Hostname: page-component-76fb5796d-vfjqv Total loading time: 0 Render date: 2024-04-26T06:20:11.818Z Has data issue: false hasContentIssue false

Seroepidemiology of human herpesvirus 8 (HHV-8) infection in injecting drug users

Published online by Cambridge University Press:  24 August 2009

A. ZAVITSANOU
Affiliation:
Department of Hygiene, Epidemiology and Medical Statistics, Athens University Medical School, Athens, Greece
M. MALLIORI
Affiliation:
Department of Psychiatry, Athens University Medical School, Eginition Hospital, Athens, Greece
V. SYPSA
Affiliation:
Department of Hygiene, Epidemiology and Medical Statistics, Athens University Medical School, Athens, Greece
M. PETRODASKALAKI
Affiliation:
Department of Hygiene, Epidemiology and Medical Statistics, Athens University Medical School, Athens, Greece
M. PSICHOGIOU
Affiliation:
Department of Hygiene, Epidemiology and Medical Statistics, Athens University Medical School, Athens, Greece
C. ROKKA
Affiliation:
Department of Hygiene, Epidemiology and Medical Statistics, Athens University Medical School, Athens, Greece
A. GIANNOPOULOS
Affiliation:
First Department of Surgery, Athens University Medical School, Laiko General Hospital, Athens, Greece
V. KALAPOTHAKI
Affiliation:
Department of Hygiene, Epidemiology and Medical Statistics, Athens University Medical School, Athens, Greece
D. WHITBY
Affiliation:
Viral Oncology Section, AIDS and Cancer Virus Program, SAIC-Frederick, National Cancer Institute–Frederick, Frederick, MD, USA
A. HATZAKIS*
Affiliation:
Department of Hygiene, Epidemiology and Medical Statistics, Athens University Medical School, Athens, Greece
*
*Author for correspondence: Professor A. Hatzakis, M.D., Ph.D., Department of Hygiene, Epidemiology and Medical Statistics, Athens University Medical School, 75 Mikras Asias Street, GR-11527, Athens, Greece. (Email: ahatzak@med.uoa.gr)
Rights & Permissions [Opens in a new window]

Summary

A cross-sectional study was carried out in injecting drug users (IDUs) from Greece to assess the seroprevalence of human herpesvirus 8 (HHV-8) and to identify potentially associated risk factors. A total of 288 IDUs were tested for K8.1 antibodies to HHV-8 lytic antigen. Associations between HHV-8 serostatus and potential risk factors were examined using univariate and multivariate logistic regression analysis. Seroprevalence of HHV-8 was 24·3% (95% CI 19·5–29·7), increasing with age from 19·4% in those aged <30 years to 52·9% in those aged ⩾40 years (P for trend=0·003). No statistically significant associations between HHV-8-positive status and gender, educational level, age at first drug injection, needle sharing, number of imprisonments, complications from drug overdose, HIV and HCV were observed. In the multivariate logistic regression analysis, older age (⩾40 vs. <40 years, OR 3·30, 95% CI 1·14–9·56) and report of septicaemia/abscess (yes vs. no, OR 1·80, 95% CI 1·01–3·18) were each independently associated with higher HHV-8 seroprevalence. HHV-8 is highly prevalent in the IDU population in Greece. The independent association between HHV-8 and reported abscess or septicaemia supports the hypothesis that poor hygiene conditions in the setting of drug injection may contribute to HHV-8 transmission.

Type
Original Papers
Copyright
Copyright © Cambridge University Press 2009

INTRODUCTION

Human herpesvirus 8 (HHV-8) is an oncogenic virus with a causal role in several diseases, such as Kaposi's sarcoma (KS), primary effusion lymphoma, and multicentric Castelman's disease [Reference Chang1Reference Carbone4]. Although the mode of HHV-8 transmission has been investigated extensively, it is still not understood. Transmission appears to occur by both sexual and non-sexual routes, and epidemiological patterns differ by population and geographical location [Reference Chatlynne and Ablashi5].

