Self-reported whole-grain intake and plasma alkylresorcinol concentrations in combination in relation to the incidence of colorectal cancer

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Standard

Self-reported whole-grain intake and plasma alkylresorcinol concentrations in combination in relation to the incidence of colorectal cancer. / Knudsen, Markus Dines; Kyrø, Cecilie; Olsen, Anja; Dragsted, Lars Ove; Skeie, Guri; Lund, Eiliv; Aman, Per; Nilsson, Lena M; Bueno-de-Mesquita, H B; Tjønneland, Anne; Landberg, Rikard.

I: American Journal of Epidemiology, Bind 179, Nr. 10, 2014, s. 1188-1196.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Knudsen, MD, Kyrø, C, Olsen, A, Dragsted, LO, Skeie, G, Lund, E, Aman, P, Nilsson, LM, Bueno-de-Mesquita, HB, Tjønneland, A & Landberg, R 2014, 'Self-reported whole-grain intake and plasma alkylresorcinol concentrations in combination in relation to the incidence of colorectal cancer', American Journal of Epidemiology, bind 179, nr. 10, s. 1188-1196. https://doi.org/10.1093/aje/kwu031

APA

Knudsen, M. D., Kyrø, C., Olsen, A., Dragsted, L. O., Skeie, G., Lund, E., Aman, P., Nilsson, L. M., Bueno-de-Mesquita, H. B., Tjønneland, A., & Landberg, R. (2014). Self-reported whole-grain intake and plasma alkylresorcinol concentrations in combination in relation to the incidence of colorectal cancer. American Journal of Epidemiology, 179(10), 1188-1196. https://doi.org/10.1093/aje/kwu031

Vancouver

Knudsen MD, Kyrø C, Olsen A, Dragsted LO, Skeie G, Lund E o.a. Self-reported whole-grain intake and plasma alkylresorcinol concentrations in combination in relation to the incidence of colorectal cancer. American Journal of Epidemiology. 2014;179(10):1188-1196. https://doi.org/10.1093/aje/kwu031

Author

Knudsen, Markus Dines ; Kyrø, Cecilie ; Olsen, Anja ; Dragsted, Lars Ove ; Skeie, Guri ; Lund, Eiliv ; Aman, Per ; Nilsson, Lena M ; Bueno-de-Mesquita, H B ; Tjønneland, Anne ; Landberg, Rikard. / Self-reported whole-grain intake and plasma alkylresorcinol concentrations in combination in relation to the incidence of colorectal cancer. I: American Journal of Epidemiology. 2014 ; Bind 179, Nr. 10. s. 1188-1196.

Bibtex

@article{415c23e3b9054acdbcb568a2b3f62e3e,
title = "Self-reported whole-grain intake and plasma alkylresorcinol concentrations in combination in relation to the incidence of colorectal cancer",
abstract = "Self-reported food frequency questionnaires (FFQs) have occasionally been used to investigate the association between whole-grain intake and the incidence of colorectal cancer, but the results from those studies have been inconsistent. We investigated this association using intakes of whole grains and whole-grain products measured via FFQs and plasma alkylresorcinol concentrations, a biomarker of whole-grain wheat and rye intake, both separately and in combination (Howe's score with ranks). We conducted a nested case-control study in a cohort from a research project on Nordic health and whole-grain consumption (HELGA, 1992-1998). Incidence rate ratios and 95% confidence intervals were calculated using conditional logistic regression. Plasma alkylresorcinol concentrations alone and Howe's score with ranks were inversely associated with the incidence of distal colon cancer when the highest quartile was compared with the lowest (for alkylresorcinol concentrations, incidence rate ratio = 0.34, 95% confidence interval: 0.13, 0.92; for Howe's score with ranks, incidence rate ratio = 0.35, 95% confidence interval: 0.15, 0.86). No association was observed between whole-grain intake and any colorectal cancer (colon, proximal, distal or rectum cancer) when using an FFQ as the measure/exposure variable for whole-grain intake. The results suggest that assessing whole-grain intake using a combination of FFQs and biomarkers slightly increases the precision in estimating the risk of colon or rectal cancer by reducing the impact of misclassification, thereby increasing the statistical power of the study.",
author = "Knudsen, {Markus Dines} and Cecilie Kyr{\o} and Anja Olsen and Dragsted, {Lars Ove} and Guri Skeie and Eiliv Lund and Per Aman and Nilsson, {Lena M} and Bueno-de-Mesquita, {H B} and Anne Tj{\o}nneland and Rikard Landberg",
note = "CURIS 2014 NEXS 175",
year = "2014",
doi = "10.1093/aje/kwu031",
language = "English",
volume = "179",
pages = "1188--1196",
journal = "American Journal of Epidemiology",
issn = "0002-9262",
publisher = "Oxford University Press",
number = "10",

