Impact of metabolism-related mutations on the heart rate of gastric cancer patients after peritoneal lavage.

BACKGROUND: During surgery for gastric cancer, peritoneal lavage using warm distilled water can cause temporary hemodynamic changes. AIM: To examine the associations between changes in heart rate and single nucleotide polymorphisms (SNPs).
METHODS: This was a prospective observational study of patients with gastric cancer who underwent gastrectomy and peritoneal hypotonic lavage at the Third Affiliated Hospital of Soochow University from March 2018 to March 2019. Related SNPs were selected, and the verified exons were analyzed. Heart rate and blood pressure (BP) were measured before and after lavage. The patients were grouped as heart rate change ≥ 30% vs < 30%. Comparison and regression analyses of the selected SNPs were performed between the two groups.
RESULTS: According to the inclusion/exclusion criteria, 194 patients were included in the analysis. Of these patients, 138 were male, with a mean age of 65.9 ± 0.8 years, and 56 were female, with a mean age of 65.0 ± 1.3 years. Heart rate dropped by 0%-10% in 65 participants, by 10%-15% in 29, by 15%-20% in 23, by 20%-50% in 39, by 50%-100% in four, six had a cardiac arrest, and 28 had an increase in heart rate. Considering the possible impact of exonic SNPs on the phenotypes, TEP1 (rs938886), TEP1 (rs1713449), and RECQL5 (rs820196) were analyzed. The haplotype analysis suggested that the haplotypes CTT [odds ratio (OR) = 2.018, 95% confidence interval (CI): 1.012-4.025, P = 0.0430] and GCC (OR = 2.293, 95%CI: 1.174-4.477, P = 0.0131) of TEP1 (rs938886), TEP1 (rs1713449), and RECQL5 (rs820196) increased the risk of a drop in heart rate > 30%.
CONCLUSION: The TEP1 (rs938886), TEP1 (rs1713449), and RECQL5 (rs820196) SNPs were associated with changes in heart rate ≥ 30% during intraperitoneal lavage using distilled water after gastrectomy for gastric cancer. ©The Author(s) 2021. Published by Baishideng Publishing Group Inc. All rights reserved.

Core Tip: Haplotype analysis suggested that the haplotypes CTT and GCC of TEP1, TEP1, and RECQL5 increased the risk of a drop in heart rate > 30%. The TEP1 (rs938886), TEP1 (rs1713449), and RECQL5 (rs820196) single nucleotide polymorphisms were associated with changes in heart rate ≥ 30% during intraperitoneal lavage using distilled water after gastrectomy for gastric cancer.

INTRODUCTION

Gastric adenocarcinomas are tumors of the stomach, including tumors of the noncardia and the subcardia (Siewert type III), with the center starting 2-5 cm below the esophagogastric junction (EGJ)[1,2]. The estimated global incidence of gastric cancer was 1033701 in 2018, with a mortality of 782685[3]. The incidence of gastric cancer is highest in Eastern Asia, Eastern Europe, and South America[3-5]. Men are twice more affected than women[2]. The direct cause of gastric cancer is not clear, but Helicobacter pylori infection and some hereditary cancer predisposition syndromes may play a role[1,2,6,7]. Patients often present with nonspecific symptoms, which may include anorexia, weight loss, abdominal pain, dyspepsia, vomiting, and early satiety[2,7]. The 5-year survival of gastric cancer is 31%; patients with localized disease will have a 5-year survival of 67%, while those with distant disease will have a 5-year survival of 5%[8].

The management of gastric cancer is multidisciplinary and includes surgery, chemotherapy, targeted therapy, and radiation therapy[1]. Gastric cancer spreads regionally to peritoneal lymph nodes, and the Japanese Gastric Cancer Association includes the cytology results of the peritoneal lavage fluid in the staging of gastric cancer[9,10], guiding treatments and chemotherapy[11,12].

Beyond its role for staging, peritoneal lavage can also be used in curative intent. Indeed, peritoneal metastasis is a major cause of relapse after gastrectomy in patients with gastric cancer[1]. Tumor cells can easily disseminate into the abdominal cavity due to the anatomical structures and then serve as seeds for metastases and relapse. Damage to the peritoneum and the exposure of connective tissue during the operation favor tumor cell growth by creating an inflammatory microenvironment[13,14]. Therefore, it is difficult to prevent tumor cells from spreading into the blood and the abdominal cavity[15]. The detection rate of tumor cells after surgery at the operation site or inside the peritoneum can be as high as 93.4%[16]. To address this issue, various methods for peritoneal lavage have been tried to destroy these tumor cells, including high temperature, hypotonic solution, and chemotherapy[17,18]. The value of intraperitoneal chemotherapy is still being debated[19,20]. High-temperature lavage shows some efficacy[21], as well as extensive lavage[18]. Hypotonic lavage emerged in the 1960s. Distilled water with an osmolarity close to 0 is used; since the osmolarity of human tissues is around 280-310 mmol/L, the difference in osmolarity causes the tumor cell to expand and eventually degenerate[22,23].

