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. 2020 Feb 21;2020:2946541. doi: 10.1155/2020/2946541

Clonorchiasis in Patients with Biliary and Pancreatic Diseases: Diagnosis and Risk Factors

Guolin Liao 1, Huaqiang Ruan 1, Peng Peng 1, Shiquan Liu 1, Jianfu Qin 1, Zhihai Liang 2, Guodu Tang 2, Mengbin Qin 1,, Jie'an Huang 1,
PMCID: PMC7060427  PMID: 32185201

Abstract

Background

Many epidemiological studies have investigated the risk factors for clonorchiasis, but endoscopic findings of this disease in endoscopic retrograde cholangiopancreatography (ERCP) have not been well characterized. In this study, we evaluated clonorchiasis in ERCP in patients with biliary and pancreatic diseases.

Methods

This was a retrospective two-center study in hospitalized patients who received ERCP between January 2012 and October 2018. All patients were divided into clonorchiasis and nonclonorchiasis groups. Data were analyzed using univariate analysis and multivariate analyses.

Results

A total of 1119 patients were included, and clonorchiasis was diagnosed in 19.2% patients. Detection of Clonorchis sinensis eggs in bile samples was higher than that in fecal samples (85.9% vs. 58.7%; P = 0.001). In multivariate analysis, male patients (95% confidence interval (CI): 1.945–4.249, P = 0.001). In multivariate analysis, male patients (95% confidence interval (CI): 1.945–4.249, P = 0.001). In multivariate analysis, male patients (95% confidence interval (CI): 1.945–4.249, P = 0.001). In multivariate analysis, male patients (95% confidence interval (CI): 1.945–4.249, P = 0.001). In multivariate analysis, male patients (95% confidence interval (CI): 1.945–4.249, P = 0.001). In multivariate analysis, male patients (95% confidence interval (CI): 1.945–4.249,

Conclusions

The detection of C. sinensis eggs was significantly higher in bile than in fecal samples; thus, bile samples represent a preferable sample for the diagnosis of clonorchiasis in patients with biliary obstruction. We found that male, age ≤ 60 years old, and CBD diameter < 12 mm were independent risk factors for clonorchiasis, while papilla fistula was a protective factor.C. sinensis eggs was significantly higher in bile than in fecal samples; thus, bile samples represent a preferable sample for the diagnosis of clonorchiasis in patients with biliary obstruction. We found that male, age ≤ 60 years old, and CBD diameter < 12 mm were independent risk factors for clonorchiasis, while papilla fistula was a protective factor.

1. Introduction

Clonorchiasis, which is caused by Clonorchis sinensis, globally affects more than 15 million people, 13 million of whom live in China and other parts of East Asia [13]. An investigation conducted from 2005 to 2014 in Guangxi Province, southern China, showed that the prevalence of clonorchiasis in the general population reached 9.9% [4]. Clonorchiasis causes mechanical and chemical injury, resulting in inflammation [57], obstruction [58], and cancerogenesis [1, 2, 9] in the intrahepatic and extrahepatic biliary tracts [8, 10]. Common assays for diagnosing clonorchiasis include serologic detection of parasite-specific antibody and DNA [1115], egg detection in bile and fecal samples [16, 17], and imaging [18]. The detection of C. sinensis eggs in fecal samples is specific, but with low sensitivity [19, 20], and requires skillful technique [21], especially when the infection is mild or there is biliary obstruction. Endoscopic retrograde cholangiopancreatography (ERCP) is not only a method for angiography but also a safe and effective tool for the treatment of biliary and pancreatic disorders. C. sinensis eggs are detectable in bile [6, 7, 19], but few studies have compared the detection of C. sinensis between bile and fecal samples.

It is important to evaluate independent risk factors for clonorchiasis in a large cohort of patients. Although several general risk factors for clonorchiasis have been reported [22, 23], no study to date has examined the risk factors associated with endoscopic findings. Various biliary or pancreatic disorders require different endoscopic interventions. ERCP procedures are generally safe and effective, but endoscopists must have a thorough understanding of indications for the selected procedures. However, there are no published data that compare endoscopic manipulation with outcomes between patients with and without clonorchiasis.

This retrospective two-center study analyzed the diagnostic sensitivity by detecting C. sinensis eggs in bile and fecal samples and the risk factors associated with endoscopic procedures. Furthermore, endoscopic manipulation and outcomes were compared between patients with and without clonorchiasis.

