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Epidemiology of chronic inflammatory demyelinating polyradiculoneuropathy in The Netherlands

Chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) is a rare but disabling disorder that often requires long‐term immunomodulatory treatment. Background incidence rates and prevalence and risk factors for developing CIDP are still poorly defined. In the current study, we used a longitu...

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Autores principales: Broers, Merel C., de Wilde, Marcel, Lingsma, Hester F., van der Lei, Johan, Verhamme, Katia M.C., Jacobs, Bart C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wiley Periodicals, Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9545265/
https://www.ncbi.nlm.nih.gov/pubmed/35567759
http://dx.doi.org/10.1111/jns.12502
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author Broers, Merel C.
de Wilde, Marcel
Lingsma, Hester F.
van der Lei, Johan
Verhamme, Katia M.C.
Jacobs, Bart C.
author_facet Broers, Merel C.
de Wilde, Marcel
Lingsma, Hester F.
van der Lei, Johan
Verhamme, Katia M.C.
Jacobs, Bart C.
author_sort Broers, Merel C.
collection PubMed
description Chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) is a rare but disabling disorder that often requires long‐term immunomodulatory treatment. Background incidence rates and prevalence and risk factors for developing CIDP are still poorly defined. In the current study, we used a longitudinal population‐based cohort study in The Netherlands to assess these rates and demographic factors and comorbidity associated with CIDP. We determined the incidence rate and prevalence of CIDP between 2008 and 2017 and the occurrence of potential risk factors in a retrospective Dutch cohort study using the Integrated Primary Care Information (IPCI) database. Cases were defined as CIDP if the diagnosis of CIDP was described in the electronic medical file. In a source population of 928 030 persons with a contributing follow‐up of 3 525 686 person‐years, we identified 65 patients diagnosed with CIDP. The overall incidence rate was 0.68 per 100 000 person‐years (95% CI 0.45‐0.99). The overall prevalence was 7.00 per 100 000 individuals (95% CI 5.41‐8.93). The overall incidence rate was higher in men compared to woman (IRR 3.00, 95% CI 1.27‐7.11), and higher in elderly of 50 years or older compared with people <50 years of age (IRR 17 95% CI 4‐73). Twenty percent of CIDP cases had DM and 9% a co‐existing other auto‐immune disease. These background rates are important to monitor changes in the frequency of CIDP following infectious disease outbreaks, identify potential risk factors, and to estimate the social and economic burden of CIDP.
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spelling pubmed-95452652022-10-14 Epidemiology of chronic inflammatory demyelinating polyradiculoneuropathy in The Netherlands Broers, Merel C. de Wilde, Marcel Lingsma, Hester F. van der Lei, Johan Verhamme, Katia M.C. Jacobs, Bart C. J Peripher Nerv Syst Research Reports Chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) is a rare but disabling disorder that often requires long‐term immunomodulatory treatment. Background incidence rates and prevalence and risk factors for developing CIDP are still poorly defined. In the current study, we used a longitudinal population‐based cohort study in The Netherlands to assess these rates and demographic factors and comorbidity associated with CIDP. We determined the incidence rate and prevalence of CIDP between 2008 and 2017 and the occurrence of potential risk factors in a retrospective Dutch cohort study using the Integrated Primary Care Information (IPCI) database. Cases were defined as CIDP if the diagnosis of CIDP was described in the electronic medical file. In a source population of 928 030 persons with a contributing follow‐up of 3 525 686 person‐years, we identified 65 patients diagnosed with CIDP. The overall incidence rate was 0.68 per 100 000 person‐years (95% CI 0.45‐0.99). The overall prevalence was 7.00 per 100 000 individuals (95% CI 5.41‐8.93). The overall incidence rate was higher in men compared to woman (IRR 3.00, 95% CI 1.27‐7.11), and higher in elderly of 50 years or older compared with people <50 years of age (IRR 17 95% CI 4‐73). Twenty percent of CIDP cases had DM and 9% a co‐existing other auto‐immune disease. These background rates are important to monitor changes in the frequency of CIDP following infectious disease outbreaks, identify potential risk factors, and to estimate the social and economic burden of CIDP. Wiley Periodicals, Inc. 2022-05-29 2022-09 /pmc/articles/PMC9545265/ /pubmed/35567759 http://dx.doi.org/10.1111/jns.12502 Text en © 2022 The Authors. Journal of the Peripheral Nervous System published by Wiley Periodicals LLC on behalf of Peripheral Nerve Society. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Reports
Broers, Merel C.
de Wilde, Marcel
Lingsma, Hester F.
van der Lei, Johan
Verhamme, Katia M.C.
Jacobs, Bart C.
Epidemiology of chronic inflammatory demyelinating polyradiculoneuropathy in The Netherlands
title Epidemiology of chronic inflammatory demyelinating polyradiculoneuropathy in The Netherlands
title_full Epidemiology of chronic inflammatory demyelinating polyradiculoneuropathy in The Netherlands
title_fullStr Epidemiology of chronic inflammatory demyelinating polyradiculoneuropathy in The Netherlands
title_full_unstemmed Epidemiology of chronic inflammatory demyelinating polyradiculoneuropathy in The Netherlands
title_short Epidemiology of chronic inflammatory demyelinating polyradiculoneuropathy in The Netherlands
title_sort epidemiology of chronic inflammatory demyelinating polyradiculoneuropathy in the netherlands
topic Research Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9545265/
https://www.ncbi.nlm.nih.gov/pubmed/35567759
http://dx.doi.org/10.1111/jns.12502
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