Skip to main content
World Journal of Gastroenterology logoLink to World Journal of Gastroenterology
. 2005 Mar 7;11(9):1292–1296. doi: 10.3748/wjg.v11.i9.1292

Hepatitis B virus infection and coronary atherosclerosis: Results from a population with relatively high prevalence of hepatitis B virus

De-Yan Tong 1,2, Xiao-Hua Wang 1,2, Cong-Feng Xu 1,2, Ying-Zhen Yang 1,2, Si-Dong Xiong 1,2
PMCID: PMC4250675  PMID: 15761966

Abstract

AIM: To investigate the possible association between hepatitis B virus (HBV) infection and angiographically proven coronary artery disease (CAD) in a population with relatively high prevalence of HBV.

METHODS: Sera from 434 patients who underwent coronary angiography were tested for HBV antigens (HBsAg, HBeAg) and antibodies (Anti-HBs, Anti-HBc and Anti-HBe) by ELISA.

RESULTS: Seventy-seven percent (224/291) of the patients with CAD and 73.4% (105/143) of the patients without angiographic evidence of atherosclerosis were seropositive for HBV (P>0.05). However, C-reactive protein (CRP) levels were significantly higher in patients with CAD (P = 0.008), while lower in HBV seropositive population (P = 0.043 and P = 0.021 after adjustment for conventional risk factors).

CONCLUSION: Our results suggested HBV infection negatively correlates with CRP levels, but seems not to be associated with coronary atherosclerosis.

Keywords: Coronary artery disease, Hepatitis B virus, C-reactive protein, Infection

INTRODUCTION

As one of the most prevalent infectious disease worldwide[1], hepatitis B Virus (HBV) has been threatening the public health of the Chinese. Researches had revealed several abnormal immune responses in hepatitis B patients[2], which might further contribute other complications such as liver cirrhosis, hepatocellular carcinoma, etc., while it is still controversial whether these HBV induced inflammation status correlates with disease in organ other than liver.

A possible role for infections in atherogenesis has been deeply scrutinized since the demonstration of herpes virus-induced atherosclerosis in chickens in 1978[3]; however, the bulk of supportive evidence has been accumulated in the past few decades[4-7]. The results of several published studies suggested a link between infection with microorganisms such as bacteria, Chlamydia, pneumoniae[8-10], Helicobacter pylori[11-13], or Porphyromonas gingivalis[14,15] and with the viruses cytomegalovirus[16-18], herpes simplex virus[19,20], or hepatitis A virus[20,21], and an increased risk of cardiovascular and cerebrovascular diseases. However, the atherogenic effects of certain infective agents remain controversial[22-25]. Nevertheless, at present, assessment of possible associations between infective agents and the risk of atheromatous disease might be still useful for the identification of individuals at higher risk of future cardiovascular and cerebrovascular events.

We reasoned that HBV would be a rational candidate pathogen among stimuli that contribute to atherosclerosis. It shares almost all the characteristics of the infectious agents implicated in the development of atherosclerosis. For example, it is one of the intracellular pathogens and can produce persistent liver disease, establish long-term, persistent infection, which induce long-lasting effects on host, such as persistent circulating antibodies. In a recently published study from a health-screening test cohort, a strong association between HBsAg carrier and carotid atherosclerosis was reported[26]. Although the concept behind this association seems to be plausible and attractive, an accumulative collection of data is clearly required to confirm the hypothesis in a different study population. The high endemicity of HBV infection and liver disease in China mainland made it possible for us to assess whether coronary atherogenesis was association of HBV serologic markers in a population with greater prevalence of HBV.

Substantial evidence now exists indicating that inflammation plays an important role in atherogenesis[27-30]. Accordingly, we used elevated serum levels of C-reactive protein (CRP) as a marker of an underlying inflammatory process and determined whether prior HBV infection was involved in inducing chronic inflammation.

Therefore, the aim of the present investigation was to test (1) whether the association between HBV infection and atherosclerosis still remained in a HBV-predisposed study population; (2) whether HBV infection was involved in triggering and sustaining the chronic inflammation process that had been proved to be critical in atherogenesis.

