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Review

Radiologic Definition of Sarcopenia in Chronic Liver Disease

by
Chul-min Lee
,
Bo Kyeong Kang
and
Mimi Kim
*
Department of Radiology, College of Medicine, Hanyang University, Seoul 04763, Korea
*
Author to whom correspondence should be addressed.
Life 2021, 11(2), 86; https://doi.org/10.3390/life11020086
Submission received: 16 December 2020 / Revised: 18 January 2021 / Accepted: 21 January 2021 / Published: 25 January 2021
(This article belongs to the Special Issue Sarcopenia and Liver Disease: Current and Future Perspectives)
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Abstract

:
Sarcopenia is prevalent in patients with chronic liver disease, and affected patients tend to have worse clinical outcomes and higher mortality. However, relevant analyses are limited by heterogeneity in the definition of sarcopenia and in the methodological approaches in assessing it. We reviewed several radiologic methods for sarcopenia in patients with chronic liver disease. Dual energy X-ray absorptiometry (DXA) can measure muscle mass, but it is difficult to evaluate muscle quality using this technique. Computed tomography, known as the gold standard for diagnosing sarcopenia, enables the objective measurement of muscle quantity and quality. The third lumbar skeletal muscle index (L3 SMI) more accurately predicted the mortality of subjects than the psoas muscle index (PMI). Few studies have evaluated the sarcopenia of chronic liver disease using ultrasonography and magnetic resonance imaging, and more studies are needed. Unification of the measurement method and cut-off value would facilitate a more systematic and universal prognosis evaluation in patients with chronic liver disease.

1. Introduction

Sarcopenia is defined as reduced skeletal muscle mass and reduced muscle functionality [1]. Primary sarcopenia is a naturally occurring phenomenon with aging; however, when its severity is due to chronic illness beyond what can be justified by aging alone, it is called secondary sarcopenia [2]. It is also prevalent in patients with chronic liver disease. Sarcopenia is associated with a higher incidence of hepatocellular carcinoma, significant liver fibrosis, hepatic encephalopathy after transjugular intrahepatic portosystemic shunt (TIPS), high list mortality, postoperative mortality, and complications in patients with end-stage liver disease [3,4,5]. Sarcopenia is recognized as a disease entity in the International Classification of Disease (ICD-10) [6].
Despite growing research on sarcopenia, progress is hampered by the lack of unified definitions. Several imaging modalities, such as dual energy X-ray absorptiometry (DXA), ultrasonography (US), computed tomography (CT), and magnetic resonance imaging (MRI) have made it possible to use body composition assessments for patients with chronic liver disease. Measuring muscle mass with several forms of imaging is less affected by acute illness or cognitive dysfunction compared with measuring strength or physical performance and can be objectively employed in clinical practice [7]. This review evaluates studies related to the definitions of, and methodological approaches to diagnose, sarcopenia in adults with chronic liver disease.