2. Patients and Methods

2.1. Patients

Patients who had biliary or pancreatic disorders (including jaundice caused by biliary obstruction; clinical and biochemical or imaging data suggestive of biliary stones, tumors, and sclerosing cholangitis; pancreatic diseases including tumors, chronic pancreatitis, and pancreatic abscess; and pancreatitis of unknown etiology and sphincter of Oddi manometry) and received ERCP procedures between January 2012 and October 2018 at both the First and Second Affiliated Hospitals, Guangxi Medical University (Nanning, China), were included. Indications for ERCP followed the guidelines of the American Society of Gastrointestinal Endoscopy [24]. Patients were excluded if age < 18 years old, no detection of C. sinensis in both fecal and bile samples, prior ERCP, or loss of clinical data. This study protocol was approved by the Institutional Review Boards of both hospitals. Written informed consent was obtained from all participants.

2.2. Procedures

All ERCP procedures were conducted by well-trained and experienced endoscopists, who are certified to perform procedures of ERCP difficulty Grade 3 per the ERCP core curriculum [25]. The ERCP equipment involved a therapeutic duodenoscope (TJF-260V; Olympus Optical, Tokyo, Japan). Selective cannulation of the common bile duct (CBD) was performed by using a guidewire or standard catheter if patients had a preexisting sphincterotomy. All duodenoscopes were disinfected and decontaminated per the guidelines and confirmed by regular smear tests. Once guidewire cannulation was successfully established after duodenoscope entry, bile was aspirated by inserting a disposable 5 F standard sphincterotome catheter into the bile duct before injection of a contrast agent for the ERCP procedure. Approximately 2–8 mL of bile (average 4 mL) was collected from patients with a clinical diagnosis of cholangitis, as suggested by clinical manifestations (jaundice, fever, and right upper quadrant pain) or radiological manifestations of biliary obstruction. The aspirated bile was immediately transferred into a sterile tube. After the injection of contrast agent, the length of the widest part of the CBD was documented and the diameter, number, and position of any CBD stone were recorded. The endoscopist on site selected endoscopic procedures including cannulation, endoscopic sphincterotomy (EST), bile culture, endoscopic papillary balloon dilation (EPBD), bougie dilatation, basket, lithotripsy basket, balloon, brush, biopsy, stent implantation, and endoscopic nasobiliary drainage (ENBD) based on the patient's conditions and the Chinese guidelines for ERCP (2010). In this study, we used the formalin-ether concentration technique (FEC) to detect C. sinensis eggs in bile and/or feces for the pathogen diagnosis of clonorchiasis. The first detection of eggs in fecal samples was made before ERCP, and two more tests were repeated during hospitalization if the first detection was negative.

2.3. Observational Index

Biochemical and hematological markers were examined within 72 hours of admission before ERCP including leukocyte (white blood cell (WBC))/amylase (AMS)/total bilirubin (TBil)/direct bilirubin (DBil)/alanine aminotransferase (ALT)/aspartate transaminase (AST)/gamma glutamyl transpeptidase (GGT)/alkaline phosphatase (ALP)/carcinoembryonic antigen (CEA)/carbohydrate antigen 199 (CA-199). Demographics and clinical findings during hospitalization were collected including gender, age, endoscopic diagnosis, papilla types, CBD diameter, and CBD stone characteristics (shape, size, position, number, and color). The collection procedure and outcome data included the cannulation method, EST/EPBD/bougie dilatation/ENBD/stent implantation/brush/biopsy/bile culture, the cut size of the EST, basket/balloon/lithotripsy basket, bile culture results, brush results, immediate complications, post-ERCP pancreatitis (PEP), post-ERCP cholangitis (PEC), and serological baseline data. PEP was defined as having new or worsened abdominal pain for more than 24 h after persistent ERCP, accompanied by elevated serum amylase level more than three times the upper limit of normal. PEC was defined as having a fever > 38°C and lasting >24 h due to biliary causes after ERCP.

2.4. Statistical Analysis

Continuous variables were expressed as the mean and standard deviation or median and interquartile range, and differences were computed using the Student's t-test or nonparametric test. Categorical variables were analyzed by the Pearson's chi-square test or Fisher's exact test. The test level in univariate was unrestricted to 0.10 if the factors underscored the clinical importance. Multivariate regression analyses were used to identify independent risk factors. Logistic regression models were employed to calculate odds ratios with 95% confidence intervals (CIs). A two-tailed P value < 0.05 was considered statistically significant (SPSS 22.0 for Windows, SPSS, Chicago, IL, USA).

3. Results

3.1. Baseline Characteristics

A total of 2171 consecutive patients who underwent ERCP in two hospitals between January 2012 and October 2018 were initially screened. Patients were excluded if age < 18 years old (n = 33), no detection of C. sinensis eggs in both bile and fecal samples (n = 822), prior ERCP (n = 161), or no clinical data (n = 36). Finally, 1119 patients were included and analyzed (Figure 1); 36.6% were female with a mean age of 57.2 ± 14.2 years (range: 20–92 years). Clonorchiasis was diagnosed in 19.2% of the 1119 patients as a result of detected C. sinensis eggs in the fecal and/or bile samples (Table 1).

