Obesity and cancer are the two most serious emerging health problems, and their interrelationship has also been known.¹ Obesity is a well-known risk factor for the development of colorectal cancer (CRC) and is also associated with higher risks of postoperative complication rates and recurrence after adjuvant chemotherapy.^2,3 Although the underlying mechanisms of their interaction remain unclear, recent data suggests an important role of visceral fat in this relationship.^4,5 Visceral adipose tissue (VAT) has higher hormonal and metabolic activities than subcutaneous adipose tissue (SAT).⁶ Visceral adipocyte-induced insulin-like growth factor, inflammatory adipokines like interleukin-6 and tumor necrosis factor-α, and angiogenic factors are reported as mediators related with the tumorigenesis of obesity-related tumors.^7-9 Furthermore, insulin resistance, commonly found in obesity, results in compensatory hyperinsulinemia. As key growth factors for colonic epithelial cells, insulin and C-peptide are well known mitogens of tumor cell growth.^10-12

Previous studies have revealed the relationship between CRC and visceral obesity (VO). However, most studies have focused on the risk of complications after surgery, rather than recurrence or survival of CRC patients.^13-16 A few studies have shown the oncologic outcomes of CRC in viscerally obese patients; however, the results and conclusions of such studies vary. Some studies have shown that VO is related to poor progression-free survival and poor response to adjuvant chemotherapy^17-19 while other studies have argued that there is no convincing relationship between VO and survival or tumor stage of CRC.^20,21 The role of VAT in CRC progression and recurrence remains to be elucidated and the numbers of studies concerning the association between metastasis and recurrence of CRC and VAT are very few.

We investigated the associations between VAT and oncologic outcomes, including overall survival, CRC-specific survival, progression-free survival, and metastasis sites, such as the liver, lung, or peritoneum, in stage III CRC.

1. Patients and data collection

The medical records of patients with colon or rectal cancer, who had undergone surgical bowel resection on account of CRC, and who had been seen at Severance Hospital, Yonsei University, Seoul, Korea, between January 1, 2007, and December 31, 2009, were identified. Among those identified, patients with metastasis at the time of diagnosis were excluded, as they were likely to have undergone significant weight loss, thus lowering the reliability of estimates on obesity and fat distribution. Patients were also excluded from the study if preoperative abdominal computed tomography (CT) could not be evaluated or if patients were diagnosed with any other type of cancer prior to the diagnosis of CRC. Finally, 472 patients diagnosed with stage III CRC were included.

Patient demographics and clinical characteristics, including age at diagnosis, gender, tumor stage at diagnosis and surgical diagnosis, and underlying medical conditions were obtained from medical records. Data regarding the history of use of drugs, family history of CRC, smoking history, drinking history, date of death and recurrence, cause of death, and received treatment were also obtained. The date of CRC diagnosis was defined as the day of pathologic diagnosis. Deaths were identified through medical records, and cause of death was determined in all cases. Height and weight recorded before surgery were used to calculate body mass index (BMI; weight in kg divided by height in m²). BMI was stratified into “underweight” (BMI <18.5 kg/m²), “normal” (BMI 18.5–24.9 kg/m²), “overweight” (BMI 25.0–29.9 kg/m²), and “obese” (BMI ≥30.0 kg/m²) based on the World Health Organization BMI classification.²²

The Institutional Review Board of Severance Hospital, Yonsei University, Seoul, Korea, approved this study in accordance with the Declaration of Helsinki, and IRB review and informed consent were exempted after review of study design.

2. Measurements of abdominal adipose tissue

Preoperative abdomen CT (Siemens Medical Systems, Forchheim, Germany) was performed on all patients. VAT and SAT areas were retrospectively measured from three axial slices at the L3–L4, L4–L5, and L5–S1 intervertebral space. The CT attenuation level was set between –190 to –30 Hounsfield units, regions of adipose tissue were delineated, and areas of total adipose tissue, VAT, and SAT were calculated. The VAT area referred to the intra-abdominal fat bound by the parietal peritoneum or transversalis fascia, excluding the vertebral column and paraspinal muscles (Supplementary Fig. 1A). SAT area was the fat superficial to the abdominal and back muscles (Supplementary Fig. 1B). Free hand-driving mode program was used to measure fat volume. Automated fat segmentation was performed after adjusting the boundaries for subcutaneous and visceral compartments at each level. Then, we manipulated the fat segments to either include or exclude focal regions as required. A skilled radiologist, blinded to the patient’s data, measured all data.

