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Verfasst von:Khankari, Nikhil K. [VerfasserIn]   i
 Banbury, Barbara L. [VerfasserIn]   i
 Borges, Maria C. [VerfasserIn]   i
 Haycock, Philip [VerfasserIn]   i
 Albanes, Demetrius [VerfasserIn]   i
 Arndt, Volker [VerfasserIn]   i
 Berndt, Sonja I. [VerfasserIn]   i
 Bezieau, Stephane [VerfasserIn]   i
 Brenner, Hermann [VerfasserIn]   i
 Campbell, Peter T. [VerfasserIn]   i
 Casey, Graham [VerfasserIn]   i
 Chan, Andrew T. [VerfasserIn]   i
 Chang-Claude, Jenny [VerfasserIn]   i
 Conti, David V. [VerfasserIn]   i
 Cotterchio, Michelle [VerfasserIn]   i
 English, Dallas R. [VerfasserIn]   i
 Figueiredo, Jane C. [VerfasserIn]   i
 Giles, Graham G. [VerfasserIn]   i
 Giovannucci, Edward L. [VerfasserIn]   i
 Gunter, Marc J. [VerfasserIn]   i
 Hampe, Jochen [VerfasserIn]   i
 Hoffmeister, Michael [VerfasserIn]   i
 Ulrich, Cornelia [VerfasserIn]   i
Titel:Mendelian randomization of circulating polyunsaturated fatty acids and colorectal cancer risk
Verf.angabe:Nikhil K. Khankari, Barbara L. Banbury, Maria C. Borges, Philip Haycock, Demetrius Albanes, Volker Arndt, Sonja I. Berndt, Stephane Bezieau, Hermann Brenner, Peter T. Campbell, Graham Casey, Andrew T. Chan, Jenny Chang-Claude, David V. Conti, Michelle Cotterchio, Dallas R. English, Jane C. Figueiredo, Graham G. Giles, Edward L. Giovannucci, Marc J. Gunter, Jochen Hampe, Michael Hoffmeister, John L. Hopper, Mark A. Jenkins, Amit D. Joshi, Loic Le Marchand, Mathieu Lemire, Christopher I. Li, Li Li, Annika Lindblom, Vicente Martin, Victor Moreno, Polly A. Newcomb, Kenneth Offit, Paul D. P. Pharoah, Gad Rennert, Lori C. Sakoda, Clemens Schafmayer, Stephanie L. Schmit, Martha L. Slattery, Mingyang Song, Stephen N. Thibodeau, Cornelia M. Ulrich, Stephanie J. Weinstein, Emily White, Aung Ko Win, Alicia Wolk, Michael O. Woods, Anna H. Wu, Qiuyin Cai, Joshua C. Denny, Todd L. Edwards, Harvey J. Murff, Stephen B. Gruber, Ulrike Peters, and Wei Zheng
E-Jahr:2020
Jahr:February 12, 2020
Umfang:11 S.
Fussnoten:Gesehen am 28.07.2020
Titel Quelle:Enthalten in: Cancer epidemiology, biomarkers & prevention
Ort Quelle:Philadelphia, Pa. : AACR, 1991
Jahr Quelle:2020
Band/Heft Quelle:29(2020), 4, Seite 860-870
ISSN Quelle:1538-7755
Abstract:Background: Results from epidemiologic studies examining polyunsaturated fatty acids (PUFA) and colorectal cancer risk are inconsistent. Mendelian randomization may strengthen causal inference from observational studies. Given their shared metabolic pathway, examining the combined effects of aspirin/NSAID use with PUFAs could help elucidate an association between PUFAs and colorectal cancer risk. Methods: Information was leveraged from genome-wide association studies (GWAS) regarding PUFA-associated SNPs to create weighted genetic scores (wGS) representing genetically predicted circulating blood PUFAs for 11,016 non-Hispanic white colorectal cancer cases and 13,732 controls in the Genetics and Epidemiology of Colorectal Cancer Consortium (GECCO). Associations per SD increase in the wGS were estimated using unconditional logistic regression. Interactions between PUFA wGSs and aspirin/NSAID use on colorectal cancer risk were also examined. Results: Modest colorectal cancer risk reductions were observed per SD increase in circulating linoleic acid [ORLA = 0.96; 95% confidence interval (CI) = 0.93-0.98; P = 5.2 x 10(-4)] and alpha-linolenic acid (ORA(LA) = 0.95; 95% CI = 0.92-0.97; P = 5.4 x 10(-5)), whereas modest increased risks were observed for arachidonic (ORAA = 1.06; 95% CI = 1.03-1.08; P = 3.3 x 10(-5)), eicosapentaenoic (OREPA = 1.04; 95% CI = 1.01-1.07; P = 2.5 x 10(-3)), and docosapentaenoic acids (ORDPA = 1.03; 95% CI = 1.01-1.06; P = 1.2 x 10(-2)). Each of these effects was stronger among aspirin/NSAID nonusers in the stratified analyses. Conclusions: Our study suggests that higher circulating shorter-chain PUFAs (i.e., LA and ALA) were associated with reduced colorectal cancer risk, whereas longer-chain PUFAs (i.e., AA, EPA, and DPA) were associated with an increased colorectal cancer risk. Impact: The interaction of PUFAs with aspirin/NSAID use indicates a shared colorectal cancer inflammatory pathway. Future research should continue to improve PUFA genetic instruments to elucidate the independent effects of PUFAs on colorectal cancer.
DOI:doi:10.1158/1055-9965.EPI-19-0891
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext: http://doi.org/10.1158/1055-9965.EPI-19-0891
 DOI: https://doi.org/10.1158/1055-9965.EPI-19-0891
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:adenomas
 aspirin
 colon-cancer
 dietary-intake
 epidemiology
 genome-wide association
 pleiotropic genetic-variants
 prevention
 prostaglandin e-2
 stratification
K10plus-PPN:1725685264
Verknüpfungen:→ Zeitschrift

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