2. Methods to Evaluate the Quantity and/or Quality of Skeletal Muscle Mass in Chronic Liver Disease

2.1. DXA

Measurements of skeletal mass are provided by DXA, which allows for the quantification of three body compartments (bone mass, fat mass, and bone fat-free mass (or lean mass)) based upon the differential tissue attenuation of X-ray photons (Figure 1).
Lean mass includes muscle and other components such as skin, tendons, and connective tissues. DXA is biased by the fluid overload that is frequently present in decompensated cirrhosis [8]. Lean mass, moreover, cannot differentiate muscle from water and can be overestimated in patients with cirrhosis who are experiencing water retention, such as ascites and peripheral edema. To minimize confounding by the fluid, both appendicular (arms and legs) and upper limb lean masses have been proposed as tools to analyze the muscle mass in cirrhosis [9]. The abdominal compartment is excluded from appendicular skeletal muscle measurements. This approach may not be influenced by ascites and thus may be useful for skeletal muscle mass estimations in patients with cirrhosis [10]. Low lean mass and appendicular limb lean mass assessed by DXA predict the risk of muscle weakness and limited mobility but are not associated with significant clinical outcomes, such as mortality [11]. Muscle mass is correlated with body size. The International Society for Clinical Densitometry recommended adjusting these values to body size. Muscle mass can be adjusted by height [9], weight [12], or body mass index (BMI) [13,14], although it is not known which of these methods is superior. The appendicular skeletal mass index (ASMI), adjusted by height, is calculated as follows:
Appendicular   skeletal   mass   index   ASMI = A p p e n d i c u l a r   s k e l e t a l   m a s s   K g h e i g h t m × h e i g h t m
Lindqvist et al. noted that ASMI showed similar results to SMI (skeletal muscle index) based on CT (γ = 0.66, p < 0.001), but the correlation between the lean mass index and SMI was weaker (γ = 0.29, p = 0.035) and falsely high in patients with ascites in the image analysis of patients before liver transplantation (LT) [15]. To date, several consensus definitions using DXA have been proposed by the International Working Group on Sarcopenia (IWGS), Asian Working Group for Sarcopenia (AWGS), and European Working Group on Sarcopenia in Older People (EWGSOP) (Table 1) [1,16,17]. The cut-off was based on the general population and should also be validated in patients with chronic liver disease (Table 1).
The limitation of DXA is its inability to assess muscle quality in contrast to CT and MRI. DXA cannot quantify intramuscular adipose tissue within and around muscles, and DXA-measured ASMI has shown only moderate correlation with SMI based on CT (γ = 0.41–0.66), which is considered to be the gold standard for estimating muscle mass in research [15,18]. Despite these limitations, DXA is commonly used in primary care in both clinical and research settings, as it has the advantages of being safe, inexpensive, and reproducible, as well as providing low radiation exposure.

2.2. US

US has also been applied to measure muscle size and myosteatosis. US is easy, inexpensive, and uses portable equipment, allowing it to be performed at the bedside, with no harm to the patient from radiation. US-based measurements have shown positive correlations with DXA-, CT-, and MRI-based measurements [19,20,21]. However, the reference standards used in each study were different, and there remains no standardization of the measurement technique. Perkisas et al. provided a standardization method for assessing appendicular muscle with US [22], but there was no clear cut-off for appendicular muscles in diagnosing sarcopenia. Only a few studies have evaluated the sarcopenia of chronic liver disease using US (Table 2).
Tandon et al. demonstrated that a nomogram based on body mass index and right thigh muscle thickness can identify male and female patients with sarcopenia defined by cross-sectional CT [23]. Hari et al. showed the possibility of using US for the evaluation of sarcopenia in patients with chronic liver disease by measuring the diameter of the right psoas muscle [24] (Figure 2). The authors reported that the success rate of measuring the psoas muscle was 72%. Technical failure was due to a poor sonic window with a high abdominal circumference or the presence of ascites. US can be used as a screening tool for sarcopenia in situations where other imaging methods are not available because of their radiation, high cost, and lack of portability.

