| |
Increased rate of death related to presence of viremia among hepatitis C virus antibody-positive subjects in a community-based cohort study
|
| |
| |
-
Hepatology Aug 2009
from Jules: in the past few years several studies have found HBV viral load levels associated with increased risk for disease and death, the higher the viral load the greater the risk for disease. Now this study is reporting similar findings in HCV, higher viral load & persisting ALT elevations increase risk for HCC and death.
"high HCVcAg (viral load) and ALT levels were important predictors of liver-related death in this population. Monitoring HCV load and ALT level in HCV carriers may be important for identifying those individuals at increased risk for HCC or other liver disease, particularly among older carriers who are less likely to respond to HCV treatment."
"persistently elevated alanine aminotransferase levels were important predictors of liver-related mortality"...."The presence of viremia increases the rate of mortality"....."Our study indicated that liver-related mortality is strongly associated with the presence of HCV viremia among persons who are seropositive for anti-HCV antibodies and that HCVcAg and ALT levels were predictors of liver-related mortality in HCV carriers"...."HCC burden in the United States will likely increase in the next two or three decades, possibly to a level equal to that currently experienced in Japan"....."Several studies have demonstrated that genotype 1b is associated with severe liver disease, including cirrhosis and HCC.[37][38] In this study, there was an apparent association between HCV serotype I infection and mortality due to HCC. Other studies, however, have not found an effect of HCV genotype on liver disease development."....."HCV RNA levels have also been reported to be associated with the progression of chronic hepatitis C.[41][42] Although the level of HCV RNA was not quantified in this study, HCVcAg levels, which are known to correlate with HCV RNA levels,[21] were assessed by fluorescence enzyme immunoassay. We observed that high HCVcAg levels were predictive of liver-related mortality, including death due to HCC, in the HCV carriers"...."In the current analysis, ALT, aspartate aminotransferase, and GGT levels at enrollment were significantly higher in subjects who died due to a liver-related disease compared with subjects who died from other causes (data not shown). In addition, after adjusting for age and sex, overall mortality (HR, 2.23) and liver-related death (HR, 11.0) were significantly higher for HCV carriers with persistently elevated ALT than for those with persistently normal ALT."
"Anti-HCV-seropositive subjects with detectable HCV core antigen (HCVcAg) or HCV RNA were considered to be persistently infected with HCV and were classified as HCV carriers. Anti-HCV-positive subjects who were negative for HCVcAg and HCV RNA were assumed to have had a prior HCV infection and were classified as noncarriers."
Hirofumi Uto 1 *, Sherri O. Stuver 2 3, Katsuhiro Hayashi 4, Kotaro Kumagai 1, Fumisato Sasaki 1, Shuji Kanmura 1, Masatsugu Numata 1, Akihiro Moriuchi 1, Susumu Hasegawa 1, Makoto Oketani 1, Akio Ido 1, Kazunori Kusumoto 5, Satoru Hasuike 5, Kenji Nagata 5, Michinori Kohara 6, Hirohito Tsubouchi 1
1Department of Digestive and Life-style related Disease, Health Research Human and Environmental Sciences, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan
2Department of Epidemiology, Boston University School of Public Health, Boston, MA
3Department of Epidemiology, Harvard School of Public Health, Boston, MA
4Center for Medical Education, Faculty of Medicine, University of Miyazaki, Kiyotake, Japan
5Gastroenterology and Hematology, Faculty of Medicine, University of Miyazaki, Kiyotake, Japan
6Department of Microbiology and Cell Biology, Tokyo Metropolitan Institute of Medical Science, Tokyo, Japan
Abstract
