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Volume 2012 (2012), Article ID 325743, 4 pages
Primary Sclerosing Cholangitis Associated with Elevated Immunoglobulin-G4: A Preliminary Study
Research Center for Gastroenterology and Liver Disease, Taleghani Educational Hospital, Shahid Beheshti University of Medical Sciences, Tehran 19857, Iran
Received 25 May 2012; Accepted 12 July 2012
Academic Editors: A. J. Karayiannakis and S. Odegaard
Copyright © 2012 Baran Parhizkar et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Background. Immunoglobulin IgG4-associated cholangitis (IAC) disease is a systemic disease histologically characterized by extensive T lymphocytes and IgG4 positive plasma cell infiltration in various organs. Prevalence of IAC in PSC patients was reported to be between 7% and 11.6% in a few previous studies. This study was carried out to evaluate frequency of serum IgG4 level in PSC patient referred to the gastroenterology ward of Taleghani educational hospital in Tehran, Iran. Material and Methods. This study was a prospective analytical cross-sectional study. Clinical presentation, laboratory values, imaging changes, inflammatory bowel disease (IBD), esophageal varices, ascites, and child score in newly PSC patients with elevated IgG4 were determined and compared with PSC patients with normal levels of IgG4. Data was analyzed by using SPSS software. The frequency and standard deviations were calculated. Differences among groups were evaluated by using the chi-square, fisher exact, and Mann-Whitney U tests. Results. 34 patients with PSC were examined in the study period, of which 9 cases (26.5%) had high IgG4 levels. Most of the patients were male, 23 cases (67.6%) and nonsmoker, 26 cases (76.5%). Patient average age was 47 years old (range 21–67 years). There was not any significant relationship among patients with IAC and PSC patients in terms of variables such as age, smoking, presence of IBD, ascites, esophageal varices, child score, and imaging findings (). Conclusion. IAC should be suspected in cases of unexplained biliary strictures with increased serum IgG4. Testing PSC patients for IgG4 and treating those who have high levels with corticosteroids in clinical trials should be considered in future studies.
Primary sclerosing cholangitis (PSC) is a chronic cholestatic disease of intrahepatic and extrahepatic biliary ducts, characterized by chronic periductal inflammation and sclerosing of the ducts, which results in segmental stenosis of bile ducts, cholestasis, and fibrosis .
During two last decades, patients with steroid responsive PSC have been presented in some case reports and a few studies .
In 1999, Erkelens et al.  described 4 cases of PSC with good response to corticosteroid therapy; therefor, posing idea of presumable autoimmune basis for this type of sclerosing cholangitis and it is named later Immunoglobulin G4- (IgG4-) Associated Cholangitis (IAC) .
IAC disease is a systemic disease histologically characterized by extensive T lymphocytes and IgG4 positive plasma cell infiltration of various organs . Most frequent clinical signs and symptoms at presentation included jaundice (77%), weight loss (51%), and abdominal pain (26%) . Despite of increasing recognition of IAC as an independent disease entity, its pathogenesis still remains unknown , and the sensitivity and specificity of IgG4 levels for the diagnosis of IAC are not known, at present time .
This study was carried out to evaluate frequency of serum IgG4 level in PSC patient referred to referral gastroenterology ward of Taleghani educational hospital in Tehran/Iran for the first time.
2. Material and Methods
This study was a cross-sectional prospective, descriptive and analytical study on 34 patients with PSC (23 were male and 11 were female with median age 43.2 years (range 21–67 years)). Newly PSC patients which were diagnosed according to the (1) chronic cholestasis of unknown etiology for at least 6 months, (2) biliary strictures typical for PSC was seen in cholangiography (MRCP or ERCP) by observation of beading appearance, and (3) appropriate exclusion of other hepatic or biliary disease using standard clinical, imaging, and laboratory criteria were included in the study by census method in Tehran Taleghani educational hospital during January, 2011 to January, 2012.
Data on clinical presentation, laboratory values, extent of the cholangiographic changes, inflammatory bowel disease (IBD), esophageal varices, ascites, and child score was collected in questioners. The IgG4 levels, CA 19-9 antigen, AMA, ASMA, and ALKM antibodies were measured and recorded in questioner too.
Patients with elevated IgG4 were determined and their laboratory and other variables were compared with PSC patients with normal levels of IgG4.
Data was analyzed by using SPSS version 16 software. The frequency and standard deviations were calculated. Differences among groups were evaluated by chi-square or fisher exact tests for qualitative variables, and nonparametric quantitative variables (such as median IgG4 levels) were compared by Mann-Whitney U test.
Thirty-four patients with PSC were examined in the study period; that 9 cases (26.5%) had high IgG4 level (>157 mg/dL, normal range 10–157 mg/dL). The mean of IgG4 levels in IAC patients was (159–292 mg/dL). Out of 34 cases, 23 of them were male (67.6%) and 26 cases were nonsmoker (76.5%).