2.3. CT

CT imaging is increasingly used as the gold standard to quantify skeletal muscle mass along with MRI and constitutes a good resource for the objective identification of sarcopenia. However, CT suffers from the disadvantage of radiation exposure. Nevertheless, patients with chronic liver disease frequently receive CTs to evaluate hepatocellular carcinoma or the complications of portal hypertension.
Generally, the cross-sectional areas of the psoas or abdominal muscle mass of the third (L3) or fourth (L4) lumbar vertebra levels that are not affected by activity are used. Although the cross-sectional area of the level of the umbilicus has previously been used [26], this area may be measured at different levels of the vertebra. Moreover, the umbilicus may become flat and unable to be found on axial CTs in patients with ascites or obesity [43]. Measuring should be conducted at the cross-sectional area of the skeletal muscles at the level of L3, which accurately represents the whole-body skeletal muscle mass [44]. At the L3 transverse section, muscle groups include the rectus abdominis, transverse abdominis, internal and external obliques, quadratus lumborum, psoas major and minor, and erector spinae. These measurements were computed by summing the tissue pixels and multiplying them by the pixel surface area. A threshold range of 29 to 150 HU is commonly used to define the muscle (Figure 3).
Most of the measured area is corrected with height and sometimes with BMI [45]. Height correction is necessary to determine the relative muscle mass because of the linear relationship between skeletal muscle and height [46]. The SMI is calculated as follows:
Skeletal   muscle   index   ( SMI )   of   L 3 = T o t a l   m u s c l e   a r e a   o f   L 3   l e v e l   cm 2 h e i g h t ( m )   × h e i g h t m
Occasionally, the psoas muscle is selected from other skeletal muscles of the region because it is located centrally, is easily identified, and is not directly affected by abdominal distension in the presence of ascites. There are several methods for measuring the area of the psoas muscle:
(1) Transverse psoas muscle thickness (TPMT), where the greatest transverse diameter of the psoas muscle runs perpendicular to the long axis (anterior–posterior oblique) of the psoas muscle diameter [27]. The results were normalized to body height and are shown as mm/m:
TPMT / height   =   T r a n s v e r s e   p s o a s   m u s c l e   t h i c k n e s s   m m h e i g h t   m
(2) The psoas muscle index (PMI), where the estimated or measured psoas muscle area is adjusted by height [33]. The estimated psoas muscle area is the sum of the product of the long axis and the short axis of the iliopsoas muscles on both sides [2]. The estimated psoas muscle area and PMI are calculated as follows:
Estimated psoas muscle area = (a × b) + (c × d)
where a is the TPMT of the right psoas muscle, b is the longitudinal psoas muscle thickness (LPMT) of the right psoas muscle, c is the TPMT of the left psoas, and d is the LPMT of the left psoas muscle.
Psoas   muscle   index   ( PMI )   of   L 3 = T o t a l   p s o a s   m u s c l e   a r e a   o f   L 3   l e v e l   cm 2 h e i g h t ( m )   ×   h e i g h t m
A consensus definition using PMI was proposed by the Japan Society of Hepatology guidelines for sarcopenia. This definition includes a cut-off value for the measured psoas muscle area of 6.36 cm2/m2 in males and 3.92 cm2/m2 in females and a cut-off value for the estimated psoas muscle of 6.0 cm2/m2 in males and 3.4 cm2/m2 in females [2] . Other studies used the cut-off value derived from mortality or morbidity [29,30,39] or from the sex-specific lowest quartile or fifth percentile of the subjects [32,33].
However, there is no evidence confirming that the cross-sectional area of the psoas muscles has a good correlation with the whole-lumbar or the whole-body muscle volume. Among 396 patients with end-stage liver disease, PMI was less likely to predict mortality than SMI in male patients. Male patients who died had a lower SMI but not a lower PMI compared to male patients who were alive [39]. Therefore, the entire skeletal muscle at the L3 vertebra level should be measured.
The attenuation of muscle was additionally measured to evaluate muscle quality. Low muscle attenuation, referred to as myosteatosis, indicates increased intramuscular fat content, which contributes to muscle weakness independent of the age-associated loss in muscle mass [47,48]. Wang et al. showed that myosteatosis, but not muscle mass, is related to mortality in a study of 292 patients with end-stage liver disease [36].
The same cut-off value cannot be uniformly applied because the muscle mass varies according to age, sex, BMI, and ethnicity. There is wide heterogeneity in the cut-off values of SMI used to defined sarcopenia in chronic liver disease: A sex-specific cut-off value derived in patients with solid tumors related to mortality [34,35,49,50], a cut-off value according to BMI [36,37], a cut-off according to age [33], a cut-off defined from control subjects [33], and a cut-off from subjects using the sex-specific lowest quartile/tertile [32,38,40]. The North American Working group on Sarcopenia in Liver Transplantation suggested that the definition of sarcopenia in patients with end-stage liver disease waiting for LT should be defined as SMI less than 50 cm2/m2 for males and less than 39 cm2/m2 for females at the L3 level [7]. In their study, there were no statistically significant differences in SMI according to ethnicity.

