We use cookies to understand how you use our site and to improve your experience. This includes personalizing content and advertising. To learn more, click here. By continuing to use our site, you accept our use of cookies. Cookie Policy.

LabMedica

Download Mobile App
Recent News Expo Clinical Chem. Molecular Diagnostics Hematology Immunology Microbiology Pathology Technology Industry Focus

Protein Biomarkers Aid Detection of Prodromal Alzheimer Disease

By LabMedica International staff writers
Posted on 17 Jan 2012
Cerebrospinal fluid (CSF) biomarkers can predict future development of Alzheimer Disease (AD) dementia within 10 years in patients with mild cognitive impairment (MCI).

The CSF biomarkers, total tau (T-tau), phosphorylated tau (P-tau), and β-amyloid 1-42 (Aβ42), have been compared for their ability to distinguish between early and late converters to AD.

Scientists at Skåne University (Malmö; Sweden) carried out an extended follow-up of the cohort from a previous study involving 137 patients with mild cognitive impairment (MCI) at baseline for an average follow-up period of 9.2 years. Lumbar punctures were performed at base line and during follow up on the 137 patients and 39 human volunteers. They analyzed CSF concentrations of Aβ42, T-tau, and phosphorylated tau P-tau181 using xMAP technology.

Systems using xMAP technology (Luminex; Austin, TX, USA) perform discrete bioassays on the surface of color-coded beads known as microspheres, which are then read in a compact analyzer. The results of the study showed an equal reduction in baseline CSF Aβ42 levels in patients with MCI who converted to AD within five years, the early converters, compared with those who converted later, such as between five and 10 years, whilst T-tau and P-tau levels were substantially higher in early converters compared to later ones. As many as 91% of the patients with mild memory impairment who had these risk markers went on to develop Alzheimer's within a ten-year period. In contrast, those who had memory impairment but normal values for the markers did not run a higher risk of getting Alzheimer's than healthy individuals

By observing how the levels of the biomarkers develop over the ten years before the patient's diagnosis, the scientists have also been able to map the progression of the disease in the brain. The results indicate that it starts with a modified turnover of beta-amyloid. Only later is this followed by changes in the tau protein and damage to nerve cells. This can be important information for those developing new therapies for Alzheimer's. Senior author of the study Oskar Hansson, MD, PhD, said, "This is a very important finding with regard to the development of new therapies against the disease. All prospective therapies have so far shown to be ineffective in stopping the disease, and many people are concerned that the pharmaceutical companies will give up their efforts in this field." The study was published in the January 2012 edition of the Archives of General Psychiatry.

Related Links:

Skåne University
Luminex



Platinum Member
Xylazine Immunoassay Test
Xylazine ELISA
Verification Panels for Assay Development & QC
Seroconversion Panels
Anti-Cyclic Citrullinated Peptide Test
GPP-100 Anti-CCP Kit
Gold Member
Automated Staining Unit
RAL Stainer

Latest Clinical Chem. News

Mass Spectrometry-Based Monitoring Technique to Predict and Identify Early Myeloma Relapse
17 Jan 2012  |   Clinical Chem.

‘Brilliantly Luminous’ Nanoscale Chemical Tool to Improve Disease Detection
17 Jan 2012  |   Clinical Chem.

Low-Cost Portable Screening Test to Transform Kidney Disease Detection
17 Jan 2012  |   Clinical Chem.