Journal of Alzheimer's Disease - Volume 46, issue 3

Authors: Ahmed, Rebekah M. | Kaizik, Cassandra | Irish, Muireann | Mioshi, Eneida | Dermody, Nadene | Kiernan, Matthew C. | Piguet, Olivier | Hodges, John R.

Article Type: Research Article

Abstract: Background: Frontotemporal dementia (FTD) is characterized by a number of prominent behavioral changes. While FTD has been associated with the presence of aberrant or unusual sexual behaviors in a proportion of patients, few studies have formally investigated changes in sexual function in this disease. Objective: We aimed to systematically quantify changes in sexual behavior, including current symptoms and changes from prior diagnoses, in behavioral-variant (bvFTD) and semantic dementia (SD), compared to Alzheimer’s disease (AD). Methods: Carers of 49 dementia patients (21 bvFTD, 11 SD, 17 AD) were interviewed using the Sexual Behavior …and Intimacy Questionnaire (SIQ), a survey designed to assess changes in sexual function across multiple domains including initiating, level of affection, and aberrant or unusual sexual behavior. Results: BvFTD patients show prominent hyposexual behavior including decreased affection, initiation, and response to advances by partners, and decreased frequency of sexual relations, compared to AD and to SD patients. The greatest changes in sexual behavior compared to pre-diagnoses were found in the bvFTD group with a 90–100% decrease in initiation, response, and frequency of sexual relations. Notably, aberrant or unusual sexual behavior was reported in a minority of bvFTD and SD patients and occurred in patients who also showed hyposexual behavior toward their partner. Conclusion: Overall loss of affection, reduced initiation of sexual activity, and responsiveness is an overwhelming feature of bvFTD. In contrast, aberrant or unusual sexual behavior is observed in the minority of bvFTD patients. The underlying pathophysiology of these changes likely reflects structural and functional changes in frontoinsular and limbic regions including the hypothalamus. Show more

Keywords: Alzheimer’s disease, frontotemporal dementia, sexual function

DOI: 10.3233/JAD-150034

Citation: Journal of Alzheimer's Disease, vol. 46, no. 3, pp. 677-686, 2015

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

Article Type: Research Article

Abstract: Background/objective: There are few reports on the effects of anti-Alzheimer’s disease (AD) drugs on older AD patients, and possible differences based on gender in a real world setting. Methods: “Okayama Late Dementia Study (OLDS)” is a retrospective clinical cohort study focusing on older AD patients (n  = 373; age≥75 years) treated with monotherapy donepezil (n  = 55), galantamine (n  = 222), rivastigmine (n  = 63), or memantine (n  = 33). The patients were evaluated as an entire group and separated by gender, using seven batteries for dementia assessment at baseline and at 3, 6, and 12 months of drug therapy. Results: …All four drugs preserved cognitive and affective functions until 12 months, except for Frontal Assessment Battery (FAB) with memantine ( * p  <  0.05 versus baseline). Donepezil monotherapy significantly improved Hasegawa Dementia Rating Scale-Revised (HDS-R) at 3 months ( * p  <  0.05), and memantine (3 and 6 months,  * p  <  0.05) and rivastigmine (3 months,  ** p  <  0.01) improved Abe’s Behavior and Psychological Symptom of Dementia Score (ABS), respectively. Activities of daily living (ADL) became significantly worse with galantamine at 12 months ( * p  <  0.05). Male Mini-Mental State Examination scores became worse at 12 months with donepezil ( * p  <  0.05), as did female Geriatric Depression Scale scores at 6 months ( * p  <  0.05). Male HDS-R and ABS scores were preserved in the galantamine group until 12 months. Female ABS scores with memantine improved at 6 months ( * p  <  0.05), while male ADL scores became worse with rivastigmine at 12 months ( * p  <  0.05). Conclusion: OLDS revealed that anti-AD drugs were effective even for older AD patients, and the clinical benefits of each drug showed a small difference with regard to gender. Show more

Keywords: Activities of daily living, affective function, Alzheimer’s disease, cognitive function, gender difference, late elder patients

DOI: 10.3233/JAD-150175

Citation: Journal of Alzheimer's Disease, vol. 46, no. 3, pp. 687-693, 2015

Authors: Kong, Dehan | Giovanello, Kelly S. | Wang, Yalin | Lin, Weili | Lee, Eunjee | Fan, Yong | Murali Doraiswamy, P | Zhu, Hongtu | and for the Alzheimer’s Disease Neuroimaging Initiative

