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High Blood Glucose Levels Correlate with Tumor Malignancy in Colorectal Cancer Patients
BACKGROUND: Research shows that type 2 diabetes mellitus (T2DM) affects the risk and prognosis of colorectal cancer (CRC). Here, we conducted a retrospective study to investigate whether the clinicopathological features of CRC patients correlate with their blood glucose levels. MATERIAL/METHODS: We...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Scientific Literature, Inc.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4677694/ https://www.ncbi.nlm.nih.gov/pubmed/26644185 http://dx.doi.org/10.12659/MSM.894783 |
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author | Cui, Ge Zhang, Ting Ren, Fan Feng, Wen-Ming Yao, Yunliang Cui, Jie Zhu, Guo-Liang Shi, Qi-Lin |
author_facet | Cui, Ge Zhang, Ting Ren, Fan Feng, Wen-Ming Yao, Yunliang Cui, Jie Zhu, Guo-Liang Shi, Qi-Lin |
author_sort | Cui, Ge |
collection | PubMed |
description | BACKGROUND: Research shows that type 2 diabetes mellitus (T2DM) affects the risk and prognosis of colorectal cancer (CRC). Here, we conducted a retrospective study to investigate whether the clinicopathological features of CRC patients correlate with their blood glucose levels. MATERIAL/METHODS: We enrolled 391 CRC patients hospitalized in our center between 2008 and 2013. Data of their first fasting plasma glucose (FPG) and 2-h postprandial glucose (2hPPG) level after admission, their clinicopathological features, and survival were collected. The correlations between blood glucose level and clinicopathological features were analyzed by Pearson chi-square analysis. Patient survival was analyzed by Kaplan-Meier and Cox-regression analysis. RESULTS: There were 116 out of the 391 CRC patients who had high blood glucose level (H-G group, 29.67%), among which 58 (14.83%), 18 (4.60%), and 40 (10.23%) were diabetes mellitus (DM), impaired glucose tolerance (IGT), and impaired fasting glucose (IFG), respectively, while 275 (70.33%) patients had normal glucose level (N-G group). Compared with the N-G group, patients in the H-G group had larger tumor diameters and lower tumor differentiation (p<0.05). A higher ratio of patients in the H-G group also had more advanced TNM staging and more ulcerative CRC gross type (p<0.05). No significant difference was observed in patient overall survival among different glucose groups. No effect of insulin therapy on CRC development and patient survival was observed. CONCLUSIONS: Blood glucose level in CRC patients correlates significantly with local tumor malignancy, but no significant effect on distant metastasis and patient overall survival was observed. |
format | Online Article Text |
id | pubmed-4677694 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | International Scientific Literature, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-46776942015-12-18 High Blood Glucose Levels Correlate with Tumor Malignancy in Colorectal Cancer Patients Cui, Ge Zhang, Ting Ren, Fan Feng, Wen-Ming Yao, Yunliang Cui, Jie Zhu, Guo-Liang Shi, Qi-Lin Med Sci Monit Clinical Research BACKGROUND: Research shows that type 2 diabetes mellitus (T2DM) affects the risk and prognosis of colorectal cancer (CRC). Here, we conducted a retrospective study to investigate whether the clinicopathological features of CRC patients correlate with their blood glucose levels. MATERIAL/METHODS: We enrolled 391 CRC patients hospitalized in our center between 2008 and 2013. Data of their first fasting plasma glucose (FPG) and 2-h postprandial glucose (2hPPG) level after admission, their clinicopathological features, and survival were collected. The correlations between blood glucose level and clinicopathological features were analyzed by Pearson chi-square analysis. Patient survival was analyzed by Kaplan-Meier and Cox-regression analysis. RESULTS: There were 116 out of the 391 CRC patients who had high blood glucose level (H-G group, 29.67%), among which 58 (14.83%), 18 (4.60%), and 40 (10.23%) were diabetes mellitus (DM), impaired glucose tolerance (IGT), and impaired fasting glucose (IFG), respectively, while 275 (70.33%) patients had normal glucose level (N-G group). Compared with the N-G group, patients in the H-G group had larger tumor diameters and lower tumor differentiation (p<0.05). A higher ratio of patients in the H-G group also had more advanced TNM staging and more ulcerative CRC gross type (p<0.05). No significant difference was observed in patient overall survival among different glucose groups. No effect of insulin therapy on CRC development and patient survival was observed. CONCLUSIONS: Blood glucose level in CRC patients correlates significantly with local tumor malignancy, but no significant effect on distant metastasis and patient overall survival was observed. International Scientific Literature, Inc. 2015-12-08 /pmc/articles/PMC4677694/ /pubmed/26644185 http://dx.doi.org/10.12659/MSM.894783 Text en © Med Sci Monit, 2015 This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License |
spellingShingle | Clinical Research Cui, Ge Zhang, Ting Ren, Fan Feng, Wen-Ming Yao, Yunliang Cui, Jie Zhu, Guo-Liang Shi, Qi-Lin High Blood Glucose Levels Correlate with Tumor Malignancy in Colorectal Cancer Patients |
title | High Blood Glucose Levels Correlate with Tumor Malignancy in Colorectal Cancer Patients |
title_full | High Blood Glucose Levels Correlate with Tumor Malignancy in Colorectal Cancer Patients |
title_fullStr | High Blood Glucose Levels Correlate with Tumor Malignancy in Colorectal Cancer Patients |
title_full_unstemmed | High Blood Glucose Levels Correlate with Tumor Malignancy in Colorectal Cancer Patients |
title_short | High Blood Glucose Levels Correlate with Tumor Malignancy in Colorectal Cancer Patients |
title_sort | high blood glucose levels correlate with tumor malignancy in colorectal cancer patients |
topic | Clinical Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4677694/ https://www.ncbi.nlm.nih.gov/pubmed/26644185 http://dx.doi.org/10.12659/MSM.894783 |
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