Improvement of energy substrate metabolism by late evening snack supplementation in patients with liver cirrhosis: a meta-analysis
Authors Yao J, Han W, Ren X, Yuan L, Xu J, Duan Z
Received 14 January 2019
Accepted for publication 8 April 2019
Published 15 May 2019 Volume 2019:15 Pages 659—668
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 2
Editor who approved publication: Professor Deyun Wang
Jia Yao,1,* Weijia Han,2,3,* Xiaojing Ren,1 Lili Yuan,1 Jun Xu,1 Zhongping Duan2,3
1Department of Gastroenterology and General Surgery, Shanxi Dayi Hospital, Taiyuan, People’s Republic of China; 2Difficult & Complicated Liver Diseases and Artificial Liver Center, Beijing Youan Hospital, Capital Medical University, Beijing, People’s Republic of China; 3Beijing Municipal Key Laboratory of Liver Failure and Artificial Liver Treatment Research, Beijing, People’s Republic of China
*These authors contributed equally to this work
Aim: Malnutrition is one of the most common complications in patients with liver cirrhosis. Abnormal energy substrate metabolism may contribute to aggravation of malnutrition. Late evening snack (LESs) supplementation has been recommended as an intervention to reduce starvation time and improve nutritional status. Published studies have analyzed the effect of LESs on the branched-chain amino acid (BCAA)/tyrosine ratio (BTR) and oxidation rate of fat and carbohydrate in patients with liver cirrhosis.
Methods: We searched PubMed, Cochrane Library, Web of Science and Embase for relevant research from January 2000 to October 2018. The primary outcome for this analysis was changes in BTR and fat and carbohydrate oxidation in patients with liver cirrhosis.
Results: A total of 9 articles, containing 211 patients, were included in this analysis. The results supported that supplementation with BCAA-enriched LESs improved BTR, and long-term supplementation with BCAAs (>1 month) may be more beneficial than short-term supplementation (<1 month) in patients with liver cirrhosis. In addition, supplementation with BCAAs may increase the oxidation rate of carbohydrates and decrease the oxidation rate of fat. Furthermore, compared with liquid-enriched LESs, BCAA was a better choice for increasing the oxidation of carbohydrates and decreasing the rate of fat oxidation.
Conclusion: BCAA-enriched LES supplementation is an appropriate nutritional intervention to improve abnormal energy substrate metabolism, which may improve malnutrition in patients with liver cirrhosis. Further research is needed on the long-term benefit and improved survival in patients with liver cirrhosis.
Keywords: cirrhosis, late evening snack, branched-chain amino acid, energy metabolism
Malnutrition is one of the most common complications in patients with liver cirrhosis and is associated with an increased risk of morbidity and mortality.1 As an important part of the comprehensive treatment of liver cirrhosis, nutritional intervention can help to improve the nutritional status and quality of life of patients with liver cirrhosis.2 The liver is an important organ for maintaining normal energy and nutrient metabolism. Therefore, it is important to explore appropriate nutritional interventions for patients with liver cirrhosis.
Abnormal energy substrate metabolism is characteristic of patients with liver cirrhosis, which may aggravate malnutrition.3 In particular, after overnight fasting, patients with liver cirrhosis show increased rates of fat oxidation and decreased rates of carbohydrate oxidation compared to normal controls. In addition, previous studies on the correlation between lifestyle and liver disease have shown that lower daily frequency of meals is associated with nonalcoholic fatty liver disease, which is a risk factor for the development of liver cirrhosis, and a high daily eating frequency is associated with healthy lifestyle.4,5 Therefore, increasing the frequency of eating is used as intervention. Late evening snacks (LESs), which add an extra meal before sleep, has been recommended as an intervention to reduce the starvation time and improve nutritional status.6,7
LESs are currently an effective method to improve the metabolic status of patients with end-stage liver disease.6 However, published studies have had small sample sizes. It is also unclear whether long-term intervention with LESs and whether branched-chain amino acids (BCAAs) are more suitable for patients with liver cirrhosis. In patients with liver cirrhosis, due to the decline in glycogen reserves and activated glutamine synthesis in muscle, the consumption of BCAAs increases, which can lead to an imbalanced ratio of BCAA to aromatic amino acids (AAAs).8 Clinically, the BCAA/tyrosine ratio (BTR) reflects the ratio of BCAAs to AAAs, and changes are closely related to liver dysfunction.9 Previous studies have shown that BTR is a prognostic factor for hepatocellular carcinoma.10 In addition, the rate of fat and carbohydrate oxidation is closely related to prognosis of cirrhosis.11 Therefore, this study summarizes the currently published literature that has analyzed the effects of LESs on BTR and the oxidation rate of fat and carbohydrate in patients with liver cirrhosis. It may provide evidence for the clinical application of LESs in patients with liver cirrhosis.