2.4. MRI

MRI can also be used to evaluate muscle quantity and quality. MRI provides high resolution and permits the separation and quantification of muscle compartments and fat distribution. It can be used to evaluate detailed anatomical changes of muscle, including muscular atrophy, fatty degeneration, and edema. In contrast to CT, MRI carries no risk of ionizing radiation exposure or kidney injury due to iodine contrast media administration. MRI can be performed without the administration of contrast media because of its high soft-tissue contrast and multiparametric characteristics.
With advances in MRI techniques, the assessment of the chemical composition of tissue has also become possible. MR spectroscopy (MRS) is a representative MR technique that assesses the chemical composition of tissue [51,52]. DIXON-based MRI is a recent MRI technique challenging MRS by using a chemical shift to enable the selective reconstruction of fat signal- and water signal-only images [53,54]. Quantitative analysis using DIXON-based MRI showed an excellent correlation in MRS, which outperformed visual assessment in the detection of muscle fat content [55]. These fat quantification MRI techniques could be applied to the evaluation of sarcopenia in terms of muscle quality assessments in patients with chronic liver disease (Figure 4).
Compared with CT, which is the gold standard for the evaluation of sarcopenia in several guidelines, MRI has shown similar performance in the evaluation of sarcopenia in healthy subjects [56,57]. Traditionally, MRIs have been used for muscle quality and quantity evaluations of neuromuscular disorders [58,59,60]. Furthermore, an MRI-only assessed sarcopenia is an important prognostic factor in many types of cancer, including breast cancer, head and neck cancer, and colorectal cancer [61,62,63]. However, this method remains in the early stages for studying sarcopenia in chronic liver disease. There are two studies on the adverse effects of decreased muscle mass diagnosed by TPMT-adjusted height and the spinae muscle area (Table 2) [41,42]. To our knowledge, there has been no study on the adverse effects of reduced muscle mass at the L3 level, and there is also a lack of research articles on myosteatosis in patients with chronic liver disease, so further studies and validations are needed. The concern regarding the high cost of MRI can be considered negligible because patients with chronic liver disease are frequently subjected to MRIs for several clinical reasons.

3. Considerations for the Radiologic Evaluation of Sarcopenia

The radiologic evaluation of sarcopenia has the advantage of being able to measure muscle mass objectively and quantitatively. CT and MRI, which are considered to be gold standards for muscle mass measurements, showed high interobserver agreement with Pearson’s correlation coefficient [39,63]. The measurements of skeletal muscle mass on CT and MRI were also found to be interchangeable. Park et al. showed very good agreement between CT and MRI measurements of skeletal muscle mass at the level of the L3 vertebra (the ICC of reader 1 was 0.928 and that of reader 2 was 0.853) [64]. This result is also consistent with studies carried out at the level of the superior mesenteric artery (mostly the first lumbar vertebra) and the level of the third cervical vertebra (C3) [57,63]. In addition, it is possible to measure skeletal muscle retrospectively because most patients with chronic liver disease frequently undergo radiologic evaluations.
In previous studies, different cut-off values were applied according to sex, etiology of the disease, ethnicity, and the modality used. The SMI values of male patients were significantly higher than those of female patients; however, the frequency of sarcopenia among male patients was higher than that in female patients when sex-specific cut-offs were applied [31,35,39]. Previous studies have examined the association between non-alcoholic fatty liver disease (NAFLD) and hepatitis B or C viral cirrhosis with sarcopenia using DXA as the assessment tool [12,13,25,65]. A study from Korea reported the association of NAFLD with sarcopenia using CT [45], with a cut-off value defined as 1 standard deviation below the sex-specific mean value for a young healthy population: 8.37 cm2/(kg/m2) for men and 7.47 cm2/(kg/m2) for women. After the publication of the EWGSOP guidelines, some studies were designed to determine specific cut-off values for sarcopenia assessment using CT for Japanese and Asian adults. Two studies provided PMI cut-off values of 3.74 and 6.36 cm2/m2 for men and 2.29 and 3.92 cm2/m2 for women, respectively, based on Japanese liver donor data. The authors suggested that that the cut-off values in Western studies could be different from the actual values in Asian populations due to differences in body sizes, lifestyles, and ethnicities [25,66]. Further studies to define sarcopenia should be conducted according to ethnicity and the etiology of hepatic disease.
There is a need for standardized CT, as CT parameters such as tube potential, the use of a contrast agent, and slide thickness also affect the assessment of skeletal muscle. A reduction in tube potential from 140 to 80 kV leads to a 5.2% decrease in SMI [67], and the use of contrast media overestimates the average SMI by up to 2.8% [68]. Differences in slice thickness of 10 and 2 mm can result in a 1.9% smaller SMI [68]. Contrast enhancement, moreover, strongly influences the value of skeletal muscle density [69,70].
Moreover, radiological assessment does not always reflect strength or physical performance [71,72,73,74]. However, further research is needed to determine which parameters of muscle strength and physical performance are complemented by radiological assessment. In 2018, EWGSOP recommended that if a patient has low muscle strength, is defined as probable sarcopenia, and has low muscle quantity or quality, they can be diagnosed as sarcopenia [1] because it is recognized that strength is better than muscle mass in predicting adverse outcomes. Sinclair et al. showed that the model for the end-stage liver disease (MELD)-handgrip strength bivariate Cox model is superior to the MELD-CT muscle Cox model (p < 0.001) in predicting mortality [18]. For muscle strength, the use of a handheld dynamometer is a valid and reliable method with high interrater and intrarater reliability. Further, the short physical performance battery and gait speed provide good measurement properties for the assessment of physical performance [1,75].