The VAT to SAT ratio (VS ratio) and VAT to TAT ratio (VT ratio) were calculated to provide a single representative measure of abdominal fat.

3. Assessment of CRC staging and treatment

All patients with pathologically confirmed CRC were evaluated for appropriate staging based on 7th version of the American Joint Committee on Cancer TNM staging system. Treatment modality was determined based on the tumor extent and location at diagnosis and recurrence during follow-up. According to the National Comprehensive Cancer Network guideline, patients with locally advanced stage III CRC or recurrent advanced tumors with resectable metastatic lesions were treated by surgical resection, followed by adjuvant chemotherapy (FOLFOX regimen). Some patients with recurrent advanced tumors with metastasis were treated by neoadjuvant chemotherapy (FOLFIRI or FOLFOX with cetuximab or bevacizumab, based on primary tumor location and the result of KRAS mutation), followed by surgery. In case of rectal cancer, preoperative chemoradiation or postoperative radiation were added. Recurrent unresectable metastatic CRC were treated by palliative chemotherapy (FOFIRI or FOLFOX regimens) with target agent, such as cetuximab or bevacizumab, according to primary tumor location and the result of KRAS mutation analysis.

4. Statistical analysis

Descriptive statistics are presented as absolute (n) and relative (%) frequencies for categorical variables, and median or mean±standard deviation for quantitative variables. In comparison of covariates between non-overweight and overweight groups, the Pearson chi-square test or Student t-test were used for analyzing categorical or continuous data, respectively. Relationships between fat parameters and clinical outcomes were examined with Cox proportional hazards regression model, which was used to estimate hazard ratios (HRs) and 95% confidence intervals (95% CIs) after adjusting patient-related variables, including age at diagnosis, gender, and family history of CRC with medication, smoking, and alcohol history, when indicated. The Kaplan-Meier analysis was used for survival curves, which were compared by the log-rank test. Given well-known sex differences in fat distribution, we adjusted for sex in bivariate and multivariate analyses. Statistical analysis was performed using the software package SPSS 21.0 (IBM Corp., Armonk, NY, USA). A difference of p<0.05 was considered statistically significant.

1. Patients’ demographics and clinical characteristics

Four hundred and seventy-two patients diagnosed with stage III CRC underwent colorectal surgery. CT scans for evaluation of disease extent and staging were performed in all 472 patients. Among the enrolled, 154 patients were overweight, while 318 were not. Demographics and baseline clinical characteristics were mostly similar between the two groups, except for factors associated with fat distribution (Table 1). Median age at diagnosis was 59 years (range, 26 to 86 years), and 272 patients were men (57.6%). As for age, gender, family history of cancer, chronic disease, and medication status, smoking history, and drinking history, there was no significant difference between the two groups. Tumor location, T and N stage, histologic type, and treatment type also showed no difference between the two groups. Average VAT area (83.89±30.85 cm² vs 57.62±26.53 cm², p<0.001) and SAT area (178.01±66.22 cm² vs 125.25±55.18 cm², p<0.001) were both significantly higher in the overweight group than in the non-overweight group. However, the VT and VS ratios did not show significant differences between the two groups.

Table 1 . Patient Demographics and Baseline Clinical Characteristics (n=472).

