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Although the independent effects of smoking status and HAART are reported as lower risks against KS, their combined effects have not been explored. We examined whether there is an interaction between smoking status and HAART use on the risk of KS development in an on-going US cohort of HIV-infected men.
Cox proportional hazards regression was used to analyse a total sample of 2736 participants of the Multicenter AIDS Cohort Study (MACS).
We identified 530 incident KS cases with a total follow-up time of 26594 person-years (incidence rate: 2.00 out of 100 person-years). Current smoking status and HAART use were independently associated with a lower risk of KS development (hazard ratio – HR=0.56, 95% CI: 0.35–0.90, P=0.02 and HR=0.27, 95% CI: 0.16–0.48, P<0.0001, respectively). There was no evidence of multiplicative interaction between current smoking status and HAART use on KS risk (HR=2.14, 95% CI: 0.97–4.73, Pinteraction=0.06). Lower effect of smoking was only present among those not on HAART (HR=0.57, 95% CI: 0.35–0.92, P=0.02).
The inverse association of cigarette smoking on KS risk may be limited to those not on HAART. The biological mechanism of smoking in KS carcinogenesis should be elucidated.
Kaposi's sarcoma (KS) is caused by human herpesvirus-8 (HHV-8) (Chang et al, 1994) and is one of the most common cancers in HIV-infected persons (Beral, 1991; Grulich et al, 2007). Highly active antiretroviral therapy (HAART) is reported to decrease KS incidence, (Jacobson et al, 2000; Portsmouth et al, 2003; Shiels et al, 2011) and to prolong time to treatment failure (Bower et al, 1999). Recently, an inverse association between cigarette smoking and infection with HHV-8 or KS development has also been reported (Goedert et al, 2002; Nawar et al, 2005; Mbulaiteye et al, 2006; Anderson et al, 2008). However, the biological mechanism of smoking in the pathogenesis of KS has not yet been defined. From the Multicenter AIDS Cohort Study (MACS), Hoover et al. (1993) reported that cigarette smoking is a protective factor against the risk of KS development in HIV-infected men and hypothesised that smoking induces inflammatory cytokines that lower the risk of AIDS-associated KS.
Although the independent roles of cigarette smoking and HAART have been reported, the interaction between them has not been examined, to our knowledge. The current analysis aimed to determine whether there is an interaction between smoking status and HAART use on the risk of KS development in a cohort of HIV-infected men who have sex with men (MSM) in the United States.
The current analysis used a public dataset obtained from the MACS, an on-going cohort study of HIV-infected and HIV-uninfected MSM in the United States (Kaslow et al, 1987). Briefly, a total of 6972 participants were recruited from four USA cities (Baltimore, MD; Chicago, IL, USA; Pittsburgh, PA, USA and Los Angeles, CA, USA) over three enrolment periods from April 1984 to August 2003: 4954 between 1984-1985, 668 between 1987–1991, and 1351 from 2001–2003. At the baseline visit and follow-up visits every 6 months, study participants were interviewed with a standardized questionnaire by trained interviewers, were examined by a clinician, and also consented to donate blood for various laboratory tests, including confirmation of HIV status (Kaslow et al, 1987; Lazo et al, 2007; Desquilbet et al, 2011). The Institutional Review Board of each participating institution approved the MACS protocol. Moreover, all MACS participants agreed to provide written consent.
The outcome of interest was KS development. Cancer ascertainment and classification were described in detail elsewhere (Seaberg et al, 2010). In the current analysis, the ICD-O-3 code 9140.4 was used to identify KS cases (World Health Organisation – WHO, 2000). We defined KS incident cases as men who did not have KS at the baseline visit or at the seroconversion visit (if HIV-negative at baseline) but developed KS subsequently.
Two independent variables were used for the current analysis: current smoking status (yes/no) at baseline and subsequent visits from the standardized questionnaire and HAART use (ever/never), according to the 2008 DHHS/Kaiser Panel on Clinical Practices for the Treatment of HIV infection guidelines (Supplementary File 1).