Material and methods
This meta-analysis was conducted and reported according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA).12 We selected articles from January 2000 to October 2018 using the databases of PubMed, Cochrane Library, Web of Science and Embase. All of the articles were about LESs in patients with liver cirrhosis. The following search terms were used: (“late evening snack” [Title/Abstract] or “nocturnal nutritional supplementation” [Title/Abstract] or “nocturnal snack” [Title/Abstract] or “evening snack” [Title/Abstract] or “nocturnal meal” [Title/Abstract]) or (“bedtime snack” [Title/Abstract]) and (“Liver Cirrhosis” [Title/Abstract] or “Cirrhosis,Liver” [Title/Abstract]) or “Cirrhoses, Liver”[Title/Abstract] or “Liver Cirrhoses” [Title/Abstract] or “Hepatic Cirrhosis” [Title/Abstract] or “Cirrhoses, Hepatic” [Title/Abstract] or “Cirrhosis, Hepatic” [Title/Abstract] or “Hepatic Cirrhoses”[Title/Abstract]) or “Cirrhosis, Hepatic” [Title/Abstract] or “Hepatic Cirrhoses” [Title/Abstract] or “Fibrosis, Liver” [Title/Abstract] or “Fibroses, Liver” [Title/Abstract] or “Liver Fibroses” [Title/Abstract] or “Liver Fibrosis” [Title/Abstract]).
Two investigators (J.Y. and W.H.) conducted a preliminary search separately, deleted duplicate records, sifted through relevant headings and abstracts, and identified relevant terms for further evaluation. References to retrieved articles were also reviewed to identify other eligible studies.
The study protocol was approved by the Ethics Committee of Beijing YouAn Hospital, Beijing, China.
Definition and study endpoints
Liver cirrhosis was diagnosed by clinical and laboratory profiles and by histological examination of liver biopsy specimens.13 The primary endpoint of this study was whether BTR and oxidation rate of carbohydrate and fat were affected by LESs.
Data extraction and quality assessment
Two investigators (J.Y. and W.H.) extracted the following information from the selected researches independently: first author, year of publication, intervention of experimental group, total numbers of patients enrolled, time of intervention for each event, levels of BTR, and oxidation rate of carbohydrate and fat before and after intervention. When research on the same patients appeared in multiple articles, to avoid duplication of information, we selected the study with the largest sample.
The US Agency for Healthcare Research and Quality (AHRQ) was used to evaluate bias risks in each study.
Inclusion criteria: liver cirrhosis was diagnosed on the basis of pathological examination findings and Child–Pugh classification. Exclusion criteria: patients had a history of other organ diseases, such as chronic heart failure or chronic respiratory, pancreatic or renal diseases.
We used Review Manager 5.2 and Stata 12.0 software for statistical analysis. Differences were expressed as mean ± standard deviation with 95% CI. Heterogeneity was tested using the I2 statistic. Heterogeneity was considered to be low in studies with I2 25–50%, moderate in studies with I2 50–75%, and high in studies with I2>75%. I2>50% represented significant heterogeneity. A fixed-effects model was used when study heterogeneity was not significant and a random-effects model when heterogeneity was significant. Begg’s test was used to estimate publication bias and sensitivity analysis was used to test stability.
Study selection and characteristics
The selection process is illustrated in Figure 1. A total of 9 articles met the inclusion criteria.14–22 The main characteristics of the included studies are described in Table 1. The meta-analysis included 221 patients from Japan, aged 42–85 years. One study was a randomized controlled trial (RCT)18 and the others were single-arm studies. Three of the 9 studies supplied a pack of LESs (210 kcal),14,17,22 others gave a pack of LESs and 1 or more supplements during the daytime. Three of the 9 studies used long-term LESs (>1 month)14,15,17 and the others used short-term LESs. Six of the 9 studies reported changes in BTR14–17,19,21 and 5 reported changes in fat and carbohydrate oxidation.18–22
Table 1 Characteristics of included researches
Figure 1 Flow diagram of study selection.
