|Year : 2013 | Volume
| Issue : 1 | Page : 40-44
Is there any relationship between Chlamydophila pneumoniae and coronary atherosclerosis among Iranians?
Mohammad Hadi Sadeghian1, Seyed Abbas Tabatabaee Yazdi2, Hossein Ayatollahi1, Mohammad Reza Keramati3, Kiarash Ghazvini4, Ali Reza Rezai5, Nasrin Heidari6, Maryam Sheikhi1, Gohar Shaghayegh1
1 Faculty of Medicine, Cancer Molecular Pathology Research Centre, Ghaem Medical Centre, Mashhad, Iran
2 Department of Pathology, Ghaem Medical Centre, Mashhad, Iran
3 Neonatal Research Centre, Faculty of Medicine, Imam Reza Medical Centre, Mashhad, Iran
4 Department of Microbiology, Ghaem Medical Centre, Mashhad, Iran
5 Department of Hematology and Blood Bank, Ghaem Medical Centre, Mashhad, Iran
6 Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran
|Date of Web Publication||16-Mar-2013|
Cancer Molecular Pathology Research Centre, Ghaem Medical Center, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad
Source of Support: Research Vice Chancellor of Mashhad University of Medical Sciences,, Conflict of Interest: None
| Abstract|| |
Background: Atherosclerosis is a coronary heart disease, andis the most common cause of death in the industrialized world. Some studies suggested that atherosclerosis may be triggered by infectious agents, mostly Chlamydophila pneumoniae. However, the role of C. pneumoniae in the pathogenesis of coronary atherosclerosis is still controversial. Objectives: This study was performed to evaluate whether there is a significant association between coronary artery atherosclerosis and C. pneumoniae by the polymerase chain reaction (PCR) method. Materials and Methods: This case-control study was carried out on formalin-fixed paraffin-embedded tissue biopsies of the coronary arteries obtained from 30 patients with coronary atherosclerosis and 30 subjects without atherosclerosis living in Northeast of Iran. All subjects' weight and height were determined, and the body mass index was calculated. We also reviewed the medical history and previous laboratory reports of patients. Deoxyribonucleic acid (DNA) was extracted, and C. pneumonia DNA was amplified and detected using PCR assay. Results: The age of the patients in the study group was from 18 to 50 years, and the male to female ratio was 5:1. Only oneout of the 30 coronary tissue samples had positive PCR for C. pneumoniae (3.3%), while it was negative for patients in the control group. Conclusions: This study showed that C. pneumoniae infection is not strongly associated with coronary artery atherosclerosis in Northeast of Iran.
Keywords: Atherosclerosis, Chlamydophila pneumonia, coronary artery, Iran
|How to cite this article:|
Sadeghian MH, Yazdi ST, Ayatollahi H, Keramati MR, Ghazvini K, Rezai AR, Heidari N, Sheikhi M, Shaghayegh G. Is there any relationship between Chlamydophila pneumoniae and coronary atherosclerosis among Iranians?. Niger Med J 2013;54:40-4
|How to cite this URL:|
Sadeghian MH, Yazdi ST, Ayatollahi H, Keramati MR, Ghazvini K, Rezai AR, Heidari N, Sheikhi M, Shaghayegh G. Is there any relationship between Chlamydophila pneumoniae and coronary atherosclerosis among Iranians?. Niger Med J [serial online] 2013 [cited 2016 Feb 10];54:40-4. Available from: http://www.nigeriamedj.com/text.asp?2013/54/1/40/108894
| Introduction|| |
Atherosclerosis is a coronary heart disease (CHD), and is the most common cause of death in the industrialized world. High blood pressure (BP), hypercholesterolemia, diabetes mellitus (DM) and smoking are considered as the major risk factors for the development of atherosclerosis. In addition, increasing age, male sex, family history and genetic factors predispose patients to CHD.  There is some data that have suggested the possible potential role of some infectious agents in the pathogenesis of atherosclerosis. ,,,, The possibility of infectious agents may trigger the process of atherosclerosis by direct or indirect inflammatory effects, especially at younger ages. 
