Literature DB >> 23766866

Plasma Amyloid-β Peptides and Homocysteine in Depression in the Homebound Elderly.

Wei Qiao Qiu1, Xiaoyan Sun, D Mkaya Mwamburi, Jacqueline Haker, David Lisle, Abishek Rizal, Yu-Min Lin, Liyan Qiao, Paul Summergrad, Marshal Folstein, Irwin Rosenberg.   

Abstract

OBJECTIVES: Both plasma amyloid-β peptide 40 (Aβ40) and homocysteine (tHcy) are linked to vascular disease, which is related to depression in the elderly. We sought to study whether the relationship between tHcy and plasma Aβ40 differs in those with and without depression. STUDY DESIGN AND METHODS: In a cross-sectional study of 1058 homebound elders, vascular depression was defined as a score ≥ 16 on the Center for Epidemiological Studies Depression scale (CES-D) along with self-reported cardiovascular disease (CVD). Plasma Aβ40 and Aβ42, and serum tHcy and creatinine were measured.
RESULTS: Elders with high tHcy had higher concentrations of plasma Aβ40 (median: 147.5 vs. 123.1 pg/ml, P < 0.0001) and Aβ42 (median: 20.2 vs. 16.6 pg/ml, P < 0.0001) than those with low tHcy. In elders with depression, the relationship between logarithm of plasma Aβ40 (LogAβ40), but not LogAβ42, and tHcy was significant (β = +0.010, SE = 0.004, P = 0.007); in contrast, this relationship was not observed in those without depression. Subjects with vascular depression had the highest concentration of tHcy (mean ± SD: 12.8 ± 4.6 vs. 11.7 ± 4.5 vs. 11.9 + 5.5, P = 0.008) compared to those without CVD and those without depression. Depressed subjects without CVD had the lowest concentration of plasma Aβ42 (median: 15.5 vs. 19.1 vs. 18.7, P = 0.01) compared to those with CVD and those without depression.
CONCLUSIONS: Vascular depression, which is associated with tHcy and Aβ40 in blood, appears to be different from depression that is associated with low plasma Aβ42. This suggests that reducing tHcy and Aβ40 may be an adjunct treatment for vascular depression.

Entities:  

Keywords:  Aβ; Depression; Homocysteine

Year:  2010        PMID: 23766866      PMCID: PMC3678954     

Source DB:  PubMed          Journal:  N Am J Med Sci (Boston)        ISSN: 1946-9357


  56 in total

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