The high incidence of AIDS-associated KS in men who have sex with men [Reference Beral6Reference Jones8] and the high seroprevalence of HHV-8 in this group [Reference Martin9Reference Smith11] have provided evidence for sexual transmission in homosexual men, whereas evidence of heterosexual spread of the virus is inconsistent [Reference Martin9, Reference Tedeschi12Reference Whitby15]. Other possible transmission routes, such as blood-borne exposures, are being investigated [Reference Hladik16]. In this regard, studies on HHV-8 infection and injecting drug use have yielded conflicting results. Some studies have found an association with frequency of drug injection [Reference Cannon14, Reference Sosa17, Reference Diamond18], whereas an investigation of HHV-8 in Dutch injecting drug users (IDUs) found little evidence of viral transmission through drug injection [Reference Renwick19]. Furthermore, results of another survey involving IDUs from San Francisco, after controlling for sexual behaviour, suggested that HHV-8 seroprevalence increased with duration of drug use [Reference Atkinson20]. An additional investigation conducted in HIV-infected pregnant women found that HHV-8 was associated with injecting drug use [Reference Goedert21].

Very few studies of HHV-8 seroprevalence have been conducted in Greece [Reference Simpson22, Reference Zavitsanou23], which along with other Mediterranean areas is known to have a high incidence of KS [Reference Stratigos, Katoulis and Stavrianeas24, Reference Touloumi25]. In addition, data are lacking for rates of HHV-8 infection in the IDU population in this area. The objective of the current study was to assess the seroprevalence of HHV-8 infection in a group of IDUs from Greece. To elucidate modes of HHV-8 transmission in this population in Greece, we also attempted to identify the associations between HHV-8 seropositivity and potential risk factors, including injecting drug use.

METHODS

Subjects – study design

This cross-sectional seroprevalence study involved a sample of 288 heroin IDUs from Greece participating in a drug-treatment programme at the Eginitio Psychiatric Hospital. All participants were asked to provide a blood sample. Trained staff obtained informed consent and interviewed participants and data were collected anonymously. The Ethics Committee of the Athens University Medical School approved the study. Participants were asked about demographic characteristics and their injecting drug history, including age at first injection, duration of injecting drug use, and use of shared needles. Additional information included the number of imprisonments since their first injection and complications associated with drug-use overdose. In addition, participants were asked whether they had ever suffered abscess/septicaemia and whether they had hepatitis. Serum samples were stored at −80°C until required.

Laboratory methods

All sera were analysed for antibodies against HHV-8 as previously described [Reference Zavitsanou23, Reference Engels26]. Specifically, a second-generation ELISA was used to detect antibodies directed against the lytic phase glycoprotein K8.1. Briefly, Escherichia coli-expressed K8.1 recombinant protein was diluted 1:5000 in 0·05 m carbonate/bicarbonate buffer at pH 10·0. Serum samples were diluted 1:20. A sample was considered to be seropositive if the optical density (OD) was ⩾0·174. In a previous evaluation of the performance characteristics of the present assay in the Greek population, the sensitivity and specificity of the test for this specific cut-off value were 94% and 100%, respectively [Reference Zavitsanou23].

Hepatitis B core antibody (anti-HBc) was tested by Axsym-MEIA (Abbott Diagnostics Division, USA). Participants were also tested for HCV antibodies (anti-HCV) using a third-generation MEIA (Abbott Laboratories, USA); antibody testing for HIV (anti-HIV) was performed using Axsym-MEIA (Abbott Diagnostics Division) with confirmation by Western blot (GeneLabs Diagnostics, 2.2 assay).

Statistical analysis

The prevalence of antibodies to HHV-8 was calculated and expressed as a percentage together with the 95% confidence interval (CI). Furthermore, age-specific prevalence rates (along with 95% CI) for the Greek IDUs were calculated and compared to the corresponding prevalences of 955 healthy urban workers from Greece; this group of healthy urban workers was previously tested for the presence of anti-HHV-8 by the same laboratory using the same immunoenzyme assay [Reference Zavitsanou23].