Figure 1.

Figure 1

Flowchart of patients included in the study.

Table 1.

Demographics and clonorchiasis in this cohort.

Study population 1119
Mean age (years, SD) 57.2 ± 14.2
Females 409 (36.6%)
Clonorchiasis 215 (19.2%)
C. sinensis eggs detected in feces 58.7%
C. sinensis eggs detected in bile 85.9%

3.2. Comparison of C. sinensis Egg Positivity in Bile and Feces

Among the 215 patients diagnosed with clonorchiasis, both bile and feces were collected from 92 patients for the detection of C. sinensis eggs. The eggs were detected in 85/92 (85.9%) bile samples, which was significantly higher than the 58.7% (54/92) detected in feces samples (P = 0.001), suggesting that the sensitivity of detecting eggs in bile was significantly higher than that in feces (Tables 1 and 2).

Table 2.

Comparison of egg detection between fecal and bile aspiration.

Eggs in bile aspiration Eggs in feces Total P
+
+ 41 38 92 0.001
13 0

4. Risk Factors for Clonorchiasis

4.1. Univariate Analysis

Univariate analysis showed that gender, age (≤60 and >60), endoscopic diagnosis, papilla types, CBD diameter (<12 mm and ≥12 mm), and CBD stone shape were associated with clonorchiasis (P < 0.05, Table 3).

Table 3.

Univariate analysis of risk factors for clonorchiasis.

Characteristic N = 1119 χ 2 P value
Clonorchiasis Nonclonorchiasis
Gender 42.93 0.0001
 Male 178 532
 Female 37 372
Age in years 23.58 0.0001
 ≤60 155 487
 >60 60 417
Endoscopic diagnosis 56.26 0.0001
 Cholelithiasis 152 624
 Malignant strictures 19 153
 Benign strictures 10 44
 Clonorchiasis 15 3
 Bile duct expansions for unknown reasons 7 35
 Pancreatic disorders 2 11
 Normal cholangiopancreatography 6 24
 Else 4 10
Papilla types 21.10 0.0001
 Normal 178 619
 Minor papilla 5 40
 Papillary carcinoma 2 43
 Papillary fistula 3 47
 Papillary diverticulum 27 155
CBD diameter 24.13 0.0001
 <12 mm 118 331
 ≥12 mm 97 573
CBD stone shape 10.60 0.001
 Stone 94 468
 Sludge 58 156

4.2. Multivariate Analysis

Multivariate logistic regression analysis showed that gender, age, endoscopic diagnosis, papilla type, and CBD diameter were independent risk factors for clonorchiasis. The clonorchiasis prevalence in male was 2.875 times higher than that in females (95% confidence interval (CI): 1.945–4.249, P = 0.0001). The clonorchiasis incidence in patients ≤ 60 years old was 1.732 times higher than that in patients > 60 years old (95% CI: 1.212–2.474, P = 0.003). Patients with papillary fistula were less susceptible to clonorchiasis compared to those with normal papilla (95% CI: 0.081–0.900, P = 0.033). However, minor papilla, papillary diverticulum, and papillary carcinoma did not correlate with clonorchiasis. Patients with CBD diameter < 12 mm had a 1.526-fold higher incidence compared to those with CBD ≥ 12 mm (95% CI: 1.093–2.130, P = 0.013). Although endoscopic diagnosis of clonorchiasis was significantly different between the two groups (95% CI: 3.774–84.822, P = 0.0001), other endoscopically diagnosed diseases were not (P > 0.05; Table 4).

Table 4.

Multivariate analysis of risk factors for clonorchiasis.

Factors Wald P value OR 95% CI
Gender
 Male 28.080 0.0001 2.875 1.945-4.249
 Female 1
Age in years
 ≤60 9.095 0.003 1.732 1.212-2.474
 >60 1
Endoscopic diagnosis
 Cholelithiasis 0.899 0.343 1.582 0.613-4.081
 Malignant strictures 0.108 0.742 0.838 0.291-2.409
 Benign strictures 0.007 0.932 1.051 0.329-3.358
 Clonorchiasis 13.196 0.0001 17.892 3.774-84.822
 Idiopathic bile duct expansions 0.191 0.662 1.321 0.379-4.606
 Pancreatic disorders 0.088 0.767 0.763 0.127-4.588
 Else 1.463 0.226 2.555 0.559-11.679
 Normal cholangiopancreatography 1
Papilla types
 Minor papilla 2.121 0.145 0.486 0.184-1.283
 Papillary carcinoma 1.742 0.187 0.362 0.080-1.637
 Papillary fistula 4.544 0.033 0.270 0.081-0.900
 Papillary diverticulum 2.099 0.147 0.703 0.436-1.133
 Normal papilla 1
CBD diameter
 <12 mm 6.147 0.013 1.526 1.093-2.130
 ≥12 mm 1