}

RIS

TY - JOUR

T1 - Self-reported whole-grain intake and plasma alkylresorcinol concentrations in combination in relation to the incidence of colorectal cancer

AU - Knudsen, Markus Dines

AU - Kyrø, Cecilie

AU - Olsen, Anja

AU - Dragsted, Lars Ove

AU - Skeie, Guri

AU - Lund, Eiliv

AU - Aman, Per

AU - Nilsson, Lena M

AU - Bueno-de-Mesquita, H B

AU - Tjønneland, Anne

AU - Landberg, Rikard

N1 - CURIS 2014 NEXS 175

PY - 2014

Y1 - 2014

N2 - Self-reported food frequency questionnaires (FFQs) have occasionally been used to investigate the association between whole-grain intake and the incidence of colorectal cancer, but the results from those studies have been inconsistent. We investigated this association using intakes of whole grains and whole-grain products measured via FFQs and plasma alkylresorcinol concentrations, a biomarker of whole-grain wheat and rye intake, both separately and in combination (Howe's score with ranks). We conducted a nested case-control study in a cohort from a research project on Nordic health and whole-grain consumption (HELGA, 1992-1998). Incidence rate ratios and 95% confidence intervals were calculated using conditional logistic regression. Plasma alkylresorcinol concentrations alone and Howe's score with ranks were inversely associated with the incidence of distal colon cancer when the highest quartile was compared with the lowest (for alkylresorcinol concentrations, incidence rate ratio = 0.34, 95% confidence interval: 0.13, 0.92; for Howe's score with ranks, incidence rate ratio = 0.35, 95% confidence interval: 0.15, 0.86). No association was observed between whole-grain intake and any colorectal cancer (colon, proximal, distal or rectum cancer) when using an FFQ as the measure/exposure variable for whole-grain intake. The results suggest that assessing whole-grain intake using a combination of FFQs and biomarkers slightly increases the precision in estimating the risk of colon or rectal cancer by reducing the impact of misclassification, thereby increasing the statistical power of the study.

AB - Self-reported food frequency questionnaires (FFQs) have occasionally been used to investigate the association between whole-grain intake and the incidence of colorectal cancer, but the results from those studies have been inconsistent. We investigated this association using intakes of whole grains and whole-grain products measured via FFQs and plasma alkylresorcinol concentrations, a biomarker of whole-grain wheat and rye intake, both separately and in combination (Howe's score with ranks). We conducted a nested case-control study in a cohort from a research project on Nordic health and whole-grain consumption (HELGA, 1992-1998). Incidence rate ratios and 95% confidence intervals were calculated using conditional logistic regression. Plasma alkylresorcinol concentrations alone and Howe's score with ranks were inversely associated with the incidence of distal colon cancer when the highest quartile was compared with the lowest (for alkylresorcinol concentrations, incidence rate ratio = 0.34, 95% confidence interval: 0.13, 0.92; for Howe's score with ranks, incidence rate ratio = 0.35, 95% confidence interval: 0.15, 0.86). No association was observed between whole-grain intake and any colorectal cancer (colon, proximal, distal or rectum cancer) when using an FFQ as the measure/exposure variable for whole-grain intake. The results suggest that assessing whole-grain intake using a combination of FFQs and biomarkers slightly increases the precision in estimating the risk of colon or rectal cancer by reducing the impact of misclassification, thereby increasing the statistical power of the study.

U2 - 10.1093/aje/kwu031

DO - 10.1093/aje/kwu031

M3 - Journal article

C2 - 24699786

VL - 179

SP - 1188

EP - 1196

JO - American Journal of Epidemiology

JF - American Journal of Epidemiology

SN - 0002-9262

IS - 10

ER -

ID: 116550159