Marine ω-3 polyunsaturated fatty acid intake and survival after colorectal cancer diagnosis.
| Authors | |
| Abstract | OBJECTIVE: Experimental evidence supports an antineoplastic activity of marine ω-3 polyunsaturated fatty acids (ω-3 PUFAs; including eicosapentaenoic acid, docosahexaenoic acid and docosapentaenoic acid). However, the influence of ω-3 PUFAs on colorectal cancer (CRC) survival is unknown. DESIGN: Within the Nurses' Health Study and Health Professionals Follow-up Study, we prospectively studied CRC-specific and overall mortality in a cohort of 1659 patients with CRC according to intake of marine ω-3 PUFAs and its change after diagnosis. RESULTS: Higher intake of marine ω-3 PUFAs after CRC diagnosis was associated with lower risk of CRC-specific mortality (p for trend=0.03). Compared with patients who consumed 0.10 g/day of marine ω-3 PUFAs, those consuming at least 0.30 g/day had an adjusted HR for CRC-specific mortality of 0.59 (95% CI 0.35 to 1.01). Patients who increased their marine ω-3 PUFA intake by at least 0.15 g/day after diagnosis had an HR of 0.30 (95% CI 0.14 to 0.64, p for trend 0.001) for CRC deaths, compared with those who did not change or changed their intake by 0.02 g/day. No association was found between postdiagnostic marine ω-3 PUFA intake and all-cause mortality (p for trend=0.47). CONCLUSIONS: High marine ω-3 PUFA intake after CRC diagnosis is associated with lower risk of CRC-specific mortality. Increasing consumption of marine ω-3 PUFAs after diagnosis may confer additional benefits to patients with CRC. |
| Year of Publication | 2016
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| Journal | Gut
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| Date Published | 2016 Jul 19
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| ISSN | 1468-3288
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| DOI | 10.1136/gutjnl-2016-311990
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| PubMed ID | 27436272
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| Links | |
| Grant list | K07 CA188126 / CA / NCI NIH HHS / United States
K24 DK098311 / DK / NIDDK NIH HHS / United States
P01 CA055075 / CA / NCI NIH HHS / United States
P01 CA087969 / CA / NCI NIH HHS / United States
P50 CA127003 / CA / NCI NIH HHS / United States
R01 CA137178 / CA / NCI NIH HHS / United States
R01 CA151993 / CA / NCI NIH HHS / United States
R03 CA176717 / CA / NCI NIH HHS / United States
R35 CA197735 / CA / NCI NIH HHS / United States
UM1 CA167552 / CA / NCI NIH HHS / United States
UM1 CA186107 / CA / NCI NIH HHS / United States
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