MATERIALS AND METHODS

Study subjects

A total of 434 patients of both genders were recruited at Zhongshan Hospital (Shanghai, China). Written informed consent was obtained from all study subjects, who approved the collection of blood samples for scientific research. The study cohort consisted of individuals referred for coronary angiography because of chest pain or noninvasive tests compatible with myocardial ischemia. We defined a patient as having coronary stenosis if there was an angiographic evidence of atherosclerosis; CAD with evidence of ≥50% stenosis of ≥1 major coronary artery by coronary angiography. Patients with myocardial infarction within previous 6 mo, valvular heart disease or nonatherosclerotic cardiomyopathy were excluded. Blood samples were taken for various measurements in these patients.

Atherosclerosis risk factors

Analyzed risk factors for atherosclerosis included age, sex, smoking (those who had stopped smoking 20 years ago and who were <30 years old when they stopped smoking were considered as non-smokers), diabetes (who were taking insulin, oral hypoglycemic agents, had previously received such treatment, or were currently using dietary modification to control the condition), hypercholesterolemia (who had a serum cholesterol value >6.2 mmol/L or were receiving cholesterol-lowering treatment), hypertension (who had received such a diagnosis with arterial pressure >140/90 mmHg or were being treated with antihypertensive medications or dietary modification.), family history and elevated CRP levels.

Laboratory testing

Serum samples obtained from all study subjects were frozen at -70 °C, and aliquots were thawed when needed for specific tests. Serum antigens (HBsAg, HBeAg) and antibodies (anti-HBs, anti-HBc, anti-HBe) for HBV were measured by ELISA (HBV-kit, KeHua, China) according to the manufacturer’s instructions. A quantitative ELISA was used to determine serum CRP (CRP-kit, DSL, USA). A set of CRP standards was used to plot a standard curve of absorbance vs CRP concentration from which the CRP concentrations in the unknown can be calculated.

Statistical analysis

Categorical data were analyzed by the χ2 test (Fisher’s exact test for small samples), with all tests double-sided. Analyses of CRP serum level in relation to HBV and other factors were made by the unpaired t-test between different groups as a continuous variable and further adjusted using partial correlation investigation. Estimated Pearson correlation value (r) was used to indicate the strength of the relationship. The covariates considered here included age, male sex, cigarette smoking, diabetes, hypercholesterolemia, hypertension and family history. Results for normally distributed continuous variables are expressed as mean±SD.

RESULTS

Study population

Four hundred and thirty four subjects were studied. Their ages ranged from 27 to 88 years (mean 62.2±10.36 years). There were 308 (71%) men and 291 (67.1%) with coronary atherosclerosis. All the traditional CAD risk factors (age, male sex, diabetes, hypertension and smoking) but hypercholesterolemia were also proved to be associated with the risk of CAD (Table 1). Besides, elevated CRP levels were demonstrated significantly higher in those with CAD compared to those without CAD (5.70±0.55 mg/L vs 3.23±0.37 mg/L, P = 0.008).

Table 1.

Traditional risk factors and CAD.

Characteristics Frequency of factors%
P
CAD (n = 291) Non-CAD (n = 143)
Age (yr) 63.0510.46 59.4810.43 0.005
Male Sex 78.7 57.4 <0.0001
Smoking 42.6 18.9 <0.0001
Diabetes 19.6 7.8 0.001
Hypertension 72.5 57.3 0.002
Hypercholesterolemia 25.8 21.7 0.351
Family history 12.9 11.9 0.877
CRP (mg/L) 5.700.55 3.230.37 0.008

HBV seropositivity and risk factors of CAD

HBV seropositive subjects were defined as samples with any of the five serological markers of HBV (HBsAg, anti-HBs, HBeAg, anti-HBe and anti-HBc) proved to be positive. Of all the study population, there were totally 329 (75.8%) HBV-seropositive individuals, 22 (5.1%) positive for HBsAg, 213 (49.1%) for anti-HBs, 285 (65.7%) for anti-HBc, 2 (0.5%) for HBeAg and 93 (21.4%) for anti-HBe. Although seropositivity (Table 2) and most of the single HBV serological markers were not relative with any of the traditional factors respectively, anti-HBc was negatively associated with hypercholesterolemia (r = -0.106, P = 0.025, OR = 0.614, 95% CI 0.401-0.941).

