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SYSTEMATIC REVIEW article

Front. Oncol., 21 August 2023
Sec. Gastrointestinal Cancers: Colorectal Cancer

Visceral obesity and anastomotic leakage rates in colorectal cancer: a systematic review and meta-analysis

Linchong YuLinchong YuWenjiang Wu*Wenjiang Wu*Shijun XiaShijun XiaYue LiYue LiZhigang XuZhigang Xu
  • Shenzhen Hospital of Guangzhou University of Chinese Medicine, Shenzhen, China

Background: Numberous studies have heatedly discussed whether obesity is a risk factor for anastomotic leakage (AL) because of the increasing number of colorectal cancer (CRC) cases and high incidence of CRC in patients with obesity.

Objective: We aimed to explore the relationship between visceral obesity(VO) and AL after CRC surgery. The databases of Pubmed, Embase, and the Cochrane Library were searched for relevant data and articles published until November 1, 2022. We identified the difference in the incidence of AL after CRC surgery between patients with and without VO. The quality of included studies was evaluated using the Newcastle- Ottawa Scale, and odds ratio (OR) and 95% CI were used to assess the association between VO and AL.

Results: This meta-analysis included 7 studies with 2,136 patients. The OR of patients with VO versus those without VO was 2.15 (95%CIs = 1.46–3.15, test for heterogeneity: P = 0.29, I2 = 18%) based on the fixed-effect model in seven studies. Notably, the difference between the two groups was statistically significant (Z = 3.91 P < 0.0001). Patients with VO in the colon cancer group exhibited a higher incidence of AL (OR = 2.88, 95% CIs = 1.38–5.99, test for heterogeneity: P = 0.27, I2 = 20%) than those in the rectal cancer group (OR = 2.74, 95% CIs = 1.13–6.65, test for heterogeneity: P = 0.20, I2 = 38%). In the studies in the relevant literature, heterogeneity was low. Regarding patients with VO, four Asian studies reported increased morbidity due to AL (OR = 2.79, 95% CIs = 1.35–5.78, test for heterogeneity: P = 0.35, I2 = 9%) compared with three non-Asian studies.

Conclusions: Our findings confirmed the significant relationship between VO and AL. Thus, VO could be considered a reliable risk factor of surgery for colon cancer.

Introduction

Anastomotic leakage(AL) is one of the most common postoperative complications of colorectal cancer(CRC) surgery that has concerned surgeons or patients for several decades. The incidence rate of AL in patients with CRC resection has been reported to be 1.2%–14.9% (17).

Eliminating the risk factor for AL is globally recognized as one of the effective ways to decrease the incidence of AL. In several studies, many risk factors, such as sex, neoadjuvant chemotherapy, anastomosis level from the anal margin, and operating time, have been linked to AL. In addition, numerous studies have heatedly discussed whether obesity is a risk factor for an AL because of the increasing number of CRC cases and high incidence of CRC in patients with obesity. Therefore, whether obesity has an impact on AL morbidity following CRC surgery remains debatable.

There are currently two measures to evacuate the extent of obesity in patients: BMI and VFA. Obesity has been linked to postoperative complication technical challenges after CRC surgeries. Moreover, it is often defined by a body mass index (BMI) of >25 (8) or 30 (9)kg/m2 in many studies. However, several studies have reported that BMI is not necessarily associated with visceral obesity (VO) (8, 10, 11) and does not always adequately reflect the regional fat distribution. Therefore, it is still debatable whether BMI is an effective tools for the preoperative assessment of the CRC procedure. According to various recent studies, VO is debased on abdominal CT scan at the level of L3–L4, and this finding is thought to be a better option for the prediction of the AL morbidity in the management of CRC surgery (12, 13). However, the impact of VO on the incidence of AL after CRC resection still remains inconclusive.

Thus, given the insufficient statistical power of the existing studies, The primary aim of our study was to incorporate results of the relevant comparative studies to examine the link between VO and AL following CRC surgery given that the existing studies lack appropriate statistical power.

Materials and methods

This systematic review and meta-analysis is based on the Preferred Reporting Items for Systematic Reviews and Meta-Analyses statements. Given that the present study is a meta-analysis, neither informed consent from the patients nor approval from the institutional review board was necessary.

Study strategy

The Pubmed, Medline, and Embase databases were searched for studies evaluating the association between VO and the AL following CRC surgery, for example, studies evaluating the effect of VO on CRC resection and those evaluating the effect of association between VO and AL on CRC surgery, from inception until November 1, 2022.

We used the combination of terms as follows: either MeSH terms or terms in title/abstract related to (“Abdominal Visceral” or “Retroperitoneal Fats” or “VO”or “obesity”) and (“anastomotic leak” or “anasotomosis leak” or “anastomosis leakage” or “AL”). Only studies published in English were considered. Additionally, we manually searched and obtained reference lists of retrieved articles and review articles. The quality of the included studies was evaluated using Newcastle–Ottawa Scale (NOS) score.

