Objective: To better understand the seemingly contradictory plasma beta-amyloid (A beta) results in Alzheimer's disease (AD) patients by using a newly developed plasma A beta assay, the INNO-BIA plasma A beta forms, in a multicenter study. Methods: A combined retrospective analysis of plasma A beta isoforms on mild cognitive impairment (MCI) from three large cross-sectional studies involving 643 samples from the participating German and Swedish centers. Results: Detection modules based on two different amino (N)-terminal specific A beta monoclonal antibodies demonstrated that A beta in plasma could be reliable quantified using a sandwich immunoassay technology with high precision, even for low A beta 42 plasma concentrations. A beta 40 and A beta 42 concentrations varied consistently with the ApoE genotype, while the A beta 42/A beta 40 ratio did not. Irrespective of the decrease of the A beta 42/A beta 40 ratio with age and MMSE, this parameter was strongly associated with AD, as defined in this study by elevated hyperphosphorylated (P-tau181P) levels in cerebrospinal fluid (CSF). Conclusion: A highly robust assay for repeatedly measuring A beta forms in plasma such as INNO-BIA plasma A beta forms might be a useful tool in a future risk assessment of AD.
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Univ Calif Los Angeles, Inst Mol Biol, Dept Neurol, Brain Res Inst, Los Angeles, CA USAUniv Calif Los Angeles, Inst Mol Biol, Dept Neurol, Brain Res Inst, Los Angeles, CA USA
Tran, Joyce
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Chang, Dennis
Hsu, Frederick
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Univ Calif Los Angeles, Inst Mol Biol, Dept Neurol, Brain Res Inst, Los Angeles, CA USAUniv Calif Los Angeles, Inst Mol Biol, Dept Neurol, Brain Res Inst, Los Angeles, CA USA
Hsu, Frederick
Wang, Hongsu
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Univ Calif Los Angeles, Inst Mol Biol, Dept Neurol, Brain Res Inst, Los Angeles, CA USAUniv Calif Los Angeles, Inst Mol Biol, Dept Neurol, Brain Res Inst, Los Angeles, CA USA
Wang, Hongsu
Guo, Zhefeng
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Univ Calif Los Angeles, Inst Mol Biol, Dept Neurol, Brain Res Inst, Los Angeles, CA USAUniv Calif Los Angeles, Inst Mol Biol, Dept Neurol, Brain Res Inst, Los Angeles, CA USA
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Shiga Univ Med Sci, Med Innovat Res Ctr, Pioneering Res Div, Seta Tsukinowa Cho, Otsu, Shiga 5202192, JapanShiga Univ Med Sci, Med Innovat Res Ctr, Pioneering Res Div, Seta Tsukinowa Cho, Otsu, Shiga 5202192, Japan
Hashim, Khairun Nisa Binti
Matsuba, Yukio
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Shiga Univ Med Sci, Med Innovat Res Ctr, Pioneering Res Div, Seta Tsukinowa Cho, Otsu, Shiga 5202192, Japan
RIKEN Ctr BrainScience, Lab Proteolyt Neurosci, 2-1 Hirosawa, Wako, Saitama 3510198, JapanShiga Univ Med Sci, Med Innovat Res Ctr, Pioneering Res Div, Seta Tsukinowa Cho, Otsu, Shiga 5202192, Japan
Matsuba, Yukio
Takahashi, Mika
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RIKEN Ctr BrainScience, Lab Proteolyt Neurosci, 2-1 Hirosawa, Wako, Saitama 3510198, JapanShiga Univ Med Sci, Med Innovat Res Ctr, Pioneering Res Div, Seta Tsukinowa Cho, Otsu, Shiga 5202192, Japan
Takahashi, Mika
Kamano, Naoko
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RIKEN Ctr BrainScience, Lab Proteolyt Neurosci, 2-1 Hirosawa, Wako, Saitama 3510198, JapanShiga Univ Med Sci, Med Innovat Res Ctr, Pioneering Res Div, Seta Tsukinowa Cho, Otsu, Shiga 5202192, Japan
Kamano, Naoko
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Tooyama, Ikuo
Saido, Takaomi C.
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RIKEN Ctr BrainScience, Lab Proteolyt Neurosci, 2-1 Hirosawa, Wako, Saitama 3510198, JapanShiga Univ Med Sci, Med Innovat Res Ctr, Pioneering Res Div, Seta Tsukinowa Cho, Otsu, Shiga 5202192, Japan
Saido, Takaomi C.
Hashimoto, Shoko
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Shiga Univ Med Sci, Med Innovat Res Ctr, Pioneering Res Div, Seta Tsukinowa Cho, Otsu, Shiga 5202192, Japan
RIKEN Ctr BrainScience, Lab Proteolyt Neurosci, 2-1 Hirosawa, Wako, Saitama 3510198, JapanShiga Univ Med Sci, Med Innovat Res Ctr, Pioneering Res Div, Seta Tsukinowa Cho, Otsu, Shiga 5202192, Japan