Table 2.

Baseline characteristics of study population with or without HBV seropositivity.

Characteristics HBV seropositive(n = 329) Non-HBV seropositive(n = 105) P
Age (yr) 62.12±10.06 62.49±11.18 0.29
Male (%) 70.2 73.3 0.622
Smoking (%) 32.8 40.9 0.158
Diabetes (%) 14.6 15.2 0.515
Hypertension (%) 62.3 64.8 0.812
Family history (%) 13.7 7.6 0.123
Hypercholesterolemia (%) 21.6 22.9 0.787

CRP and HBV seropositivity

Mean CRP levels were lower in HBV seropositive (4.29±0.44 mg/L) than in HBV seronegative individuals (6.60±1.04 mg/L) (r = -0.130, P = 0.043). Individual serological markers such as anti-HBc and anti-HBs also relate to a low level of CRP (Table 3). Besides smoking age, male sex and hypertension, etc. was shown to be associated with the increased CRP level (r = 0.108, P = 0.039) as reported previously[24]. However, the significant association between elevated CRP levels and HBV seropositivity maintained after adjustment for smoking (P = 0.015).

Table 3.

Association between HBV serological markers and CRP level.

HBV serological markers Pearson correlation (r) P P1
HBsAg -0.036 0.511 0.406
Anti-HBs -0.126 0.027 0.029
HbeAg2 0.000 1 1
Anti-HBe -0.014 0.795 0.643
Anti-HBc -0.115 0.049 0.032
HBV seropositive -0.13 0.043 0.01

1After adjustment for smoking.

2

Fisher’s exact test was used.

HBV seropositivity and CAD

The HBV seropositive as well as single HBV serological marker was not significantly related with CAD (Table 4). Other stages of infection inferred by serological test such as healthy carriers (with HBsAg, anti-HBc and anti-HBeAg positive) (r = -0.052, P = 0.262), resolved HBV infection (with anti-HBs, anti-HBc and anti-HBe positive) (r = 0.037, P = 0.421) and HBsAg-negative HBV infection (anti-HBc positive only) (r = 0.019, P = 0.676) showed no significant correlation with CAD either.

Table 4.

HBV serological markers and CAD.

HBV serum factor Positive frequency of factors (%)
P
CAD Non-CAD
HbsAg 4.5 6.3 0.415
Anti-HBs 49.8 46.9 0.56
HbeAg 0.7 0 1
Anti-Hbe 22 21.7 0.969
Anti-HBc 69.4 59.4 0.066
Healthy carriers1 2.8 4.9 0.27
Resolved HBV infection2 11.7 9.1 0.474
HBsAg (-) HBV infection3 16.8 15.4 0.7
HBV seropositive 77 73.4 0.417
1

Healthy carriers: HBsAg (+), anti-HBc (+) and anti-HBeAg (+).

2

Resolved HBV infection: anti-HBs (+), anti-HBc (+) and anti-HBe (+).

3

HBsAg (-) HBV infection: anti-HBc positive only.

In addition, since the HBV seropositivity was proven to be negatively associated with CRP level in our study population, we further analyzed two subgroups of patients (one with CRP levels at or below the median and the other with CRP values above the median) to try to exclude the influence on the association of HBV seropositivity and CAD from its interaction with CRP levels. The estimated pearson correlation value were 0.034 and -0.051 respectively with both P>0.05.