Nevertheless, observations during the procedure revealed that peritoneal lavage using warm distilled water can cause temporary changes in the cardiovascular system of the patients, such as lowering heart rate and altering blood pressure. In this study, we examined the changes in heart rate in patients with gastric cancer who underwent proximal or total gastrectomy before and after peritoneal lavage using distilled water, and we explored the associations between changes in heart rate and single nucleotide polymorphisms (SNPs) of genes that are involved in metabolism. The results could help identify patients who might be at risk of hemodynamic changes during hypotonic intraperitoneal lavage.

MATERIALS AND METHODS

Study design and patients

This was a prospective observational study of patients with gastric cancer who underwent gastrectomy at the Third Affiliated Hospital of Soochow University from March 2018 to March 2019. The study was approved by the ethics committee of the Third Affiliated Hospital of Soochow University. All participants signed an informed consent form.

The inclusion criteria were as follows: (1) 30-90 years of age; (2) Gastric cancer stage I-III; and (3) Scheduled to undergo proximal or total gastrectomy. The exclusion criteria were as follows: (1) Scheduled to undergo distal gastrectomy; (2) Arrhythmia or other underlying conditions that may affect the heart rate; or (3) Incomplete data.

Clinical data collection

Peripheral blood (2 mL) was obtained from the ulnar vein before the operation for subsequent DNA extraction. The surgery was performed by two teams. Both teams had professional experience of over 10 years. Distilled water was used for peritoneal lavage during the operation[24]. After gastrectomy and abdominal lymphadenectomy, warm distilled water at 42°C was used for peritoneal lavage at the xiphoid process within 10 cm from the chest wall. Lavage duration was 3-5 s.

The heart rate and blood pressure were recorded before lavage and around 40-60 s after lavage. The change in heart rate = (the ultimate value of heart rate after lavage - heart rate before lavage)/heart rate before lavage × 100%.

DNA extraction, polymerase chain reaction, and whole exon sequencing

Peripheral blood (2 mL) was obtained from each patient. All the samples were preserved at -80°C until use. Genomic DNA was extracted using the TIANamp blood DNA kit (Tiangen Biotech, Beijing, China) according to the manufacturer's instructions. The concentration and purity of the DNA sample met the polymerase chain reaction (PCR) requirements. The DNA concentration was > 50 ng/μL, and A260/A280 was 1.8-2.0. Primer Premier 5.0 software (Premier Biosoft, Palo Alto, CA, United States) was used to design the primers according to the sequence in NCBI (Table 1). The primers were synthesized and purified by Sangon (Shanghai, China). Genotyping for the gene polymorphisms was examined by real-time PCR on a Light Cycler480® II system (Roche Diagnostics, Basel, Switzerland). The real-time PCR reaction for each gene was performed in a 25-μL volume, containing 0.1 μL of 100 μmol/L each primer, 2 μL of DNA, 2.5 μL of 10 × buffer, 2.5 μL of MgCl2 (25 mmol/L), 0.25 μL of dNTP (10 mmol/L), and 0.5 μL of Taq DNA polymerase. The thermal cycling conditions included the following steps: initial denaturation at 95°C for 3 min, followed by 40 cycles at 95°C for 5 s and 60°C for 15 s.

Table 1

Validation of the mutation sites in six patients with a sudden drop in heart rate during distilled water lavage

