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1.
Neurology ; 78(5): 342-51, 2012 Jan 31.
Article in English | MEDLINE | ID: mdl-22282647

ABSTRACT

OBJECTIVE: Although incidence rates for mild cognitive impairment (MCI) have been reported, few studies were specifically designed to measure the incidence of MCI and its subtypes using published criteria. We estimated the incidence of amnestic MCI (aMCI) and nonamnestic MCI (naMCI) in men and women separately. METHODS: A population-based prospective cohort of Olmsted County, MN, residents ages 70-89 years on October 1, 2004, underwent baseline and 15-month interval evaluations that included the Clinical Dementia Rating scale, a neurologic evaluation, and neuropsychological testing. A panel of examiners blinded to previous diagnoses reviewed data at each serial evaluation to assess cognitive status according to published criteria. RESULTS: Among 1,450 subjects who were cognitively normal at baseline, 296 developed MCI. The age- and sex-standardized incidence rate of MCI was 63.6 (per 1,000 person-years) overall, and was higher in men (72.4) than women (57.3) and for aMCI (37.7) than naMCI (14.7). The incidence rate of aMCI was higher for men (43.9) than women (33.3), and for subjects with ≤12 years of education (42.6) than higher education (32.5). The risk of naMCI was also higher for men (20.0) than women (10.9) and for subjects with ≤12 years of education (20.3) than higher education (10.2). CONCLUSIONS: The incidence rates for MCI are substantial. Differences in incidence rates by clinical subtype and by sex suggest that risk factors for MCI should be investigated separately for aMCI and naMCI, and in men and women.


Subject(s)
Cognitive Dysfunction/epidemiology , Age Factors , Aged , Aged, 80 and over , Cognitive Dysfunction/classification , Cognitive Dysfunction/psychology , Cohort Studies , Educational Status , Female , Follow-Up Studies , Humans , Longitudinal Studies , Male , Memory Disorders/epidemiology , Memory Disorders/psychology , Minnesota/epidemiology , Neuropsychological Tests , Population , Prospective Studies , Risk Factors , Sex Factors , Socioeconomic Factors
2.
Eur J Neurol ; 19(1): 38-46, 2012 Jan.
Article in English | MEDLINE | ID: mdl-21518145

ABSTRACT

BACKGROUND AND PURPOSE: Our objective was to document the clinical and imaging features of Othello's syndrome (delusional jealousy). METHODS: The study design was a retrospective case series of 105 patients with Othello's syndrome that were identified using the Electronic Medical Record system of Mayo Clinic. RESULTS: The average age at onset of Othello's syndrome was 68 (25-94) years with 61.9% of patients being male. Othello's syndrome was most commonly associated with a neurological disorder (73/105) compared with psychiatric disorders (32/105). Of the patients with a neurological disorder, 76.7% had a neurodegenerative disorder. Seven of eight patients with a structural lesion associated with Othello's syndrome had right frontal lobe pathology. Voxel-based morphometry showed greater gray matter loss predominantly in the dorsolateral frontal lobes in the neurodegenerative patients with Othello's compared to matched patients with neurodegenerative disorders without Othello's syndrome. Treatment success was notable for patients with dopamine agonist induced Othello's syndrome in which all six patients had improvement in symptoms following decrease in medication. CONCLUSIONS: This study demonstrates that Othello's syndrome occurs most frequently with neurological disorders. This delusion appears to be associated with dysfunction of the frontal lobes, especially the right frontal lobe.


Subject(s)
Frontal Lobe/pathology , Schizophrenia, Paranoid/pathology , Adult , Aged , Aged, 80 and over , Dopamine Agonists/adverse effects , Female , Humans , Jealousy , Magnetic Resonance Imaging , Male , Middle Aged , Neurodegenerative Diseases/complications , Neurodegenerative Diseases/drug therapy , Retrospective Studies , Schizophrenia, Paranoid/complications
3.
Neurology ; 78(4): 232-40, 2012 Jan 24.
Article in English | MEDLINE | ID: mdl-22189452

