Prognostic Significance of the L3 Skeletal Muscle Index and Advanced Lung Cancer Inflammation Index in Elderly Patients with Esophageal Cancer.

OBJECTIVE: To evaluate the correlation between the advanced lung cancer inflammation index (ALI) and the L3 skeletal muscle index (L3SMI) and their prognostic value in elderly patients with esophageal cancer (EC).
MATERIALS AND METHODS: The clinical data of 158 elderly patients with EC were collected retrospectively. The L3SMI measures the area of skeletal muscle at the level of the third lumbar (L3) vertebra using computed tomography (CT). A high L3SMI and low L3SMI group were created using sex-based quartiles. The ALI, prognostic nutrition index (PNI), and geriatric nutrition risk index (GNRI) were calculated according to standard laboratory protocols.
RESULTS: The CT diagnostic criteria for senile sarcopenia in South China are height ≤32.96 cm2/m2 for females and height ≤35.4 cm2/m2 for males. The logistic regression analysis showed that a low L3SMI was significantly associated with a low ALI. Survival analysis revealed EC patients with a low L3SMI and a low ALI had poorer overall survival (OS) than patients with a high L3SMI and a high ALI. Univariate and multivariate Cox analyses showed that the L3SMI and ALI were independent predictors of EC prognosis in elderly individuals.
CONCLUSION: There was a significant correlation between the PNI, GNRI, ALI, and L3SMI. Overall, our findings show the L3SMI and ALI are clinical indicators that can potentially be used to independently predict the prognosis of elderly EC patients and display good predictive value.

Introduction

Esophageal cancer (EC) is a tumor with the seventh and sixth highest morbidity and mortality rates worldwide, respectively.1 With the aging population and the acceleration of population growth, the occurrence of EC has increased.2 EC is primarily divided into squamous cell carcinoma and adenocarcinoma. In East Asia, EC cases are primarily squamous cell carcinoma. The early symptoms of EC are not typical and because EC is aggressive and progresses rapidly,3 most patients are at an advanced stage when they are first diagnosed.4,5 Esophageal obstruction caused by the progressive growth of EC makes eating difficult for EC patients, which in turn leads to malnutrition and even cachexia.6 Many studies have focused on the nutritional status of cancer patients. The geriatric nutritional risk index (GNRI) is a simplified screening parameter calculated based on serum albumin and body weight that can be used to assess nutrition-related risks.7 The prognostic nutritional index (PNI) is calculated using the serum albumin concentration and the total number of peripheral blood lymphocytes.8 The PNI reflects the nutritional and immune status of patients. With the increasing aging population, the number of elderly EC patients is growing. Owing to the heterogeneity of the health status of the elderly, EC patients in this age group lack accurate prognostic predictors. The treatment of EC is still managed using a comprehensive strategy based on surgical intervention.9 With improvements in diagnosis and treatment technologies, the prognosis of EC has also improved, but the prognosis of EC patients is still poor.5,10 Therefore, exploring reliable indicators for predicting patient survival can help to identify patients with poor prognoses and allow the early adoption of better prevention and treatment methods and reduce mortality.

Skeletal muscle not only plays a role during exercise or movement but also participates in complex immune and inflammatory processes of the body by secreting a variety of cytokines. Hence, some people refer to it as a “secretory organ”.11 Sarcopenia was first proposed by Rosenberg as the gradual loss of skeletal muscle mass associated with aging.12 The L3 skeletal muscle index (L3SMI) assessed using computed tomography (CT) is the primary method for diagnosing sarcopenia. In recent years, sarcopenia has been confirmed to be significantly related to malnutrition and the poor prognosis of various malignant tumors.13–16 The commonly used diagnostic criteria for sarcopenia have been primarily formulated by European and American specialists, although there are obvious ethnic differences among Asian, European, and American populations.17,18 Thus, the diagnostic criteria in Europe and America may not be applicable to Asian populations. In addition, given to the features of the elderly population, the current diagnostic criteria are not suitable for elderly Asian individuals.

