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Dietary Intake of Heterocyclic Amines, Meat-derived Mutagenic Activity, and Risk of Colorectal Adenomas

Meats cooked well-done by high temperature techniques produce mutagenic compounds such as heterocyclic amines (HCAs), but the amounts of these compounds vary by cooking techniques, temperature, time, and type of meat. We investigated the role of HCAs in the etiology of colorectal adenomas and the ex...

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Published in:Cancer epidemiology, biomarkers & prevention biomarkers & prevention, 2001-05, Vol.10 (5), p.559-562
Main Authors: SINHA, Rashmi, KULLDORFF, Martin, CHOW, Wong-Ho, DENOBILE, John, ROTHMAN, Nathaniel
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KULLDORFF, Martin
CHOW, Wong-Ho
DENOBILE, John
ROTHMAN, Nathaniel
description Meats cooked well-done by high temperature techniques produce mutagenic compounds such as heterocyclic amines (HCAs), but the amounts of these compounds vary by cooking techniques, temperature, time, and type of meat. We investigated the role of HCAs in the etiology of colorectal adenomas and the extent to which they may explain the previously observed risk for red meat and meat-cooking methods. In a case-control study of colorectal adenomas, cases ( n = 146) were diagnosed with colorectal adenomas at sigmoidoscopy or colonoscopy, and controls ( n = 228) were found not to have colorectal adenomas at sigmoidoscopy. Using a meat-derived HCA and mutagen database and responses from a meat-cooking questionnaire module, we estimated intake of 2-amino-3,4,8-trimethylimidazo[4,5-f]quinoxaline (DiMeIQx), 2-amino-3,8-dimethylimidazo[4,5-f]quinoxaline (MeIQx), 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP) and mutagenic activity. We calculated odds ratios and 95% confidence intervals using logistic regression adjusting for several established risk factors for colorectal adenomas or cancer. The odds ratios (95% confidence interval; P for trend test) fifth versus first quintiles are: 2.2 (1.2–4.1; P = 0.02) for DiMeIQx; 2.1 (1.0–4.3; P = 0.002) for MeIQx; 2.5(1.1–5.5; P = 0.02) for PhIP; and 3.1 (1.4–6.8; P = 0.001) for mutagenic activity. When the three HCAs were adjusted for the other two, only the trend for MeIQx ( P = 0.04) remained statistically significant. When we tried to disentangle the relative contribution of the three HCAs from the meat variables, we found that MeIQx remained significantly associated with risk even when adjusted for red meat but not vice versa . When MeIQx and well-done meat were analyzed in the same model, the risks were attenuated for both. Mutagenic activity from meat remained significantly associated with increased risk even when adjusted for intake of red meat or well-done red meat, whereas the red meat and well-done red meat associations were no longer significant when adjusted for total mutagenic activity. In conclusion, we found an elevated risk of colorectal adenomas associated with high intake of certain HCAs. Further, mutagenic activity from cooked meat consumption, a measure that integrates all of the classes of mutagens, was strongly associated with risk and explained the excess risk with intake of well-done red meat.
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We investigated the role of HCAs in the etiology of colorectal adenomas and the extent to which they may explain the previously observed risk for red meat and meat-cooking methods. In a case-control study of colorectal adenomas, cases ( n = 146) were diagnosed with colorectal adenomas at sigmoidoscopy or colonoscopy, and controls ( n = 228) were found not to have colorectal adenomas at sigmoidoscopy. Using a meat-derived HCA and mutagen database and responses from a meat-cooking questionnaire module, we estimated intake of 2-amino-3,4,8-trimethylimidazo[4,5-f]quinoxaline (DiMeIQx), 2-amino-3,8-dimethylimidazo[4,5-f]quinoxaline (MeIQx), 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP) and mutagenic activity. We calculated odds ratios and 95% confidence intervals using logistic regression adjusting for several established risk factors for colorectal adenomas or cancer. The odds ratios (95% confidence interval; P for trend test) fifth versus first quintiles are: 2.2 (1.2–4.1; P = 0.02) for DiMeIQx; 2.1 (1.0–4.3; P = 0.002) for MeIQx; 2.5(1.1–5.5; P = 0.02) for PhIP; and 3.1 (1.4–6.8; P = 0.001) for mutagenic activity. When the three HCAs were adjusted for the other two, only the trend for MeIQx ( P = 0.04) remained statistically significant. When we tried to disentangle the relative contribution of the three HCAs from the meat variables, we found that MeIQx remained significantly associated with risk even when adjusted for red meat but not vice versa . When MeIQx and well-done meat were analyzed in the same model, the risks were attenuated for both. Mutagenic activity from meat remained significantly associated with increased risk even when adjusted for intake of red meat or well-done red meat, whereas the red meat and well-done red meat associations were no longer significant when adjusted for total mutagenic activity. In conclusion, we found an elevated risk of colorectal adenomas associated with high intake of certain HCAs. 