A k-means cluster analysis requested a 3-group solution from neuropsychological data acquired from individuals diagnosed clinically with AD/VaD. MRI measures of hippocampal, caudate, ventricular, subcortical lacunar infarction, whole brain volume, and leukoaraiosis (LA) were analyzed. Three regions of LA volumes were quantified and these included …the periventricular (5 mm around the ventricles), infracortical (5 mm beneath the gray matter), and deep (between periventricular and infracortical) regions. Results: Cluster analysis sorted AD/VaD patients into single domain amnestic (n  = 41), single-domain dysexecutive (n  = 26), and multi-domain (n  = 26) phenotypes. Multi-domain patients exhibited worst performance on language tests; however, multi-domain patients were equally impaired on memory tests when compared to amnestic patients. Statistically-determined groups dissociated using neuroradiological parameters: amnestic and multi-domain groups presented with smaller hippocampal volume while the dysexecutive group presented with greater deep, periventricular, and whole brain LA. Neither caudate nor lacunae volume differed by group. Caudate nucleus volume negatively correlated with total LA in the dysexecutive and multi-domain groups. Conclusions: There are at least three distinct subtypes embedded within patients diagnosed clinically with AD/VaD spectrum dementia. We encourage future research to assess a) the neuroradiological substrates underlying statistically-determined AD/VaD spectrum dementia and b) how statistical modeling can be integrated into existing diagnostic criteria. Show more

Keywords: Caudate nucleus, executive function, hippocampus, lacune, learning, leukoaraiosis, memory, Philadelphia (repeatable) Verbal Learning Test, ventricles, white matter abnormalities

DOI: 10.3233/JAD-150407

Citation: Journal of Alzheimer's Disease, vol. 48, no. 3, pp. 833-847, 2015

Authors: Kuntz, Mélanie | Candela, Pietra | Saint-Pol, Julien | Lamartinière, Yordenca | Boucau, Marie-Christine | Sevin, Emmanuel | Fenart, Laurence | Gosselet, Fabien

Article Type: Research Article

Abstract: One of the prime features of Alzheimer’s disease (AD) is the excessive accumulation of amyloid-β (Aβ) peptides in the brain. Several recent studies suggest that this phenomenon results from the dysregulation of cholesterol homeostasis in the brain and impaired bidirectional Aβ exchange between blood and brain. These mechanisms appear to be closely related and are controlled by the blood-brain barrier (BBB) at the brain microvessel level. In animal models of AD, the anticancer drug bexarotene (a retinoid X receptor agonist) has been found to restore cognitive functions and decrease the brain amyloid burden by regulating cholesterol homeostasis. However, the drug’s …therapeutic effect is subject to debate and the exact mechanism of action has not been characterized. Therefore, the objective of this present study was to determine bexarotene’s effects on the BBB. Using an in vitro model of the human BBB, we investigated the drug’s effects on cholesterol exchange between abluminal and luminal compartments and the apical-to-basolateral transport of Aβ peptides across the BBB. Our results demonstrated that bexarotene induces the expression of ABCA1 but not ApoE. This upregulation correlates with an increase in ApoE2-, ApoE4-, ApoA-I-, and HDL-mediated cholesterol efflux. Regarding the transport of Aβ peptides, bexarotene increases the expression of ABCB1, which in turn decreases Aβ apical-to-basolateral transport. Our results showed that bexarotene not only promotes the cholesterol exchange between the brain and the blood but also decreases the influx of Aβ peptides across BBB, suggesting that bexarotene is a promising drug candidate for the treatment of AD. Show more

Keywords: ABCA1, ABCB1, Aβ peptide, bexarotene, blood-brain barrier, cholesterol, RAGE, RXR

DOI: 10.3233/JAD-150469

Citation: Journal of Alzheimer's Disease, vol. 48, no. 3, pp. 849-862, 2015

Authors: You, S. Christine | Walsh, Christine M. | Chiodo, Louis A. | Ketelle, Robin | Miller, Bruce L. | Kramer, Joel H.

Article Type: Research Article

Abstract: Background: Cognitive deficits are presumed to be the primary driver of functional impairment in Alzheimer’s disease (AD); however, functional impairment is likely multifactorially determined. Objective: Our objective was to determine the relative contribution of neuropsychiatric symptoms in predicting ratings of functional status. Methods: A total of 223 patients received routine neurological and neuropsychological evaluations and met criteria of probable AD dementia based on the McKhann criteria. Demographic, cognitive, and neuropsychiatric variables were entered in a hierarchical linear regression analysis to predict functional status as measured by the Functional Activities Questionnaire (FAQ). …Results: The total model explained 29.7% of the variance (p  <  0.001) in FAQ. Importantly, neuropsychiatric variables explained 12.7% of the unique variance, with apathy and sleep as significant contributors. Conclusion: Two neuropsychiatric variables, apathy and changes in sleep/nighttime behaviors, predicted ratings of functional status in AD patients independent of age, global cognition, memory and executive function measures, and depressive symptoms. These results highlight the importance of neuropsychiatric symptoms in understanding and potentially treating the functional limitations so prevalent in AD. Show more

Keywords: Alzheimer’s disease, apathy, neuropsychology, sleep disorders

DOI: 10.3233/JAD-150018

Citation: Journal of Alzheimer's Disease, vol. 48, no. 3, pp. 863-869, 2015

Article Type: Other

DOI: 10.3233/JAD-150647

Citation: Journal of Alzheimer's Disease, vol. 48, no. 3, pp. 871-874, 2015

Authors: Huang, Rong | Wang, Pin | Han, Jing | Xia, Wenqing | Cai, Rongrong | Sun, Haixia | Sun, Jie | Wang, Shaohua

Article Type: Correction

DOI: 10.3233/JAD-159003

Citation: Journal of Alzheimer's Disease, vol. 48, no. 3, pp. 875-875, 2015

Authors: Arab, L. | Sabbagh, M.N.

Article Type: Correction

DOI: 10.3233/JAD-159004

Citation: Journal of Alzheimer's Disease, vol. 48, no. 3, pp. 877-877, 2015