An increasing number of studies have confirmed that tumor-related inflammation plays a vital role in the occurrence and development of tumors.19 Recently, many studies have shown that a new inflammation-related index, the advanced lung cancer inflammation index (ALI), can be used to evaluate the prognosis of various malignant tumors, such as non-small-cell lung cancer,20 small-cell lung cancer,21 and diffuse large B cell lymphoma.22 The ALI was first used to assess the prognosis of lung cancer patients. However, researchers have found that the ALI is also a good independent prognostic indicator in head and neck and gastrointestinal tumors. The ALI is associated with poor prognosis in EC,23 head and neck squamous cell carcinoma,24 and in colorectal cancer.25,26

The purpose of this study was to establish the L3SMI cut-off value to be used for diagnosis of sarcopenia in elderly EC patients in southern China (Guangxi Province). In addition, we explored the relationship between the L3SMI and PNI, GNRI, and ALI and their prognostic value in elderly EC patients.

Materials and Methods

Study Population

Data on 189 elderly EC patients who underwent surgical treatment at the First Affiliated Hospital of Guangxi Medical University (Nanning, China) from September 2013 to July 2018 were collected. The inclusion criteria were as follows: (a) EC diagnosis confirmed by pathology; (b) radical esophageal cancer surgery performed; (c) no radiotherapy or chemotherapy conducted prior to surgery; (d) patients aged ≥65 years;27 and (e) patients with complete clinical and follow-up data. We used the 8th edition of the American Joint Committee on Cancer (AJCC) TNM grading system to stage patients after surgery. The ethics committee of the First Affiliated Hospital of the Guangxi Medical College approved the study (approval number: 2021(KY-E-046)). All patients in this study provided written informed consent. This study was performed in accordance with the Declaration of Helsinki.

Data Collection

The clinical data collected from patients was as follows: sex, age, height, and weight. The preoperative laboratory serological examinations of all patients were completed within 1 week prior to surgery. The primary preoperative laboratory serological tests included assessment of lymphocyte counts, neutrophils, and albumin levels. The neutrophil/lymphocyte ratio (NLR) was defined as the neutrophil count divided by the lymphocyte count. Hypoalbuminemia was defined as an albumin level <35 g/L. According to the median NLR, patients were divided into two subgroups: high NLR and low NLR values. The body mass index (BMI) was calculated using the square of weight (kg)/height (m2). BMI values were divided into three subgroups: low <18.5, normal = 18.5–24, and high ≥24.28 The PNI was calculated using the following formula: 10 × serum albumin value (g/dL) +0.005 × total lymphocyte count in the peripheral blood (per mm3).8 The GNRI was calculated as follows: GNRI = 1.489 × serum albumin (g/dL) + 41.7 × weight/ideal body weight.7 The ALI was defined as BMI (kg/m2) × albumin (g/dL)/NLR. Time-dependent receiver operating characteristic (ROC) curves were plotted to establish the cutoff values for the GNRI, PNI, and ALI and to establish the high/low GNRI, high/low PNI, and high/low ALI subgroups.

Skeletal Muscle Tissue Measurement

Enhanced CT imaging of the abdomen of patients the week before treatment was used to collect two consecutive images at the L3 level. The L3 skeletal muscles included the paraspinal, psoas major, rectus abdominis, internal oblique, external oblique, and transverse abdominal muscles.18 The L3SMI was calculated as the square of skeletal muscle area (cm2)/height (m2).

Follow-Up

All patients in the cohort received telephone or outpatient follow-up after surgery. The deadline for follow-up was 1 January 2021. Overall survival (OS) was defined as the time from surgery to death or the last follow-up.