Univariate analysis using the χ2 test and t test, as appropriate, was performed to examine the presence of associations between HHV-8 serostatus and all questionnaire variables. A multivariate logistic regression model was used to identify risk factors independently associated with the presence of HHV-8 antibodies. Specifically, a model containing all variables whose univariate test had a P value <0·25 was considered. Then, variables that did not contribute to the model, based on their Wald statistic, were eliminated and the new model was compared to the old through the likelihood ratio statistic. With the exception of the duration of injecting drug use, variables whose exclusion gave a non-significant likelihood ratio statistic (P<0·05) were omitted from the model.

RESULTS

Characteristics of the study population and HHV-8 seroprevalence

Of the 288 IDUs included in the study, 230 were males (79·9%) and 58 (20·1%) were females. The age of the study population ranged from 17 to 58 years with a mean value (s.d.) of 29·3 (6·2) years. A total of 15·6% of the study population had an education level above high school. Most participants reported a relatively long history of injecting drug use. In this regard, the mean (s.d.) duration of injecting drug use was 8·2 (5·9) years, whereas the mean age at first drug injection was 21·0 (5·0) years. The majority of the study population (52·8%) reported that they had never injected with a used syringe, and 35 (12·1%) reported having been in prison more than 10 times since their first drug injection. A total of 34·1% reported a history of abscess/septicaemia. Anti-HBc was detected in 53·0% of the study population, and 20·0% reported having suffered from hepatitis. The majority of the study population (90·5%) was HCV positive, while the HIV prevalence rate was extremely low with only one patient being HIV positive (0·35%); as a result of this low frequency, this variable was not considered for further analyses.

Of the 288 participants, 70 were reactive for anti-HHV-8 antibodies, indicating an overall seroprevalence of HHV-8 in IDUs from Greece of 24·3% (95% CI 19·5–29·7). The age-specific prevalence of HHV-8 in IDUs compared to healthy workers was 19·4% vs. 6·5% (<30 years old); 27·7% vs. 5·7% (30–39 years old); and 52·9% vs. 9·1% (⩾40 years old), with no overlap in the corresponding 95% CI [Reference Zavitsanou23].

Univariate analysis

Table 1 illustrates the univariate associations between HHV-8 serostatus and participant characteristics. In the univariate analysis, few variables were associated with positive HHV-8 serology. HHV-8 infection was associated with advancing age (P for trend=0·003). More specifically, HHV-8 seroprevalence increased with age from 19·4% in participants aged <30 years to 52·9% in those aged ⩾40 years. Furthermore, seroprevalence was higher in IDUs with a history of abscess/septicaemia (32·6% vs. 20·1%, P=0·019). An association of borderline significance was detected between HHV-8 seropositivity and duration of injecting drug use (P for trend=0·073).

Table 1. Univariate analysis of HHV-8 seroprevalence according to demographic variables, reported behaviour and status of HIV, HCV and anti-HBc

* Missing values because of lack of response from some participants.

The P value is for a test for linear trend.

No significant associations were observed between HHV-8 infection and gender, educational level, age at first drug injection, needle sharing, number of imprisonments since first drug injection, or complications from drug overdose. Moreover, self-reported hepatitis, anti-HBc, anti-HCV, and anti-HIV were not significantly associated with HHV-8 status.

Independent risk factors for HHV-8 infection

A multiple logistic regression model was used to identify independent risk factors for HHV-8 infection (Table 2). In this model, HHV-8 was significantly more prevalent in individuals aged ⩾40 years compared to those aged <40 years (OR 3·30, 95% CI 1·14–9·56, P=0·03). Moreover, a history of septicaemia or abscess (OR 1·80, 95% CI 1·01–3·18, P=0·05) was independently associated with higher HHV-8 seroprevalence. There was no association between duration of drug injection and HHV-8 infection in the multiple logistic regression model.

