Screening for hepatitis C in a general adult population in a low-prevalence area: the Tromsø study

The study was part of the seventh survey of the Tromsø Study (Tromsø 7) in 2015–2016. The Tromsø Study is a longitudinal population-based, prospective study with repeated health surveys since 1974 in the municipality of Tromsø in Northern Norway [23]. Tromsø is the largest city in Northern Norway, harbouring the world’s northernmost university, thus having a high proportion of young people. The present population (per 2nd quarter of 2018) is 76,062 inhabitants, predominantly of Norwegian origin (14% immigrants) [24].

Tromsø 7 included more than 50 research projects, covering various health issues, symptoms and chronic diseases. HCV detection was included for the first time. Based on the official population registry, residents of the municipality of Tromsø aged 40 years and older were invited to participate. A personal invitation was sent about 2 weeks before a suggested time of appointment at one permanent study site. The subjects were free to attend whenever suitable within the opening hours of the study site and within the one year duration of the study. The invitation leaflet included all necessary information, and a questionnaire was enclosed, as well as username and password for an optional online response. Non-attenders were given one reminder. Information about the survey and invitation to participate were repeatedly provided in the local newspapers.

All 32,591 citizens aged 40 years and above were invited, and 21,083 (65%) attended. Sera from 20,946 participants (64.3% of invited citizens) were tested for anti-HCV, of whom 11,004 (52.5%) were women and 9942 (47.5%) were men. The participation rate was highest in the age group 60 to 69 years for both women and men, somewhat lower in younger age groups, and lowest among those older than 80 years (Table 1).

The participants responded to a self-administered questionnaire with questions about health, psychological problems triggering contact to professional health care, anxiety or depression, smoking habits, alcohol consumption, the use of drugs other than alcohol, level of education, marital status and main occupation/activity. There were two questions regarding hepatitis C (translated from Norwegian): “Have you been infected with the liver virus hepatitis C?”, and “If you have been infected with the liver virus hepatitis C: have you ever received treatment?”

Sera from 20,946 participants were stored frozen at − 20 °C and tested for anti-HCV (ARCHITECT Anti-HCV Assay, Abbott System, Wiesbaden, Germany) at the Department of Microbiology and Infection Control, University Hospital of North Norway, Tromsø, Norway. Individuals with a positive anti-HCV test received an information letter with their test results, describing the requirement for a second blood test to discriminate between current infection and previous exposure to HCV. The second blood test was performed at the University Hospital in Tromsø, where the result was followed up by the responsible medical doctor at the Department of Gastroenterology, and compared to any existing HCV test results. Two reminders were sent to those who did not have the follow-up test. The follow-up samples were retested for anti-HCV and further tested for the presence of HCV RNA (ROCHE RT-PCR Cobas Amplicor Hepatitis C Viral Polymerase Chain Reaction, Roche Molecular System Inc., Branchburg NJ, USA). Samples positive for the anti-HCV test and negative to the HCV RNA test were analyzed with a recombinant immunoblot assay (RIBA HCV 3.0 SIA test, Chiron Cooperation, Emeryville, CA, USA) as a secondary confirmation test of the first line anti-HCV test to rule out unspecific positive tests. Samples were considered anti-HCV positive with reactivity to two or more antigens in the RIBA test, indeterminate when reactivity to only one antigen was present, which may represent previous resolved HCV-infection or unspecific antibody reactions [25], and negative when no antigen-specific reactivity was observed. The RIBA test was not carried out in cases were existing laboratory results were consistent with either spontaneous clearance (previous positive RIBA test or positive HCV RNA test followed by at least two consecutive negative HCV RNA tests with at least three months interval) or obtained sustained virologic response (SVR) after antiviral treatment. HCV genotyping was performed as a hybridization assay on products from the HCV RNA PCR according to the manufacturer’s instructions (INNO-LIPA HCV II kit, INNOGENETICS, Ghent, Belgium).

The term HCV exposure is used in Tables 2 and 3 to include individuals with the following characteristics: (1) persons with chronic (viraemic) HCV infection; i.e. with positive HCV RNA: (2) persons with treatment-recovered HCV infection: (3) persons with spontaneously resolved HCV infection; i.e. with positive RIBA test or positive HCV RNA test followed by at least two consecutive negative HCV RNA tests with at least three months interval: (4) persons with positive anti-HCV test, negative HCV RNA and indeterminate RIBA test.

