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Innate and Acquired Cellular Immunity in Children with Familial Hypercholesterolemia Treated with Simvastatin

The aim of this cross-sectional study was to assess the influence of simvastatin treatment in children with familial hypercholesterolemia (FH) on parameters of cellular immunity. Twenty-six children with FH were included, of which thirteen were treated with 10 mg simvastatin for at least 26 weeks, a...

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Autores principales: Motkowski, Radosław, Alifier, Marek, Abramowicz, Paweł, Konstantynowicz, Jerzy, Mikołuć, Bożena, Stasiak-Barmuta, Anna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9147505/
https://www.ncbi.nlm.nih.gov/pubmed/35629051
http://dx.doi.org/10.3390/jcm11102924
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author Motkowski, Radosław
Alifier, Marek
Abramowicz, Paweł
Konstantynowicz, Jerzy
Mikołuć, Bożena
Stasiak-Barmuta, Anna
author_facet Motkowski, Radosław
Alifier, Marek
Abramowicz, Paweł
Konstantynowicz, Jerzy
Mikołuć, Bożena
Stasiak-Barmuta, Anna
author_sort Motkowski, Radosław
collection PubMed
description The aim of this cross-sectional study was to assess the influence of simvastatin treatment in children with familial hypercholesterolemia (FH) on parameters of cellular immunity. Twenty-six children with FH were included, of which thirteen were treated with 10 mg simvastatin for at least 26 weeks, and thirteen were age- and sex-matched with a low-cholesterol diet only. Total WBC count and lipid profile were measured. Flow cytometry was used to identify lymphocyte subsets and determine the expression of adhesion molecules (AM) and toll-like receptors (TLRs) on leukocytes. No differences were found in the basic values of peripheral blood count and subpopulations of lymphocytes between groups. The percentage of granulocytes with the expression of AM was higher in those treated with statins. The TLR-2 expression on granulocytes and monocytes showed higher values, whereas the TLR-4 expression was lower on lymphocytes and granulocytes in simvastatin-treated children. Treatment with simvastatin in children with FH is not associated with alterations in the amounts of granulocytes and monocytes. There is no association between statin treatment and the pattern of peripheral blood lymphocyte subpopulations. The role of AM and TLRs needs further investigation, given the effect of statins on the innate immunity may be important for their efficacy and safety during growth.
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spelling pubmed-91475052022-05-29 Innate and Acquired Cellular Immunity in Children with Familial Hypercholesterolemia Treated with Simvastatin Motkowski, Radosław Alifier, Marek Abramowicz, Paweł Konstantynowicz, Jerzy Mikołuć, Bożena Stasiak-Barmuta, Anna J Clin Med Article The aim of this cross-sectional study was to assess the influence of simvastatin treatment in children with familial hypercholesterolemia (FH) on parameters of cellular immunity. Twenty-six children with FH were included, of which thirteen were treated with 10 mg simvastatin for at least 26 weeks, and thirteen were age- and sex-matched with a low-cholesterol diet only. Total WBC count and lipid profile were measured. Flow cytometry was used to identify lymphocyte subsets and determine the expression of adhesion molecules (AM) and toll-like receptors (TLRs) on leukocytes. No differences were found in the basic values of peripheral blood count and subpopulations of lymphocytes between groups. The percentage of granulocytes with the expression of AM was higher in those treated with statins. The TLR-2 expression on granulocytes and monocytes showed higher values, whereas the TLR-4 expression was lower on lymphocytes and granulocytes in simvastatin-treated children. Treatment with simvastatin in children with FH is not associated with alterations in the amounts of granulocytes and monocytes. There is no association between statin treatment and the pattern of peripheral blood lymphocyte subpopulations. The role of AM and TLRs needs further investigation, given the effect of statins on the innate immunity may be important for their efficacy and safety during growth. MDPI 2022-05-22 /pmc/articles/PMC9147505/ /pubmed/35629051 http://dx.doi.org/10.3390/jcm11102924 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Motkowski, Radosław
Alifier, Marek
Abramowicz, Paweł
Konstantynowicz, Jerzy
Mikołuć, Bożena
Stasiak-Barmuta, Anna
Innate and Acquired Cellular Immunity in Children with Familial Hypercholesterolemia Treated with Simvastatin
title Innate and Acquired Cellular Immunity in Children with Familial Hypercholesterolemia Treated with Simvastatin
title_full Innate and Acquired Cellular Immunity in Children with Familial Hypercholesterolemia Treated with Simvastatin
title_fullStr Innate and Acquired Cellular Immunity in Children with Familial Hypercholesterolemia Treated with Simvastatin
title_full_unstemmed Innate and Acquired Cellular Immunity in Children with Familial Hypercholesterolemia Treated with Simvastatin
title_short Innate and Acquired Cellular Immunity in Children with Familial Hypercholesterolemia Treated with Simvastatin
title_sort innate and acquired cellular immunity in children with familial hypercholesterolemia treated with simvastatin
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9147505/
https://www.ncbi.nlm.nih.gov/pubmed/35629051
http://dx.doi.org/10.3390/jcm11102924
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