Nutritional assessment in patients with liver cirrhosis

Sara Haj Ali, Awni Abu Sneineh, Reem Hasweh

Sara Haj Ali, Reem Hasweh, Department of Internal Medicine, Faculty of Medicine, Al-Balqa Applied University, Salt 19117, Jordan

Awni Abu Sneineh, Department of Gastroenterology and Hepatology, University of Jordan, Faculty of Medicine, Amman 11942, Jordan

Abstract Malnutrition is a liver cirrhosis complication affecting more than 20%-50% of patients. Although the term can refer to either nutrient deficiency or excess, it usually relates to undernutrition in cirrhosis settings. Frailty is defined as limited physical function due to muscle weakness, whereas sarcopenia is defined as muscle mass loss and an advanced malnutrition stage. The pathogenesis of malnutrition in liver cirrhosis is multifactorial, including decreased oral intake, maldigestion/malabsorption, physical inactivity, hyperammonemia, hypermetabolism, altered macronutrient metabolism and gut microbiome dysbiosis. Patients with chronic liver disease with a Body Mass Index of ＜ 18.5 kg/m2 and/or decompensated cirrhosis or Child-Pugh class C are at the highest risk of malnutrition. For patients at risk of malnutrition, a detailed nutritional assessment is required, typically including a history and physical examination, laboratory testing, global assessment tools and body composition testing. The latter can be done using anthropometry, cross-sectional imaging including computed tomography or magnetic resonance, bioelectrical impedance analysis and dual-energy X-ray absorptiometry. A multidisciplinary team should screen for and treat malnutrition in patients with cirrhosis. Malnutrition and sarcopenia are associated with an increased risk of complications and a poor prognosis in patients with liver cirrhosis; thus, it is critical to diagnose these conditions early and initiate the appropriate nutritional therapy. In this review, we describe the prevalence and pathogenesis of malnutrition in liver cirrhosis patients and discuss the best diagnostic approach to nutritional assessment for them.

Key Words: Malnutrition; Cirrhosis; Nutritional assessment; Sarcopenia; Nutrition; Frailty

lNTRODUCTlON

Malnutrition is defined as nutrient imbalance (deficiency or excess) with adverse effects on the body’s form, function or outcome. According to the European Association for the Study of Liver Disease (EASL), the term “malnutrition” refers to “undernutrition”[1]. Frailty is defined as limited physical function due to muscle weakness and diminished muscle contractility, while sarcopenia is defined as the generalized loss of muscle mass. Malnutrition is a common complication of liver cirrhosis, with a prevalence rate of 5-92%[2]. The prevalence of malnutrition increases with worsening liver disease[3]. It has been reported that one-fifth of patients with compensated cirrhosis and more than half the patients with decompensated cirrhosis have malnutrition[4]. Additionally, even patients with chronic liver disease who are not cirrhotic can have malnutrition. In this group of patients, malnutrition may be masked by obesity[5]. Due to the increasing prevalence of non-alcoholic fatty liver disease, overweight and obesity are becoming more common in cirrhotic patients. In this review, we describe the pathophysiology of malnutrition in liver cirrhosis and discuss the best diagnostic approach to assess the nutritional status of patients in clinical practice.

METHODS

A PubMed web-based search was conducted to review the literature published from its inception until January 1, 2022, using the keywords ‘malnutrition’, ‘nutritional assessment,’ ‘liver cirrhosis,’ and ‘sarcopenia.’ All relevant articles published in the English language were reviewed, and data on epidemiology, pathogenesis, diagnosis and prognosis were extracted.