Statistical Analysis

All the statistical analyses were performed using SPSS version 19.0. GraphPad Prism version 5.0 and R version 4.0.2 were used to draw the graphs. Time-dependent ROC curves were plotted to establish the cutoff values for the GNRI, PNI, and ALI. The correlations between the L3SMI, ALI, clinicopathological data, and nutritional risk, and the correlations between the L3SMI and ALI and its components were analyzed using a logistic regression. Kaplan–Meier analysis was used to construct a survival curve, and the Log rank test was used for comparisons. The hazard ratios (HRs) and 95% confidence intervals (CIs) were calculated using univariate and multivariate Cox proportional hazards regression models to evaluate the relationship between the L3SMI and the ALI and prognosis. The important factors in the multivariate Cox analysis were used to construct a nomogram, the coordination index (C index), and a calibration curve were used to evaluate the predictive accuracy of the nomogram. A P-value <0.05 was considered to indicate statistical significance.

Results

Patient Characteristics

A total of 189 elderly EC patients were enrolled from September 2013 to July 2018, of which 10 patients did not have preoperative CT images available, 8 patients did not have complete clinical data, and 13 patients were lost to follow-up. The clinical characteristics of the patients are shown in Table 1. The median age of the patients was 69.5 years (range 65–86 years; mean age 70.7±4.49 years). According to the ROC curve (Figure 1), the cutoff value, sensitivity, specificity, and area under the ROC curve (AUC) values for the GNRI and PNI of the 158 elderly EC patients were determined. The cutoff, sensitivity, specificity, and AUC values of the GNRI were 96.60, 60.8%, 62.0%, and 0.602 (95% CI = 0.513–0.691), respectively. The cutoff, sensitivity, specificity, and AUC values of the PNI were 45.35, 75.9%, 44.3%, and 0.606 (95% CI = 0.517–0.694), respectively. The cutoff, sensitivity, specificity, and AUC values of the ALI were 31.24, 62.0%, 63.3% and 0.638 (95% CI = 0.552–0.725), respectively.

Table 1

Baseline Characteristics of Patients and Tumors

Characteristics	n	%
Age
≤70	84	53.16%
>70	74	46.84%
Gender
Female	32	20.25%
Male	126	79.75%
BMI
Low	39	24.68%
Normal	99	62.66%
High	20	12.66%
Cancer embolus
No	123	77.85%
Yes	35	22.15%
Perineural invasion
No	141	89.24%
Yes	17	10.76%
Smoke
No	96	60.76%
Yes	62	39.24%
Alcohol drinking
No	88	55.70%
Yes	70	44.30%
Lymphatic metastasis
No	82	51.90%
Yes	76	48.10%
Differentiation
Poor	41	25.95%
Moderately	66	41.77%
Well	51	32.28%
Tumor depth
pT1	20	12.66%
pT2	49	31.01%
pT3	86	54.43%
pT4	3	1.90%
Tumor location
Upper	10	6.33%
Middle	89	56.33%
Lower	59	37.34%
Pathology
Squamous cell carcinoma	148	93.67%
Adenocarcinoma	10	6.33%
Tumor size
≤4cm	82	51.90%
>4cm	76	48.10%

Abbreviation: BMI, body mass index.

Figure 1

The receiver-operating characteristic (ROC) curves for GNRI, ALI, and PNI.

L3SMI Grouping of the Elderly EC Patients

The L3SMI was divided into four sex-based quartiles: G1, G2, G3, and G4. The Kaplan–Meier survival curves showed that the OS of the G1 group was significantly worse than that of the G2, G3, and G4 groups (Figure 2), and the survival curve of the G1 group was significantly separated from that of the other groups. Thus, the G1 group cutoff appeared more suitable as a threshold for elderly EC sarcopenia. Therefore, based on the above analysis, the 158 elderly EC patients were divided into high and low L3SMI groups. The G2, G3, and G4 groups were combined and represented the high L3SMI group, and the G1 group represented the low L3SMI group.

Figure 2

Kaplan–Meier survival curve of the sex-based quartile method (G1–4) of L3SMI in EC patients.