The overall mortality of patients infected with hepatitis C virus (HCV) has not been fully elucidated. This study analyzed mortality in subjects positive for antibody to HCV (anti-HCV) in a community-based, prospective cohort study conducted in an HCV hyperendemic area of Japan. During a 10-year period beginning in 1995, 1125 anti-HCV-seropositive residents of Town C were enrolled into the study and were followed for mortality through 2005. Cause of death was assessed by death certificates. Subjects with detectable HCV core antigen (HCVcAg) or HCV RNA were considered as having hepatitis C viremia and were classified as HCV carriers; subjects who were negative for both HCVcAg and HCV RNA (i.e., viremia-negative) were considered as having had a prior HCV infection and were classified as HCV noncarriers. Among the anti-HCV-positive subjects included in the analysis, 758 (67.4%) were HCV carriers, and 367 were noncarriers. A total of 231 deaths occurred in these subjects over a mean follow-up of 8.2 years: 176 deaths in the HCV carrier group and 55 in the noncarrier group. The overall mortality rate was higher in HCV carriers than in noncarriers, adjusted for age and sex (hazard ratio, 1.53; 95% confidence interval, 1.13-2.07). Although liver-related deaths occurred more frequently among the HCV carriers (hazard ratio, 5.94; 95% confidence interval, 2.58-13.7), the rates of other causes of death did not differ between HCV carriers and noncarriers. Among HCV carriers, a higher level of HCVcAg (>100 pg/mL) and persistently elevated alanine aminotransferase levels were important predictors of liver-related mortality. Conclusion: The presence of viremia increases the rate of mortality, primarily due to liver-related death, among anti-HCV-seropositive persons in Japan.
Hepatitis C virus (HCV) was identified 20 years ago. It is now known that between 50% and 85% of acute HCV infections become chronic[1-3]; after developing chronic infection, spontaneous HCV clearance is very rare. Approximately 170 million people worldwide are infected with HCV, and chronic HCV infection is a major health problem. HCV is a common cause of fatal liver disease, including liver cirrhosis and hepatocellular carcinoma (HCC). However, the liver-related mortality rate associated with chronic HCV infection is highly variable across different populations. In patients that have been infected for more than 20 years, the occurrence of liver cirrhosis, HCC, and liver disease-related mortality are reported to be 10%-50%, 1%-23%, and 4%-15%, respectively.[4-6]
The range in published HCV-related mortality rates is due in part to the variability in the natural history of HCV infection as well as in the subjects studied. Some HCV-positive individuals have persistently normal alanine aminotransferase (ALT) levels and exhibit no clinical symptoms. Persons with this phenotype were often not included in previous hospital-based studies that focused on liver-related mortality in patients with HCV-associated liver disease/cirrhosis.[4][5] A few studies have systematically examined the risk of causes of death after HCV infection in a community-based setting[7-9]; however, the status of HCV viremia was not clear in these studies. In addition, the age range of HCV-infected subjects followed for mortality can vary considerably, with some cohort studies conducted in subjects whose average age was younger than 45 years[1][10-13] and others among older individuals.[9][14][15] To overcome some of these limitations, we analyzed mortality in 1125 subjects positive for antibody to HCV (anti-HCV) with data on viremia status, who were enrolled in a population-based cohort study in an HCV hyperendemic area of Japan between 1995 and 2005. These subjects were followed prospectively until death or until the end of the study in December 2005.
Discussion
Our study indicated that liver-related mortality is strongly associated with the presence of HCV viremia among persons who are seropositive for anti-HCV antibodies and that HCVcAg and ALT levels were predictors of liver-related mortality in HCV carriers. In this study population, the age distribution of anti-HCV-positive subjects, the prevalence of viremia, and the frequency of HCV serotype I were similar to previously reported data in Japan.[22-25] Japan has the highest incidence rate of HCC attributed to HCV infection among developed countries. Tanaka et al. estimated that HCV infection was spread in Japan during the 1920s, whereas HCV was widely disseminated in the United States in the 1960s.[26] The authors suggested that the HCC burden in the United States will likely increase in the next two or three decades, possibly to a level equal to that currently experienced in Japan.