Inclusion and exclusion criteria

Studies that met the following eligibility criteria were included following the Cochrane recommendations (PICOS schema): a) those discussing the association between the VO and the AL after CRC surgery (either open or laparoscopic); b) those discussing both VO group and non-VO groups; c) retrospective, prospective, or cohort studies included patients with CRC; d) those with clear definition of VO; e) those with clear data on both VO group and non-VO groups as well as AL.f) The study reported odds ration (OR) with a 95%CI: alternatively, the data were used to calculate OR. g) the primary outcome of this meta-analysis was to compared the morbidity of AL between VO groups and non-VO groups.

Exclusion criteria were as follows: studies involving non-human populations, review articles, experimental studies, case reports, and studies without controls were excluded. Moreover, studies on gastric and small intestinal surgery as well as emergency surgery were excluded.

Data extraction

Two reviewers (L.Y. and SJ.X.) independently extracted the following parameters from each study: (i) journal title, author name and year of publication; (ii) population characteristics of studies; (iii) study design and inclusion/exclusion criteria; (iv) type of the surgery and the disease; (v) numbers of individuals in the obese groups and non-obese groups; and (vi) outcomes of AL.

Any disagreements were resolved by consensus between the two reviewers.

Quality assessment

The Newcastle–Ottawa Scale (NOS) (14) was used to rate the quality of the included studies. The scale takes into account the selection of the study groups, comparability of the groups and determination of the exposure or the outcome of interest for both case–control and cohort studies. Two investigators (L.Y. and SJ.X.) conducted this evaluation. The high quality of the study was indicated by a total score of ≥6. Table 1 shows the NOS for the seven studies.

TABLE 1
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Table 1 Characteristics of included studies.

Outcomes

The primary aim of our analysis was to combine the result of comparative studies to determine the relationship between VO and AL after CRC surgery.

Statistical analysis

All statistical analyses were performed using the Review Manager (RevMan) version 5.4 provided by Cochrane Collaboration. The values of ORs with 95% CIs were pooled using generic inverse variance methods for describing dichotomous variables. Heterogeneity was evaluated using the statistical values of Q and I2. For P < 0.1 or I2 > 50%, heterogeneity was considered to be present, and the random-effects model was performed. Alternatively, the fixed-effects model was performed. P–values of < 0.05 were considered statistically significant.

Result

The selection procedure has been shown in the Figure 1. The database search yielded 297 studies. Of these, seven studies were ultimately included after exclusion based on the inclusion and exclusion criteria (1521).

FIGURE 1
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Figure 1 Flowchart of the selection process.

The characteristics of the included studies are summarized in Table 1. We identified seven studies published during 2006-2021 involving 2136 patients with 144 leakages. Among these studies, 1035 patients with visceral obesity (visceral fat area [VFA] of ≥100 cm2 or 130 cm2) and 1101 patients with nonvisceral obesity were included. Of those with visceral obesity, 87 (8.41%) and 948 (91.59%) cases were associated with and without AL.

Table 1 presents information about the seven studies, including that about the year of publication, country, types of the study design, definition of VO, type of surgery and disease, and specified controls for patient with obesity. Notably, three papers were of retrospective studies, whereas the others were of prospective studies. Of the seven studies, four published from 2005 to 2018 were from Asia, one was from North America, and two published from 2015-2020 were from European institutions. Although the remaining studies reported clear data to calculate the ORs with 95% CI, only three (16, 20, 21) of the included studies directly published the ORs with 95% CI.

Two measures that are most commonly used to evaluate an individual’s level of obesity are BMI and VFA. A single-slice CT scan was used to quantify VFA in the current meta-analysis at the level of the navel (L3–L4) (22, 23). Additionally, many studies used alternative cutoffs, such as 130 cm2 (24), 100 cm2 (23), and 90 cm2 (25), to define VO and treat VFA as a dichotomous variable.

Details of the numerous definitions of VO are summarized in Table 2. The study from Mexico (21) only used the VFA rather than BMI to describe the obesity as its objective was to evaluate the relationship between skeletal muscle index and VFA with 30-day mortality in CRC surgery. Four Asian studies used VFA to describe the VO, whereas the specific cutoffs for diagnosing VO (VFA > 100 cm2) were different between two Japanese studies and the Chinese and Korean study according to the VFA cutoff line of the Japan Society for the Study of Obesity. Although most studies simply use same cutoff for both males and females, Chinese studies use distinct cutoffs for males and females. Moreover, the number of the lumbar CT scan is different among seven studies. Korean studies defined obesity as VFA of >130 cm2, whereas other five studies defined it as VFA of > 100 cm2.

TABLE 2
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Table 2 Details of the various definitions of VO.