4. Conclusions

The evaluation of sarcopenia is crucial in patients with chronic liver disease, as well as other chronic illness, because sarcopenia is one of the important prognostic factors [4,5]. Overall, CT and MRI are considered the gold standard for evaluating sarcopenia and are frequently performed in patients with chronic liver disease for the evaluation of hepatocellular carcinoma or complications of portal hypertension. CT shows excellent performance in estimating the quality and quantity of muscle, and many studies have reported variable measurement methods and cut-off values in patients with chronic liver disease. MRI could be a competent imaging modality for muscle quality evaluation by measuring intramuscular fat content with MRS or DIXON-based MRI, as well as muscle mass by measuring the area, which requires further validations in chronic liver disease. DXA is a reliable alternative for clinical use when a CT scan is not clinically indicated or available. Unification of the measurement method and cut-off value would facilitate more systematic and universal prognosis evaluations in patients with chronic disease.

Author Contributions

Conceptualization: M.K.; data curation: C.-m.L., B.K.K.; supervision: M.K.; writing–original draft: C.-m.L.; review and editing: M.K. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

No new data were created or analyzed in this study. Data sharing is not applicable to this article.

Acknowledgments

None of the authors have any financial relationships to disclose.

Conflicts of Interest

We declare that we have no financial and personal relationships with other people or organizations that can inappropriately influence our work, and there is no professional or other personal interest of any nature or kind in any product, service, and/or company.