The current analysis included 2736 participants (HIV-seropositive or seroconverters) as we excluded 3514 HIV non-infected participants and 722 participants in enrolment 3. As there were only four incident cases of KS in enrolment period 3 and all cases in enrolment period 3 received HAART, it was not possible to examine the interaction. Overall time of follow-up was from April 1, 1984 to October 1, 2005 (cutoff of the dataset). The follow-up time was defined as the time from the entry date (HIV-infected men) or the seroconversion date (HIV-seroconverters) to the KS diagnosis date for subjects who developed KS or to the last recorded visit date for subjects who did not develop KS. In the current analysis, those who died before the development of KS were censored.
As CD4+ cell count and HIV viral load were significantly associated (i.e, collinearity – P<0.0001), we did not include both of them in the adjusted model. Current smoking status at baseline visit and HAART ever-use were included because these variables did not change over time. The covariates included in the adjusted models as categorised in Table 1 were: age, race/ethnicity, employment status, education level, individual gross income, CD4 cell count, and enrolment period (D'Souza et al, 2008; Desquilbet et al, 2011). CD4 cell count was treated as a time-dependent variable in adjusted models. Enrolment period was adjusted for because there was difference in HAART adherence between whites and African Americans between the two enrolment periods (Lazo et al, 2007).
We used Cox proportional hazards regression to determine the interaction between smoking status and HAART use on KS development. The interaction between current smoking status and HAART use-ever was a product of these two binary variables. In the modelling process, besides the interaction terms, both current smoking status and HAART use-ever were also presented. We also performed stratified analyses to determine the relationship between current smoking status and KS risk by HAART use and the relationship between HAART use and KS risk by current smoking status. All statistical analyses were performed using SAS 9.2 (Cary, NC, USA) (SAS Institute 2000). All tests were two-sided, and P=0.05 was used as the significance level.
More than 40% of participants were current smokers. The proportion of ever HAART use was 23 and 41% among HIV-seropositive and HIV-seroconverters, respectively (Table 1). We identified 530 incident KS cases with a total follow-up time of 26594 person-years. The incidence rate was, therefore, 2.00 out of 100 person-years (2.40 out of 100 person-years in HIV-seropositive persons and 0.88 out of 100 person-years in HIV-seroconverters; data not shown). Although current smoking status and HAART use were independently associated with a lower risk of KS development (HR=0.56, 95% CI: 0.35–0.90, P=0.02 and HR=0.27, 95% CI: 0.16–0.48, P<0.0001, respectively), there was no evidence of interaction on the multiplicative scale between current smoking status and HAART use on the risk of KS (HR=2.14, 95% CI: 0.97–4.73, Pinteraction=0.13) (data not shown).
HAART use showed a protective effect in lowering the risk of KS development in non-current smokers (HR=0.28, 95% CI: 0.16–0.49, P<0.0001). In stratified analyses by HAART use (Table 2), the inverse association with smoking was only present among those not using HAART (HR=0.75, 95% CI: 0.35–0.92, P=0.02).
In this analysis, we found that current smoking status and HAART use were independently associated with a lower risk of KS development, and there was no evidence of multiplicative interaction between current smoking status and HAART use. However, we also found that the inverse association of smoking was only present among those who had never been on HAART. The inverse association between HAART use and the risk of KS found in our analysis is consistent with previous literature (Jones et al, 2000; Carrieri et al, 2003). The importance of immunosuppression in KS carcinogenesis is highlighted by these findings. HIV seropositivity among HHV-8 infected persons seems to facilitate cytokine production that induces angiogenesis, stimulates the growth of endothelial cells, and promotes the growth of KS spindle cells (Albini et al, 1995; Fiorelli et al, 1995; Gallo, 1998).