Mutation type	Chr	Start	End	Ref	Alt	Location	Gene name	FOC	Primers for sequencing (5’-3’)
									Forward	Reverse
SNP
1	chr14	20757383	20757383	A	G	UTR3	TTC5	0/6	CCAAAGAAGAGGAAGGACCTAAAG	CTGTCTCTTCCACTGCTCTCTATGTT
2	chr14	20818983	20818983	C	T	intronic	PARP2-920	0/6	TTTATGAGTTGGCATTCAGAAAGTC	GAAAGGTGAAAGGATTTAGGGAAC
3	chr14	20824859	20824859	T	C	intronic	PARP2-156	0/6	ATAAGAGGGAGTCAGAGGAAGGTGT	AGCACTGAGAACATTACTGTATCCCT
4	chr14	20837701	20837701	G	C	exonic	TEP1-886	0/6	GTGTCTTTAGATGTGGTGTTGGCT	TGGCAGAGTCCTCATTTTTGTGT
5	chr14	20841162	20841162	C	T	intronic	TEP1-0948	0/6	CCTCTAACGCCCAGTAAATACACAG	TCTCTTATCCCAGCAGTATCCCAG
6	chr14	20841313	20841313	G	A	intronic	TEP1-0948	0/6
7	chr14	20841707	20841707	C	T	exonic	TEP1-449	0/6	TATTCCGCATACCTTCCCCAC	CCCTGCTCCGTCCCTTCTT
8	chr16	1756178	1756178	T	C	upstream	MAPK8IP3	0/6	GGAAGCGACCACTGCCG	CATCTGGATCTCCATCATCGC
9	chr17	8161149	8161149	C	T	exonic	PFAS	0/6	GAAAGCCTGTGTAACTCTGATTGC	ATTACTGGCTTCAATGGCAACC
10	chr17	73627539	73627539	T	C	exonic	RECQL5	0/6	GCAATGTCCCTGATGTCCTACC	CTGGAGCAAGACCTGCATCG
11	chr21	35470291	35470291	-	T	UTR3	SLC5A3	0/6	CGAATGTGCTTGTGTGATACTTGTT	GGCAGACTTGTTGGTCATTTCAG
12	chr9	98691137	98691137	T	C	exonic	ERCC6L2	1/6	CTTGATTACCGACGACTTGATGG	ATGTTGATAAAGGAAATGAGAGAAAAGC
Indel
13	chr17	8052526	8052532	AAAAACA	-	intronic	PER1	0/6	TGAAACCCCGTCTCTACTGAAAATAC	TCCCTTAGTGGATTCTTCGCAG
14	chr12	133417982	133417982	-	AA	UTR3	CHFR	1/6	GAAAGGCTTCGTCTCTGCTGC	TGGAGGTGAAGAGAGCGTGTTT

Chr: Chromosome number; Ref: Reference sequence; Alt: Alteration sequence; FOC: Frequency of mutation in the control group; SNP: Single nucleotide polymorphism; Indel: Insertion or deletion; TTC5: Tetratricopeptide repeat domain 5; PARP2: Poly (ADP-ribose) polymerase 2; TEP1: Telomerase associated protein 1; MAPK8IP3: Mitogen-activated protein kinase 8 interacting protein 3; PFAS: Phosphoribosylformylglycinamidine synthase; RECQL5: RecQ like helicase 5; SLC5A3: Solute carrier family 5 member 3; ERCC6L2: ERCC excision repair 6 like 2; PER1: Period circadian regulator 1; CHFR: Checkpoint with forkhead and ring finger domains.

The PCR products were purified from 1.5% agarose gel using the SanPrep column DNA Agarose Gel Extraction Kit (Sangon Biotech Co., Ltd., Shanghai, China) and were then directly sequenced using PCR primers as sequencing primers by Sangon Biotech Company. For sequence comparison and identification, the chromatogram sequences were inspected using Chromas 2.2 (Technelysium, Queensland, Australia) and searched against the GenBank by the BLAST program provided by the NCBI. Whole exon sequencing (WES) was performed by Shanghai GMINIX Information Technology Co., Ltd., China, according to their standard protocols.

SNP selection

We first screened the genetic mutations (SNP, insertion, or deletion) that occurred in all patients with heart rate changes of over 50% compared with those with changes < 10%, and then performed validation in all the patients included in the study.

Grouping

We used a 30% change in heart rate as a cutoff, based on clinical experience, to assign the patients into two groups: Patients with changes in heart rate < 30% were considered the control group, while those with changes in heart rate ≥ 30% were considered the observation group. Comparison and regression analyses of the selected SNPs were performed between the two groups.

Statistical analysis

Statistical analyses were performed using GraphPad Prism 6.0 (GraphPad Software, Inc., San Diego, CA, United States). A normality test was performed for all continuous variables using the Kolmogorov-Smirnov test. For the variables that followed normal distribution, the data were displayed as mean ± SD and analyzed using the independent-sample t-test. For those that did not follow normal distribution, the data were displayed as medians (ranges) and analyzed by the Mann-Whitney U-test. The categorical variables were displayed as frequencies and percentages and analyzed by the chi-square or Fisher’s exact test. The Hardy-Weinberg equilibrium test was performed for the SNPs. Logistic regression was performed using a 30% change in the heart rate as the outcome indicator to identify the associated haplotype. Two-sided (except for the chi-square test) P values < 0.05 were considered statistically significant.

