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INTRODUCTION
Primary sclerosing cholangitis (PSC) is a chronic disease that affects the biliary tract. Progressive inflammation and fibrosis cause intrahepatic and extrahepatic bile duct obstruction and dilatation. The diagnosis of PSC is based on cholestatic biochemical profile and cholangiography. The annual incidence of PSC was 0.5–1.3 per 100,000 individuals in Western countries [1,2], whereas no relative information is available in Asian countries. The prevalence of PSC was approximately 0.095–0.13 per 10,000 inhabitants in Asian countries, which is 10-fold lower than the prevalence in Western countries [3].
Although the exact etiology and pathogenesis of PSC are still unknown, several studies have shown an association of PSC with certain genetic, environmental, and immunologic factors. There is no curative treatment for PSC, and a considerable number of patients develop severe clinical sequelae, such as portal hypertension, liver cirrhosis, and end-stage liver disease, eventually requiring liver transplantation (LT). Moreover, patients with PSC have a higher lifetime risk of cholangiocarcinoma and gall bladder cancer.
PSC is strongly associated with inflammatory bowel disease (IBD), especially ulcerative colitis (UC). Approximately 47%–76% and 20%–37% of patients with PSC had IBD in Western and Asian countries, respectively [1]. The proportion of UC was over 75% in these cases [4]. By contrast, PSC was less commonly diagnosed in patients with IBD, occurring in approximately 2.4%–7.5% of patients with UC and approximately 3% of patients with Crohn’s disease (CD) in Western countries [4]. With regard to Asian countries, PSC was identified in 0.3% and 0.2% of Korean patients with UC and CD, respectively [5]. Approximately 25% of patients with IBD and PSC developed PSC before the diagnosis of IBD [6].
Patients with IBD and concomitant PSC were characterized by pancolitis, backwash ileitis, rectal sparing, and increased risk of colorectal cancer (CRC) and cholangiocarcinoma [7-9] in Western countries, whereas the relationship between PSC and IBD was less frequently reported in Asian countries. Previously, both IBD [10] and PSC [5,11] were less prevalent in Taiwan as well as in overall Asia. Therefore, limited data were available regarding PSC and IBD among Asians. With the increasing prevalence of IBD in Taiwan in recent decades [10], we sought to evaluate possible factors associated with PSC that can aid earlier diagnosis of PSC in IBD. Compared with patients with IBD and without PSC, those with concomitant IBD and PSC have a higher risk of hepatic failure. Earlier identification and preparation for LT might be helpful for improving outcomes in such patients.
METHODS
1. Patients
This retrospective study was conducted to review patients with IBD admitted to National Taiwan University Hospital from January 1, 1996, to December 31, 2018. This study was approved by the Institutional Review Board of National Taiwan University Hospital (IRB No. 201912236RINC). This study is a retrospective study using anonymous clinical data review and so informed consent was waived. The International Classification of Diseases, Ninth Revision, Clinical Modification (ICD-9-CM) codes were used for the detection of UC (ICD-9-CM code 556.9) and CD (ICD-9-CM code 555.9). The type of IBD and the extent and severity of colitis were recorded. The diagnosis of IBD was based on a combination of clinical, endoscopic, and histologic features and the exclusion of an infectious etiology. The extent of colitis was classified as proctitis (E1), left sided (E2), and extensive (E3) in UC [12] according to the Montreal classification. The severity of disease (mild, moderate, or severe) was determined according to Truelove and Witts criteria [8]. Patients with IBD with concomitant PSC were identified from the radiology information system of National Taiwan University Hospital. All types of radiological reports with the keyword “sclerosing” and “cholangitis” were searched, and the charts of patients who repeatedly underwent computed tomography, magnetic resonance imaging, or percutaneous biliary procedures were reviewed. The diagnostic criteria of PSC were based on cholestatic biochemical profile and cholangiography. Studies involving patients with IgG4-associated cholangitis and secondary causes of sclerosing cholangitis were excluded. Clinical information, including demographic data, laboratory and pathologic reports, treatment regimens, the area involved in PSC, the disease course, and a history of cancer or LT, was assessed. A total of 12 patients with concomitant IBD and PSC were identified. Adult patients with IBD and PSC were matched with those with IBD but without PSC, as a comparison group, with a 1:4 ratio, according to sex, age, and time of hospital admission. Because the number of patients in the pediatric group (patients aged below 18 years) was small, pediatric patients with IBD and PSC were matched with those with IBD but without PSC in a 1:2 ratio. Differences in clinical information and outcomes between patients with IBD and PSC and those with IBD but without PSC were compared.
2. Statistical Analysis
Continuous variables are expressed as the mean ± standard deviation. Categorical variables are expressed as the frequency (percentage). Student t-test was used to compare quantitative variables, and the chi-square statistic or Fisher exact test was used to compare categorical variables between the 2 cohorts. A P-value less than 0.05 was considered statistically significant. Statistical analyses were performed using SPSS 11.0 program (SPSS Inc., Chicago, IL, USA).
