Plasma levels of C-reactive protein and serum amyloid A and gastric cancer in a nested case-control study: Japan Public Health Center-based prospective study

被引:35
作者
Sasazuki, Shizuka [1 ]
Inoue, Manami [1 ]
Sawada, Norie [1 ]
Iwasaki, Motoki [1 ]
Shimazu, Taichi [1 ]
Yamaji, Taiki [1 ]
Tsugane, Shoichiro [1 ]
机构
[1] Natl Canc Ctr, Epidemiol & Prevent Div, Res Ctr Canc Prevent & Screening, Tokyo 1040045, Japan
基金
日本学术振兴会;
关键词
HELICOBACTER-PYLORI INFECTION; CYTOKINE GENE POLYMORPHISMS; CORONARY HEART-DISEASE; ACUTE-PHASE PROTEINS; A PROTEIN; INCREASED RISK; CARCINOMA; INFLAMMATION; PROGNOSIS; SAA;
D O I
10.1093/carcin/bgq010
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Gastric carcinogenesis may be under the combined influence of factors related to the host, Helicobacter pylori bacterial virulence and the environment. One possible host-related factor is the inflammatory or immune response. To clarify this point, we investigated the association between plasma levels of C-reactive protein (CRP) and serum amyloid A (SAA) and the subsequent risk of gastric cancer in a population-based nested case-control study. Subjects were observed from 1990 to 2004. Among 36 745 subjects who answered the baseline questionnaire and provided blood samples, 494 gastric cancer cases were identified and matched to 494 controls for our analysis. The overall distribution of CRP and SAA was not apparently associated with the development of gastric cancer. However, a statistically significant increased risk was observed when subjects were categorized dichotomously. The adjusted odds ratio (OR) for the development of gastric cancer for the CRP-positive group (CRP > 0.18 mg/dl) compared with the CRP-negative group was 1.90 [95% confidence interval (CI): 1.19-3.02, P = 0.007]. The OR for the SAA-positive group (SAA > 8 mu g/ml) compared with the SAA-negative group was 1.93 (95% CI: 1.22-3.07, P = 0.005). In conclusion, our results suggest that those who react strongly to inflammation or who have a high host immune response, as reflected by extremely elevated plasma levels of CRP and SAA, are at a high risk to develop gastric cancer.
引用
收藏
页码:712 / 718
页数:7
相关论文
共 39 条
[1]  
[Anonymous], INT CLASS DIS ONC
[2]  
[Anonymous], 1993, GEN RUL GASTR CANC S
[3]   SERUM AMYLOID-A (SAA) VARIATIONS IN PATIENTS WITH CANCER - CORRELATION WITH DISEASE-ACTIVITY, STAGE, PRIMARY SITE, AND PROGNOSIS [J].
BIRAN, H ;
FRIEDMAN, N ;
NEUMANN, L ;
PRAS, M ;
SHAINKINKESTENBAUM, R .
JOURNAL OF CLINICAL PATHOLOGY, 1986, 39 (07) :794-797
[4]   Evaluation of serum amyloid A as a biomarker for gastric cancer [J].
Chan, De-Chuan ;
Chen, Cheng-Jueng ;
Chu, Heng-Cheng ;
Chang, Wei-Kuo ;
Yu, Jyh-Cherng ;
Chen, Yu-Ju ;
Wen, Li-Li ;
Huang, Su-Ching ;
Ku, Chih-Hung ;
Liu, Yao-Chi ;
Chen, Jenn-Han .
ANNALS OF SURGICAL ONCOLOGY, 2007, 14 (01) :84-93
[5]   Identification of serum amyloid a protein as a potentially useful biomarker to monitor relapse of nasopharyngeal cancer by serum proteomic profiling [J].
Cho, WCS ;
Yip, TTC ;
Yip, C ;
Yip, V ;
Thulasiraman, V ;
Ngan, RKC ;
Yip, TT ;
Lau, WH ;
An, JSK ;
Law, SCK ;
Cheng, WW ;
Ma, VWS ;
Lim, CKP .
CLINICAL CANCER RESEARCH, 2004, 10 (01) :43-52
[6]   Discriminative value of serum amyloid A and other acute-phase proteins for coronary heart disease [J].
Delanghe, JR ;
Langlois, MR ;
De Bacquer, D ;
Mak, R ;
Capel, P ;
Van Renterghem, LV ;
De Backer, G .
ATHEROSCLEROSIS, 2002, 160 (02) :471-476
[7]   Interleukin-1 polymorphisms associated with increased risk of gastric cancer [J].
El-Omar, EM ;
Carrington, M ;
Chow, WH ;
McColl, KEL ;
Bream, JH ;
Young, HA ;
Herrera, J ;
Lissowska, J ;
Yuan, CC ;
Rothman, N ;
Lanyon, G ;
Martin, M ;
Fraumeni, JF ;
Rabkin, CS .
NATURE, 2000, 404 (6776) :398-402
[8]   Mechanisms of disease: Acute-phase proteins and other systemic responses to inflammation [J].
Gabay, C ;
Kushner, I .
NEW ENGLAND JOURNAL OF MEDICINE, 1999, 340 (06) :448-454
[9]   Serum amyloid A protein (SAA) in colorectal carcinoma [J].
Glojnaric, I ;
Casl, MT ;
Simic, D ;
Lukac, J .
CLINICAL CHEMISTRY AND LABORATORY MEDICINE, 2001, 39 (02) :129-133
[10]  
Ilhan N, 2004, WORLD J GASTROENTERO, V10, P1115