The OR of patients with VO versus without VO was 2.15 (95%CIs = 1.46–3.15, test for heterogeneity: P = 0.29, I2 = 18%; Figure 2) based on the fixed-effect model in seven studies; the difference between the two groups was statistically significant (Z = 3.91 P < 0.0001).

FIGURE 2
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Figure 2 Shows a forest plot comparing the incidence of AL in visceral and non-visceral groups.

Regarding subgroup analyses in terms of study design, the OR of the patients with VO versus those without VO was 3.25 (95%CIs = 1.71–6.17, test for heterogeneity: P = 0.40, I2 = 1%; Figure 2) based on the fixed-effect model in prospective studies. The OR in terms of VO in the subgroup analyses was 1.70 (95%CIs = 1.06–2.75; Figure 2) based on the fixed-effects model in retrospective studies, without significant heterogeneity (P = 0.39, I2 = 0%).Similarly, difference between the two groups were statistically significant in terms of prospective studies and retrospective studies.

We divided AL risk in patients with VO according to the factor of colon and rectal cancers because these cancers may have different effects on the outcomes of AL. Patients with VO have a higher incidence of AL in the colon cancer group (OR = 2.88, 95%CIs = 1.38–5.99, test for heterogeneity: P = 0.27, I2 = 20%, Figure 3) than those in the rectal group (OR = 2.74, 95%CIs = 1.13–6.65, test for heterogeneity: P = 0.20, I2 = 38%, Figure 3). Heterogeneity between the two groups was low. This suggest that VO is be a reliable tool for predicting morbidity due to AL in cases of major intestinal CRC, particularly cancer localized in the colon.

FIGURE 3
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Figure 3 Forest plot of AL morbidity in patients with visceral obesity stratified by the factor of different location of cancer.

Regarding patients with VO, four Asian studies reported higher morbidity due to AL (OR = 2.79, 95%CIs = 1.35–5.78: test for heterogeneity: P = 0.35, I2 = 9%; Figure 4) compared with three non-Asian studies. Although Moon HG et al. (26), Cecchini S et al. (27), and Ballian N et al. (28) reported no increase in morbidity among patients with VO, nevertheless, we believed that VO is better suitable for Asian patients regarded as an assessment for morbidity due to AL.

FIGURE 4
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Figure 4 Forest plot of AL morbidity in patients with VO stratified by Asian and non-Asian studies.

Publication bias and sensitive analysis

In accordance with the Cochrane Handbook for Systematic Reviews of Interventions, we did not examine publication bias because the number of the included studies was <10. Sensitivity analysis was performed to evaluate the stability of the results in subgroup of Rectal cancer and Non-asian, resulting in the omission of one study from the meta-analysis at a time. The results revealed no significant change in the group of Non-asian. However, we discover the heterogeneity decreased after the removal of Y. Ishii in the group of Rectal cancer, because the number of total cases and AL cases in Y. Ishii were lower than those of the other two articles, and there was no case of AL in the VO group in Y. Ishii. Thus, the result of Y. Ishii had a great impact on the heterogeneity in subgroup of Rectal cancer. With Y. Ishii excluded, we derive the result showing a large correlation between VO and AL in the subgroup of Rectal cancer. The results of sensitivity analysis are presented in Table 3.

TABLE 3
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Table 3 Sensitivity analysis results after removing one study at a time.

Discussion

Obesity is a global health issue that impacts the surgical outcome of patients with CRC as a risk factor (2935). Both BMI and VFA could be considered as measures of obesity in humans. Specifically, VO was defined as an intra-abdominal VFA of >100 cm2 in a horizontal slide in the umbilical plane on a CT-scan at the level of the navel (L3–L4) whereas general obesity was defined as BMI of >30kg/m2 based on height and weight. Moreover, the cutoff line of the VFA varies for Asian and European populations. Based on the review of the seven papers in the present study, studies in China (17) use two separate cutoff lines for male and female patients, but other studies in other countries only use one cutoff for patients with VO. Two distinct cutoff lines (130 cm2 and 100 cm2), four different planimetric cross-sectional scan levels of CT (L3–L4, L3, L4, L4–L5) and four different attenuation ranges (–190 to –30, –140 to –50, –150 to –50, –150 to –30 HU) were utilized in all studies, except for one. According to the result of our study, there is some agreement on the cutoff line for BMI obesity owing to differences in obesity prevalence and body fat distribution between Asian and European populations; however, there is still disagreement about the criteria of the cutoff line and the plane of the planimetric cross-sectional scan level for VFA in defining VO. We could not analyze the differences between the various of scale listed above in the current study because of the small number of total investigations. Accordingly, it is critical to establish an appropriate VFA cutoff line, cross-sectional scan level and attenuation range for all ethnics in the preoperative assessment and future studies.