Several studies have examined mortality in patients with HCV. Seeff et al. provided mortality data for 222 transfusion-associated hepatitis C cases and 377 control patients after approximately 25 years of follow-up.[27] Kamitsukasa et al. also reported mortality data for 302 HCV-infected patients with tuberculosis sequelae who had received a blood transfusion.[15] Although both studies showed that liver-related mortality was significantly higher in the disease groups than in the control groups, liver-related mortality was not the main cause of death. Kamitsukasa et al. reported that the main cause of death for approximately 45% of the patients in their study was tuberculosis sequelae.[15] Similar results were obtained in patients with inherited bleeding disorders and hepatitis C, where the main cause of death was human immunodeficiency virus (HIV)/acquired immune deficiency syndrome (AIDS).[28] Moreover, there was no significant difference between patients with and without hepatitis C in the overall mortality rates in the study by Seeff et al. In contrast, our study showed that all-cause mortality and liver-related mortality with or without HCC were significantly higher in the HCV carrier group than in the noncarrier group. The incidence of HCC in Caucasian patients with HCV-related cirrhosis has been reported to be 1.2% in the United States,[29] whereas the incidence in Japanese patients is reportedly between 6% and 7%.[30] Furthermore, HCV-related cases in some studies included subjects with previous HCV infections.[15][27] Ethnic-dependent and racial-dependent variation in the rates of HCC, the composition of the comparisons groups, and/or complications unrelated to liver disease, such as tuberculosis sequelae or HIV/AIDS, may have resulted in differences in the patient prognoses between our study and previous studies.
It has been reported that HCC was the main cause of liver-related death in patients with compensated cirrhosis due to HCV infection.[31][32] Kasahara et al. found that 74% of liver-related death in patients with chronic hepatitis C who had not received IFN therapy was due to HCC.[33] Although HCC was more frequently observed than other liver-related deaths in our study, the proportion of HCC among all liver disease deaths (59% in the HCV carrier group) was relatively low compared to that study.[33] This occurrence may have been because the causes of death were obtained from death certificates in our study and cases of severe hepatic failure due to HCC may have been classified as liver disease excluding HCC.
A large community-based linkage study that included 78,438 individuals with hepatitis C indicated that the risk of dying from drug-related causes was significantly greater than from liver-related causes; however, the incidence of liver-related deaths was greater than that of drug-related deaths in patients older than 45 years.[7] In addition, other studies have shown that age appears to be an important risk factor that affects HCC development[14] and that the risk of cirrhosis is related to the patient's age at the time of infection and to disease activity.[34][35] These reports, which focused on patients with transfusion-associated chronic hepatitis C, suggest that the younger the patients are at the time of infection, the lower the rate of progression. Although the exact dates of infection and HCC diagnosis were not clear in our study population, the median age at enrollment was older than 60 years. Thus, the incidence of liver-related deaths might be expected to be greater than deaths from other causes.
In our study, HCV serotype I, which included HCV genotypes 1a and 1b, was found in 64.5% of the HCV carrier subjects in whom serotype was measured, whereas serotype 2, which included genotypes 2a and 2b, was detected in 30.6% of patients. These results agree with the overall distributions of HCV genotypes and serotypes in the entire Japanese population, which show that genotype 1b is the most prevalent genotype at 70%.[36] Several studies have demonstrated that genotype 1b is associated with severe liver disease, including cirrhosis and HCC.[37][38] In this study, there was an apparent association between HCV serotype I infection and mortality due to HCC. Other studies, however, have not found an effect of HCV genotype on liver disease development.[39][40] In addition, although an association of indeterminate serotype with mortality was observed (HR = 3.6), the reason for this finding is not clear. A larger study is needed to elucidate the role of genotype in the prognosis of HCV infection.