Article Type: Research Article

Abstract: The growing public threat of Alzheimer’s disease (AD) has raised the urgency to discover and validate prognostic biomarkers in order to predicting time to onset of AD. It is anticipated that both whole genome single nucleotide polymorphism (SNP) data and high dimensional whole brain imaging data offer predictive values to identify subjects at risk for progressing to AD. The aim of this paper is to test whether both whole genome SNP data and whole brain imaging data offer predictive values to identify subjects at risk for progressing to AD. In 343 subjects with mild cognitive impairment (MCI) enrolled in the …Alzheimer’s Disease Neuroimaging Initiative (ADNI-1), we extracted high dimensional MR imaging (volumetric data on 93 brain regions plus a surface fluid registration based hippocampal subregion and surface data), and whole genome data (504,095 SNPs from GWAS), as well as routine neurocognitive and clinical data at baseline. MCI patients were then followed over 48 months, with 150 participants progressing to AD. Combining information from whole brain MR imaging and whole genome data was substantially superior to the standard model for predicting time to onset of AD in a 48-month national study of subjects at risk. Our findings demonstrate the promise of combined imaging-whole genome prognostic markers in people with mild memory impairment. Show more

Keywords: Alzheimer’s disease, genetics, magnetic resonance imaging, proportional hazards models, risk

DOI: 10.3233/JAD-150164

Citation: Journal of Alzheimer's Disease, vol. 46, no. 3, pp. 695-702, 2015

Authors: Chiang, Hsueh-Sheng | Mudar, Raksha A. | Pudhiyidath, Athula | Spence, Jeffrey S. | Womack, Kyle B. | Cullum, C. Munro | Tanner, Jeremy A. | Eroh, Justin | Kraut, Michael A. | Hart Jr., John

Article Type: Research Article

Abstract: Deficits in semantic memory in individuals with amnestic mild cognitive impairment (aMCI) have been previously reported, but the underlying neurobiological mechanisms remain to be clarified. We examined event-related potentials (ERPs) associated with semantic memory retrieval in 16 individuals with aMCI as compared to 17 normal controls using the Semantic Object Retrieval Task (EEG SORT). In this task, subjects judged whether pairs of words (object features) elicited retrieval of an object (retrieval trials) or not (non-retrieval trials). Behavioral findings revealed that aMCI subjects had lower accuracy scores and marginally longer reaction time compared to controls. We used a multivariate analytical technique …(STAT-PCA) to investigate similarities and differences in ERPs between aMCI and control groups. STAT-PCA revealed a left fronto-temporal component starting at around 750 ms post-stimulus in both groups. However, unlike controls, aMCI subjects showed an increase in the frontal-parietal scalp potential that distinguished retrieval from non-retrieval trials between 950 and 1050 ms post-stimulus negatively correlated with the performance on the logical memory subtest of the Wechsler Memory Scale-III. Thus, individuals with aMCI were not only impaired in their behavioral performance on SORT relative to controls, but also displayed alteration in the corresponding ERPs. The altered neural activity in aMCI compared to controls suggests a more sustained and effortful search during object memory retrieval, which may be a potential marker indicating disease processes at the pre-dementia stage. Show more

Keywords: Cognition, electroencephalography, event-related potentials, memory, mild cognitive impairment, semantics

DOI: 10.3233/JAD-142781

Citation: Journal of Alzheimer's Disease, vol. 46, no. 3, pp. 703-717, 2015

Authors: Chang, Ki Jung | Lee, Soojin | Lee, Yunhwan | Lee, Kang Soo | Hwan Back, Joung | Jung, Young Ki | Lim, Ki Young | Noh, Jai Sung | Kim, Hyun Chung | Roh, Hyun Woong | Choi, Seong Hye | Kim, Seong Yoon | Joon Son, Sang | Hong, Chang Hyung

