key: cord-0024695-m926kn69
authors: Yang, Tao; Yan, Xuhong; Cao, Yibo; Bao, Tiantian; Li, Guangsong; Gu, Shengliang; Xiong, Kai; Xiao, Tianbao
title: Meta-analysis of Glutamine on Immune Function and Post-Operative Complications of Patients With Colorectal Cancer
date: 2021-12-06
journal: Front Nutr
DOI: 10.3389/fnut.2021.765809
sha: b04ecd81023e19a609fbaee8f5bf50cce668e21e
doc_id: 24695
cord_uid: m926kn69

The aim of this meta-analysis was to evaluate the clinical significance of glutamine in the management of patients with colorectal cancer (CRC) after radical operation. Electronic databases, including PubMed, EMBASE, MEDLINE, Cochrane Library, Chinese Biomedical Database (CBM), China National Knowledge Infrastructure (CNKI), VIP medicine information system (VIP), and Wanfang electronic databases were comprehensively searched from inception to 30, July 2021. Prospective randomized trials with glutamine vs. routine nutrition or blank therapy were selected. The immune function related indicators (including IgA, IgG, IgM, CD4+, CD8+, and the ratio of CD4+/CD8+), post-operative complications [including surgical site infection (SSI), anastomotic leakage, and length of hospital stay (LOS)], and corresponding 95% confidence intervals (CIs) were assessed in the pooled analysis. Subsequently, the heterogeneity between studies, sensitivity, publication bias, and meta-regression analysis were performed. Consequently, 31 studies which contained 2,201 patients (1,108 in the glutamine group and 1,093 in the control group) were included. Results of pooled analysis indicated that glutamine significantly improved the humoral immune function indicators [including IgA (SMD = 1.15, 95% CI: 0.72–1.58), IgM (SMD = 0.68, 95% CI: 0.48–0.89), and IgG (SMD = 1.10, 95% CI: 0.70–1.50)], and the T cell immune function indicators [including CD4+ (SMD = 0.76, 95% CI: 0.53–0.99) and the ratio of CD4+/CD8+ (SMD = 0.92, 95% CI: 0.57–1.28)]. Meanwhile, the content of CD8+ was decreased significantly (SMD = −0.50, 95% CI: −0.91 to −0.10) followed by glutamine intervention. Pooled analysis of SSI (RR = 0.48, 95% CI: 0.30–0.75), anastomotic leakage (RR = 0.23, 95% CI: 0.09–0.61), and LOS (SMD = −1.13, 95% CI: −1.68 to −0.58) were decreased significantly in glutamine group compared with control group. Metaregression analysis revealed that the covariate of small-sample effects influenced the robustness and reliability of IgG outcome potentially. Findings of the present work demonstrated that glutamine ought to be applied as an effective immunenutrition therapy in the treatment of patients with CRC after radical surgery. The present meta-analysis has been registered in PROSPERO (no. CRD42021243327). Systematic Review Registration: https://www.crd.york.ac.uk/PROSPERO, Identifier: CRD42021243327.

Colorectal cancer (CRC) is the most malignant tumors in digestive system and has become a serious threat to human health. Statistically, the global data showed that newly increased patients with CRC ∼1,880,725 (including 1,148,515 cases of colon cancer and 732,210 cases of rectum cancer), and the fatality rate of CRC was estimated to be ∼9.4% (1) . Furthermore, the death rate from CRC is predicted to increase by 60% (colon cancer) and 71.5% (rectum cancer), respectively, in 2035 (2) . Data from the American Cancer Society indicates that CRC is the third most common cancer diagnosed in both men and women in the United States. The number of CRC cases in the US for 2021 are: 1,04,270 new cases of colon cancer and 45,230 new cases of rectal cancer (3) . From 2012 through 2016, CRC increased every year by 2% in people younger than 50 and 1% in people 50-64 in the US (3) .

