Total and high-molecular weight adiponectin and risk of colorectal cancer: the European Prospective Investigation into Cancer and Nutrition Study.

نویسندگان

  • Krasimira Aleksandrova
  • Heiner Boeing
  • Mazda Jenab
  • H Bas Bueno-de-Mesquita
  • Eugene Jansen
  • Fränzel J B van Duijnhoven
  • Veronika Fedirko
  • Sabina Rinaldi
  • Isabelle Romieu
  • Elio Riboli
  • Dora Romaguera
  • Sabine Westphal
  • Kim Overvad
  • Anne Tjønneland
  • Marie Christine Boutron-Ruault
  • Françoise Clavel-Chapelon
  • Rudolf Kaaks
  • Annekatrin Lukanova
  • Antonia Trichopoulou
  • Pagona Lagiou
  • Dimitrios Trichopoulos
  • Claudia Agnoli
  • Amalia Mattiello
  • Calogero Saieva
  • Paolo Vineis
  • Rosario Tumino
  • Petra H Peeters
  • Marcial Argüelles
  • Catalina Bonet
  • María-José Sánchez
  • Miren Dorronsoro
  • Jose-María Huerta
  • Aurelio Barricarte
  • Richard Palmqvist
  • Göran Hallmans
  • Kay-Tee Khaw
  • Nick Wareham
  • Naomi E Allen
  • Francesca L Crowe
  • Tobias Pischon
چکیده

Adiponectin-an adipose tissue-derived protein-may provide a molecular link between obesity and colorectal cancer (CRC), but evidence from large prospective studies is limited. In particular, no epidemiological study explored high-molecular weight (HMW) and non-HMW adiponectin fractions in relation to CRC risk, despite them being hypothesized to have differential biological activities, i.e. regulating insulin sensitivity (HMW adiponectin) versus inflammatory response (non-HMW adiponectin). In a prospective, nested case-control study, we investigated whether prediagnostic serum concentrations of total, HMW and non-HMW adiponectin are associated with risk of CRC, independent of obesity and other known CRC risk factors. A total of 1206 incident cases (755 colon and 451 rectal) were matched to 1206 controls using incidence-density sampling. In conditional logistic regression, adjusted for dietary and lifestyle factors, total adiponectin and non-HMW adiponectin concentrations were inversely associated with risk of CRC [relative risk (RR) comparing highest versus lowest quintile = 0.71, 95% confidence interval (CI) = 0.53-0.95, P(trend) = 0.03 for total adiponectin and RR = 0.45, 95% CI = 0.34-0.61, P(trend) < 0.0001 for non-HMW adiponectin]. HMW adiponectin concentrations were not associated with CRC risk (RR = 0.91, 95% CI = 0.68-1.22, P(trend) = 0.55). Non-HMW adiponectin was associated with CRC risk even after adjustment for body mass index and waist circumference (RR = 0.39, 95% CI = 0.26-0.60, P(trend) < 0.0001), whereas the association with total adiponectin was no longer significant (RR = 0.81, 95% CI = 0.60-1.09, P(trend) = 0.23). When stratified by cancer site, non-HMW adiponectin was inversely associated with both colon and rectal cancer. These findings suggest an important role of the relative proportion of non-HMW adiponectin in CRC pathogenesis. Future studies are warranted to confirm these results and to elucidate the underlying mechanisms.

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عنوان ژورنال:
  • Carcinogenesis

دوره 33 6  شماره 

صفحات  -

تاریخ انتشار 2012