Evidence map›Paper›PMID 41892013›Full record

ArticleDiseases (Basel, Switzerland)2026

Clinical and Demographic Features of Primary Biliary Cholangitis in Kazakhstan.

Aisulu Gainutdin, Alexander Nersesov, Komori Atsumasa, Aigul Raissova, Saltanat Madenova, Laura Yerdaliyeva, Dinara Suleimenova, Balday Issenova

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Article in Diseases (Basel, Switzerland), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Aisulu GainutdinAsfendiyarov Kazakh National Medical University, Almaty 05000, Kazakhstan.
Alexander NersesovAsfendiyarov Kazakh National Medical University, Almaty 05000, Kazakhstan.ORCID 0000-0002-8601-3966
Komori AtsumasaNHO Nagasaki Medical Center, Nagasaki 856-8562 , Japan.
Aigul RaissovaAsfendiyarov Kazakh National Medical University, Almaty 05000, Kazakhstan.
Saltanat MadenovaAsfendiyarov Kazakh National Medical University, Almaty 05000, Kazakhstan.
Laura YerdaliyevaAsfendiyarov Kazakh National Medical University, Almaty 05000, Kazakhstan.
Dinara SuleimenovaAsfendiyarov Kazakh National Medical University, Almaty 05000, Kazakhstan.
Balday IssenovaAsfendiyarov Kazakh National Medical University, Almaty 05000, Kazakhstan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

objectivesPrimary biliary cholangitis (PBC) is a chronic immune-mediated cholestatic liver disease with increasing global prevalence. However, data on this disease from Central Asia are lacking. We aimed to describe the clinical, serological, and treatment characteristics of PBC patients in Kazakhstan.

methodsThis study was a multicenter, retrospective, observational study including adults diagnosed with PBC between 2014 and 2022 across seven hepatology centers in Kazakhstan. Clinical presentation, laboratory parameters, autoimmune comorbidities, liver disease severity, and ursodeoxycholic acid (UDCA) treatment response were assessed. Biochemical response at 1 year was evaluated using Paris-1 and Barcelona criteria.

resultsA total of 230 patients were included; 93.9% were female and 91.3% were of Asian ethnicity, with a median age at diagnosis of 53 years. Cirrhosis was present at diagnosis in 50.2% of the patients. PBC with autoimmune hepatitis (AIH) features was identified in 56.1% of the patients and was associated with higher rates of cirrhosis, portal hypertension complications, antinuclear antibody (ANA) positivity, and higher elastography indices compared with isolated PBC. Overall, approximately 55% of the patients achieved a biochemical response to UDCA at 1 year, with similar response rates between patients with PBC and those with PBC with AIH features.

conclusionsThis first comprehensive study of PBC in Kazakhstan demonstrates late disease presentation with a high burden of cirrhosis and frequent AIH features. Despite advanced disease, about half of the patients achieved biochemical remission on UDCA. These findings underscore the need for earlier diagnosis and optimized management strategies for PBC in Kazakhstan and similar settings in Central Asia.

Indexed as

autoimmune hepatitisepidemiologyKazakhstanprimary biliary cholangitis

Identifiers

PMID41892013
PMCPMC13025080

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.