Relationship Between the L3SMI and ALI and Clinical Pathological Characteristics of the Patients

A logistic regression analysis was conducted to determine the correlations between patient clinical and pathological characteristics and the L3SMI and ALI (Table 2). ALI and sex (P = 0.009; OR = 0.349, 95% CI = 0.158–0.771), GNRI (P < 0.001; OR = 8.468, 95% CI = 3.943–18.186), PNI (P = 0.001; OR = 3.628, 95% CI = 1.650–7.976), and tumor size (P = 0.035; OR = 0.488, 95% CI = 0.251–0.949) were significantly correlated. L3SMI and lymphatic metastasis (P = 0.035, OR = 0.446, 95% CI = 0.210–0.946), cancer embolus (P=0.004; OR=0.307, 95% CI = 0.137–0.688), tumor depth (P = 0.006, OR = 0.310, 95% CI = 0.135–0.711), GNRI (P < 0.001, OR = 5.992, 95% CI = 2.445–14.685), and PNI (P=0.007, OR = 2.810, 95% CI = 1.327–5.952) were all significantly related.

Table 2

The Relationships Between the ALI, L3SMI and Clinicopathological Factors of Elderly EC Patients

Characteristics	ALI		L3SMI
	OR(95% CI)	P	OR(95% CI)	P
Gender (Male)	0.349(0.158–0.771)	0.009	0.858(0.338–2.177)	0.747
Age (>70)	1.439(0.750–2.763)	0.274	0.736(0.354–1.530)	0.412
Smoke (Yes)	0.674(0.343–1.328)	0.254	0.855(0.407–1.795)	0.678
Alcohol drinking (Yes)	0.551(0.282–1.077)	0.081	0.850(0.409–1.767)	0.663
Lymphatic metastasis (Yes)	0.685(0.356–1.319)	0.258	0.446(0.210–0.946)	0.035
Cancer embolus (Yes)	0.447(0.188–1.066)	0.069	0.307(0.137–0.688)	0.004
Perineural invasion (Yes)	0.713(0.238–2.138)	0.546	0.733(0.241–2.234)	0.585
Differentiation (Poor)	0.631(0.293–1.358)	0.239	0.722(0.325–1.606)	0.425
Tumor depth(pT3+pT4)	1.105(0.573–2.129)	0.766	0.310(0.135–0.711)	0.006
GNRI(>96.6)	8.468(3.943–18.186)	<0.001	5.992(2.445–14.685)	<0.001
PNI(>45.35)	3.628(1.650–7.976)	0.001	2.810(1.327–5.952)	0.007
Tumor size(>4cm)	0.488(0.251–0.949)	0.035	1.039(0.501–2.158)	0.917
Pathology (Adenocarcinoma)	0.423(0.087–2.063)	0.287	0.287(0.078–1.051)	0.060
Tumor location		0.344		0.923
Upper	1		1
Middle	1.019(0.268–3.868)	0.978	0.810(0.159–4.111)	0.799
Lower	0.607(0.152–2.425)	0.480	0.733(0.140–3.844)	0.714

Note: Bold values indicate statistically significant values.

Abbreviations: GNRI, Geriatric Nutritional Risk Index; PNI, prognostic nutritional index; L3SMI, L3 skeletal muscle index; ALI, advanced lung cancer inflammation index; EC, esophageal cancer; OR, odds ratio.

Relationships Between the L3SMI and ALI and Its Components

The relationships between the L3SMI and ALI and its components (Table 3) were explored. The L3SMI was significantly related to the ALI (P = 0.004, OR = 3.942, 95% CI = 1.534–10.133). The relationship between the L3SMI and the ALI components was further explored. The L3SMI was significantly correlated with the BMI (P = 0.005) and NLR (P = 0.008, OR = 0.185, 95% CI = 0.054–0.639).