RESULTS
1. Demographic Characteristics of Patients with UC
A total of 763 patients were diagnosed with IBD (380 with CD and 383 with UC); 12 of them with UC had concomitant PSC. The incidence of PSC was 1.57% in patients with IBD and 3.1% in patients with UC. Patients with UC and PSC were significantly younger than those with UC but without PSC (median age: 22.5 and 49.0 years, respectively; P=0.001). Male predominance was noted in both the groups (83.3% and 58.5%, respectively; P=0.085). After the subgroup analysis of pediatric patients with UC, a significantly higher proportion of male patients was observed in the PSC group than in the non-PSC group (100% and 38.2%, respectively; P=0.015). The demographics of patients with IBD with and without PSC are summarized in Table 1. The basic characteristics of 12 patients with UC and PSC are listed in Table 2. The majority (75%) of these patients were diagnosed with PSC along with or after the diagnosis of UC. The typical PSC magnetic resonance imaging images were shown in Supplementary Fig. 1.
2. Comparison of Clinical Characteristics between Patients with UC with and without PSC
Among the 12 patients who had concomitant UC and PSC, 7 were adults. They were matched with patients with UC but without PSC according to sex, age, and the year of admission as a control group, at a 1:4 ratio in the adult group and 1:2 ratio in the pediatric group. Finally, a total of 38 matched patients (28 adults and 10 children) with UC were included as controls. The clinical characteristics of these patients are listed in Table 3. Underlying diseases, namely hypertension (8.3% vs. 5.3%, P=0.696), diabetes mellitus (0% vs. 5.3%, P=0.417), hyperlipidemia (0% vs. 2.6%, P=0.570), coronary artery disease (0% vs. 5.3%, P=0.417), chronic kidney disease (8.3% vs. 5.3%, P=0.696), and chronic viral hepatitis, were comparable between the groups (all P>0.05). Moreover, there was no statistical difference in the colitis-involved area and disease severity between the groups, whereas patients with UC and PSC had higher proportion of rectal sparing, compared with patients with UC but without PSC (25% and 0%, respectively; P=0.001). The frequency of backwash ileitis did not differ between the 2 groups (33.3% vs. 9.1%, P=0.133). However, the endoscope reached the terminal ileum in only 28 of 50 patients (6 in the PSC group and 22 in the non-PSC group). Furthermore, compared with patients in the non-PSC group, those in the PSC group presented more severe liver-associated symptoms and imaging findings. Patients in the PSC group had higher risks of jaundice (50.0% and 2.6%, respectively; P<0.001), liver cirrhosis (41.7% and 2.6%, respectively; P<0.001), hepatic decompensation (25.0% and 2.6%, respectively; P=0.013), and requiring LT (25.0% and 0%, respectively; P=0.001) than did patients in the non-PSC group. Among the 3 patients who received LT for the PSC, 1 patient passed away 7 years after LT due to septic shock. All of them, their UC disease activity were stable during the follow-up period. With regarding to treatment, all patients with UC and PSC received ursodeoxycholic acid (100% vs. 0%, P<0.001), whereas those without PSC did not. Otherwise, the frequency of administering 5-aminosalicylic acid (83.3% vs. 100%, P=0.054), steroids (58.3% vs. 52.6%, P=0.730), thiopurine (41.7% vs. 47.4%, P=0.730), and anti-tumor necrosis factor-α (0% vs. 21.0%, P=0.083) did not significantly differ between the groups. Patients with UC and PSC did not have a significantly higher risk of cancer (8.3% vs. 7.9%, P=0.679) or higher mortality (16.7% vs. 7.9%, P=0.377) than did patients with UC but without PSC. In the PSC-UC group, 1 patient developed colon cancer and 2 patients died (1 patient owing to hepatic failure and the other owing to colon cancer). In the non-PSC-UC group, 2 patients developed colon cancer and 1 patient developed acute myeloid leukemia. Three patients died (1 owing to HCV-related hepatic failure, 1 owing to colon cancer, and 1 owing to pneumonia), all of whom were aged over 60 years. The mortality rate did not significantly differ between the pediatric and adult groups (8.6% vs. 13.3%, P=0.629).
3. Comparison of Laboratory Characteristics between Patients with and without PSC
Compared with patients with UC but without PSC, those with UC and PSC had higher levels of serum total bilirubin (0.54 and 1.26 mg/dL, respectively; P=0.001), alanine aminotrans-ferase (12 and 73 U/L, respectively; P<0.001), alkaline phosphatase (75.5 and 275.5 U/L, respectively; P<0.001), γ-glutamyl transpeptidase (24.5 and 165 U/L, respectively; P=0.005), and prothrombin time (10.9 and 11.4 seconds, respectively; P=0.042). Furthermore, the hemoglobin level was significantly lower in the PSC-UC group than in the non-PSC-UC group (10.6 and 12.4 g/dL, respectively; P=0.002). The relevant data are listed in Table 4.