Although different studies have been carried out to prove this hypothesis some infections may contribute in the pathogenesis of atherosclerosis; nothing has ever been conclusively proven. The possible role of some agents such as Chlamydophila pneumoniae,  hepatitis C. virus, Human immunodeficiency virus, hepatitis B virus, cytomegalovirus, herpes virus,  Epstein-Barr virus, Mycobacterium tuberculosis, and helicobacter pylori, have been considered in the pathogenesis of atherosclerosis. Among these pathogens, C. pneumoniae is important, because it could be effectively treated by antibiotics.  C. pneumoniae is an obligatory intracellular organism, and is responsible for at least 10% of community-acquired pneumonias. This bacterium has also been associated with pharyngitis, bronchitis, otitis, influenza-like illness, sinusitis and myocarditis. ,,
Conflicting results have been reported about the relationship between C. pneumonia and atherosclerosis. West et al. Apfalter et al., and Zibaeenezhad et al. reported no association between C. pneumoniae and atherosclerosis but others found significant association between C. pneumoniae and atherosclerosis. ,, The results of Jha et al.,  Dabiri et al.  and Sessa et al.  support the idea that C. pneumoniae may have a role in the development of atherosclerosis. This controversy about the role C. pneumoniae in the pathogenesis of atherosclerosis emphasizes the importance of more research works.
The aim of this study was to demonstrate whether there is any difference between two group of patients with coronary atherosclerotic plaque and subjects without coronary atherosclerosis for the presence of C. pneumoniae DNA by polymerase chain reaction (PCR) method.
| Materials and Methods|| |
This case-control study was carried out on 60 formalin-fixed paraffin-embedded (FFPE) coronary artery biopsies in the molecular pathology laboratory, Ghaem Hospital, Mashhad, Iran in 2010.
Coronary artery tissues were selected from another study that was performed previously by our colleagues for determining prevalence of atherosclerotic plaques in autopsy cases with non-cardiac death in northeast Iran. In this study, left coronary artery (LCA), right coronary artery (RCA) and left circumflex artery (LCX) had been evaluated grossly and microscopically.
Our materials included 30 coronary artery tissues with atherosclerotic plaques that were defined as study group, and 30 coronary artery tissues without atherosclerotic plaques that served as the control group. Archived slides of the two groups were reviewed by two pathologists for confirmation of diagnosis, tissue adequacy and selection of the best paraffin blocks for DNA extraction. For all subjects, the weight and height were determined, and the body mass index (BMI) was calculated. We also reviewed the medical history and the previous laboratory reports of patients.
Five to seven, 5-μm-thick sectionswere cut from each FFPE specimen under sterile conditions, and then the DNA was extracted by using proteinase K and non-heating DNA extraction method.  DNA concentration was determined by using the Thermo Scientific NanoDrop 2000 spectrophotometer, and specimens with low DNA content (<20 ng/μL) were excluded from the study.
PCR was performed for detecting C. pneumoniae DNA by using the PCR Kits (DNA Technology (JSC), PCR Kit, Moscow, Russia). 10 μl of PCR master mix and 0.5 μl unit of Taqpolymerase (Hot Start Taq DNA Polymerase) were added into each paraffin sealed tube and were mixed, then 5 μl (100 ng) of DNA samples were added (except for positive and negative controls) and were spun at 1,000 rpm for 3-5 s. The tubes were placed into applied biosystems (ABI) Veriti Thermal Cycler and PCR was performed with the program of 180 s at 94°C for the first step and then 45 cycles was run as follows: 50 s at 94°C, 50 s at 64°C, 50 s at 72°C.
Amplified PCR products were electrophoresed on a 2% agarose gel, stained with ethidium bromide, and photographed under ultraviolet light by gel documentation instrument. PCR was interpreted as positive when the DNA band corresponds to the band of the positive control (254bp) in addition to the internal control band (IC:370 bp).
