Evolution of Abeta42 and Abeta40 levels and Abeta42/Abeta40 ratio in plasma during progression of Alzheimer's disease: a multicenter assessment.

Standard

Evolution of Abeta42 and Abeta40 levels and Abeta42/Abeta40 ratio in plasma during progression of Alzheimer's disease: a multicenter assessment. / Blennow, K; De Meyer, G; Hansson, O; Minthon, L; Wallin, A; Zetterberg, H; Lewczuk, P; Vanderstichele, H; Vanmechelen, E; Kornhuber, J; Wiltfang, J; Heuser, I; Maier, W; Luckhaus, C; Rüther, E; Hüll, M; Jahn, Holger; Gertz, H J; Frölich, L; Hampel, H; Pernetzki, R.

in: J NUTR HEALTH AGING, Jahrgang 13, Nr. 3, 3, 2009, S. 205-208.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Blennow, K, De Meyer, G, Hansson, O, Minthon, L, Wallin, A, Zetterberg, H, Lewczuk, P, Vanderstichele, H, Vanmechelen, E, Kornhuber, J, Wiltfang, J, Heuser, I, Maier, W, Luckhaus, C, Rüther, E, Hüll, M, Jahn, H, Gertz, HJ, Frölich, L, Hampel, H & Pernetzki, R 2009, 'Evolution of Abeta42 and Abeta40 levels and Abeta42/Abeta40 ratio in plasma during progression of Alzheimer's disease: a multicenter assessment.', J NUTR HEALTH AGING, Jg. 13, Nr. 3, 3, S. 205-208. <http://www.ncbi.nlm.nih.gov/pubmed/19262954?dopt=Citation>

APA

Blennow, K., De Meyer, G., Hansson, O., Minthon, L., Wallin, A., Zetterberg, H., Lewczuk, P., Vanderstichele, H., Vanmechelen, E., Kornhuber, J., Wiltfang, J., Heuser, I., Maier, W., Luckhaus, C., Rüther, E., Hüll, M., Jahn, H., Gertz, H. J., Frölich, L., ... Pernetzki, R. (2009). Evolution of Abeta42 and Abeta40 levels and Abeta42/Abeta40 ratio in plasma during progression of Alzheimer's disease: a multicenter assessment. J NUTR HEALTH AGING, 13(3), 205-208. [3]. http://www.ncbi.nlm.nih.gov/pubmed/19262954?dopt=Citation

Vancouver

Bibtex

@article{ba46ac711f104d98acdd8efdf1178c11,
title = "Evolution of Abeta42 and Abeta40 levels and Abeta42/Abeta40 ratio in plasma during progression of Alzheimer's disease: a multicenter assessment.",
abstract = "OBJECTIVE: To better understand the seemingly contradictory plasma beta-amyloid (Abeta) results in Alzheimer's disease (AD) patients by using a newly developed plasma Abeta assay, the INNO-BIA plasma Abeta forms, in a multicenter study. METHODS: A combined retrospective analysis of plasma Abeta 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 Abeta monoclonal antibodies demonstrated that Abeta in plasma could be reliable quantified using a sandwich immunoassay technology with high precision, even for low Abeta42 plasma concentrations. Abeta40 and Abeta42 concentrations varied consistently with the ApoE genotype, while the Abeta42/Abeta40 ratio did not. Irrespective of the decrease of the Abeta42/Abeta40 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 Abeta forms in plasma such as INNO-BIA plasma Abeta forms might be a useful tool in a future risk assessment of AD.",
author = "K Blennow and {De Meyer}, G and O Hansson and L Minthon and A Wallin and H Zetterberg and P Lewczuk and H Vanderstichele and E Vanmechelen and J Kornhuber and J Wiltfang and I Heuser and W Maier and C Luckhaus and E R{\"u}ther and M H{\"u}ll and Holger Jahn and Gertz, {H J} and L Fr{\"o}lich and H Hampel and R Pernetzki",
year = "2009",
language = "Deutsch",
volume = "13",
pages = "205--208",
journal = "J NUTR HEALTH AGING",
issn = "1279-7707",
publisher = "Springer Paris",
number = "3",

}

RIS

TY - JOUR

T1 - Evolution of Abeta42 and Abeta40 levels and Abeta42/Abeta40 ratio in plasma during progression of Alzheimer's disease: a multicenter assessment.

AU - Blennow, K

AU - De Meyer, G

AU - Hansson, O

AU - Minthon, L

AU - Wallin, A

AU - Zetterberg, H

AU - Lewczuk, P

AU - Vanderstichele, H

AU - Vanmechelen, E

AU - Kornhuber, J

AU - Wiltfang, J

AU - Heuser, I

AU - Maier, W

AU - Luckhaus, C

AU - Rüther, E

AU - Hüll, M

AU - Jahn, Holger

AU - Gertz, H J

AU - Frölich, L

AU - Hampel, H

AU - Pernetzki, R

PY - 2009

Y1 - 2009

N2 - OBJECTIVE: To better understand the seemingly contradictory plasma beta-amyloid (Abeta) results in Alzheimer's disease (AD) patients by using a newly developed plasma Abeta assay, the INNO-BIA plasma Abeta forms, in a multicenter study. METHODS: A combined retrospective analysis of plasma Abeta 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 Abeta monoclonal antibodies demonstrated that Abeta in plasma could be reliable quantified using a sandwich immunoassay technology with high precision, even for low Abeta42 plasma concentrations. Abeta40 and Abeta42 concentrations varied consistently with the ApoE genotype, while the Abeta42/Abeta40 ratio did not. Irrespective of the decrease of the Abeta42/Abeta40 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 Abeta forms in plasma such as INNO-BIA plasma Abeta forms might be a useful tool in a future risk assessment of AD.

AB - OBJECTIVE: To better understand the seemingly contradictory plasma beta-amyloid (Abeta) results in Alzheimer's disease (AD) patients by using a newly developed plasma Abeta assay, the INNO-BIA plasma Abeta forms, in a multicenter study. METHODS: A combined retrospective analysis of plasma Abeta 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 Abeta monoclonal antibodies demonstrated that Abeta in plasma could be reliable quantified using a sandwich immunoassay technology with high precision, even for low Abeta42 plasma concentrations. Abeta40 and Abeta42 concentrations varied consistently with the ApoE genotype, while the Abeta42/Abeta40 ratio did not. Irrespective of the decrease of the Abeta42/Abeta40 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 Abeta forms in plasma such as INNO-BIA plasma Abeta forms might be a useful tool in a future risk assessment of AD.

M3 - SCORING: Zeitschriftenaufsatz

VL - 13

SP - 205

EP - 208

JO - J NUTR HEALTH AGING

JF - J NUTR HEALTH AGING

SN - 1279-7707

IS - 3

M1 - 3

ER -