4.3. Comparison of Endoscopic Procedures with Clonorchiasis Incidence

Univariate analysis showed that endoscopic procedures including the cannulation method, EST, ENBD, stent implantation, and balloon and bile culture were significantly associated with clonorchiasis (P < 0.05). Among the 215 patients with clonorchiasis, 202 received guidewire cannulation, 11 received dual guidewire, 1 received precut papillotomy, and 1 had failed cannulation. EST and ENBD were performed for removing stones, C. sinensis detection, or keeping bile drainage in 178 cases. Stent was implanted in 29 cases for biliary stenosis or for drainage (28 with single plastic stent and 1 with metal stent). Ballooning was used in 164 cases for dilating the bile duct. Bile was obtained in 150 cases for culture. Other procedures showed no correlation with clonorchiasis including bougie dilatation, brush, biopsy, the cut size of EST, basket, lithotripsy basket, bile culture results, brush results, immediate complications, PEP, and PEC (P > 0.05; Tables 5 and 6).

Table 5.

Comparison of endoscopic procedures performed between clonorchiasis and nonclonorchiasis.

Characteristic N = 1119 χ 2 P value
Clonorchiasis Nonclonorchiasis
Cannulation method 10.47 0.011
 Guidewire 202 850
 Dual guidewire 11 24
 Precut papillotomy 1 29
 Fail 1 1
EST 13.55 0.0001
 Yes 178 636
 No 37 268
Cut size of EST 0.36 0.835
 Big 4 11
 Medium 20 65
 Small 154 558
EPBD 0.09 0.759
 Yes 110 452
 No 105 452
Bougie dilatation 1.93 0.165
 Yes 10 66
 No 205 838
ENBD 23.42 0.0001
 Yes 178 595
 No 37 309
Stent implantation 20.25 0.0001
 Single plastic stent 28 189
 Metal stent 1 10
 Multiple stent 0 42
 No 186 663
Basket 0.67 0.414
 Yes 77 351
 No 138 553
Balloon 17.45 0.0001
 Yes 164 552
 No 51 352
Lithotripsy basket 2.19 0.139
 Yes 11 73
 No 204 831
Bile culture 7.71 0.005
 Yes 150 538
 No 65 366
Brush 0.02 0.903
 Yes 22 90
 No 193 814
Biopsy 2.44 0.119
 Yes 1 22
 No 214 882

Table 6.

Comparison of endoscopic procedure outcomes between clonorchiasis and nonclonorchiasis.

Characteristic N = 1119 χ 2 P value
Clonorchiasis Nonclonorchiasis
Bile culture results 2.94 0.086
 Positive 39 181
 Negative 110 358
Brush results 0.234 0.628
 Malignant 3 16
 Benign 19 73
Immediate complications 1.40 0.237
 Yes 2 23
 No 213 881
PEP 0.23 0.629
 Yes 11 54
 No 204 850
PEC 0.0001 1.000
 Yes 1 4
 No 214 900

4.4. Analysis Characteristics of the CBD Stone

CBD stones in 562 cholelithiasis patients were nonsludge. Univariate analysis showed that size, location, number, and color of these stones were not significantly associated with clonorchiasis incidence (P > 0.05; Table 7).

Table 7.

Analysis of characteristics of CBD stones between clonorchiasis and nonclonorchiasis.

Characteristic N = 562 χ 2 P value
Clonorchiasis Nonclonorchiasis
Stone size 3.26 0.196
 ≤5 mm 15 52
 ≤15 mm 69 339
 >15 mm 10 77
Stone position in CBD 9.76 0.135
 Upper 17 80
 Intermediate 17 61
 Lower 35 159
 Upper & intermediate 13 44
 Lower & intermediate 7 75
 Upper & lower 1 19
 Dispersion 4 30
Stone number 0.39 0.532
 <3 65 308
 ≥3 29 160
Stone color 5.38 0.129
 Yellow 16 57
 Black 5 24
 Brown 45 230
 White 2 1

5. Comparison of Biochemical and Hematological Findings between Patients with and without Clonorchiasis

The analyses showed that patients in both groups had elevated liver enzymes and jaundice. WBC, DBil, and ALT levels before ERCP in patients diagnosed with clonorchiasis were significantly higher than those in nonclonorchiasis patients (P = 0.001, 0.022, and 0.032, respectively). AMS, TBil, AST, ALP, GGT, CEA, and CA-199 levels showed no significant correlation with clonorchiasis (P > 0.05; Table 8).

Table 8.

Comparison of biochemical and hematologic findings between clonorchiasis and nonclonorchiasis.