HCV RNA levels have also been reported to be associated with the progression of chronic hepatitis C.[41][42] Although the level of HCV RNA was not quantified in this study, HCVcAg levels, which are known to correlate with HCV RNA levels,[21] were assessed by fluorescence enzyme immunoassay. We observed that high HCVcAg levels were predictive of liver-related mortality, including death due to HCC, in the HCV carriers. The precise mechanism underlying HCV infection-dependent hepatocarcinogenesis is not clear. However, a study of transgenic mice that express the HCV core protein demonstrated that this protein was important in HCC development.[43] Of interest, Moucari et al. reported that insulin resistance is a specific feature of chronic hepatitis C and associated with high serum HCV RNA levels.[44] A significant increase in the incidence of diabetes has also been seen in subjects with high titer of HCV core protein compared to subjects who were negative for anti-HCV.[45] Moreover, significant fibrosis is associated with insulin resistance,[44] and diabetes mellitus is known to increase the risk of primary liver cancer in the presence of other risk factors such as hepatitis C.[46] Thus, HCVcAg levels might be associated with liver-related mortality through the development of HCV-induced insulin resistance or diabetes mellitus.
We have previously shown that elevated ALT levels are an important predictor of HCC among HCV carriers in this study population.[19] In the current analysis, ALT, aspartate aminotransferase, and GGT levels at enrollment were significantly higher in subjects who died due to a liver-related disease compared with subjects who died from other causes (data not shown). In addition, after adjusting for age and sex, overall mortality (HR, 2.23) and liver-related death (HR, 11.0) were significantly higher for HCV carriers with persistently elevated ALT than for those with persistently normal ALT.
Our study had several limitations. First, data regarding liver histology were lacking. It is likely that HCV carriers had more cirrhosis than did HCV noncarriers, given that more HCV carriers died of HCC and non-HCC liver deaths (Table 2). However, we were unable to examine this possibility directly. Information on platelet counts, which are generally inversely correlated with hepatic fibrosis, was available for a subset of subjects. Based on data obtained in 1996, mean platelet counts were significantly lower in HCV carriers (n = 539; 18.4 x 104/uL ± 5.6 x 104/uL) than in HCV noncarriers (n = 277; 21.3 ± 6.0). In addition, data from the last examination attended after 2001 showed that the persistently elevated ALT group had lower mean platelet counts (n = 94; 14.5 x 104/uL ± 5.5 x 104/uL) than did the persistently normal ALT group (n = 123; 21.8 ± 7.3). These findings suggest that the presence of viremia may increase the rate of hepatic fibrosis, especially in HCV carriers with high ALT levels.
Second, although the effect of IFN therapy may have implications with respect to the overall death rates in the study population, information on treatment was limited. However, the proportion of treated subjects with an observed sustained viral response to IFN was small (7%). Data on socioeconomic factors, which are strongly related to mortality outcomes,[47] also were not available in this study. We would not expect much variation in socioeconomic status in the study population, because the cohort included only Japanese subjects who resided in a small rural community where farming is the principal occupation. In addition, all subjects in the study population had health insurance. Thus, we believe that socioeconomic factors and IFN therapy likely did not greatly affect the rate of mortality in our study population.
In conclusion, the results of this prospective 10-year follow-up study showed a strong effect of HCV carrier status on liver-related mortality among anti-HCV-seropositive individuals. Moreover, high HCVcAg and ALT levels were important predictors of liver-related death in this population. Monitoring HCV load and ALT level in HCV carriers may be important for identifying those individuals at increased risk for HCC or other liver disease, particularly among older carriers who are less likely to respond to HCV treatment.
Results
Demographic Characteristics of Study Subjects.
As shown in Table 1, 758 (67.4%) of the anti-HCV-positive subjects were HCV carriers (i.e., positive for HCVcAg or HCV RNA), with a mean age at enrollment of 64.9 years. The HCV noncarrier group, who were considered to have had a prior HCV infection, included 367 subjects whose mean age at enrollment was 62.6 years. On average, the HCV carriers were older and had higher levels of ALT and gamma-glutamyltransferase (GGT) than the noncarriers, at baseline. In contrast, there were no significant differences between the two groups with respect to sex, alcohol intake, or history of blood transfusions. The number of subjects positive for hepatitis B surface antigen was small and not significantly different between the two groups. Sixty-seven subjects reported that they had previously received interferon (IFN) therapy, all of whom were categorized as HCV carriers when they entered the study. Fifteen of these subjects were treated prior to entering the study, five were treated during the study, and one was treated both prior to and during the study; for the other 46 subjects, the timing of IFN treatment was unknown. Although the results of IFN therapy could not be fully determined for these 67 subjects, 41 of 44 with available data in 2005 were positive for HCV RNA at that time and only three (7%) were negative for HCV RNA.
