| Literature DB >> 29377173 |
Julia Butt1, Mazda Jenab2, Martina Willhauck-Fleckenstein1, Angelika Michel1, Michael Pawlita1, Cecilie Kyrø3, Anne Tjønneland3, Marie-Christine Boutron-Ruault4,5, Franck Carbonnel4,5,6, Gianluca Severi4,5, Rudolf Kaaks7, Tilman Kühn7, Heiner Boeing8, Antonia Trichopoulou9,10, Carlo la Vecchia9,11, Anna Karakatsani9,12, Salvatore Panico13, Rosario Tumino14, Claudia Agnoli15, Domenico Palli16, Carlotta Sacerdote17, H B As Bueno-de-Mesquita18,19,20,21, Elisabete Weiderpass22,23,24,25, Maria-José Sánchez26,27, Catalina Bonet Bonet28, José María Huerta27,29, Eva Ardanaz27,30,31, Kathryn Bradbury32, Marc Gunter2, Neil Murphy2, Heinz Freisling2, Elio Riboli20, Kostas Tsilidis20,33, Dagfinn Aune20, Tim Waterboer1, David J Hughes34.
Abstract
The gut microbiome is increasingly implicated in colorectal cancer (CRC) development. A subgroup of patients diagnosed with CRC show high antibody responses to Streptococcus gallolyticus subspecies gallolyticus (SGG). However, it is unclear whether the association is also present pre-diagnostically. We assessed the association of antibody responses to SGG proteins in pre-diagnostic serum samples with CRC risk in a case-control study nested within a prospective cohort. Pre-diagnostic serum samples from 485 first incident CRC cases (mean time between blood draw and diagnosis 3.4 years) and 485 matched controls in the European Prospective Investigation into Nutrition and Cancer (EPIC) study were analyzed for antibody responses to 11 SGG proteins using multiplex serology. Odds ratios (OR) and 95% confidence intervals (CI) were estimated using multivariable conditional logistic regression models. Antibody positivity for any of the 11 SGG proteins was significantly associated with CRC risk with 56% positive controls compared to 63% positive cases (OR: 1.36, 95% CI: 1.04-1.77). Positivity for two or more proteins of a previously identified SGG 6-marker panel with greater CRC-specificity was also observed among 9% of controls compared to 17% of CRC cases, corresponding to a significantly increased CRC risk (OR: 2.17, 95% CI: 1.44-3.27). In this prospective nested case-control study, we observed a positive association between antibody responses to SGG and CRC development in serum samples taken before evident disease onset. Further work is required to establish the possibly etiological significance of these observations and whether SGG serology may be applicable for CRC risk stratification.Entities:
Keywords: Streptococcus gallolyticus; antibodies; bacterial serology; colorectal neoplasms; prospective cohort
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Year: 2018 PMID: 29377173 DOI: 10.1002/ijc.31283
Source DB: PubMed Journal: Int J Cancer ISSN: 0020-7136 Impact factor: 7.396