ArticleMolecular neurobiology2018
Detection of CSF 14-3-3 Protein in Sporadic Creutzfeldt-Jakob Disease Patients Using a New Automated Capillary Western Assay.
Article in Molecular neurobiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
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6 citing papers in PubMed, 18 citations in OpenAlex.
- Characterization of variably protease-sensitive prionopathy by capillary electrophoresis.Scientific reports · 2024Article
- Cerebrospinal fluid biomarkers in SARS-CoV-2 patients with acute neurological syndromes.Revue neurologique · 2023Article
- Capillary Western Immunoassay Optimization of Estrogen Related Factors in Human Subcutaneous Adipose Tissue.Methods and protocols · 2022Article
- Sporadic Creutzfeldt-Jakob disease presenting as dizziness and cognitive decline: A case report.Medicine · 2019Article
- Application of high-throughput, capillary-based Western analysis to modulated cleavage of the cellular prion protein.The Journal of biological chemistry · 2019Article
- Detection of Dystrophin Dp71 in Human Skeletal Muscle Using an Automated Capillary Western Assay System.International journal of molecular sciences · 2018Article
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Authors and funding
4 authors at 1 institution in 1 country.
Funding
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Abstract
Sporadic Creutzfeldt-Jakob disease (sCJD) is a fatal rapidly progressive dementia. The detection of 14-3-3 protein in cerebrospinal fluid (CSF) is included in the WHO diagnostic criteria for the pre-mortem diagnosis of CJD. The aim of this study is to assess CSF 14-3-3 protein analytical and diagnostic performances using a new automated capillary Western technology (Simple Western technology-SW). For the validation of this assay, samples from a cohort of 268 patients suspected from sCJD were analyzed: 77 sCJD (including 40 definite sCJD) and 191 non-CJD samples were tested using both SW and the current Western Blot (WB) assays. Automated capillary Western determination provided better analytical performances than WB with a lower intra- and inter-assay variability. Analytical interferences such as hemolysis and high total protein concentration known to lead to false positive WB results were also assessed using SW assay: unfortunately, these interferences still remain confounders of CSF 14-3-3 protein determination. Finally, automated capillary Western assay's sensitivity and specificity were superior to those of WB assay (93.5 and 95.3%, respectively, compared to 92.2 and 84.8% for WB). In conclusion, with a shorter time of analysis than WB assays' (4 h versus 1.5 day), automated capillary Western assay is an excellent routine alternative method to the currently performed WB assay for CSF 14-3-3 protein detection in patients suspected of sporadic Creutzfeldt-Jakob disease.
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