Plasma amyloid β-protein and C-reactive protein in relation to the rate of progression of Alzheimer disease
Plasma amyloid β-protein and C-reactive protein in relation to the rate of progression of Alzheimer disease
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DOI:
10.1001/archneur.65.6.776
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发表时间:
2008-06-01
影响因子:
--
通讯作者:
Irizarry, Michael C.
中科院分区:
文献类型:
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作者:
Locascio, Joseph J.;Fukumoto, Hiroaki;Irizarry, Michael C.
Objective: To examine whether plasma markers of amyloid precursor protein metabolism (amyloid beta-protein ending in Val-40 [A beta 40] and Ala-42 [A beta 42]), inflammation (high-sensitivity C-reactive protein), and folic acid metabolism (folic acid, vitamin B-12, and total homocysteine levels) are associated with the rate of cognitive and functional decline in persons with Alzheimer disease.Design: Longitudinal study across a mean (SD) of 4.2 (2.6) years with assessments at approximately 6-to 12-month intervals.Setting: Outpatient care.Patients: A cohort of 122 patients having a clinical diagnosis of probable Alzheimer disease, each with at least 2 assessments across time.Main Outcome Measures: Scores on the cognitive Information-Memory- Concentration subscale of the Blessed Dementia Scale and the functional Weintraub Activities of Daily Living Scale.Results: Low plasma levels of A beta 40, A beta 42, and high-sensitivity C-reactive protein were associated with a significantly more rapid cognitive decline, as indexed using the Blessed Dementia Scale, than were high levels. Low levels of A beta 42 and high-sensitivity C-reactive protein were significantly associated with more rapid functional decline on the Weintraub Activities of Daily Living Scale than were high levels. These plasma markers contributed about 5% to 12% of the variance accounted for on the Blessed Dementia Scale and the Activities of Daily Living Scale by fixed-effects predictors. Measures of folic acid metabolism were not associated with changes on either the Blessed Dementia Scale or the Activities of Daily Living Scale.Conclusions: Plasma markers of amyloid precursor protein metabolism and C-reactive protein may be associated with the rate of cognitive and functional decline in patients with Alzheimer disease.