Volume 23, Number 7—July 2017
Concurrent Infection with Hepatitis C Virus and Streptococcus pneumoniae
Hepatitis C virus (HCV) is a flavivirus that can cause a chronic hepatic infection in 75%–85% of persons initially infected (1). This virus is present worldwide, infects 130–175 million persons, and causes sequelae that include cirrhosis, end-stage liver disease, and hepatocellular cancer (1). In some patients infected with HCV, bacterial infections are more common and more severe than in patients not infected with HCV (2–6). Co-infection with HIV is also common among HCV-infected patients and can lead to higher mortality rates from sepsis than infection with either virus alone (4). Bacteremia has also been shown to be higher in hemodialysis patients infected with HCV (38.3%) than those not infected (21.8%), and mortality rates are higher for bacteremic patients infected with HCV than in those not infected (3).
Streptococcus pneumoniae is a gram-positive bacterium found in the nasopharynx and is a common cause of bacteremia. This microorganism can cause a variety of diseases ranging from noninvasive disease, such as pneumonia without bacteremia, to invasive pneumococcal disease (IPD), such as pneumonia with bacteremia, primarily in young or elderly persons (5,6). The virulence of this bacterium is driven by its wide assortment (currently 97) of polysaccharide capsule types (serotypes) (7).
To improve understanding of IPD and the effects of the use of pneumococcal protein conjugate vaccines introduced into Alberta, Canada, in 2002 and 2010, we began a 15-year longitudinal study of IPD in 2000. We took advantage of this prospective cohort to examine the prevalence, correlates, and outcomes of IPD patients co-infected with HCV. We hypothesized that IPD patients co-infected with HCV would have higher mortality rates and more complications than IPD patients not infected with HCV.
In Canada, the national case definition for IPD is isolation of S. pneumoniae from a normally sterile site, such as blood, cerebrospinal fluid, pleural fluid, biopsy tissue, joint aspiration, pericardial fluid, or peritoneal fluid (8). IPD is a provincially reportable disease in Alberta. Therefore, all invasive pneumococcal isolates are submitted to the Provincial Laboratory for Public Health (Edmonton, Alberta, Canada) for further characterization. Access to these isolates enabled us to prospectively identify all cases of IPD in northern Alberta. However, the study was limited to persons >17 years of age. HCV infection was defined as a positive antibody test result for this virus documented in the chart of a patient as part of usual care (i.e., we did not specifically test each patient for HCV for purposes of this study).
Clinical Data Collection
Research nurses collected sociodemographic, clinical, functional, and laboratory data from the medical record of each patient by using a standardized case report form (Tables 1, 2). These nurses received training on data collection before the start of the study. In addition to the case report form, standard operating procedures documents, definitions, drug classification, and underlying illness categorization were part of working documents. With respect to concurrent illnesses, if the attending physician recorded such an illness, it was accepted. Complete data were available for sociodemographic and functional status. If there was no record of a concurrent illness, it was assumed that the illness was not present. Additional details of the methods used in the study have been reported (9). This study was approved by the institutional research review committees of the Alberta Health Regions and the ethics review board of the University of Alberta.
Identification and Serotyping of S. pneumoniae Isolates
S. pneumoniae isolates were received at the Provincial Laboratory for Public Health from acute diagnostic laboratories in Alberta as per requirements of provincial notifiable disease regulations. S. pneumoniae isolates were confirmed as S. pneumoniae on the basis of characteristic morphology and optochin susceptibility before serotyping (10). All pneumococcal isolates that showed a positive Quellung reaction with commercial type-specific antisera (Statens Serum Institute, Copenhagen, Denmark) were assigned a serotype designation (11). Strains that were susceptible to optochin but that could not be serotyped by the Quellung assay were assayed by using the AccuProbe S. pneumoniae Culture Identification Test (Gen-Probe, San Diego, CA, USA) to confirm species identification.