Results of PCR in control and atherosclerotic groups were analyzed with SPSS version 11.5 by a statistician. We used Fisher's exact test for comparison of categorical variables and independent sample t-test for continuous variable in patients and control groups. A P value below 0.05 (P0 < 0.05) was considered significant.
| Results|| |
The age range in the control group was 20-46 years with a mean (standard deviation) age of 26.0 (6.41) years. In the study group, it ranges from 18 to 50 years with a mean (SD) age of 32.0 (9.46) years and the t-test showed no significant difference between the ages of patients in the study and control groups (P=0.97). Twenty-five patients (83.3%) were males and five patients (16.7%) were females. The male to female ratio was 5:1 and no significant difference was seen between study and control groups for gender (P0 = 1.00) by Fisher's exact test. The mean BMI of the patients in the study and control groups were 24.4 (3.77) and 23.9 (2.62) kg/m  respectively [Table 1]. The frequency of atherosclerotic plaques in the different vessels of heart of the patients in the study is as shown in [Table 2]. As a result, the possibility of the appearance of advanced atherosclerotic plaques s in LCA was higher than the two other vessels. Concurrent occurrences of different stages of atherosclerosis were seen in our patients. Only one vessel involvement with fibro-fatty morphology (mild) was seen in five patients (16.7%), one vessel with advanced plaque was observed in three patients (10.0%), seven patients (23.3%) had one vessel with fibro-fatty and one vessel with advanced plaque, Two vessels with advanced plaque were noticed in six patients (20.0%), Three vessels with advanced plaque were observed in five patients (16.7%) and four patients (13.3%) had two vessels with advanced plaque and one fibro-fatty morphology.
|Table 1: Comparisons between patients with coronary atherosclerosis and controls for weight, height and body mass index|
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|Table 2: The frequency of atherosclerotic plaques in different vessels of the heart in the study group|
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Positive PCR result for C. pneumonia was seen in one (3.3%) sample among the 30 coronary artery tissues with atherosclerosis (advanced plaque), while all the control samples were negative. Fisher's exact test showed no significant difference for detection of C. pneumoniae between samples of coronary artery with and without atherosclerotic plaque (P = 1).
| Discussion|| |
Ischemic heart disease could be observed in the absence of its major risk factors such as increasing age, male gender, hypertension, hyperlipidemia, smoking and DM. It was postulated that inflammation contributes to the initiation and progression of atherosclerotic lesions. Inflammatory cells are seen during all steps of atherogenesis, and some infectious agents may trigger this inflammation. ,
Although some studies showed that C. pneumoniae can increase the risk of atherosclerosis, ,, but we did not find any significant difference in the frequency of C. pneumoniae DNA isolation in the coronary arteries with and without atherosclerosis by PCR method. We believe that at least two important factors can account for this discrepancy in the results from previous studies: Methodology and epidemiology. C pneumonia infection can be diagnosed by various methods such as serology with an increase in serum antibodies against the organism, DNA detectionby PCR, Immunocytochemistry, electron microscopyand C. pneumonia isolation by culture. 
In other studies, the most widely used method for identifying of C. pneumoniae infection was based on antibody detection. The frequency of antibody against C. pneumoniae starts to rise in children and is observed approximately in 50% of adolescents. ,, Somesero-epidemiologic studies have shown a relationship between C. pneumoniae and atherosclerosis. Saikku et al., Podsiad≥y et al. and Romano et al. detected a higher level of antibody against C. pneumoniae in CHD compared to control group but Zibaeenezhad et al., Romeo et al., and Ericson et al., found that the presence of antibodies was unable to predict coronary artery events.