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Figure 1. Dual energy X-ray absorptiometry (DXA) scan with body composition analysis. The subject’s height was 1.59 m, and the lean and appendicular lean masses were 39.1 and 16.6 kg, respectively. The Appendicular Lean Mass Index (ALMI) was calculated as 6.6 kg/m2.
Figure 1. Dual energy X-ray absorptiometry (DXA) scan with body composition analysis. The subject’s height was 1.59 m, and the lean and appendicular lean masses were 39.1 and 16.6 kg, respectively. The Appendicular Lean Mass Index (ALMI) was calculated as 6.6 kg/m2.
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Figure 2. Left side: Example of an ultrasound measurement of the psoas muscle diameter. Right side: the corresponding CT image.
Figure 2. Left side: Example of an ultrasound measurement of the psoas muscle diameter. Right side: the corresponding CT image.
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Figure 3. Abdominal CT images taken at the third lumbar vertebra with cirrhosis applied to quantify transverse psoas muscle thickness (TPMT), psoas muscle, and total muscle areas. The psoas muscle in panels (c,d) and total muscle area in panels (e,f) are colored in red. Panels (a,c,e) present a female patient with low TPMT (5.9 mm/m), psoas muscle index (PMI) (2.3 cm2/m2), and skeletal muscle index (SMI) (35.7 cm2/m2). Panels (b,d,f) present a male patient with high TPMT (23.3 mm/m), PMI (6.8 cm2/m2), and SMI (51.6 cm2/m2). The mean density of muscle in (c–f) is 34.7, 38.2, 26.2, and 36.6 HU, respectively.
Figure 3. Abdominal CT images taken at the third lumbar vertebra with cirrhosis applied to quantify transverse psoas muscle thickness (TPMT), psoas muscle, and total muscle areas. The psoas muscle in panels (c,d) and total muscle area in panels (e,f) are colored in red. Panels (a,c,e) present a female patient with low TPMT (5.9 mm/m), psoas muscle index (PMI) (2.3 cm2/m2), and skeletal muscle index (SMI) (35.7 cm2/m2). Panels (b,d,f) present a male patient with high TPMT (23.3 mm/m), PMI (6.8 cm2/m2), and SMI (51.6 cm2/m2). The mean density of muscle in (c–f) is 34.7, 38.2, 26.2, and 36.6 HU, respectively.
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Figure 4. Example MR images (fat fraction) of cross-section of the spinal muscles at the Superior Mesenteric Artery level in two patients with low fatty degeneration (a) and high fatty degeneration (b). (a) The area and fat fraction of the left spinal muscle were 3150 mm2 and 10.3%. (b) The area and fat fraction of the left spinal muscle were 1394 mm2 and 44.3%. An axial three-dimensional multi-echo-modified Dixon gradient echo sequence was used for the MRI. Imaging parameters for the sequence were as follows: six Echo Time (TE)s (first TE shortest automatic (0.9–1.2ms), delta TE 0.8–1.01ms); Repetition Time (TR) shortest automatic (5.8–6.3 ms); flip angle =3; field of view = 35 × 35 cm2; 3 mm slice thickness with no gap; matrix size = 300 × 300; number of slices = 60; scan time = 14.1 s; parallel imaging SENSE factor = 2; number of signal average = 1. The sequence automatically produces water, fat, fat fraction, R2*, and T2* maps.
Figure 4. Example MR images (fat fraction) of cross-section of the spinal muscles at the Superior Mesenteric Artery level in two patients with low fatty degeneration (a) and high fatty degeneration (b). (a) The area and fat fraction of the left spinal muscle were 3150 mm2 and 10.3%. (b) The area and fat fraction of the left spinal muscle were 1394 mm2 and 44.3%. An axial three-dimensional multi-echo-modified Dixon gradient echo sequence was used for the MRI. Imaging parameters for the sequence were as follows: six Echo Time (TE)s (first TE shortest automatic (0.9–1.2ms), delta TE 0.8–1.01ms); Repetition Time (TR) shortest automatic (5.8–6.3 ms); flip angle =3; field of view = 35 × 35 cm2; 3 mm slice thickness with no gap; matrix size = 300 × 300; number of slices = 60; scan time = 14.1 s; parallel imaging SENSE factor = 2; number of signal average = 1. The sequence automatically produces water, fat, fat fraction, R2*, and T2* maps.
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Table