Variable	Total (n=472)	Non-overweight (BMI <25 kg/m2) (n=318)	Overweight (BMI ≥25 kg/m2) (n=154)	p-value
Age, yr	59 (26–86)	59 (26–86)	58 (29–80)	0.355
Male sex	272 (57.6)	177 (55.7)	95 (61.7)	0.214
Smoking status				0.836
Current smoker	285 (60.4)	191 (60.1)	94 (61.0)
Former smoker	91 (19.3)	60 (18.9)	31 (20.1)
Never smoker	96 (20.3)	67 (21.1)	29 (18.8)
Daily drinker	39 (8.3)	28 (8.8)	11 (7.1)	0.539
Family history of colorectal cancer	35 (7.4)	23 (7.2)	12 (7.8)	0.828
Chronic disease and medication
Hypertension	159 (33.7)	103 (32.4)	56 (36.4)	0.392
Diabetes mellitus	81 (17.2)	56 (17.6)	25 (16.2)	0.710
Regular use of metformin	44 (9.3)	32 (10.1)	12 (7.8)	0.426
Regular use of low-dose aspirin	94 (19.9)	58 (18.2)	36 (23.4)	0.190
Fatty liver	45 (9.5)	20 (6.3)	25 (16.2)	0.001
Cancer location				0.545
Colon	285 (60.4)	189 (59.4)	96 (62.3)
Rectum	187 (39.6)	129 (40.6)	56 (37.7)
T-stage				0.090
Tis	2 (0.4)	0	2 (1.3)
T1	19 (4.0)	11 (3.5)	8 (5.2)
T2	46 (9.7)	28 (8.8)	18 (11.7)
T3	346 (73.3)	234 (73.5)	112 (72.7)
T4	59 (12.5)	45 (14.2)	14 (9.1)
N-stage				0.796
N0	1 (0.2)	1 (0.3)	0
N1a	177 (37.5)	123 (38.7)	54 (35.1)
N1b	150 (31.8)	96 (30.2)	54 (35.1)
N1c	0	0	0
N2a	92 (19.5)	63 (19.8)	29 (18.8)
N2b	52 (11.0)	35 (11.0)	17 (11.0)
Histologic type				0.497
Well differentiated	45 (9.5)	27 (8.5)	18 (11.7)
Moderately differentiated	388 (82.2)	265 (83.3)	123 (79.9)
Poorly/undifferentiated	22 (4.7)	14 (4.4)	8 (5.2)
Unknown	17 (3.6)	12 (3.8)	5 (3.2)
Treatment
Neoadjuvant CCRT	32 (6.8)	23 (7.2)	9 (5.8)	0.574
Adjuvant CTx	460 (97.5)	309 (97.2)	151 (98.1)	0.568
Adjuvant CCRT	95 (20.1)	63 (19.8)	32 (20.8)	0.806
Postoperative RT	1 (0.2)	0	1 (0.7)	0.150
Measures of obesity*
VAT area, cm2	66.20±30.57	57.62±26.53	83.89±30.85	<0.001
SAT area, cm2	142.46±63.92	125.25±55.18	178.01±66.22	<0.001
VAT to TAT ratio	32.46±9.81	32.32±9.89	32.76±9.65	0.634
VAT to SAT ratio	51.42±23.60	51.13±23.56	52.04±23.74	0.696

Data are presented as median (range), number (%), or mean±SD..

BMI, body mass index; CCRT, chemoradiation; CTx, chemotherapy; RT, radiation therapy; VAT, visceral adipose tissue; SAT, subcutaneous adipose tissue; TAT, total adipose tissue..

*VAT area and SAT area: the average value for area at each of the three vertebral levels: L3–L4, L4–L5, and L5–S1..

2. Fat distribution and survival analysis

Among the entire cohort, there were total of 111 deaths, of which 67 cases were CRC-related. There were 114 cases of recurrence, with the lung being the most frequent site of recurrence (34 cases), followed by the liver and peritoneum, with 33 and 25 cases of recurrence, respectively. The median follow-up duration was 60 months (range, 12 to 84 months).

Overall survival and CRC-specific survival were investigated according to the obesity index (Tables 2 and 3). The Cox hazard regression analysis for overall survival showed that BMI was an independent risk factor for overall mortality. Higher BMI tended to display a lower risk of overall mortality in univariate analysis (HR, 0.939; 95% CI, 0.884 to 0.998; p=0.043), and this result was consistent after adjusting for age at diagnosis, sex, and familial history of CRC (HR, 0.915; 95% CI, 0.840 to 0.997; p=0.044). Regarding CRC-specific survival analysis, BMI was not a significant independent factor associated with CRC-specific mortality (HR, 1.006; 95% CI, 0.904 to 1.120; p=0.908). Interestingly, neither average VAT nor SAT area was associated with overall mortality. Meanwhile, the VT ratio (HR, 1.020; 95% CI, 1.001 to 1.039; p=0.043) and VS ratio (HR, 1.008; 95% CI, 1.001 to 1.016; p=0.027) were both related to higher overall mortality in univariate analysis. However, after adjustment for clinical factors, the results were not statistically significant. Nonetheless, VT and VS ratios were both independent predictors for CRC-specific mortality in stage III CRC after surgical resection (Table 3). In univariate analysis, both VT ratio (HR, 1.031; 95% CI, 1.006 to 1.056; p=0.014) and VS ratio (HR, 1.013; 95% CI, 1.004 to 1.022; p=0.005) were significantly associated with higher cancer-specific mortality; after adjustment of clinically relevant factors, the results maintained statistical significance (VT ratio: HR, 1.041; 95% CI, 1.008 to 1.075; p=0.015 and VS ratio: HR, 1.016; 95% CI, 1.005 to 1.028; p=0.006).

