Diabetes and Insulin Therapy, but Not Metformin, Are Related to Hepatocellular Cancer Risk

Miele, Luca; Bosetti, Cristina; Turati, Federica; Rapaccini, Gianlodovico; Gasbarrini, Antonio; La Vecchia, Carlo; Boccia, Stefania; Grieco, Antonio

doi:https://doi.org/10.1155/2015/570356

Gastroenterology Research and Practice

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Research Article | Open Access

Volume 2015 | Article ID 570356 | https://doi.org/10.1155/2015/570356

Diabetes and Insulin Therapy, but Not Metformin, Are Related to Hepatocellular Cancer Risk

Luca Miele,^1,2Cristina Bosetti,³Federica Turati,³Gianlodovico Rapaccini,^1,2Antonio Gasbarrini,¹Carlo La Vecchia,⁴Stefania Boccia,⁵and Antonio Grieco¹

Academic Editor: Roberto César P. Lima-Júnior

Received21 Jan 2015

Revised24 Apr 2015

Accepted27 Apr 2015

Published13 May 2015

Abstract

Introduction. Metabolic conditions, including type 2 diabetes, have been related to hepatocellular carcinoma (HCC) risk. We have further analyzed the role of diabetes and antidiabetic treatments on HCC. Methods. Data derived from a hospital-based case-control study (Italy, 2005–2012) on 224 HCC patients and 389 controls. Odds ratios (ORs) were estimated using multiple logistic regression models. Results. Sixty-nine (30.9%) cases versus 52 (13.5%) controls reported a diabetes diagnosis, corresponding to a multivariate OR of 2.25 (95% confidence interval, CI = 1.42–3.56). A stronger excess risk emerged for a longer time since diabetes diagnosis (OR = 2.96 for <10 years and 5.33 for ≥10 years). Oral therapies were inversely, though not significantly, related to HCC risk, OR being 0.44 for metformin and 0.88 for sulfonylureas; conversely, insulin was nonsignificantly directly associated (OR = 1.90). Compared to nondiabetic subjects who were never smokers, those who were diabetics and ever smokers had an OR of 6.61 (95% CI 3.31–13.25). Conclusion. Our study confirms an over 2-fold excess HCC risk in diabetics, with a stronger excess risk in diabetic subjects who are also tobacco smokers. Metformin may decrease the risk of HCC, whereas insulin may increase the risk.

1. Introduction

Liver cancer is the seventh most common cancer and the third cause of cancer deaths worldwide [1, 2]. In Italy, 2950 deaths from liver cancer were registered in 2008 in men (3% of all cancer deaths) and 1500 (2% of all cancer deaths) in women [3].

Hepatocellular carcinoma (HCC) is the most common histological type of liver cancer, accounting for up to 85% of cases [4]. The major recognized factors for HCC are chronic hepatitis B virus (HBV) and hepatitis C virus (HCV) infections, heavy alcohol drinking, and tobacco smoking [4–8].

Several epidemiological studies have indicated that type 2 diabetes mellitus is also associated with an increased risk of HCC [9–15]. A meta-analysis of epidemiological studies published up to February 2011 reported a significant relative risk (RR) of 2.4 from 17 case-control studies, 2.2 from 25 cohort studies, and a RR of 2.4 from 7 cohort studies on mortality from HCC [13]. A significant trend with duration of diabetes was observed in 6 studies, with a RR of 3.3 for 10 years since diabetes diagnosis. Moreover, the presence of diabetes has been associated with metastatic HCC and with worse prognosis [16, 17].

Although data on the role of drugs for the treatment of type 2 diabetes in HCC are limited, there are indications that metformin, sulfonylureas [18], and thiazolidinediones [19] are associated with a reduced risk of HCC, whereas insulin may increase the risk [20].

We have further analyzed the role of diabetes and antidiabetic treatments in HCC risk using data from a hospital-based case-control study conducted in Italy.