Estimated prevalence numbers of HCV exposure and chronic (viraemic) HCV infection in the Tromsø population were calculated based on the observed prevalence in each age group and corrected for different attendance rates between the groups. An equal prevalence between attenders and non-attenders was presumed for the calculation of expected numbers of infected individuals.

All subjects with a positive HCV RNA test were offered a clinical evaluation, which included a thorough medical examination, the recording of the medical history and the assessment of risk factors for HCV infection. An estimate of the time-point of transmission was made based on information on the first year of high-risk behaviour, such as injecting drug use (IDU), tattoos or transfusion of blood products prior to 1992 [26]. At this stage, an additional blood sample was analysed for platelet count, alanine aminotransferase (ALT), and aspartate aminotransferase (AST) in order to calculate the Fibrosis-4 (FIB-4) index [27]. The blood sample was also analysed for hepatitis B surface antigen (HBsAg), hepatitis B core antibody (HBcAb) and antigens/antibodies to human immunodeficiency virus (HIV Ag/Ab combo). Liver stiffness (kPa) was measured with transient elastography (FibroScan® 402, Echosens, Paris, France). Significant fibrosis and cirrhosis was defined as liver stiffness values ≥7 kPa and ≥ 12,5 kPa, respectively, equivalent to METAVIR fibrosis stage ≥F2 and F4, respectively [28]. Ultrasound was performed at the responsible medical doctor’s discretion. Treatment was offered to all HCV RNA positive patients who met for clinical follow-up.

Figure 1 shows a flowchart of the study with associated results. The anti-HCV screening test was positive in 217 (1.0%) of 20,946 individuals. The follow-up test was negative for anti-HCV and/or RIBA in 83 samples. Thus, the prevalence of confirmed anti-HCV was 0.6% (95% CI: 0.5–0.7%) (n = 134), with a sex distribution of 71 (53%) men and 63 (47%) women. HCV RNA was detected in 33 (0.2%; 95% CI: 0.1–0.3) of 20,946 participants, 18 male (54.5%). Of these viraemic cases, 13 (39.4%; 95% CI: 22.7–56.1) were not aware of their infection. Two of the 33 persons with current positive HCV RNA reported that they had received antiviral treatment earlier, one of whom had interrupted the treatment before scheduled treatment-end and was considered to be a treatment failure. The second person did not meet for clinical follow up, rendering it unclear whether the vireaemia represents reinfection or treatment failure. Overall, current or treatment-recovered HCV infection was found in 85 (0.4%; 95% CI: 0.3–0.5) of 20,946 individuals, 48 (56.5%) men and 37 (43.5%) women. Of those, 52 (61.2%) had previously received antiviral treatment with achieved SVR.

Spontaneous clearance of HCV was demonstrated in 33 (24.6, 95% CI: 17.3–31.9) of 134 anti-HCV positive individuals. The RIBA test was indeterminate in 16 of the cases that were anti- HCV positive and HCV RNA negative.

Table 2 shows the observed prevalence of HCV exposure and chronic (viraemic) HCV infection according to sex and 10-year age groups, as well as the estimated over-all prevalence. The highest prevalence of HCV exposure (1.2%) and chronic HCV infection (0.4%) was seen in the age group 50–59 years.

Data on HCV genotype (GT) was available in 75 of the 85 persons with current or recovered chronic HCV infection. HCV GT 1a was detected in 19 (25.3%) individuals, GT 1b in 10 (13.3%), GT 2b in 10 (13.3%), GT 3a in 33 (44%), GT 4 in one (1.3%) and GT 1 not available for subtyping in 2 (2.7%).

Thirteen of the 33 (39.4%) individuals with viraemic HCV infection were not aware of their infectious status, corresponding to a population prevalence of 0.06% (95% CI: 0.03–0.09). Nine of the 13 were women and the median age was 55 years. The distribution of genotypes 1 through 3 was six GT 1a, two GT 2 and five GT 3a. The median ALT value was 48 U/L (range 21–276 U/L), with eight of thirteen persons demonstrating a normal ALT value. The median liver stiffness value was 6.7 kPa (range 4.1–17.6). Liver stiffness values were < 7 kPa in five persons and between 7 and 12 kPa in six persons. Two persons had liver stiffness > 12.5 kPa, one of whom was considered to have established liver cirrhosis based on liver stiffness of 17.6 kPa and signs of cirrhosis on ultrasound. The second person had probable liver cirrhosis based on liver stiffness of 12.6 kPa and a FIB-4 index of 3.86. HBsAg was negative in all, and HBcAb was detected in three of the 13 persons. In the self-administered questionnaire, six of the 13 individuals reported current (n = 2) or past (n = 4) drug injection. In the follow-up examination, an additional three persons reported past drug injection, thus 69.2% reported a history of IDU. The median estimated time from infection to diagnosis was 30 years (range 10–40 years). Extrapolating the observed proportion of individuals who were unaware of their HCV infection to the whole population of Northern Norway (484,001 inhabitants) implies that 290 persons above 40 years of age in this region could be unaware of ongoing HCV infection.

