Impaired glucose metabolism in colorectal cancer

被引:29
作者
Ehrmann-Josko, Agnieszka
Sieminska, Jolanta
Gornicka, Barbara
Ziarkiewicz-Wroblewska, Bogna
Ziolkowski, Bartlomiej
Muszynski, Jacek
机构
[1] Med Univ Warsaw, Dept Gastroenterol & Metab Dis, PL-02097 Warsaw, Poland
[2] Med Univ Warsaw, Dept Expt Physiol & Clin Physiol, PL-02097 Warsaw, Poland
[3] Med Univ Warsaw, Dept Pathol, PL-02097 Warsaw, Poland
关键词
colorectal cancer; diabetes;
D O I
10.1080/00365520600587444
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Objective. Some studies have found that people with type 2 diabetes mellitus are at increased risk of neoplasms, especially colorectal cancer ( CRC). In other studies it is also suggested that there is a higher incidence of diabetes mellitus in patients with CRC. The aims of this study were to assess whether the incidence of type 2 diabetes mellitus and impaired glucose tolerance ( IGT) are higher in subjects with CRC and to determine the difference between diabetic subjects and healthy controls regarding glucose metabolism ( glycaemia, insulinaemia, serum levels of C-peptide) as well as insulin resistance and sensitivity. Material and methods. The study included a total of 80 subjects: 40 enrolled patients ( 20 M, 20 F) with newly diagnosed sporadic colorectal cancer and 40 subjects with endoscopically excluded CRC or adenomas serving as controls. Subjects were matched for gender, age and body mass index ( BMI) ( age +/- 5 years BMI +/- 1 kg/m(2)). A 75-g oral glucose tolerance test was performed after an overnight fast. Samples for glycaemia, serum levels of C-peptide and insulin were taken at 0, 30, 60, 90, 120 and 150 min of the study. HOMA-IR, EIR, EIR/HOMA-IR indexes were calculated. Results. There was a significantly higher incidence of impaired glucose metabolism ( IGM - diabetes mellitus or IGT) in CRC subjects. No differences were found in levels of glucose, insulin or C-peptide. Insulinaemia and C-peptide curves showed a shift typical of diabetes, in the form of a delayed insulin release peak. The HOMA-IR, EIR as well as the EIR/HOMA-IR indexes showed no differences between groups. Conclusions. A significantly higher incidence of IGM appears to occur in CRC patients than in the healthy population. This phenomenon is not dependent on age and body-weight, which may suggest that it is cancer that predisposes to diabetes rather than the other way round. The neoplastic process in the colon is not associated with hyperinsulinaemia or insulin resistance, but in CRC patients, pancreatic B-cell dysfunction typical of the early stages of diabetes is seen.
引用
收藏
页码:1079 / 1086
页数:8
相关论文
共 39 条
[1]   Excess risk of primary liver cancer in patients with diabetes mellitus [J].
Adami, HO ;
Chow, WH ;
Nyren, O ;
Berne, C ;
Linet, MS ;
Ekbom, A ;
Wolk, A ;
McLaughlin, JK ;
Fraumeni, JF .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1996, 88 (20) :1472-1477
[2]   CANCER RISK IN PATIENTS WITH DIABETES-MELLITUS [J].
ADAMI, HO ;
MCLAUGHLIN, J ;
EKBOM, A ;
BERNE, C ;
SILVERMAN, D ;
HACKER, D ;
PERSSON, I .
CANCER CAUSES & CONTROL, 1991, 2 (05) :307-314
[3]   Attributable risks for hepatocellular carcinoma in Northern Italy [J].
Braga, C ;
LaVecchia, C ;
Negri, E ;
Franceschi, S .
EUROPEAN JOURNAL OF CANCER, 1997, 33 (04) :629-634
[4]  
Colangelo LA, 2002, CANCER EPIDEM BIOMAR, V11, P385
[5]  
CZYZYK A, 1997, PATOFIZJOLOGIA KLIN
[6]  
DOERING CR, 1935, PREVENTIVE MED HYGIE, P1221
[7]   INSULIN AND COLON-CANCER [J].
GIOVANNUCCI, E .
CANCER CAUSES & CONTROL, 1995, 6 (02) :164-179
[8]   Insulin, insulin-like growth factors and colon cancer: A review of the evidence [J].
Giovannucci, E .
JOURNAL OF NUTRITION, 2001, 131 (11) :3109S-3120S
[9]   Risk factors for primary breast cancer in Japan: 8-year follow-up of atomic bomb survivors [J].
Goodman, MT ;
Cologne, JB ;
Moriwaki, H ;
Vaeth, M ;
Mabuchi, K .
PREVENTIVE MEDICINE, 1997, 26 (01) :144-153
[10]   Prospective study of adult onset diabetes mellitus (type 2) and risk of colorectal cancer in women [J].
Hu, FB ;
Manson, JE ;
Liu, SM ;
Hunter, D ;
Colditz, GA ;
Michels, KB ;
Speizer, FE ;
Giovannucci, E .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1999, 91 (06) :542-547