Table 2 . Cox Hazard Regression Analysis for Overall Mortality According to Obesity Index.

Obesity index	Univariate HR (95% CI)	p-value	Adjusted HR (95% CI)*	p-value
BMI	0.939 (0.884–0.998)	0.043	0.915 (0.840–0.997)	0.044
Average VAT area	1.000 (0.994–1.006)	0.888	1.003 (0.995–1.011)	0.506
Average SAT area	0.999 (0.996–1.002)	0.405	1.002 (0.997–1.007)	0.453
VAT to TAT ratio	1.020 (1.001–1.039)	0.043	1.022 (0.997–1.049)	0.091
VAT to SAT ratio	1.008 (1.001–1.016)	0.027	1.009 (1.000–1.019)	0.058

HR, hazard ratio; CI, confidence interval; BMI, body mass index; VAT, visceral adipose tissue; SAT, subcutaneous adipose tissue; TAT, total adipose tissue..

*Adjusted for age at diagnosis, sex, familial history of colorectal cancer..

Table 3 . Cox Hazard Regression Analysis for Colorectal Cancer-Specific Mortality According to Obesity Index.

Obesity index	Univariate HR (95% CI)	p-value	Adjusted HR (95% CI)*	p-value
BMI	0.980 (0.907–1.059)	0.613	1.006 (0.904–1.120)	0.908
Average VAT	1.001 (0.993–1.008)	0.895	1.004 (0.993–1.014)	0.493
Average SAT	0.997 (0.993–1.001)	0.197	0.996 (0.990–1.003)	0.278
VAT to TAT ratio	1.031 (1.006–1.056)	0.014	1.041 (1.008–1.075)	0.015
VAT to SAT ratio	1.013 (1.004–1.022)	0.005	1.016 (1.005–1.028)	0.006

HR, hazard ratio; CI, confidence interval; BMI, body mass index; VAT, visceral adipose tissue; SAT, subcutaneous adipose tissue; TAT, total adipose tissue..

*Adjusted for age at diagnosis, sex, familial history of colorectal cancer..

Additionally, according to the VT ratios of each intervertebral level, overall survival, cancer-specific survival, and recurrence-free survival were analyzed. There were no significant results regarding the overall survival and recurrence-free survival (Supplementary Tables 1 and 2). However, all three VT ratios (at L3–L4, L4–L5, and L5–S1) showed significant results, as higher VT ratios were associated with higher cancer-specific mortality, in analyses both unadjusted and adjusted for clinically relevant factors (Supplementary Table 3).

3. Fat distribution and recurrence

Recurrence-free survival analysis was also performed according to obesity index (Table 4); however, there were no statistically significant results. BMI (HR, 0.978; 95% CI, 0.898 to 1.065; p=0.612), VAT (HR, 0.995; 95% CI, 0.986 to 1.003; p=0.234), and VT ratio (HR, 0.989; 95% CI, 0.963 to 1.015; p=0.387) were not associated with recurrence after treatment of stage III CRC. We performed additional analyses concerning the location of tumor recurrence. First, we investigated the relationship between fatty liver and liver recurrence; however, no significant association was found between these two factors (Supplementary Fig. 2). Liver and lung metastases according to obesity index were also evaluated separately; however, the analysis showed no significant results (Supplementary Tables 4 and 5). Analysis regarding peritoneal seeding recurrence provided interesting results (Table 5). In the multivariate analysis for peritoneal seeding recurrence according to obesity index and after adjusting for clinically relevant factors, BMI, VT ratio, and VS ratio showed statistically significant results. Higher VT (HR, 1.069; 95% CI, 1.010 to 1.131; p=0.020) and VS ratio (HR, 1.024; 95% CI, 1.003 to 1.045; p=0.023) were both associated with a higher risk of peritoneal seeding recurrence, but higher BMI (HR, 0.877; 95% CI, 0.774 to 0.994; p=0.040) was associated with a lower risk of peritoneal seeding recurrence. When VT ratio was divided into two groups by the highest and lowest 25 percentile number, VT ratio of the highest 25 percentile group had a 5-time higher risk of peritoneal recurrence than the lowest 25 percentile group (HR, 5.587; 95% CI, 1.048 to 29.789; p=0.044). However, results regarding VS ratio showed an irrelevant outcome (HR, 2.206; 95% CI, 0.616 to 7.895; p=0.224).

Table 4 . Cox Hazard Regression Analysis for Recurrence According to Obesity Index.

