Exposure to bacterial products lipopolysaccharide and flagellin and hepatocellular carcinoma: a nested case-control study

نویسندگان

  • Veronika Fedirko
  • Hao Quang Tran
  • Andrew T. Gewirtz
  • Magdalena Stepien
  • Antonia Trichopoulou
  • Krasimira Aleksandrova
  • Anja Olsen
  • Anne Tjønneland
  • Kim Overvad
  • Franck Carbonnel
  • Marie-Christine Boutron-Ruault
  • Gianluca Severi
  • Tilman Kühn
  • Rudolf Kaaks
  • Heiner Boeing
  • Christina Bamia
  • Pagona Lagiou
  • Sara Grioni
  • Salvatore Panico
  • Domenico Palli
  • Rosario Tumino
  • Alessio Naccarati
  • Petra H. Peeters
  • H. B. Bueno-de-Mesquita
  • Elisabete Weiderpass
  • José María Huerta Castaño
  • Aurelio Barricarte
  • María-José Sánchez
  • Miren Dorronsoro
  • J. Ramón Quirós
  • Antonio Agudo
  • Klas Sjöberg
  • Bodil Ohlsson
  • Oskar Hemmingsson
  • Mårten Werner
  • Kathryn E. Bradbury
  • Kay-Tee Khaw
  • Nick Wareham
  • Konstantinos K. Tsilidis
  • Dagfinn Aune
  • Augustin Scalbert
  • Isabelle Romieu
  • Elio Riboli
  • Mazda Jenab
چکیده

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.

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عنوان ژورنال:

دوره 15  شماره 

صفحات  -

تاریخ انتشار 2017