All 13 persons with previously undiagnosed chronic HCV infection have been successfully treated with achieved SVR 12 or 24 weeks after completed treatment.

Frequencies of socio-demographic characteristics in the HCV-exposed cohort compared to the background population are shown in Table 3. In univariate analysis, there was a positive association between HCV exposure and self-reported bad health, daily smoking, the use of drugs other than alcohol, lower level of education, living without a spouse/partner, being disabled or unemployed, and having psychological problems triggering contact to professional health care. In a separate question about anxiety or depression, the HCV-exposed cohort scored higher than the background population (data not shown). We found no association between alcohol consumption and HCV infection. In a multivariate logistic regression analysis including significant variables from the univariate analysis and adjusting for age and gender, significant independent predictors of being exposed to HCV were: Being disabled or unemployed (OR 2.5; 95% CI 1.7–3.7), current daily smoking (OR 4.4; 95% CI 2.2–8.6), previous daily smoking (OR 2.7; 95% CI 1.4–5.1), current use of drugs other than alcohol (OR 35,4; 95% CI 17.4–71.9), and previous use of drugs other than alcohol (OR 15.7; 95% CI 10.2–24.2).

Table 4 shows the estimated costs for the screening project. The total cost for screening of 20,946 individuals was NOK 1177705 (€ 125,175), and the cost per newly detected chronic HCV infection (n = 13) was NOK 90593 (€ 9629).

The strength of this study is the large sample size in a general population, which enhances the probability that the study population is representative of the general population. However, there are important limitations. First, The Tromsø 7 study only included individuals aged 40 years and older. This age restriction was inherent to the overreaching study design of Tromsø 7, but clearly introduces a selection bias. IDU is the main mode of transmission of HCV [31], and it is estimated that 29.8% (range 25.0–34.8) of PWIDs in Western Europe are younger than 25 years [32]. In the municipality of Tromsø, it is estimated that the number of PWIDs is approximately 300 (personal communication, Inger Hilde Trandem, MD, Social Medical Center, Tromsø, May 28, 2018). There is no clear data on their age distribution, but it is reasonable to assume that the proportion of young PWID in Tromsø is comparable to the findings in the above mentioned study. Due to the age restriction, the prevalence of HCV infection in our study is most likely underestimated.

Second, even if participation rates were generally high across all age groups, self-selection is still an important issue that may affect the representativeness of the study sample. The attenders in population surveys tend to be more educated and have a healthier life style than non-attenders [33]. The second survey of the Tromsø study (Tromsø 2) showed that various psychiatric disorders and alcohol abuse were significant predictors of nonattendance in health surveys [34], and a Canadian study demonstrated that non-response bias is a problem in alcohol and drug use surveys [35]. It is therefore reasonable to assume that current and former PWIDs are less likely to participate in health surveys, also resulting in underestimation of the true HCV prevalence and reducing the efficiency of screening in the general population.

The interpretation and significance of indeterminate RIBA reactions are unclear. In one study, 4.9% of RIBA indeterminate cases were found to be HCV RNA positive [36]. Still, most individuals with indeterminate RIBA have a negative HCV RNA test, which may represent previous resolved HCV-infection as well as unspecific antibody reactions [25]. Reports have shown that approximately half of those with indeterminate RIBA have a resolved HCV infection [37, 38]. In this study, we have chosen to include persons with RIBA indeterminate result in the HCV-exposed cohort, which could have led to overestimation of anti-HCV positive. However, the number of RIBA-indeterminate records was low, making the contribution of these less important.