Surgical treatment in the management of non-metastatic or resectable CRC is irreplaceable and recommended as the firstline for radical treatment by the National Comprehensive Cancer Network (NCCN) Guidelines (4, 5) and European Society for Medical Oncology (ESMO) Guidelines (6, 7) . However, due to the long-term consumption of tumor before the radical resection of CRC, insufficient nutritional intake, and the stress responses caused by surgical trauma the patients are most likely to suffer from malnutrition, decreased immune function, intestinal dysfunction, and post-operative complications. Previous studies have reported that malnutrition prevalence has been widely reported to reach 15-40% in patients with cancer at the time of diagnosis, and up to 80-90% in advanced cases of the disease (8) . The prevalence of malnutrition in CRC patients also ranged from 45 to 60% (9) and these rates significantly increased followed by radical surgery (10) . In addition, immune dysfunction or immunosuppression caused by surgery acted as the main inducement of post-operative complications. Many studies have attributed post-operative complications such as surgical site infection (SSI), anastomotic leak, ureteral injury, intraabdominal abscess, enteric fistula, bleeding, and post-operative bowel obstruction to immune dysfunction and malnutrition (11) (12) (13) (14) . Consequently, these complications not only significantly affected the short-term outcomes, such as the prolonging length of hospital stay (LOS) and increasing associated health costs, but it also deteriorated the long-term oncological results, including declining patients' quality of life and cancer recrudescence (15, 16) .

Increasing evidences from clinical researches demonstrated that immunonutrition therapy was very likely to improve the immune function and decrease complications or recrudescence in patients after CRC surgery (17) (18) (19) (20) . Glutamine, a critical substance of immunenutrition, is an important source of energy for the intestinal tract and could improve intestinal function. Many studies have revealed the positive role of glutamine in CRC patients who underwent radical surgery (21) (22) (23) . Furthermore, glutamine levels in serum could affect overall survival (OS) and progression-free survival (PFS) significantly, and serum glutamine levels may be applied as a prognostic indicator in patients with CRC (24, 25) . However, other studies indicated that glutamine applied in CRC patients did not significantly improve the survival outcomes or post-operative complications (26) (27) (28) .

These evidences were hard to match due to the heterogeneity of study designs, study populations, sample quantities, and systematic approaches based upon current clinical studies. To address those ambiguities and to evaluate the actual clinical significance of glutamine in patients with CRC, a meta-analysis of randomized, prospective clinical trials about glutamine applied in CRC patients who underwent radical surgery was conducted. This meta-analysis provided essential evidence of the effects of glutamine on immune functions and post-operative complications of patients with CRC.

We have registered this protocol previously in PROSPERO in April 2021 (number: CRD42021243327, https://www.crd.york. ac.uk/PROSPERO).

The Cochrane Handbook for Systematic Reviews of Interventions and the PRISMA statement was referred by this study and the "PICOS" principles was employed for developing the inclusion and exclusion criteria. Studies that meet the following inclusion criteria were included: (1) the design of study was a prospectively randomized controlled trial (RCT); (2) patients with CRC (including colon cancer and rectal cancer) and undergone radical surgery; (3) glutamine was set as experiment group and routine nutrition or blank therapy (fluid supporting therapy) as control group; (4) at least one of the investigated outcomes was reported in original researches. The exclusion criteria were as follows: (i) irrelevant studies and duplicated literatures; (ii) unavailable data literatures; (iii) letters, reviews, comments, case-report, laboratory studies, and meta-analysis.

The PubMed, EMBASE, MEDLINE, Cochrane Library, Chinese Biomedical Database (CBM), China National Knowledge Infrastructure (CNKI), VIP medicine information system (VIP), and Wanfang electronic databases were comprehensively searched up to July 30, 2021. The search terms were in the combination of medical subject headings (MeSH) terms and the following free words: (Colon/Rectal/colorectal/cancer/ tumor/carcinoma/neoplasm) AND (glutamine/nutrition/ immunenutrition) AND (complication/infection/leakage) AND (immune/immunity/IgA/IgG/IgM/CD4+/CD8+/CD4+/CD8+) AND (random/randomized/RCTs/clinical trial). In addition, potentially relevant references were also obtained manually. The language of all the publications was not limited.

All search results were combined in Endnote TM , Version X8 (Thompson Reuters). Duplicates were removed manually. Two investigators (Tao Yang and Xuhong Yan) filtered the original studies independently. If the literature meets the eligibility criteria, the two investigators will further read the full text to screen the study. Any discrepancies were tackled by discussion or third-party consensus.

All data were collected independently by two investigators (Tao Yang and Yibo Cao) from eligible RCTs using a standardized form. The following information were extracted including: (i) Study ID, including the name of the first author and publication year; (ii) study subjects, number of participants, and their ages; (iii) treatment regimens for the treatment and control groups; and (iv) the primary endpoint, the immune function related indicators (including IgA, IgG, IgM, CD4+, CD8+, and the ratio of CD4+/CD8+) and the secondary endpoint, the post-operative complications (including SSI, anastomotic leakage, and LOS). If insufficient details were reported, we would contact authors for further information. Disagreements between two investigators were tackled by discussion and consensus.