Table 2. Multiple logistic regression: determinants of HHV-8 seropositivity

OR, Odds ratio; CI, confidence interval.

DISCUSSION

Non-AIDS-related KS is more frequent in Greece [Reference Stratigos, Katoulis and Stavrianeas24, Reference Touloumi25] than in northern Europe or the USA. In the current cross-sectional study, we observed a high HHV-8 seroprevalence in Greek IDUs (24·3%), a much higher rate than that reported in healthy urban workers from Greece. The higher prevalence persisted even after we controlled for age. Moreover, HHV-8 prevalence reported for Greek IDUs was considerably higher than the rate observed in the majority of studies performed with IDUs [Reference Sosa17, Reference Atkinson20, Reference Goedert21, Reference Gambus27Reference Larocca31]. However, these differences could be in part attributed to the fact that these studies employ different serological assays – with different sensitivity and specificity – to detect HHV-8 antibodies; research indicates that HHV-8 seroprevalence estimates, measured in absolute terms, depend strongly on test performance [Reference Engels26].

The seroprevalence of HHV-8 was independently associated with advancing age, a pattern consistent with results from previous age-specific prevalence studies [Reference Lavreys32Reference Baillargeon34]. We also identified an independent association between HHV-8 serostatus and self-reported abscess/septicaemia. Skin abscess and septicaemia are frequent medical complications of intravenous drug use [Reference Haverkos and Lange35, Reference Stein36]. Potential sources of infection include the skin, dirty syringes, contaminated drugs, and solutions used to clean equipment and dissolve drugs [Reference Haverkos and Lange35, Reference Stein36]. In the present study, IDUs who self-reported abscess/septicaemia had an increased risk of being HHV-8 infected compared to those reporting no evidence of these complications. One possibility is that the study population used injection practices without following fundamental hygiene conditions (e.g. having unsterile skin before injection or using dirty syringes). Such conditions might contribute to transmission of HHV-8 infection.

The prevalence of HCV infection was high in this group (90·5%) and this high rate is in accord with findings from other studies conducted in Greek incarcerated IDUs [Reference Malliori37]. Because HCV was highly prevalent in this study population, a possible association between HCV and HHV-8 infection could not be assessed, but this association between the two infections has already been suggested in previous studies [Reference Fiore38, Reference Mbulaiteye39]. Earlier authors have suggested that transmission of HHV-8 might occur through needle sharing [Reference Cannon14], but we did not identify sharing as a risk factor for transmission in the current study. However, in view of the high prevalence of anti-HCV in our study group, the validity of this negative finding should be viewed with caution. Although we found an independent association between self-reported abscess and HHV-8 infection, injection with a used syringe did not emerge as being associated with HHV-8-positive status.

In conclusion, we identified a high seroprevalence of HHV-8 infection in IDUs from Greece. Evidence suggests that inappropriate hygiene conditions in the setting of drug injection may contribute to HHV-8 transmission. Understanding the epidemiology of HHV-8 is critical for designing interventions to decrease the transmission of this virus.

ACKNOWLEDGEMENTS

This project was funded by the Hellenic Scientific Society for AIDS and Sexually Transmitted Diseases.

DECLARATION OF INTEREST

None.

