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Prediagnostic plasma testosterone, sex hormone-binding globulin, IGF-I and hepatocellular carcinoma: Etiological factors or risk markers?

Authors :
Lukanova, Annekatrin Becker, Susen Huesing, Anika Schock, Helena Fedirko, Veronika Trepo, Elisabeth Trichopoulou, Antonia Bamia, Christina Lagiou, Pagona Benetou, Vassiliki and Trichopoulos, Dimitrios Noethlings, Ute Tjonneland, Anne and Overvad, Kim Dossus, Laure Teucher, Birgit Boeing, Heiner and Aleksandrova, Krasimira Palli, Domenico Pala, Valeria and Panico, Salvatore Tumino, Rosario Ricceri, Fulvio and Bueno-De-Mesquita, H. Bas Siersema, Peter D. Peeters, Petra H. M. Quiros, Jose Ramon Duell, Eric J. Molina-Montes, Esther and Chirlaque, Maria-Dolores Gurrea, Aurelio Barricarte and Dorronsoro, Miren Lindkvist, Bjoern Johansen, Dorthe Werner, Marten Sund, Malin Khaw, Kay-Tee Wareham, Nick Key, Timothy J. Travis, Ruth C. Rinaldi, Sabina Romieu, Isabelle and Gunter, Marc J. Riboli, Elio Jenab, Mazda Kaaks, Rudolf
Publication Year :
2014

Abstract

Elevated prediagnostic testosterone and insulin-like growth factor I (IGF-I) concentrations have been proposed to increase risk of hepatocellular carcinoma (HCC). However, the metabolism of these hormones is altered as a consequence of liver damage and they may have clinical utility as HCC risk markers. A case-control study was nested within the European Prospective Investigation into Cancer and Nutrition cohort and included 125 incident HCC cases and 247 individually matched controls. Testosterone, sex hormone-binding globulin (SHBG) and IGF-I were analyzed by immunoassays. Odds ratios (ORs) and 95% confidence intervals (CIs) were estimated by conditional logistic regression. The area under the receiver operating curves (AUC) was calculated to assess HCC predictive ability of the tested models. After adjustments for epidemiological variables (body mass index, smoking, ethanol intake, hepatitis and diabetes) and liver damage (a score based on albumin, bilirubin, aspartate aminotransaminase, alanine aminotransaminase, gamma-glutamyltransferase and alkaline phosphatase concentrations), only SHBG remained significantly associated with risk [OR for top versus bottom tertile of 3.86 (1.32-11.3), p(trend) = 0.009]. As a single factor SHBG had an AUC of 0.81 (0.75-0.86). A small, but significant increase in AUC was observed when SHBG was added to a model including the liver damage score and epidemiological variables (from 0.89 to 0.91, p = 0.02) and a net reclassification of 0.47% (0.45-0.48). The observed associations of HCC with prediagnostic SHBG, free testosterone and IGF-I concentrations are in directions opposite to that expected under the etiological hypotheses. SHBG has a potential to be tested as prediagnostic risk marker for HCC. (c) 2013 UICC What’s new? Testosterone and insulin-like growth factor-1 (IGF-1) are implicated in the development of hepatocellular carcinoma (HCC), though their involvement may be more complex than previously thought. Here, in a unique study population with low prevalence of hepatitis infections, an association was detected between HCC risk and increased levels of sex hormone binding globulin (SHBG) and IGF-1 prior to diagnosis. Neither testosterone nor IGF-1, however, was found to have an etiological influence in the decade before diagnosis. The results suggest that SHBG and IGF-I should be considered in the clinical evaluation of patients at increased risk of HCC.

Details

Language :
English
Database :
OpenAIRE
Accession number :
edsair.od......2127..0970ffd068f160dde829298fba8f1b34