Table 1. Recommended cut-off values for muscle mass using dual energy X-ray absorptiometry (DXA).
Table 1. Recommended cut-off values for muscle mass using dual energy X-ray absorptiometry (DXA).
IWGS, 2011AWGS, 2014EWGSOP, 2018
ASMI7.23 kg/m2 for men
5.67 kg/m2 for women		7.0 kg/m2 for men
5.4 kg/m2 for women		7.0 kg/m2 for men
5.5 kg/m2 for women
Table
Table 2. Summary of studies investigating radiologic sarcopenia in chronic liver disease.
Table 2. Summary of studies investigating radiologic sarcopenia in chronic liver disease.
AuthorSubjects
(M/F)		Mean Age
(Years)		Country
/Ethnicity (%)		Etiology (%)Body Composition MethodsDefinition of SarcopeniaPrevalenceAdverse Effects
Lee 2016 [13]2,761
(1,240:1,520)		55.8KoreaNAFLDDXA, ASMI (ASM adjusted by BMI)0.789 for men, 0.521 for women12.2%
M: 10.6%
F: 13.5%		Sarcopenia was associated with significant liver fibrosis (OR = 0.52–0.67, p < 0.01)
Han 2018 [25]506 (258:248)50.7KoreaChronic hepatitis BDXA, ASMI (ASM adjusted by BMI)0.89 for men, 0.58 for women24.9%Sarcopenia was associated with significant liver fibrosis (OR = 2.01–3.62, p < 0.05)
Belarmino 2018 [10]144 (144:0)54.0BrazilCirrhosis
59 alcoholic
20 viral
12 cryptogenic
9 other		DXA, ASMI (ASM adjusted by height)Tertile of patients (<7 Kg/m2) plus nondominant handgrip strength < 25 Kg13.2%Patient with sarcopenia showed higher mortality (p < 0.001)
Sinclair 2019 [9]420 (420:0)55.4 (median)AustraliaESLD
28.3 HCC
24.3 HCV,
12.6 alcoholic
10.2 PSC,
6.2 NAFLD
18.3 other		DXA, ALMI (ALM adjusted by height)<7.26 Kg/m2 30.9%ALM and lean mass of the arms were inversely associated with mortality (HR = 0.78, p = 0.03 for ALM and HR = 0.37, p = 0.02 for lean mass of the arms)
Hari 2019 [24]75 (39:36)63SloveniaCirrhosis
67 alcohol
15 NAFLD
18 other		US,
(1) psoas to height ratio (right psoas muscle diameter divided by height)
(2) right PMI (π · psoas2/height2)		NANAPsoas to height ratio was related to hospitalization (HR = 0.72, p < 0.001) and mortality (HR = 0.82, p = 0.022)
PMI was related to hospitalization (HR = 0.88, p < 0.001) and mortality (HR = 0.93, p = 0.017)
Durand 2014 [26]562 (455:107)5388 Caucasian
10 Afrian
2 Asian 		ESLD
42 alcohol
15 HBV
30 HCV
5 biliary disease
8 others		CT at level of umbilicus, TPMT/heightNANATPMT/height was an independent predictive factor of waiting list mortality (HR = 0.87, p = 0.001).
Kim 2014 [27]65 (41:24)55KoreaCirrhosis
56.9 alcohol
26.1 viral
9.3 mixed
7.7 other		CT, L4, TPMT/heightNANAMortality with TPMT/height ≥14 mm/m was higher than TPMT/height <14 mm/m (HR = 5.4, p < 0.001)
Krell 2013 [28]207 (129:78)51.781.2 White
11.1 African American
7.7 Other		Patients with LT
26.1 HCV
25.1 HCC
14.5 alcohol
34.3 other		CT, L4, total psoas areaSex-specific tertiles 33%Patients in the lowest tertile had a greater than 4-fold higher change in developing a severe infection in comparison with patients with in the highest tertile (OR = 4.6, 95 % CI = 2.25–9.53)
Tateyama 2020 [29]99 (61:38)70JapanCirrhosis
52.5 HCV
18.2 HBV
29.3 other		CT, L3, PMI, SMI<4.3 cm2/m235.4%The incidence of minor hepatic encephalopathy was frequent in patients with lower PMI than higher PMI (p = 0.001)
Hou 2020 [30]251 (129:122)62.6ChinaCirrhosis
38.3 viral
15.9 alcohol
8.4 autoimmune
37.5 other		CT, L3, PMIMale: <3.5 cm2/m2
Female: <2.6 cm2/m2		NAPMI was associated with 3-year mortality in male (HR = 0.673, p = 0.020) and in female (HR = 0.586, p = 0.013).
Masuda
2013 [31]		204 (103:101)54AsianPatients with LT
12.7 HBV,
50.5 HCV
13.2 PBC
4.9 alcoholic
18.6 other		CT, L3, psoas muscle area Lowest 5th percentile
<800 cm2 for men
<380 cm2 for women		47.1%
M: 58.3%
F: 35.6%		Sarcopenia was an independent predictor of postoperative sepsis (HR = 5.31, p = 0.009)
Kalafateli 2017 [32]232 (162:70) 5376.3 Caucasian
5.6 African
16.8 Asian
1.3 Other		Patients with LT
20.3 autoimmune
34.9 viral
23.7 alcohol
21.1 other		CT, L3, PMILowest quartile
<340 mm2/m2 for male
<264 mm2/m2 for female		24.6%
M: 24.7%
F: 24.3%		L3-PMI was associated with longer hospital stay (OR = 0.996, 95% CI = 0.9940.999) and 1-year mortality (OR = 0.996, p = 0.05).
Tsien 2014 [33]53 (41:12)56.9USAPatients with LT
41.5 viral
22.6 mixed
7.5 NASH
28.3 other		CT, mid L4 level, PMI and muscle attenuation.5th percentile of control subjects
