Correlation of growth differentiation factor 15 level in esophageal cancer with cachectic indicators and postoperative infectious complication

TL;DR

This study shows that higher levels of GDF15 in esophageal cancer patients are linked to worse health and more post-surgery infections.

Contribution

The study identifies GDF15 as a potential biomarker for cachexia and postoperative complications in esophageal cancer.

Findings

GDF15 levels correlated with age, diabetes, and markers of organ dysfunction and muscle loss.

Higher GDF15 was an independent risk factor for postoperative infectious complications.

A GDF15 cut-off of 930 pg/mL predicted infectious complications with moderate accuracy.

Abstract

Patients with esophageal cancer (EC) usually have multiple comorbidities, particularly, high cachexia incidence, which may lead to increased postoperative complications. A novel inflammatory marker, growth differentiation factor 15 (GDF15), was recently reported to be associated with cancer cachexia. This study evaluated the correlation between clinical data suggestive of cachexia in patients with EC and circulating GDF15 levels.

Eighty patients with EC were enrolled in this study. Plasma samples were collected before initiating any cancer treatment. GDF15 was quantified using ELISA. Clinical information, including age, comorbidities, biochemical data, Controlling Nutritional Status score, and Psoas muscle index (PMI), was collected from the clinical records. Clinical impact of GDF15 was then evaluated and compared with cachectic indicators or postoperative results.

The median value of GDF15 was 1168 pg/mL (range 298–9100 pg/mL). GDF15 values statistically correlated with age, prevalence of diabetes, serum level of aspartate aminotransferase/γ-glutamyltransferase/creatinine/blood sugar/albumin, and PMI. Sixty-three patients finally underwent curative esophagectomy with right thoracic approach and gastric tube reconstruction. Patients with infectious complications had a statistically higher GDF15 than those without. The cut-off value was 930 pg/mL for detecting infectious complications, with an area under the receiver operating characteristic curve value of 0.685, and high GDF15 was detected as an independent risk factor for postoperative infectious complications.

GDF15 is potentially suggestive of general condition deterioration from aging, organ dysfunction, and decreased muscle mass, which may lead to cachexia in patients with EC. Moreover, patients with higher GDF15 are at a risk of postoperative infectious complications.

The online version contains supplementary material available at 10.1007/s10388-025-01157-0.

Figures

Selected treatment and analysis cohort in this study. a The patients of overall case analysis were used for comparison between GDF15 level and patient’s characteristics, nutritional status, blood test, and tumor progression. b The patients of preoperative chemotherapy case analysis were used for comparison between GDF15 level and chemotherapeutic adverse events and its response. c The patients of surgical case analysis were used for comparison between GDF15 level and surgical complications

GDF15 distribution and correlation between continuous variables. a Plasma GDF15 distribution. b Correlation between age, blood biochemical data, and circulating growth differentiation factor 15 (GDF15). GDF15 escalations are seen well correlated with escalation of age, and serum levels of aspartate aminotransferase (AST), γ-glutamyltransferase (γ-GTP), creatinine, uric acid (UA), and blood sugar (BS)

Full text

Introduction

Cachexia was first defined as “a complex metabolic syndrome associated with underlying illness and characterized by loss of muscle with or without loss of fat mass” by Evans et al. [1]. Cachexia is seen in patients with various underlying diseases and is known to be an important prognostic indicator in patients with cancer. However, the condition of patients with cachexia is difficult to qualify because it is formed by a complex interaction of various factors. Although there are several well-known indicators that can estimate the cachectic condition, including several symptoms such as loss of appetite, loss of body weight, decreased body mass index, decreased grip strength, and increased C-reactive protein [2–4], there are only few single blood markers that can reflect cancer cachexia caused by complex triggers.

Growth differentiation factor 15 (GDF15) also known as macrophage inhibitory cytokine-1 (MIC-1) is in a member of the transforming growth factor beta super family. DGF15 is weakly expressed in the most organs including liver, lung, and kidneys under normal conditions, but its expression is known to be elevated in inflammatory condition such as organ failure or cancer bearing patients. Therefore, GDF15 was recently reported to be associated with cancer cachexia. In basic research, circulating GDF15 levels have been correlated with the loss of food intake, tumor size, and skeletal muscle atrophy in tumor-bearing animals [5–7]. In the clinical field, several investigators have reported that circulating GDF15 levels in patients with cachectic cancer are much higher than those in non-cachectic patients, and this was correlated with cancer-associated weight loss [7, 8]. These previous studies suggest that GDF15 is potentially useful as a clinical cachectic biomarker for patients with cancer, particularly those facing highly invasive surgery. However, there are a few reports on the impact on perioperative outcomes. Therefore, in this study, we evaluated the correlation between clinical data suggesting cachexia in patients with Esophageal Cancer (EC) and plasma GDF15 to assess the usefulness of GDF15 as a potential biomarker for cachexia and risk factors for postoperative complications.

