Impact of APOE in mild cognitive impairment

M. R. Farlow, Y. He, S. Tekin, J. Xu, R. Lane, H. C. Charles

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Abstract

Objective: The authors aimed to use baseline data of an ongoing large, prospective study in subjects with mild cognitive impairment (MCI) to investigate the impact of APOE genotype on the symptom profile of the condition. Methods: Cognitive assessments included the AD Assessment Scale cognitive subscale (ADAS-cog), the Mini-Mental State Examination (MMSE), and a cognitive battery for assessment of memory, attention, and executive function. Behavioral assessments included the Neuropsychiatric Inventory and Beck Depression Inventory. Activities of daily living were assessed by the AD Cooperative Study Activities of Daily Living (ADCS-ADL) scale. Hippocampal volumes were measured with MRI. Results: A total of 494 of 1,018 study subjects provided APOE data. Approximately 40% of the subjects were APOE ε4 carriers. APOE ε4 carriers had lower MMSE (p = 0.01) and higher ADAS-cog (p < 0.0001) scores than noncarriers, indicating worse cognitive impairment. APOE ε4 carriers also had greater deficits on New York University delayed paragraph recall and Buschke free and cued selective reminding tests, and on the ADCS-ADL scale (p < 0.001). They also had smaller hippocampal volumes (p = 0.002). Behavioral scores were similar across the subgroups. Conclusion: MCI subjects carrying the APOE ε4 allele showed distinct cognitive and imaging profiles, which appeared to resemble those of early Alzheimer patients. APOE ε4 genotype was associated with greater impairments in memory and functional activities as well as hippocampal atrophy.

Original languageEnglish (US)
Pages (from-to)1898-1901
Number of pages4
JournalNeurology
Volume63
Issue number10
DOIs
StatePublished - Nov 23 2004

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ASJC Scopus subject areas

  • Clinical Neurology

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Farlow, M. R., He, Y., Tekin, S., Xu, J., Lane, R., & Charles, H. C. (2004). Impact of APOE in mild cognitive impairment. Neurology, 63(10), 1898-1901. https://doi.org/10.1212/01.WNL.0000144279.21502.B7