Exposure and Outcomes
Our independent exposure of interest was a dichotomous variable representing the presence or absence of concurrent HCV infection. Our primary outcome was in-hospital deaths as recorded in patient records. Secondary outcomes included prespecified complications of IPD, defined as the presence of >1 of the following features: cellulitis, osteomyelitis, septic arthritis, endocarditis, empyema, meningitis, acute kidney injury requiring dialysis, liver failure, peritonitis, and need for mechanical ventilation.
Descriptive data are shown as mean (SD) for continuous variables and number (%) for categorical variables. Differences were evaluated by using the χ2test for categorical variables and the t-test for continuous variables. Pneumococcal serotypes according to HCV status were summarized descriptively.
For our main outcome, we completed a series of multivariate logistic regression analyses to evaluate the association between HCV and in-hospital deaths after accounting for increasing degrees of clinical and prognostic data known to be associated with HCV infection or IPD-related outcomes in an effort to examine risk factor stacking. First, we calculated unadjusted estimates of death for HCV-positive patients compared with estimates for HCV-negative patients (reference group). Second, we adjusted for sociodemographic information (i.e., age, sex, Aboriginal status, and residence at time of admission). Third, we adjusted for the following concurrent conditions: solid organ cancer, HIV, diabetes, coronary heart disease, and chronic obstructive pulmonary disease. In addition, we included a marker for the presence of >2 other chronic conditions as a measure of additional illnesses as reported (12,13). Fourth, we included functional status in our model (independently walking versus not walking before hospital admission) because this factor has better prognostic value than age and disease severity and acts as a proxy for frailty (14). Fifth, we included several health behaviors associated with increased risk for HCV infection, including current smoking status, illicit drug use, and alcoholism.
In addition to our primary analysis, we conducted analyses for patients with a history of cirrhosis and for those infected with HIV. Infection with HIV is associated with cirrhosis, and both factors are associated with increased risk for IPD.
We report adjusted odds ratios (ORs) from logistic regression models with their respective 95% CIs and associated p values. All analyses were conducted by using Stata version 14 (StataCorp LLC, College Station, TX, USA).
During the 15 years of the study, 3,251 adults >17 years of age were identified as having cases of IPD. Of these adults, 355 (11%) had HCV infections. We obtained sociodemographic characteristics of the 2 population groups, those infected with HCV and those not infected (Table 1). The population with HCV infections had a mean age that was 10 years younger than that for persons without HCV infections (p<0.001). Persons with HCV infections were significantly (all p<0.001) more likely to be Aboriginal, homeless, have concomitant HIV infection and cirrhosis of the liver, have alcoholism, and be current smokers and illicit drug users (Table 1).
Inpatient Mortality Rates and Complications
Overall, 486 (15%) patients died in a hospital: higher mortality rates were observed for those with concurrent HCV infections (57, 16%) versus no HCV infections (429, 15%). This absolute increased risk for death of 1% was statistically significant in models sequentially adjusted for sociodemographic variables, concurrent conditions, and lifestyle factors (fully adjusted OR [aOR] 1.71, 95% CI 1.15–2.54; p<0.001) (Table 2; Figure). For sequential models, age had the largest effect on the association between HCV and death (OR 1.10 for unadjusted analyses, OR 1.93 when age was added to model). The risk for death by infection with HCV was similar between age groups (persons <65 years of age, OR 1.76 and persons >65 years of age, OR 1.45; p for interaction = 0.86).
Other variables had minor influence on the point estimate for HCV by sequential analyses. Additional variables independently associated with death in a hospital in the final fully adjusted model included increasing age, history of cancer, functional status, smoking status, and alcoholism (p<0.05). Furthermore, patients infected with HCV alone (aOR 1.60) and those infected with HCV who had cirrhosis (aOR 2.85) had an increased risk for death compared with patients who were not infected with HCV and did not have cirrhosis (p for interaction >0.05). Patients infected with HIV alone (aOR 1.71) and those infected with HCV and HIV (aOR 1.46) also had an increased risk for death compared with patients not infected with HCV or HIV (p for interaction >0.05).
