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Статья

Reduction of β‐amyloid peptide<sub>42</sub> in the cerebrospinal fluid of patients with Alzheimer's disease

Ruth MotterAthena Neurosciences, Inc, South San Francisco, CACarmen Vigo‐PelfreyAthena Neurosciences, Inc, South San Francisco, CADora KholodenkoAthena Neurosciences, Inc, South San Francisco, CARobin BarbourAthena Neurosciences, Inc, South San Francisco, CAKelly Johnson‐WoodAthena Neurosciences, Inc, South San Francisco, CADouglas GalaskoL. ChangUCLA Harbor Medical Center, Department of Neurology, Torrance, CABruce L. MillerUCLA Harbor Medical Center, Department of Neurology, Torrance, CAChristopher M. ClarkUniversity of Pennsylvania, Graduate Hospital, Department of Neurology, Philadelphia, PAR. GreenNeurobehavior Program of Neurology, Wesley Woods Center and Emory University School of Medicine, Atlanta, GADarin E. OlsonNeurobehavior Program of Neurology, Wesley Woods Center and Emory University School of Medicine, Atlanta, GAPaula C. SouthwickR. WolfertB.S. Alelia E. MunroeIvan LieberburgAthena Neurosciences, Inc, South San Francisco, CAPeter SeubertAthena Neurosciences, Inc, South San Francisco, CADale SchenkAthena Neurosciences, Inc, South San Francisco, CA
1995en
ABI

Аннотация

Abstract In this clinical study, the cerebrospinal fluid (CSF) level of a Novemberel form of the β‐amyloid peptide (Aβ) extending to position 42 (Aβ 42 ) was determined in patients with Alzheimer's disease (AD) as well as controls. In addition to measurement of CSF Aβ 42 levels, total Aβ peptides, microtubule‐associated protein τ, and apolipoprotein E (ApoE) genotype were also assessed. It is interesting that CSF Aβ 42 levels were found to be significantly lower in AD patients relative to controls, whereas total Aβ levels were not. Aβ 42 has recently been shown to preferentially deposit in the brain tissue of patients with AD, suggesting that diminished clearance may account for its reduction in CSF. As previously reported, τ levels were increased in AD patients; however, neither Aβ 42 nor τ levels were apparently influenced by the ApoE genotype.

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