Baseline serum C‐reactive protein and death from colorectal cancer in the NHANES III cohort
Several prospective studies suggest that C‐reactive protein (CRP), a nonspecific serologic marker of inflammation, might be linked to risk of colorectal cancer (CRC), whereas others have reported null or protective effects. We analyzed data from 7,072 participants (50–85 years) in the U.S. National...
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Published in | International journal of cancer Vol. 134; no. 8; pp. 1862 - 1870 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Hoboken, NJ
Wiley-Blackwell
15.04.2014
Wiley Subscription Services, Inc |
Subjects | |
Online Access | Get full text |
ISSN | 0020-7136 1097-0215 1097-0215 |
DOI | 10.1002/ijc.28504 |
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Summary: | Several prospective studies suggest that C‐reactive protein (CRP), a nonspecific serologic marker of inflammation, might be linked to risk of colorectal cancer (CRC), whereas others have reported null or protective effects. We analyzed data from 7,072 participants (50–85 years) in the U.S. National Health and Nutrition Examination Survey III (1988–1994), a nationally representative cohort (n = 33,994; 2 months–85 years) with vital status follow‐up to 2000. Hazard ratios (HRs) for mortality associated with baseline clinically raised (≥1.00 mg/dL) and intermediate (≥0.22–0.99 mg/dL) CRP levels were estimated using Cox proportional hazards regression controlling for CRC risk factors. There were 59 deaths from CRC, 106 from other obesity‐related cancers (other‐ORCs) and 1,130 from cardiovascular disease (CVD). Participants with clinically raised CRP at baseline were found to have a statistically significant greater risk of CRC death (HRs = 2.36–2.47) in comparison to persons with undetected levels. HRs were lower for death from other‐ORC and CVD (1.82, 95% CI 1.05–3.15; 1.53, 95% CI 1.29–1.81, respectively). Intermediate CRP level was associated with a nonsignificant 10–21% increased risk for CRC death. HR for CRC death was higher among persons with a normal BMI (2.16, 95% 0.96–4.87, p = 0.06) compared to those who were overweight (1.22, 95% CI 0.53–2.78) or obese (1.23, 95% CI, 0.37–4.08). A similar pattern was observed for waist circumference. This effect modification suggests that the impact of chronic inflammation may be independent of excess body fat. Future research is recommended to confirm emerging data that elevated serologic CRP might reflect underlying colonic inflammation.
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The correlation between C‐Reactive Protein (CRP) and risk of colorectal cancer (CRC) has been unclear. In this study, the authors analyzed data from the long‐term NHANES III survey in order to clarify this association. They found that high levels of serum CRP more than doubled the risk of death from CRC. Surprisingly, this risk was much higher among subjects with a normal BMI than among those who were obese. These results indicate that elevated serum CRP may reflect underlying colonic inflammation, which could, in turn, aid in clinical assessment of CRC risk. |
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Bibliography: | Conflicts of interest Nothing to report Study concept and design (H.S. and A.M.H.); analysis and interpretation of data (H.S., A.M.H., J.S., S.R., A.T.V. and R.G.S.); drafting of manuscript (All); critical revision of manuscript for important intellectual content (All) and statistical analysis (H.S. and A.M.H.) Author contributions ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 ObjectType-Article-2 ObjectType-Feature-1 |
ISSN: | 0020-7136 1097-0215 1097-0215 |
DOI: | 10.1002/ijc.28504 |