Our finding on the independent inverse association of current smoking status on the risk of KS development is also consistent with previous studies (Hoover et al, 1993; Goedert et al, 2002; Nawar et al, 2005; Anderson et al, 2008). For example, Hoover et al. (1993) found that in HIV-infected men, KS was 30–39% less likely among smokers than among non-smokers and hypothesised that smoking regulates key inflammatory cytokines, thus reducing KS risk among AIDS patients. In fact, Nouri-Shirazi and Guinet (2003), and Nouri-Shirazi et al. (2007) reported that nicotine influences the immune system by modifying the differentiation of dendritic cells (DCs) into atypical DCs. Specifically, the DCs alter the regulation of interleukin (IL)-10, 12 and interferon-γ-producing effector cells as well as the stimulation of antigen-presenting cell-dependent T-cell responses. Although the biological mechanism of smoking on carcinogenesis is not fully understood, this evidence provides a rationale for further investigation of the role of cigarette-smoking (i.e., nicotine) on KS risk.
We also observed that the inverse association of smoking was only present among those not on HAART. As Hoover et al. (1993) found the impact of smoking status on KS incidence before the HAART era, we thought that the potential protective effects on KS development by smoking and HAART use might be due to separate biological mechanisms and deserve to be studied further.
The major strength of our study is the use of MACS, a well-designed large cohort study of HIV-infected men in the United States, to accurately identify KS cases. The main limitation in our analysis is that because most MACS participants are Caucasian males, we cannot generalise our findings to HIV-infected women or to other racial/ethnic groups. Another limitation is that we could not analyse specific HAART regimens individually due to the change of its definition over time. Although there were no associated found (data not shown) between smoking intensity as measured by the ‘number of packs smoked per day when smoked most', >25% of subjects were missing data on smoking duration. Therefore, a more accurate representation of smoking intensity measured in pack-years could not be calculated.
To our knowledge, this is the first attempt to determine the possible interaction between smoking status and HAART use on KS risk. We also thought that if this interaction is true, the underlying biological or statistical mechanism deserves further investigation. We found independent associations between current smoking status and HAART use with a lower risk of KS development but no evidence of multiplicative interaction between current smoking status and HAART use. However, the inverse association between cigarette smoking and KS risk may be limited to those not using HAART. Our findings should be interpreted cautiously, given the negative impact of smoking on general health and the null results from a previous clinical trial examining nicotine use on KS development (Goedert et al, 2008). We, however, still think that to fully appreciate the impact that this finding might have on KS incidence among HIV-infected populations, the comprehensive biological mechanism of smoking in KS carcinogenesis needs to be elucidated.
Data in this manuscript were collected by the Multicenter AIDS Cohort Study (MACS) with centres (Principal Investigators) at The Johns Hopkins Bloomberg School of Public Health (Joseph B Margolick, Lisa P Jacobson), Howard Brown Health Centre, Feinberg School of Medicine, Northwestern University, Cook County Bureau of Health Services (John P Phair, Steven M. Wolinsky), University of California, Los Angeles (Roger Detels), and University of Pittsburgh (Charles R Rinaldo). The MACS is funded by the National Institute of Allergy and Infectious Diseases, with additional supplemental funding from the National Cancer Institute. UO1-AI-35042, UL1-RR025005, UO1-AI-35043, UO1-AI-35039, UO1-AI-35040, UO1-AI-35041. Website located at http://www.statepi.jhsph.edu/macs/macs.html. HNL received funding from the UTHealth Innovation for Cancer Prevention Research Postdoctoral Fellowship, the University of Texas School of Public Health Cancer Prevention and Research Institute of Texas, grant #RP101503. MES received partial funding from the Dan L Duncan Cancer Centre (DLDCC), Baylor College of Medicine, under the DLDCC Scholar Award. We thank Dr Wenyaw Chan (UT SPH) and Ms Renke Zhou (Baylor College of Medicine) for their advice on statistical analysis.
Supplementary Information accompanies this paper on British Journal of Cancer website (http://www.nature.com/bjc)
The contents of this publication are solely the responsibility of the authors and do not necessarily represent the official views of the National Institutes of Health or the Cancer Prevention and Research Institute of Texas.