PATHOGENESlS

There are multiple factors that contribute to the development of malnutrition and sarcopenia in liver cirrhosis (Figure 1). First, the principal cause of malnutrition is reduced oral intake, and this can be due to anorexia, early satiety, nausea and cognitive impairment in the setting of hepatic encephalopathy. Patients with liver cirrhosis often have altered taste and smell, which can cause anorexia due to changes in the oral flora, use of antibiotics, dry mouth, zinc or magnesium deficiency[6]. Additionally, imbalances between orexigenic and anorexigenic hormones and chronic elevations in cytokines like tumor necrosis factor (TNF)-α can also trigger anorexia[7,8]. Early satiety can be explained by abdominal distension secondary to ascites or altered intestinal motility, which is common in cirrhosis[9]. Furthermore, unpalatable low-salt diets followed by the patients with ascites, alcohol abuse, and frequent tests requiring fasting for hours can all contribute to decreased oral intake[8]. Second, nutrient maldigestion and malabsorption can occur due to reduced bile production, altered intestinal motility with subsequent small bowel bacterial overgrowth, portal hypertensive gastropathy/ enteropathy and long-term lactulose use[8]. Furthermore, pancreatic insufficiency frequently coexists with alcoholic liver cirrhosis, contributing to decreased nutrient uptake. Third, alteration in macronutrient metabolism is an important factor affecting nutritional status in cirrhosis. Carbohydrate metabolism is characterized by increased gluconeogenesis, elevated fasting serum insulin levels, insulin resistance, decreased glycogen synthesis and storage and the early use of lipids and proteins as substrates for energy production and gluconeogenesis[7]. It has been observed that the rate of fat and protein catabolism after a short overnight fast in patients with liver cirrhosis is similar to that of healthy individuals who underwent 2-3 d of starvation[10]. Abnormal protein metabolism manifests itself as more protein catabolism and less synthesis, low levels of branched-chain amino acids (BCAA), and higher levels of aromatic amino acids (AAA), resulting in a lower Fischer’s ratio (BCAA/AAA ratio) which has been associated with complications such as hepatic encephalopathy[11]. Hyperammonemia promotes muscle breakdown and sarcopenia by upregulating myostatin which inhibits protein synthesis[12]. Testosterone levels are decreased in cirrhotic males and this further contributes to decreased protein synthesis and loss of muscle mass[13].

Figure 1 Factors contributing to malnutrition and sarcopenia in liver cirrhosis.

Lipid metabolism exhibits increased lipolysis, lipid oxidation and ketogenesis[14]. Fourth, hypermetabolism affecting one-third of cirrhotic patients, contributes to malnutrition. It is defined as having a resting energy expenditure ＞ 120% of the predictive value, and it can be caused by infections or chronic inflammation and is not associated with sex, underlying cause or severity of liver disease[15]. Fifth, an imbalance of gut microbiota (dysbiosis) in liver cirrhosis has been suggested as a contributing factor in malnutrition. Short-chain fatty acid-producing bacteria such as Bacteroides are reduced in patients with cirrhosis, and there is a higher abundance of Campylobacterales in moderately malnourished cirrhotics; findings have been associated with malnutrition in children[16-19]. The alteration in gut microbiome composition leads to increased intestinal permeability, bacterial translocation and infectious complications like spontaneous bacterial peritonitis[20]. This results in increased protein catabolism and muscle mass loss mediated by inflammation. Finally, physical inactivity, which is common in patients with significant ascites or hepatic encephalopathy may contribute to reduced muscle mass[21].

Beta blockers have been suggested as a possible external factor contributing to malnutrition in cirrhosis. However, a recent study found that patients who received non-selective beta blockers had actually better skeletal muscle index and improvement in sarcopenia[22].

The role of portal hypertension in malnutrition and sarcopenia is not clear. There is very limited literature about the prevalence of malnutrition and sarcopenia in non-cirrhotic portal hypertension. A study by Lattanziet al[23] found that the prevalence of sarcopenia in non-cirrhotic portal hypertension was similar to that in patients with compensated cirrhosis. This could suggest that portal hypertension per se may play a role in the development of malnutrition and sarcopenia given the fact that those patients have less liver damage compared to cirrhotic patients. This theory could be supported by the fact that nutritional status improves after transjugular intrahepatic portosystemic shunt (TIPS) and resolution of portal hypertension[24,25].