Characteristics Clonorchiasis Nonclonorchiasis P value
WBC (109/L) 8.8 (6.6–11.2) 7.6 (5.6–9.9) 0.001
AMS 90.0 (52.0–193.3) 74.0 (51.0–123.0) 0.090
TBil (μmol/L) 96.9 (26.6–171.9) 58.0 (20.1–160.2) 0.054
DBil (μmol/L) 68.9 (16.4–126.9) 39.4 (10.1–117.3) 0.022
ALT (U/L) 87.0 (34.3–190.0) 67.0 (30.0–134.0) 0.032
AST (U/L) 65.0 (33.5–109.5) 53.0 (30.0–100.0) 0.086
ALP (U/L) 189.5 (120.3–284.5) 193.0 (118.0–334.0) 0.464
GGT (U/L) 310.5 (162.8–570.5) 297.0 (128.0–576.0) 0.890
CEA (ng/mL) 2.3 (1.4–3.0) 2.0 (1.2–3.6) 0.542
CA-199 (U/mL) 32.9 (10.3–139.1) 28.3 (9.0–133.4) 0.526

All data are represented by median and interquartile range (IQR).

6. Discussion

Clonorchiasis mainly occurs in East Asia and is associated with eating raw freshwater fish that carry the parasite [22]. Guangxi Province, where our patients resided, is part of southern China, and residents enjoy raw freshwater fish. In this study, clonorchiasis was diagnosed in 19.2% of the 1119 patients as a result of detected C. sinensis eggs in the fecal and/or bile samples. In addition, clonorchiasis mainly occurred in patients younger than 60 years old (155/215, 72.1%), with a 2.875-fold higher incidence in male than female patients. Clonorchiasis incidence in this cohort was significantly higher than that reported in the general Chinese population. Fang et al. [26] reported that clonorchiasis prevalence was 2.94% and 1.84% in males and females, respectively, with the highest prevalence found in the 50- to 59-year-old age group. Hoang et al. [27] reported that the prevalence in the male was 2.33 times higher than that in females in Vietnam, which supports our finding that more male clonorchiasis patients identified in southern China were susceptible to biliary or pancreatic disorders, including jaundice and elevated hepatic biochemical markers of TBil, DBil, ALT, AST, ALP, and GGT.

Detected C. sinensis eggs is direct evidence of clonorchiasis. The egg detection methods include Kato-Katz method (KK) and direct smear microscopy (DM) [18, 28]. The sensitivities of KK, FEC, and DM reported by Manuel et al. [29] were 71%, 50%, and 3%, respectively. The so-called “gold” standard combines the following four methods: KK, spontaneous sedimentation, FEC, and DM. However, Men et al. [19] referred to a combination of six KK plus two FECT methods as the “gold” standard. However, those standards involve multiple detection methods and a collection of consecutive fecal sample detection methods, which make them difficult to apply. Furthermore, when the infection activity is low or biliary obstruction is present, the probability of detecting eggs in fecal samples is extremely low. In our study, FEC was used for the detection of C. sinensis eggs in fecal and bile samples. We found that C. sinensis eggs were significantly more frequently detected in bile (79/92, 85.9%) than in fecal (54/92, 58.7%) samples, indicating that bile detection of C. sinensis eggs is preferable to fecal detection for the diagnosis of clonorchiasis in patients with biliary obstruction. Thus, bile detection should be incorporated into the established gold standards for diagnosing clonorchiasis.

Previous studies have identified male, eating raw fish, lower educational levels, and location of the villages as demographic or epidemiologic risk factors for clonorchiasis [22, 23, 30, 31]. Multivariate analysis showed that endoscopic diagnosis of clonorchiasis was significantly different between two groups, but it was not an independent risk factor for clonorchiasis. In addition, it could be influenced by subjective judgment (such as flocs and other parasites), resulting in a low sensitivity for direct diagnosis (15/41, 36.6%). Our research suggested both demographic factors of male and age ≤ 60 years old and CBD diameter < 12 mm as independent risk factors for clonorchiasis, while papilla fistula emerged as protective factor in the analysis. These findings are expected to identify a group of patients at high risk for clonorchiasis if they develop biliary or pancreatic disorders, especially in endemic regions.

When infected raw or undercooked fish is ingested by humans, the metacercariae excyst in the duodenum migrates into the intrahepatic bile ducts where eggs are laid. We wondered whether the excyst migration efficiency is related to papilla type. Our results showed that patients with normal papilla more frequently had clonorchiasis than patients with papillary fistula. As recently reported, positron emission tomography-computed tomography [32] can view the migration route within the host. This device may help investigate this issue among subjects with or without normal papilla.

