Back to Search Start Over

Immunoglobulin M: A Neglected Serum Biomarker in Treatment‐Naive Primary Biliary Cholangitis With Normal Alkaline Phosphatase.

Authors :
Ding, Dawei
Xuan, Guoyun
Hu, Yinan
Yu, Jiahao
Liu, Yansheng
Guo, Guanya
Ma, Shuoyi
Yang, Fangfang
Tian, Siyuan
Ma, Gang
Chen, Ling
Zhou, Xinmin
Shang, Yulong
Han, Ying
Source :
Hepatology Communications; Jun2022, Vol. 6 Issue 6, p1403-1412, 10p
Publication Year :
2022

Abstract

The diagnosis of primary biliary cholangitis (PBC) in patients with seropositive anti‐mitochondrial antibody (AMA) but normal alkaline phosphatase (ALP) depends on a liver biopsy. We aimed to reveal potential serum biomarkers that could suggest the necessity of a liver biopsy in such patients. Retrospective analysis was performed. Subjects who were treatment naive with seropositive AMA but normal ALP and who underwent at least one liver biopsy between 2008 and 2020 were included in this study. Histologic biopsies were evaluated by two experienced pathologists blinded to the serum tests. A total of 115 patients who were treatment naive were included in this study. Of these, 77 patients (67%) exhibited histologic PBC features and nonspecific histologic features were found in the remaining 38 (33%) patients. Multivariate analysis suggested that baseline serum immunoglobulin M (IgM) >0.773 × upper limit of normal (ULN) (P < 0.001) and age >42 years (P = 0.002) were associated with the diagnosis of PBC through liver biopsies. A significant decrease in the median levels of gamma‐glutamyl transpeptidase (GGT) and IgM was found in 54 patients with PBC who received ursodeoxycholic acid (UDCA). Conclusion: For patients who were treatment naive with seropositive AMA but normal ALP, baseline serum IgM >0.773 × ULN and age >42 years were the factors that strongly suggested a diagnosis of PBC. In these patients receiving UDCA, a dynamic monitoring of GGT and IgM might be helpful in evaluating therapeutic responses. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
2471254X
Volume :
6
Issue :
6
Database :
Complementary Index
Journal :
Hepatology Communications
Publication Type :
Academic Journal
Accession number :
157112301
Full Text :
https://doi.org/10.1002/hep4.1907