Obesity index	Univariate HR (95% CI)	p-value	Adjusted HR (95% CI)*	p-value
BMI	0.971 (0.915–1.031)	0.342	0.978 (0.898–1.065)	0.612
Average VAT	0.996 (0.990–1.003)	0.249	0.995 (0.986–1.003)	0.234
Average SAT	0.999 (0.996–1.002)	0.372	1.002 (0.997–1.007)	0.541
VAT to TAT ratio	1.000 (0.981–1.019)	0.978	0.989 (0.963–1.015)	0.387
VAT to SAT ratio	1.000 (0.992–1.008)	0.976	0.996 (0.986–1.006)	0.446

HR, hazard ratio; CI, confidence interval; BMI, body mass index; VAT, visceral adipose tissue; SAT, subcutaneous adipose tissue; TAT, total adipose tissue..

*Adjusted for age at diagnosis, sex, familial history of colorectal cancer..

Table 5 . Cox Hazard Regression Analysis for Peritoneal Seeding According to Obesity Index.

Obesity index	Univariate HR (95% CI)	p-value	Adjusted HR (95% CI)*	p-value
BMI	0.884 (0.780–1.002)	0.054	0.877 (0.774–0.994)	0.040
Average VAT	1.003 (0.990–1.016)	0.671	1.007 (0.991–1.021)	0.369
Average SAT	0.999 (0.992–1.006)	0.797	0.997 (0.990–1.004)	0.393
VAT to TAT ratio	1.017 (0.977–1.059)	0.413	1.069 (1.010–1.131)	0.020
VAT to TAT ratio (top vs bottom 25th percentile)
≤24.53%	1.000		1.000
>38.85%	1.657 (0.479–5.729)	0.425	5.587 (1.048–29.789)	0.044
VAT to SAT ratio	1.007 (0.991–1.024)	0.373	1.024 (1.003–1.045)	0.023
VAT to SAT ratio (top vs bottom 25th percentile)
≤32.50%	1.000		1.000
>63.53%	1.900 (0.564–6.395)	0.300	2.206 (0.616–7.895)	0.224

HR, hazard ratio; CI, confidence interval; BMI, body mass index; VAT, visceral adipose tissue; SAT, subcutaneous adipose tissue; TAT, total adipose tissue..

*Adjusted for age at diagnosis, sex, familial history of colorectal cancer..

Since the VAT and SAT areas used in survival and recurrence analyses were the average values of three intervertebral levels, another subgroup analysis, comparing peritoneal recurrence risk of these three intervertebral levels, was performed. Peritoneal seeding recurrence rate according to VT ratio of each spine level in stage III CRC patients was best explained when applying the area of adipose tissue from the L3 to L4 intervertebral level (Fig. 1A). When VT ratio of the L3–L4 level was divided into two groups by 50 percentile number, VT ratio of higher than 50 percentile had almost a 5-time higher risk of peritoneal recurrence than the lower than 50 percentile group (HR, 4.969; 95% CI, 1.303 to 18.949; p=0.019). However, VT ratio of higher than 50 percentile at the L4–L5 level (HR, 0.514; 95% CI, 0.091 to 2.892; p=0.450) or L5–S1 level (HR, 2.617; 95% CI, 0.413 to 16.57; p=0.307) was not associated with a higher risk of peritoneal recurrence (Fig. 1B and C).

Figure 1. Peritoneal seeding rate according to the visceral adipose tissue to total adipose tissue area ratio at each level of the lumbar spine in stage III colorectal cancer patients. (A) Visceral to total adipose tissue (VT) ratio at the L3–L4 level, (B) VT ratio at the L4–L5 level, (C) VT ratio at the L5–S1 level.

Obesity is known to be a risk factor for the development of several cancers, including CRC. However, the influence of VAT distribution on the outcomes of patients with CRC remains controversial. The objective of this study was to examine the outcome of CRC patients according to obesity indices including BMI, VAT area, SAT area, and their corresponding ratios.

Compared to SAT, VAT is known to be more biologically active and therefore related to obesity-related diseases including cancer.^7,15,23 Most of VAT is distributed within the omentum, mesentery, and retroperitoneum.²⁴ Then, we considered CT scan as a better method for measurement of fat because CT scan is mandatory examination before treatment of all newly diagnosed CRC. We focused on VAT distribution and its relative ratio to total adipose tissue or SAT distribution.