2. Materials and Methods

2.1. Selection of Cases and Controls

Study subjects were recruited among patients admitted to the Teaching Hospital “Agostino Gemelli” of the Università Cattolica del Sacro Cuore, Rome, Italy, from January 2005 until July 2012, and eligibility was restricted to Caucasian individuals born in Italy. In particular, cases were 224 patients with HCC recruited among subjects referred to the Outpatient Liver Unit of the hospital. The diagnosis of HCC was performed according to the AASLD guidelines [21]. Controls were 389 patients from the same hospital, enrolled during the same time period. Around 50% of the controls were outpatients, and the remaining were patients undergoing surgical interventions (laparoscopic cholecystectomy, appendicitis, and inguinal hernia) or admitted for a wide spectrum of other acute nonneoplastic diseases. The study was conducted according to the Declaration of Helsinki and was approved by the Ethical Committee of Università Cattolica del Sacro Cuore. A written informed consent was obtained from all study subjects.

2.2. Data Collection

HCC cases and controls were interviewed by trained interviewers using a structured questionnaire to collect information on demographics, lifestyle habits (including tobacco smoking and alcohol drinking), and medical history. In particular, the questionnaire included information on history and duration of diabetes and use of antidiabetic drugs (metformin, sulfonylureas, and insulin). Questions focused on the time period ending one year prior to diagnosis for cases and on the year prior to the interview date for controls.

2.3. Data Analysis

Odds ratios (ORs) for HCC and their corresponding 95% confidence intervals (CI) were estimated using multiple logistic regression models [22] including terms for age, sex, tobacco smoking, and alcohol drinking. To test for multiplicative interaction between diabetes and tobacco smoking, we compared the difference in −2 log likelihood of the models with and without an interaction term with the distribution with one degree of freedom. Moreover, we tested for additive interaction using the relative excess risk due to interaction (RERI) and the synergy index () [23] and tested their significance using the delta method [24].

3. Results

Table 1 shows the distribution of HCC cases and corresponding controls according to selected factors. Cases were somewhat older than controls, more frequently of male sex and ever smokers. History of hepatitis was reported by 71% of cases and 3% of controls.

The distribution of HCC cases and controls and corresponding ORs according to history of diabetes and use of antidiabetic drugs are given in Table 2. Sixty-nine (30.9%) cases versus 52 (13.5%) controls reported a diagnosis of diabetes, corresponding to a multivariate OR of 2.25 (95% CI = 1.42–3.56). A stronger excess risk was observed for a longer time since diagnosis of diabetes (OR = 2.96 for <10 years and 5.33 for ≥10 years). Subjects using oral antidiabetic drugs had a nonsignificantly reduced HCC risk as compared to nonusers: the OR was 0.51 for use of any oral antidiabetic drug, 0.44 for metformin, and 0.88 for sulfonylureas. Conversely, subjects using insulin had a nonsignificantly higher risk of HCC as compared to nonusers (OR = 1.90).

The combined effect of diabetes and tobacco smoking on HCC risk is shown in Table 3. Compared to nondiabetic subjects who were never smokers, those who were diabetics and ever smokers had an OR of 6.61 (95% CI = 3.31–13.25). The interaction was significant on an additive scale (RERI = 4.27, and , ), and also borderline significant on a multiplicative one (; ).

4. Discussion

In this study, subjects with diabetes have an over 2-fold excess risk of HCC, in line with the evidence from several other case-control and cohort studies [11–13]. Further, HCC risk was higher in subjects with a longer history of diabetes. Again this is in agreement with the evidence from a few other investigations [13, 20, 25].

The mechanistic role of diabetes in HCC cancerogenesis is not straightforward. Diabetes may be a consequence of chronic liver diseases (such as cirrhosis, nonalcoholic fatty liver disease, and steatosis) [26, 27]. However, the persistence of an excess risk many years since diagnosis suggests that diabetes may be a real cause of HCC. Hyperinsulinemia and insulin resistance, which characterize diabetes, and the consequent upregulation of the insulin-like growth factor-1/insulin receptor substrate-1 system, may also explain the association between diabetes and HCC [28, 29]. Changes in the hepatic activity and mitosis related to metabolic alterations or to impaired liver function in diabetics are other possible explanations of the association observed [30].