We also compared the endoscopic procedures and outcomes between patients with and without clonorchiasis and found significant differences in conducting procedures including the cannulation method, EST, ENBD, stent implantation, balloon, and bile culture between the two groups. Patients with clonorchiasis were inclined to require guidewire cannulation, EST, ENBD, a single plastic stent, balloon, and bile culture. It is established that infection with C. sinensis is one of the most important factors for cholangiocarcinoma [33, 34], but our study found no significant differences in the brush results between clonorchiasis and nonclonorchiasis. The reason could be that patients with biliary or pancreatic disorders may not be representative; thus, future studies are needed to investigate the relationship between clonorchiasis and cholangiocarcinoma in a population without biliary or pancreatic disorders. There was no correlation between clonorchiasis and bile duct stones. As noted in this study, patients with clonorchiasis did not show special endoscopic features, so endoscopists must choose procedures after fully evaluating patients.

A few limitations of this study are worth mentioning. First, this was a retrospective study; thus, it may inevitably produce bias in data collection and selection. Prospective, large-cohort, multicenter studies are needed to confirm our findings. Second, only one assay (i.e., FEC) was used for the detection of C. sinensis in our study, and additional methods like KK were not used. Third, as bile samples were obtained during the ERCP procedure, the presence of C. sinensis eggs near the duodenal papilla may cause a positive bile finding, and ERCP procedures may have also increased the positive fecal finding. Fourth, the cohort we studied represented patients with biliary or pancreatic disorders, so these findings cannot be directly inferred to the general population.

7. Conclusions

In summary, our data showed that the detection of C. sinensis eggs was significantly higher in bile than in fecal samples; thus, the detection of C. sinensis in bile represents a preferable sample for the diagnosis of clonorchiasis in patients with biliary obstruction. We also found that male, age ≤ 60 years old, and CBD diameter < 12 mm were independent risk factors for clonorchiasis while papilla fistula as protective factor, indicating that patients with normal biliary or pancreatic tract are likely to be at high risk for clonorchiasis, in addition to age and gender, especially in endemic region.

Abbreviations

ERCP:

Endoscopic retrograde cholangiopancreatography

CBD:

Common bile duct

EST:

Endoscopic sphincterotomy

EPBD:

Endoscopic papillary balloon dilation

ENBD:

Endoscopic nasobiliary drainage

WBC:

White blood cell

AMS:

Amylase

TBil:

Total bilirubin

DBil:

Direct bilirubin

ALT:

Alanine aminotransferase

AST:

Aspartate transaminase

GGT:

Gamma glutamyl transpeptidase

ALP:

Alkaline phosphatase

CEA:

Carcinoembryonic antigen

CA-199:

Carbohydrate antigen 199

PEP:

Post-ERCP pancreatitis

PEC:

Post-ERCP cholangitis

FEC:

Formalin-ether concentration technique

KK:

Kato-Katz method

DM:

Direct smear microscopy.

Contributor Information

Mengbin Qin, Email: dr.mmbin@hotmail.com.

Jie'an Huang, Email: hjagxmu@163.com.

Data Availability

The data used to support the findings of this study are available from the corresponding author upon request.

Ethical Approval

This study was approved by the Ethics Committee of the Second Affiliated Hospital and the First Affiliated Hospital of Guangxi Medical University, Nanning, China.

Conflicts of Interest

The authors declare no conflict of interest.

Authors' Contributions

Qin MB and Huang JA conceived the study. Liao GL conducted the study and wrote the manuscript. Liao GL, Ruan HQ, Peng P, Liu SQ, Qin JF, Liang ZH, Tang GD, and Qin MB collected and analyzed the data. All authors contributed to the design and interpretation of the results and manuscript preparation. Liao GL and Ruan HQ contributed equally to this study. Qin MB and Huang JA were the guarantors and corresponding authors.

