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Effects of glutamine on plasma protein and inflammation in postoperative patients with colorectal cancer: a meta-analysis of randomized controlled trials

OBJECTIVE: To evaluate the effects of glutamine on the plasma protein and inflammatory responses in colorectal cancer (CRC) patients following radical surgery. METHODS: We thoroughly retrieved online databases (EMBASE, MEDLINE, PubMed, and others) and selected the randomized controlled trials (RCTs)...

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Autores principales: Xiong, Kai, Li, Guangsong, Zhang, Yu, Bao, Tiantian, Li, Ping, Yang, Xiangdong, Chen, Jiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10421765/
https://www.ncbi.nlm.nih.gov/pubmed/37566134
http://dx.doi.org/10.1007/s00384-023-04504-8
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author Xiong, Kai
Li, Guangsong
Zhang, Yu
Bao, Tiantian
Li, Ping
Yang, Xiangdong
Chen, Jiang
author_facet Xiong, Kai
Li, Guangsong
Zhang, Yu
Bao, Tiantian
Li, Ping
Yang, Xiangdong
Chen, Jiang
author_sort Xiong, Kai
collection PubMed
description OBJECTIVE: To evaluate the effects of glutamine on the plasma protein and inflammatory responses in colorectal cancer (CRC) patients following radical surgery. METHODS: We thoroughly retrieved online databases (EMBASE, MEDLINE, PubMed, and others) and selected the randomized controlled trials (RCTs) with glutamine vs. conventional nutrition or blank treatment up until March 2023. The plasma protein associated markers indicators (consisting of albumin (ALB), prealbumin (PA), nitrogen balance (NB), total protein (TP)), inflammatory indicators (including TNF-α, CRP, infectious complications (ICs)), and matching 95% confidence intervals (CIs) were evaluated utilizing the pooled analysis. Subsequently, meta-regression analysis, contour-enhanced funnel plot, Egger’s test, and sensitivity analysis were carried out. RESULTS: We discovered 26 RCTs, included an aggregate of 1678 patients, out of which 844 were classified into the glutamine group whereas 834 were classified into the control group. The findings recorded from pooled analysis illustrated that glutamine substantially enhanced the plasma protein markers (ALB [SMD([random-effect]) = 0.79, 95% CI: 0.55 to 1.03, I(2) = 79.4%], PA [SMD([random-effect]) = 0.94, 95% CI: 0.69 to 1.20, I(2) = 75.1%], NB [SMD([random-effect]) = 1.11, 95% CI: 0.46 to 1.75, I(2) = 86.9%). However, the content of TP was subjected to comparison across the 2 groups, and no statistical significance was found (SMD([random-effect]) = − 0.02, 95% CI: − 0.60 to 0.57, P = 0.959, I(2) = 89.7%). Meanwhile, the inflammatory indicators (including TNF-α [SMD([random-effect]) = − 1.86, 95% CI: − 2.21 to − 1.59, I(2) = 56.7%], CRP [SMD([random-effect]) = − 1.94, 95% CI: − 2.41 to − 1.48, I(2) = 79.9%], ICs [RR([fixed-effect]) = 0.31, 95% CI: 0.21 to 0.46, I(2) = 0.00%]) were decreased significantly followed by the treatment of glutamine. CONCLUSIONS: The current study’s findings illustrated that glutamine was an effective pharmaco-nutrient agent in treating CRC patients following a radical surgical operation. PROSPERO registration number: CRD42021243327. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00384-023-04504-8.
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spelling pubmed-104217652023-08-13 Effects of glutamine on plasma protein and inflammation in postoperative patients with colorectal cancer: a meta-analysis of randomized controlled trials Xiong, Kai Li, Guangsong Zhang, Yu Bao, Tiantian Li, Ping Yang, Xiangdong Chen, Jiang Int J Colorectal Dis Review OBJECTIVE: To evaluate the effects of glutamine on the plasma protein and inflammatory responses in colorectal cancer (CRC) patients following radical surgery. METHODS: We thoroughly retrieved online databases (EMBASE, MEDLINE, PubMed, and others) and selected the randomized controlled trials (RCTs) with glutamine vs. conventional nutrition or blank treatment up until March 2023. The plasma protein associated markers indicators (consisting of albumin (ALB), prealbumin (PA), nitrogen balance (NB), total protein (TP)), inflammatory indicators (including TNF-α, CRP, infectious complications (ICs)), and matching 95% confidence intervals (CIs) were evaluated utilizing the pooled analysis. Subsequently, meta-regression analysis, contour-enhanced funnel plot, Egger’s test, and sensitivity analysis were carried out. RESULTS: We discovered 26 RCTs, included an aggregate of 1678 patients, out of which 844 were classified into the glutamine group whereas 834 were classified into the control group. The findings recorded from pooled analysis illustrated that glutamine substantially enhanced the plasma protein markers (ALB [SMD([random-effect]) = 0.79, 95% CI: 0.55 to 1.03, I(2) = 79.4%], PA [SMD([random-effect]) = 0.94, 95% CI: 0.69 to 1.20, I(2) = 75.1%], NB [SMD([random-effect]) = 1.11, 95% CI: 0.46 to 1.75, I(2) = 86.9%). However, the content of TP was subjected to comparison across the 2 groups, and no statistical significance was found (SMD([random-effect]) = − 0.02, 95% CI: − 0.60 to 0.57, P = 0.959, I(2) = 89.7%). Meanwhile, the inflammatory indicators (including TNF-α [SMD([random-effect]) = − 1.86, 95% CI: − 2.21 to − 1.59, I(2) = 56.7%], CRP [SMD([random-effect]) = − 1.94, 95% CI: − 2.41 to − 1.48, I(2) = 79.9%], ICs [RR([fixed-effect]) = 0.31, 95% CI: 0.21 to 0.46, I(2) = 0.00%]) were decreased significantly followed by the treatment of glutamine. CONCLUSIONS: The current study’s findings illustrated that glutamine was an effective pharmaco-nutrient agent in treating CRC patients following a radical surgical operation. PROSPERO registration number: CRD42021243327. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00384-023-04504-8. Springer Berlin Heidelberg 2023-08-11 2023 /pmc/articles/PMC10421765/ /pubmed/37566134 http://dx.doi.org/10.1007/s00384-023-04504-8 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Review
Xiong, Kai
Li, Guangsong
Zhang, Yu
Bao, Tiantian
Li, Ping
Yang, Xiangdong
Chen, Jiang
Effects of glutamine on plasma protein and inflammation in postoperative patients with colorectal cancer: a meta-analysis of randomized controlled trials
title Effects of glutamine on plasma protein and inflammation in postoperative patients with colorectal cancer: a meta-analysis of randomized controlled trials
title_full Effects of glutamine on plasma protein and inflammation in postoperative patients with colorectal cancer: a meta-analysis of randomized controlled trials
title_fullStr Effects of glutamine on plasma protein and inflammation in postoperative patients with colorectal cancer: a meta-analysis of randomized controlled trials
title_full_unstemmed Effects of glutamine on plasma protein and inflammation in postoperative patients with colorectal cancer: a meta-analysis of randomized controlled trials
title_short Effects of glutamine on plasma protein and inflammation in postoperative patients with colorectal cancer: a meta-analysis of randomized controlled trials
title_sort effects of glutamine on plasma protein and inflammation in postoperative patients with colorectal cancer: a meta-analysis of randomized controlled trials
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10421765/
https://www.ncbi.nlm.nih.gov/pubmed/37566134
http://dx.doi.org/10.1007/s00384-023-04504-8
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