We used PCR for detection of C. pneumonia; this assay appears to be more sensitive than cell culture. , Our finding was in concordance with those of West et al., Jantos et al. and Satpathy et al.  Similarly, Reszka et al., studied presence of C. pneumonia DNA in aortic vessels, Voorend et al. in cerebral vessels, and Kwon et al. in carotid arteries and could not establish any significant difference in PCR results between the study and control groups. These findings suggest that serology could detect past as well as present infection, whereas PCR detects current C. pnuemoniae infection. Considering the study of West et al. and Satpathy et al. who showed a higher C. pnuemoniae IgG antibody in patients with CHD compared to control group but could not detect the organism by nested PCR assay in any specimen strengthens our hypothesis. We believe that the lack of standardized methods for the detection of C. pnuemoniae infection used in the aforementioned studies is probably one of the important reasons for the discrepancies in their results.
C. pnuemoniae is a common human pathogen; the majority of infected subjects have few or no symptoms. It seems that this infection has endemic and epidemic distribution. The frequency of antibodies to C. pneumoniae is approximately 50% in the northern hemisphere. , Exposure to C. pneumoniae is probably common in Iran. Moghaddam et al. reported 38% seropositivity for C. pneumonia antibodies (IgG and IgM) in healthy subjects by ELISA method in Tehran, Iran. Studies carried out in Iran on the association between C. pneumonia infection, and atherosclerosis revealed conflicting results; while some studies showed the association between C. pneumonia infection, and atherosclerosis , others didn't demonstrate any significant associationbetween C. pneumonia and atherosclerosis. ,
The anatomical localization of vessels may also be a factor influencing the results from previous studies. Jha et al. showed that C. pneumoniae may be associated with CHD and coronary artery was more susceptible to C. pneumoniae as compared with carotid artery.
Bahrmand et al. and Ericson et al. examined the relationship of C. pneumoniae infection to the severity of coronary atherosclerosis by PCR and serology respectively. They examined coronary artery samples with two different methods, and both revealed a high rate of reactivity to this bacterium in severe atherosclerosis and a much lower rate in mild atherosclerosis; therefore, they concluded that severity (stage) of atherosclerosis can be presumed as an important factor in diagnosis of C. pneumoniae infection.
Our study was performed on 30 archived FFPE coronary artery tissues of patients with atherosclerosis. This sample size may be too small for final decision; therefore, future study with a larger number of case groups and also using fresh specimens are helpful.
In conclusion, we did not find any significant association between C. pneumoniae infection and coronary artery atherosclerosis by PCR method. Further studies involving a greater number of patients and also using more specific methods for detecting living C. Pneumonia organisms by culture can be helpful.
| Acknowledgments|| |
This study was the result of an M.D. student thesis proposal and financially supported by the Research Vice Chancellor of Mashhad University of Medical Sciences. The authors are thankful to them and to Dr. Mohammad Khajeh Daluei for the statistical advice.
| References|| |