Our study suggests that use of oral antidiabetic drugs, in particular metformin, reduces the risk of HCC, while insulin is associated with an increased risk. A few other investigations found an inverse association with metformin [31–34] and a direct one with insulin [35–37] and also sulfonylureas [31, 32]. This is in line with the observation that metformin reduces insulin resistance, suppresses tumour formation, and inhibits cell growth, while insulin may promote carcinogenesis [38, 39]. However, potential confounders, such as the severity of diabetes and the variable baseline characteristics of patients using different drugs may influence the association between antidiabetic drugs and the subsequent risk of developing HCC.

Cases and controls in our study came from comparable catchment areas, were interviewed by uniformly trained interviewers, and were unaware of a possible link between diabetes and liver cancer, thereby reducing the likelihood of potential selection and recall bias. Our study has however some limitations. First, our questionnaire recorded frequency of alcohol consumption one year before cancer diagnosis (for cases) or interview date (for controls), and we have no information on duration of use or lifetime alcohol intake. Thus, alcohol information was not interpretable in our database due to frequent cessation of alcohol consumption in subjects with hepatitis and other chronic liver diseases. Consequently, we used information on alcohol only as a covariate for multivariate analysis, though we recognize that this may have led to some underadjustment. In the absence of allowance for alcohol, the OR for diabetes was 2.46 (95% CI 1.60–3.79), thus suggesting that even more accurate allowance for alcohol is unlikely to largely or totally explain the association with diabetes. Anyway, alcohol consumption was moderately associated with liver cancer [40]. Second, information on hepatitis was valid in cases, since it was based on third generation immunoassay; this does not apply to all controls, though the almost 3% prevalence of hepatitis is in broad agreement with data from the Italian general population [5]. When we added a term for hepatitis to the model, the OR for diabetes became 4.75 (95% CI, 2.54–8.86). This indicates that the association between diabetes and HCC cannot be explained by a greater frequency of HBV/HCV infections among diabetic subjects. The increase of the RR is due to the fact that no control with hepatitis reported a history of diabetes. Thus, the models including a term for hepatitis were largely unstable and consequently were not considered in the main analyses. Third, in our models, we were unable to allow for overweight and obesity, which are strongly related to type 2 diabetes and have been positively associated with the risk of liver cancer [41, 42]. Such an association is partially or largely due to hyperinsulinemia and diabetes in overweight subjects, and may therefore represent an overadjustment. Further, history of diabetes and use of antidiabetic drugs was self-reported, and only a few subjects reported information on duration of diabetes. Our findings, however, were in agreement with those reported in other case-control and cohort studies. Moreover, self-reported history of diabetes has been reported to be satisfactorily reliable [43] and the overall prevalence of diabetes among controls is consistent with estimates from national population-based surveys [44]. Finally, concerns have been recently raised about a possible link between long-acting insulin analogue (glargine) and increased risk of selected cancers [39]. Information on the type of insulin was available for 41 out of 51 patients reporting insulin use. Among them, 19 used rapid-acting (e.g., insulin aspart, insulin lispro, and insulin glulisine) or regular/short-acting insulin, 9 used intermediate-acting (e.g., NPH) or long-acting insulin (e.g., insulin detemir, insulin glargine), and the remaining 13 patients used different types of insulin simultaneously. In particular, only 7 patients used insulin glargine, alone or in combination with other types of insulin. Therefore, numbers were too limited to analyze the different insulin types separately.

5. Conclusions

Our study confirms the over 2-fold excess risk of HCC in diabetics and suggests that use of metformin may reduce the risk of HCC, while insulin may increase the risk. The diabetes-related excess risk is even greater in diabetic subjects who are also tobacco smokers, the two factors combined yielding an over 6-fold increased risk. The attributable risk in this population is 17% for diabetes alone and 37% for diabetes and tobacco combined. This is an additional reason confirming the importance of stopping smoking in diabetics.

Conflict of Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

Authors’ Contribution

Stefania Boccia and Antonio Grieco equally contributed to this work.

Acknowledgments

This work was conducted with the contribution of the Italian Association for Cancer Research (AIRC, Grant no. 13203). Federica Turati was supported by a fellowship from the Italian Foundation for Cancer Research (FIRC). The authors thank Mrs. I. Garimoldi for editorial assistance.

