Literature DB >> 17445286

Magnetic resonance imaging correlates of set shifting.

Joel H Kramer1, Lovingly Quitania, David Dean, John Neuhaus, Howard J Rosen, Cathra Halabi, Michael W Weiner, Vincent A Magnotta, Dean C Delis, Bruce L Miller.   

Abstract

The purpose of this study was to examine the relationships between lobar volumes and set shifting. We studied 101 subjects, including 36 normal controls, 16 patients with probable Alzheimer's disease, 30 patients with frontotemporal dementia (FTD), and 19 patients with semantic dementia (SD), using a shifting paradigm that carefully controlled for component abilities. Subjects were administered two conditions of the Delis-Kaplan Executive Function System (D-KEFS) Design Fluency Test. In the control condition (DF:Control), examinees generated as many unique designs as possible in 60 s by drawing lines connecting only unfilled dots. In the switching condition (DF:Switch), examinees generated designs by drawing lines alternating between filled and unfilled dots. We used BRAINS2 software to generate volumes of the right and left frontal, temporal, and parietal lobes. Partial correlations and multiple regressions showed that, after controlling for Mini-Mental State Examination and DF:Control, only the right and left frontal lobe volumes significantly correlated with the DF:Switch, most clearly in the FTD and SD groups. Follow-up analyses indicated that frontal contributions to shifting were not related to working memory. Results highlight the importance of carefully controlling for component cognitive processes when studying executive functioning.

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Year:  2007        PMID: 17445286      PMCID: PMC2443737          DOI: 10.1017/S1355617707070567

Source DB:  PubMed          Journal:  J Int Neuropsychol Soc        ISSN: 1355-6177            Impact factor:   2.892


  38 in total

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  25 in total

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Review 7.  Language, executive function and social cognition in the diagnosis of frontotemporal dementia syndromes.

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8.  Voxel and surface-based topography of memory and executive deficits in mild cognitive impairment and Alzheimer's disease.

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9.  Longitudinal rates of lobar atrophy in frontotemporal dementia, semantic dementia, and Alzheimer's disease.

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