Risk Factors and Adverse Events Poorly Predict Infections and Hypogammaglobulinemia in Granulomatosis with Polyangiitis Patients Receiving Rituximab

Background. 29 GPA patients from the Northern Norway vasculitis disease registry received rituximab (RTX) induction and maintenance. 24% and 31% had, respectively, severe and chronic infections while 45% had hypogammaglobulinemia and 28% discontinued RTX due to hypogammaglobulinemia. The aim of the...

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Published in:Autoimmune Diseases
Main Author: Besada, Emilio
Format: Article in Journal/Newspaper
Language:English
Published: Hindawi Publishing Corporation 2016
Subjects:
Online Access:https://hdl.handle.net/10037/8940
https://doi.org/10.1155/2016/8095695
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author Besada, Emilio
author_facet Besada, Emilio
author_sort Besada, Emilio
collection University of Tromsø: Munin Open Research Archive
container_start_page 1
container_title Autoimmune Diseases
container_volume 2016
description Background. 29 GPA patients from the Northern Norway vasculitis disease registry received rituximab (RTX) induction and maintenance. 24% and 31% had, respectively, severe and chronic infections while 45% had hypogammaglobulinemia and 28% discontinued RTX due to hypogammaglobulinemia. The aim of the study was to examine how known predictors and adverse events interacted with adverse events using structural statistical methods. Methods. Five predictors (age, cyclophosphamide, total Ig and CD4/CD8 ratio prior RTX, and type of RTX maintenance regimen) and 4 adverse events (severe and chronic infections, hypogammaglobulinemia, and RTX discontinuation) were modeled in principal component and redundancy analyses. Results. The 5 predictors explained 51% of the variance of the GPA cohort. Models including cyclophosphamide exposure and total Ig level predicted best adverse events. However total Ig level has low R squared. The 2 best combinations of adverse events explained 13% of the variance of the predictors and adverse events. Only chronic infections were associated with combination of all adverse events (P= 0.014). Hypogammaglobulinemia did not seem associated with the other adverse events. Conclusions. Traditional risk factors for infections and hypogammaglobulinemia seemed to poorly predict adverse events in our GPA cohort.
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Autoimmune Diseases 2016, 2016: 8095695
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spelling ftunivtroemsoe:oai:munin.uit.no:10037/8940 2025-04-13T14:24:31+00:00 Risk Factors and Adverse Events Poorly Predict Infections and Hypogammaglobulinemia in Granulomatosis with Polyangiitis Patients Receiving Rituximab Besada, Emilio 2016 https://hdl.handle.net/10037/8940 https://doi.org/10.1155/2016/8095695 eng eng Hindawi Publishing Corporation http://dx.doi.org/10.1155/2016/8095695 Autoimmune Diseases 2016, 2016: 8095695 FRIDAID 1317022 doi:10.1155/2016/8095695 https://hdl.handle.net/10037/8940 openAccess VDP::Medisinske fag: 700::Klinisk medisinske fag: 750::Reumatologi: 759 VDP::Midical sciences: 700::Clinical medical sciences: 750::Rheumatology: 759 Journal article Tidsskriftartikkel Peer reviewed 2016 ftunivtroemsoe https://doi.org/10.1155/2016/8095695 2025-03-14T05:17:55Z Background. 29 GPA patients from the Northern Norway vasculitis disease registry received rituximab (RTX) induction and maintenance. 24% and 31% had, respectively, severe and chronic infections while 45% had hypogammaglobulinemia and 28% discontinued RTX due to hypogammaglobulinemia. The aim of the study was to examine how known predictors and adverse events interacted with adverse events using structural statistical methods. Methods. Five predictors (age, cyclophosphamide, total Ig and CD4/CD8 ratio prior RTX, and type of RTX maintenance regimen) and 4 adverse events (severe and chronic infections, hypogammaglobulinemia, and RTX discontinuation) were modeled in principal component and redundancy analyses. Results. The 5 predictors explained 51% of the variance of the GPA cohort. Models including cyclophosphamide exposure and total Ig level predicted best adverse events. However total Ig level has low R squared. The 2 best combinations of adverse events explained 13% of the variance of the predictors and adverse events. Only chronic infections were associated with combination of all adverse events (P= 0.014). Hypogammaglobulinemia did not seem associated with the other adverse events. Conclusions. Traditional risk factors for infections and hypogammaglobulinemia seemed to poorly predict adverse events in our GPA cohort. Article in Journal/Newspaper Northern Norway University of Tromsø: Munin Open Research Archive Norway Autoimmune Diseases 2016 1 6
spellingShingle VDP::Medisinske fag: 700::Klinisk medisinske fag: 750::Reumatologi: 759
VDP::Midical sciences: 700::Clinical medical sciences: 750::Rheumatology: 759
Besada, Emilio
Risk Factors and Adverse Events Poorly Predict Infections and Hypogammaglobulinemia in Granulomatosis with Polyangiitis Patients Receiving Rituximab
title Risk Factors and Adverse Events Poorly Predict Infections and Hypogammaglobulinemia in Granulomatosis with Polyangiitis Patients Receiving Rituximab
title_full Risk Factors and Adverse Events Poorly Predict Infections and Hypogammaglobulinemia in Granulomatosis with Polyangiitis Patients Receiving Rituximab
title_fullStr Risk Factors and Adverse Events Poorly Predict Infections and Hypogammaglobulinemia in Granulomatosis with Polyangiitis Patients Receiving Rituximab
title_full_unstemmed Risk Factors and Adverse Events Poorly Predict Infections and Hypogammaglobulinemia in Granulomatosis with Polyangiitis Patients Receiving Rituximab
title_short Risk Factors and Adverse Events Poorly Predict Infections and Hypogammaglobulinemia in Granulomatosis with Polyangiitis Patients Receiving Rituximab
title_sort risk factors and adverse events poorly predict infections and hypogammaglobulinemia in granulomatosis with polyangiitis patients receiving rituximab
topic VDP::Medisinske fag: 700::Klinisk medisinske fag: 750::Reumatologi: 759
VDP::Midical sciences: 700::Clinical medical sciences: 750::Rheumatology: 759
topic_facet VDP::Medisinske fag: 700::Klinisk medisinske fag: 750::Reumatologi: 759
VDP::Midical sciences: 700::Clinical medical sciences: 750::Rheumatology: 759
url https://hdl.handle.net/10037/8940
https://doi.org/10.1155/2016/8095695