DlAGNOSlS

Malnutrition screening tools

The EASL released clinical practice guidelines in 2019 on nutritional assessment and management in chronic liver disease patients[1]. They recommended the screening of all patients with chronic liver disease for the risk of malnutrition using two tests: The body mass index (BMI) and Child-Pugh classification. Patients with a BMI ＜ 18.5 kg/m2and/or those with Child-Pugh class C or decompensated cirrhosis are considered at higher risk for malnutrition. On the other hand, patients with BMI 18.5-29.9 kg/m2and are Child-Pugh class A or B should undergo nutritional screening using one of the following liver disease-specific malnutrition screening tools: The Royal Free Hospital-nutritional prioritizing tool (RFH-NPT) or the liver disease undernutrition screening tool. Those who are at low risk for malnutrition need follow-up and re-assessment every year, while patients with moderate or high risk for malnutrition should have a detailed nutritional assessment. In addition, patients with a high risk for malnutrition need to be assessed for sarcopenia as well (Figure 2).

Figure 2 Algorithm for nutritional screening and assessment in liver cirrhosis. Adapted from the European Association for the Study of the Liver (EASL) clinical practice guidelines (with permission from Elsevier). Citation: European Association for the Study of the Liver. EASL Clinical Practice Guidelines on nutrition in chronic liver disease. J. Hepatol. 2019, 70, 172-193. Copyright© 2018 European Association for the Study of the Liver. Published by Elsevier. BMI: Body mass index (Supplementary material).

RFH-NPT uses simple clinical questions that take less than 3 minutes to complete and can be used by non-specialist staff. It classifies patients into low (0 points), medium (1 point), or high risk (2-7 points) for malnutrition. It considers the patient’s nutritional history (unplanned weight loss, dietary intake, BMI) and the presence or absence of fluid overload (ascites and/or peripheral edema). Although it has been validated in a multicenter trial in the United Kingdom, it requires further testing[26]. RFH-NPT was reported to correlate with clinical deterioration, the severity of liver disease, and complications of liver cirrhosis and was found to be an independent predictor of clinical deterioration and transplant-free survival. Furthermore, improvement in RFH-NPT score was associated with improved survival[27]. RFH-NPT is recommended by the European Society of Parenteral Enteral Nutrition guidelines as the best available tool for malnutrition screening in liver disease[28].

The liver disease undernutrition screening tool uses six patient-directed questions about nutritional intake, weight loss, subcutaneous fat loss, muscle mass loss, fluid accumulation and decline in functional status. Its limitation is that it is entirely dependent on the patient’s subjective judgment and has a low negative predictive value[29]. As with RFH-NPT, it needs further validation.

Detailed nutritional assessment

Patients who are at risk of malnutrition during screening should undergo comprehensive nutritional evaluation for confirmation of malnutrition and characterization of their nutritional status. This should ideally be done by a registered dietician or nutritionist. The evaluation process includes history taking, physical examination, laboratory tests, subjective global assessment and specialized methods for body composition assessment.

HlSTORY

Patients should be asked about their dietary intake; recent weight loss; use of supplements; alcohol consumption; any eating barriers such as anorexia, nausea, altered taste or smell, abdominal distension or pain, or any socioeconomic barrier; and symptoms of nutritional deficiency such as dermatitis (zinc, niacin, vitamin A), sore tongue (folate, vitamin B12), or paresthesia (thiamine, pyridoxine, vitamin B12). Dietary intake can be assessed using 24-h dietary recall, which is simple to use and does not require a high level of literacy. However, one significant disadvantage is that it is dependent on the patient’s recall skills and may not be representative of daily meal selection or eating behavior[30]. Another option is a 3-d food diary, which requires patients to cooperate and follow standardized instructions; however, it may be burdensome for patients and difficult to implement in those with advanced disease. It is the preferred method because it relies the least on patient recall[31]. Repeated 24-h dietary recalls are another option[32]. At a minimum, the patients should be asked if their relative food intake has changed over time and, if so, how much.

