Tier 4 — mechanistic

Choline and betaine intake and colorectal cancer risk in Chinese population: a case-control study

Min-Shan Lu, Yu-Jing Fang, Zhi-Zhong Pan, Xiao Zhong, Mei-Chun Zheng, Yu-Ming Chen, Cai-Xia Zhang
PloS one 2015 10(3):e0118661

Bibliography

PubMed
PMID 25785727
PubMed Central
PMC4364675
Funding
Reported funding/support: This study was jointly supported by the Sun Yat-sen University Hundred Talents Program (51000-3181301) and Danone Nutrition Research and Education Foundation (No: DIC2011-03). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests
Reported disclosure: Competing Interests: The authors have declared that no competing interests exist.

Study snapshot

DesignCase-control study
ModelHuman participants
Sample890 colorectal-cancer cases and 890 controls
InterventionHabitual dietary choline and/or betaine intake; no randomized TMG treatment
Duration2010-2013 recruitment
EndpointsColorectal-cancer odds

What the study showed, in plain terms

Published in 2015, this source examined human observational and biomarker research. Design: Case-control study. Sample/model: 890 colorectal-cancer cases and 890 controls. The exposure or intervention was Habitual dietary choline and/or betaine intake; no randomized TMG treatment. Follow-up or treatment period: 2010-2013 recruitment.

Betaine intake was not significantly associated with colorectal-cancer odds; some choline measures showed inverse associations.

Observational exposure analysis: residual confounding and reverse causation remain possible. Associations do not establish that betaine supplementation causes the same outcome. Diet recall, case selection or illness-related metabolite changes may introduce bias.

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Key findings

  • Betaine intake was not significantly associated with colorectal-cancer odds; some choline measures showed inverse associations.
  • The recorded outcome domains were Colorectal-cancer odds.
  • The exposure was observed rather than assigned as an isolated supplement treatment.

What this study can and cannot tell us

  • Observational exposure analysis: residual confounding and reverse causation remain possible. Associations do not establish that betaine supplementation causes the same outcome. Diet recall, case selection or illness-related metabolite changes may introduce bias.
  • Confounding, dietary patterns, illness, medication use and reverse causation can influence an association. Blood or dietary concentrations do not identify the effect of starting a capsule.
  • Source basis: Accessible full-text extract plus indexed bibliographic data. Missing method details, funding information or participant denominators are not inferred.

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