In addition to an increased mortality rate, the prevalence of most IPD-related complications, including cellulitis, acute kidney injury, liver failure, peritonitis, and requirement for mechanical ventilation, were higher in HCV-positive patients, but meningitis was significantly lower in HCV-positive patients (p<0.05 for all comparisons) (Table 2).
We identified the 10 most common pneumococcal serotypes causing IPD in the 2 study groups (Table 3). There were notable differences between the 2 groups. Serotype 5 caused 19% of infections in HCV-positive patients and 7% of infections in HCV-negative patients. Serotypes 12F, 20, and 9N were approximately twice as common in HCV-positive patients, and 22F was twice as common in HCV-negative patients (Table 3). Overall, 40 serotypes were found in HCV-positive patients and 51 serotypes in HCV-negative patients. Serotypes in 7-valent pneumococcal conjugate vaccine (PCV7), 13-valent pneumococcal conjugate vaccine (PCV13), and 23-valent pneumococcal polysaccharide vaccine caused 18%, 47%, and 71% of infections, respectively, in HCV-positive patients and 24%, 48%, and 70% of infections, respectively, in HCV-negative patients.
In a prospective cohort of patients with IPD, we found that concurrent infection with HCV was common, as were risk factors for acquisition of HCV, such as Aboriginal status, alcoholism, and illicit drug use. Furthermore, adjusted analyses showed that HCV infection was associated with a 70% increased risk of death. In addition to an increased mortality rate, patients infected with HCV were more likely to have serious complications of IPD other than meningitis.
A recent health technology report from the University of Calgary (Calgary, Alberta, Canada) indicated a prevalence of diagnosed hepatitis C of ≈0.7% in adults in Alberta and a prevalence as high as 3% in Aboriginal persons (15). Thus, the overall prevalence rate for hepatitis C of 11% for those with IPD is 15-fold higher than that for the general population and 3.6-fold higher than that for the Aboriginal population. The reasons for this increased prevalence are complicated by known risk factors, such as concurrent tobacco smoking, alcoholism, and homelessness (16–19). Whether HCV infection only confers a higher risk for IPD requires further study.
We have shown that cirrhosis of the liver is a risk factor for death in patients with IPD (9). A rat model of cirrhosis showed multiple impairments of pulmonary defenses against S. pneumoniae, including impairment of extrapulmonary killing of the infecting organism before arrival of neutrophils (20). Levels of lysozyme and C3 were decreased in bronchoalveolar lavage washings, and neutrophil-mediated killing of the virulent type 3 strain of S. pneumoniae was also impaired (20).
The prevalence of peritonitis for HCV-positive patients (5%) versus that for HCV-negative patients (1%) in our study was expected, given the likely higher amount of ascites in HCV-positive patients. Empyema complicated the course of 8% of HCV-positive patients compared with 3.4% and 3.3% of HCV-positive patients in previous studies of IPD (21–23).
A cellulitis prevalence of 7% in HCV-positive patients was ≈3 times the prevalence of 2% for HCV-negative patients. Cellulitis caused by S. pneumoniae was reported in 1917 and seems to be an uncommon entity; only 45 cases had been reported as of 2006 (23–26). Our data indicated that cellulitis complicates IPD much more frequently than previously recognized. In our study, we detected 83 cases of cellulitis. This finding strongly suggests that HCV infection is associated with pneumococcal cellulitis, especially given the aOR of 3.4 we documented (27). Moreover, although HCV-positive patients were more likely to be homeless, occurrence of cellulitis was similar irrespective of underlying place of residence and could not explain these findings. A higher rate of liver failure among HCV-positive patients probably indicates that these patients had cirrhosis at time of hospitalization, and IPD triggered liver failure in patients with compromised liver function.
Renal failure was more common in IPD patients infected with HCV. There are several mechanisms whereby renal involvement occurs in HCV-infected patients, including glomerular immune complex disease, direct viral invasion of renal parenchyma, and nephrotoxicity of some drugs used to treat HCV infection (28).