|1.||Kumar V, Abbas AK, Fausto N, Acter JC, editors. Robbins and Cotran Pathologic Basis of Disease. 8 th ed. Philadelphia: Saunders Elsevier; 2010. p. 496-506. |
|2.||Campbell LA, Yaraei K, Van Lenten B, Chait A, Blessing E, Kuo CC, et al. The acute phase reactant response to respiratory infection with Chlamydia pneumoniae: Implications for the pathogenesis of atherosclerosis. Microbes Infect 2010;12:598-606. |
|3.||Ayada K, Yokota K, Hirai K, Fujimoto K, Kobayashi K, Ogawa H, et al. Regulation of cellular immunity prevents Helicobacter pylori-induced atherosclerosis. Lupus 2009;18:1154-68. |
|4.||Stassen FR, Vainas T, Bruggeman CA. Infection and atherosclerosis. An alternative view on an outdated hypothesis. Pharmacol Rep 2008;60:85-92. |
|5.||Alviar CL, Echeverri JG, Jaramillo NI, Figueroa CJ, Cordova JP, Korniyenko A, et al. Infectious atherosclerosis: Is the hypothesis still alive? A clinically based approach to the dilemma. Med Hypotheses 2011;76:517-21. |
|6.||Jha HC, Srivastava P, Divya A, Prasad J, Mittal A. Prevalence of Chlamydophila pneumoniae is higher in aorta and coronary artery than in carotid artery of coronary artery disease patients. APMIS 2009;117:905-11. |
|7.||Tien PC, Schneider MF, Cole SR, Cohen MH, Glesby MJ, Lazar J, et al. Association of hepatitis C virus and HIV infection with subclinical atherosclerosis in the women's interagency HIV study. AIDS 2009;23:1781-4. |
|8.||Ghotaslou R, Aslanabadi N, Ghojazadeh M. Hepatitis B virus infection and the risk of coronary atherosclerosis. Ann Acad Med Singapore 2008;37:913-5. |
|9.||Müller BT, Huber R, Henrich B, Adams O, Berns G, Siebler M, et al. Chlamydia pneumoniae, herpes simplex virus and cytomegalovirus in symptomatic and asymptomatic high-grade internal carotid artery stenosis. Does infection influence plaque stability? Vasa 2005;34:163-9. |
|10.||Apostolou F, Gazi IF, Lagos K, Tellis CC, Tselepis AD, Liberopoulos EN, et al. Acute infection with Epstein-Barr virus is associated with atherogenic lipid changes. Atherosclerosis 2010;212:607-13. |
|11.||Rota S, Rota S. Mycobacterium tuberculosis complex in atherosclerosis. Acta Med Okayama 2005;59:247-51. |
|12.||Woods GL, Walker DH, McPherson RA, Pincus MR. Henry's Clinical Diagnosis and Management by Laboratory Methods. 21 st ed. Pennsylvania: Elsevier Saunders; 2007. p. 1002-3. |
|13.||Fazio G, Giovino M, Gullotti A, Bacarella D, Novo G, Novo S. Atherosclerosis, inflammation and Chlamydia pneumoniae. World J Cardiol 2009;1:31-40. |
|14.||Forbes BA, Sahm DF, Weissfeld AS. editors. Bailey and Scott's Diagnostic Microbiology. 11 th ed. Mosby Elsevier; 2002. p. 578-9. |
|15.||West SK, Kohlhepp SJ, Jin R, Gleaves CA, Stamm W, Gilbert DN. Detection of circulating Chlamydophila pneumoniae in patients with coronary artery disease and healthy control subjects. Clin Infect Dis 2009;48:560-7. |
|16.||Apfalter P, Barousch W, Nehr M, Willinger B, Rotter M, Hirschl AM. No evidence of involvement of Chlamydia pneumoniae in severe cerebrovascular atherosclerosis by means of quantitative real-time polymerase chain reaction. Stroke 2004;35:2024-8. |
|17.||Zibaeenezhad MJ, Amanat A, Alborzi A, Obudi A. Relation of Chlamydia pneumoniae infection to documented coronary artery disease in Shiraz, Southern Iran. Angiology 2005;56:43-8. |
|18.||Dabiri H, Rezadehbashi M, Badami N, Aghanouri R, Ahmadi H, Khoramizadeh MR, et al. Detection of Chlamydia pneumoniae in atherosclerotic plaques of patients in Tehran, Iran. Jpn J Infect Dis 2009;62:195-7. |