Excessive peri-visceral adipose tissue, a disproportionately large omentum and a thickened mesentery are observed in patients with VO. In these cases, VO—as opposed to subcutaneous deposits—has been postulated as a superior predictor of technical operating difficulty and patient outcomes (12, 36). In case of rectal cancer surgery, the technical difficulties associated with surgery in the narrow pelvis may be better reflected by VFV than BMI. As an intraoperative factor, intra-abdominal fat increases the technical challenges leading to compaction of VO to AL rates. Obesity causes chronically increased intra-abdominal pressures (37), which could impair micro-circulation of the anastomosis. In addition, obesity is associated with metabolic abnormalities, which cause an inflammatory state that may have a negative effect on normal tissue repair and anastomotic healing (38, 39). However, some (12, 13, 16, 40) studies reported that although BMI (linearly correlated with BMI) cannot explain intra-abdominal adiposity, VO can.

We investigated the effect of VO on rates of anastomosis leakage following laparoscopic or open surgery for CRC in the current meta-analysis, which included seven studies that used the VFA value as a method to determine VO for different groups of patients. The curent meta-analysis sheds light on the controversially reported association between VO and AL risk in CRC surgery. Our analysis of the AL result revealed that VO was significantly associated with increased morbidity due to AL; this finding is consistent with other prior studies (16, 18, 41, 42).

Many studies found no significant link between obesity and the development of AL after the surgery for rectal cancer (2, 17, 4345). However, some studies reported that the measuring visceral fat on a CT scan is a more sensitive factor than BMI in predicting the development of anastomotic dehiscence (16, 20, 32, 34, 35, 46). In contrast, some studies on CRC surgery identified a remarkable association between obesity and AL (16, 20, 42, 47,). According to our findings, the VO group exhibited a greater incidence of AL after both rectal and colon cancer surgery. Thus, it is convincing that VFA, which is strongly associated with a higher incidence of AL, is a reliable tool for analyzing the effects of adiopse tissue deposition on incidences of AL. Obesity may be a risk factor for leaks in extremely low rectal anastomosis because it may be related to tension at the anastomotic site, but technical challenges associated with surgery in the narrow pelvis may be better reflected by VFV(visceral fat volume) than BMI. These could be some of the reasons why VO is superior to BMI obesity in terms of the association with the morbidity of AL.

Our study suggests that VO is related to AL in CRC surgery, so preoperative evaluation of patients’ VO by CT may help the surgeon to acknowledge the morbidity of postoperative AL and develop relevant preoperative strategies to reduce the morbidity of AL. Since it’s unrealistic to change the situation of VO before the surgery in the short term, the only thing we can to is to prevent and intervene AL from other perspectives. For example, it is still common practice to place a drainage tube near the anastomosis or drainage in the colon and pelvic cavity, and reducing the time of using the cutting closure device is also considered to reduce the incidence of AL after laparoscopic rectal cancer (48). The fluorescent angiography (indocyanine green-fluorescence angiography, ICG-FA) is a detection technology that can be detected by the imaging system and can detect the insufficient blood supply of the anastomosis early. After ICG-FA, the transection line can be transferred to the site of good blood perfusion, and the anastomosis here can ensure the blood supply of the anastomosis (49). To reduce the incidence of CRC postoperative AL measures above, we strongly believe that prevention is more meaningful than treatment. As for low location rectal cancer surgery, preventive ileostomy or in anastomosis local use absorbable suture reinforcement can be regarded as effective measures, but the disadvantage of preventive stoma is possible to bring preventive stoma complications and the second operation. The early appearance of AL means the failure of the suture procedure, resulting in an immediate rupture of the anastomosis. The advanced AL is more likely caused by the physiological condition and the vulnerability of anastomotic tissue of the patients, which are the crucial point and bottleneck problem of reducing the incidence of AL from our point of view. There is no optimal treatment for AL and the associated high morbidity and fatality, but with further study and improvement of variable risk factors, the care of preoperative CRC patients will be best optimized (50).

To the best of our knowledge, this is the first study to compare the relationship between VO and morbidity due to AL in patients who had undergone CRC surgery for malignant tumors. The study has some limitations. First, some of the included studies were retrospective; thus, the final result could have been influenced by confounding factors. Nevertheless, all the studies included in this meta-analysis were rated as high quality. Second, as several studies included data on different cancer foci as well as different ethnicities, we tended to address this issue by performing a stratified analysis depending on these criteria. Third, the cutoff of the VFA can differ between studies depending on the research institution from different locations. Fourth, owing to the unclear group data, we could not examine the relationship between obesity and AL across different types of the surgery (open or laparoscopic). Fifth, studies analyzing the influence of VO on the outcome of AL in patients with CRC are insufficient; hence, only seven studies meet our eligibility standards. In future, risk analyses for AL in CRC surgery should include visceral fat levels and account for subgroup differences.