There was not any significant relationship among patients with IAC and PSC patients in terms of variables such as age, smoking, presence of IBD, ascites, esophageal varices, child score, and laboratory and imaging findings () (Table 1).
33.3% of IAC patients and 44% of PSC patients with normal IgG4 levels had IBD ().
Intrahepatic involvement and extrahepatic involvement were seen in 55.6% and 11.1% of IAC patients, and in 33.3% of them both intra- and extrahepatic involvement were seen ().
High CA19-9 was seen in 77.8% of IAC patients. Serum value of CA19-9 among patients with PSC was between 11 and 347, and 7 patients have high level of CA19-9 (above 347 mg/dL).
Laboratory findings in IAC patients including liver enzyme and serum IgG4 levels, CA 19-9 antigen, AMA, ASMA, and ALKM antibodies are listed in Table 2.
Elevated serum IgG4 levels (IAC) were seen in 26.5% of PSC patients in our study. So far, few studies have been published which evaluated the increase in IgG4 in patients with PSC [2, 7], the highest previous reported prevalence was 11.6% which has been mentioned in the Björnsson et al. study . It seems that our achieved frequency is the highest figure reported in PSC patients with increased IgG4 levels. Meanwhile, a few previous studies evaluated an increase in IgG4 in patients with PSC [2, 7] and other studies have been conducted on patients with AIP [1, 6].
Our results suggest that IgG4 measurement should be considered in all patients with PSC and should be a part of the diagnostic criteria in these patients.
The first case report of IgG4-related systemic disease (ISD-) like disorders date backs to the sixties .
Two autoimmune and allergic mechanisms are proposed in the pathogenesis of IAC , but whether induced responses by T-helper 1 cells (as an autoimmune disease)  or dominant semiallergic response of T-helper 2 cells can induce inflammatory reaction in IAC patients is unclear yet [10–12].
Increased IgG4 titers can be seen in both types of allergic diseases such as asthma and atopic dermatitis [11, 13] and autoimmune diseases such as pemphigus vulgaris, myastenia gravis, vasculitis, and systemic lupus erythematous . The role of IgG4 in pathogenesis of IAC is not clearly clarified yet.
Now HISORt criteria, which is provided by the Mayo Clinic, has been recognized as the most useful diagnostic criteria of IgG4-SC .
It is well known that IAC is a manifestation of a systemic fibroinflammatory process involving the bile duct, pancreas, salivary and lacrimal glands, retroperitoneum, and lymph nodes. The association of IAC with autoimmune pancreatitis (AIP) is of particular clinical relevance. Studies from the Mayo Clinic revealed that 92.5% of patients with IAC suffer from AIP whereas IAC may occur in 20%–90% of cases of AIP. In fact, unexplained pancreatic disease and other organ involvement are important clues in the diagnosis of IAC .
In Mendes et al. study , patients with increased IgG4 levels have higher levels of bilirubin, alkaline phosphatase, and Mayo risk score and less time for liver transplantation. Also in the Björnsson et al. study  liver cirrhosis was seen in 50% of patients. How ever, in our study there was not any significant relationship among bilirubin, alkaline phosphatase, AST, ALT levels, and child score in patients with elevated IgG4 levels (IAC) compared to PSC patients with normal IgG4 levels.
The number of reviewed PSC patients in the Mendes et al.  and Björnsson  studies was 127 and 285 cases respectively, whereas in our study this figure was 34 cases; it seems, despite of the same age range of our patients and the two previous studies, especially Björnsson et al. study , restrictions on the sample size in our study could partly be effective in the absence of statistical difference in factors listed previously.
On the other hand as we did not include the control in this study and according to our results, we cannot certainly comment on severity of illness in IAC patients compared to those with normal serum IgG4 levels.
In our study there was not any association among clinical statuses, such as the presence of ascites and esophageal varices, with presence of IAC which result is coordinated with the results of previous studies [13, 16]. These findings indicate that there was not any specific clinical sign suggestive for IAC in patients with PSC.
In this study, IBD was seen in 41.2% of all PSC patients and 33.3% of IAC patients. The only previous study that has evaluated IBD in PSC patients with elevated IgG4 was Björnsson et al. study , which indicated IBD in 75% of their cases and had higher figure in comparison with our study.
IAC is characterized by bile duct wall thickening and biliary strictures, which are, in contrast to primary sclerosing cholangitis, predominantly located in the lower bile ducts. In a review of 53 patients with IAC, Ghazale et al.  reported that IAC is associated with radiologic findings of AIP in 92% and elevated serum IgG4 in 74%. Therefore, more information on the cholangiographic findings might be useful along with a comment on the higher incidence of intrahepatic compared with extrahepatic biliary tract involvement among IAC patients in this study.
