Application of Atomic Dielectric Resonance Spectroscopy for the screening of blood samples from patients with clinical variant and sporadic CJD.

J Transl Med

National CJD Surveillance Unit & Division of Pathology, University of Edinburgh School of Molecular and Clinical Medicine, Western General Hospital, Edinburgh EH4 2XU, UK.

Published: August 2007

AI Article Synopsis

  • Researchers are addressing the safety of blood transfusions by developing assays to detect sub-clinical vCJD infections, which are challenging due to the sensitivity required for accurate detection.
  • The innovative method used, Atomic Dielectric Resonance Spectroscopy (ADRS), analyzes blood samples to identify unique signatures from vCJD patients compared to other groups.
  • The study found that ADRS can classify blood samples with 100% accuracy, suggesting it could serve as an effective screening tool alongside existing methods for detecting vCJD.

Article Abstract

Background: Sub-clinical variant Creutzfeldt-Jakob disease (vCJD) infection and reports of vCJD transmission through blood transfusion emphasise the need for blood screening assays to ensure the safety of blood and transplanted tissues. Most assays aim to detect abnormal prion protein (PrPSc), although achieving required sensitivity is a challenge.

Methods: We have used innovative Atomic Dielectric Resonance Spectroscopy (ADRS), which determines dielectric properties of materials which are established by reflectivity and penetration of radio/micro waves, to analyse blood samples from patients and controls to identify characteristic ADR signatures unique to blood from vCJD and to sCJD patients. Initial sets of blood samples from vCJD, sCJD, non-CJD neurological diseases and normal healthy adults (blood donors) were screened as training samples to determine group-specific ADR characteristics, and provided a basis for classification of blinded sets of samples.

Results: Blood sample groups from vCJD, sCJD, non-CJD neurological diseases and normal healthy adults (blood donors) screened by ADRS were classified with 100% specificity and sensitivity, discriminating these by a co-variance expert analysis system.

Conclusion: ADRS appears capable of recognising and discriminating serum samples from vCJD, sCJD, non-CJD neurological diseases, and normal healthy adults, and might be developed to provide a system for primary screening or confirmatory assay complementary to other screening systems.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2008164PMC
http://dx.doi.org/10.1186/1479-5876-5-41DOI Listing

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