Article Type: Research Article

Abstract: Background & Objective: White matter hyperintensities (WMHs) contribute to aggravation of dementia or geriatric syndrome, thereby resulting in functional impairment. However, evidence of direct association between WMHs and medical resource utilization indicated by length of hospital stay (LOS) is scarce in patients with cognitive impairment. This study aimed to examine the relationship between the severity of WMHs and LOS in patients with cognitive impairment. Methods: 4,253 older adults with cognitive impairment were enrolled in this study. We defined LOS as the total sum of days from January 1, 2008 to December 31, 2012. The severity …of periventricular (PVWMHs), deep (DWMHs), and overall white matter hyperintensities (Overall WMHs) was evaluated by a visual rating scale. We conducted multinomial logistic regression to demonstrate the relationship between LOS and severity of PVWHMs, DWHMs, and Overall WMHs, respectively. Results: The median LOS was 20 days. Severe PVWMHs had a higher likelihood of longer LOS (Q3: odd ratio/OR = 1.32, 95% confidence interval/CI = 1.06–1.64; Q4: OR = 1.33, 95% CI = 1.07–1.65; Q5: OR = 1.55, 95% CI = 1.26–1.91). As for DWMHs, moderate DWMHs were related to longer LOS (Q4: OR = 1.33, 95% CI = 1.03–1.71; Q5: OR = 1.63, 95% CI = 1.26–2.11). Finally, severity of overall WMHs was independently associated with LOS, which was similar to the results of DWMHs. Conclusion: These findings would advocate for prevention of WMHs to stave off excess medical resource utilization in patients with cognitive impairment. Show more

Keywords: Cognitive impairment, dementia, length of hospital stay, white matter hyperintensities

DOI: 10.3233/JAD-142823

Citation: Journal of Alzheimer's Disease, vol. 46, no. 3, pp. 719-726, 2015

Authors: Munro, Catherine E. | Donovan, Nancy J. | Guercio, Brendan J. | Wigman, Sarah E. | Schultz, Aaron P. | Amariglio, Rebecca E. | Rentz, Dorene M. | Johnson, Keith A. | Sperling, Reisa A. | Marshall, Gad A.

Article Type: Research Article

Abstract: Background: Neuropsychiatric symptoms (NPS), such as apathy and depression, commonly accompany cognitive and functional decline in early Alzheimer’s disease (AD). Prior studies have shown associations between affective NPS and neurodegeneration of medial frontal and inferior temporal regions in mild cognitive impairment (MCI) and AD dementia. Objective: To investigate the association between functional connectivity in four brain networks and NPS in elderly with MCI. Methods: NPS were assessed using the Neuropsychiatric Inventory in 42 subjects with MCI. Resting-state functional connectivity in four networks (default mode network, fronto-parietal control network (FPCN), dorsal attention network, and ventral attention …network) was assessed using seed-based magnetic resonance imaging. Factor analysis was used to identify two factors of NPS: Affective and Hyperactivity. Linear regression models were utilized with the neuropsychiatric factors as the dependent variable and the four networks as the predictors of interest. Covariates included age, gender, premorbid intelligence, processing speed, memory, head movement, and signal-to-noise ratio. These analyses were repeated with the individual items of the affective factor, using the same predictors. Results: There was a significant association between greater Affective factor symptoms and reduced FPCN connectivity (p  = 0.03). There was no association between the Hyperactivity factor and any of the networks. Secondary analyses revealed an association between greater apathy and reduced FPCN connectivity (p  = 0.005), but none in other networks. Conclusions: Decreased connectivity in the FPCN may be associated with greater affective symptoms, particularly apathy, early in AD. These findings extend prior studies, using different functional imaging modalities in individuals with greater disease severity. Show more

Keywords: Alzheimer’s disease, apathy, functional magnetic resonance imaging, mild cognitive impairment, neuropsychiatric symptoms

DOI: 10.3233/JAD-150017

Citation: Journal of Alzheimer's Disease, vol. 46, no. 3, pp. 727-735, 2015

Authors: Milano, Nicholas J. | Heilman, Kenneth M.

Article Type: Research Article

Abstract: Background and Objective: Primary progressive aphasia (PPA) is a neurodegenerative disorder characterized by progressive language impairment. The three variants of PPA include the nonfluent/agrammatic, semantic, and logopenic types. The goal of this report is to describe two patients with a loss of speech initiation that was associated with bilateral medial frontal atrophy. Methods and Results: Two patients with progressive speech deficits were evaluated and their examinations revealed a paucity of spontaneous speech; however their naming, repetition, reading, and writing were all normal. The patients had no evidence of agrammatism or apraxia of speech but did …have impaired speech fluency. In addition to impaired production of propositional spontaneous speech, these patients had impaired production of automatic speech (e.g., reciting the Lord’s Prayer) and singing. Structural brain imaging revealed bilateral medial frontal atrophy in both patients. Conclusion: These patients’ language deficits are consistent with a PPA, but they are in the pattern of a dynamic aphasia. Whereas the signs-symptoms of dynamic aphasia have been previously described, to our knowledge these are the first cases associated with predominantly bilateral medial frontal atrophy that impaired both propositional and automatic speech. Thus, this profile may represent a new variant of PPA. Show more

