White matter fractional anisotropy is related to processing speed in metabolic syndrome patients: a case-control study

<p>Abstract</p> <p>Background</p> <p>Metabolic Syndrome (MetSd) is a cluster of vascular risk factors that may influence cerebrovascular pathology during aging. Recently, microstructural white matter (WM) changes detected by diffusion tensor imaging (DTI) and processing...

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Main Authors: Bargalló Núria, Freixenet Núria, Jurado María, Segura Bàrbara, Junqué Carme, Arboix Adrià
Format: Article
Language:English
Published: BMC 2010-07-01
Series:BMC Neurology
Online Access:http://www.biomedcentral.com/1471-2377/10/64
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spelling doaj-722265143be445dca8f90560ee1c79712020-11-25T01:00:41ZengBMCBMC Neurology1471-23772010-07-011016410.1186/1471-2377-10-64White matter fractional anisotropy is related to processing speed in metabolic syndrome patients: a case-control studyBargalló NúriaFreixenet NúriaJurado MaríaSegura BàrbaraJunqué CarmeArboix Adrià<p>Abstract</p> <p>Background</p> <p>Metabolic Syndrome (MetSd) is a cluster of vascular risk factors that may influence cerebrovascular pathology during aging. Recently, microstructural white matter (WM) changes detected by diffusion tensor imaging (DTI) and processing speed deficits have been reported in MetSd patients. We aimed to test the relationship between WM alteration and cognitive impairment in these patients.</p> <p>Methods</p> <p>The sample comprised 38 subjects (19 patients aged between 50 and 80 years old, and 19 controls). All patients fulfilled National Cholesterol Education Program Adult Treatment Panel III (NCEP ATP-III) criteria for MetSd. Speed of information processing was measured by the Symbol Digit Modalities Test (SDMT) and reaction time (RT) on the Continuous Performance Test (CPT-II) and the Grooved Pegboard Test (GPT). DTI images were acquired in a 3 Tesla Siemens Trio scanner. Voxelwise statistical analysis of the fractional anisotropy (FA) data was performed using the Tract-Based Spatial Statistics part of the FMRIB Software Library. A correlation analysis was performed between processing speed variables and FA values.</p> <p>Results</p> <p>There was a larger proportion of slow subjects (percentile below 25<sup>th</sup>) in the patient group (Chi<sup>2 </sup>= 7.125 p = 0.008). FA values correlated positively with SDMT in anterior and posterior parts of the corpus callosum, and RT CPT-II correlated negatively with FA values in the anterior corpus callosum (p < 0.05 corrected) in the patient group.</p> <p>Conclusion</p> <p>We found significant correlations between WM alterations and cognitive impairment in MetSd patients, especially in the frontal lobe. These findings highlight the importance of MetSd prevention and control due to its association with structural and functional damage in the central nervous system.</p> http://www.biomedcentral.com/1471-2377/10/64
collection DOAJ
language English
format Article
sources DOAJ
author Bargalló Núria
Freixenet Núria
Jurado María
Segura Bàrbara
Junqué Carme
Arboix Adrià
spellingShingle Bargalló Núria
Freixenet Núria
Jurado María
Segura Bàrbara
Junqué Carme
Arboix Adrià
White matter fractional anisotropy is related to processing speed in metabolic syndrome patients: a case-control study
BMC Neurology
author_facet Bargalló Núria
Freixenet Núria
Jurado María
Segura Bàrbara
Junqué Carme
Arboix Adrià
author_sort Bargalló Núria
title White matter fractional anisotropy is related to processing speed in metabolic syndrome patients: a case-control study
title_short White matter fractional anisotropy is related to processing speed in metabolic syndrome patients: a case-control study
title_full White matter fractional anisotropy is related to processing speed in metabolic syndrome patients: a case-control study
title_fullStr White matter fractional anisotropy is related to processing speed in metabolic syndrome patients: a case-control study
title_full_unstemmed White matter fractional anisotropy is related to processing speed in metabolic syndrome patients: a case-control study
title_sort white matter fractional anisotropy is related to processing speed in metabolic syndrome patients: a case-control study
publisher BMC
series BMC Neurology
issn 1471-2377
publishDate 2010-07-01
description <p>Abstract</p> <p>Background</p> <p>Metabolic Syndrome (MetSd) is a cluster of vascular risk factors that may influence cerebrovascular pathology during aging. Recently, microstructural white matter (WM) changes detected by diffusion tensor imaging (DTI) and processing speed deficits have been reported in MetSd patients. We aimed to test the relationship between WM alteration and cognitive impairment in these patients.</p> <p>Methods</p> <p>The sample comprised 38 subjects (19 patients aged between 50 and 80 years old, and 19 controls). All patients fulfilled National Cholesterol Education Program Adult Treatment Panel III (NCEP ATP-III) criteria for MetSd. Speed of information processing was measured by the Symbol Digit Modalities Test (SDMT) and reaction time (RT) on the Continuous Performance Test (CPT-II) and the Grooved Pegboard Test (GPT). DTI images were acquired in a 3 Tesla Siemens Trio scanner. Voxelwise statistical analysis of the fractional anisotropy (FA) data was performed using the Tract-Based Spatial Statistics part of the FMRIB Software Library. A correlation analysis was performed between processing speed variables and FA values.</p> <p>Results</p> <p>There was a larger proportion of slow subjects (percentile below 25<sup>th</sup>) in the patient group (Chi<sup>2 </sup>= 7.125 p = 0.008). FA values correlated positively with SDMT in anterior and posterior parts of the corpus callosum, and RT CPT-II correlated negatively with FA values in the anterior corpus callosum (p < 0.05 corrected) in the patient group.</p> <p>Conclusion</p> <p>We found significant correlations between WM alterations and cognitive impairment in MetSd patients, especially in the frontal lobe. These findings highlight the importance of MetSd prevention and control due to its association with structural and functional damage in the central nervous system.</p>
url http://www.biomedcentral.com/1471-2377/10/64
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