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Monitoring of Lymphocyte Populations During Treatment with Interferon-β-1b to Predict Multiple Sclerosis Disability Progression
M. Vališ, O. Vyšata, L. Sobíšek, B. Klímová, C. Andrýs, D. Vokurková, Z. Pavelek,
Language English Country United States
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
30592627
DOI
10.1089/jir.2018.0100
Knihovny.cz E-resources
- MeSH
- Adult MeSH
- Interferon-beta therapeutic use MeSH
- Middle Aged MeSH
- Humans MeSH
- Lymphocytes pathology MeSH
- Young Adult MeSH
- Lymphocyte Count MeSH
- Multiple Sclerosis blood drug therapy MeSH
- Aged MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Young Adult MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
The authors aim to understand how lymphocyte populations could predict the course of multiple sclerosis (MS) in people treated with interferon-β (IFN-β). Twenty-five male patients and 72 female patients were analyzed in the study. Peripheral blood samples were taken before and 5 years after the treatment with IFN-β. Lymphocyte subsets were analyzed by flow cytometry. The authors compared lymphocyte parameters between confirmed sustained progression (CSP) and non-CSP groups by using Welch's one-way analysis of means or a chi-square test of independence. A penalized (lasso) logistic regression model was fitted to identify the combination of lymphocyte parameters for potential biomarkers. The combination of lymphocyte counts, relative CD3+/CD25+ cells, absolute CD8 T cells, absolute CD8+/CD38+ cells, absolute CD38+ cells, and relative CD5+/CD19+ cells was identified as potential biomarker for the IFN-β treatment to monitor MS development in relation to CSP. The results suggest that other biomarkers aid in patient observation, predict a favorable outcome, and assist in the decision-making process for the early therapy escalation.
References provided by Crossref.org
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