DISCUSSION
In this hospital-based cohort study, 1.57% prevalence of PSC was observed among Taiwanese patients with IBD; the prevalence was 3.1% in patients with UC and 0% in those with CD. Thus, all these IBD patients were diagnosed with UC. This finding is compatible with that of our previously published nationwide population-based study that showed a 1.6% prevalence of cholangitis in Taiwanese patients with IBD [13]. The prevalence of PSC in Indian patients with UC and CD was 0.4% and 0%, respectively [14], and that in Korean patients was 0.3% and 0.2%, respectively [5]. Meanwhile, 2.4% to 7.5% of patients with UC were diagnosed with PSC in Western countries [4]. The lower prevalence of PSC along with IBD in Asian countries than in Western countries may be attributed to underdiagnosis; alternatively, the prevalence could have actually been low. To the best of our knowledge, PSC was more common among patients with IBD in Taiwan than in other Asian countries.
We observed that patients with IBD and PSC were much younger than those with IBD but without PSC; in addition, men were more likely to develop PSC, especially in the pediatric group. Male predominance of PSC in children and adolescents was previously reported [15]. According to Vavricka et al. [6], 25% of patients with IBD and PSC developed PSC before the diagnosis of IBD, which indicates that in the majority of cases, PSC would be diagnosed after the diagnosis of IBD. Our results also demonstrated that in 25% of patients, PSC was diagnosed before IBD, in 33% of patients, PSC and IBD were simultaneously diagnosed, and in 42% of patients, PSC was diagnosed after IBD. Interestingly, in the majority of pediatric patients (60%), PSC and UC were simultaneously diagnosed. Our study also revealed that patients with UC and PSC had a higher risk of liver decompensation and increased requirement for LT. Therefore, routine survey and regular follow-up of liver and biliary profile function are recommended in pediatric male patients with IBD for early diagnosis and accurate management of PSC.
Our data demonstrated that underlying systemic disease or the extent or severity of colitis did not significantly differ between the PSC-UC and non-PSC-UC groups. Compared with patients with IBD alone, those with IBD and PSC have been reported to show predominant extensive colitis [16,17]. Even in the current study, patients with IBD and PSC presented with more extensive colitis (75%). Approximately 57.9% of patients in our matched control group presented with extensive colitis, whereas another hospital-based study conducted in Taiwan demonstrated that left-sided colitis was the predominant disease (42.7%), followed by extensive colitis (39.1%), in patients with UC [18]. There was no difference in the area of colitis between the 2 patient groups in this study, which may be attributed to the fact that our control group patients had more extensive colitis, as our hospital was a referral center for this condition. More rectal-sparing type (RST) UC was identified in our PSC group than in the non-PSC group (25% and 0%, respectively; P=0.001). In the study conducted by Park et al. [19], RST was detected in 3.3% of Korean patients with UC. RST was a relative disease status and could develop during disease progression [20]. Currently, it is well established that RST UC is associated with PSC [21]. Backwash ileitis was also reported as a distinct phenotype of patients with IBD and PSC [22]. In our study, although the proportion of ileitis seems higher in the group of patients with PSC, there was no statistical difference between the groups as terminal ileum intubation was achieved only in 28 patients (56%). Complete ileocolonoscopy was recommended for all patients with an initial diagnosis of IBD.
Compared with patients with UC but without PSC, those with PSC had higher levels of bilirubin, liver enzymes, biliary enzymes, and prothrombin time and a lower level of hemoglobin. The majority of these laboratory profiles were associated with liver reserve and could be prognostic factors for hepatic failure. Thus, it is reasonable that these patients with PSC had higher risks of liver cirrhosis and hepatic failure and were more likely to require LT.
In the PSC-UC group, 1 patient developed colon cancer, whereas in the non-PSC-UC group, 2 patients developed colon cancer. UC was associated with a 2- to 4-fold increased risk of CRC [23]. Compared with patients with IBD alone, those with IBD and PSC had an increased risk of CRC (odds ratio, 3.41; 95% confidence interval, 2.13–5.48) [24]. The low rate of cancer in the PSC-UC group might be attributed to the small number of patients in this group. We recommend annual surveillance colonoscopy for patients with IBD and PSC according to guidelines [25].
This study has some limitations. First, this was a retrospective study. Although we speculated that data regarding comprehensive laboratory studies would be available for hospitalized patients, not all patients had complete laboratory profiles or underwent cholangiography; hence, the prevalence of PSC might have been underestimated. Second, owing to the limited number of pediatric patients with IBD, the ratio of the PSC group to the control group was 1:2. The small patient number also led to a nonsignificant statistical result. Despite these limitations, the findings of this study help understand the characteristics of PSC concomitant with IBD in patients from Asian countries.
In conclusion, 1.57% prevalence of PSC was observed in Taiwanese patients with IBD, which was the highest in Asia. Pediatric male patients with UC had a higher risk of PSC. In the majority of patients, PSC was diagnosed along with or after IBD. Compared with patients with UC but without PSC, those with UC and PSC had higher levels of liver and biliary enzymes and higher risks of liver cirrhosis and hepatic failure. Routine survey and regular follow-up of hepatic and biliary profile function are recommended in pediatric male patients with IBD for early diagnosis and proper management of PSC to improve the outcomes of these patients.
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