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Brief Report |
Received December 23, 2003; revised November 23, 2004; accepted January 31, 2005. From the Geriatric Psychiatry Program, Nathan Kline Institute for Psychiatric Research, Orangeburg, NY (NP, LMW, JJS), the Dept. of Psychiatry, New York Univ. School of Medicine, New York, NY (NP, JJS), and the Dept. of Immunology, Institute for Basic Research in Developmental Disabilities, Staten Island, NY (PDM). Send correspondence and reprint requests to Nunzio Pomara, M.D., Geriatric Psychiatry Program, Nathan S. Kline Institute, 140 Old Orangeburg Rd., Bldg. 35, Orangeburg, NY 10962. e-mail: pomara{at}nki.rfmh.org
© 2005 American Association for Geriatric Psychiatry
Objective: Longitudinal changes in plasma beta amyloid protein 1-42 and 1-40 (Aß42 and Aß40) levels and possible relationships with cognitive decline and apolipoprotein (APOE) genotype were studied in healthy elderly individuals. Methods: Authors determined cognitive level and plasma Aß40 and Aß42 levels twice, approximately 4 years apart, in 34 elderly subjects. Results: Analyses revealed a selective reduction in Aß42 levels at follow-up, which were not modulated by the
4 allele. Greater reductions and higher baseline plasma Aß42 levels were associated with reductions in cognitive scores. Conclusions: Alterations in plasma Aß42 levels may be associated with subtle cognitive decline in elderly subjects without dementia.
Key Words: Amyloid Beta Proteins Longitudinal Studies Dementia Apolipoprotein
4 Alleles
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