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Introduction: Primary biliary cholangitis (PBC) is a chronic autoimmune cholestatic liver disease. Despite established first-line therapy with ursodeoxycholic acid (UDCA), many patients do not achieve biochemical remission. Data on the characteristics of PBC in Poland remain limited.
Objectives: To characterize demographic, clinical, and serological features of Polish patients with PBC and effect of treatment in a multicenter retrospective study.
Patients And Methods: A total of 364 patients from 10 hepatology centers were included. Data on demographics, laboratory tests, autoantibodies, and markers of disease severity were collected between January 6 and March 8, 2025 and analyzed according to the duration of UDCA treatment (<2 vs. ≥2 years).
Results: Women constituted 92.3% of the cohort. Most patients were aged 60-80 years, but male patients were relatively more common in the <50 and >80 age groups. Cirrhosis was diagnosed in 35.2% of patients. Anti-mitochondrial antibodies were present in 94.4%, and anti-Ro52 antibodies in 34.1%. Anti-gp210 and anti-sp100 antibodies were more frequent in patients with longer disease duration. No substantial differences in liver biochemistry were found between short- and long-term UDCA groups, except for lower GGT activity with longer treatment. Despite pruritus in 46% of patients, antipruritic therapy was rarely used.
Conclusions: This is the first national study to characterize PBC in Poland. Findings suggest limited long-term efficacy of UDCA, potential diagnostic delay in men, and unmet needs in symptom management. Anti-gp210, anti-sp100, and anti-Ro52 antibodies may serve as important serologic markers. Prospective studies are needed to confirm these observations.
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http://dx.doi.org/10.20452/pamw.17071 | DOI Listing |
Med Sci (Paris)
September 2025
Service des maladies de l'appareil digestif. Centre de compétence Maladies rares « Maladies inflammatoires des voies biliaires et hépatites autoimmunes », Hôpital Huriez, Lille, France.
Primary biliary cholangitis (PBC) is a rare disease for which management long consisted of a single treatment: ursodeoxycholic acid. In 2015-2016, this disease regained interest with the first studies on obeticholic acid (FXR agonist) and then on bezafibrate (PPAR agonist). Subsequently, over the past five years, significant progress has been made in the management of PBC.
View Article and Find Full Text PDFCureus
August 2025
Gastroenterology, Medica Superspecialty Hospital, Kolkata, IND.
Before the period of endoscopic retrograde cholangiopancreatography (ERCP), individuals with biliary tract diseases would undergo side-to-side choledochoduodenostomy, and sump syndrome used to develop as a complication of this procedure. There is retention of bile along with debris or calculi, and refluxed duodenal contents in the common bile duct, which leads to biliary and pancreatic complications. This syndrome's pathophysiology often results when the distal common bile duct below the anastomosis becomes a blind pouch (), leading to stasis of bile, food debris, and bacteria, which can lead to obstruction and infection.
View Article and Find Full Text PDFTherap Adv Gastroenterol
September 2025
Department of Gastroenterology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, China.
Background: Managing patients with primary biliary cholangitis (PBC) who demonstrate an inadequate response to ursodeoxycholic acid or experience intolerable side effects remains a significant clinical challenge.
Objectives: This study aims to investigate the efficacy and safety of peroxisome proliferator-activated receptor (PPAR) agonists in the treatment of PBC.
Design: Meta-analysis and systematic review.
ACG Case Rep J
October 2024
Department of Internal Medicine, Division of Gastroenterology, University of Texas Medical Branch, Galveston, TX.
Biliary enteric fistulas are rare form of internal biliary fistula encountered in <1% of patients with biliary disease while cholecystocolic fistulas are even rarer with reported incidence of 0.06%-0.14% in patients undergoing cholecystectomy.
View Article and Find Full Text PDFCurr Opin Rheumatol
September 2025
Yale School of Medicine, Department of Internal Medicine, Section of Digestive Diseases, New Haven, Connecticut, USA.
Purpose Of Review: To synthesize current knowledge on the genetic, immunopathogenic, and clinical presentations of systemic sclerosis (SSc) and primary biliary cholangitis (PBC) with a focus on their co-occurrence as a clinically relevant overlap syndrome. This narrative review summarizes preclinical and clinical studies addressing SSc-PBC overlap.
Recent Findings: Genomic studies highlight shared susceptibility loci between SSc and PBC.