Table 3

The Relationships Between the L3SMI and ALI (and Its Components) of Elderly EC Patients

Characteristics	Case	L3SMI
	No.(%)	Low(%)	High(%)	OR(95% CI)	P
ALI
Low	101	32	69	1
High	57	6	51	3.942(1.534–10.133)	0.004
BMI (Kg/m2)					0.005
Low	39	17	22	1
Normal	99	19	80	3.254(1.452–7.290)	0.004
High	20	2	18	6.955(1.415–34.174)	0.017
Albumin (g/dl)
Low	23	7	16	1
Normal	135	31	104	1.468(0.554–3.889)	0.440
NLR
Low	79	13	66	1
High	79	25	54	0.185(0.054–0.639)	0.008

Note: Bold values indicate statistically significant values.

Abbreviations: L3SMI, L3 skeletal muscle index; ALI, advanced lung cancer inflammation index; EC, esophageal cancer; BMI, body mass index; NLR, neutrophil-lymphocyte ratio; OR, odds ratio.

Survival Analysis and Risk Factors for OS

As of 1 January 2021, a total of 79 patients had died. According to the Kaplan–Meier analysis, patients with a low L3SMI had significantly worse OS than those with a high L3SMI (P < 0.0001) (Figure 3A). Patients with a low ALI had significantly worse OS than those with a high ALI (P = 0.001) (Figure 3B). To evaluate the combined prognostic value of the L3SMI and ALI, 158 elderly EC patients were divided into four subgroups according to combinations of L3SMI and ALI values: low L3SMI/low ALI, low L3SMI/high ALI, high L3SMI/low ALI, and high L3SMI/high ALI. Compared with the other groups, the prognosis of the high L3SMI/high ALI group was significantly better (P < 0.0001) (Figure 4). Univariate and multivariate Cox analyses were used to identify independent prognostic factors for the elderly EC patients (Table 4). The univariate Cox analysis indicated that lymphatic metastasis (P < 0.001; HR = 2.756, 95% CI = 1.728–4.396), cancer embolus (P < 0.001; HR = 2.564, 95% CI = 1.589–4.137), tumor differentiation (P = 0.003, HR = 2.042, 95% CI = 1.281–3.256), tumor depth (P = 0.005; HR = 1.961, 95% CI = 1.225–3.139), L3SMI (P < 0.001; HR = 0.366, 95% CI = 0.232–0.577), GNRI (P = 0.007; HR = 0.535, 95% CI = 0.338–0.845), PNI (P = 0.009, HR = 0.555, 95% CI = 0.356–0.865), and ALI (P = 0.002, HR = 0.434, 95% CI = 0.256–0.735) were significantly associated with OS. A multivariate Cox analysis was performed including factors found to significantly affect OS in the univariate analysis. Lymphatic metastasis (P = 0.013; HR = 1.905, 95% CI = 1.146–3.166), tumor differentiation (P = 0.025; HR = 1.781, 95% CI = 1.075–2.950), L3SMI (P=0.019; HR = 0.536, 95% CI = 0.318–0.903), and ALI (P = 0.037, HR = 0.537, 95% CI = 0.300–0.962) were independent prognostic factors affecting the OS.

Figure 3

Kaplan–Meier survival curve of overall survival in patients: (A) L3SMI; (B) ALI.

Figure 4

Kaplan–Meier survival curves of patients in subgroups differentiated by L3SMI and ALI.

Table 4

Univariate and Multivariate Analyses of Overall Survival (OS) in the Elderly EC Patients