RESULTS

Characteristics of the participants

According to the inclusion/exclusion criteria, 201 patients were included in the study. Seven patients were subsequently excluded due to incomplete data. Finally, 194 patients were included in the analysis (Table 2). Of these patients, 138 were male, with a mean age of 65.9 ± 0.8 years, and 56 were female, with a mean age of 65.0 ± 1.3 years. The patients’ heart rate changed during peritoneal lavage using warm distilled water. The heart rate dropped by 0%-10% in 65 patients, by 10%-15% in 29 patients, by 15%-20% in 23 patients, by 20%-50% in 39 patients, by 50%-100% in four patients, six patients had a cardiac arrest, and 28 patients had an increase in their heart rate.

Table 2

Baseline clinical information

Characteristics	HR decreased < 30% (n = 172)	HR deceased ≥ 30% (n = 22)	P value
Age (years), mean ± SD	65.6 ± 9.1	65.8 ± 10.4	0.62
Sex, n (%)
Male	72.7	59.1	0.2136
Female	27.3	40.9
Smoking, n (%)	14.0	4.6	0.3190
Drinking, n (%)	7.0	0	0.3668
Hypertension, n (%)	34.3	40.9	0.6361
Diabetes, n (%)	8.1	13.6	0.4171
Hemodynamics before lavage, mean ± SD
Heart rate (bpm)	61 ± 10	62 ± 13	0.511
Diastolic pressure (mmHg)	66 ± 10	65 ± 12	0.6207
Systolic pressure (mmHg)	122 ± 18	119 ± 19	0.3159
Hemodynamics after lavage, mean ± SD
Heart rate (bpm)	56 ± 12	27 ± 20	< 0.0001
Diastolic pressure (mmHg)	76 ± 14	53 ± 23	< 0.0001
Systolic pressure (mmHg)	141 ± 24	92 ± 48	< 0.0001
Change in heart rate (%), mean ± SD	8.3 ± 12.4	59.3 ± 27.7	< 0.0001
Change in diastolic pressure (mmHg), mean ± SD	10.0 ± 13.1	-11.8 ± 18.9	< 0.0001
Change in systolic pressure (mmHg), mean ± SD	17.5 ± 21.8	-26.0 ± 41.5	< 0.0001

HR: Heart rate; SD: Standard deviation.

WES analysis

According to the changes in heart rate, we randomly selected six patients among those with heart rate change > 50%, and those with heart rate change of < 10%, respectively, for WES analysis. Compared to the reference genome, the former patients had 4986 SNPs and 258 insertions or deletions; the latter patients had 22294 SNPs and 1065 insertions/deletions. There were 16192 SNPs and 700 insertions/deletions shared among these 12 patients.

We selected 14 SNPs and insertions/deletions that occurred in all the patients with heart rate change > 50% but did not occur or only occurred once in the patients with heart rate change of < 10% for further validation in a larger population. These SNPs and insertions/deletions included the point mutation in the 3’-untranslated region (UTR) of TTC5 and the AA insertion in CHFR; the exonic point mutations of TEP1-886, TEP1-449, and RECQL5; the intronic mutations in PARAP2-920, PARAP2-156, TEP1-0948, MAPK8IP3, PFA, SLC5A3, ERCC6L2, and PER1; the point mutation in CHFR; and the deletion in PER1. Finally, we successfully validated the point mutations in one of TTC5, TEP1-886, TEP1-449, and two of TEP1-0948, and one of RECQL5, a total of six SNPs.

SNPs associated with changes in heart rate

Considering the possible impact of exonic SNPs on the phenotypes, we decided to compare the following SNPs in all patients: TEP1 (rs938886), TEP1 (rs1713449), and RECQL5 (rs820196). There were no statistically significant differences in the allele frequency and genotype frequency between the two groups (Table 3). The linkage disequilibrium tests suggested a strong disequilibrium between TEP1 (rs938886) and TEP1 (rs1713449) (Figure 1). The haplotype analysis suggested that the haplotypes CTT [odds ratio (OR) = 2.018, 95% confidence interval (CI): 1.012-4.025, P = 0.0430) and GCC (OR = 2.293, 95%CI: 1.174-4.477, P = 0.0131) of TEP1 (rs938886), TEP1 (rs1713449), and RECQL5 (rs820196) increased the risk of a drop in heart rate > 30% (Table 4).