Our study was integrated in an established population-based survey with repeated health surveys since 1974. The attendance rate was 64.3% and the estimated cost per newly detected chronic HCV infection was approximately NOK 90000 (€ 9629). HCV-screening of the general population outside such an established population survey would have been more laborious and at an expected considerably higher costs, thus making it less feasible. As discussed above, it is likely that persons belonging to risk groups for HCV infection attended the study to a lesser degree than the general population, reducing the efficiency of such an approach. On the other hand, the study has unmasked several individuals with chronic HCV infection that did not define themselves as belonging to known risk groups. A recent Spanish pilot study for an eventual population-based screening program included the adult population (20–75 years) in a small health area with a participation rate of 46.2% (2637/5706) [39]. HCV RNA was detected in 13 persons (0.5%), of whom five were unaware of the disease.

In low-prevalence countries, routine screening of the entire population has not been considered to be cost-effective [15‐18], and screening are limited to high-risk populations. However, the high proportion of undiagnosed HCV infection clearly underscores the limitations of the risk-based screening approach and the need to reconsider screening strategies in order to achieve the diagnosis rate of 90% promoted by the WHO.

In the US, it is recommended a one-time screening of persons in the high-prevalence 1945–1965 birth cohort, in addition to targeted risk-based testing [40]. In the present study, the highest prevalence of anti-HCV and viraemic HCV infection was found in the age group 50–59 years, i.e. in people born between 1956 and 1965, which may be explained by a later onset of the epidemic of IDU in Norway, with a gradual increase in the number of PWID from the onset of IDU in 1973 until a peak was reached in 2000 [7]. In a birth-cohort analysis, 73% of the HCV-infected population in Norway was born between 1955 and 1980 [41]. A systematic review including several countries concluded that screening of birth cohorts, drug users, and high-risk populations was cost-effective [18]. However, recent studies indicate that universal screening of the general population may be an effective strategy. In France, where the prevalence of chronic HCV infection is 0.3% [2], a modelling study showed that universal screening of all individuals aged 18–80 years was the most effective screening strategy, and also the most cost-effective, assuming rapid initiation of treatment after diagnosis [19]. Likewise, in Spain with an HCV RNA prevalence 0.35–0.41%, a recent modelling study concluded that screening of the general adult population would identify a larger number of additional individuals with chronic HCV infection than screening high-risk groups or screening the age-cohort with the highest anti-HCV prevalence plus high-risk groups [20].

Others suggest strategies to improve targeted screening of people in high-risk groups in various settings. Primary care practitioners can play an important role in targeted screening, especially in former PWID, whereas screening of current PWID is more appropriate in settings like outpatient clinics, opioid substitution programs, jails, and psychiatric clinics [17, 42‐46]. In a screening and medical follow-up programme in Northern Norway, primary care practitioners were encouraged to screen patients with former or present risk factors for HCV infection, which led to an increase in the number of newly diagnosed HCV infections in the subsequent years [47]. Technical bottlenecks in HCV testing can lead to missed opportunities in the HCV cascade of care, e.g., when a high proportion of anti-HCV positive individuals are not followed up with a confirmatory test for HCV RNA [48]. The availability of a new point-of-care (PoC) test with high sensitivity and specificity (close to 100%) for detection of HCV RNA might contribute to simplification of HCV testing and thus enable decentralisation of HCV care and treatment [49]. New technology, such as the use of dried blood spot and saliva sampling could increase access to HCV testing, e.g. in people with difficult venous access [50, 51].

There are potential negative effects associated with screening large numbers of persons in a population with low prevalence of HCV infection. In our study, the proportion of false positive anti-HCV tests was 38.2% (83/217). False-positive results can cause harm by way of anxiety and stigmatization, although such effects are difficult to quantify [52].

Modelling studies have indicated that screening in the general adult population may be an effective screening strategy [19, 20]. Universal screening may allow diagnosis and treatment of asymptomatic infected persons, avoiding the development of complications and onward transmission, thus saving health costs. To be effective, people with the highest risk of infection must also attend the screening project. Based on this, strategies to improve targeted screening of people in high-risk groups in various settings, including primary care-based interventions, may still be the most effective approach in low-prevalence regions. To overcome the high costs associated with screening in the general population, the use of a birth-cohort screening strategy could be considered, which in our case would be based on the finding of the highest prevalence of anti-HCV and chronic HCV infection in people born between 1956 and 1965. Finally, implementation of simplified testing methods may increase access to HCV testing in both risk groups and birth cohorts.