Methods

Patient selection and information

Eighty patients with EC who first visited our outpatient ward between July 2021 and March 2023 were enrolled in this study. After careful additional examination, the treatment was determined based on EC practice guidelines 2022 edited by the Japanese esophageal society [9, 10]. Patient information, including age, sex, comorbidities, social history, and blood test results at the time of pre-treatment, were collected from clinical records. Alcohol consumption was defined only for patients who habitually consumed alcohol. Chronic obstructive pulmonary disease was defined as the patients < 70% of FEV1.0%. The tumor stage was diagnosed according to the TNM classification of malignant tumors, 8th edition [11]. In case patients who underwent surgery, postoperative complications according to the Clavien–Dindo classification of surgical complications and results of neoadjuvant chemotherapy (NAC) were also collected. Adverse event for NAC was determined by Common Terminology Criteria for Adverse Events version 5.0. The response to NAC was determined using the Japanese classification of esophageal cancer [12]. We created three different cohorts for each purpose of our analysis, namely, an "Overall case analysis" to examine the background and GDF15 levels of esophageal cancer patients, a “Preoperative chemotherapy case analysis” to examine adverse events of NAC, and a “Surgical case analysis” to examine surgical complications (Fig. 1). The patients with “Surgical case analysis” were limited to right thoracic approach and gastric tube reconstruction. All patients consented to pre-treatment blood collection for research purposes and the study protocol prior to blood collection. The study protocol was approved by the Ethics Committee of the Tohoku University Graduate School of Medicine (accession no. 2021-1-167).Fig. 1. Selected treatment and analysis cohort in this study. a The patients of overall case analysis were used for comparison between GDF15 level and patient’s characteristics, nutritional status, blood test, and tumor progression. b The patients of preoperative chemotherapy case analysis were used for comparison between GDF15 level and chemotherapeutic adverse events and its response. c The patients of surgical case analysis were used for comparison between GDF15 level and surgical complications

Collection of plasma samples

Plasma samples were collected from all patients at the time of their first visit or admission. All samples were obtained prior to any treatment for EC and these were stored at 4 °C before dispensing 200 μL each and then stored at − 80 °C until further analysis.

ELISA for GDF-15

Plasma GDF15 concentrations were quantified using a Human GDF-15 Quantikine ELISA Kit (R&D Systems, Inc., Minneapolis, MN, USA). After defrosting samples on ice, each 13 µL of samples and 50 µL of standards adjusted concentration were put into each well which pre-aliquoted assay diluent and incubated at room temperature for 2 h. Subsequently, after aspiration and washing each well, 200 µL conjugate was put into each well and incubated at room temperature for 1 h. Finally, each standard and sample were reacted with the substrate and stop solutions, and the absorbance was read using a spectrometer with a wavelength correction set to 540 nm. Detailed measurement methods were obtained from the manufacturer’s instructions and previous reports [13, 14].

Parameters for patient’s malnutrition and sarcopenia

To evaluate the correlation between GDF-15 levels and malnutrition and sarcopenia, we chose the controlling nutritional status (CONUT) score and psoas muscle index (PMI) as the parameters of malnutrition and sarcopenia, respectively. CONUT score was calculated by using serum total cholesterol, albumin, and total lymphocyte at the time of pre-treatment and malnutrition was defined as CONUT score ≥ 2. Sarcopenia was measured using the cross-sectional areas of both psoas muscles at the caudal part of the third lumbar vertebra on pre-treatment computed tomography images. PMI was calculated as follows:

\documentclass[12pt]{minimal} \usepackage{amsmath} \usepackage{wasysym} \usepackage{amsfonts} \usepackage{amssymb} \usepackage{amsbsy} \usepackage{mathrsfs} \usepackage{upgreek} \setlength{\oddsidemargin}{-69pt} \begin{document}$${\mathrm{PMI}} = {\mathrm{cross}} {\mathrm{-}} {\text{sectional area of both psoas muscles }}({\mathrm{cm}}^{{2}} )/{\mathrm{height}}^{{2}}\; ({\mathrm{m}}^{{2}} ).$$\end{document}

Sarcopenia was defined as that lower than the sex-specific 25th percentile [15].

