Pre-diagnostic circulating resistin concentrations and mortality among individuals with colorectal cancer: Results from the European Prospective Investigation into Cancer and Nutrition study

Thu Thi Pham, Katharina Nimptsch, Krasimira Aleksandrova, Mazda Jenab, Veronika Fedirko, Kana Wu, Anne Kirstine Eriksen, Anne Tjønneland, Gianluca Severi, Joseph Rothwell, Rudolf Kaaks, Verena Katzke, Alberto Catalano, Claudia Agnoli, Giovanna Masala, Maria Santucci De Magistris, Rosario Tumino, Roel Vermeulen, Amaia Aizpurua, Camino Trobajo-SanmartínMaría Dolores Chirlaque, Maria Jose Sánchez, Sai San Moon Lu, Amanda J. Cross, Sofia Christakoudi, Elisabete Vainio Weiderpass, Tobias Pischon

Research output: Contribution to journalArticlepeer-review

Abstract

Resistin is a protein involved in inflammation and angiogenesis processes and may play a role in the progression of colorectal cancer (CRC). However, it remains unclear whether resistin is associated with increased mortality after CRC diagnosis. We examined pre-diagnostic serum resistin concentrations in relation to CRC-specific and all-cause mortality among 1343 incident CRC cases from the European Prospective Investigation into Cancer and Nutrition cohort. For CRC-specific mortality as the primary outcome, hazard ratios (HRs) and 95% confidence intervals (95% CI) were estimated from competing risk analyses based on cause-specific Cox proportional hazards models and further in sensitivity analyses using Fine–Gray proportional subdistribution hazards models. For all-cause mortality as the secondary outcome, Cox proportional hazards models were used. Subgroup analyses were performed by sex, tumor subsite, tumor stage, body mass index and time to CRC diagnosis. Resistin was measured on a median of 4.8 years before CRC diagnosis. During a median follow-up of 8.2 years, 474 deaths from CRC and 147 deaths from other causes were observed. Resistin concentrations were not associated with CRC-specific mortality (HRQ4vsQ1 = 0.95, 95% CI: 0.73–1.23; Ptrend =.97; and HRper doubling of resistin concentration = 1.00; 95% CI: 0.84–1.19; P =.98) or all-cause mortality. Results from competing risk (sensitivity) analysis were similar. No associations were found in any subgroup analyses. These findings suggest no association between pre-diagnostic circulating resistin concentrations and CRC-specific or all-cause mortality among persons with CRC, and the potential insignificance of resistin in CRC progression.

Original languageEnglish (US)
Pages (from-to)1596-1606
Number of pages11
JournalInternational journal of cancer
Volume154
Issue number9
DOIs
StatePublished - May 1 2024

Keywords

  • colorectal cancer
  • EPIC
  • mortality
  • pre-diagnostic
  • resistin
  • survival

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

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