The Cochrane Collaboration's tool for assessing risk of bias were employed for quality evaluation. Any disagreements during assessment were resolved by iteration, discussion, and consensus.

All data were analyzed using Stata version 14.0 (Stata Corporation). Heterogeneity amongst studies was assessed using a Q-test and an I²-test before determining the pooled effect. A Frontiers in Nutrition | www.frontiersin.org fixed effects model or a random effects model was based on the results of the Q-test and I²-test. A fixed effects model was adopted if I² < 50% and p > 0.1. Otherwise, a random effects model was used. The primary endpoint was immune function related indicators (IgA, IgG, IgM, CD4 + , CD8 + , and CD4 + /CD8 + ) and LOS was a continuous variable. The pooled analysis of these indicators was expressed as standard mean difference (SMD). The SSI and anastomotic leakage were dichotomous variables, and the pooled analysis of these complications was expressed as relative risks (RR). The significance of pooled effects was determined using a Z-test; p < 0.05 was considered to indicate a statistically significant difference. Sensitivity analysis was utilized to investigate the influence of a highrisk study on overall meta-analysis. Possible publication bias and the detailed reasons underlying publication bias were determined by contour-enhanced funnel plot. Possible source of heterogeneity was explored by metaregression performing via random effect model, and the restricted maximum likelihood (REML) estimation method proposed by Harbord et al. (29) was applied in metaregression.

A total of 444 relevant articles were retrieved ultimately. Among these, 304 were repeated articles. Totally, 84 literatures were excluded by screening the titles and abstracts due to reviews, conference abstract, animal experiments, case report, with 56 articles remaining. Then 25 articles were excluded by examining the abstracts or full-texts. Finally, this meta-analysis included 31 studies that fulfilled the inclusion criteria (Figure 1 ).

Totally, 2,201 patients were involved in 31 studies (21) (22) (23) . Among these, 1,108 were allocated to the glutamine group and 1,093 patients were allocated to the control group. 

Methodological quality assessment and outline of the included 31 studies were presented in Figures 2A,B . The generation of randomized sequence was identified adequately in all trials. The allocation concealment was unclear according to all trials. These trials were neither single nor double blinding design. Consequently, the evaluation of detection bias was high risk (Figure 2B) . Incomplete outcomes and selective reporting were not detected in all studies. Conclusively, the methodological quality of all included trials stayed at a lower level due to the lack of blinding.

Glutamine on Humoral Immune Function of Patients With CRC

The pooled analysis of humoral immune function indicators (IgA, IgM, IgG) is presented in Figure 3 and SMD presentation. Heterogeneity was examined firstly before pooled analysis of these indicators. Test results revealed that there was a significant heterogeneity for IgA (I²-test = 89.3% and Q-test p = 0.000, Figure 3A ), moderate heterogeneity for IgM (I²-test = 65.2% and Q-test p = 0.000, Figure 3B) , and significant heterogeneity for IgG (I²-test = 89.9% and Q-test p = 0.000, Figure 3C) between included studies. Thus, a random effect model was selected for pooled analysis. Results revealed that IgA content was significantly increased (Z = 5.27, p = 0.000; SMD = 1.15, 95% CI: 0.72-1.58; Figure 3A ) in the glutamine group compared with the control group. Meanwhile, the indicator of IgM was also increased (Z = 6.47, p = 0.000; SMD = 0.68, 95% CI: 0.48-0.89; Figure 3B ) in glutamine group. In addition, the indicator of IgG was significantly increased (Z = 5.34, p = 0.000; SMD = 1.10, 95% CI: 0.70-1.50; Figure 3C ) in glutamine group compared with control group. These results demonstrated that glutamine improved the humoral immune function effectively for patients with CRC after radical operation.