Overall and Cause-Specific Mortality.
Over an average of 8.2 years of follow-up, 231 deaths occurred among the 1125 subjects (Table 2). The overall mortality rate was 25.0 per 1000 person-years in this study population. Most deaths were liver-related, with 45 due to HCC and 31 to other liver diseases including cirrhosis, hepatic failure, and ruptured esophageal varix. The next most frequent cause of death was other neoplasms (n = 41), followed by pulmonary disease excluding lung cancer (n = 32), stroke (n = 30), other/unknown causes (n = 30), and heart disease (n = 22).
Of the 231 deaths, 176 were in the HCV carrier group and 55 were in the noncarrier group (Table 2). After adjusting for age and sex, HCV carriers had a significantly higher overall mortality rate (HR, 1.53; 95% CI, 1.13-2.07), compared to HCV noncarriers (Table 3). The elevated mortality rate among the subjects with evidence of HCV viremia was due to a much higher occurrence of liver-related deaths (HR, 5.94; 95% CI, 2.58-13.7). In contrast, HCV viremia was not significantly associated with death from other malignancies, stroke, heart disease, or pulmonary disease. The cumulative risk of death, based on Kaplan-Meier estimates, was 28.0% for the HCV carrier group and 17.9% for the HCV noncarrier group over 10.3 years (Fig. 1), a statistically significant difference (P < 0.001).
Predictors of Mortality Among HCV Carriers.
The age-adjusted and sex-adjusted association between HCV serotype and HCVcAg level and mortality was examined among the subjects with HCV viremia. Compared to HCV serotype II, those with serotype I infection did not have a higher rate of overall (HR, 1.04) or liver-related mortality (HR, 1.12); however, having an indeterminate HCV serotype was related to both overall (HR, 3.59; 95% CI, 2.1-6.1) and liver-related death (HR, 2.12; 95% CI, 0.78-5.75). Of note, both serotype I infection (HR, 2.21; 95% CI, 0.91-5.33) and indeterminate HCV infection (HR, 3.89; 95% CI, 0.97-15.7) appeared to increase HCC mortality. In addition, a significantly increased rate of liver-related death was associated with a higher level (100 pg/mL) of HCVcAg (HR, 1.81; 95% CI, 1.08-3.06); the effect of higher HCVcAg level was stronger with respect to other liver-related death (HR, 2.58; 95% CI, 1.04-6.41) than to HCC death (HR, 1.48; 95% CI, 0.77-2.82). HCVcAg level had no effect on overall mortality among the HCV carriers (HR, 1.06).
In a subgroup analysis of 719 HCV carrier subjects who had data for at least three separate ALT measurements, 173 had persistently normal ALT levels while 141 had persistently abnormal levels. Subjects whose ALT levels fluctuated were not included in the analysis. Adjusting for age and sex, overall mortality (HR, 2.23; 95% CI, 1.37-3.61) and liver-related death (HR, 11.0; 95% CI, 4.35-27.9) were significantly higher for HCV carriers with persistently elevated ALT than for those with persistently normal ALT. The strongly elevated rate of liver-related mortality was evident for death due to both HCC (HR, 11.1) as well as other liver-related disease (HR, 14.5).
Patients and Methods
Study Population.
Since 1993, we have been following anti-HCV-seropositive residents in a hyperendemic area (Town C) of Japan. The overall prevalence of anti-HCV positivity is higher (20.6%) in this region than in the surrounding area.[16] Town C is a small town in midwestern Miyazaki Prefecture, Japan, and the Town C HCV Study is a cohort study examining the natural course of HCV infection.[17-20] A general health examination program, begun in 1993, has been conducted annually for residents over 20 years of age. An ultrasonography-based liver disease screening program was initiated in 1994 to detect HCC in Town C residents who were identified as positive for anti-HCV. A total of 1321 anti-HCV-positive residents were enrolled into the cohort from 1994 through the last liver disease screening in 2006. Informed consent was obtained from subjects at the time of enrollment. The study was approved by the human subjects committees of the Harvard School of Public Health, the University of Miyazaki Faculty of Medicine, the Boston University School of Public Health, and the Kagoshima University Graduate School of Medical and Dental Sciences.
