C-reactive protein levels are not associated with increased risk for colorectal cancer in women

被引:102
作者
Zhang, SMM
Buring, JE
Lee, IM
Cook, NR
Ridker, PM
机构
[1] Harvard Univ, Sch Med, Brigham & Womens Hosp, Div Prevent Med, Boston, MA 02115 USA
[2] Harvard Univ, Sch Publ Hlth, Boston, MA 02115 USA
关键词
D O I
10.7326/0003-4819-142-6-200503150-00008
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Observations that risk for colorectal cancer is elevated in patients with inflammatory bowel disease and that longterm use of anti-inflammatory drugs may reduce colorectal cancer risk have raised the possibility that inflammation may play a role in the development of colorectal cancer. While a recent prospective study observed a positive association between C-reactive protein (CRP), a marker of inflammation, and risk for colon cancer, data testing this hypothesis are sparse. Objective: To evaluate whether plasma CRP levels predict colorectal cancer risk in women. Design: Prospective cohort study, with 97% morbidity follow-up and 100% mortality follow-up within the past 2 years. Setting: women's Health Study. Participants: 27 913 apparently healthy women age 45 years or older who had CRP measured at entry into a trial of low-dose aspirin and vitamin E. Maximum length of intervention and follow-up was 10.8 years. Measurements: self-reported incident colorectal adenocarcinoma confirmed by medical record review. Results: 169 women developed colorectal adenocarcinomas during follow-up. Baseline CRP levels were not significantly associated with colorectal cancer risk. The multivariate hazard ratios according to cutoff points for CRP proposed in clinical guidelines were 0.79 (95% CI, 0.53 to 1.17) for the category of 1 to 3 mg/L and 0.66 (CI, 0.43 to 1.03) for the category of greater than 3 mg/L (P for trend = 0.09), as compared with the category of less than 1 mg/L. High CRP levels were also not associated with increased risk in analyses done according to tumor location and stage at diagnosis, according to alternative cutoff points for CRP, or in any of the subgroups evaluated. Limitations: Despite multivariate analysis, residual confounding might still be present. Although this study was prospective, we cannot completely exclude undetected cancer at baseline. Measurements for CRP were available for only 71% of women in the cohort; however, the women who did and those who did not provide blood were mostly similar. Conclusions: Plasma CRP levels do not appear to predict an increased risk for developing colorectal cancer in apparently healthy women. Low-grade inflammation may not play an important role in increasing the risk for colorectal cancer.
引用
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页码:425 / 432
页数:8
相关论文
共 45 条
[1]  
[Anonymous], 1975, SEER CANC STAT REV
[2]  
Baron JA, 2003, PROG EXP TUMOR RES, V37, P1
[3]   Interleukin-6 blood level is associated with circulating carcinoembryonic antigen and prognosis in patients with colorectal cancer [J].
Belluco, C ;
Nitti, D ;
Frantz, M ;
Toppan, P ;
Basso, D ;
Plebani, M ;
Lise, M ;
Jessup, JM .
ANNALS OF SURGICAL ONCOLOGY, 2000, 7 (02) :133-138
[4]   Progress in cancer screening over a decade: Results of cancer screening from the 1987, 1992, and 1998 National Health Interview Surveys [J].
Breen, N ;
Wagener, DK ;
Brown, ML ;
Davis, WW ;
Ballard-Barbash, R .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2001, 93 (22) :1704-1713
[5]   Tumor necrosis factor antagonist therapy and lymphoma development - Twenty-six cases reported to the Food and Drug Administration [J].
Brown, SL ;
Greene, MH ;
Gershon, SK ;
Edwards, ET ;
Braun, MM .
ARTHRITIS AND RHEUMATISM, 2002, 46 (12) :3151-3158
[6]   Serum interleukin-6 levels reflect the disease status of colorectal cancer [J].
Chung, YC ;
Chang, YF .
JOURNAL OF SURGICAL ONCOLOGY, 2003, 83 (04) :222-226
[7]   Serum C-reactive protein correlates with survival in colorectal cancer patients but is not an independent prognostic indicator [J].
Chung, YC ;
Chang, YF .
EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY, 2003, 15 (04) :369-373
[8]   Inflammation and cancer [J].
Coussens, LM ;
Werb, Z .
NATURE, 2002, 420 (6917) :860-867
[9]   Hormone replacement therapy and its relationship to lipid and glucose metabolism in diabetic and nondiabetic postmenopausal women [J].
Crespo, CJ ;
Smit, E ;
Snelling, A ;
Sempos, CT ;
Andersen, RE .
DIABETES CARE, 2002, 25 (10) :1675-1680
[10]   Effect of postmenopausal hormones on inflammation-sensitive proteins - The Postmenopausal Estrogen/Progestin Interventions (PEPI) Study [J].
Cushman, M ;
Legault, C ;
Barrett-Connor, E ;
Stefanick, ML ;
Kessler, C ;
Judd, HL ;
Sakkinen, PA ;
Tracy, RP .
CIRCULATION, 1999, 100 (07) :717-722