Before pooled analysis of T cell immune function indicators (CD4+, CD8+, CD4+/CD8+), heterogeneity across studies was tested conventionally. Heterogeneity test results revealed there was moderate heterogeneity for CD4+ (I²-test = 71.2% and Qtest p = 0.000, Figure 4A ), significant heterogeneity for CD8+ (I²-test = 89.9% and Q-test p = 0.000, Figure 4B) , and significant heterogeneity for CD4+/CD8+ (I²-test = 85.9% and Q-test p = 0.000, Figure 4C ). So, a random effect model was selected for pooled analysis. In the pooled meta-analysis, the content of CD4+ was increased significantly (Z = 6.47, p = 0.000; SMD = 0.76, 95% CI: 0.53-0.99; Figure 4A ) in the glutamine group compared with the control group. On the contrary, the content of CD8+ was decreased significantly (Z = 2.44, p = 0.015; SMD = −0.50, 95% CI: −0.91 to −0.10; Figure 4B ) in the glutamine group. Meanwhile, the ratio of CD4+/CD8+ was increased significantly (Z = 5.07, p = 0.000; SMD = 0.92, 95% CI: 0.57-1.28; Figure 4C ) in the glutamine group compared with the control group. Results are shown in Figure 4 and SMD presentation.

Heterogeneity was examined prior to pooled analysis of SSI, anastomotic leakage, and LOS. Test results revealed there were no significant heterogeneity across 12 studies (I²-test = 0.0% and Q-test p = 0.909, Figure 5A ) that reported SSI outcome, seven studies (I²-test = 0.0% and Q-test p = 0.944, Figure 5B ) that reported anastomotic leakage. Thus, a fixed effects model was applied for the pooled analysis. However, results revealed there was significant heterogeneity for LOS outcome (I²-test = 85.6% and Q-test p = 0.000, Figure 5C ). So, a random effect model was employed for pooled analysis. In the pooled metaanalysis, the rates of SSI were decreased significantly (Z 

Sensitivity analysis via leave-one-out procedure each time was carried out to verify robustness of pooled results (LOS, IgA, IgG, CD8+, and CD4+/CD8+) with significant heterogeneity (≥80%) across included studies. Results are shown in Figure 6 . Sensitivity analysis of LOS outcome ( Figure 6A ) indicated that exclusion of any study did not account for heterogeneity significantly, which demonstrated the pooled result of LOS was robust to some extent. Meanwhile, the same conclusions were retrieved from the sensitivity analysis of IgA (Figure 6B) , IgG (Figure 6C) , CD8+ (Figure 6D) , and CD4+/CD8+ ( Figure 6E ).

All results of sensitivity analysis demonstrated that the pooled results were robust to some extent.

Contour-enhanced funnel plot, which added conventional milestones in levels of statistical significance (p < 0.01, p < 0.05, p < 0.1 or p > 0.1) to funnel plots, was utilized to distinguish detail reasons of publication bias. Results of SSI ( Figure 7A ) indicated many studies were in areas of none-statistical significance (p > 0.1), which suggested that the origin of asymmetry may be more likely due to publication bias. Furthermore, results of IgA (Figure 7B) , IgM (Figure 7C) , IgG (Figure 7D) , CD4+ (Figure 7E) , CD8+ (Figure 7F) , and CD4+/CD8+ (Figure 7G) presented that a great majority of missing studies were in areas of higher statistical significance (p < 0.01), which indicated the origin of asymmetry was most likely to be due to undetected factors rather than publication bias. Subsequently, we traced the original researches again, speculating that studies with a small sample size, ITT analysis, and missing blinding in many studies may account for those undetected bias. These factors may influence our conclusions potentially.

Metaregression was performed to assess the effect of underlying confounding factors on pooled effect estimation and to seek the sources of heterogeneity. The following covariates were predicted as potential factors premeditatedly: x Administration route (PN or EN) of glutamine; y Tumor type (Colon/rectal/CRC); z Total sample size (<100 or ≥100). Overall, univariate analysis indicated the administration route (PN or EN) of glutamine (Table 2, Figure 8A ) and type of tumor (Table 2, Figure 8B ) had no significant influence on the results of SSI, IgA, IgM, IgG, CD4+, CD8+, and CD4+/CD8+ outcomes (p > 0.05). The remaining variable of total sample size had significant influences on the pooled effects of IgM (p = 0.03, Table 2 , Figure 8C ) and IgG (p = 0.01, Table 2, Figure 8C ). Then, multivariate metaregression was utilized to evaluate the impact of multicovariates on the pooled effects. Three mentioned covariates (administration route of glutamine, tumor type, and total sample size) did not affect the pooled effects of SSI, IgA, IgM, CD4+, CD8+, and CD4+/CD8+, and the heterogeneity did not stem from this model (p > 0.05, Table 2, Figure 8D ). However, multivariate analysis revealed that the endpoint of IgG was influenced by the covariate of total sample size (P = 0.02, Table 2 , Figure 8D) , which indicated the heterogeneity may originate from this covariate.