PHYSlCAL EXAMlNATlON

It should include measuring the BMI; examination for ascites and edema; muscle wasting, which is usually done by assessing the temporalis muscle, quadriceps and deltoids; and loss of subcutaneous fat which can be assessed in the chest, eye sockets and triceps areas. The BMI divides patients into four categories: Underweight, normal weight, overweight, and obese. In cirrhotic patients, it can be used to diagnose obesity in the absence of fluid retention. In the case of fluid retention, the patient's dry weight should be used, which can be estimated using the documented patient’s weight prior to the development of fluid retention if available, the patient’s weight post paracentesis, or by subtracting a percentage of weight based on the severity of ascites (5% for mild, 10% for moderate and 15% for severe) with an additional 5% subtracted if bilateral lower limb edema is present[33,34]. This has not been validated yet but has demonstrated excellent inter-observer agreement.

LAΒORATORY TESTS

The use of serum biomarkers for the diagnosis of malnutrition is controversial and currently they only complement the nutritional assessment[35]. Complete blood count; serum creatinine; serum albumin, Creactive protein (CRP); levels of vitamins and minerals like zinc, phosphorus, magnesium and iron are included in laboratory tests. Serum protein measurements may be limited in patients with advanced liver cirrhosis and synthetic dysfunction because they do not always reflect nutritional status. CRP may be useful in assessing catabolism and interpreting the results of nutrient levels. It is important to tailor testing according to the patient’s underlying liver disease and comorbidities.

GLOΒAL ASSESSMENT TOOLS

Subjective global assessment

It consists of five historical parameters (weight loss, dietary changes, gastrointestinal symptoms, functional capacity and metabolic demand associated with the underlying disease) and three physical examination parameters (loss of subcutaneous fat, muscle wasting and edema/ascites)[36]. Based on the results of these parameters, the patient gets a rating of A (well-nourished), B (moderately malnourished) or C (severely malnourished). Although subjective global assessment (SGA) is simple to administer, has fair to good interobserver reproducibility[37] and correlates with post-operative outcomes in patients without liver cirrhosis, it underestimates the prevalence of sarcopenia and has a low agreement with other methods of nutritional assessment[34,38].

Royal free hospital-SGA

Due to the limitations of the SGA, the royal free hospital-SGA (RFH-SGA) was developed[39]. It consists of dietary intake, BMI based on dry weight and mid-arm muscle circumference. Patients are stratified into three groups: adequately nourished, moderately malnourished and severely malnourished. The RFH-SGA is reproducible, correlates with other measurements of body composition and has shown promise in predicting survival and post-transplant outcomes[40,41]. However, it takes a longer time than SGA and requires additional validation.

Assess for frailty

There are currently no standardized criteria for diagnosing frailty in cirrhosis. There are several geriatric measures that have been used to assess frailty in cirrhotic patients. The Liver Frailty Index measures hand grip strength, balance, and timed chair stands and has been found to be correlated with mortality[42]. The Fried frailty criteria include unintentional weight loss, self-reported exhaustion, grip strength, slow walking speed and low physical activity. An increase in the Fried frailty score was found to be associated with an increased risk of waiting list mortality[43]. The short physical performance battery measures repeated chair stands, balance, and timed 13-foot walk and has been shown to predict transplant waiting list mortality[43].

ΒODY COMPOSlTlON TESTlNG

Body composition testing is summarized in Table 1.

Anthropometry

These are simple and quick bedside methods for determining body fat and muscle mass that are unaffected by fluid retention. Triceps skin fold (TSF) and mid-arm muscle circumference (MAMC) are the most commonly used measurements [MAMC = mid-arm circumference - (TSF × 0.314)]. Both MAMC and TSF have been found to correlate with survival in cirrhotic patients, with MAMC having higher prognostic power than TSF[44]. These tests have interobserver variability and low accuracy.

Bioelectrical impedance analysis

It determines the water content of the body by measuring the resistance to electrical current flow within the body which is then used to estimate muscle mass. Bioelectrical impedance analysis (BIA) is measured with a special scale or by attaching electrodes to an arm and a leg. It is inexpensive, portable and simple to use; however, the results are influenced by the patient’s volume status which can change in cirrhosis[45].