Conclusion

In the current study, we investigated the relationship between VO and morbidity due to AL following surgery for CRC. Our findings confirmed the remarkable relationship between VO and AL. Furthermore, the incidence of AL after the surgery for colon cancer in patients with VO was high in all cancer groups, demonstrating that VO maybe a valid risk factor of surgery for colon cancer.

Data availability statement

The original contributions presented in the study are included in the article/supplementary material. Further inquiries can be directed to the corresponding author.

Author contributions

First author: LY (analysis and interpretation of data, drafting the article or revising it critically for important intellectual content). The corresponding author: WW (conception and design, final approval of the version to be published). Other author: SX, ZX, and YL (acquisition of data). All authors contributed to the article and approved the submitted version.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

1. Smith JD, Butte JM, Weiser MR, D'Angelica MI, Paty PB, Temple LK, et al. Anastomotic leak following low anterior resection in stage IV rectal cancer is associated with poor survival. Ann Surg Oncol (2013) 20:2641. doi: 10.1245/s10434-012-2854-9

PubMed Abstract | CrossRef Full Text | Google Scholar

2. Rutten HJ, den Dulk M, Lemmens VE, van de Velde CJ, Marijnen CA. Controversies of total mesorectal excision for rectal cancer in elderly patients. Lancet Oncol (2008) 9:494. doi: 10.1016/S1470-2045(08)70129-3

PubMed Abstract | CrossRef Full Text | Google Scholar

3. Reisinger KW, van Vugt JL, Tegels JJ, Snijders C, Hulsewé KW Hoofwijk AG, et al. Functional compromise reflected by sarcopenia, frailty, and nutritional depletion predicts adverse postoperative outcome after colorectal cancer surgery. Ann Surg (2015) 261:345. doi: 10.1097/SLA.0000000000000628

PubMed Abstract | CrossRef Full Text | Google Scholar

4. Manceau G, Karoui M, Werner A, Mortensen NJ, Hannoun L. Comparative outcomes of rectal cancer surgery between elderly and non-elderly patients: a systematic review. Lancet Oncol (2012) 13:e525. doi: 10.1016/S1470-2045(12)70378-9

PubMed Abstract | CrossRef Full Text | Google Scholar

5. Kartheuser AH, Leonard DF, Penninckx F, Paterson HM, Brandt D, Remue C, et al. Waist circumference and waist/hip ratio are better predictive risk factors for mortality and morbidity after colorectal surgery than body mass index and body surface area. Ann Surg (2013) 258:722. doi: 10.1097/SLA.0b013e3182a6605a

PubMed Abstract | CrossRef Full Text | Google Scholar

6. Kang SB, Park JW, Jeong SY, Nam BH, Choi HS, Kim DW, et al. Open versus laparoscopic surgery for mid or low rectal cancer after neoadjuvant chemoradiotherapy (COREAN trial): short-term outcomes of an open-label randomised controlled trial. Lancet Oncol (2010) 11:637. doi: 10.1016/S1470-2045(10)70131-5

PubMed Abstract | CrossRef Full Text | Google Scholar

7. Fujita S, Akasu T, Mizusawa J, Saito N, Kinugasa Y, Kanemitsu Y, et al. Postoperative morbidity and mortality after mesorectal excision with and without lateral lymph node dissection for clinical stage II or stage III lower rectal cancer (JCOG0212): results from a multicentre, randomised controlled, non-inferiority trial. Lancet Oncol (2012) 13:616. doi: 10.1016/S1470-2045(12)70158-4

PubMed Abstract | CrossRef Full Text | Google Scholar

8. Examination Committee of Criteria for ‘Obesity Disease’ in Japan; Japan Society for the Study of Obesity. New criteria for ‘obesity disease’ in Japan. Circ J (2002) 66:987–92. doi: 10.1253/circj.66.987

PubMed Abstract | CrossRef Full Text | Google Scholar

9. Organization WH. The asia-pacifc perspective: redefining obesity and its treatment. Australia: Health Communications Australia (2000) 2000:10–1.

Google Scholar

10. Chen Z, Yang J, Liu Z, Zhang Y, Sun J, Wang P. Which obesity-associated parameters can better reflect the risk of the occurrence of the AL? Scand J Gastroenterol (2020) 55(4):466–71. doi: 10.1080/00365521.2020.1748223

PubMed Abstract | CrossRef Full Text | Google Scholar

11. WHO expert consultation. Appropriate body-mass index for Asian populations and its implications for policy and intervention strategies. Lancet (2004) 363:157–63. doi: 10.1016/S0140-6736(03)15268-3