References

  • 1.Furst T., Keiser J., Utzinger J. Global burden of human food-borne trematodiasis: a systematic review and meta-analysis. The Lancet Infectious Diseases. 2012;12(3):210–221. doi: 10.1016/S1473-3099(11)70294-8. [DOI] [PubMed] [Google Scholar]
  • 2.Qian M. B., Chen Y. D., Liang S., Yang G. J., Zhou X. N. The global epidemiology of clonorchiasis and its relation with cholangiocarcinoma. Infectious Diseases of Poverty. 2012;1(1):p. 4. doi: 10.1186/2049-9957-1-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Qian M. B., Chen Y. D., Yan F. Time to tackle clonorchiasis in China. Infectious Diseases of Poverty. 2013;2(1) doi: 10.1186/2049-9957-2-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Lai D. H., Hong X. K., Su B. X., et al. Current status of Clonorchis sinensis and clonorchiasis in China. Transactions of the Royal Society of Tropical Medicine and Hygiene. 2016;110(1):21–27. doi: 10.1093/trstmh/trv100. [DOI] [PubMed] [Google Scholar]
  • 5.Choi D., Lim J. H., Lee K. T., et al. Gallstones and Clonorchis sinensis infection: a hospital-based case-control study in Korea. Journal of Gastroenterology and Hepatology. 2008;23, 8 Part 2:e399–e404. doi: 10.1111/j.1440-1746.2007.05242.x. [DOI] [PubMed] [Google Scholar]
  • 6.Qiao T., Ma R. H., Luo X. B., Luo Z. L., Zheng P. M. Cholecystolithiasis is associated with Clonorchis sinensis infection. PLoS One. 2012;7(8):p. e42471. doi: 10.1371/journal.pone.0042471. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Qiao T., Ma R. H., Luo Z. L., Yang L. Q., Luo X. B., Zheng P. M. Clonorcis sinensis eggs are associated with calcium carbonate gallbladder stones. Acta Tropica. 2014;138:28–37. doi: 10.1016/j.actatropica.2014.06.004. [DOI] [PubMed] [Google Scholar]
  • 8.Choi B. I., Han J. K., Hong S. T., Lee K. H. Clonorchiasis and cholangiocarcinoma: etiologic relationship and imaging diagnosis. Clinical Microbiology Reviews. 2004;17(3):540–552. doi: 10.1128/CMR.17.3.540-552.2004. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Shin H. R., Oh J. K., Lim M. K., et al. Descriptive epidemiology of cholangiocarcinoma and clonorchiasis in Korea. Journal of Korean Medical Science. 2010;25(7):1011–1016. doi: 10.3346/jkms.2010.25.7.1011. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Sripa B., Kaewkes S., Intapan P. M., Maleewong W., Brindley P. J. Food-borne trematodiases in Southeast Asia epidemiology, pathology, clinical manifestation and control. Advances in Parasitology. 2010;72:305–350. doi: 10.1016/S0065-308X(10)72011-X. [DOI] [PubMed] [Google Scholar]
  • 11.Choi M. H., Park I. C., Li S., Hong S. T. Excretory-secretory antigen is better than crude antigen for the serodiagnosis of clonorchiasis by ELISA. The Korean Journal of Parasitology. 2003;41(1):35–39. doi: 10.3347/kjp.2003.41.1.35. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Kim Y. J., Lee S. M., Choi G. E., et al. Performance of an enzyme-linked immunosorbent assay for detection of Clonorchis sinensis infestation in high- and low-risk groups. Journal of Clinical Microbiology. 2010;48(7):2365–2367. doi: 10.1128/JCM.02506-09. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Kim T. Y., Cho P. Y., Na J. W., Hong S. J. Molecular cloning and phylogenetic analysis of Clonorchis sinensis elongation factor-1α. Parasitology Research. 2007;101(6):1557–1562. doi: 10.1007/s00436-007-0676-7. [DOI] [PubMed] [Google Scholar]
  • 14.Shen C., Lee J. A., Allam S. R., et al. Serodiagnostic applicability of recombinant antigens of Clonorchis sinensis expressed by wheat germ cell-free protein synthesis system. Diagnostic Microbiology and Infectious Disease. 2009;64(3):334–339. doi: 10.1016/j.diagmicrobio.2009.03.003. [DOI] [PubMed] [Google Scholar]
  • 15.Ju J. W., Joo H. N., Lee M. R., et al. Identification of a serodiagnostic antigen, legumain, by immunoproteomic analysis of excretory-secretory products of Clonorchis sinensis adult worms. Proteomics. 2009;9(11):3066–3078. doi: 10.1002/pmic.200700613. [DOI] [PubMed] [Google Scholar]
  • 16.Traub R. J., Macaranas J., Mungthin M., et al. A new PCR-based approach indicates the range of Clonorchis sinensis now extends to Central Thailand. PLoS Neglected Tropical Diseases. 2009;3(1):p. e367. doi: 10.1371/journal.pntd.0000367. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Le T. H., Van De N., Blair D., Sithithaworn P., McManus D. P. Clonorchis sinensis and Opisthorchis viverrini: Development of a mitochondrial-based multiplex PCR for their identification and discrimination. Experimental Parasitology. 2006;112(2):109–114. doi: 10.1016/j.exppara.2005.09.012. [DOI] [PubMed] [Google Scholar]