Our analysis focuses on the 1125 subjects with hepatitis C viremia data between 1995 and February of 2005, who were followed for mortality from the beginning of 1996 through the end of 2005. Anti-HCV-seropositive subjects with detectable HCV core antigen (HCVcAg) or HCV RNA were considered to be persistently infected with HCV and were classified as HCV carriers. Anti-HCV-positive subjects who were negative for HCVcAg and HCV RNA were assumed to have had a prior HCV infection and were classified as noncarriers. Subjects who underwent oral or intravenous administration of medical herbs or other palliative therapies or who had received interferon therapy were not excluded from the analyses. A subgroup analysis was conducted on HCV carrier subjects with at least three independent ALT measurements obtained at an annual general health examination or liver disease screening; ALT levels 35 were considered abnormal.
Follow-Up.
For this analysis, follow-up started at the date of first HCV viremia measurement (baseline) and ended at date of death or December 31, 2005. During the course of the study, 12 residents moved to other areas, and their follow-up time was censored at that point; no other subjects were lost to follow-up. Cause of death was based on the information from the death certificate and was classified into one of seven categories: HCC, liver disease excluding HCC, neoplasms excluding HCC (i.e., other neoplasms), stroke, heart disease, pulmonary disease excluding lung cancer, and other/unknown causes.
Laboratory Methods.
Serum anti-HCV antibodies were detected using second-generation enzyme immunoassay testing (Immunocheck F-HCV antibody; International Reagents Co., Kobe, Japan) or third-generation chemiluminescence enzyme immunoassays (Lumipulse Ortho II; Ortho-Clinical Diagnostics, Tokyo, Japan). In the anti-HCV-positive residents, serum levels of HCVcAg were tested with a fluorescence enzyme immunoassay (Immunocheck F-HCV Ag Core; International Reagents Co., Kobe, Japan),[21] with a detection threshold of 8 pg/mL. The presence of HCV RNA was determined by reverse transcription polymerase chain reaction (Amplicor HCV Monitor, version 1.0 [Nippon Roche, Tokyo, Japan] or version 2.0 [Nippon Roche or Roche Diagnostics K.K., Tokyo, Japan]) in study subjects whose HCVcAg levels were below the detection threshold.
Serologically defined HCV genotype (HCV serotype) was determined with a serological genotyping assay kit (Immunocheck F-HCV Grouping; International Reagents Co., Tokyo, Japan). If the HCV serotype could not be determined, the HCV genotype was examined (HCV Core Genotype; SRL, Tokyo, Japan). HCV genotype 1b was included with serotype I, and genotypes 2a and 2b with serotype II. No other HCV genotype was detected in this study population.
Statistical Analysis.
One-factor analysis of variance, X2 tests, Fisher's exact tests, and the Mann-Whitney U tests were used, when appropriate, for statistical comparisons of the baseline characteristics of the HCV carrier and noncarrier groups of subjects. Cox proportional hazards regression was used to obtain hazard ratios (HRs) and 95% confidence intervals (CIs) that were adjusted for age and sex; for the analyses of cause-specific mortality, subjects who died from a different cause were censored at the time of death. The cumulative incidence of death was analyzed by the Kaplan-Meier method, and differences in the survival curves were evaluated by the log-rank test. Statistical analyses were performed using Statistical Analysis System (SAS, version 9.1; SAS Institute, Cary, NC), STATVIEW (version 5.0; Abacus Concepts, Berkeley, CA), or SPSS (SPSS Inc., Chicago, IL) software programs. A P value less than 0.05 was considered to be statistically significant.
|
|
| |
| |
|
|
|