PubMed Abstract | CrossRef Full Text | Google Scholar

12. Seki Y, Ohue M, Sekimoto M, Takiguchi S, Takemasa I, Ikeda M, et al. Evaluation of the technical difficulty performing laparoscopic resection of a rectosigmoid carcinoma: visceral fat reflects technical difficulty more accurately than body mass index. Surg Endosc (2007) 21:929–34. doi: 10.1007/s00464-006-9084-9

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Tsujinaka S, Konishi F, Kawamura YJ, Saito M, Tajima N, Tanaka O, et al. VO predicts surgical outcomes after laparoscopic colectomy for sigmoid colon cancer. Dis Colon Rectum (2008) 51:1757–1765, discussion 1765–1757. doi: 10.1007/s10350-008-9395-0

PubMed Abstract | CrossRef Full Text | Google Scholar

14. Stang A. Critical evaluation of the Newcastle-Ottawa scale for the assessment of the quality of nonrandomized studies in meta-analyses. Eur J Epidemiol (2010) 25(9):603–5. doi: 10.1007/s10654-010-9491-z

PubMed Abstract | CrossRef Full Text | Google Scholar

15. Giani A, Famularo S, Riva L, Tamini N, Ippolito D, Nespoli L, et al. Association between specific presurgical anthropometric indexes and morbidity in patients undergoing rectal cancer resection. Nutrition (2020) 75-76:110779. doi: 10.1016/j.nut.2020.110779

PubMed Abstract | CrossRef Full Text | Google Scholar

16. Cakir H, Heus C, Verduin WM, Lak A, Doodeman HJ, Bemelman WA, et al. VO, body mass index and risk of complications after colon cancer resection: A retrospective cohort study. Surgery (2015) 157(5):909–15. doi: 10.1016/j.surg.2014.12.012

PubMed Abstract | CrossRef Full Text | Google Scholar

17. Chen WZ, Chen XD, Ma LL, Zhang FM, Lin J, Zhuang CL, et al. Impact of VO and sarcopenia on short-term outcomes after colorectal cancer surgery. Dig Dis Sci (2018) 63(6):1620–30. doi: 10.1007/s10620-018-5019-2

PubMed Abstract | CrossRef Full Text | Google Scholar

18. Kang J, Baek SE, Kim T, Hur H, Min BS, Lim JS, et al. Impact of fat obesity on laparoscopic total mesorectal excision: more reliable indicator than body mass index. Int J Colorectal Dis (2012) 27(4):497–505. doi: 10.1007/s00384-011-1333-2

PubMed Abstract | CrossRef Full Text | Google Scholar

19. Ishii Y, Hasegawa H, Nishibori H, Watanabe M, Kitajima M. Impact of VO on surgical outcome after laparoscopic surgery for rectal cancer. Br J Surg (2005) 92(10):1261–2. doi: 10.1002/bjs.5069

PubMed Abstract | CrossRef Full Text | Google Scholar

20. Watanabe J, Tatsumi K, Ota M, Suwa Y, Suzuki S, Watanabe A, et al. The impact of VO on surgical outcomes of laparoscopic surgery for colon cancer. Int J Colorectal Dis (2014) 29(3):343–51. doi: 10.1007/s00384-013-1803-9

PubMed Abstract | CrossRef Full Text | Google Scholar

21. Moctezuma-Velázquez P, Vergara-Fernández O, Salgado-Nesme N, Aguilar-Frasco JL, Sainz-Hernández JC, Moctezuma-Velázquez C. Influence of muscle mass area and VO on 30-day mortality after colorectal surgery with primary anastomosis. Rev Invest Clin (2021) 73(6):379–87. doi: 10.24875/RIC.21000108

PubMed Abstract | CrossRef Full Text | Google Scholar

22. Kuritzkes BA, Pappou EP, KIran RP, Baser O, Fan L, Guo X, et al. Visceral fat area, not body mass index, predicts postoperative 30-day morbidity in patients undergoing colon resection for cancer. Int J Colorectal Dis (2018) 33:1019–28. doi: 10.1007/s00384-018-3038-2

PubMed Abstract | CrossRef Full Text | Google Scholar

23. Heus C, Cakir H, Lak A, Doodeman HJ, Houdijk AP. VO, muscle mass and outcome in rectal cancer surgery after neo-adjuvant chemo-radiation. Int J Surg (2016) 29:159–64. doi: 10.1016/j.ijsu.2016.03.066

PubMed Abstract | CrossRef Full Text | Google Scholar

24. Ding Z, Wu XR, Remer EM, Lian L, Stocchi L, Li Y, et al. Association between high visceral fat area and postoperative complications in patients with Crohn’s disease following primary surgery. Colorectal Dis (2016) 18:163–72. doi: 10.1111/codi.13128

PubMed Abstract | CrossRef Full Text | Google Scholar

25. Yu H, Joh YG, Son GM, Kim HS, Jo HJ, Kim HY. Distribution and impact of the visceral fat area in patients with colorectal cancer. Ann Coloproctol (2016) 32:20–6. doi: 10.3393/ac.2016.32.1.20