Keywords: Abulia, dementia, dynamic aphasia, primary progressive aphasia

DOI: 10.3233/JAD-142112

Citation: Journal of Alzheimer's Disease, vol. 46, no. 3, pp. 737-745, 2015

Authors: Henrique de Gobbi Porto, Fábio | Martins Novaes Coutinho, Artur | Lucia de Sá Pinto, Ana | Gualano, Bruno | Luís de Souza Duran, Fabio | Prando, Silvana | Rachel Ono, Carla | Spíndola, Lívia | Okada de Oliveira, Maira | Helena Figuerêdo do Vale, Patrícia | Nitrini, Ricardo | Alberto Buchpiguel, Carlos | Maria Dozzi Brucki, Sonia

Article Type: Research Article

Abstract: Background: Aerobic training (AT) is a promising intervention for mild cognitive impairment (MCI). Objective: To evaluate the effects of AT on cognition and regional brain glucose metabolism (rBGM) in MCI patients. Methods: Subjects performed a twice-a-week, moderate intensity, AT program for 24 weeks. Assessment with ADAS-cog, a comprehensive neuropsychological battery, and evaluation of rBGM with positron emission tomography with 18 F-fluorodeoxyglucose ([18 F]FDG-PET) were performed before and after the intervention. Aerobic capacity was compared using the maximal oxygen consumption VO2 max (mL/Kg/min). [18 F]FDG-PET data were analyzed on a voxel-by-voxel basis with …SPM8 software. Results: Forty subjects were included, with a mean (M) age of 70.3 (5.4) years and an initial Mini-Mental State Exam score of 27.4 (1.7). Comparisons using paired t -tests revealed improvements in the ADAS-cog (M difference: −2.7 (3.7), p  <  0.001) and VO2 max scores (M difference: 1.8 (2.0) mL/kg/min, p  <  0.001). Brain metabolic analysis revealed a bilateral decrease in the rBGM of the dorsal anterior cingulate cortex, pFWE = 0.04. This rBGM decrease was negatively correlated with improvement in a visuospatial function/attentional test (rho =−0.31, p  = 0.04). Several other brain areas also showed increases or decreases in rBGM. Of note, there was an increase in the retrosplenial cortex, an important node of the default mode network, that was negatively correlated with the metabolic decrease in the dorsal anterior cingulate cortex (r  =−0.51, p  = 0.001). Conclusion: AT improved cognition and changed rBGM in areas related to cognition in subjects with MCI. Show more

Keywords: Aerobic physical exercise, aerobic training, anterior cingulate cortex, cognition, mild cognitive impairment, non-pharmacological interventions, positron emission tomography with 18F-fluorodeoxyglucose

DOI: 10.3233/JAD-150033

Citation: Journal of Alzheimer's Disease, vol. 46, no. 3, pp. 747-760, 2015

Authors: Tedone, Enzo | Arosio, Beatrice | Colombo, Federico | Ferri, Evelyn | Asselineau, Delphine | Piette, Francois | Gussago, Cristina | Belmin, Joel | Pariel, Sylvie | Benlhassan, Khadija | Casati, Martina | Bornand, Anne | Rossi, Paolo Dionigi | Mazzola, Paolo | Annoni, Giorgio | Doulazmi, Mohamed | Mariani, Jean | Porretti, Laura | Bray, Dorothy H. | Mari, Daniela