ABSTRACT

OBJECTIVE: To determine the relationship between ß-amyloid (Aß) load as measured by [(11)C]-Pittsburgh compound B (PiB) PET and cognitive function in cognitively normal older adults. METHODS: We studied 408 cognitively normal older adults who participated in the population-based Mayo Clinic Study of Aging (MCSA) from January 2009 through March 2011. The participants underwent PiB PET and neuropsychometric testing within 6 months. The association between PiB retention and cognitive function was measured by partial correlation and an interaction with APOE status was tested using linear regression after adjusting for age, sex, and education. RESULTS: Higher PiB retention was associated with cognitive performance (Spearman partial r = -0.18; p < 0.01), specifically the memory, language, attention/executive, and visual-spatial processing domains in the whole group of participants. The association between PiB retention and cognition was modified by the APOE status on linear regression analysis even after controlling for the differences in the distribution of PiB values among APOE ε4 carriers and noncarriers (p = 0.02). Cognitive performance was associated with the Aß deposition in the frontal, temporal, and parietal lobe association cortices in APOE ε4 carriers on SPM analysis (p < 0.001). CONCLUSION: There is a modest association between PiB retention and cognitive function in cognitively normal older adults and this relationship between Aß load and cognitive function is modified by APOE status. Whereas Aß load is associated with greater cognitive impairment in APOE ε4 carriers, the cognitive function in APOE ε4 noncarriers is influenced less by the Aß load, suggesting that APOE isoforms modulate the harmful effects of Aß on cognitive function.


Subject(s)
Amyloid beta-Peptides/metabolism , Apolipoproteins E/genetics , Apolipoproteins E/physiology , Cognition/physiology , Aged , Aged, 80 and over , Cohort Studies , Executive Function/physiology , Female , Genotype , Heterozygote , Humans , Magnetic Resonance Imaging , Male , Memory/physiology , Neuropsychological Tests , Positron-Emission Tomography , Psychomotor Performance/physiology
4.
Neurology ; 77(10): 951-8, 2011 Sep 06.
Article in English | MEDLINE | ID: mdl-21865577

ABSTRACT

OBJECTIVE: To determine the relationship between proton magnetic resonance spectroscopy ((1)H MRS) metabolites and ß-amyloid (Aß) load and the effects of Aß load on the association between (1)H MRS metabolites and cognitive function in cognitively normal older adults. METHODS: We studied 311 cognitively normal older adults who participated in the population-based Mayo Clinic Study of Aging from January 2009 through September 2010. Participants underwent (11)C-Pittsburgh compound B (PiB) PET, (1)H MRS from the posterior cingulate gyri, and neuropsychometric testing to assess memory, attention/executive, language, and visual-spatial domain functions within 6 months. Partial Spearman rank order correlations were adjusted for age, sex, and education. RESULTS: Higher PiB retention was associated with abnormal elevations in myoinositol (mI)/creatine (Cr) (partial r(s) = 0.17; p = 0.003) and choline (Cho)/Cr (partial r(s) = 0.13; p = 0.022) ratios. Higher Cho/Cr was associated with worse performance on Auditory Verbal Learning Test Delayed Recall (partial r(s) = -0.12; p = 0.04), Trail Making Test Part B (partial r(s) = 0.12; p = 0.04), Wechsler Adult Intelligence Scale-Revised (WAIS-R) Digit Symbol (partial r(s) = -0.18; p < 0.01), and WAIS-R Block Design (partial r(s) = -0.12; p = 0.03). Associations between (1)H MRS metabolites and cognitive function were not different among participants with high vs low PiB retention. CONCLUSION: In cognitively normal older adults, the (1)H MRS metabolite ratios mI/Cr and Cho/Cr are associated with the preclinical pathologic processes in the Alzheimer disease cascade. Higher Cho/Cr is associated with worse performance on domain-specific cognitive tests independent of Aß load, suggesting that Cho/Cr elevation may also be dependent on other preclinical dementia pathologies characterized by Cho/Cr elevation such as Lewy body or ischemic vascular disease in addition to Aß load.


Subject(s)
Amyloid beta-Peptides/metabolism , Cognition/physiology , Magnetic Resonance Spectroscopy , Population Surveillance , Aged , Aged, 80 and over , Amyloid beta-Peptides/adverse effects , Choline/biosynthesis , Choline/metabolism , Cognition Disorders/diagnosis , Cognition Disorders/metabolism , Cognition Disorders/psychology , Creatinine/metabolism , Female , Humans , Magnetic Resonance Spectroscopy/methods , Male , Neuropsychological Tests , Population Surveillance/methods , Prospective Studies , Protein Stability
5.
Neurology ; 75(10): 889-97, 2010 Sep 07.
Article in English | MEDLINE | ID: mdl-20820000