Although one study was an RCT, the baseline characteristics of each group were not comparable. We, therefore, compared the changes before and after LES treatment in each group, and we divided this RCT into 3 groups of one-arm study. Assessment of the single-arm studies by the AHRQ methodology checklist is shown in Table 2. All included single-arm studies described the source of data and patient inclusion and exclusion criteria clearly, provided detailed explanation for excluded data, and presented measurements for the primary study endpoints.
Table 2 The US Agency for Healthcare Research and Quality checklist for quality assessment of one-arm research
Effects of less on BTR
We selected 6 studies that measured the changes in BTR before and after LESs.14–17,19,21 BTR was increased after LESs (MD=0.79, 95% CI [0.15, 1.43]). The heterogeneity was significant (I2=90%) with publication bias (P<0.00001) (Figure 2A). In order to find the reason, subgroup analysis was performed by treatment period. Three of the studies had short-term LESs (<1 month) compared with >1 month in the others. BTR in the long-term LES group was increased with no heterogeneity (I2=0%), but BTR in the short-term LES group was increased with high heterogeneity (I2=96%) (Figure 2B). The differences between the groups were significant (P=0.02). The changes in BTR after long-term LESs were superior to that after short-term LESs.
In the long-term treatment subgroup, BACCs were given besides LESs in one study,15 and BACCs were given once a day as LESs in 2 studies.14,17 Subgroup analysis showed that BTR was increased in the two groups, but there was no difference between these 2 treatments (P=0.48) (Figure 2C).
Analysis of sensitivity was conducted to evaluate the robustness of the effect. The results showed that sensitivity was low (MD=0.58, 95% CI [0.35, 0.81], the range for all articles was 95% CI [0.27, 0.93]). Begg’s test showed publication bias in the 6 studies, although it was not significant (Pr > |z| =0.296, continuity corrected).
Effects of less on oxidation rate of fat
We selected 5 studies that measured changes in fat oxidation before and after LESs.18–22 Fat oxidation was decreased after LESs (MD= −13.21, 95% CI [−15.34, −11.07]) with low heterogeneity (I2=23%) (Figure 3A).
Patients in two studies17,22 were treated with a pack of liquid nutrients as LESs, and the others received a pack of BCAAs. Subgroup analysis showed that BCAAs and liquid nutrients decreased fat oxidation, although there was no significant difference between the 2 groups (P=0.15). There was no heterogeneity in the BCAA group, but the heterogeneity in the liquid nutrient group was significant (I2=73%) (Figure 3B), so this was an important source of heterogeneity. The results indicated BCAA was a better choice for reducing the oxidation rate of fat.
Analysis of sensitivity was conducted to evaluate the robustness of the effect. The results showed that sensitivity was low (mean estimate= −1.11, 95% CI [−1.42, −0.80]), and the range for all articles was 95% CI [−1.78, −0.65]). Begg’s test showed publication bias in the 5 studies, although it was not significant (Pr > |z| =0.086, continuity corrected).
Effects of less on oxidation rate of carbohydrate
We selected 5 studies that measured the oxidation rate of carbohydrate before and after LESs.18–22 The level of carbohydrate oxidation was increased after LESs (MD=11.92, 95% CI [9.88, 13.96]) with no heterogeneity (I2=0%) (Figure 4A).
Patients from two studies17,22 received LESs as liquid nutrients and the others received a pack of BCAAs. Subgroup analysis showed that BCAAs and liquid nutrients both increased the oxidation rate of carbohydrate, although there was no significant difference between the two treatment groups (P=0.18). There was no heterogeneity in the BCAA group, but the heterogeneity in the liquid nutrient group was significant (I2=59%) (Figure 4B), so this was an important source of heterogeneity. The result indicated that BCAA was a better choice for increasing the oxidation rate of carbohydrate.
Analysis of sensitivity was conducted to evaluate the robustness of the effect. The results showed that sensitivity was low (MD=1.09, 95% CI [0.78, 1.4]), the range for all articles was 95% CI [0.63, 1.67]). Begg’s test showed publication bias in the 5 studies, although it was not significant (Pr > |z| =0.086, continuity corrected).