The important point that should be considered is that cholangiographic changes in IAC, pancreatic cancer, PSC, and cholangiocarcinoma are more similar and if diagnosis of IAC will be neglected, it can lead to invasive intervention for patients. Therefore, based on cholangiographic findings we suggest that evaluation of serum IgG4 is useful in diagnosis of IAC cases and changing therapeutic process in these patients.
In this regards, Nakazawa and colleges  in their study which was published in 2012 evaluated diagnostic criteria of IgG4-related cholangitis based on cholangiographic findings and noticed different diagnostic factors for any of PSC, pancreatic cancer, and cholangiocarcinoma.
It seems that future studies in this field can be considered as the next research step.
Limited sample size and impossibility for follow-up response to corticosteroid treatment in our patients due to restrictions on access to patients were the major limitation of our study.
Based on the findings of this study, measured serum IgG4 level in all patients with PSC should be considered especially at diagnose time.
Future studies in this field especially studies with control groups and also multicenter clinical trials in the field of corticosteroid therapy and other useful therapies are suggested.
- A. Ghazale, S. T. Chari, L. Zhang et al., “Immunoglobulin G4-associated cholangitis: clinical profile and response to therapy,” Gastroenterology, vol. 134, no. 3, pp. 706–715, 2008.
- E. Björnsson, S. T. Chari, T. C. Smyrk, and K. Lindor, “Immunoglobulin G4 associated cholangitis: description of an emerging clinical entity based on review of the literature,” Hepatology, vol. 45, no. 6, pp. 1547–1554, 2007.
- G. W. Erkelens, F. P. Vleggaar, W. Lesterhuis, H. R. Van Buuren, and S. D. J. Van Der Werf, “Sclerosing pancreato-cholangitis responsive to steroid therapy,” The Lancet, vol. 354, no. 9172, pp. 43–44, 1999.
- Y. A. Alderlieste, B. D. J. Van Den Elzen, E. A. J. Rauws, and U. Beuers, “Immunoglobulin G4-associated cholangitis: one variant of immunoglobulin G4-related systemic disease,” Digestion, vol. 79, no. 4, pp. 220–228, 2009.
- H. Takikawa, Y. Takamori, A. Tanaka, H. Kurihara, and Y. Nakanuma, “Analysis of 388 cases of primary sclerosing cholangitis in Japan. Presence of a subgroup without pancreatic involvement in older patients,” Hepatology Research, vol. 29, no. 3, pp. 153–159, 2004.
- F. D. Mendes, R. Jorgensen, J. Keach et al., “Elevated serum IgG4 concentration in patients with primary sclerosing cholangitis,” American Journal of Gastroenterology, vol. 101, no. 9, pp. 2070–2075, 2006.
- E. Björnsson, “the prevalence of IgG4 levels in patients with Primary Sclerosing Cholangitis,” Gastroenterology, 2009, DDW abstract.
- H. Sarles, J. C. Sarles, R. Muratore, and C. Guien, “Chronic inflammatory sclerosis of the pancreas-An autonomous pancreatic disease?” American Journal of Digestive Diseases, vol. 6, no. 7, pp. 688–698, 1961.
- K. Okazaki, K. Uchida, M. Ohana et al., “Autoimmune-related pancreatitis is associated with autoantibodies and a Th1/Th2-type cellular immune response,” Gastroenterology, vol. 118, no. 3, pp. 573–581, 2000.
- T. Umemura, Y. Zen, H. Hamano, S. Kawa, Y. Nakanuma, and K. Kiyosawa, “Immunoglobin G4-hepatopathy: association of immunoglobin G4-bearing plasma cells in liver with autoimmune pancreatitis,” Hepatology, vol. 46, no. 2, pp. 463–471, 2007.
- Y. Zen, T. Fujii, K. Harada et al., “Th2 and regulatory immune reactions are increased in immunoglobin G4-related sclerosing pancreatitis and cholangitis,” Hepatology, vol. 45, no. 6, pp. 1538–1546, 2007.
- I. Zandieh and M. F. Byrne, “Autoimmune pancreatitis: a review,” World Journal of Gastroenterology, vol. 13, no. 47, pp. 6327–6332, 2007.
- E. Björnsson, “Immunoglobulin G4-associated cholangitis,” Current Opinion in Gastroenterology, vol. 24, no. 3, pp. 389–394, 2008.
- S. Mihai, M. T. Chiriac, J. E. Herrero-González et al., “IgG4 autoantibodies induce dermal-epidermal separation,” Journal of Cellular and Molecular Medicine, vol. 11, no. 5, pp. 1117–1128, 2007.
- T. Nakazawa, I. Naitoh, K. Hayashi et al., “Diagnostic criteria for IgG4-related sclerosing cholangitis based on cholangiographic classification,” Journal of Gastroenterology, vol. 47, no. 1, pp. 79–87, 2012.
- U. Broomé, R. Olsson, L. Lööf et al., “Natural history and prognostic factors in 305 Swedish patients with primary sclerosing cholangitis,” Gut, vol. 38, no. 4, pp. 610–615, 1996.