DISCUSSION

So far there is still few data available to prove the association between HBV infection and atherogenesis. Kiechl et al[31] found no significant association between chronic hepatitis and the development of new carotid atheromatous plaques, although they did not specify the type of hepatitis virus. However, another study in Japan demonstrated an increased prevalence of carotid atherosclerosis in HBV carriers[26]. Differences in study design, frequency of individuals with chronic HBV infection, and possibly region differences might explain the difference results of their study and ours.

Since serologic markers of HBV provide tools to follow the natural course of the disease and hitherto, there were no concrete evidence supporting the infection of HBV in endothelial cells, we examined the five widely used serologic markers instead of more sensitive HBV-DNA detection with the hypothesis that circulating HBV-associated antigens and antibodies might be the risk factors for atherogenesis. In our investigation, we found no evidence to support an association of HBV seropositivity and CAD prevalence. Subgroups used in clinic such as healthy carriers, those resolved HBV infection and those with HBsAg-negative HBV infection did not show correlation to coronary stenosis either, despite suggestive evidence from some clinical reports[32] and plausible mechanisms[33-35].

Although HBV seropositivity failed to be relative with CAD prevalence, one observation needed emphasis in this study. anti-HBs, anti-HBc and HBV seropositivity were all negatively related with elevated CRP levels, which were independent of other risk factors for atherosclerosis (Table 3). As CRP had been suggested as a cardiovascular risk factor, all these results hinted a possible protective trend of HBV on atherogenesis derived from a study in HBV high-risk region. This tendency is quite interesting and might be expected through several possible evidences: (1) HBV infection is highly prevalent in China and some developing regions compared to European countries; in contrast, the incidence of cardiovascular diseases is remarkably higher in Europe; (2) In general, the clinical course of chronic HBV infection may lead to hepatic decompensation, progression of liver disease, and the development of cirrhosis. It was reported that liver cirrhosis appears to be associated with a decreased risk of atherosclerosis, which may be attributed to the reduction of some traditional risk factors for atherosclerosis, such as high lipoprotein A and total cholesterol[36]. It is reasonable to hypothesize that the expression of CRP, a liver-specific protein, may also be influenced by hepatic dysfunction during chronic HBV infection; (3) A recent study demonstrated that there was no relationship between HBV carrier or seropositivity and increased pulse wave velocity, which suggested HBV infection did not seem to be able to contribute to increase arterial stiffness. Although it was reported by Ishizaka et al[26] that HBsAg seropositivity was a risk factor for carotid atherosclerosis, which was not associated with CRP level, the conclusion might be limited by the relatively low prevalence of HBV carriers (0.9%) in that population, compared to 5.1% seropositivity for HBsAg in this study.

There are several caveats relating to our study that must be noted. First, the study design was cross-sectional in nature, which cannot establish causality. It can only establish an association. Therefore, any conclusion derived from such study must be considered preliminary and hypothesis-generating, rather than hypothesis-proving. Second, the present study is relatively small in size. As a result, we may have missed a very weak association between HBV seropositivity and coronary stenosis. Nevertheless this study is one of the largest studies on HBV infection and CAD to date. Third, the individuals of control group might still be consisted of suspected CAD who may not be representative of other individuals without clinical features triggering the decision to perform coronary angiography. Fourth, the effects of reducing the CRP levels, a widely accepted atherosclerosis risk, in HBV seropositive population, might cover the relationship between HBV seropositivity and coronary atherosclerosis.

In conclusion, our results indicated that there is no statistical relationship between HBV infection and coronary atherosclerosis. We disagree with previously reported findings[26] that hepatitis B infection is probably an important contributor to CAD. And the role of HBV-associated reduction of CRP levels during the development of coronary atherosclerosis is still a disputed issue.