Adverse effects of less
There were no adverse events related to LESs in any of the 9 articles.
This study evaluated the published literature on the effects of LESs, especially BCAA-based LESs. The results of the analysis supported that supplementation with BCAAs can improve BTR, and long-term supplementation with BCAAs (>1 month) may be more beneficial than short-term supplementation (<1 month) in patients with liver cirrhosis. In addition, supplementation with BCAAs may increase the oxidation rate of carbohydrates and decrease the oxidation rate of fat, thereby significantly improving abnormal energy substrate metabolism in patients with liver cirrhosis. LESs are one of the commonly used nutritional interventions, but there is a scarcity of high-quality research among published studies. The results of the present study may provide evidence for BCAAs as a major component of LESs to improve substrate metabolism in patients with liver cirrhosis.
Since the glycogen reserve of liver cells in patients with cirrhosis is less than that of normal people, short-term hunger can induce gluconeogenesis.3 Therefore, after a natural sleep cycle, fat and protein are the main energy-supplying substances, which is inclined to cause malnutrition in patients with liver cirrhosis.23,24 Therefore, to improve this condition, previous studies have proposed LESs as an intervention method, that is, giving a certain amount of calories at nighttime can reduce the time of hunger, thereby improving the abnormal substrate energy supply.25 Similar to previous studies, the present study supports the idea that LESs may improve the oxidation rate of carbohydrates and reduce the oxidation rate of fat in patients with liver cirrhosis. Furthermore, the BCAA-based LESs are better than fat-based LESs for increasing carbohydrate oxidation rate and reducing fat oxidation rate. Therefore, BCAA is considered to be a good choice for LES intervention.
Patients with liver cirrhosis often have amino acid metabolism disorder, which is often associated with a variety of complications such as hepatic encephalopathy and sarcopenia.14 Most studies have shown that BCAA supplementation improves amino acid profile, albumin level, and hepatic encephalopathy,26 and may also promote regeneration of liver cells.27 There is also research indicating that BCAAs can reduce the risk of liver cancer recurrence.28 However, to date, there has been no large study on BCAA supplementation in patients with liver cirrhosis. A total of 9 studies were pooled in the present study. The results showed that in patients with liver cirrhosis, BTR was significantly higher after than before oral BCAA supplementation. More importantly, there has been no study on the duration of BCAA supplementation. We showed that long-term BCAA supplementation (>1 month) may be more beneficial than short-term supplementation (<1 month) in patients with liver cirrhosis.
There were some limitations to this study, most of which were related to the quality of the research papers included. First, only 1 of the 9 studies was an RCT and the others were single-arm studies. Second, most of the studies had small samples. Third, most of the patients included in this study were Asians. Therefore, a large, multicenter RCT is needed to further analyze the effects of LESs, especially BCAA-based LESs, on patients with liver cirrhosis.
LESs based on BCAAs can improve BTR, increase the oxidation rate of carbohydrates, and decrease the oxidation rate of fat in patients with liver cirrhosis, which may improve the malnutrition in these patients. Long-term supplementation with BCAAs is more efficient and better than fat-based LESs. Our results may provide evidence for the clinical application of LESs in patients with liver cirrhosis. When patients are supplemented with BCAAs, one should also consider the individual choice of the patient and the detailed status of their condition. Therefore, further research requires a larger sample of more individualized and standardized treatments.
This study was funded by the Shanxi Province 136 revitalization medical project (General Surgery Department); Science Foundation of China, Grant/Award Number: 81600561; National Key R&D Program of China (No. 2017YFA0103000); Beijing Municipal Administration of Hospitals Clinical Medicine Development of Special Funding Support (No. ZYLX201806); “Beijing Municipal Administration of Hospitals” Ascent Plan (No. DFL20151601); National Science and Technology Key Project on “Major Infectious Diseases such as HIV/AIDS, Viral Hepatitis Prevention and Treatment” (Nos. 2012ZX10002004-006, 2017ZX10203201-005, 2017ZX10201201-001-001, 2017ZX10201201-002-002, 2017ZX10202203-006-001, 2017ZX10302201-004-002).
The authors report no conflicts of interest in this work.
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