Overall, findings from this study illustrated that immune functions (including humoral immune function and T cell immune function) can be improved significantly with glutamine in sufferers with CRC. Meanwhile, the main post-operative complications also reduced by glutamine in patients with CRC after surgery. The certainty of conclusion from current study is mainly reflected in the following three aspects. First were decreased significantly in glutamine group compared with control group. All supporting evidence mentioned above demonstrated that glutamine should be applied as an effective immunenutrition therapy in the treatment of CRC patients after radical surgery. Immunenutrition support for patients who underwent radical surgery for CRC is widely accepted for reducing the incidence and severity of post-operative complications. However, appropriate assessment and application of immunenutrition therapies were largely neglected (58) . Until to now, immunenutrition support is generally recommended by the European Society for Clinical Nutrition and Metabolism (ESPEN) for malnourished patients with cancer (59) , and it also coincided with the program of enhanced recovery after surgery (ERAS) (60) . Glutamine, a substance of immunenutrition, as the major fuel source for macrophages, lymphocytes, and enterocytes, could increase the immune cell responses and decrease inflammations evidently (61, 62) . For lymphocytes, glutamine activates the expression of T cell surface markers CD25, CD45RO, and CD71, promotes directly the proliferation of CD3+ (marker for mature lymphocytes) and T regulatory cells (T-reg) (63, 64) . Furthermore, glutamine also reduces lymphokine-activated killer cell activity (64, 65) . For monocytes and macrophages, glutamine stimulates antigen presentation, increases expression of surface antigens, and improves antioxidant defenses (66, 67) . Due to the high rates of glutamine utilization in lymphocytes, macrophages, and neutrophils, the deficiency of glutamine is mostly like to arise immune dysfunction (68, 69) . Previous study has indicated that glutamine could promote T cells differentiated into three subsets (Th1, Th17, and Treg). Meanwhile, glutaminase (GLS), which converts glutamine to glutamate, can promote Th17 but constrain Th1 and CTL effector cell differentiation (70) . In addition, a clinical trial reported that glutamine and omega-3 fatty acids not only increased the total lymphocyte count, CD4+, CD8+, complement C3, IgG, IgA in all patients, but also decreased C-reactive protein (CRP) and the rates of wound infection (71) . Thus, we come to the conclusion that deficiency of glutamine may lead to impaired immune function and ampliative inflammatory responses of CRC patients after radical surgery. On the contrary, glutamine supplementation could improve immune function and decrease complications after radical surgery in CRC patients.

This current work exerts more attention to the clinical benefits of glutamine in CRC patients after radical surgery. However, it is noteworthy that potential limitations of this integrated analysis should be emphasized. Thirty-one included trials were neither single nor double blinding design, which increases the risk of detection bias. Meanwhile, undetected bias predicted by contourenhanced funnel plot showed studies with a small sample size and missing ITT analysis may account for potential bias. These factors may have a potential impact on final conclusions. Metaregression by univariate and multivariate analysis found sample size included in original studies was a potential covariate causing significant heterogeneity, and deescalating validity of results in this pooled analysis.

All in all, this meta-analysis with 2,201 patients from 31 RCTs provide pivotal evidence that glutamine supplementation could improve immune function and decrease post-operative complications of CRC patients after radical surgery effectively. When accepting the conclusions of this study, the methodological limitations should be noticed at the same time. It is widely recognized that the management CRC in pre-or post-operative stages is very much needed in the participation of multiple disciplinary team (MDT) and requires long-term medication. Thus, increasing RCTs with larger scale and multidimensional efficacy and nutritional status assessment are extensively required to balance the risk-benefit profile of glutamine in the management of CRC.

The original contributions presented in the study are included in the article/supplementary material, further inquiries can be directed to the corresponding author/s.

TY, XY, and YC performed the search and drafted the manuscript. TY and XY performed the data extraction and analyzed the data. YC, TB, and TX designed the study and amended the original draft. GL, SG, and KX equally involved and contributed into the study conduction. All authors contributed to the article and approved the submitted version. 

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Our greatest acknowledgment to the authors who made detailed data available for this meta-analysis and all our colleagues in this study for their hard work.

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.