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

J Gerontol A Biol Sci Med Sci. 2000 Feb;55(2):M103-9. doi: 10.1093/gerona/55.2.m103.

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.

Publication types

  • Comparative Study
  • Research Support, U.S. Gov't, P.H.S.
  • Twin Study

MeSH terms

  • Aged
  • Aged, 80 and over
  • Algorithms
  • Alleles
  • Apolipoprotein E4
  • Apolipoproteins E / genetics*
  • Brain / pathology*
  • Cerebrospinal Fluid
  • Cognition / physiology
  • Cognition Disorders / physiopathology*
  • Cohort Studies
  • Data Interpretation, Statistical
  • Disabled Persons
  • Follow-Up Studies
  • Gait / physiology
  • Humans
  • Leg / physiology*
  • Longitudinal Studies
  • Magnetic Resonance Imaging*
  • Male
  • Memory / physiology
  • Neuropsychological Tests
  • Postural Balance / physiology
  • Psychomotor Performance / physiology*
  • Risk Factors

Substances

  • Apolipoprotein E4
  • Apolipoproteins E