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The protective effect of dietary folate intake on gastric cancer is modified by alcohol consumption: A pooled analysis of the StoP Consortium.

Sandra González-PalaciosLaura-María Compañ-GabucioLaura Torres-ColladoAlejandro Oncina-CanovasManuela García-de-la-HeraGiulia CollatuzzoEva NegriClaudio PelucchiMatteo RotaLizbeth López-CarrilloNuno LunetSamantha MoraisMary H WardVicente MartinMacarena Lozano-LorcaReza MalekzadehMohammadreza PaksereshtRaúl Ulises Hernández-RamírezRossella BonziLinia PatelMalaquias López-CervantesCharles S RabkinShoichiro TsuganeAkihisa HidakaAntonia TrichopoulouAnna KarakatsaniM Constanza CamargoMaria Paula CuradoZuo-Feng ZhangCarlo La VecchiaPaolo BoffettaJesús Vioque
Published in: International journal of cancer (2024)
Dietary folate intake has been identified as a potentially modifiable factor of gastric cancer (GC) risk, although the evidence is still inconsistent. We evaluate the association between dietary folate intake and the risk of GC as well as the potential modification effect of alcohol consumption. We pooled data for 2829 histologically confirmed GC cases and 8141 controls from 11 case-control studies from the international Stomach Cancer Pooling Consortium. Dietary folate intake was estimated using food frequency questionnaires. We used linear mixed models with random intercepts for each study to calculate adjusted odds ratios (OR) and 95% confidence interval (CI). Higher folate intake was associated with a lower risk of GC, although this association was not observed among participants who consumed >2.0 alcoholic drinks/day. The OR for the highest quartile of folate intake, compared with the lowest quartile, was 0.78 (95% CI, 0.67-0.90, P-trend = 0.0002). The OR per each quartile increment was 0.92 (95% CI, 0.87-0.96) and, per every 100 μg/day of folate intake, was 0.89 (95% CI, 0.84-0.95). There was a significant interaction between folate intake and alcohol consumption (P-interaction = 0.02). The lower risk of GC associated with higher folate intake was not observed in participants who consumed >2.0 drinks per day, OR Q4v Q1  = 1.15 (95% CI, 0.85-1.56), and the OR 100 μg/day  = 1.02 (95% CI, 0.92-1.15). Our study supports a beneficial effect of folate intake on GC risk, although the consumption of >2.0 alcoholic drinks/day counteracts this beneficial effect.
Keyphrases
  • alcohol consumption
  • weight gain
  • case control
  • clinical trial
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  • risk assessment
  • body mass index
  • mass spectrometry
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  • drug induced