PubMed Abstract | CrossRef Full Text | Google Scholar

26. Moon HG, Ju YT, Jeong CY, Jung EJ, Lee YJ, Hong SC, et al. VO may affect oncologic outcome in patients with colorectal cancer. Ann Surg Oncol (2008) 15:1918–22. doi: 10.1245/s10434-008-9891-4

PubMed Abstract | CrossRef Full Text | Google Scholar

27. Cecchini S, Cavazzini E, Marchesi F, Sarli L, Roncoroni L. Computed tomography volumetric fat parameters versus body mass index for predicting short-term outcomes of colon surgery. World J Surg (2011) 35:415–23. doi: 10.1007/s00268-010-0888-3

PubMed Abstract | CrossRef Full Text | Google Scholar

28. Ballian N, Lubner MG, Munoz A, Harms BA, Heise CP, Foley EF, et al. VO is associated with outcomes of total mesorectal excision for rectal adenocarcinoma. J Surg Oncol (2012) 105:365–70. doi: 10.1002/jso.22031

PubMed Abstract | CrossRef Full Text | Google Scholar

29. McDermott FD, Heeney A, Kelly ME, Steele RJ, Carlson GL, Winter DC. Systematic review of preoperative, intraoperative and postoperative risk factors for colorectal anastomotic leaks. Br J Surg (2015) 102:462–79. doi: 10.1002/bjs.9697

PubMed Abstract | CrossRef Full Text | Google Scholar

30. Buchs NC, Gervaz P, Secic M, Bucher P, Mugnier-Konrad B, Morel P. Incidence, consequences, and risk factors for anastomotic dehiscence after colorectal surgery: a prospective monocentric study. Int J Colorectal Dis (2008) 23:265–70. doi: 10.1007/s00384-007-0399-3

PubMed Abstract | CrossRef Full Text | Google Scholar

31. Zhang X, Wu Q, Gu C, Hu T, Bi L, Wang Z. The effect of increased body mass index values on surgical outcomes after radical resection for low rectal cancer. Surg Today (2019) 49:401–9. doi: 10.1007/s00595-019-01778-w

PubMed Abstract | CrossRef Full Text | Google Scholar

32. Frasson M, Flor-Lorente B, Rodriguez JL, Granero-Castro P, Hervás D , Alvarez Rico MA, et al. Risk factors for anastomotic leak after colon resection for cancer: multivariate analysis and nomogram from a multicentric, prospective, national study with 3193 patients. Ann Surg (2015) 262:321–30. doi: 10.1097/SLA.0000000000000973

PubMed Abstract | CrossRef Full Text | Google Scholar

33. Makela JT, Kiviniemi H, Laitinen S. Risk factors for AL after left-sided colorectal resection with rectal anastomosis. Dis Colon Rectum (2003) 46:653–60. doi: 10.1007/s10350-004-6627-9

PubMed Abstract | CrossRef Full Text | Google Scholar

34. Nikolian VC, Kamdar NS, Regenbogen SE, Morris AM, Byrn JC, Suwanabol PA, et al. Anastomotic leak after colorectal resection: A population-based study of risk factors and hospital variation. Surgery (2017) 161:1619–27. doi: 10.1016/j.surg.2016.12.033

PubMed Abstract | CrossRef Full Text | Google Scholar

35. Akiyoshi T, Ueno M, Fukunaga Y, Nagayama S, Fujimoto Y, Konishi T, et al. Effect of body mass index on short-term outcomes of patients undergoing laparoscopic resection for colorectal cancer. Surg Laparosc Endosc.Percutaneous Tech (2011) 21:409–14. doi: 10.1097/SLE.0b013e31822e5fdc

CrossRef Full Text | Google Scholar

36. Ellulu MS, Patimah I, Khaza’ai H, Rahmat A, Abed Y. Obesity and inflammation: the linking mechanism and the complications. Arch Med Sci (2017) 13(4):851–63. doi: 10.5114/aoms.2016.58928

PubMed Abstract | CrossRef Full Text | Google Scholar

37. Nguyen N, Wolfe B. The physiologic effects of pneumoperitoneum in the morbidly obese. Ann Surg (2005) 241:219–26. doi: 10.1097/01.sla.0000151791.93571.70

PubMed Abstract | CrossRef Full Text | Google Scholar

38. Sciuto A, Merola G, De Palma GD, Sodo M, Pirozzi F, Bracale UM, et al. Predictive factors for AL after laparoscopic colorectal surgery. World J Gastroenterol (2018) 24(21):2247–60. doi: 10.3748/wjg.v24.i21.2247

PubMed Abstract | CrossRef Full Text | Google Scholar

39. Low S, Chin MC, Ma S, Heng D, Deurenberg-Yap M. Rationale for redefining obesity in Asians. Ann Acad Med Singap (2009) 38(1):66–9. doi: 10.47102/annals-acadmedsg.V38N1p66

