Literature DB >> 10737693

The joint effect of apolipoprotein E epsilon4 and MRI findings on lower-extremity function and decline in cognitive function.

D Carmelli1, C DeCarli, G E Swan, M Kelly-Hayes, P A Wolf, T Reed, J M Guralnik.   

Abstract

BACKGROUND: Cognitive decline and poor physical function are risk factors for disability in old age and may occur more often in subjects with the apolipoprotein E epsilon4 (ApoE-epsilon4) allele. The objective of this study was to investigate the joint effect of ApoE-epsilon4 and structural changes detected on MRI brain scans on cognitive decline and lower-extremity function.
METHODS: Brain MRI (1.5 T), neuropsychological tests, and lower-extremity physical function tests were administered to World War II male veteran twins ages 69 to 80. Quantification of MRI scans used a previously published algorithm to segment brain images into total cerebral brain (TCB), cerebrospinal fluid (CSF), and white-matter hyperintensity (WMH) volumes. A short battery of physical performance tests was used to assess lower-extremity function. Ten-year changes in performance on the Mini-Mental State Exam (MMSE), the Benton Visual Retention Test (BVRT), and the Digit Symbol Substitution (DSS) test were used to assess cognitive decline.
RESULTS: For the sample as a whole, the comparison of subjects by median split of total cerebral brain volume found that those with brain volumes below the median performed worse on tests of gait and balance (p < .01) and experienced greater cognitive decline on the MMSE and BVRT cognitive test batteries (both p < .01). In addition, subjects with WMH volumes above the median had poor performance on the standing balance tasks and experienced greater decline on the DSS test (p < .01). Stratified analyses revealed that the joint effect of radiological findings and the ApoE-epsilon4 allele on cognitive decline and lower-extremity function was often greater than that expected from the separate effects combined.
CONCLUSIONS: We conclude that radiological findings in conjunction with ApoE-epsilon4 may single out a group at higher risk for dementia. We speculate that the observed interaction effect may be due to increased susceptibility to brain injury or impaired repair mechanisms in subjects with ApoE-epsilon4.

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Year:  2000        PMID: 10737693     DOI: 10.1093/gerona/55.2.m103

Source DB:  PubMed          Journal:  J Gerontol A Biol Sci Med Sci        ISSN: 1079-5006            Impact factor:   6.053


  27 in total

1.  Apolipoprotein E e4 allele is associated with more rapid motor decline in older persons.

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2.  Cognitive status and future risk of frailty in older Mexican Americans.

Authors:  Mukaila A Raji; Soham Al Snih; Glenn V Ostir; Kyriakos S Markides; Kenneth J Ottenbacher
Journal:  J Gerontol A Biol Sci Med Sci       Date:  2010-07-09       Impact factor: 6.053

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Review 5.  Clinically asymptomatic vascular brain injury: a potent cause of cognitive impairment among older individuals.

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Review 7.  Genetic vulnerability following traumatic brain injury: the role of apolipoprotein E.

Authors:  N Nathoo; R Chetty; J R van Dellen; G H Barnett
Journal:  Mol Pathol       Date:  2003-06

8.  Apolipoprotein E genotype and risk of developing physical limitations in elderly people.

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Journal:  J Am Geriatr Soc       Date:  2009-07       Impact factor: 5.562

9.  Age-related changes in memory and fluid reasoning in a sample of healthy old people.

Authors:  Geoff Der; Mike Allerhand; John M Starr; Scott M Hofer; Ian J Deary
Journal:  Neuropsychol Dev Cogn B Aging Neuropsychol Cogn       Date:  2009-07-01

10.  Evaluation of a home-based exercise program in the treatment of Alzheimer's disease: the Maximizing Independence in Dementia (MIND) study.

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