Serum YKL-40 in Risk Assessment for Colorectal Cancer: A Prospective Study of 4,496 Subjects at Risk of Colorectal Cancer

被引:44
作者
Johansen, Julia S. [1 ,2 ,3 ]
Christensen, Ib J. [4 ,5 ]
Jorgensen, Lars N. [6 ]
Olsen, Jesper [7 ]
Rahr, Hans B. [8 ]
Nielsen, Knud T. [9 ]
Laurberg, Soren [10 ]
Brunner, Nils [11 ]
Nielsen, Hans Jorgen [1 ,12 ]
机构
[1] Univ Copenhagen, Fac Hlth & Med Sci, Inst Clin Med, Copenhagen, Denmark
[2] Univ Copenhagen, Herlev Hosp, Dept Oncol, Copenhagen, Denmark
[3] Univ Copenhagen, Herlev Hosp, Dept Med, Copenhagen, Denmark
[4] Rigshosp, Finsen Lab, DK-2100 Copenhagen, Denmark
[5] Univ Copenhagen, Biotech Res & Innovat Ctr, Copenhagen, Denmark
[6] Bispebjerg Hosp, Dept Surg Gastroenterol, DK-2400 Copenhagen, Denmark
[7] Glostrup Cty Hosp, Dept Surg, Copenhagen, Denmark
[8] Odense Univ Hosp, Dept Surg Gastroenterol, DK-5000 Odense, Denmark
[9] Randers Cent Hosp, Dept Surg, Randers, Denmark
[10] Aarhus Univ Hosp, Dept Surg, DK-8000 Aarhus, Denmark
[11] Univ Copenhagen, Mol Dis Biol Sect, Copenhagen, Denmark
[12] Univ Copenhagen, Hvidovre Hosp, Dept Surg Gastroenterol, DK-2650 Hvidovre, Denmark
关键词
PLASMA YKL-40; CHITINASE; 3-LIKE-1; TISSUE RESPONSES; PROTEIN; CELLS; INFLAMMATION; EXPRESSION;
D O I
10.1158/1055-9965.EPI-13-1281
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The aim of the present study was to test the hypothesis that high serum YKL-40 associates with colorectal cancer in subjects at risk of colorectal cancer. We measured serum YKL-40 in a prospective study of 4,496 Danish subjects [2,064 men, 2,432 women, median age 61 years (range, 18-97)] referred to endoscopy due to symptoms or other risk factors for colorectal cancer. Blood samples were collected just before large bowel endoscopy. Serum YKL-40 was determined by ELISA. Serum YKL-40 was higher (P < 0.0001, unadjusted for confounding covariates) in subjects diagnosed with colon cancer (median 126 mu g/L, 25%-75%: 80-206 mu g/L) and rectal cancer (104, 72-204 mu g/L) compared with subjects with adenoma (84, 53-154 mu g/L), other nonmalignant findings (79, 49-138 mu g/L), and no findings (62, 41-109 mu g/L). Serum YKL-40 independently predicted colorectal cancer [OR, 1.53; 95% confidence interval (CI), 1.40-1.67; AUC = 0.68, P < 0.0001]. Restricting the analysis to subjects with no comorbidity increased the OR for serum YKL-40 to predict colorectal cancer (OR, 1.82; 1.58-2.08; AUC = 0.73, P < 0.0001). Combining serum YKL-40 and CEA demonstrated that both were significant [(YKL-40, OR, 1.27; 95% CI, 1.16-1.40); (CEA, OR, 1.92; 1.75-2.10; AUC = 0.75, P < 0.0001; OR for a 2-fold difference in marker level)]. Multivariable analysis (YKL-40, CEA, age, gender, body mass index, and center) showed that serum YKL40 was a predictor for colorectal cancer in individuals without comorbidity (OR, 1.25; 95% CI, 1.05-1.40; P = 0.012), whereas this was not the case for those with comorbidity (OR, 0.98; 95% CI, 0.84-1.14; P = 0.80). In conclusion, high serum YKL-40 in subjects suspected of colorectal cancer and without comorbidity associates with colorectal cancer. Determination of serum YKL-40 may be useful in combination with other biomarkers in risk assessment for colorectal cancer. (c) 2015 AACR.
引用
收藏
页码:621 / 626
页数:6
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