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prevention</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>SINHA, Rashmi</au><au>KULLDORFF, Martin</au><au>CHOW, Wong-Ho</au><au>DENOBILE, John</au><au>ROTHMAN, Nathaniel</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dietary Intake of Heterocyclic Amines, Meat-derived Mutagenic Activity, and Risk of Colorectal Adenomas</atitle><jtitle>Cancer epidemiology, biomarkers &amp; prevention</jtitle><addtitle>Cancer Epidemiol Biomarkers Prev</addtitle><date>2001-05-01</date><risdate>2001</risdate><volume>10</volume><issue>5</issue><spage>559</spage><epage>562</epage><pages>559-562</pages><issn>1055-9965</issn><eissn>1538-7755</eissn><abstract>Meats cooked well-done by high temperature techniques produce mutagenic compounds such as heterocyclic amines (HCAs), but the amounts of these compounds vary by cooking techniques, temperature, time, and type of meat. We investigated the role of HCAs in the etiology of colorectal adenomas and the extent to which they may explain the previously observed risk for red meat and meat-cooking methods. In a case-control study of colorectal adenomas, cases ( n = 146) were diagnosed with colorectal adenomas at sigmoidoscopy or colonoscopy, and controls ( n = 228) were found not to have colorectal adenomas at sigmoidoscopy. Using a meat-derived HCA and mutagen database and responses from a meat-cooking questionnaire module, we estimated intake of 2-amino-3,4,8-trimethylimidazo[4,5-f]quinoxaline (DiMeIQx), 2-amino-3,8-dimethylimidazo[4,5-f]quinoxaline (MeIQx), 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP) and mutagenic activity. We calculated odds ratios and 95% confidence intervals using logistic regression adjusting for several established risk factors for colorectal adenomas or cancer. The odds ratios (95% confidence interval; P for trend test) fifth versus first quintiles are: 2.2 (1.2–4.1; P = 0.02) for DiMeIQx; 2.1 (1.0–4.3; P = 0.002) for MeIQx; 2.5(1.1–5.5; P = 0.02) for PhIP; and 3.1 (1.4–6.8; P = 0.001) for mutagenic activity. When the three HCAs were adjusted for the other two, only the trend for MeIQx ( P = 0.04) remained statistically significant. When we tried to disentangle the relative contribution of the three HCAs from the meat variables, we found that MeIQx remained significantly associated with risk even when adjusted for red meat but not vice versa . When MeIQx and well-done meat were analyzed in the same model, the risks were attenuated for both. Mutagenic activity from meat remained significantly associated with increased risk even when adjusted for intake of red meat or well-done red meat, whereas the red meat and well-done red meat associations were no longer significant when adjusted for total mutagenic activity. In conclusion, we found an elevated risk of colorectal adenomas associated with high intake of certain HCAs. Further, mutagenic activity from cooked meat consumption, a measure that integrates all of the classes of mutagens, was strongly associated with risk and explained the excess risk with intake of well-done red meat.</abstract><cop>Philadelphia, PA</cop><pub>American Association for Cancer Research</pub><pmid>11352869</pmid><tpages>4</tpages></addata></record>
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ispartof Cancer epidemiology, biomarkers & prevention, 2001-05, Vol.10 (5), p.559-562
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1538-7755
language eng
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source Free E-Journal (出版社公開部分のみ)
subjects Adenoma - epidemiology
Adenoma - etiology
Adult
Aged
Amines - adverse effects
Biological and medical sciences
Carcinogenesis, carcinogens and anticarcinogens
Case-Control Studies
Colorectal Neoplasms - epidemiology
Colorectal Neoplasms - etiology
Confidence Intervals
Diet - adverse effects
Female
Food Handling - methods
Foods and miscellaneous
Heterocyclic Compounds - adverse effects
Hot Temperature
Humans
Logistic Models
Male
Meat - adverse effects
Medical sciences
Middle Aged
Mutagenicity Tests
Mutagens - adverse effects
Mutagens - chemistry
Odds Ratio
Reference Values
Risk Assessment
Risk Factors
Tumors
title Dietary Intake of Heterocyclic Amines, Meat-derived Mutagenic Activity, and Risk of Colorectal Adenomas
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