Statistical analysis

Mann–Whitney U test was used to analyze the relationship between GDF15 levels, patient characteristics, and postoperative complications. Linear regression analysis was performed to estimate the relationship between patients’ age or blood data and GDF15 levels. Multivariate analysis was performed using logistic regression, and the variables used for the multivariate analyses were determined using stepwise regression. Receiver operating characteristic (ROC) curves and the area under the curve (AUC) were calculated to determine the optimal cut-off value for predicting postoperative infectious complications. Statistical significance was set at P < 0.05. All statistical analyses were performed using JMP Pro 16 software (SAS Institute, Cary, NC, USA).

Results

Patient’s characteristics

A total of 80 patients were enrolled in this study. The mean age was 68.3 years and 80.0% were male. The number of patients diagnosed with cStages I, II, III, and IV was 21, 10, 32, and 17, respectively. Histological subtypes were classified as squamous cell carcinoma, adenocarcinoma, and others (including basaloid squamous cell carcinoma, and carcinoma), with 61, 17, and 2, respectively. Surgery alone, NAC, and other treatments (including chemoradiotherapy, chemotherapy alone, and radiotherapy alone) were selected for 35, 38, and 7 patients, respectively. The number of patients with malnutrition diagnosed using CONUT was 24 (30.0%) and that of patients with sarcopenia was 21 (26.3%). The median value of GDF15 was 1168 pg/mL (range 298–9100 pg/mL). The patient characteristics are presented in Table 1. Table 1. Patient’s characteristicsOverall case analysis(N = 80)%Surgical case analysis(N = 63)%Age, years Mean ± SD68.3 ± 8.868.5 ± 8.3Sex Male6480.04977.8 Female1620.01422.2Performance status PS07087.55790.5 PS11012.569.5Smoking history6480.04876.2Alchohol consumption^a^6885.05384.1Comorbidities COPD^b^2025.01523.8 Hypertension5467.54469.8 Diabetes1215.0711.1Dysphagia^c^4252.53352.4cT stage T1–23543.83047.6 T3–44556.33352.4cN stage N negative2733.82438.1 N positive (N1, N2, N3)53 (33, 20, 0)66.339 (25, 14, 0)61.9cM stage M06783.85790.5 M11316.369.5cStage I–II31 (21, 10)38.828 (20, 8)44.4 III–IV49 (32, 17)61.335 (27, 8)55.6Tumor location CeUtMt (Ce, Ut, Mt)40 (1, 10, 29)50.032 (1, 8, 23)50.8 LtAeG (Lt, Ae, G)40 (26, 13, 1)50.031 (22, 9, 0)49.2Histological subtype Squamous cell carcinoma6176.34977.8 Adenocarcinoma1721.31320.6 Other22.511.6Initial treatment Surgery3543.82844.4 Neoadjuvant chemotherapy (FP, DCF)38 (15, 23)47.53454.0 Other78.811.6Neoadjuvant chemotherapy FP1518.51544.1 DCF2328.41955.9BMI, kg/m^2^ Mean ± SD22.5 ± 3.022.6 ± 3.0CONUT 0–15670.04266.7 2–122430.02133.3Sarcopenia Sarcopenia2126.31625.4 Non-sarcopenia5973.84774.6GDF-15, pg/mL Median (range)1168 (298–9100)1103 (413–9100)^a^Habtal alchohol consumption^b^COPD defined as < 70% of FEV1.0%^c^Dysphagia score ≥ 1