Characteristics	Univariate Analysis		Multivariate Analysis
	HR(95% CI)	P	HR(95% CI)	P
Gender (Male)	1.029(0.594–1.781)	0.920
Age(>70)	1.402(0.902–2.180)	0.133
Smoke (Yes)	1.013(0.645–1.592)	0.956
Alcohol drinking (Yes)	0.842(0.538–1.316)	0.450
BMI (Normal+High)	0.669(0.414–1.081)	0.101
Lymphatic metastasis (Yes)	2.756(1.728–4.396)	<0.001	1.905(1.146–3.166)	0.013
Cancer embolus (Yes)	2.564(1.589–4.137)	<0.001	1.540(0.900–2.635)	0.115
Perineural invasion (Yes)	1.334(0.666–2.673)	0.416
Differentiation (Poor)	2.042(1.281–3.256)	0.003	1.781(1.075–2.950)	0.025
Tumor depth(pT3+pT4)	1.961(1.225–3.139)	0.005	1.184(0.715–1.962)	0.241
L3SMI (high-L3SMI)	0.366(0.232–0.577)	<0.001	0.536(0.318–0.903)	0.019
GNRI(>96.6)	0.535(0.338–0.845)	0.007	1.017(0.562–1.838)	0.957
PNI(>45.35)	0.555(0.356–0.865)	0.009	0.807(0.483–1.346)	0.410
Tumor size(>4cm)	1.096(0.705–1.704)	0.683
Pathology (Adenocarcinoma)	1.156(0.467–2.860)	0.754
ALI (high)	0.434(0.256–0.735)	0.002	0.537(0.300–0.962)	0.037
Tumor location		0.611
Upper	1
Middle	0.736(0.314–1.727)	0.482
Lower	0.647(0.268–1.565)	0.334

Note: Bold values indicate statistically significant values.

Abbreviations: GNRI, Geriatric Nutritional Risk Index; PNI, prognostic nutritional index; L3SMI, L3 skeletal muscle index; ALI, advanced lung cancer inflammation index; EC, esophageal cancer; HR, hazard ratio.

Nomogram Model

Based on the results of the multivariate Cox analysis, a nomogram was constructed for the prediction of patient prognosis. The results indicated that the most important factor for prognosis was lymphatic metastasis, followed by the L3SMI, ALI, and degree of differentiation (Figure 5). By calculating the score of each factor, the 1- to 5-year OS of the EC patients could be predicted for individual patients. The C index for predicting the OS was 0.707. The calibration curve showed that the 5-year OS predictions using the nomogram showed the best agreement with the actual observations (Figure 6).

Figure 5

Nomogram for elderly EC patients. The points identified on the top scale for each independent covariate were added to determine the estimated overall survival and the probability of 1-, 3- and 5- year survival.

Figure 6

The calibration plot for 5-year survival of elderly EC patients. The X-axis presents the predicted probability and the Y-axis shows the actual probability.

Discussion

This study found a significant correlation between the L3SMI and ALI. Moreover, the L3SMI and ALI were identified as independent prognostic factors for elderly EC patients. Using our nomogram, we found that the most important factor affecting prognosis was lymphatic metastasis, followed by L3SMI, ALI, and degree of differentiation. In this study, we first proposed possible CT diagnostic criteria to distinguish sarcopenia in elderly EC patients in South China (for females with L3SMI ≤32.96 cm2/m2 and males with L3SMI≤35.4 cm2/m2). Prior to this study, the diagnostic label for sarcopenia was mainly based on sex-specific cutoff values for the L3SMI (males ≤52.4 cm2/m2, females ≤38.5 cm2/m2).18 These cutoff values were based on the racial characteristics of Europeans and Americans. However, due to ethnic differences between Asians, Europeans, and Americans, there are also differences in the pathological types of EC, especially for the elderly. Therefore, the diagnostic criteria for sarcopenia should be updated.