ABSTRACT

OBJECTIVE: We investigated the prevalence of mild cognitive impairment (MCI) in Olmsted County, MN, using in-person evaluations and published criteria. METHODS: We evaluated an age- and sex-stratified random sample of Olmsted County residents who were 70-89 years old on October 1, 2004, using the Clinical Dementia Rating Scale, a neurologic evaluation, and neuropsychological testing to assess 4 cognitive domains: memory, executive function, language, and visuospatial skills. Information for each participant was reviewed by an adjudication panel and a diagnosis of normal cognition, MCI, or dementia was made using published criteria. RESULTS: Among 1,969 subjects without dementia, 329 subjects had MCI, with a prevalence of 16.0% (95% confidence interval [CI] 14.4-17.5) for any MCI, 11.1% (95% CI 9.8-12.3) for amnestic MCI, and 4.9% (95% CI 4.0-5.8) for nonamnestic MCI. The prevalence of MCI increased with age and was higher in men. The prevalence odds ratio (OR) in men was 1.54 (95% CI 1.21-1.96; adjusted for age, education, and nonparticipation). The prevalence was also higher in subjects who never married and in subjects with an APOE epsilon3epsilon4 or epsilon4epsilon4 genotype. MCI prevalence decreased with increasing number of years of education (p for linear trend <0.0001). CONCLUSIONS: Our study suggests that approximately 16% of elderly subjects free of dementia are affected by MCI, and amnestic MCI is the most common type. The higher prevalence of MCI in men may suggest that women transition from normal cognition directly to dementia at a later age but more abruptly.


Subject(s)
Cognition Disorders/epidemiology , Dementia/epidemiology , Sex Characteristics , Aged , Aged, 80 and over , Aging , Cognition Disorders/diagnosis , Dementia/diagnosis , Executive Function , Female , Humans , Male , Minnesota , Neuropsychological Tests , Odds Ratio , Prevalence , Sex Factors
6.
Encephale ; 36(4): 314-25, 2010 Sep.
Article in French | MEDLINE | ID: mdl-20850603

ABSTRACT

INTRODUCTION: The early diagnosis of Alzheimer's disease is a new challenge. This study concerns 50 patients, 34 females (68 %) and 16 males (32 %) with Alzheimer (AD), according to NINCDS-ADRDA diagnostic criteria. OBJECTIVES: To systematically evaluate in all patients behavioral and psychological signs and symptoms of dementia (BPSSD), according to the stage of AD, with the patients of our population separated into two MMS groups. METHODS: The first group was composed of patients with an MMS score from 10 to 20 (eight males and 19 females). Patients of the second group had an MMS score between 21 and 28 (eight males and 19 females). The Neuro-Psychiatric Inventory (NPI) was used to collect information on the presence of BPSSD in AD patients. NPI scores were correlated to the cognitive part of the Alzheimer's Disease Assessment Scale (ADAS-Cog) that permits evaluation of the severity of cognitive impairment in AD patients. Before starting the study, all patients gave their informed consent to participate in the study of BPSSD in AD. Statistical treatment of data was performed using STATVIEW. RESULTS: Our study demonstrates that BPSSD are present not only in early but also in moderate stages of AD. As cognitive impairment, BPSSD are an integrate part of the clinical picture. With a frequency of 74 % for the whole population, "anxiety" represented the more predominant BPSSD for all our patients at all stages of AD. At the very early stages of AD, BPSSD appeared to precede cognitive disorders. CONCLUSION: The symptomatic association of "depression", "agitation", and "irritability of mood" may remain in a steady state for a few months before the appearance of verbal episodic memory impairment, which is characteristic of hippocampus involvement. "Irritability" seems to specifically characterise the initial phase of AD. On the other hand, two BPSSD are characteristic of the late stages of AD: "sleep disorder" and "hallucinations".


Subject(s)
Alzheimer Disease/diagnosis , Alzheimer Disease/psychology , Mental Disorders/diagnosis , Mental Disorders/psychology , Aged , Aged, 80 and over , Alzheimer Disease/classification , Alzheimer Disease/pathology , Cognition Disorders/classification , Cognition Disorders/diagnosis , Cognition Disorders/pathology , Cognition Disorders/psychology , Delusions/classification , Delusions/diagnosis , Delusions/pathology , Delusions/psychology , Depressive Disorder/classification , Depressive Disorder/diagnosis , Depressive Disorder/pathology , Depressive Disorder/psychology , Disease Progression , Female , Frontal Lobe/pathology , Hallucinations/classification , Hallucinations/diagnosis , Hallucinations/pathology , Hallucinations/psychology , Hippocampus/pathology , Humans , Irritable Mood , Magnetic Resonance Imaging , Male , Mental Disorders/classification , Mental Disorders/pathology , Mental Status Schedule , Middle Aged , Neocortex/pathology , Neuropsychological Tests/statistics & numerical data , Psychometrics , Psychomotor Agitation/classification , Psychomotor Agitation/diagnosis , Psychomotor Agitation/pathology , Psychomotor Agitation/psychology , Sleep Wake Disorders/classification , Sleep Wake Disorders/diagnosis , Sleep Wake Disorders/pathology , Sleep Wake Disorders/psychology
7.
Neurology ; 75(4): 349-57, 2010 Jul 27.
Article in English | MEDLINE | ID: mdl-20660865