Article Type: Research Article

Abstract: Background: Age and short leukocyte telomeres have been associated with a higher risk of Alzheimer’s disease (AD). Inflammation is involved in AD and it is suggested that anti-inflammatory interleukin-10 (IL-10) may partly antagonize these processes. Objective: The aim is to correlate telomere length (TL) in peripheral blood mononuclear cells (PBMC) from patients with AD to disease progression rate. Moreover, we evaluated whether TL was associated with IL-10 production by unstimulated or amyloid-β (Aβ)-stimulated PBMC. Methods: We enrolled 31 late-onset AD and 20 age-matched healthy elderly (HE). After a two-year follow-up period, patients …were retrospectively evaluated as slow-progressing (ADS) (Mini Mental State Examination (MMSE) decline over the two years of follow-up ≤3 points) or fast progressing AD (ADF) (MMSE decline ≥5 points). TL was measured by flow cytometry and in vitro IL-10 production by enzyme-linked immunosorbent assay. Results: TL (mean±SD) for HE, ADS, and ADF was 2.3±0.1, 2.0±0.1, and 2.5±0.1 Kb, respectively. ADS showed a shorter TL compared to HE (p  = 0.034) and to ADF (p  = 0.005). MMSE decline correlated with TL in AD (R2  = 0.284; p  = 0.008). We found a significant difference in IL-10 production between unstimulated and Aβ-stimulated PBMC from ADS (40.7±13.7 versus 59.0±27.0; p  = 0.004) but not from ADF (39.7±14.4 versus 42.2±22.4). HE showed a trend toward significance (47.1±25.4 versus 55.3±27.9; p  = 0.10). Conclusion: PBMC from ADF may be characterized by an impaired response induced by Aβ and by a reduced proliferative response responsible for the longer telomeres. TL might be a contributing factor in predicting the rate of AD progression. Show more

Keywords: Alzheimer’s disease, disease progression, interleukin-10, peripheral blood mononuclear cells, telomere

DOI: 10.3233/JAD-142808

Citation: Journal of Alzheimer's Disease, vol. 46, no. 3, pp. 761-769, 2015

Authors: Piscopo, Paola | Tosto, Giuseppe | Belli, Chiara | Talarico, Giuseppina | Galimberti, Daniela | Gasparini, Marina | Canevelli, Marco | Poleggi, Anna | Crestini, Alessio | Albani, Diego | Forloni, Gianluigi | Lucca, Ugo | Quadri, Pierluigi | Tettamanti, Mauro | Fenoglio, Chiara | Scarpini, Elio | Bruno, Giuseppe | Vanacore, Nicola | Confaloni, Annamaria

Article Type: Research Article

Abstract: Several studies have established the sortilin-related receptor gene (SORL1 ) as a susceptibility locus for Alzheimer’s disease (AD). Single nucleotide polymorphisms of SORL1 reported in literature as being associated with AD were investigated in an Italian case-control data set, and their role as a risk factor of conversion to AD was studied in an independent sample of subjects diagnosed with mild cognitive impairment (MCI) at baseline. rs641120, rs2070045, and rs1010159 were genotyped in 734 subjects diagnosed with AD (n  = 338) and MCI (n  = 181) and in healthy controls (n  = 215). Our results confirmed the association between rs641120 and AD …(p  = 0.01). In the MCI cohort, rs1010159 was associated with conversion to AD (HR = 1.56, p  = 0.002). Taken together, these findings confirm that SORL1 is associated with AD and might be a potential tool for identifying MCI subjects at high risk of conversion to AD. Show more

Keywords: Alzheimer’s disease, mild cognitive impairment, single nucleotide polymorphisms, SORL1

DOI: 10.3233/JAD-141551

Citation: Journal of Alzheimer's Disease, vol. 46, no. 3, pp. 771-776, 2015

Authors: Shen, Liang | Ji, Hong-Fang

Article Type: Research Article

Abstract: The associations between homocysteine (Hcy), folic acid, and vitamin B12 and Alzheimer’s disease (AD) have gained much interest, while remaining controversial. We aim to perform meta-analyses to evaluate comprehensively: i) Hcy, folic acid, and vitamin B12 levels in AD patients in comparison with controls; and ii) the association between Hcy, folic acid, and vitamin B12 levels and risk of AD. A literature search was performed using Medline and Scopus databases. A total of 68 studies were identified and included in the meta-analyses. Stata 12.0 statistical software was used to perform the meta-analyses. First, AD patients may have higher level of …Hcy, and lower levels of folate and vitamin B12 in plasma than controls. Further age-subgroup analysis showed no age effect for Hcy levels in plasma between AD patients and matched controls, while the differences in folate and vitamin B12 levels further enlarged with increased age. Second, data suggests that high Hcy and low folate levels may correlate with increased risk of AD occurrence. The comprehensive meta-analyses not only confirmed higher Hcy, lower folic acid, and vitamin B12 levels in AD patients than controls, but also implicated that high Hcy and low folic acid levels may be risk factors of AD. Further studies are encouraged to elucidate mechanisms linking these conditions. Show more

Keywords: Alzheimer’s disease, folic acid, homocysteine, meta-analysis, vitamin B12