The most interesting finding in our study was that a higher VT ratio and a higher VS ratio were both associated with a higher risk of peritoneal seeding recurrence. To our knowledge, this is the first study to find a relationship between peritoneal seeding recurrence and visceral fat. Several studies have provided evidence of the significant contribution of VO to cancer development and aimed to understand the role of omental fat in intraperitoneal tumorigenesis. Using coculture system to simulate the crosstalk between adipocytes and cancer cells, Xiang et al.²⁵ showed that omental adipocytes induced a significant increase of lipid uptake in gastric cancer cells, and enhanced their invasiveness. Similarly, another study using coculture of adipocyte and ovarian cancer cells demonstrated the direct transfer of lipids from adipocytes to cancer cells and an increase of tumor growth.²⁶ In addition to the adipocytes, stimulation of peritoneal tumors is also associated with omental adipose tissue-derived stem cells (ASCs). Nowicka et al.²⁷ reported that ASCs significantly promoted proliferation, migration, and resistance to chemotherapy and radiation in ovarian cancer cell lines by providing cancer cells with lactose and ATP generated in the glycolytic pathway. Another series of experiments using ASCs isolated from mice showed that cells isolated from the visceral fat of obese animals were able to increase the development of intraperitoneal tumors, whereas cells obtained from SAT lacked this activity.²⁸

Along with these reports, the traditional “insulin hypothesis” has also been used to explain the relationship between obesity or visceral adiposity and CRC.^11,29 Prospective studies have shown an increased risk of CRC in individuals with higher levels of postprandial insulin,³⁰ C-peptide,³¹ and fasting glucose.³⁰ However, Renehan et al.³² showed that not only the insulin/insulin-like growth factor molecular pathway, but also metabolic syndrome, aging, endogenous sex hormones, adiponectin, and leptin are all very complexly connected with inter-related regulation. Therefore, the insulin hypothesis, sex hormones and adiponectin, adipocyte-promoted lipid internalization of cancer cells, and ASCs affect and regulate each other in the process of peritoneal metastasis.

However, our assessment regarding peritoneal seeding recurrence and overall survival has shown that higher BMI was related to a lower risk of peritoneal seeding recurrence and overall mortality. In a recent review article regarding BMI, obesity, and their association with cardiovascular diseases, the authors claimed that BMI does not explain fat distribution or degree of VO.³³ The metabolically healthy obese phenotype refers to a subgroup of obese individuals in which high BMI is associated with a healthy metabolic profile, characterized by high insulin sensitivity, favorable lipid profile, low VAT, and high lean mass. The “metabolically health” with healthy obese phenotype was not considered in our study, but this might have affected the results of our study, showing a low risk of peritoneal seeding and overall mortality in patients with higher BMI.

Our study has some limitations. First, given the retrospective nature of this study, the results require cautious interpretation. In addition, there is currently no established threshold of VAT area or VS ratio for defining VO. However, our findings might provide additional supportive evidence in this research area. Further, although our study includes a very heterogeneous patient population, it also includes a large number of subjects with stage III CRC, which improves the reliability of the results. Finally, the results of this study should be confirmed among the general population because patients of this study were from a tertiary medical institute.

In conclusion, VO is closely related to the increased risk of CRC-specific mortality and, most intriguingly, to higher risk of peritoneal seeding metastasis in patients with stage III CRC. These findings could be useful in strategy making process of diet and physical care for the patient group in actual clinical field. Further studies are needed to clarify the physiologic and biologic mechanisms mediating the link between visceral adiposity and CRC metastasis. The assimilation of quantitative measures of VO and corresponding clinical studies is needed to integrate these results with therapeutic and epidemiologic studies.

Supplementary materials can be accessed at https://doi.org/10.5009/gnl20266.

This research was supported by a grant from the National R&D Program for Cancer Control, Ministry of Health and Welfare, Republic of Korea (grant number: 1631020).

This abstract was presented in a poster session at Asian Pacific Digestive Week 2018 (APDW 2018), on November 15-18, 2018, in Seoul, Korea.

S.J.P. and J.H.C. are editorial board members of the journal but were not involved in the peer reviewer selection, evaluation, or decision process of this article. No other potential conflicts of interest relevant to this article were reported.

Study concept and design: T.I.K. Data acquisition: J.W.P., S.Y.C., S.J.P., J.J.P., J.H.C., J.S.L., W.H.K. Data analysis and interpretation: J.W.P., S.Y.C., J.S.L., T.I.K. Statistical analysis: J.W.P., S.Y.C. Drafting of the manuscript: J.W.P., S.Y.C. Critical revision of the manuscript: S.J.P., J.J.P., J.H.C., W.H.K., T.I.K.