PMID- 20649818 OWN - NLM STAT- PubMed-not-MEDLINE DCOM- 20110714 LR - 20200929 IS - 1872-034X (Electronic) IS - 1386-6346 (Linking) VI - 40 IP - 8 DP - 2010 Aug TI - Clinical characteristics of patients with autoimmune hepatitis seropositive for anticentromere antibody. PG - 786-92 LID - 10.1111/j.1872-034X.2010.00684.x [doi] AB - AIM: Recent studies have revealed that primary biliary cirrhosis patients with anticentromere antibody (ACA) commonly develop portal hypertension. However, the clinical characteristics of autoimmune hepatitis (AIH) remain uncertain. We investigated the clinical features of patients with AIH seropositive for ACA (ACA-AIH), comparing them with those of patients with AIH seropositive for other immunofluorescent patterns of antinuclear antibodies (ANA) (other-AIH). METHODS: AIH was diagnosed on the basis of the scoring system proposed by the International Autoimmune Hepatitis Group. Seropositivity for ACA was determined by a discrete speckled pattern on HEp-2 cells by an immunofluorescent technique. The severity of histological grading and staging was evaluated by the histological activity index (HAI) score. RESULTS: Eight (17%) of 47 patients with AIH had ACA. No significant differences in age, sex, onset pattern of the disease, progression to hepatic failure and relapse rate were present between the ACA-AIH and other-AIH groups. The frequency of concurrent autoimmune diseases in ACA-AIH was significantly higher than that in other-AIH (75% vs 36%, P = 0.0406). Biochemical analysis revealed a significantly lower mean immunoglobulin G (IgG) level than that in other-AIH (2176 +/- 641 vs 3013 +/- 923 mg/dL, P = 0.0150). However, there were no differences in serum alanine aminotransferase levels, titers of ANA, HAI scores or the positive rate of human leukocyte antigen (HLA)-DR4 between the groups. CONCLUSION: These results suggest that the emergence of ACA is not a distinct entity of AIH, despite its clinical characteristics of a significantly higher frequency of concurrent autoimmune diseases and lower serum IgG levels. FAU - Himoto, Takashi AU - Himoto T AD - Departments of Gastroenterology and Neurology, Kagawa University School of Medicine, Kagawa, Japan. FAU - Murota, Masayuki AU - Murota M FAU - Yoneyama, Hirohito AU - Yoneyama H FAU - Deguchi, Akihiro AU - Deguchi A FAU - Kurokochi, Kazutaka AU - Kurokochi K FAU - Senda, Shoichi AU - Senda S FAU - Haba, Reiji AU - Haba R FAU - Watanabe, Seishiro AU - Watanabe S FAU - Nishioka, Mikio AU - Nishioka M FAU - Masaki, Tsutomu AU - Masaki T LA - eng PT - Journal Article PL - Netherlands TA - Hepatol Res JT - Hepatology research : the official journal of the Japan Society of Hepatology JID - 9711801 EDAT- 2010/07/24 06:00 MHDA- 2010/07/24 06:01 CRDT- 2010/07/24 06:00 PHST- 2010/07/24 06:00 [entrez] PHST- 2010/07/24 06:00 [pubmed] PHST- 2010/07/24 06:01 [medline] AID - HEP684 [pii] AID - 10.1111/j.1872-034X.2010.00684.x [doi] PST - ppublish SO - Hepatol Res. 2010 Aug;40(8):786-92. doi: 10.1111/j.1872-034X.2010.00684.x.