TY - JOUR
T1 - Exposure to bacterial products lipopolysaccharide and flagellin and hepatocellular carcinoma
T2 - A nested case-control study
AU - Fedirko, Veronika
AU - Tran, Hao Quang
AU - Gewirtz, Andrew T.
AU - Stepien, Magdalena
AU - Trichopoulou, Antonia
AU - Aleksandrova, Krasimira
AU - Olsen, Anja
AU - Tjønneland, Anne
AU - Overvad, Kim
AU - Carbonnel, Franck
AU - Boutron-Ruault, Marie Christine
AU - Severi, Gianluca
AU - Kühn, Tilman
AU - Kaaks, Rudolf
AU - Boeing, Heiner
AU - Bamia, Christina
AU - Lagiou, Pagona
AU - Grioni, Sara
AU - Panico, Salvatore
AU - Palli, Domenico
AU - Tumino, Rosario
AU - Naccarati, Alessio
AU - Peeters, Petra H.
AU - Bueno-de-Mesquita, H. B.
AU - Weiderpass, Elisabete
AU - Castaño, José María Huerta
AU - Barricarte, Aurelio
AU - Sánchez, María José
AU - Dorronsoro, Miren
AU - Quirós, J. Ramón
AU - Agudo, Antonio
AU - Sjöberg, Klas
AU - Ohlsson, Bodil
AU - Hemmingsson, Oskar
AU - Werner, Mårten
AU - Bradbury, Kathryn E.
AU - Khaw, Kay Tee
AU - Wareham, Nick
AU - Tsilidis, Konstantinos K.
AU - Aune, Dagfinn
AU - Scalbert, Augustin
AU - Romieu, Isabelle
AU - Riboli, Elio
AU - Jenab, Mazda
N1 - Publisher Copyright:
© 2017 The Author(s).
PY - 2017/4/4
Y1 - 2017/4/4
N2 - Background: Leakage of bacterial products across the gut barrier may play a role in liver diseases which often precede the development of liver cancer. However, human studies, particularly from prospective settings, are lacking. Methods: We used a case-control study design nested within a large prospective cohort to assess the association between circulating levels of anti-lipopolysaccharide (LPS) and anti-flagellin immunoglobulin A (IgA) and G (IgG) (reflecting long-term exposures to LPS and flagellin, respectively) and risk of hepatocellular carcinoma. A total of 139 men and women diagnosed with hepatocellular carcinoma between 1992 and 2010 were matched to 139 control subjects. Multivariable rate ratios (RRs), including adjustment for potential confounders, hepatitis B/C positivity, and degree of liver dysfunction, were calculated with conditional logistic regression. Results: Antibody response to LPS and flagellin was associated with a statistically significant increase in the risk of hepatocellular carcinoma (highest vs. lowest quartile: RR = 11.76, 95% confidence interval = 1.70-81.40; P trend = 0.021). This finding did not vary substantially by time from enrollment to diagnosis, and did not change after adjustment for chronic infection with hepatitis B and C viruses. Conclusions: These novel findings, based on exposures up to several years prior to diagnosis, support a role for gut-derived bacterial products in hepatocellular carcinoma development. Further study into the role of gut barrier failure and exposure to bacterial products in liver diseases is warranted.
AB - Background: Leakage of bacterial products across the gut barrier may play a role in liver diseases which often precede the development of liver cancer. However, human studies, particularly from prospective settings, are lacking. Methods: We used a case-control study design nested within a large prospective cohort to assess the association between circulating levels of anti-lipopolysaccharide (LPS) and anti-flagellin immunoglobulin A (IgA) and G (IgG) (reflecting long-term exposures to LPS and flagellin, respectively) and risk of hepatocellular carcinoma. A total of 139 men and women diagnosed with hepatocellular carcinoma between 1992 and 2010 were matched to 139 control subjects. Multivariable rate ratios (RRs), including adjustment for potential confounders, hepatitis B/C positivity, and degree of liver dysfunction, were calculated with conditional logistic regression. Results: Antibody response to LPS and flagellin was associated with a statistically significant increase in the risk of hepatocellular carcinoma (highest vs. lowest quartile: RR = 11.76, 95% confidence interval = 1.70-81.40; P trend = 0.021). This finding did not vary substantially by time from enrollment to diagnosis, and did not change after adjustment for chronic infection with hepatitis B and C viruses. Conclusions: These novel findings, based on exposures up to several years prior to diagnosis, support a role for gut-derived bacterial products in hepatocellular carcinoma development. Further study into the role of gut barrier failure and exposure to bacterial products in liver diseases is warranted.
KW - Endotoxins
KW - Flagellin
KW - Hepatocellular carcinoma
KW - Lipopolysaccharide
KW - Prospective studies
UR - http://www.scopus.com/inward/record.url?scp=85016932578&partnerID=8YFLogxK
U2 - 10.1186/s12916-017-0830-8
DO - 10.1186/s12916-017-0830-8
M3 - Article
C2 - 28372583
AN - SCOPUS:85016932578
SN - 1741-7015
VL - 15
JO - BMC Medicine
JF - BMC Medicine
IS - 1
M1 - 72
ER -