Footnotes

Supported by Major State Basic Research Development Program of China, No. G2000056903 and the National High Technology Research and Development Program of China, No. 2004AA215242

Co-first-author: Xiao-Hua Wang

Assistant Editor Li WZ Edited by Gabbe M

References

  • 1.Lok AS, McMahon BJ. Chronic hepatitis B. Hepatology. 2001;34:1225–1241. doi: 10.1053/jhep.2001.29401. [DOI] [PubMed] [Google Scholar]
  • 2.Wang JY, Liu P. Abnormal immunity and gene mutation in patients with severe hepatitis-B. World J Gastroenterol. 2003;9:2009–2011. doi: 10.3748/wjg.v9.i9.2009. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Fabricant CG, Fabricant J, Litrenta MM, Minick CR. Virus-induced atherosclerosis. J Exp Med. 1978;148:335–340. doi: 10.1084/jem.148.1.335. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Libby P, Egan D, Skarlatos S. Roles of infectious agents in atherosclerosis and restenosis: an assessment of the evidence and need for future research. Circulation. 1997;96:4095–4103. doi: 10.1161/01.cir.96.11.4095. [DOI] [PubMed] [Google Scholar]
  • 5.Muhlestein JB, Anderson JL, Hammond EH, Zhao L, Trehan S, Schwobe EP, Carlquist JF. Infection with Chlamydia pneumoniae accelerates the development of atherosclerosis and treatment with azithromycin prevents it in a rabbit model. Circulation. 1998;97:633–636. doi: 10.1161/01.cir.97.7.633. [DOI] [PubMed] [Google Scholar]
  • 6.Mayr M, Kiechl S, Willeit J, Wick G, Xu Q. Infections, immunity, and atherosclerosis: associations of antibodies to Chlamydia pneumoniae, Helicobacter pylori, and cytomegalovirus with immune reactions to heat-shock protein 60 and carotid or femoral atherosclerosis. Circulation. 2000;102:833–839. doi: 10.1161/01.cir.102.8.833. [DOI] [PubMed] [Google Scholar]
  • 7.Strachan DP, Carrington D, Mendall MA, Ballam L, Morris J, Butland BK, Sweetnam PM, Elwood PC. Relation of Chlamydia pneumoniae serology to mortality and incidence of ischaemic heart disease over 13 years in the caerphilly prospective heart disease study. BMJ. 1999;318:1035–1039. doi: 10.1136/bmj.318.7190.1035. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Saikku P, Leinonen M, Tenkanen L, Linnanmäki E, Ekman MR, Manninen V, Mänttäri M, Frick MH, Huttunen JK. Chronic Chlamydia pneumoniae infection as a risk factor for coronary heart disease in the Helsinki Heart Study. Ann Intern Med. 1992;116:273–278. doi: 10.7326/0003-4819-116-4-273. [DOI] [PubMed] [Google Scholar]
  • 9.Melnick SL, Shahar E, Folsom AR, Grayston JT, Sorlie PD, Wang SP, Szklo M. Past infection by Chlamydia pneumoniae strain TWAR and asymptomatic carotid atherosclerosis. Atherosclerosis Risk in Communities (ARIC) Study Investigators. Am J Med. 1993;95:499–504. doi: 10.1016/0002-9343(93)90332-j. [DOI] [PubMed] [Google Scholar]
  • 10.Kuo CC, Shor A, Campbell LA, Fukushi H, Patton DL, Grayston JT. Demonstration of Chlamydia pneumoniae in atherosclerotic lesions of coronary arteries. J Infect Dis. 1993;167:841–849. doi: 10.1093/infdis/167.4.841. [DOI] [PubMed] [Google Scholar]
  • 11.Pasceri V, Cammarota G, Patti G, Cuoco L, Gasbarrini A, Grillo RL, Fedeli G, Gasbarrini G, Maseri A. Association of virulent Helicobacter pylori strains with ischemic heart disease. Circulation. 1998;97:1675–1679. doi: 10.1161/01.cir.97.17.1675. [DOI] [PubMed] [Google Scholar]