References

REFERENCES

1.Chang, Y, et al. Identification of herpesvirus-like DNA sequences in AIDS-associated Kaposi's sarcoma. Science 1994; 266: 18651869.CrossRefGoogle ScholarPubMed
2.Cesarman, E, et al. Kaposi's sarcoma-associated herpesvirus-like DNA sequences in AIDS-related body-cavity-based lymphomas. New England Journal of Medicine 1995; 332: 11861191.Google Scholar
3.Soulier, J, et al. Kaposi's sarcoma-associated herpesvirus-like DNA sequences in multicentric Castelman's disease. Blood 1995; 86: 12761280.CrossRefGoogle Scholar
4.Carbone, A, et al. Kaposi's sarcoma-associated herpesvirus DNA sequences in AIDS-related and AIDS-unrelated lymphomatous effusions. British Journal of Haematology 1996; 94: 533543.CrossRefGoogle ScholarPubMed
5.Chatlynne, L, Ablashi, D. Seroepidemiology of Kaposi's sarcoma-associated herpesvirus (KSHV). Seminars in Cancer Biology 1999; 9: 175185.Google Scholar
6.Beral, V, et al. Kaposi's sarcoma among persons with AIDS: a sexually transmitted infection? Lancet 1990; 335: 123128.Google Scholar
7.Hoover, DR, et al. Epidemiologic analysis of Kaposi's sarcoma as an early and later AIDS outcome in homosexual men. American Journal of Epidemiology 1993; 138: 266278.CrossRefGoogle ScholarPubMed
8.Jones, JL, et al. Incidence and trends in Kaposi's sarcoma in the era of effective antiretroviral therapy. Journal of Acquired Immune Deficiency Syndromes 2000; 24: 270274.CrossRefGoogle ScholarPubMed
9.Martin, JN, et al. Sexual transmission and the natural history of human herpesvirus 8 infection. New England Journal of Medicine 1998; 338: 948954.Google Scholar
10.Kedes, DH, et al. The seroepidemiology of human herpesvirus 8 (Kaposi's sarcoma-associated herpesvirus): distribution of infection in KS risk groups and evidence for sexual transmission. Nature Medicine 1996; 2: 918924.Google Scholar
11.Smith, NA, et al. Serologic evidence of human herpesvirus 8 transmission by homosexual but not heterosexual sex. Journal of Infectious Diseases 1999; 180: 600606.CrossRefGoogle Scholar
12.Tedeschi, R, et al. Seropositivity to human herpesvirus 8 in relation to sexual history and risk of sexually transmitted among women. International Journal of Cancer 2000; 87: 232235.Google Scholar
13.Eltom, MA, et al. Transmission of human herpesvirus 8 by sexual activity among adults in Lagos, Nigeria. AIDS 2002; 16: 24732478.CrossRefGoogle ScholarPubMed
14.Cannon, MJ, et al. Blood-borne and sexual transmission of human herpesvirus 8 in women with or at risk for human immunodeficiency virus infection. New England Journal of Medicine 2001; 344: 637643.CrossRefGoogle ScholarPubMed
15.Whitby, D, et al. Human herpesvirus 8: seroepidemiology among women and detection in the genital tract of seropositive women. Journal of Infectious Diseases 1999; 179: 234236.CrossRefGoogle ScholarPubMed
16.Hladik, W, et al. Transmission of human herpesvirus 8 by blood transfusion. New England Journal Medicine 2006; 355: 13311338.CrossRefGoogle ScholarPubMed
17.Sosa, C, et al. Human herpesvirus 8 can be transmitted through blood in drug addicts. Medicina 2001; 61: 291294.Google ScholarPubMed
18.Diamond, C, et al. Seroepidemiology of human herpesvirus 8 among young men who have sex with men. The Seattle Young Men's Survey Team. Sexually Transmitted Diseases 2001; 28: 176183.Google Scholar
19.Renwick, N, et al. Risk factors for human herpesvirus 8 infection in a cohort of drug users in the Netherlands, 1985–1996. Journal of Infectious Diseases 2002; 185: 18081812.Google Scholar
20.Atkinson, J, et al. Seroprevalence of human herpesvirus among injection drug users in San Francisco. Journal of Infectious Diseases 2003; 187: 974981.Google Scholar
21.Goedert, JJ, et al. Women and infants transmission study. Risk factors for Kaposi's sarcoma-associated herpesvirus infection among HIV-1 infected pregnant women in the USA. AIDS 2003; 17: 425433.Google Scholar