A finding that is more difficult to explain is the lower rate of meningitis for HCV-positive than for HCV-negative patients. However, whether meningitis is less frequent in HCV-positive patients remains uncertain. In France, a reduction in pneumococcal meningitis was observed after introduction of PCV13 for children and adults (29). Conversely, Moore et al. found that the rate of meningitis for adults increased during the post-PCV13 era when compared with the pre-PCV13 era (30).
To explain why meningitis rates were different for HCV-positive and HCV-negative patients in our study cohort, rates of vaccination with PCV13 would also have to be different between HCV-positive and HCV-negative patients. Although possible, we believe that this suggestion is unlikely. An alternative explanation that we believe is more plausible might be that HCV-positive patients are at substantially increased risk for all-cause and IPD-related deaths and that the HCV-positive patients who do not die during hospitalization end up also being at a lower risk for meningitis (e.g., a form of healthy survivor bias) and therefore appear as if this complication is less likely to develop in them. Thus, those patients infected with HCV who died during hospitalization probably also had clinically unrecognized meningitis, rather than having HCV being protective against this complication. Alternatively, it might be possible that patients infected with HCV tended to have lower platelet counts and were therefore less likely to have cerebrospinal fluid collected and a diagnosis of meningitis confirmed.
With respect to serotypes, serotype 5 was most common in the HCV group because of an outbreak of serotype 5 infections that occurred in western Canada and preferentially infected the homeless population (31). We also observed an outbreak of infections with serotype 20 among middle-age homeless persons in Edmonton, Alberta, starting in 2012 (G.J. Tyrrell, unpub. data). Serotypes contained in PCV7, PCV13, and 23-valent pneumococcal polysaccharide vaccines had a similar occurrence in HCV-positive and HCV-negative patients, except that HCV-positive patients were less likely to be infected with serotypes in PCV7.
The strengths of this study include the large number of patients with IPD studied over a long period and the richness of the clinical data obtained for each patient. However, our study had limitations. First, we identified HCV-positive patients on the basis of a positive antibody test result. Thus, some patients who were antibody positive but HCV RNA negative would be falsely identified as having active infection with HCV. Second, we were unable to categorize the severity of liver disease. Third, we did not have detailed information regarding the vaccination status of all patients. Fourth, we examined only patients who had a diagnosis of HCV and did not prospectively obtain serologic data for all patients admitted to a hospital with IPD.
In conclusion, we have shown that concurrent HCV infection in patients with IPD is common, and HCV infection in this population portends an increased risk for death and more serious complication of IPD, such as cellulitis and peritonitis (but not meningitis) than for patients not infected with HCV. Because many HCV-infected patients have risk factors that are indications for pneumococcal vaccination, additional studies of IPD in patients infected with HCV are needed to determine whether HCV without other risk factors is an indication for vaccination.
Dr. Marrie is an infectious diseases specialist in the Department of Medicine, Dalhousie University, Halifax, Nova Scotia, Canada. His research interests are community-acquired pneumonia, outcomes, and health services.
We thank Ibrahim Quazi and Lilly Yusho for data management and Carol Mangan for data collection.
This study was supported by grants-in-aid from Pfizer Canada, and Merck Canada, Inc. S.R.M. holds the Endowed Chair in Patient Health Management and is supported by the Faculties of Medicine and Dentistry and Pharmacy and Pharmaceutical Sciences at the University of Alberta. D.T.E. holds a Canada Research Chair and is supported by the Government of Canada.
T.J.M. and G.J.T. designed the study, organized data collection, and had full access to all data; D.T.E. performed analyses and had full access to all data; T.J.M., G.J.T., D.T.E., and S.R.M. wrote the article; and all authors contributed to interpretation of data, revising the article for content, and approved the final version of the article.
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TablesCite This Article
1All authors contributed equally to this article.