  • 12.Mendall MA, Goggin PM, Molineaux N, Levy J, Toosy T, Strachan D, Camm AJ, Northfield TC. Relation of Helicobacter pylori infection and coronary heart disease. Br Heart J. 1994;71:437–439. doi: 10.1136/hrt.71.5.437. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Danesh J, Collins R, Peto R. Chronic infections and coronary heart disease: is there a link? Lancet. 1997;350:430–436. doi: 10.1016/S0140-6736(97)03079-1. [DOI] [PubMed] [Google Scholar]
  • 14.Chiu B. Multiple infections in carotid atherosclerotic plaques. Am Heart J. 1999;138:S534–S536. doi: 10.1016/s0002-8703(99)70294-2. [DOI] [PubMed] [Google Scholar]
  • 15.Deshpande RG, Khan MB, Genco CA. Invasion of aortic and heart endothelial cells by Porphyromonas gingivalis. Infect Immun. 1998;66:5337–5343. doi: 10.1128/iai.66.11.5337-5343.1998. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Nieto FJ, Adam E, Sorlie P, Farzadegan H, Melnick JL, Comstock GW, Szklo M. Cohort study of cytomegalovirus infection as a risk factor for carotid intimal-medial thickening, a measure of subclinical atherosclerosis. Circulation. 1996;94:922–927. doi: 10.1161/01.cir.94.5.922. [DOI] [PubMed] [Google Scholar]
  • 17.Chiu B, Viira E, Tucker W, Fong IW. Chlamydia pneumoniae, cytomegalovirus, and herpes simplex virus in atherosclerosis of the carotid artery. Circulation. 1997;96:2144–2148. doi: 10.1161/01.cir.96.7.2144. [DOI] [PubMed] [Google Scholar]
  • 18.Zhu J, Quyyumi AA, Norman JE, Csako G, Epstein SE. Cytomegalovirus in the pathogenesis of atherosclerosis: the role of inflammation as reflected by elevated C-reactive protein levels. J Am Coll Cardiol. 1999;34:1738–1743. doi: 10.1016/s0735-1097(99)00410-6. [DOI] [PubMed] [Google Scholar]
  • 19.Siscovick DS, Schwartz SM, Corey L, Grayston JT, Ashley R, Wang SP, Psaty BM, Tracy RP, Kuller LH, Kronmal RA. Chlamydia pneumoniae, herpes simplex virus type 1, and cytomegalovirus and incident myocardial infarction and coronary heart disease death in older adults: the Cardiovascular Health Study. Circulation. 2000;102:2335–2340. doi: 10.1161/01.cir.102.19.2335. [DOI] [PubMed] [Google Scholar]
  • 20.Zhu J, Nieto FJ, Horne BD, Anderson JL, Muhlestein JB, Epstein SE. Prospective study of pathogen burden and risk of myocardial infarction or death. Circulation. 2001;103:45–51. doi: 10.1161/01.cir.103.1.45. [DOI] [PubMed] [Google Scholar]
  • 21.Zhu J, Quyyumi AA, Norman JE, Costello R, Csako G, Epstein SE. The possible role of hepatitis A virus in the pathogenesis of atherosclerosis. J Infect Dis. 2000;182:1583–1587. doi: 10.1086/317613. [DOI] [PubMed] [Google Scholar]
  • 22.Wald NJ, Law MR, Morris JK, Bagnall AM. Helicobacter pylori infection and mortality from ischaemic heart disease: negative result from a large, prospective study. BMJ. 1997;315:1199–1201. doi: 10.1136/bmj.315.7117.1199. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Ridker PM, Hennekens CH, Stampfer MJ, Wang F. Prospective study of herpes simplex virus, cytomegalovirus, and the risk of future myocardial infarction and stroke. Circulation. 1998;98:2796–2799. doi: 10.1161/01.cir.98.25.2796. [DOI] [PubMed] [Google Scholar]
  • 24.Rohde LE, Hennekens CH, Ridker PM. Survey of C-reactive protein and cardiovascular risk factors in apparently healthy men. Am J Cardiol. 1999;84:1018–1022. doi: 10.1016/s0002-9149(99)00491-9. [DOI] [PubMed] [Google Scholar]
