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Age increases MCP‐1 level in association with bariatric surgery operating time and metabolic risk severity

OBJECTIVE: Assess the role of inflammation on operating time in younger vs. older bariatric surgery patients. METHODS: Fifty‐five younger (F: 46, Age: 34.9 ± 4.0 years, body mass index [BMI]: 48.2 ± 1.0 kg m(−2)) and 48 older (F: 34, Age: 57.0 ± 5.1 years, BMI: 46.8 ± 1.0 kg m(−2)) adults were studi...

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Autores principales: Malin, S. K., Kaplan, J. L., Meng, L., Garmey, J. C., Kirby, J. L., Taylor, A. M., Hallowell, P. T., McNamara, C. A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5478804/
https://www.ncbi.nlm.nih.gov/pubmed/28706732
http://dx.doi.org/10.1002/osp4.105
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author Malin, S. K.
Kaplan, J. L.
Meng, L.
Garmey, J. C.
Kirby, J. L.
Taylor, A. M.
Hallowell, P. T.
McNamara, C. A.
author_facet Malin, S. K.
Kaplan, J. L.
Meng, L.
Garmey, J. C.
Kirby, J. L.
Taylor, A. M.
Hallowell, P. T.
McNamara, C. A.
author_sort Malin, S. K.
collection PubMed
description OBJECTIVE: Assess the role of inflammation on operating time in younger vs. older bariatric surgery patients. METHODS: Fifty‐five younger (F: 46, Age: 34.9 ± 4.0 years, body mass index [BMI]: 48.2 ± 1.0 kg m(−2)) and 48 older (F: 34, Age: 57.0 ± 5.1 years, BMI: 46.8 ± 1.0 kg m(−2)) adults were studied prior to surgery. Blood pressure, glycaemic control (fasting glucose/insulin, HbA(1c)), lipids (high‐density lipoprotein and triglycerides) and inflammation (monocyte chemoattractant protein‐1 [MCP‐1]) were assessed. Metabolic risk severity z‐scores were calculated from clinical outcomes. Omental adipose biopsies were collected at surgery for MCP‐1 protein analysis. Operating time was used to characterize surgical difficulty. RESULTS: Older vs. younger adults had higher HbA(1c) (P = 0.03). There was no difference in BMI, lipids, metabolic risk severity or insulin between groups, but operating time was longer in older vs. younger individuals (P = 0.04). Circulating MCP‐1 was also elevated in older vs. younger adults (P = 0.04) independent of HbA(1c), although this was not explained by omental fat. Nevertheless, serum MCP‐1 was associated with increased metabolic risk severity (R = 0.27, P = 0.01). In addition, operating time was linked to HbA(1c) (R = 0.30, P = 0.01) and omental MCP‐1 protein (R = 0.31, P < 0.01). CONCLUSIONS: MCP‐1 is associated with longer operating time and increased metabolic risk severity in older bariatric patients independent of glycaemic control. Pre‐operative treatment of inflammation may be required to enhance surgery effectiveness.
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spelling pubmed-54788042017-07-11 Age increases MCP‐1 level in association with bariatric surgery operating time and metabolic risk severity Malin, S. K. Kaplan, J. L. Meng, L. Garmey, J. C. Kirby, J. L. Taylor, A. M. Hallowell, P. T. McNamara, C. A. Obes Sci Pract Original Articles OBJECTIVE: Assess the role of inflammation on operating time in younger vs. older bariatric surgery patients. METHODS: Fifty‐five younger (F: 46, Age: 34.9 ± 4.0 years, body mass index [BMI]: 48.2 ± 1.0 kg m(−2)) and 48 older (F: 34, Age: 57.0 ± 5.1 years, BMI: 46.8 ± 1.0 kg m(−2)) adults were studied prior to surgery. Blood pressure, glycaemic control (fasting glucose/insulin, HbA(1c)), lipids (high‐density lipoprotein and triglycerides) and inflammation (monocyte chemoattractant protein‐1 [MCP‐1]) were assessed. Metabolic risk severity z‐scores were calculated from clinical outcomes. Omental adipose biopsies were collected at surgery for MCP‐1 protein analysis. Operating time was used to characterize surgical difficulty. RESULTS: Older vs. younger adults had higher HbA(1c) (P = 0.03). There was no difference in BMI, lipids, metabolic risk severity or insulin between groups, but operating time was longer in older vs. younger individuals (P = 0.04). Circulating MCP‐1 was also elevated in older vs. younger adults (P = 0.04) independent of HbA(1c), although this was not explained by omental fat. Nevertheless, serum MCP‐1 was associated with increased metabolic risk severity (R = 0.27, P = 0.01). In addition, operating time was linked to HbA(1c) (R = 0.30, P = 0.01) and omental MCP‐1 protein (R = 0.31, P < 0.01). CONCLUSIONS: MCP‐1 is associated with longer operating time and increased metabolic risk severity in older bariatric patients independent of glycaemic control. Pre‐operative treatment of inflammation may be required to enhance surgery effectiveness. John Wiley and Sons Inc. 2017-04-26 /pmc/articles/PMC5478804/ /pubmed/28706732 http://dx.doi.org/10.1002/osp4.105 Text en © 2017 The Authors. Obesity Science & Practice published by John Wiley & Sons Ltd, World Obesity and The Obesity Society. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Malin, S. K.
Kaplan, J. L.
Meng, L.
Garmey, J. C.
Kirby, J. L.
Taylor, A. M.
Hallowell, P. T.
McNamara, C. A.
Age increases MCP‐1 level in association with bariatric surgery operating time and metabolic risk severity
title Age increases MCP‐1 level in association with bariatric surgery operating time and metabolic risk severity
title_full Age increases MCP‐1 level in association with bariatric surgery operating time and metabolic risk severity
title_fullStr Age increases MCP‐1 level in association with bariatric surgery operating time and metabolic risk severity
title_full_unstemmed Age increases MCP‐1 level in association with bariatric surgery operating time and metabolic risk severity
title_short Age increases MCP‐1 level in association with bariatric surgery operating time and metabolic risk severity
title_sort age increases mcp‐1 level in association with bariatric surgery operating time and metabolic risk severity
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5478804/
https://www.ncbi.nlm.nih.gov/pubmed/28706732
http://dx.doi.org/10.1002/osp4.105
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