Higher incidence of persistent chronic infection of Chlamydia pneumoniae among coronary artery disease patients in India is a cause of concern

被引:26
作者
Jha, Hem C.
Vardhan, Harsh
Gupta, Rishein
Varma, Rakesh
Prasad, Jagdish
Mittal, Aruna
机构
[1] Inst Pathol, ICMR, Div Tissue Culture Mikrobiol, New Delhi, India
[2] Dept Cardiol, New Delhi, India
[3] Dept Cardiovasc Thorac & Vasc Surg, New Delhi, India
关键词
D O I
10.1186/1471-2334-7-48
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: There is growing evidence that Chlamydia pneumoniae may be involved in the pathogenesis of atherosclerosis, as several studies have demonstrated the presence of the organism in atherosclerotic lesions. C. pneumoniae infections, which are especially persistent infections, have been difficult to diagnose either by serological methods or isolation of the organism from the tissue. Nucleic Acid Amplification tests (NAATs) has emerged as an important method for detecting C. pneumoniae. Inspite of high prevalence of C. pneumoniae specific antibodies in coronary heart disease patients, direct detection of C. pneumoniae in circulating blood of coronary artery disease (CAD) patients by sensitive nucleic acid amplification tests nested PCR (nPCR), multiplex PCR (mPCR) has not been carried out is required. Further correlation of the presence of C. pneumoniae in blood of CAD patients with C. pneumoniae specific IgA and IgG antibodies, which may indicative of the status of infection with the progression of atherosclerosis. This will help in order to prepare strategies for the antibiotic intervention to avoid the progression towards CAD. Methods: Venous blood was obtained from 91 CAD patients and 46 healthy controls. Nucleic acid amplification tests viz. nested -, semi-nested- and multiplex PCR were used for detection of C. pneumoniae. ELISA carried out prevalence of C. pneumoniae specific IgG and IgA antibodies. Results: 29.67% (27/ 91) patients were positive for C. pneumoniae using nested PCR. The sensitivity and specificity of semi-nested and multiplex PCR were 37.03%, 96.96% and 22.22%, 100% with respect to nested PCR. Positive nPCR patients were compared with presence of C. pneumoniae specific IgA, IgA+IgG and IgG antibodies. Among 27 (29.67%) nPCR C. pneumoniae positive CAD patients, 11(12%) were IgA positive, 13(14.2%) were IgA+IgG positive and only1 (1.1%) was IgG positive. A significant presence of C. pneumoniae was detected in heavy smokers, non-alcoholics and with family histories of diabetes and blood pressure group of CAD patients by nPCR. Conclusion: The results indicate synergistic association of C. pneumoniae infection and development of CAD with other risk factors. We also detected increased positivity for C. pneumoniae IgA than IgG in nPCR positive CAD patients. Positive nPCR findings in conjunction with persisting high C. pneumoniae specific antibody strongly suggest an ongoing infection.
引用
收藏
页数:8
相关论文
共 33 条
[1]   Multicenter comparison trial of DNA extraction methods and PCR assays for detection of Chlamydia pneumoniae in endarterectomy specimens [J].
Apfalter, P ;
Blasi, F ;
Boman, J ;
Gaydos, CA ;
Kundi, M ;
Maass, M ;
Makristathis, A ;
Meijer, A ;
Nadrchal, R ;
Persson, K ;
Rotter, ML ;
Tong, CYW ;
Stanek, G ;
Hirschl, AM .
JOURNAL OF CLINICAL MICROBIOLOGY, 2001, 39 (02) :519-524
[2]   In-house nucleic acid amplification assays in research: How much quality control is needed before one can rely upon the results? [J].
Apfalter, P ;
Reischl, U ;
Hammerschlag, MR .
JOURNAL OF CLINICAL MICROBIOLOGY, 2005, 43 (12) :5835-5841
[3]   Evidence of Chlamydia pneumoniae in human arteriosclerotic lesions:: Insights into its possible pathogenic role [J].
Bauriedel, G ;
Schmücking, I ;
Hutter, R ;
Schmidt, T ;
Welsch, U .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1998, 31 (02) :390A-391A
[4]  
CHRISTIAN AJ, 1998, J CLIN MICROBIOL, V36, P1890
[5]   Intrathecal antibody production against Chlamydia pneumoniae in multiple sclerosis is part of a polyspecific immune response [J].
Derfuss, T ;
Gürkov, R ;
Bergh, FT ;
Goebels, N ;
Hartmann, M ;
Barz, C ;
Wilske, B ;
Autenrieth, I ;
Wick, M ;
Hohlfeld, R ;
Meinl, E .
BRAIN, 2001, 124 :1325-1335
[6]  
Enas EA, 2001, INTERNET J CARDIOL, V1, P2
[7]   IDENTIFICATION OF CHLAMYDIA-PNEUMONIAE BY DNA AMPLIFICATION OF THE 16S RIBOSOMAL-RNA GENE [J].
GAYDOS, CA ;
QUINN, TC ;
EIDEN, JJ .
JOURNAL OF CLINICAL MICROBIOLOGY, 1992, 30 (04) :796-800
[8]   Ethanol inhibits fibroblast growth factor-induced proliferation of aortic smooth muscle cells [J].
Ghiselli, G ;
Chen, J ;
Kaou, M ;
Hallak, H ;
Rubin, R .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2003, 23 (10) :1808-1813
[9]   INFECTIONS CAUSED BY CHLAMYDIA-PNEUMONIAE STRAIN TWAR [J].
GRAYSTON, JT .
CLINICAL INFECTIOUS DISEASES, 1992, 15 (05) :757-763
[10]  
Gupta S, 1997, CIRCULATION, V96, P404