References

J. Ferlay, H. R. Shin, F. Bray, D. Forman, C. Mathers, and D. M. Parkin, GLOBOCAN 2008. Cancer Incidence and Mortality Worldwide, IARC CancerBase no. 10, 2008, http://globocan.iarc.fr/.
J. Ferlay, H.-R. Shin, F. Bray, D. Forman, C. Mathers, and D. M. Parkin, “Estimates of worldwide burden of cancer in 2008: GLOBOCAN 2008,” International Journal of Cancer, vol. 127, no. 12, pp. 2893–2917, 2010.
View at: Publisher Site | Google Scholar
T. Rosso, M. Malvezzi, P. Bertuccio, E. Negri, C. La Vecchia, and A. Decarli, “Cancer mortality in Italy, 2008, and predictions for 2012,” Tumori, vol. 98, no. 5, pp. 559–567, 2012.
View at: Publisher Site | Google Scholar
S. Stuver and D. Trichopoulos, “Cancer of the liver and biliary tract,” in Cancer Epidemiology, H.-O. Adami, D. Hunter, and D. Trichpoulos, Eds., pp. 308–332, Oxford Universiy Press, New York, NY, USA, 2nd edition, 2008.
View at: Google Scholar
S. Franceschi, M. Montella, J. Polesel et al., “Hepatitis viruses, alcohol, and tobacco in the etiology of hepatocellular carcinoma in Italy,” Cancer Epidemiology Biomarkers and Prevention, vol. 15, no. 4, pp. 683–689, 2006.
View at: Publisher Site | Google Scholar
W. T. London and K. A. McGlynn, “Liver cancer,” in Cancer Epidemiology and Prevention, D. Schottenfeld and J. F. Fraumeni Jr., Eds., pp. 763–786, Oxford University Press, New York, NY, USA, 3rd edition, 2006.
View at: Google Scholar
H. B. El-Serag, “Hepatocellular carcinoma,” The New England Journal of Medicine, vol. 365, no. 12, pp. 1118–1127, 2011.
View at: Publisher Site | Google Scholar
C. Bosetti, F. Turati, and C. la Vecchia, “Hepatocellular carcinoma epidemiology,” Best Practice & Research Clinical Gastroenterology, vol. 28, pp. 753–770, 2014.
View at: Google Scholar
C. La Vecchia, E. Negri, A. Decarli, and S. Franceschi, “Diabetes mellitus and the risk of primary liver cancer,” International Journal of Cancer, vol. 73, no. 2, pp. 204–207, 1997.
View at: Publisher Site | Google Scholar
H. B. El-Serag, T. Tran, and J. E. Everhart, “Diabetes increases the risk of chronic liver disease and hepatocellular carcinoma,” Gastroenterology, vol. 126, no. 2, pp. 460–468, 2004.
View at: Publisher Site | Google Scholar
H. B. El-Serag, H. Hampel, and F. Javadi, “The association between diabetes and hepatocellular carcinoma: a systematic review of epidemiologic evidence,” Clinical Gastroenterology and Hepatology, vol. 4, no. 3, pp. 369–380, 2006.
View at: Publisher Site | Google Scholar
C. Wang, X. Wang, G. Gong et al., “Increased risk of hepatocellular carcinoma in patients with diabetes mellitus: a systematic review and meta-analysis of cohort studies,” International Journal of Cancer, vol. 130, no. 7, pp. 1639–1648, 2012.
View at: Publisher Site | Google Scholar
P. Wang, D. Kang, W. Cao, Y. Wang, and Z. Liu, “Diabetes mellitus and risk of hepatocellular carcinoma: a systematic review and meta-analysis,” Diabetes/Metabolism Research and Reviews, vol. 28, no. 2, pp. 109–122, 2012.
View at: Publisher Site | Google Scholar
C. Bosetti, V. Rosato, J. Polesel et al., “Diabetes mellitus and cancer risk in a network of case-control studies,” Nutrition and Cancer, vol. 64, no. 5, pp. 643–651, 2012.
View at: Publisher Site | Google Scholar
T. M. Welzel, B. I. Graubard, S. Quraishi et al., “Population-attributable fractions of risk factors for hepatocellular carcinoma in the United States,” American Journal of Gastroenterology, vol. 108, no. 8, pp. 1314–1321, 2013.