|19.||Sessa R, Di Pietro M, Schiavoni G, Petrucca A, Cipriani P, Zagaglia C, et al. Measurement of Chlamydia pneumoniae bacterial load in peripheral blood mononuclear cells may be helpful to assess the state of chlamydial infection in patients with carotid atherosclerotic disease. Atherosclerosis 2007;195:e224-30. |
|20.||Shi SR, Cote RJ, Wu L, Liu C, Datar R, Shi Y, et al. DNA extraction from archival formalin-fixed, paraffin-embedded tissue sections based on the antigen retrieval principle: Heating under the influence of pH. J Histochem Cytochem 2002;50:1005-11. |
|21.||Saikku P, Leinonen M, Mattila K, Ekman MR, Nieminen MS, Mäkelä PH, et al. Serological evidence of an association of a novel Chlamydia, TWAR, with chronic coronary heart disease and acute myocardial infarction. Lancet 1988;2:983-6. |
|22.||Podsiad³y E, Przy³uski J, Kwiatkowski A, Kruk M, Wszo³a M, Nosek R, et al . Presence of Chlamydia pneumoniae in patients with and without atherosclerosis. Eur J Clin Microbiol Infect Dis 2005;24:507-13. |
|23.||Romano Carratelli C, Nuzzo I, Cozzolino D, Bentivoglio C, Paolillo R, Rizzo A. Relationship between Chlamydia pneumoniae infection, inflammatory markers, and coronary heart diseases. Int Immunopharmacol 2006;6:848-53. |
|24.||Romeo F, Martuscelli E, Chirieolo G, Cerabino LM, Ericson K, Saldeen TG, et al. Seropositivity against Chlamydia pneumoniae in patients with coronary atherosclerosis. Clin Cardiol 2000;23:327-30. |
|25.||Ericson K, Saldeen TG, Lindquist O, Pâhlson C, Mehta JL. Relationship of Chlamydia pneumoniae infection to severity of human coronary atherosclerosis. Circulation 2000;101:2568-71. |
|26.||Petyaev IM, Zigangirova NA, Petyaev AM, Pashko UP, Didenko LV, Morgunova EU, et al. Isolation of Chlamydia pneumoniae from serum samples of the patients with acute coronary syndrome. Int J Med Sci 2010;7:181-90. |
|27.||Jantos CA, Nesseler A, Waas W, Baumgärtner W, Tillmanns H, Haberbosch W. Low prevalence of Chlamydia pneumoniae in atherectomy specimens from patients with coronary heart disease. Clin Infect Dis 1999;28:988-92. |
|28.||Satpathy G, Bhan A, Sharma A, Kar UK. Detection of Chlamydophila pneumoniae (Chlamydia pneumoniae) in endarteroctomy specimens of coronary heart diseases patients. Indian J Med Res 2008;128:658-62. |
|29.||Reszka E, Jegier B, Wasowicz W, Lelonek M, Banach M, Jaszewski R. Detection of infectious agents by polymerase chain reaction in human aortic wall. Cardiovasc Pathol 2008;17:297-302. |
|30.||Voorend M, van der Ven AJ, Kubat B, Lodder J, Bruggeman CA. Limited role for C. pneumoniae, CMV and HSV-1 in cerebral large and small vessel atherosclerosis. Open Neurol J 2008;2:39-44. |
|31.||Kwon TW, Kim DK, Ye JS, Lee WJ, Moon MS, Joo CH, et al. Detection of enterovirus, cytomegalovirus, and Chlamydia pneumoniae in atheromas. J Microbiol 2004;42:299-304. |
|32.||Cook PJ, Honeybourne D. Clinical aspects of Chlamydia pneumoniae infection. Presse Med 1995;24:278-82. |
|33.||Moghaddam M, Feizpoor H, Noroozi AR, Doost MG. Determination of frequency rate of Chlamydia pneumonia infection in two groups of patients with and without AMI. J Tehran Faculty of Med 2004;62:79-5. |
|34.||Bahrmand AR, Bahadori M, Hossaini A, Velayati AA, Aghabozorgy S, Shakoor A, et al. Chlamydia pneumoniae DNA is more frequent in advanced than in mild atherosclerosis lesions. Scand J Infect Dis 2004;36:119-23. |
|35.||Hosseinian A, Habibzadeh SH, Ahari SS, Mokhtarpoor A. The study of previous contact with Chlamydia pneumoniae in patients with myocardial infarction. J Ardabil University Med Sci Health Services 2007;7:35-40. |
[Table 1], [Table 2]