Cargando…
Elevated Squamous Cell Carcinoma Antigen, Cytokeratin 19 Fragment, and Carcinoembryonic Antigen Levels in Diabetic Nephropathy
OBJECTIVE: We aimed to explore whether squamous cell carcinoma antigen (SCC), cytokeratin 19 fragment (Cyfra21-1), neuron-specific enolase (NSE), and carcinoembryonic antigen (CEA) are elevated in diabetic nephropathy (DN) and the association between urinary albumin-to-creatinine ratio (UACR) and tu...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5514347/ https://www.ncbi.nlm.nih.gov/pubmed/28744310 http://dx.doi.org/10.1155/2017/5304391 |
_version_ | 1783250827506352128 |
---|---|
author | Chen, Jianzhong Tao, Feng Zhang, Bin Chen, Qingguang Qiu, Yan Luo, Qian Gen, Yanna Meng, Jiali Zhang, Jue Lu, Hao |
author_facet | Chen, Jianzhong Tao, Feng Zhang, Bin Chen, Qingguang Qiu, Yan Luo, Qian Gen, Yanna Meng, Jiali Zhang, Jue Lu, Hao |
author_sort | Chen, Jianzhong |
collection | PubMed |
description | OBJECTIVE: We aimed to explore whether squamous cell carcinoma antigen (SCC), cytokeratin 19 fragment (Cyfra21-1), neuron-specific enolase (NSE), and carcinoembryonic antigen (CEA) are elevated in diabetic nephropathy (DN) and the association between urinary albumin-to-creatinine ratio (UACR) and tumor markers in diabetic patients. METHODS: Nondialysis patients with diabetes (n = 261) and 90 healthy controls were enrolled. DN was defined as an UACR ≥ 30 mg/g in the absence of a urinary tract infection or other renal abnormalities. RESULTS: Patients with DN had significantly higher serum SCC, Cyfra21-1, and CEA levels than those with normoalbuminuria and healthy controls. The rates of positive SCC, Cyfra21-1, and CEA significantly increased with increasing urinary albumin excretion (all P for trend < 0.001). In contrast, NSE was not affected by DN. SCC, Cyfra21-1, and CEA were significantly and positively correlated with UACR. In logistic regression, after multivariable adjustment, increased UACR was associated with increased odds ratio of elevated tumor marker levels (all P for trend < 0.05). CONCLUSIONS: Serum levels of SCC, Cyfra21-1, and CEA are markedly increased with increasing urinary albumin excretion, which affects the specificity for diagnosis for lung cancer. Appropriate interpretation of tumor markers in diabetic patients is mandatory to avoid unnecessary and even hazardous biopsies. |
format | Online Article Text |
id | pubmed-5514347 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-55143472017-07-25 Elevated Squamous Cell Carcinoma Antigen, Cytokeratin 19 Fragment, and Carcinoembryonic Antigen Levels in Diabetic Nephropathy Chen, Jianzhong Tao, Feng Zhang, Bin Chen, Qingguang Qiu, Yan Luo, Qian Gen, Yanna Meng, Jiali Zhang, Jue Lu, Hao Int J Endocrinol Research Article OBJECTIVE: We aimed to explore whether squamous cell carcinoma antigen (SCC), cytokeratin 19 fragment (Cyfra21-1), neuron-specific enolase (NSE), and carcinoembryonic antigen (CEA) are elevated in diabetic nephropathy (DN) and the association between urinary albumin-to-creatinine ratio (UACR) and tumor markers in diabetic patients. METHODS: Nondialysis patients with diabetes (n = 261) and 90 healthy controls were enrolled. DN was defined as an UACR ≥ 30 mg/g in the absence of a urinary tract infection or other renal abnormalities. RESULTS: Patients with DN had significantly higher serum SCC, Cyfra21-1, and CEA levels than those with normoalbuminuria and healthy