GDF15 correlated with cachectic indicators but not with tumor progression

Correlation between GDF15 and patient characteristics are shown in Table 2. Both categorical and continuous variables of age were strongly correlated with GDF15 (Fig. 2 and Table 2) (elder vs. younger: 1323 vs. 903, P < 0.001). Those with a worse tendency performance status (PS) (PS 0 vs. 1: 1116 vs. 1331, P = 0.052) were also observed. Patients with diabetes had significantly higher GDF15 than unaffected patients (1449 vs. 1117, P = 0.021). Furthermore, sarcopenia patients also had higher GDF15 than non-sarcopenia patients (1360 vs. 1076, P = 0.003). The malnutrition indicator CONUT score was not significantly correlated with GDF15, but a correlation between a worse CONUT score and GDF15 increase was observed. In each element of CONUT, namely, total lymphocyte, total cholesterol, and albumin, only serum albumin was observed negative correlation with GDF15 (P = 0.009) (Fig. 2). In correlation between GDF15 and the result of blood test, GDF15 was positively correlated with aspartate aminotransferase (P < 0.0001), γ-glutamyltransferase (P < 0.0001), creatinine (P = 0.004), uric acid (P = 0.012), and blood sugar (P = 0.031) (Fig. 2). All the results we examined are shown in Supplementary Fig. 1. Table 2. Patient’s characteristics vs GDF15GDF15, pg/mL [median (range)]P-valueAge (< 68/≥ 68)903 (298–3220)/1323 (795–9100)<** 0**.001Sex (male/female)1207 (298–9100)/1054 (583–1971)0.361Performance status (0/1)1116 (298–9100)/1331 (989–2378)0.052Smoking history (yes/no)1206 (298–9100)/978 (584–1971)0.107Alchohol consumption^a^ (yes/no)1206 (414–9100)/1030 (298–1971)0.241Comorbidities COPD^b^ (yes/no)1297 (768–2379)/1101 (298–9100)0.128 Hypertension (yes/no)1206 (414–9100)/994 (298–4743)0.071 Diabetes (yes/no)1449 (941–3220)/1117 (298–9100)0.021Dysphagia^c^ (yes/no)1102 (584–4743)/1217 (298–9100)0.603cT stage (T1–2/T3–4)1214 (298–9100)/1103 (582–4743)0.631cN stage (negative/positive)1076 (414–9100)/1199 (298–4743)0.448cM stage (M0/M1)1190 (298–9100)/1076 (642–3220)0.710cStage (I–II/III–IV)1165 (298–9100)/1170 (582–4743)0.763Tumor location (CeUtMt/LtAeG)1088 (414–9100)/1195 (298–3179)0.693Histological subtype (SCC/AC/other)1214 (414–9100)/1027 (298–3179)/1226 (1063–1390)0.254BMI, kg/m^2^ (< 23/≥ 23)1199 (298–9100)/1165 (414–3220)0.437CONUT (0–1/2–12)1117 (298–3220)/1333 (583–9100)0.156Sarcopenia (Yes/No)1360 (642–9100)/1076 (298–3220)0.003Overall case analysis^a^Habtal alchohol consumption^b^COPD defined as < 70% of FEV1.0%^c^Dysphagia score ≥ 1Fig. 2GDF15 distribution and correlation between continuous variables. a Plasma GDF15 distribution. b Correlation between age, blood biochemical data, and circulating growth differentiation factor 15 (GDF15). GDF15 escalations are seen well correlated with escalation of age, and serum levels of aspartate aminotransferase (AST), γ-glutamyltransferase (γ-GTP), creatinine, uric acid (UA), and blood sugar (BS)

In contrast, GDF15 levels did not correlate with tumor location, histological subtype, or tumor progression.

GDF15 had no statistical correlation with NAC adverse event and response

Thirty-eight patients received NAC (23 for the docetaxel, cisplatin, plus 5-FU and 15 for the cisplatin plus 5-FU regimen). GDF15 was not correlated with any adverse events, including leukopenia, neutropenia, increased creatinine, anorexia, nausea, or mucositis oral and pathological response (Table 3). Table 3NAC adverse event and response vs GDF15DCF (N = 23)FP (N = 15)GDF15 [median (range)]P-valueGDF15 [median (range)]P-valueLeukopenia (≥ G2) (yes/no)1029 (584–1860)/1310 (830–1437)0.7101392 (1099–1830)/1082 (802–1482)0.112Neutropenia (≥ G3) (yes/no)1029 (584–1860)/1355 (1355)0.6511099 (802–1830)/1102 (848–1482)1.000Creatinine increased (≥ G1) (yes/no)1364 (704–1689)/1029 (584–1860)0.2681296 (1033–1482)/1099 (802–1830)0.151Anorexia (≥ G2) (yes/no)1029 (830–1437)/1223 (584–1860)0.9511099 (848–1393)/1102 (802–1830)0.903Nausea (≥ G2) (yes/no)1373 (902–1437)/986 (584–1860)0.2241099 (1099)/1102 (802–1830)0.817Mucositis oral (≥ G2) (yes/no)902 (584–1354)/1147 (704–1860)0.3001011 (989–1033)/1103 (802–1830)0.235Overall adverse events^a^ (yes/no)1223 (796–1617)/1029 (584–1860)0.8061246 (989–1830)/1101 (802–1482)0.361Pathological response (Grade 1a/Grade 1b–2)902 (796–1360)/1355 (584–1860)0.3221033 (848–1830)/987 (802–1393)0.361Preoperative chemotherapy case analysis^a^Four or more of G2, or 3 or more G3 adverse events

