SAGE Journals Online
Advertisement
Sign In to gain access to subscriptions and/or personal tools.

 

Advanced Search

Journal Navigation

Journal Home

Subscriptions

Archive

Contact Us

Table of Contents

Advertisement

Sign In to gain access to subscriptions and/or personal tools.
American Journal of Alzheimer's Disease and Other Dementias®
This Article
Right arrow Full Text (PDF)
Right arrow References
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to Saved Citations
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Request Reprints
Right arrow Add to My Marked Citations
Citing Articles
Right arrow Citing Articles via Google Scholar
Right arrow Citing Articles via Scopus
Google Scholar
Right arrow Articles by Leszek, J.
Right arrow Articles by Gamian, A.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Leszek, J.
Right arrow Articles by Gamian, A.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?

Analysis of Serum of Patients With Alzheimer’s Disease for the Level of Advanced Glycation End Products

Jerzy Leszek, MD

Department of Psychiatry, Medical University, Wroclaw, Poland, jleszek{at}psych.am.wroc.pl

Krzysztof Malyszczak, MD

Department of Psychiatry, Medical University, Wroclaw, Poland

Adam Bartys, MSc

Institute of Immunology and Experimental Therapy, Wroclaw, Poland

Magda Staniszewska, PhD

Institute of Immunology and Experimental Therapy, Wroclaw, Poland

Andrzej Gamian, PhD

Institute of Immunology and Experimental Therapy, Wroclaw, Poland

Data on the serum level of advanced glycation end products (AGEs) in Alzheimer’s disease (AD) patients are scarce, although a specific biochemical marker easy to detect in body fluids is desired for an early diagnosis of disease and to monitor the effects of therapeutic treatment. In the current study, the content of AGEs was examined with an immunochemical assay in the sera of AD patients, in the frame of a search for a biochemical marker of disease. Subjects with AD and vascular dementia (VaD) were included in the study (n = 30; age range, 68-70 years). The results were compared to the healthy control groups. The enzyme-linked immunosorbent assay (ELISA) inhibition test for the determination of AGEs is based on a rabbit anti-AGE, affinity-purified antibody and a model AGE-myoglobin antigen, in which a serum sample treated with proteinase K is used as an inhibitor. For the measurement of immune complexes and anti-AGE antibodies, the corresponding ELISA tests have been applied. The AGE level in the VaD group (49.5 UAGE) was higher than in AD patients (46.1 UAGE). The level of total AGEs in the sera of AD patients was significantly lower than in the control group (50/51.6 UAGE). These relations were not observed with regard to the immune complexes and anti-AGE antibody levels in AD (70.2 UIC/0.027 UIgG) and VaD (83 UIC/0.034 UIgG) patients because the levels of these parameters were similar to the controls (76.2 UIC/0.042 UIgG). The work revealed the lower level of circulating serum AGEs in patients with AD in relation to healthy controls.

Key Words: Alzheimer’s disease • vascular dementia • glycation products • advanced glycation end products • AGEs • biological markers

American Journal of Alzheimer's Disease and Other Dementias®, Vol. 21, No. 5, 360-365 (2006)
DOI: 10.1177/1533317506291075


Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter    What's this?




Advertisement