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Post-Streptococcal Antibodies Are Associated with Metabolic Syndrome in a Population-Based Cohort
BACKGROUND: Streptococcal infections are known to trigger autoimmune disorders, affecting millions worldwide. Recently, we found an association between post-streptococcal autoantibodies against Protein Disulphide Isomerase (PDI), an enzyme involved in insulin degradation and insulin resistance. This...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3176794/ https://www.ncbi.nlm.nih.gov/pubmed/21949836 http://dx.doi.org/10.1371/journal.pone.0025017 |
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author | Aran, Adi Lin, Ling Finn, Laurel Ann Weiner, Karin Peppard, Paul Young, Terry Mignot, Emmanuel |
author_facet | Aran, Adi Lin, Ling Finn, Laurel Ann Weiner, Karin Peppard, Paul Young, Terry Mignot, Emmanuel |
author_sort | Aran, Adi |
collection | PubMed |
description | BACKGROUND: Streptococcal infections are known to trigger autoimmune disorders, affecting millions worldwide. Recently, we found an association between post-streptococcal autoantibodies against Protein Disulphide Isomerase (PDI), an enzyme involved in insulin degradation and insulin resistance. This led us to evaluate associations between post-streptococcal antibodies and metabolic syndrome, as defined by the updated National Cholesterol Education Program definition, 2005. METHODS AND FINDINGS: Metabolic data (HDL, triglycerides, fasting glucose, blood pressure, waist circumference, BMI, smoking), post-streptococcal antibodies (anti-Streptolysin O (ASO) and anti-PDI), and C-reactive protein (CRP, as a general inflammatory marker), were assessed in 1156 participants of the Wisconsin Sleep Cohort Study. Anti-PDI antibodies were found in 308 participants (26.6%), ASO≥100 in 258 (22.3%), and 482 (41.7%) met diagnostic criteria for metabolic syndrome. Anti-PDI antibodies but not ASO were significantly associated with metabolic syndrome [n = 1156, OR 1.463 (95% CI 1.114, 1.920), p = 0.0062; adjusted for age, gender, education, smoking]. Importantly, the anti-PDI - metabolic syndrome association remained significant after adjusting for CRP and fasting insulin. CONCLUSIONS: Post-streptococcal anti-PDI antibodies are associated with metabolic syndrome regardless of fasting insulin and CRP levels. Whereas these data are in line with a growing body of evidence linking infections, immunity and metabolism, additional studies are necessary to establish the post-streptococcal – metabolic syndrome association. |
format | Online Article Text |
id | pubmed-3176794 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-31767942011-09-26 Post-Streptococcal Antibodies Are Associated with Metabolic Syndrome in a Population-Based Cohort Aran, Adi Lin, Ling Finn, Laurel Ann Weiner, Karin Peppard, Paul Young, Terry Mignot, Emmanuel PLoS One Research Article BACKGROUND: Streptococcal infections are known to trigger autoimmune disorders, affecting millions worldwide. Recently, we found an association between post-streptococcal autoantibodies against Protein Disulphide Isomerase (PDI), an enzyme involved in insulin degradation and insulin resistance. This led us to evaluate associations between post-streptococcal antibodies and metabolic syndrome, as defined by the updated National Cholesterol Education Program definition, 2005. METHODS AND FINDINGS: Metabolic data (HDL, triglycerides, fasting glucose, blood pressure, waist circumference, BMI, smoking), post-streptococcal antibodies (anti-Streptolysin O (ASO) and anti-PDI), and C-reactive protein (CRP, as a general inflammatory marker), were assessed in 1156 participants of the Wisconsin Sleep Cohort Study. Anti-PDI antibodies were found in 308 participants (26.6%), ASO≥100 in 258 (22.3%), and 482 (41.7%) met diagnostic criteria for metabolic syndrome. Anti-PDI antibodies but not ASO were significantly associated with metabolic syndrome [n = 1156, OR 1.463 (95% CI 1.114, 1.920), p = 0.0062; adjusted for age, gender, education, smoking]. Importantly, the anti-PDI - metabolic syndrome association remained significant after adjusting for CRP and fasting insulin. CONCLUSIONS: Post-streptococcal anti-PDI antibodies are associated with metabolic syndrome regardless of fasting insulin and CRP levels. Whereas these data are in line with a growing body of evidence linking infections, immunity and metabolism, additional studies are necessary to establish the post-streptococcal – metabolic syndrome association. Public Library of Science 2011-09-20 /pmc/articles/PMC3176794/ /pubmed/21949836 http://dx.doi.org/10.1371/journal.pone.0025017 Text en Aran et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Aran, Adi Lin, Ling Finn, Laurel Ann Weiner, Karin Peppard, Paul Young, Terry Mignot, Emmanuel Post-Streptococcal Antibodies Are Associated with Metabolic Syndrome in a Population-Based Cohort |
title | Post-Streptococcal Antibodies Are Associated with Metabolic Syndrome in a Population-Based Cohort |
title_full | Post-Streptococcal Antibodies Are Associated with Metabolic Syndrome in a Population-Based Cohort |
title_fullStr | Post-Streptococcal Antibodies Are Associated with Metabolic Syndrome in a Population-Based Cohort |
title_full_unstemmed | Post-Streptococcal Antibodies Are Associated with Metabolic Syndrome in a Population-Based Cohort |
title_short | Post-Streptococcal Antibodies Are Associated with Metabolic Syndrome in a Population-Based Cohort |
title_sort | post-streptococcal antibodies are associated with metabolic syndrome in a population-based cohort |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3176794/ https://www.ncbi.nlm.nih.gov/pubmed/21949836 http://dx.doi.org/10.1371/journal.pone.0025017 |
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