Journal of the International Neuropsychological Society



Dementia, asymmetry of temporal lobe structures, and Apolipoprotein E genotype: Relationships to cerebral atrophy and neuropsychological impairment


ERIN D.  BIGLER  a1 a2 c1, DAVID F.  TATE  a1, MICHAEL J.  MILLER  a1, SARA A.  RICE  a1, CORY D.  HESSEL  a1, HEATH D.  EARL  a1, JOANN T.  TSCHANZ  a3, BRENDA  PLASSMAN  a4 and KATHLEEN A.  WELSH-BOHMER  a4
a1 Departments of Psychology and Neuroscience, Brigham Young University, Provo, Utah
a2 Departments of Psychiatry and Radiology, University of Utah, Salt Lake City, Utah
a3 Department of Psychology, Utah State University, Logan, Utah
a4 Department of Psychiatry, Duke University, Durham, North Carolina

Abstract

We examined asymmetry of hippocampal volume as well as other temporal lobe structures (temporal lobe, temporal horn of the lateral ventricular system, parahippocampal and fusiform gyri) in 194 subjects from the Cache County, Utah study, with varying disorders [85 with Alzheimer's disease (AD), 59 with some cognitive or neuropsychiatric disorder—referenced as a Mixed Neuropsychiatric group, 30 with mild ambiguous/mild cognitive impairment (MA/MCI) and 20 controls] and APOE genotypes. Asymmetry was determined by subtracting left-side volume from the right corrected by total intracranial volume. No significant asymmetry was observed to be associated with presence of the [epsilon]4 allele. Since the AD-[epsilon]4 allele risk effect may be expressed early in the course of the disorder, we also examined asymmetry indices in AD, MA/MCI and Mixed Neuropsychiatric subjects early in the course of their disorder (2 years or less) to those with longer duration illness (greater than 2 years). We observed a leftward asymmetry (i.e., left side larger) regardless of APOE genotype in hippocampal volume where both AD and MCI subjects demonstrated a leftward shift in hippocampal size when length of disease (LOD) was less but not more than 2 years. Leftward asymmetry was not associated with LOD in the Mixed Neuropsychiatric group. These findings do not support an association between [epsilon]4 and hippocampal asymmetry in dementia. We also examined whether asymmetry influenced neuropsychological performance, but minimal effects were observed. Where significance or strong trends were observed, better neuropsychological performance was associated with larger parenchymal volume of temporal lobe structures. These findings were interpreted as representing cognitive reserve effects where larger volume was protective against impairment. The role of asymmetry research in understanding neuropsychological performance in dementia is discussed. (JINS, 2002, 8, 925–933.)

(Received February 8 2002)
(Revised May 15 2002)
(Accepted May 29 2002)


Key Words: Dementing Alzheimer's disease; Hippocampus; Temporal lobe; Asymmetry; Neuropsychology.

Correspondence:
c1 Reprint requests to: Erin D. Bigler, Ph.D., Departments of Psychology and Neuroscience, 1001 SWKT, Brigham Young University, Provo, UT 84602. E-mail: erin_bigler@byu.edu


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