controls. The rates of positive SCC, Cyfra21-1, and CEA significantly increased with increasing urinary albumin excretion (all P for trend < 0.001). In contrast, NSE was not affected by DN. SCC, Cyfra21-1, and CEA were significantly and positively correlated with UACR. In logistic regression, after multivariable adjustment, increased UACR was associated with increased odds ratio of elevated tumor marker levels (all P for trend < 0.05). CONCLUSIONS: Serum levels of SCC, Cyfra21-1, and CEA are markedly increased with increasing urinary albumin excretion, which affects the specificity for diagnosis for lung cancer. Appropriate interpretation of tumor markers in diabetic patients is mandatory to avoid unnecessary and even hazardous biopsies. Hindawi 2017 2017-07-04 /pmc/articles/PMC5514347/ /pubmed/28744310 http://dx.doi.org/10.1155/2017/5304391 Text en Copyright © 2017 Jianzhong Chen et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Chen, Jianzhong Tao, Feng Zhang, Bin Chen, Qingguang Qiu, Yan Luo, Qian Gen, Yanna Meng, Jiali Zhang, Jue Lu, Hao Elevated Squamous Cell Carcinoma Antigen, Cytokeratin 19 Fragment, and Carcinoembryonic Antigen Levels in Diabetic Nephropathy |
title | Elevated Squamous Cell Carcinoma Antigen, Cytokeratin 19 Fragment, and Carcinoembryonic Antigen Levels in Diabetic Nephropathy |
title_full | Elevated Squamous Cell Carcinoma Antigen, Cytokeratin 19 Fragment, and Carcinoembryonic Antigen Levels in Diabetic Nephropathy |
title_fullStr | Elevated Squamous Cell Carcinoma Antigen, Cytokeratin 19 Fragment, and Carcinoembryonic Antigen Levels in Diabetic Nephropathy |
title_full_unstemmed | Elevated Squamous Cell Carcinoma Antigen, Cytokeratin 19 Fragment, and Carcinoembryonic Antigen Levels in Diabetic Nephropathy |
title_short | Elevated Squamous Cell Carcinoma Antigen, Cytokeratin 19 Fragment, and Carcinoembryonic Antigen Levels in Diabetic Nephropathy |
title_sort | elevated squamous cell carcinoma antigen, cytokeratin 19 fragment, and carcinoembryonic antigen levels in diabetic nephropathy |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5514347/ https://www.ncbi.nlm.nih.gov/pubmed/28744310 http://dx.doi.org/10.1155/2017/5304391 |
work_keys_str_mv | AT chenjianzhong elevatedsquamouscellcarcinomaantigencytokeratin19fragmentandcarcinoembryonicantigenlevelsindiabeticnephropathy AT taofeng elevatedsquamouscellcarcinomaantigencytokeratin19fragmentandcarcinoembryonicantigenlevelsindiabeticnephropathy AT zhangbin elevatedsquamouscellcarcinomaantigencytokeratin19fragmentandcarcinoembryonicantigenlevelsindiabeticnephropathy AT chenqingguang elevatedsquamouscellcarcinomaantigencytokeratin19fragmentandcarcinoembryonicantigenlevelsindiabeticnephropathy AT qiuyan elevatedsquamouscellcarcinomaantigencytokeratin19fragmentandcarcinoembryonicantigenlevelsindiabeticnephropathy AT luoqian elevatedsquamouscellcarcinomaantigencytokeratin19fragmentandcarcinoembryonicantigenlevelsindiabeticnephropathy AT genyanna elevatedsquamouscellcarcinomaantigencytokeratin19fragmentandcarcinoembryonicantigenlevelsindiabeticnephropathy AT mengjiali elevatedsquamouscellcarcinomaantigencytokeratin19fragmentandcarcinoembryonicantigenlevelsindiabeticnephropathy AT zhangjue elevatedsquamouscellcarcinomaantigencytokeratin19fragmentandcarcinoembryonicantigenlevelsindiabeticnephropathy AT luhao elevatedsquamouscellcarcinomaantigencytokeratin19fragmentandcarcinoembryonicantigenlevelsindiabeticnephropathy |