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Serum chemerin levels are independently associated with quality of life in colorectal cancer survivors: A pilot study

BACKGROUND: Colorectal cancer (CRC) survivors are known to experience various symptoms that significantly affect their quality of life (QOL); therefore, it is important to identify clinical markers related with CRC survivor QOL. Here we investigated the relationship between serum chemerin levels, a...

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Autores principales: Lee, Jee-Yon, Lee, Mi-Kyung, Kim, Nam-Kyu, Chu, Sang-Hui, Lee, Duk-Chul, Lee, Hye-Sun, Lee, Ji-Won, Jeon, Justin Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5419570/
https://www.ncbi.nlm.nih.gov/pubmed/28475614
http://dx.doi.org/10.1371/journal.pone.0176929
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author Lee, Jee-Yon
Lee, Mi-Kyung
Kim, Nam-Kyu
Chu, Sang-Hui
Lee, Duk-Chul
Lee, Hye-Sun
Lee, Ji-Won
Jeon, Justin Y.
author_facet Lee, Jee-Yon
Lee, Mi-Kyung
Kim, Nam-Kyu
Chu, Sang-Hui
Lee, Duk-Chul
Lee, Hye-Sun
Lee, Ji-Won
Jeon, Justin Y.
author_sort Lee, Jee-Yon
collection PubMed
description BACKGROUND: Colorectal cancer (CRC) survivors are known to experience various symptoms that significantly affect their quality of life (QOL); therefore, it is important to identify clinical markers related with CRC survivor QOL. Here we investigated the relationship between serum chemerin levels, a newly identified proinflammatory adipokine, and QOL in CRC survivors. METHODS: A data of total of 110 CRC survivors were analysed in the study. Serum chemerin levels were measured with an enzyme immunoassay analyser. Functional Assessment of Cancer Therapy (FACT) scores were used as an indicator of QOL in CRC survivors. RESULTS: Weak but not negligible relationships were observed between serum chemerin levels and FACT-General (G) (r = -0.22, p<0.02), FACT-Colorectal cancer (C) (r = -0.23, p<0.02) and FACT-Fatigue (F) scores (r = -0.27, p<0.01) after adjusting for confounding factors. Both stepwise and enter method multiple linear regression analyses confirmed that serum chemerin levels were independently associated with FACT-G (stepwise: β = -0.15, p<0.01; enter: β = -0.12, p = 0.02), FACT-C (stepwise: β = -0.19, p<0.01; enter; β = -0.14, p = 0.02) and FACT-F scores (stepwise: β = -0.23, p<0.01; enter: β = -0.20, p<0.01). CONCLUSIONS: Our results demonstrate a weak inverse relationship between serum chemerin and CRC survivor QOL. Although it is impossible to determine causality, our findings suggest that serum chemerin levels may have a significant association with CRC survivor QOL. Further prospective studies are required to confirm the clinical significance of our pilot study.
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spelling pubmed-54195702017-05-14 Serum chemerin levels are independently associated with quality of life in colorectal cancer survivors: A pilot study Lee, Jee-Yon Lee, Mi-Kyung Kim, Nam-Kyu Chu, Sang-Hui Lee, Duk-Chul Lee, Hye-Sun Lee, Ji-Won Jeon, Justin Y. PLoS One Research Article BACKGROUND: Colorectal cancer (CRC) survivors are known to experience various symptoms that significantly affect their quality of life (QOL); therefore, it is important to identify clinical markers related with CRC survivor QOL. Here we investigated the relationship between serum chemerin levels, a newly identified proinflammatory adipokine, and QOL in CRC survivors. METHODS: A data of total of 110 CRC survivors were analysed in the study. Serum chemerin levels were measured with an enzyme immunoassay analyser. Functional Assessment of Cancer Therapy (FACT) scores were used as an indicator of QOL in CRC survivors. RESULTS: Weak but not negligible relationships were observed between serum chemerin levels and FACT-General (G) (r = -0.22, p<0.02), FACT-Colorectal cancer (C) (r = -0.23, p<0.02) and FACT-Fatigue (F) scores (r = -0.27, p<0.01) after adjusting for confounding factors. Both stepwise and enter method multiple linear regression analyses confirmed that serum chemerin levels were independently associated with FACT-G (stepwise: β = -0.15, p<0.01; enter: β = -0.12, p = 0.02), FACT-C (stepwise: β = -0.19, p<0.01; enter; β = -0.14, p = 0.02) and FACT-F scores (stepwise: β = -0.23, p<0.01; enter: β = -0.20, p<0.01). CONCLUSIONS: Our results demonstrate a weak inverse relationship between serum chemerin and CRC survivor QOL. Although it is impossible to determine causality, our findings suggest that serum chemerin levels may have a significant association with CRC survivor QOL. Further prospective studies are required to confirm the clinical significance of our pilot study. Public Library of Science 2017-05-05 /pmc/articles/PMC5419570/ /pubmed/28475614 http://dx.doi.org/10.1371/journal.pone.0176929 Text en © 2017 Lee et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Lee, Jee-Yon
Lee, Mi-Kyung
Kim, Nam-Kyu
Chu, Sang-Hui
Lee, Duk-Chul
Lee, Hye-Sun
Lee, Ji-Won
Jeon, Justin Y.
Serum chemerin levels are independently associated with quality of life in colorectal cancer survivors: A pilot study
title Serum chemerin levels are independently associated with quality of life in colorectal cancer survivors: A pilot study
title_full Serum chemerin levels are independently associated with quality of life in colorectal cancer survivors: A pilot study
title_fullStr Serum chemerin levels are independently associated with quality of life in colorectal cancer survivors: A pilot study
title_full_unstemmed Serum chemerin levels are independently associated with quality of life in colorectal cancer survivors: A pilot study
title_short Serum chemerin levels are independently associated with quality of life in colorectal cancer survivors: A pilot study
title_sort serum chemerin levels are independently associated with quality of life in colorectal cancer survivors: a pilot study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5419570/
https://www.ncbi.nlm.nih.gov/pubmed/28475614
http://dx.doi.org/10.1371/journal.pone.0176929
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