ABSTRACT

OBJECTIVE: It has been suggested that people who develop Parkinson disease (PD) may have a characteristic premorbid personality. We tested this hypothesis using a large historical cohort study with long follow-up. METHODS: We conducted a historical cohort study in the region including the 120-mile radius centered in Rochester, MN. We recruited 7,216 subjects who completed the Minnesota Multiphasic Personality Inventory (MMPI) for research at the Mayo Clinic from 1962 through 1965 and we considered 5 MMPI scales to measure sensation seeking, hypomania, positive emotionality, social introversion, and constraint. A total of 6,822 subjects (94.5% of the baseline sample) were followed over 4 decades either actively (via interview and examination) or passively (via medical records). RESULTS: During follow-up, 227 subjects developed parkinsonism (156 developed PD). The 3 MMPI scales that we selected to measure the extroverted personality construct (sensation seeking, hypomania, and positive emotionality) did not show the expected pattern of higher scores associated with reduced risk of PD. Similarly, the 2 MMPI scales that we selected to measure the introverted personality construct (social introversion and constraint) did not show the expected pattern of higher scores associated with increased risk of PD. However, higher scores for constraint were associated with an increased risk of all types of parkinsonism pooled together (hazard ratio 1.39; 95% CI 1.06-1.84; p = 0.02). CONCLUSIONS: We suggest that personality traits related to introversion and extroversion do not predict the risk of PD.


Subject(s)
Exploratory Behavior , Introversion, Psychological , Parkinson Disease/epidemiology , Parkinson Disease/psychology , Personality , Adult , Aged , Cohort Studies , Extraversion, Psychological , Female , Follow-Up Studies , Humans , MMPI , Male , Middle Aged , Predictive Value of Tests , Proportional Hazards Models , Risk Factors , Young Adult
8.
Int Psychogeriatr ; 22(6): 984-94, 2010 Sep.
Article in English | MEDLINE | ID: mdl-20594384

ABSTRACT

BACKGROUND: Neuropsychiatric symptoms (NPS) affect almost all patients with dementia and are a major focus of study and treatment. Accurate assessment of NPS through valid, sensitive and reliable measures is crucial. Although current NPS measures have many strengths, they also have some limitations (e.g. acquisition of data is limited to informants or caregivers as respondents, limited depth of items specific to moderate dementia). Therefore, we developed a revised version of the NPI, known as the NPI-C. The NPI-C includes expanded domains and items, and a clinician-rating methodology. This study evaluated the reliability and convergent validity of the NPI-C at ten international sites (seven languages). METHODS: Face validity for 78 new items was obtained through a Delphi panel. A total of 128 dyads (caregivers/patients) from three severity categories of dementia (mild = 58, moderate = 49, severe = 21) were interviewed separately by two trained raters using two rating methods: the original NPI interview and a clinician-rated method. Rater 1 also administered four additional, established measures: the Apathy Evaluation Scale, the Brief Psychiatric Rating Scale, the Cohen-Mansfield Agitation Index, and the Cornell Scale for Depression in Dementia. Intraclass correlations were used to determine inter-rater reliability. Pearson correlations between the four relevant NPI-C domains and their corresponding outside measures were used for convergent validity. RESULTS: Inter-rater reliability was strong for most items. Convergent validity was moderate (apathy and agitation) to strong (hallucinations and delusions; agitation and aberrant vocalization; and depression) for clinician ratings in NPI-C domains. CONCLUSION: Overall, the NPI-C shows promise as a versatile tool which can accurately measure NPS and which uses a uniform scale system to facilitate data comparisons across studies.