DOI: 10.3233/JAD-150140

Citation: Journal of Alzheimer's Disease, vol. 46, no. 3, pp. 777-790, 2015

Authors: Oleson, Stephanie | Murphy, Claire

Article Type: Research Article

Abstract: Alzheimer’s disease (AD) is a neurodegenerative disorder characterized by progressive memory impairment and the presence of amyloid plaques and neurofibrillary tangles. The associated neuropathology originates in brain areas responsible for olfaction, which makes olfactory tasks potentially useful for assessing AD. The strongest genetic risk factor for AD is the apolipoprotein E (ApoE) ɛ4 allele that has been associated with increased cognitive and olfactory deficits. While individuals carrying one ɛ4 allele of the ApoE gene are at increased risk for AD relative to non-carriers, those with two copies of the ɛ4 allele demonstrate an even higher risk for developing AD. Furthermore, …homozygous ApoE ɛ4/4 individuals diagnosed with AD are known to have heightened amyloid burden and a more rapid rate of cognitive decline relative to heterozygous ɛ3/4 ApoE carriers. All of these factors suggest there are differences in severity and progression of AD as a function of possessing one versus two ɛ4 alleles. The current study investigated olfactory functioning in homozygous ɛ4/4 older adults diagnosed with probable AD. Compared to demographically matched ɛ3/3 and ɛ3/4 individuals, ɛ4/4 individuals showed deficits in odor identification and remote odor memory as measured by odor familiarity ratings. The current findings suggest that these particular domains of olfactory functioning may be more impaired in AD ɛ4/4 homozygotes compared to ɛ3/4 heterozygotes and ɛ3/3 homozygotes. These deficits give insight into how the presence of two ɛ4 alleles may differentially affect the progression of AD and suggest the usefulness of odor tasks in detecting those at risk for AD. Show more

Keywords: Alzheimer’s disease, ApoE, apolipoprotein E, olfaction, smell impairment

DOI: 10.3233/JAD-150089

Citation: Journal of Alzheimer's Disease, vol. 46, no. 3, pp. 791-803, 2015

Authors: Ramakers, Inez H.G.B. | Honings, Steven T.H. | Ponds, Rudolf W. | Aalten, Pauline | Köhler, Sebastian | Verhey, Frans R.J. | Visser, Pieter Jelle

Article Type: Research Article

Abstract: Background: The relation between psychological distress, personality traits, and cognitive decline in cognitively impaired patients remains unclear. Objective: To investigate the effect of psychological distress and personality traits on cognitive functioning in subjects with mild cognitive impairment (MCI); and to investigate the predictive accuracy of these factors for the development of dementia. Methods: MCI patients (n  = 343, age: 60.9±9.9 years, 38% female, and MMSE score: 28.1±1.9) were included from the Maastricht memory clinic. All patients underwent a standardized neuropsychological assessment (including tests for measuring mental speed (Trail Making Test (TMT) part A …and Stroop Color Word Test (SCWT) part I), executive functioning (TMT part B and SCWT part III), memory (15-Word Learning Tests), and verbal fluency (1-minute animals)), CT or MRI, and blood assessment. The Dutch Personality Questionnaire (DPQ) and the 90-items Symptom Check List (SCL-90) were used to measure personality traits and psychological distress. Conversion to dementia was assessed two, five, and ten years after baseline. The mean follow-up period was 6.7±3.4 years. Results: The Psychoneuroticism score of the SCL-90 was associated with slower performances on SCWT part I and TMT part A. The subdomain Neuroticism of the DPQ was also associated with slower scores on the TMT part A. At follow-up, 85 (25.9%) subjects had developed dementia. The SCL-90 total score, and the subscales, Anxiety, Somatization, Insufficiency in thought and action, and Sleeping problems were associated with a decreased risk for developing (AD-type) dementia. Conclusion: Psychological distress negatively affected information processing speed, but was not associated with an increased risk of developing dementia in patients with MCI. Show more

Keywords: Alzheimer’s disease, cognition, dementia, mild cognitive impairment, neuropsychological performances, neuroticism, personality, psychological distress

DOI: 10.3233/JAD-142493

Citation: Journal of Alzheimer's Disease, vol. 46, no. 3, pp. 805-812, 2015

Article Type: Meeting Report

DOI: 10.3233/JAD-150316

Citation: Journal of Alzheimer's Disease, vol. 46, no. 3, pp. 813-816, 2015