GDF15 correlated with infectious complication

Seventy-one patients underwent curative esophagectomy. Of these, 35 underwent robot-assisted minimally invasive esophagectomy, 33 underwent conventional (thoracoscopic) minimally invasive esophagectomy, two underwent transhiatal esophagectomy, and one underwent thoracotomy. Sixty-three (88.7%) patients underwent reconstruction via gastric conduit, five via small intestine, and three via secondary reconstruction. No perioperative mortalities were observed. To avoid the influence of surgical factors on postoperative complications as much as possible, this analysis was limited to the patients who underwent esophagectomy with right thoracic approach and gastric tube reconstruction. Cardiovascular complications, pneumonia, and anastomotic leakage were observed in 4 (6.3%), 11 (17.5%), and 5 (7.9%) patients, respectively. Cardiovascular complications were included 3 patients with atrial fibrillation and 1 patient with heart failure due to cardiac tamponade. The patients who developed infectious complications (including pneumonia, anastomotic leakage, and surgical site infection) had statistically higher GDF15 than those who did not (P = 0.024) (Table 4). Table 4. Postoperative complications vs GDF15Cases (%)GDF15, pg/mL [median (range)]P-valueCardiovascular (≥ GII) (yes/no)4 (6.3)1174 (929–1390)/1103 (414–9100)0.757Peumonia (≥ GII) (yes/no)11 (17.5)1310 (801–9100)/1099 (414–4743)0.107Anastomotic leakage (≥ GII) (yes/no)5 (7.9)1359 (1165–4743)/1099 (414–9100)0.060Surgical site infection (≥ GII) (yes/no)3 (4.8)958 (830–1103)/1148 (414–9100)0.349Infectious complication^a^ (≥ GII) (yes/no)18 (28.6)1262 (801–9100)/1071 (414–1860)0.024Overall complications (≥ GII) (yes/no)29 (46.0)1182 (584–9100)/1099 (414–1860)0.334Overall complications (≥ GIIIa) (yes/no)14 (22.2)1318 (802–4743)/1099 (298–9100)0.089Overall complications (≥ GIIIb) (yes/no)5 (7.9)1310 (1063–1390)/1102 (414–9100)0.360Surgical case analysis^a^Patients with pneumonia and/or anastomotic leakage and/or surgical site infection

Cut-off value of GDF15 for predicting infectious complication

The area under the curve of GDF15 by receiver operating characteristic curve for predicting postoperative infectious complications was 0.685 (Supplementary Fig. 2). The cut-off value was determined to be 930 pg/mL, with 41.9% sensitivity and 88.9% specificity. Stepwise multivariate logistic regression analysis estimated that tumor location (P = 0.001) and plasma GDF15 concentration (P = 0.020) were risk factors for infectious complications (Table 5). Table 5. Univariate and multivariate analysis for infectious complicationUnivariate analysisMultivariate analysisOdds ratio95% CIP-valueOdds ratio95% CIP-valueAge (≥ 68/< 68)3.2840.995–10.8410.051Sex (female/male)1.0790.285–4.0900.911Performance status (1/0)5.8570.966–35.5240.055Smoking history (yes/no)1.5150.364–6.3140.568COPD^a^ (no/yes)1.2030.326–4.4380.781Hypertension (yes/no)1.6900.469–6.0850.422Diabetes (no/yes)1.0530.185–6.0020.954Dysphagia^b^ (yes/no)3.2840.995–10.8410.051cT stage (T1–2/T3–4)1.4500.382–3.4590.804cN stage (positive/negative)2.0580.624–6.7940.236cM stage (M0/M1)1.2750.124–13.1470.838cStage (III–IV/I–II)1.0870.360–3.2850.883Tumor location (CeUtMt/LtAeG)9.3332.327–37.4420.00217.163.378–87.2060.001BMI, kg/m^2^ (< 23/≥ 23)1.6460.537–5.0480.383CONUT (2–12/0–1)1.6440.516–5.2360.400Sarcopenia (yes/no)3.5001.048–11.6900.0423.570.730–17.5570.116GDF15 (≥ 930 pg/mL/< 930)5.7601.175–28.2440.0318.5561.409–51.9540.020Surgical case analysis^a^COPD defined as < 70% of FEV1.0%^b^Dysphagia score ≥ 1

