Monoclonal gammopathy in autoimmune diseases : Analysis and follow-up of 160 cases in a tertiary center in China

Copyright © 2021 Elsevier Inc. All rights reserved.

Détails bibliographiques
Publié dans:Clinical immunology (Orlando, Fla.). - 1999. - 234(2022) vom: 02. Jan., Seite 108909
Auteur principal: Liu, Huazhen (Auteur)
Autres auteurs: Li, Pengchong, Li, Ketian, Zhou, Ziyue, Zhou, Yangzhong, Leng, Xiaomei, Zhao, Lidan, Zhang, Xuan
Format: Article en ligne
Langue:English
Publié: 2022
Accès à la collection:Clinical immunology (Orlando, Fla.)
Sujets:Journal Article Research Support, Non-U.S. Gov't Autoimmune disease Hematological neoplasm Monoclonal gammopathy Prognosis Myeloma Proteins multiple myeloma M-proteins
Description
Résumé:Copyright © 2021 Elsevier Inc. All rights reserved.
Monoclonal gammopathy (MG) is common in autoimmune diseases (AID), but its progression to hematological neoplasm (HN) and the predictors for the progression are unclear. Patients diagnosed with AID and MG in our hospital from January 2010 to June 2017 were reviewed and followed. Cox proportional hazard regression analysis was applied. Of 160 patients with AID and MG, the most common AID was primary Sjӧgren's syndrome (37, 23.1%). Thirty-nine (24.4%) patients developed HN during follow-up (median: 3.7 years, IQR: 0.3-5.5 years). The cumulative probability of HN progression was 21.8% at one year and 29.3% at six years after the finding of MG. High levels of monoclonal protein (> 14.35% of total serum protein) (HR 11.71, 95%CI: 5.37-25.54), significant weight loss (HR 6.24, 95%CI: 2.87-13.59), and reduction of other types of immunoglobulins (HR 3.02, 95%CI: 1.40-6.48) are independent risk indicators for HN whose presence warrants vigorous follow-up and monitoring
Description:Date Completed 25.02.2022
Date Revised 25.02.2022
published: Print-Electronic
Citation Status MEDLINE
ISSN:1521-7035
DOI:10.1016/j.clim.2021.108909