A high frequency of viral agents yet absence of Borrelia burgdorferi is seen within the myocardium of subjects with normal left ventricular systolic function: an electron microscopy study

. 2016 Mar ; 61 (2) : 129-35. [epub] 20150724

Jazyk angličtina Země Spojené státy americké Médium print-electronic

Typ dokumentu časopisecké články, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/pmid26205424
Odkazy

PubMed 26205424
DOI 10.1007/s12223-015-0417-8
PII: 10.1007/s12223-015-0417-8
Knihovny.cz E-zdroje

A wide range of viral agents is associated with the development of acute myocarditis and its possible chronic sequela, dilated cardiomyopathy (DCM). There is also increasing evidence that Borrelia burgdorferi (Bb) is associated with DCM in endemic regions for Bb infection. This study sought to use electron microscopy to prospectively analyze the presence of viruses and Bb within the myocardium of 40 subjects with preserved left ventricular (LV) ejection fraction and 40 patients with new-onset unexplained DCM during the same time period. Virus particles were found within the myocardium of 23 subjects (58%) of both cohorts studied, yet there was no statistically significant difference in virus family presence between those with DCM versus those with preserved LV systolic function. In contrast, Bb was detected only in those subjects with DCM (0 versus 5 subjects; p ˂ 0.05). Polymerase chain reaction was performed on samples from patients who were positive for Bb according to electron microscopy, and Bb was confirmed in 4 out of 5 individuals. Our results demonstrate that the prevalence of viral particles does not differ between subjects with preserved LV systolic function versus those with DCM and therefore suggests that the mere presence of a viral agent within the myocardium is not sufficient to establish a clear link with the development of DCM. In contrast, the presence of Bb was found only within myocardial samples of patients with DCM; this finding supports the idea of a causal relationship between Bb infection and DCM development.

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J Heart Lung Transplant. 2010 Jul;29(7):739-46 PubMed

Eur Heart J. 2008 Jan;29(2):270-6 PubMed

Med Microbiol Immunol. 2010 May;199(2):139-43 PubMed

J Am Coll Cardiol. 2003 Aug 6;42(3):466-72 PubMed

Postgrad Med J. 2014 Jan;90(1059):33-42 PubMed

J Clin Microbiol. 2008 Oct;46(10):3540-3 PubMed

Am Heart J. 2007 May;153(5):850-8 PubMed

Circulation. 2005 Feb 22;111(7):887-93 PubMed

Acta Cardiol. 1999 Apr;54(2):83-8 PubMed

Am J Pathol. 2011 Oct;179(4):1917-28 PubMed

J Heart Lung Transplant. 2005 Oct;24(10):1632-8 PubMed

Virchows Arch. 2008 Sep;453(3):233-41 PubMed

J Am Coll Cardiol. 2002 Mar 6;39(5):892-5 PubMed

Heart. 1996 Mar;75(3):295-300 PubMed

N Engl J Med. 2010 Apr 1;362(13):1248-9 PubMed

Eur J Heart Fail. 2012 Jun;14(6):588-96 PubMed

Med Klin (Munich). 1998 Apr 15;93(4):223-8 PubMed

J Med Virol. 2010 Aug;82(8):1449-57 PubMed

Clin Infect Dis. 2009 Dec 1;49(11):1660-6 PubMed

Future Microbiol. 2015;10(4):629-53 PubMed

Eur Heart J. 2007 Mar;28(6):733-40 PubMed

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