  • 25.White AD, Folsom AR, Chambless LE, Sharret AR, Yang K, Conwill D, Higgins M, Williams OD, Tyroler HA. Community surveillance of coronary heart disease in the Atherosclerosis Risk in Communities (ARIC) Study: methods and initial two years' experience. J Clin Epidemiol. 1996;49:223–233. doi: 10.1016/0895-4356(95)00041-0. [DOI] [PubMed] [Google Scholar]
  • 26.Ishizaka N, Ishizaka Y, Takahashi E, Toda Ei E, Hashimoto H, Ohno M, Nagai R, Yamakado M. Increased prevalence of carotid atherosclerosis in hepatitis B virus carriers. Circulation. 2002;105:1028–1030. doi: 10.1161/hc0902.105718. [DOI] [PubMed] [Google Scholar]
  • 27.Ross R. Atherosclerosis--an inflammatory disease. N Engl J Med. 1999;340:115–126. doi: 10.1056/NEJM199901143400207. [DOI] [PubMed] [Google Scholar]
  • 28.Epstein SE, Zhou YF, Zhu J. Infection and atherosclerosis: emerging mechanistic paradigms. Circulation. 1999;100:e20–e28. doi: 10.1161/01.cir.100.4.e20. [DOI] [PubMed] [Google Scholar]
  • 29.Mattila KJ, Valtonen VV, Nieminen MS, Asikainen S. Role of infection as a risk factor for atherosclerosis, myocardial infarction, and stroke. Clin Infect Dis. 1998;26:719–734. doi: 10.1086/514570. [DOI] [PubMed] [Google Scholar]
  • 30.Muhlestein JB. Chronic infection and coronary artery disease. Med Clin North Am. 2000;84:123–148. doi: 10.1016/s0025-7125(05)70210-8. [DOI] [PubMed] [Google Scholar]
  • 31.Kiechl S, Egger G, Mayr M, Wiedermann CJ, Bonora E, Oberhollenzer F, Muggeo M, Xu Q, Wick G, Poewe W, et al. Chronic infections and the risk of carotid atherosclerosis: prospective results from a large population study. Circulation. 2001;103:1064–1070. doi: 10.1161/01.cir.103.8.1064. [DOI] [PubMed] [Google Scholar]
  • 32.Zhu J, Quyyumi AA, Norman JE, Csako G, Waclawiw MA, Shearer GM, Epstein SE. Effects of total pathogen burden on coronary artery disease risk and C-reactive protein levels. Am J Cardiol. 2000;85:140–146. doi: 10.1016/s0002-9149(99)00653-0. [DOI] [PubMed] [Google Scholar]
  • 33.Mendall MA, Patel P, Ballam L, Strachan D, Northfield TC. C reactive protein and its relation to cardiovascular risk factors: a population based cross sectional study. BMJ. 1996;312:1061–1065. doi: 10.1136/bmj.312.7038.1061. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34.Navab M, Berliner JA, Subbanagounder G, Hama S, Lusis AJ, Castellani LW, Reddy S, Shih D, Shi W, Watson AD, et al. HDL and the inflammatory response induced by LDL-derived oxidized phospholipids. Arterioscler Thromb Vasc Biol. 2001;21:481–488. doi: 10.1161/01.atv.21.4.481. [DOI] [PubMed] [Google Scholar]
  • 35.Geiss HC, Ritter MM, Richter WO, Schwandt P, Zachoval R. Low lipoprotein (a) levels during acute viral hepatitis. Hepatology. 1996;24:1334–1337. doi: 10.1002/hep.510240602. [DOI] [PubMed] [Google Scholar]
  • 36.Marchesini G, Ronchi M, Forlani G, Bugianesi E, Bianchi G, Fabbri A, Zoli M, Melchionda N. Cardiovascular disease in cirrhosis--a point-prevalence study in relation to glucose tolerance. Am J Gastroenterol. 1999;94:655–662. doi: 10.1111/j.1572-0241.1999.00931.x. [DOI] [PubMed] [Google Scholar]

Articles from World Journal of Gastroenterology : WJG are provided here courtesy of Baishideng Publishing Group Inc

RESOURCES