  • 18.Kim J. H., Choi M. H., Bae Y. M., Oh J. K., Lim M. K., Hong S. T. Correlation between discharged worms and fecal egg counts in human clonorchiasis. PLoS Neglected Tropical Diseases. 2011;5(10):p. e1339. doi: 10.1371/journal.pntd.0001339. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Joo K. R., Bang S. J. A bile based study of Clonorchis sinensis infections in patients with biliary tract diseases in Ulsan, Korea. Yonsei Medical Journal. 2005;46(6):794–798. doi: 10.3349/ymj.2005.46.6.794. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Qian M. B., Yap P., Yang Y. C., et al. Accuracy of the Kato-Katz method and formalin-ether concentration technique for the diagnosis of Clonorchis sinensis, and implication for assessing drug efficacy. Parasites & Vectors. 2013;6(1):p. 314. doi: 10.1186/1756-3305-6-314. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Johansen M. V., Sithithaworn P., Bergquist R., Utzinger J. Towards improved diagnosis of zoonotic trematode infections in Southeast Asia. Advances in Parasitology. 2010;73:171–195. doi: 10.1016/S0065-308X(10)73007-4. [DOI] [PubMed] [Google Scholar]
  • 22.Qian M.-B., Utzinger J., Keiser J., Zhou X.-N. Clonorchiasis. The Lancet. 2016;387(10020):800–810. doi: 10.1016/S0140-6736(15)60313-0. [DOI] [PubMed] [Google Scholar]
  • 23.Phan V. T., Ersboll A. K., Do D. T., Dalsgaard A. Raw-fish-eating behavior and fishborne zoonotic trematode infection in people of northern Vietnam. Foodborne Pathogens and Disease. 2011;8(2):255–260. doi: 10.1089/fpd.2010.0670. [DOI] [PubMed] [Google Scholar]
  • 24.Baron T. H., Petersen B. T., Mergener K., et al. Quality indicators for endoscopic retrograde cholangiopancreatography. Gastrointestinal Endoscopy. 2006;63(4 Suppl):S29–S34. doi: 10.1016/j.gie.2006.02.019. [DOI] [PubMed] [Google Scholar]
  • 25.ASGE Training Committee, Jorgensen J., Kubiliun N., et al. Endoscopic retrograde cholangiopancreatography (ERCP): core curriculum. Gastrointestinal Endoscopy. 2016;83(2):279–289. doi: 10.1016/j.gie.2015.11.006. [DOI] [PubMed] [Google Scholar]
  • 26.Fang Y. Y., Chen Y. D., Li X. M., Wu J., Zhang Q. M., Ruan C. W. Current prevalence of Clonorchis sinensis infection in endemic areas of China. Chinese Journal of Parasitology & Parasitic Diseases. 2008;26(2):99–103, 109. [PubMed] [Google Scholar]
  • 27.Vinh H. Q., Phimpraphai W., Tangkawattana S., et al. Risk factors for Clonorchis sinensis infection transmission in humans in northern Vietnam: a descriptive and social network analysis study. Parasitology International. 2017;66(2):74–82. doi: 10.1016/j.parint.2016.11.018. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Hong S. T., Choi M. H., Kim C. H., Chung B. S., Ji Z. The Kato-Katz method is reliable for diagnosis of Clonorchis sinensis infection. Diagnostic Microbiology and Infectious Disease. 2003;47(1):345–347. doi: 10.1016/s0732-8893(03)00113-5. [DOI] [PubMed] [Google Scholar]
  • 29.Calvopina M., Romero-Alvarez D., Diaz F., Cevallos W., Sugiyama H. A comparison of Kato-Katz technique to three other methods for diagnosis of Amphimerus spp. liver fluke infection and the prevalence of infection in Chachi Amerindians of Ecuador. PLoS One. 2018;13(10, article e0203811) doi: 10.1371/journal.pone.0203811. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Qian M. B., Chen Y. D., Fang Y. Y., et al. Disability weight of Clonorchis sinensis infection: captured from community study and model simulation. PLoS Neglected Tropical Diseases. 2011;5(12):p. e1377. doi: 10.1371/journal.pntd.0001377. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31.Qian M. B., Chen Y. D., Fang Y. Y., et al. Epidemiological profile of Clonorchis sinensis infection in one community, Guangdong, People’s Republic of China. Parasites & Vectors. 2013;6(1):p. 194. doi: 10.1186/1756-3305-6-194. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32.Kim T. I., Yoo W. G., Kwak B. K., Seok J.–. W., Hong S.–. J. Tracing of the bile-chemotactic migration of juvenile Clonorchis sinensis in rabbits by PET-CT. PLoS Neglected Tropical Diseases. 2011;5(12):p. e1414. doi: 10.1371/journal.pntd.0001414. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.de Martel C., Plummer M., Franceschi S. Cholangiocarcinoma: descriptive epidemiology and risk factors. Gastroentérologie Clinique et Biologique. 2010;34(3):173–180. doi: 10.1016/j.gcb.2010.01.008. [DOI] [PubMed] [Google Scholar]
  • 34.Prueksapanich P., Piyachaturawat P., Aumpansub P., Ridtitid W., Chaiteerakij R., Rerknimitr R. Liver fluke-associated biliary tract cancer. Gut Liver. 2018;12(3):236–245. doi: 10.5009/gnl17102. [DOI] [PMC free article] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

The data used to support the findings of this study are available from the corresponding author upon request.


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