Table 3

Allele frequency and genotype frequency in the two groups

Characteristics	HR decreased ≥ 30% (n = 22)	HR decreased < 30% (n = 172)	Fisher's P value
TEP1 (rs938886), n (%)
C	14 (0.32)	105 (0.31)	0.8608
G	30 (0.68)	239 (0.70)
CC	1 (0.05)	16 (0.09)	0.5022
CG	12 (0.55)	73 (0.42)
GG	9 (0.41)	83 (0.48)
HWE	0.2278	0.9929
TEP1 (rs1713449), n (%)
C	30 (0.68)	236 (0.69)	0.9546
T	14 (0.32)	108 (0.31)
CC	9 (0.41)	82 (0.48)	0.4465
CT	12 (0.55)	72 (0.42)
TT	1 (0.05)	18 (0.11)
HWE	0.2278	0.7110
RECQL5 (rs820196), n (%)
C	16 (0.36)	109 (0.32)	0.5319
T	28 (0.64)	235 (0.68)
CC	1 (0.05)	19 (0.11)	0.1292
CT	14 (0.64)	71 (0.41)
TT	7 (0.32)	82 (0.48)
HWE	0.0787	0.5420

HR: Heart rate; HWE: Fisher’s P value of Hardy-Weinberg equilibrium test.

Figure 1

Linkage disequilibrium test. A and B: D' values (A) and r2 values (B) both indicated strong linkage disequilibrium between TEP1 (rs938886) and TEP1 (rs1713449).

Table 4

Haplotype analysis

Items, n (%)	HR decreased ≥ 30% (n = 22)	HR decreased < 30% (n = 172)	Fisher's P value	Odds ratio (95%CI)
CTC	0.00 (0.00)	40.98 (0.12)	0.025601	0.000 (0.000-0.008)
CTT	14.00 (0.32)	64.02 (0.19)	0.042935	2.018 (1.012-4.025)
GCC	16.00 (0.36)	68.02 (0.20)	0.013161	2.293 (1.174-4.477)
GCT	14.00 (0.32)	167.98 (0.49)	0.029281	0.481 (0.246-0.939)
GTT	0.00 (0.00)	3.00 (0.01)	-	-

All frequencies < 0.03 were ignored in the analysis. Loci selected for the hap-analysis: TEP1 (rs938886), TEP1 (rs1713449), and RECQL5 (rs820196). HR: Heart rate; CI: Confidence interval.

DISCUSSION

Peritoneal lavage can lower the relapse rate caused by peritoneal metastasis[17,18]. During surgery for gastric cancer, peritoneal lavage using warm distilled water can cause temporary hemodynamic changes. This study aimed to examine the changes in heart rate in patients with gastric cancer who underwent proximal or total gastrectomy before and after peritoneal lavage using distilled water and to explore the associations between changes in heart rate and SNPs. The results strongly suggest that the TEP1 (rs938886), TEP1 (rs1713449), and RECQL5 (rs820196) SNPs were associated with changes in heart rate ≥ 30% during intraperitoneal lavage using distilled water after gastrectomy for gastric cancer. Therefore, a genetic test for TEP1 and RECQL5 could be performed before gastrectomy and a different lavage method could be chosen for those at high risk to avoid adverse outcomes such as abnormal heart rate.

Currently, despite the improvement in surgical techniques and multimodal combination therapy, the prognosis of gastric cancer, especially advanced gastric cancer (AGC) complicated by serosal invasion (T3 or T4) is still poor[1]. The overall 5-year survival rate is less than 35%[25]. In 1998, the Japanese Gastric Cancer Association suggested using peritoneal lavage cytology to detect free malignant cells in the abdominal cavity[9]. In 2010, peritoneal lavage cytology was also recommended to stage patients with gastric cancer in the 7th edition of Cancer Tumor Node Metastasis (TNM) staging by the American Joint Cancer Committee (AJCC)[26]. Although it is currently a routine procedure to perform peritoneal lavage using warm water during gastrectomy, very few studies, focus on the mechanisms underlying the changes caused by peritoneal lavage in the internal environment and the circulation system of patients, or focus on the associated genetic mutations. These changes in hemodynamics might represent important challenges for the anesthesiologists, who are responsible for restoring the changes in hemodynamics. Therefore, to address this issue, we carefully examined vital signs during peritoneal lavage using distilled water in 194 patients with gastric cancer. We found that 22 participants had a drop in heart rate of ≥ 30%, and six of them even had a cardiac arrest. A previous study by Ohki et al[23] did not report the changes in hemodynamics. Subsequently, we performed genetic screening and investigated the underlying mechanisms.