Male, <50 years old: <12.27 cm2/ m2
Male, >50 years old:
<10.12 cm2/m2
Female: <50 years old:
<10.47 cm2/m2
Female: >50 years old:
<10.33 cm2/m2		62.3% at pre-LT
86.8% at post-LT		Pre-LT sarcopenia increased mortality (p = 0.06).
Continued sarcopenia in post-LT showed a trend of higher mortality (p = 0.08)
Tanai 2016 [34]149 (82:37)65JapanCirrhosis
53.0 HCV
22.8 alcohol
6.7 HBV
17.4 other		CT, L3 level, SMI<52.4 cm2/m2 for men
<38.5 cm2/m2 for women		63%
M: 76%
F: 48%		Relative change in skeletal muscle area (<3.1%) was associated with mortality (HR = 2.73, p < 0.001).
Nardelli 2017 [35]46 (34:12)58.6ItalyPatients with cirrhosis received TIPSCT, L3-4 disc space, SMISame as above57%Sarcopenia was associated with development of hepatic encephalopathy after TIPS (HR = 3.13, p < 0.001)
Wang 2016 [36]292 (193:99)6155 Non-hispanic white
5 Black
26 Hispanic
8 Asian
6 Other		ESLD
60 HCV
11 alcohol
8 NAFLD
10 cholestatic
12 other		CT, L3, SMI and muscle attenuationMuscle mass
<43 cm2/ m2 for men with BMI <25 Kg/m2
<53 cm2/m2 for men with BMI ≥25 Kg/m2
<41 cm2/m2 for women with any BMI
Reduced muscle attenuation
<41 HU for BMI <25 Kg/m2
<33 HU for BMI ≥25 Kg/m2		Sarcopenia: 38%
Poor muscle quality: 50%		Muscle quality was associated with waitlist mortality (HR = 0.77, p = 0.02), but muscle mass was not (HR = 0.91, p = 0.35).
Montano-Loza 2016 [37]678 (457:221)57CanadaCirrhosis
40 HCV
23 alcohol
14 NASH and cryptogenic
8 autoimmune
6 HBC
1 other		CT, L3, SMI and muscle attenuationSame as aboveSarcopenia: 43%
Poor muscle quality: 52.1%		Sarcopenia (HR= 2, p < 0.001) and poor muscle quality (HR = 1.42, p = 0.04) were associated with mortality.
Carey 2017 [38]396 (277:119)5871 Non-hispanic white
5 Black
11 Hispanic
8 Asian
7 Other		Patients with LT
48 HCV
17 alcohol
12 NAFLD
5 HBV
17 other		CT, superior aspect of L3, SMI<50 cm2/ m2 for men
<39 cm2/ m2 for women		44.9%Sarcopenia was associated with waitlist mortality (HR = 0.95, p < 0.001)
Ebadi 2018 [39]353 (246:107)56USAESLDCT, L3, PMI and SMISMI
<50 cm2/m2 for men
<39 cm2/m2 for women
PMI (cut-off calculated from subjects)
<5.1 cm2/m2 for men
<4.3 cm2/m2 for women
Sarcopenia by SMI: 47%
M: 51%
F: 36%
In women, both low SMI and PMI were predictors of mortality (HR = 2.05, p = 0.05 for low SMI and HR = 2.47, p = 0.01 for low PMI).
In men, low SMI was only significant predictor of mortality (HR = 2.46, p = 0.002).
Fujiwara 2015 [40]1,257 (828:429)68.6JapanPatients with HCC
71.2 HCV
11.3 HBV
17.5 other		CT, L3, SMI and muscle attenuationMuscle mass
<36.2 cm2/m2 for men
<29.6 cm2/m2 for women
Reduced muscle attenuation
<44.4 HU for men
<39.3 HU for women		Sarcopenia: 11.1%
M: 11.6%
F: 10.0%
Poor muscle quality: 85.0%		Sarcopenia (HR = 1.52, p = 0.001) and poor muscle quality (HR = 1.34, p = 0.020) were significant predictors of survival.
Beer 2020 [41]265 (164:101)54AustriaCLD
21 HCV
19 alcohol
9 HBV		MR, L3, TPAM/height<12mm/m for men
<8mm/m for women		27.2%Sarcopenia was risk factor for mortality (HR = 2.76, p = 0.045) for compensatory advanced chronic liver disease.
Praktiknjo 2018 [42]116 (69:47)59EUPatients with cirrhosis received TIPS
62.9 alcohol
15.5 viral
21.6 other		MR, at level of SMA, spinae muscle area and fat-free muscle areaSex specific cut-off from subjects
Total muscle <3523 mm2 and fat-free muscle <3197 mm2 for men
Total muscle <3153 mm2 and fat-free muscle <2895 mm2 for women		44.0%Persistence of sarcopenia after TIPS is associated with mortality (HR = 5.62, p = 0.001)
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Lee, C.-m.; Kang, B.K.; Kim, M. Radiologic Definition of Sarcopenia in Chronic Liver Disease. Life 2021, 11, 86. https://doi.org/10.3390/life11020086

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Lee C-m, Kang BK, Kim M. Radiologic Definition of Sarcopenia in Chronic Liver Disease. Life. 2021; 11(2):86. https://doi.org/10.3390/life11020086

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Lee, Chul-min, Bo Kyeong Kang, and Mimi Kim. 2021. "Radiologic Definition of Sarcopenia in Chronic Liver Disease" Life 11, no. 2: 86. https://doi.org/10.3390/life11020086

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