Subject(s)
Alzheimer Disease/diagnosis , Neuropsychological Tests/statistics & numerical data , Aged , Aged, 80 and over , Alzheimer Disease/classification , Alzheimer Disease/psychology , Apathy/classification , Brief Psychiatric Rating Scale/statistics & numerical data , Communication , Cross-Cultural Comparison , Delusions/classification , Delusions/diagnosis , Delusions/psychology , Depressive Disorder/classification , Depressive Disorder/diagnosis , Depressive Disorder/psychology , Female , Hallucinations/classification , Hallucinations/diagnosis , Hallucinations/psychology , Humans , Male , Mental Disorders/classification , Mental Disorders/diagnosis , Mental Disorders/psychology , Mental Status Schedule/statistics & numerical data , Observer Variation , Psychometrics/statistics & numerical data , Psychomotor Agitation/classification , Psychomotor Agitation/diagnosis , Psychomotor Agitation/psychology , Reproducibility of Results , Statistics as Topic
9.
Eur J Neurol ; 15(4): 350-4, 2008 Apr.
Article in English | MEDLINE | ID: mdl-18312405

ABSTRACT

Recent case-series studies indicated that a medication used to treat Parkinson's disease (PD), in particular Pramipexole, is associated with gambling. A case-series study cannot test this hypothesis; therefore, we need to design a case-control or cohort study to test the aforementioned hypothesis. Typical of a case-control design, we sampled on the dependent variable, which we defined as incident gambling in PD. A research neurologist, who was kept uninformed of the case-control status, retrospectively measured the exposure of interest (i.e. medications used to treat PD) by using the medical database system of Mayo Clinic Jacksonville. Eleven patients with PD without history of gambling, but had newly developed gambling, were matched by age and sex to the control group of 37 PD patients without gambling at a ratio of one case to at least three controls. Disease duration, age, and sex did not differ between cases and controls. Combined therapy with Pramipexole and levodopa did not increase the risk of gambling as compared to monotherapy with Pramipexole (OR, 0.15; 95% CI, 0.01-1.26). Treatment with Pramipexole was associated with increased risk of gambling and this association approached significance (OR, 3.6; 95% CI, 0.9-14.9). Patients with PD who newly developed gambling behavior were more likely to have been taking Pramipexole than other anti-PD medication. However, the association between Pramipexole and gambling behavior is not necessarily etiologic.


Subject(s)
Antiparkinson Agents/adverse effects , Benzothiazoles/adverse effects , Gambling , Aged , Case-Control Studies , Confidence Intervals , Humans , Male , Middle Aged , Odds Ratio , Parkinson Disease/drug therapy , Pramipexole , Retrospective Studies , Review Literature as Topic , Risk
10.
Neurology ; 67(10): 1764-8, 2006 Nov 28.
Article in English | MEDLINE | ID: mdl-17130407

ABSTRACT

OBJECTIVE: To assess the hazard of death in persons with and without amnestic mild cognitive impairment (aMCI). METHODS: From 1987 through 2003, persons with aMCI (n = 243) and an age- and gender-matched reference group of cognitively normal persons in Olmsted County, MN, were recruited through the Mayo Clinic Alzheimer's Disease Patient Registry and followed prospectively through 2004. Survival was estimated using Kaplan-Meier survival curves, and the hazard of death for the aMCI cohort vs the reference cohort was estimated using Cox proportional hazards models. RESULTS: Over a median follow-up of 5.7 years, persons with aMCI had increased mortality (hazard ratio [HR] = 1.7; 95% CI: 1.3 to 2.3) vs reference subjects. The hazard of death by aMCI subtype was 1.5 in persons with single-domain aMCI (95% CI: 1.1 to 2.1) and 2.9 in persons with multiple-domain aMCI (95% CI: 1.9 to 4.6) vs reference subjects. Analyses restricted to aMCI cases showed an interaction between aMCI subtype and APOE-epsilon4 allele status (p = 0.003). Among aMCI cases with an APOE-epsilon4 allele, there was no difference in mortality between single- and multiple-domain aMCI (HR = 1.2; 95% CI: 0.6 to 2.3). However, among aMCI cases with no APOE-epsilon4 allele, the hazard of death in multiple-domain aMCI was 4.6 (95% CI: 2.3 to 9.1) vs single-domain aMCI. CONCLUSIONS: Amnestic mild cognitive impairment is associated with increased mortality, which is greater in multiple-domain aMCI than in single-domain aMCI. Mortality in aMCI subtypes may vary by APOE-epsilon4 allele status.


Subject(s)
Amnesia/mortality , Amnesia/psychology , Apolipoprotein E4/genetics , Cognition Disorders/mortality , Cognition Disorders/psychology , Genetic Predisposition to Disease/genetics , Aged , Aged, 80 and over , Algorithms , Amnesia/genetics , Cognition Disorders/genetics , Cohort Studies , DNA Mutational Analysis , Dementia/complications , Dementia/mortality , Dementia/psychology , Diagnosis, Differential , Female , Follow-Up Studies , Gene Frequency , Genetic Testing , Genotype , Humans , Male , Neuropsychological Tests , Prospective Studies , Software Design , Survival Rate
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