In the present study, we found that TEP1 and RECQL5 were associated with a drop in heart rate of ≥ 30% during peritoneal lavage using distilled water. TEP1 (Telomerase-associated protein 1) encodes a hexamer DNA helicase that can unwind the short double-stranded DNA in the 5' -> 3' direction. TEP1, together with the mitochondrial single-stranded DNA binding protein and mtDNA polymerase, is considered to play a crucial role in mtDNA replication. TEP1 exerts its functions by binding to the mitochondrial single-stranded DNA binding protein and plays a crucial role in respiration[27]. TEP1 is located in the mitochondrial matrix and nucleoid. TEP1 mutations can cause infantile-onset spinal cerebellar ataxia (IOSCA) and progressive extraocular paralysis (PEO) and are associated with several mitochondrial disorders; alternative splicing of TEP1 results in several transcript variants, which may lead to changes in heart rate[28,29]. The human RECQL5 (RecQ protein-like 5) gene is located at 17q25.2-25.3 and contains at least 19 exons. It is alternatively spliced into three mRNA variants, RECQL5α, RECQL5β, and RECQL5γ. RECQL5 is one of the five major members of the RECQ helicase family and plays a role in suppressing sister chromatid exchange and DNA repair by homologous recombination as well as preventing double-stranded DNA breakage and the synergistic effect of TOPIIα. RECQL5 may be essential in DNA metabolism and may affect heart rate and be involved in heart diseases[30].

It is believed that emerging evidence will support the association between metabolic genes and the development and progression of heart failure. Therefore, glucose metabolism in the heart or the metabolic pathways relevant to ATP synthesis might be new research directions to prevent heart failure and cardiac arrest during surgery. In this study, some metabolic genes had SNPs that were associated with a drop in heart rate during intraperitoneal lavage using distilled water. If metabolic modulators can be found and proved to be effective in treating patients with heart failure, we could guide treatment decisions and evaluate the patients’ response via metabolic imaging or metabolic biomarkers. In this case, a multidisciplinary method should be proposed by a group of anesthetists, cardio-pathologists, endocrinologists, and geneticists[31-33].

This study has limitations. The sample size was relatively small and from a single center. Also, only a few metabolic parameters were examined. A full array of changes in metabolic parameters should be examined in future studies to better grasp what happens, metabolically, during the heart rate drop as a result of peritoneal lavage. Finally, the SNPs identified here might be specific to an ethnic group, and the results should be confirmed in other groups.

CONCLUSION

In conclusion, SNPs in TEP1 (rs938886), TEP1 (rs1713449), and RECQL5 (rs820196) were associated with changes in heart rate ≥ 30% during intraperitoneal lavage using distilled water after gastrectomy for gastric cancer. Therefore, a genetic test for TEP1 and RECQL5 could be performed before gastrectomy and a different lavage method could be chosen for those at high risk to avoid adverse outcomes such as abnormal heart rate or even cardiac arrest.

ARTICLE HIGHLIGHTS

Research background

For the first time, we found that severe cardiovascular changes occurred in patients with gastric cancer during intraoperative distilled water lavage, which was also observed in a large cohort.

Research motivation

The internal causes of this phenomenon were studied through detailed clinical case observation and a mechanistic study.

Research objectives

The target population was screened out through gene detection and verification.

Research methods

We conducted a prospective observational study of the included cases, and selected typical patients for gene screening, and the results were validated in a large cohort.

Research results

We successfully validated a site mutation in TEP1-886, TEP1-449 as well as RECQL5, and selected the heart rate change of 30% as the cut-off value for comparison and regression analysis.

Research conclusions

SNPs in TEP1 (rs938886), TEP1 (rs1713449) and RECQL5 (rs820196) were associated with changes in heart rate > 30% when peritoneal lavage with distilled water was performed after gastrectomy for gastric cancer patients.

Research perspectives

We performed pre-operative detection of TEP1 and RECQL5 genes in patients and selected different lavage methods for high-risk groups to improve peri-operative safety.

ACKNOWLEDGEMENTS

We appreciate the great help from all the members of the Department of Gastrointestinal Surgery in the Third Affiliated Hospital of Soochow University.