The aim of the present study was to evaluate whether elevated serological protein biomarker levels may identify adenoma patients, who are at increased risk of being diagnosed with subsequent primary malignancy. It is concluded that increased levels of plasma TIMP-1, CEA, CA19-9, and serum YKL-40 at large bowel endoscopy without findings may be associated with an increased risk of developing a subsequent malignant disease.īackground: Blood-based, cancer-associated biomarkers may detect subjects at risk of having neoplastic diseases. The cumulative risk of developing malignant disease within the first 5 years after endoscopy was group 0, 3.3% group 1, 5.8% group 2, 7.8%. A multivariate analysis showed that increased biomarker levels were associated with subsequent development of a malignant disease (P = 0.002). Univariatly, increase of all four biomarkers was significantly associated with subsequent development of a malignant disease. A total of 43 subjects developed a primary malignant disease in the observation period. The levels were separated into three groups: 0, none of the biomarkers increased 1, one biomarker increased 2, two or more biomarkers increased. The upper 90% limits of the reference levels of every single protein were used to differentiate between normal and increased levels. Plasma levels of TIMP-1, CEA, CA19-9, and YKL-40 were determined in samples collected just before endoscopy and compared with subsequent development of a malignant disease within a period of 7-8 years. In a major study of 4,990 subjects undergoing large bowel endoscopy, 691 were without pathology and comorbidity. The present study focused on a possible association between increased biomarker levels in such subjects and subsequent development of malignant diseases. Soluble cancer-related protein biomarker levels may be increased in subjects without findings at large bowel endoscopy performed due to symptoms associated with colorectal cancer.
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