Computed tomography

The gold standard for sarcopenia assessment is the quantification of muscle mass using cross-sectional imaging[46]. The skeletal muscle index (cm2/m2) is calculated by analyzing the abdominal skeletal muscles at the L3 vertebral level. Cut-off values based on an American study (50 cm2/m2in males and 39 cm2/m2in females) that correlated best with outcomes have been proposed, though ethnicity-specific criteria may be required given the fact that Asians have lower lean body mass compared to Western populations[47]. A meta-analysis of the impact of computed tomography (CT-assessed muscle mass on clinical outcomes in liver transplant patients showed an association between low muscle mass and mortality that was independent of the Model for End-Stage Liver Disease Score[48]. Obviously, the routine and multiple CT scans to diagnose sarcopenia are limited by the cost, availability, radiation and contrast exposures; however, since it is often used for other purposes in liver cirrhosis like evaluation of hepatocellular carcinoma and liver transplantation assessment, thus it can be used at least once for assessment of sarcopenia.

Magnetic resonance imaging

The use of magnetic resonance imaging for the assessment of sarcopenia has been suggested with the advantages of high accuracy and lack of ionizing radiation. It is only used for research purposes due to limitations of high cost and lack of cut-off values.

Ultrasonography

It has been more than two decades that the use of ultrasound for skeletal muscle mass estimation in the context of fluid retention has been proposed[49]. The biceps, anterior forearm flexors and quadriceps muscles correlated best with lean body mass. The test is radiation-free and allows bedside assessment at a low cost. A previous study showed that combining BMI with thigh muscle thickness measured by ultrasound is significantly correlated with sarcopenia diagnosedviacross-sectional imaging[34]. However, a more recent study found that ultrasound muscle thickness had no advantage over other bedside techniques (namely MAMC and BIA)[50].

Table 1 Comparison between body composition testing modalities

Dual-energy X-ray absorptiometry

It allows regional and whole-body assessment of bone mineral density, fat mass and lean mass. Even though it is less precise compared to a CT scan, it has a lower cost and radiation exposure which makes it more suitable for repeat testing during follow-up[51]. The major limitation is its validity in the case of fluid retention which can lead to the underestimation of sarcopenia. To overcome the confounding effect of ascites, use of appendicular lean mass that excludes the abdominal compartment has been proposed[52]. Other studies proposed the use of arm lean mass to further reduce the effect of lower limb edema and it was found to be superior to appendicular lean mass in terms of mortality[53,54].

lMPACT OF MALNUTRlTlON, SARCOPENlA AND FRAlLTY ON LlVER ClRRHOSlS

Malnutrition has a negative impact on cirrhosis progression and outcome[55]. For example, patients with cirrhosis who are malnourished were found to have twice the rates of hospitalizations and mortality as compared to well-nourished patients[56]. It has also been shown that malnutrition is a predictor of other complications of cirrhosis, such as infections, hepatic encephalopathy and ascites[57-59]. Malnutrition and sarcopenia are independent predictors of poor outcomes in patients with liver cirrhosis and in those undergoing liver transplantation[60-62]. In addition, sarcopenic obesity and myosteatosis are independently associated with long-term mortality in liver cirrhosis[63]. Furthermore, it has been demonstrated that the diagnosis of frailty in cirrhosis is associated with an increase in mortality[64]. Given the significant impact on morbidity and mortality, it is critical to screen all patients with liver cirrhosis for malnutrition and provide nutritional therapy to those who require it in order to improve their quality of life and survival. A multidisciplinary approach is the best way to accomplish this.

CONCLUSlON

Malnutrition is a common complication of liver cirrhosis with complex pathophysiology that adversely affects the clinical outcome. A stepwise diagnostic approach should be followed for early recognition and management.

FOOTNOTES

Author contributions:Haj Ali S collected data and wrote the draft; Abu Sneineh A critically revised the manuscript; Hasweh R collected data and wrote the draft.

Conflict-of-interest statement:All authors report no relevant conflict of interest for this article.

Open-Access:This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BYNC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is noncommercial. See: https://creativecommons.org/Licenses/by-nc/4.0/

Country/Territory of origin:Jordan

ORClD number:Sara Haj Ali 0000-0002-0825-7113; Reem Hasweh 0000-0001-8879-8659.

S-Editor:Wu YXJ

L-Editor:Filipodia

P-Editor:Wu YXJ