Discussion

In this study, we assessed the usefulness of circulating GDF15 as a potential biomarker of cachexia and a risk factor for postoperative complications in patients with EC. Our results showed that circulating GDF15 levels were significantly higher in various indicators suggesting cachexia, such as advanced age, diabetes, and skeletal muscle loss which are important factors for sarcopenia. These results indicate that the elevated GDF15 may not be caused primarily by cancer, but by chronic inflammation in multiple organs caused by the patient’s comorbidities, life history, and aging.

DGF15 is normally synthesized in the liver and is thought to be expressed in the lungs and kidneys. However, its expression is known to be elevated in cells of inflamed tissues, such as in chronic renal failure [14, 16]. Many patients with EC have an older onset, and a history of heavy smoking and alcohol consumption which may predispose them to chronic inflammation in multiple organs where GDF15 can potentially be elevated. Moreover, in the current study, blood levels of parameters such as liver function, renal function, and blood sugar were correlated with GDF15. In contrast, oncological factors such as TNM staging, tumor location, and histological subtype were not correlated with GDF15. Although several previous studies have reported that patients with advanced cancer have higher levels of circulating GDF15 which is different from the results of the current study [8], these reports mainly focused on patients with unresectable advanced cancer, which may have caused the difference in results.

In the past decade, various perioperative indicators have been reported to influence postoperative complications of curative esophagectomy. Especially, sarcopenic and malnutrition status are well-known risk factor for infectious complication as well as worse prognosis [17–23]. However, no useful single blood markers have been reported as indicators of cachexia, malnutrition, or sarcopenia. Since our current data have shown that circulating GDF15 is a risk factor for infectious complications in patients with EC, GDF15 may be useful for predicting blood biomarkers of cachexia which can lead to infectious complications in patients with EC who have undergone curative esophagectomy.

Regarding GDF15 function, Hsu et al. have reported GDF15 regulates food intake by connecting brainstem-restricted receptor named grail cell-derived neurotrophic factor receptor alpha like [24]. Additionally, in cancer field, several basic and clinical reports have shown GDF15 inducing anorexia and following weight loss [6, 8]. These reports indicate that GDF15 escalation induces anorexia and that controlling GDF15 may suppress anorexia. In other words, not only active intervention, such as nutritional therapy, rehabilitation, and diabetes control normalize GDF15, but also direct GDF15 suppression may also improve cancer inducing anorexia, one of the causes of cachexia, and decrease postoperative complications. As a first step in this validation, we are now beginning to examine pre- and postoperative GDF15 levels and mid- to long-term prognosis. In addition, GDF15 is currently receiving much attention as a biomarker for mitochondrial dysfunction [25]. The possibility that increasing GDF15 in cancer patients may reflect not only anorexia and chronic inflammation but also mitochondrial dysfunction which we currently under investigation.

In contrast, although we expected circulating GDF15 may influence NAC adverse events before this study was conducted, and there was no correlation between GDF15 and NAC adverse events, including anorexia. Because two different NAC regimens were included in this study, the number of patients in the cohort was very small, which may be one of the reasons. Therefore, re-verification is needed. This study had several limitations. First, this study was conducted retrospectively at a single institute for a single cancer type, although several histological subtypes were included. Second, only a small number of patients were included. Therefore, prospective studies targeting a larger number of patients are necessary.

In conclusion, this study suggested circulating GDF15 is potentially suggestive of deterioration of the general condition, resulting from aging, organ dysfunction, and decreased muscle mass, which may lead to cachexia in EC patients. Moreover, higher circulating GDF15 levels are associated with a risk of postoperative infectious complications.

Supplementary Information

Below is the link to the electronic supplementary material.Supplementary file1 Supplementary Fig. 1 Correlation between blood biochemical data and circulating growth differentiation factor 15 (GDF15). (PPTX 101 KB)Supplementary file2 Supplementary Fig. 2 Receiver operating characteristic curve for predicting postoperative infectious complication by circulating GDF15. The area under the curve (AUC) of GDF15 is 0.678. The cut-off value is determined to be 940 pg/mL with 42.3% sensitivity and 87.0% specificity. (PPTX 40 KB)