View at: Publisher Site | Google Scholar
G. C. Connolly, S. Safadjou, R. Chen et al., “Diabetes mellitus is associated with the presence of metastatic spread at disease presentation in hepatocellular carcinoma,” Cancer Investigation, vol. 30, no. 10, pp. 698–702, 2012.
View at: Publisher Site | Google Scholar
W.-Y. Shau, Y.-Y. Shao, Y.-C. Yeh et al., “Diabetes mellitus is associated with increased mortality in patients receiving curative therapy for hepatocellular carcinoma,” Oncologist, vol. 17, no. 6, pp. 856–862, 2012.
View at: Publisher Site | Google Scholar
D. Soranna, L. Scotti, A. Zambon et al., “Cancer risk associated with use of metformin and sulfonylurea in type 2 diabetes: a meta-analysis,” Oncologist, vol. 17, no. 6, pp. 813–822, 2012.
View at: Publisher Site | Google Scholar
C. Bosetti, V. Rosato, D. Buniato, A. Zambon, C. La Vecchia, and G. Corrao, “Cancer risk for patients using thiazolidinediones for type 2 diabetes: a meta-analysis,” The Oncologist, vol. 18, no. 2, pp. 148–156, 2013.
View at: Publisher Site | Google Scholar
S. Schlesinger, K. Aleksandrova, T. Pischon et al., “Diabetes mellitus, insulin treatment, diabetes duration, and risk of biliary tract cancer and hepatocellular carcinoma in a European Cohort,” Annals of Oncology, vol. 24, no. 9, pp. 2449–2455, 2013.
View at: Publisher Site | Google Scholar
J. Bruix and M. Sherman, “Management of hepatocellular carcinoma,” Hepatology, vol. 42, no. 5, pp. 1208–1236, 2005.
View at: Publisher Site | Google Scholar
N. E. Breslow and N. E. Day, Statistical Methods in Cancer Research. Vol. I. The Analysis of Case-Control Studies, IARC Scientific Publications no. 32, IARC, Lyon, France, 1980.
K. Rothmann, “Measuring interactions,” in Epidemiology: An Introduction, Oxford University Press, Oxford, UK, 2002.
View at: Google Scholar
D. W. Hosmer and S. Lemeshow, “Confidence interval estimation of interaction,” Epidemiology, vol. 3, no. 5, pp. 452–456, 1992.
View at: Publisher Site | Google Scholar
G. Y. Lai, Y. Park, P. Hartge, A. R. Hollenbeck, and N. D. Freedman, “The association between self-reported diabetes and cancer incidence in the NIH-AARP diet and health study,” The Journal of Clinical Endocrinology & Metabolism, vol. 98, no. 3, pp. E497–E502, 2013.
View at: Publisher Site | Google Scholar
R. P. Beasley, “Diabetes and hepatocellular carcinoma,” Hepatology, vol. 44, no. 6, pp. 1408–1410, 2006.
View at: Publisher Site | Google Scholar
M. Shibata, Y. Kihara, M. Taguchi, M. Tashiro, and M. Otsuki, “Nonalcoholic fatty liver disease is a risk factor for type 2 diabetes in middle-aged Japanese men,” Diabetes Care, vol. 30, no. 11, pp. 2940–2944, 2007.
View at: Publisher Site | Google Scholar
S. Tanaka, L. Mohr, E. V. Schmidt, K. Sugimachi, and J. R. Wands, “Biological effects of human insulin receptor substrate-1 overexpression in hepatocytes,” Hepatology, vol. 26, no. 3, pp. 598–604, 1997.
View at: Publisher Site | Google Scholar
E. Giovannucci, D. M. Harlan, M. C. Archer et al., “Diabetes and cancer: a consensus report,” Diabetes Care, vol. 33, no. 7, pp. 1674–1685, 2010.
View at: Publisher Site | Google Scholar
E. S. Dellon and N. J. Shaheen, “Diabetes and hepatocellular carcinoma: associations, biologic plausibility, and clinical implications,” Gastroenterology, vol. 129, no. 3, pp. 1132–1134, 2005.
View at: Publisher Site | Google Scholar
S. A. Oliveria, C. E. Koro, M. U. Yood, and M. Sowell, “Cancer incidence among patients treated with antidiabetic pharmacotherapy,” Diabetes and Metabolic Syndrome: Clinical Research and Reviews, vol. 2, no. 1, pp. 47–57, 2008.
