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Department of Neurology, Gertrudis Hospital, 3. Leun- Biskirchen, Germany. Copyright . This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Parkinson’s disease is characterized by a substantial cognitive heterogeneity, which is apparent in different profiles and levels of severity. To date, a distinct clinical profile for patients with a potential risk of developing dementia still has to be identified. We introduce a data- driven approach to detect different cognitive profiles and stages. Comprehensive neuropsychological data sets from a cohort of 1. Parkinson’s disease patients with and without dementia were explored by a factor analysis to characterize different cognitive domains. Based on the factor scores that represent individual performance in each domain, hierarchical cluster analyses determined whether subgroups of Parkinson’s disease patients show varying cognitive profiles. A six- factor solution accounting for 6. Cronbach’s alpha coefficients ). The cluster analyses suggested two independent patient clusters with different cognitive profiles. They differed only in severity of cognitive impairment and self- reported limitation of activities of daily living function but not in motor performance, disease duration, or dopaminergic medication. Importantly, these profiles were independent of motor progression. Introduction. Beyond the characteristic motor signs, a number of nonmotor symptoms including cognitive aspects are gaining increasing attention in Parkinson’s disease (PD). Recent work revealed a substantial heterogeneity of cognitive impairment, which is apparent in both different profiles and different levels of severity ranging from slight and early cognitive changes up to the diagnosis of PD dementia (PDD) . With the demand for an early, individualized, and better therapeutic treatment, the focus is now to identify the patients with a potentially higher risk of dementia . Already a few cognitive alterations may enhance the risk of PDD. However, it needs to be noted that exactly the same cognitive alterations can also be found in PD patients who did not develop dementia . On subtest level, some studies suggest that early executive dysfunction is predictive of the conversion to dementia . Thus, a distinct clinical profile for patients with a potential risk of developing PDD still has to be identified . Some data- driven studies on different subtypes of PD found a poor test performance in varying neuropsychological tasks, suggesting that these help to diagnose PDD . Recently, a cluster analysis on a small cohort of PD patients without dementia revealed differences in severity of cognitive deterioration but not in cognitive phenotypes . We here propose an approach to identify cognitive profiles based on performance differences within quantitatively determined domains using standardized factor scores. These standard values can be used to compare the mean performance of each single PD patient investigated here to the mean performance of the present, total PD cohort. Our study thus was designed by (i) a data- driven identification of different cognitive domains in a large cohort of both PD patients with and without dementia and (ii) a data- based subdivision of PD patients according to exactly these standardized domain scores to characterize subgroups with divers cognitive profiles and potentially different levels of cognitive impairment. Materials and Methods. Patients. We investigated 1. PD according to the UK Brain Bank criteria . All patients received their usual, optimized medication and were able to complete all cognitive tasks (Tables 1 and 2 provide all relevant details). Table 1: Demographic, clinical, and neuropsychological characteristics of the two PD groups (PDD patients included) as identified by the first hierarchical cluster analysis. Table 2: Demographic, clinical, and neuropsychological characteristics of the two PD groups (PDD patients excluded) as identified by the second hierarchical cluster analysis. Inclusion criteria were: age . Exclusion criteria were: other neurological diseases affecting the central nervous system, prior surgery for PD, medication interfering with cognition (i. Patients with identified gene mutations and those reporting more than 2 first or second degree relatives with a definitive diagnosis of PD . Most patients identified their spouse as caregiver (7. The study was approved by the local ethical committee. All patients and caregivers gave written informed consent. Neuropsychological Assessment. All examinations and expert evaluations were carried out within a week. Each patient underwent a comprehensive test battery according to the recommendations of the Movement Disorder Society (MDS) Task Force . Further, we applied the logical memory tasks (Log. I and Log. II) of the Wechsler Memory Scale- Revised (WMS- R, verbal memory) . Analyses are based on standard norms (percentile rank scores) of healthy German control subjects as published in the manuals. Data are corrected either for age (NAI, WMS- R, VOSP) or for age and education (CERAD, TAP, TMT, TL- D). Diagnostic criteria for dementia followed the recommendation of the MDS task force for probable PDD . In detail, our criteria for PDD were (i) scores 1. SD (PR < 7) in at least one test below published group norms of healthy control subjects in at least 2 of the following cognitive domains: attention (as measured by Alertness, Go- Nogo), executive function (DS, TL- D, TMT- A, TMT- B, VF), visuospatial function (praxis, praxis delay, OD), memory (Log. I, Log. II, WL, WL- I, WL delay, WL- R, FT), or language ability (BNT), (ii) cognitive decline with insidious onset and slow progression reported by either the patients or their proxies, and (iii) impairment of nonmotor activities of daily living (ADL) as verified by a structured patient and/or caregiver interview on the perception of cognitively influenced ADL function in the domestic environment. Motor Performance, Behavioral Disturbances, and ADLClinical assessment included the Hoehn and Yahr stage, the unified Parkinson disease rating scale part III (UPDRS- III) . The Parkinson’s Disease Questionnaire (PDQ- 3. Further, we calculated age- corrected standard scores of the patients’ ADL function using (i) a self- rating questionnaire (Nuernberger- Alters- Alltagsaktivitaeten- Skala, NAA) and (ii) its corresponding scale for proxies (Nuernberger- Alters- Beobachtungsskala, NAB) . Identification of Cognitive Domains: Exploratory Factor Analysis (EFA)First, we performed an EFA on all neuropsychological data to identify cognitive domains in the PD group. The factor matrix was optimized with oblique rotation, because factors were expected to be correlated . Variables with a factor loading or were considered as core variables for a given factor . The Kaiser’s criterion (eigenvalue > 1) and the corresponding scree plot results were used to determine the number of factors to be retained. Internal consistency was verified by Cronbach’s alpha () coefficient, which was required to be higher than for each factor to indicate a sufficient internal consistency structure . Identification of Characteristic Profiles in the PD Cohort: Hierarchical Cluster Analysis. Based on the factor loadings from the EFA, individual factor scores were calculated by the Anderson- Rubin algorithm, which produces factor scores that are uncorrelated and standardized with a mean of zero and a standard deviation of 1. A patient with a factor score of 0 (zero) thus shows average performance compared to the total PD cohort; a positive score indicates performance above, a negative score below the average of the whole patient group investigated here. With these individual factor scores, we performed two separate hierarchical cluster analyses to identify patient subgroups with different cognitive profiles (Ward’s- method). The first analysis was conducted on the total group of PD patients (), the second, for validation purposes, on all PD patients except those with dementia (). As PDD patients can be expected to suffer from more severe cognitive, motor, and behavioral impairment, we evaluated this specific influence on our study results by excluding them from the second HCA. Student’s - (age, disease duration, UPDRS- III motor score) or . Analyses of covariance and Mantel- Haenszel statistics accounted for differences in demographics and disease severity. Because of the number of comparisons, the significance levels were set at to optimize the trade- off between false positive protection (type 1) and sensitivity/power (type 2 error). All analyses were conducted using SPSS 1. SPSS Inc, Chicago, III, USA). Patient Characteristics. Of the 1. 21 patients, seventeen (1. L- dopa, 2. 5 (2. Both L- dopa and dopamine agonists were given to 7. Twenty- four patients (1. PDD; six of them were treated with cholinesterase inhibitors (see Table 1 for further details). Cognitive Domains. Table 3 shows the result of the EFA and the internal consistency analysis. The EFA was verified by the Bartlett’s test of sphericity (, , ) and the Kaiser- Meyer- Olkin measures of sampling adequacy (MSA = 0. A six- factor solution accounting for 6. Table 1 for information on the rejected five- factor solution). The internal consistency structure of each factor was found to be at least moderately high (). Factor 1 consisted of five neuropsychological tasks explaining 3. Factor 2 comprised four tasks on word- list memory and recall (, 8. Both Factor 3 (6. Church Employee Evaluation Template. Custom Search. Church Forms.. CDCollection of all the Church Forms, Flyers, Certificates..(8. Free. Church. Forms. CD - each form.. in PDF and MS Word 2. 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