22.Simpson, GR, et al. Prevalence of Kaposi's sarcoma-associated herpesvirus infection measured by antibodies to recombinant capsid protein and latent immunofluorescent antigen. Lancet 1996; 348: 11331138.CrossRefGoogle Scholar
23.Zavitsanou, A, et al. Human herpesvirus 8 (HHV-8) infection in healthy urban employees from Greece: seroprevalence-associated factors. Journal of Medical Virology 2007; 79: 591596.Google Scholar
24.Stratigos, JD, Katoulis, AC, Stavrianeas, NG. An overview of classic Kaposi's sarcoma in Greece. Advances in Experimental Medicine and Biology 1999; 455: 503506.Google Scholar
25.Touloumi, G, et al. The epidemiologic profile of Kaposi's sarcoma in Greece prior and during the AIDS era. International Journal of Cancer 1997; 70: 538541.3.0.CO;2-Z>CrossRefGoogle ScholarPubMed
26.Engels, EA, et al. Identifying human herpesvirus 8 infection: performance, characteristics of serologic assays. Journal of Acquired Immune Deficiency Syndromes 2000; 23: 346354.Google Scholar
27.Gambus, G, et al. Prevalence and distribution of HHV-8 in different subpopulations, with and without HIV infection, in Spain. AIDS 2001; 15: 11671174.Google Scholar
28.Perna, AM, et al. Antibodies to human herpes virus type 8 (HHV-8) in general population and in individuals at risk for sexually transmitted diseases in Western Sicily. International Journal of Epidemiology 2000; 29: 175179.Google Scholar
29.Bernstein, KT, et al. Factors associated with human herpesvirus type 8 infection in an injecting drug user cohort. Sexually Transmitted Diseases 2003; 30: 199204.Google Scholar
30.Challine, D, et al. Seroprevalence of human herpesvirus 8 antibody in populations at high or low risk of transfusion, graft, or sexual transmission of viruses. Transfusion 2001; 41: 11201125.CrossRefGoogle ScholarPubMed
31.Larocca, L, et al. Prevalence of antibodies to HHV-8 in the general population and in individuals at risk for sexually transmitted and blood-borne infections in Catania, Eastern Sicily. Infezioni in Medicina 2005; 13: 7985.Google Scholar
32.Lavreys, L, et al. Human herpesvirus 8: seroprevalence and correlates in prostitutes in Mombasa, Kenya. Journal of Infectious Diseases 2003; 187: 359363.Google Scholar
33.Mayama, S, Cuevas, L, Sheldon, J. Prevalence and transmission of Kaposi's sarcoma-associated herpesvirus (human herpesvirus 8) in Ugandan children and adolescents. International Journal of Cancer 1998; 77: 817820.3.0.CO;2-X>CrossRefGoogle ScholarPubMed
34.Baillargeon, J, et al. Seroprevalence of Kaposi's sarcoma-associated herpesvirus infection among blood donors from Texas. Annals of Epidemiology 2001; 11: 512518.Google Scholar
35.Haverkos, HW, Lange, WR. Serious infections other than human immunodeficiency virus among intravenous drug users. Journal of Infectious Diseases 1990; 161: 894902.Google Scholar
36.Stein, MD. Medical complications of intravenous drug use. Journal of General Internal Medicine 1990; 5: 249257.Google Scholar
37.Malliori, M, et al. A survey of bloodborne viruses and associated risk behaviours in Greek prisons. Addiction 1998; 93: 243251.Google Scholar
38.Fiore, JR, et al. High seroprevalence of human herpesvirus 8 (HHV-8) in HIV-1 infected pregnant women of Southeastern Italy: association with injection drug use and hepatitis C virus infection. Journal of Medical Virology 2004; 72: 656660.CrossRefGoogle ScholarPubMed
39.Mbulaiteye, SM, et al. Seroprevalence and risk factors for human herpesvirus 8 infection, rural Egypt. Emerging Infectious Diseasess 2008; 14: 586591.CrossRefGoogle ScholarPubMed
Figure 0

Table 1. Univariate analysis of HHV-8 seroprevalence according to demographic variables, reported behaviour and status of HIV, HCV and anti-HBc

Figure 1

Table 2. Multiple logistic regression: determinants of HHV-8 seropositivity