View at: Publisher Site | Google Scholar
V. Donadon, M. Balbi, M. D. Mas, P. Casarin, and G. Zanette, “Metformin and reduced risk of hepatocellular carcinoma in diabetic patients with chronic liver disease,” Liver International, vol. 30, no. 5, pp. 750–758, 2010.
View at: Publisher Site | Google Scholar
M. M. Hassan, S. A. Curley, D. Li et al., “Association of diabetes duration and diabetes treatment with the risk of hepatocellular carcinoma,” Cancer, vol. 116, no. 8, pp. 1938–1946, 2010.
View at: Publisher Site | Google Scholar
M.-S. Lee, C.-C. Hsu, M. L. Wahlqvist, H.-N. Tsai, Y.-H. Chang, and Y.-C. Huang, “Type 2 diabetes increases and metformin reduces total, colorectal, liver and pancreatic cancer incidences in Taiwanese: a representative population prospective cohort study of 800,000 individuals,” BMC Cancer, vol. 11, article 20, 2011.
View at: Publisher Site | Google Scholar
J. Luo, R. Chlebowski, S. Liu et al., “Diabetes mellitus as a risk factor for gastrointestinal cancers among postmenopausal women,” Cancer Causes and Control, vol. 24, no. 3, pp. 577–585, 2013.
View at: Publisher Site | Google Scholar
B. Carstensen, D. R. Witte, and S. Friis, “Cancer occurrence in Danish diabetic patients: duration and insulin effects,” Diabetologia, vol. 55, no. 4, pp. 948–958, 2012.
View at: Publisher Site | Google Scholar
C.-H. Chang, J.-W. Lin, L.-C. Wu, M.-S. Lai, and L.-M. Chuang, “Oral insulin secretagogues, insulin, and cancer risk in type 2 diabetes mellitus,” The Journal of Clinical Endocrinology & Metabolism, vol. 97, no. 7, pp. E1170–E1175, 2012.
View at: Publisher Site | Google Scholar
C. La Vecchia, “Diabetes mellitus, medications for type 2 diabetes mellitus, and cancer risk,” Metabolism: Clinical and Experimental, vol. 60, no. 10, pp. 1357–1358, 2011.
View at: Publisher Site | Google Scholar
E. Badrick and A. G. Renehan, “Diabetes and cancer: 5 years into the recent controversy,” European Journal of Cancer, vol. 50, pp. 2119–2125, 2014.
View at: Publisher Site | Google Scholar
F. Turati, C. Galeone, M. Rota et al., “Alcohol and liver cancer: a systematic review and meta-analysis of prospective studies,” Annals of Oncology, vol. 25, pp. 1526–1535, 2014.
View at: Publisher Site | Google Scholar
E. E. Calle, C. Rodriguez, K. Walker-Thurmond, and M. J. Thun, “Overweight, obesity, and mortality from cancer in a prospectively studied cohort of U.S. adults,” The New England Journal of Medicine, vol. 348, no. 17, pp. 1625–1638, 2003.
View at: Publisher Site | Google Scholar
S. C. Larsson and A. Wolk, “Overweight, obesity and risk of liver cancer: a meta-analysis of cohort studies,” British Journal of Cancer, vol. 97, no. 7, pp. 1005–1008, 2007.
View at: Publisher Site | Google Scholar
C. Bosetti, A. Tavani, E. Negri, D. Trichopoulos, and C. La Vecchia, “Reliability of data on medical conditions, menstrual and reproductive history provided by hospital controls,” Journal of Clinical Epidemiology, vol. 54, no. 9, pp. 902–906, 2001.
View at: Publisher Site | Google Scholar
EPICENTRO, Rapporto nazionale Passi 2009: rischio cardiovascolare, Italian Institute of Public Health, 2010, http://www.epicentro.iss.it/passi/rapporto2009/Cardiovascolare09.asp.

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Copyright © 2015 Luca Miele et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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