Many studies have shown that sarcopenia is related to the poor prognosis of many malignant tumors. In this study, it was found that patients with a low L3SMI were more likely to develop lymphatic metastasis and cancer embolus, and were more likely to have an advanced tumor stage than those with a high L3SMI. Further, lower L3SMI was also associated with a lower PNI and GNRI. A total of 60–80% of patients with EC are often unable to eat due to mechanical obstruction from the tumor, resulting in insufficient nutritional intake.6 In addition, elderly individuals are more prone to malnutrition, and their nutritional status is related to the effectiveness of cancer treatment.29,30 Poor nutritional status may be related to micro-metastasis and the growth of residual cancer cells, which may lead to a poor prognosis.31 Many studies have confirmed that patients with a low L3SMI exhibit a variety of adverse reactions, including increased hospitalization and postoperative rehabilitation costs,32 decreased independent living ability,33 and increased risk of accidental falls and even fractures caused by decreased skeletal muscle mass.34 In addition, skeletal muscle not only plays a role during exercise and movement but also participates in complex immune and inflammatory processes in the body by secreting a variety of cytokines.

Skeletal muscle exerts autocrine, paracrine, and endocrine functions. For example, skeletal muscle can secrete interleukin-6 (IL-6), IL-8, and IL-15. Skeletal muscle can also secrete other inflammatory markers, including tumor necrosis factor-α (TNF-α) and C-reactive protein (CRP), leading to systemic inflammation.35,36 IL-15 can bind natural killer (NK) lymphocytes with high affinity through a variety of signaling pathways and protect NK cells from apoptosis by upregulating Bcl-2 to ensure the normal development and survival of NK cells.37 In patients with sarcopenia, the secretion of IL-15 decreases; which leads to a decrease in the anti-tumor ability of the immune system, and may cause lymphatic metastasis, cancer embolus, and tumor progression.38

In this study, the ALI was significantly correlated with the GNRI, the PNI, and tumor size. The ALI was then combined with the BMI, albumin, NLR (BMI × albumin/NLR), and the combination of these factors allowed a better consideration of systemic inflammation and nutritional status. A low ALI score represents a decrease in BMI and serum albumin, and an increase in the NLR, indicated poor nutritional status and high inflammation. An analysis of the L3SMI and ALI (and its components), showed that the L3SMI was significantly related to the ALI, BMI, and NLR. Previous studies have confirmed that BMI is closely related to sarcopenia status,39 which is consistent with the results of this study. Inflammation plays a key role in the immune response to pathogens and tissue repair, but it can become chronic and promote the production of reactive oxygen and nitrogen species, stimulate angiogenesis, and cell proliferation, and may ultimately play a key role in the process of cancer.19

An increase in the NLR indicates an increase in the body’s inflammatory response and a decrease in the lymphocyte-mediated anti-tumor response, which can easily cause tumor progression and metastasis. These effects can ultimately lead to a poor prognosis for the patient.40,41 The relationship between sarcopenia and systemic inflammation is very tight, which is consistent with these findings. Previous studies have also found that skeletal muscle tissue secretes numerous proinflammatory factors, such as TNF-α and IL-6, which in turn lead to the progression of systemic inflammation.37 Systemic inflammation induces the release of proinflammatory cytokines and growth factors,42 which in turn exert catabolic effects on host metabolism leading to increased skeletal muscle decomposition.43,44 The muscle atrophy caused by inflammation further aggravates systemic inflammation and leads to harmful inflammatory muscle weakness.45

This study has certain limitations. First, this study only used skeletal muscle mass to define sarcopenia, ignoring changes in body function. In future, the patient’s muscle function should be evaluated in prospective studies. Second, this was a single-center retrospective study with a relatively small sample size; hence, multicenter large-scale studies are required to verify our findings. However, diagnostic criteria for sarcopenia in elderly EC patients in South China were also proposed for the first time in this study. Our findings showed that the L3SMI was significantly correlated with the ALI. Early identification of elderly EC patients with poor prognosis and timely intervention can improve the prognosis of elderly EC patients.

Conclusion

This study was the first to propose diagnostic criteria for sarcopenia specific to elderly patients with EC in South China: an L3SMI ≤32.96 cm2/m2 for females and an L3SMI ≤35.4 cm2/m2 for males. The L3SMI and ALI are significantly related, and both are independent prognostic factors in elderly EC patients. The nomogram considering the ALI and L3SMI provides a scientific basis for identifying patients with poor prognoses.