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Salicylic Acid and Risk of Colorectal Cancer: A Two-Sample Mendelian Randomization Study.

Aayah NounuRebecca C RichmondIsobel D StewartPraveen SurendranNicholas J WarehamAdam ButterworthStephanie J WeinsteinDemetrius AlbanesJohn A BaronJohn L HopperJane C FigueiredoPolly A NewcombNoralane M LindorGraham CaseyElizabeth A PlatzLoic Le MarchandCornelia M UlrichChristopher I LiFränzel J B van DujinhovenAndrea GsurPeter T CampbellVictor MorenoPavel VodickaLudmila VodickovaEfrat AmitayElizabeth AlwersJenny Chang-ClaudeLori C SakodaMartha L SlatteryRobert E SchoenMarc J GunterSergi Castellví-BelHyeong-Rok KimSun-Seog KweonAndrew T ChanLi LiWei ZhengD Timothy BishopDaniel D BuchananGraham G GilesStephen B GruberGad RennertZsofia K StadlerTabitha A HarrisonYi LinTemitope O KekuMichael O WoodsClemens SchafmayerBethany Van GuelpenSteven GallingerHeather HampelSonja I BerndtPaul D P PharoahAnnika LindblomAlicja WolkAnna H WuEmily WhiteUlrike PetersDavid A DrewDominique SchererJusto Lorenzo BermejoHermann BrennerMichael HoffmeisterAnn C WilliamsCaroline L Relton
Published in: Nutrients (2021)
Salicylic acid (SA) has observationally been shown to decrease colorectal cancer (CRC) risk. Aspirin (acetylsalicylic acid, that rapidly deacetylates to SA) is an effective primary and secondary chemopreventive agent. Through a Mendelian randomization (MR) approach, we aimed to address whether levels of SA affected CRC risk, stratifying by aspirin use. A two-sample MR analysis was performed using GWAS summary statistics of SA (INTERVAL and EPIC-Norfolk, N = 14,149) and CRC (CCFR, CORECT, GECCO and UK Biobank, 55,168 cases and 65,160 controls). The DACHS study (4410 cases and 3441 controls) was used for replication and stratification of aspirin-use. SNPs proxying SA were selected via three methods: (1) functional SNPs that influence the activity of aspirin-metabolising enzymes; (2) pathway SNPs present in enzymes' coding regions; and (3) genome-wide significant SNPs. We found no association between functional SNPs and SA levels. The pathway and genome-wide SNPs showed no association between SA and CRC risk (OR: 1.03, 95% CI: 0.84-1.27 and OR: 1.08, 95% CI: 0.86-1.34, respectively). Results remained unchanged upon aspirin use stratification. We found little evidence to suggest that an SD increase in genetically predicted SA protects against CRC risk in the general population and upon stratification by aspirin use.
Keyphrases
  • genome wide
  • low dose
  • dna methylation
  • cardiovascular events
  • antiplatelet therapy
  • gene expression
  • acute coronary syndrome
  • magnetic resonance imaging
  • cardiovascular disease
  • coronary artery disease
  • cross sectional