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Persistently elevated IgA antibodies to Mycoplasma pneumoniae in patients with internal carotid artery stenosis

Background: It has been suggested that Mycoplasma pneumoniae may play a role in the development of atherosclerosis, but to date this association is still a matter of debate due to conflicting findings. Methods: We have investigated the levels of specific IgA antibodies to M. pneumoniae in 91 patient...

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Autores principales: Daxböck, Florian, Assadian, Afshin, Watkins-Riedel, Thomas, Assadian, Ojan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: German Medical Science GMS Publishing House 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3252649/
https://www.ncbi.nlm.nih.gov/pubmed/22242085
http://dx.doi.org/10.3205/dgkh000161
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author Daxböck, Florian
Assadian, Afshin
Watkins-Riedel, Thomas
Assadian, Ojan
author_facet Daxböck, Florian
Assadian, Afshin
Watkins-Riedel, Thomas
Assadian, Ojan
author_sort Daxböck, Florian
collection PubMed
description Background: It has been suggested that Mycoplasma pneumoniae may play a role in the development of atherosclerosis, but to date this association is still a matter of debate due to conflicting findings. Methods: We have investigated the levels of specific IgA antibodies to M. pneumoniae in 91 patients with internal carotid artery (ICA) stenosis using a commercial kit (SeroMP™ IgA; Savyon Diagnostics, Israel; cut-off value: 20 binding units; BU). All patients underwent surgery for ICA stenosis. From each patient, the first serum sample (S1) was taken before surgery, and the second after an interval of 6 month (S2). Results: The S1 seroprevalence was 18.7% (17/91). Thirteen of the 17 patients with positive S1 levels also remained positive after six month, whereby no decrease of IgA level was seen (median S1 level: 34 BU, range: 22–65 BU; median S2 level: 37 BU, range: 22–58 BU). Specifically, six of the patients showed an increased level after 6 months, and six a decrease, with the level remaining constant in one patient. In contrast, only 3 of the 74 S1 negative patients became positive for anti-M. pneumoniae IgA between the taking of the first and the second serum specimen (p<0.01). None of the assessed demographic factors or risk factors for atherosclerosis was associated with IgA seropositivity, neither were the degree CAVK or the degree of stenosis. Conclusion: These findings cannot be explained throughout by the general seroprevalence, or by past respiratory tract infections with the pathogen, and therefore may suggest a role for M. pneumoniae in the development of atherosclerosis, since a chronic infection must be assumed.
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spelling pubmed-32526492012-01-12 Persistently elevated IgA antibodies to Mycoplasma pneumoniae in patients with internal carotid artery stenosis Daxböck, Florian Assadian, Afshin Watkins-Riedel, Thomas Assadian, Ojan GMS Krankenhhyg Interdiszip Article Background: It has been suggested that Mycoplasma pneumoniae may play a role in the development of atherosclerosis, but to date this association is still a matter of debate due to conflicting findings. Methods: We have investigated the levels of specific IgA antibodies to M. pneumoniae in 91 patients with internal carotid artery (ICA) stenosis using a commercial kit (SeroMP™ IgA; Savyon Diagnostics, Israel; cut-off value: 20 binding units; BU). All patients underwent surgery for ICA stenosis. From each patient, the first serum sample (S1) was taken before surgery, and the second after an interval of 6 month (S2). Results: The S1 seroprevalence was 18.7% (17/91). Thirteen of the 17 patients with positive S1 levels also remained positive after six month, whereby no decrease of IgA level was seen (median S1 level: 34 BU, range: 22–65 BU; median S2 level: 37 BU, range: 22–58 BU). Specifically, six of the patients showed an increased level after 6 months, and six a decrease, with the level remaining constant in one patient. In contrast, only 3 of the 74 S1 negative patients became positive for anti-M. pneumoniae IgA between the taking of the first and the second serum specimen (p<0.01). None of the assessed demographic factors or risk factors for atherosclerosis was associated with IgA seropositivity, neither were the degree CAVK or the degree of stenosis. Conclusion: These findings cannot be explained throughout by the general seroprevalence, or by past respiratory tract infections with the pathogen, and therefore may suggest a role for M. pneumoniae in the development of atherosclerosis, since a chronic infection must be assumed. German Medical Science GMS Publishing House 2011-12-15 /pmc/articles/PMC3252649/ /pubmed/22242085 http://dx.doi.org/10.3205/dgkh000161 Text en Copyright © 2011 Daxböck et al. http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc-nd/3.0/deed.en). You are free to copy, distribute and transmit the work, provided the original author and source are credited.
spellingShingle Article
Daxböck, Florian
Assadian, Afshin
Watkins-Riedel, Thomas
Assadian, Ojan
Persistently elevated IgA antibodies to Mycoplasma pneumoniae in patients with internal carotid artery stenosis
title Persistently elevated IgA antibodies to Mycoplasma pneumoniae in patients with internal carotid artery stenosis
title_full Persistently elevated IgA antibodies to Mycoplasma pneumoniae in patients with internal carotid artery stenosis
title_fullStr Persistently elevated IgA antibodies to Mycoplasma pneumoniae in patients with internal carotid artery stenosis
title_full_unstemmed Persistently elevated IgA antibodies to Mycoplasma pneumoniae in patients with internal carotid artery stenosis
title_short Persistently elevated IgA antibodies to Mycoplasma pneumoniae in patients with internal carotid artery stenosis
title_sort persistently elevated iga antibodies to mycoplasma pneumoniae in patients with internal carotid artery stenosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3252649/
https://www.ncbi.nlm.nih.gov/pubmed/22242085
http://dx.doi.org/10.3205/dgkh000161
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