PubMed Abstract | CrossRef Full Text | Google Scholar

40. Bouchard C, Despres JP, Mauriege P. Genetic and nongenetic determinants of regional fat distribution. Endocr Rev (1993) 14:72–93. doi: 10.1210/edrv-14-1-72

PubMed Abstract | CrossRef Full Text | Google Scholar

41. Rickles AS, Iannuzzi JC, Mironov O, Deeb AP, Sharma A, Fleming FJ, et al. VO and colorectal cancer: are we missing the boat with BMI? J Gastrointest Surg (2013) 17:133–43. doi: 10.1007/s11605-012-2045-9

PubMed Abstract | CrossRef Full Text | Google Scholar

42. Goulart A, Malheiro N, Rios H, Sousa N, Leão P. Influence of visceral fat in the outcomes of colorectal cancer. Dig Surg (2019) 36:33–40. doi: 10.1159/000486143

PubMed Abstract | CrossRef Full Text | Google Scholar

43. Baastrup NN, Christensen JK, Jensen KK, Jørgensen LN. VO and short-term outcomes after laparoscopic rectal cancer resection. Surg Endosc (2020) 34(1):177–85. doi: 10.1007/s00464-019-06748-4

PubMed Abstract | CrossRef Full Text | Google Scholar

44. Nakanishi R, Oki E, Sasaki S, Hirose K, Jogo T, Edahiro K, et al. Sarcopenia is an independent predictor of complications after colorectal cancer surgery. Surg Today (2018) 48(2):151–7. doi: 10.1007/s00595-017-1564-0

PubMed Abstract | CrossRef Full Text | Google Scholar

45. Kobayashi A, Kaido T, Hamaguchi Y, Okumura S, Shirai H, Kamo N, et al. Impact of visceral adiposity as well as sarcopenic factors on outcomes in patients undergoing liver resection for colorectal liver metastases. World J Surg (2018) 42(4):1180–91. doi: 10.1007/s00268-017-4255-5

PubMed Abstract | CrossRef Full Text | Google Scholar

46. Yang T, Wei M, He Y, Deng X, Wang Z. Impact of VO on outcomes of laparoscopic colorectal surgery: A metaanalysis. ANZ J Surg (2015) 85:507–13. doi: 10.1111/ans.13132

PubMed Abstract | CrossRef Full Text | Google Scholar

47. Verduin WM, Warps AK, van den Helder R, Doodeman HJ, Houdijk APJ. INfluences of fat and MUscle in colorectal surgery collaborative. Visceral fat and AL after colon cancer resection. Dis Colon Rectum (2021) 64(2):163–70. doi: 10.1097/DCR.0000000000001779

PubMed Abstract | CrossRef Full Text | Google Scholar

48. Balciscueta Z, Uribe N, Caubet L, López M, Torrijo I, Tabet J, et al. Impact of the number of stapler firings on anastomotic leakage in laparoscopic rectal surgery: a systematic review and meta-analysis. Tech Coloproctol (2020) 24(21):919–25. doi: 10.1007/s10151-020-02240-7

PubMed Abstract | CrossRef Full Text | Google Scholar

49. Jacqueline VDB, Jongen A, Melenhorst J, Breukink SO, Lenaerts K , Schols RM, et al. Near-infrared fluorescence image-guidance in anastomotic colorectal cancer surgery and its relation to serum markers of anastomotic leakage: a clinical pilot study. Surg Endosc (2019) 33(11):3766–74. doi: 10.1007/s00464-019-06673-6

PubMed Abstract | CrossRef Full Text | Google Scholar

50. Yu K, Chen Z. Risks of anastomotic leakage in patients with colorectal cancer after operation and how to effectively avoid it. Zhong Nan Da Xue Xue Bao Yi Xue Ban (2021) 46(9):1031–40. doi: 10.11817/j.issn.1672-7347.2021.200569

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: anastomotic leakage, visceral obesity, colorectal cancer, meta-analysis, surgery

Citation: Yu L, Wu W, Xia S, Li Y and Xu Z (2023) Visceral obesity and anastomotic leakage rates in colorectal cancer: a systematic review and meta-analysis. Front. Oncol. 13:1224196. doi: 10.3389/fonc.2023.1224196

Received: 17 May 2023; Accepted: 02 August 2023;
Published: 21 August 2023.

Edited by:

Antonio Mario Scanu, University of Sassari, Italy

Reviewed by:

Andrea Chierici, Centre Hospitalier Universitaire de Nice, France
Maria Laura Cossu, University of Sassari, Italy

Copyright © 2023 Yu, Wu, Xia, Li and Xu. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Wenjiang Wu, 1053660645@qq.com

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