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Bacterial infections in a pediatric cohort of primary and acquired complement deficiencies

BACKGROUND: Acquired complement deficiency can occur in the setting of autoimmune syndromes, such as systemic lupus erythematosus (SLE), with very low or, occasionally, undetectable C3 levels. Based on inherited complement defects, patients with transiently low complement may be at similar risk for...

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Autores principales: Al-Shaikhly, Taha, Hayward, Kristen, Basiaga, Matthew L., Allenspach, Eric J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7513499/
https://www.ncbi.nlm.nih.gov/pubmed/32972440
http://dx.doi.org/10.1186/s12969-020-00467-0
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author Al-Shaikhly, Taha
Hayward, Kristen
Basiaga, Matthew L.
Allenspach, Eric J.
author_facet Al-Shaikhly, Taha
Hayward, Kristen
Basiaga, Matthew L.
Allenspach, Eric J.
author_sort Al-Shaikhly, Taha
collection PubMed
description BACKGROUND: Acquired complement deficiency can occur in the setting of autoimmune syndromes, such as systemic lupus erythematosus (SLE), with very low or, occasionally, undetectable C3 levels. Based on inherited complement defects, patients with transiently low complement may be at similar risk for serious bacterial infection, but the degree of risk related to C3 level and temporal association is unknown. METHODS: We performed a retrospective study including pediatric patients with undetectable total complement activity or absent individual complement components measured at our institution from 2002 to 2018. We assessed annual rate of serious bacterial infection (SBI) defined as requiring hospitalization and/or parenteral antibiotics by manual chart review. Among included SLE patients, we assessed the 30-day probability of SBI for given C3 measurements using a logistic regression model to determine risk. Primary complement deficiency was analyzed for SBI rate as comparison. Covariates included age, level of immune suppression and history of lupus nephritis. RESULTS: Acquired complement deficiency secondary to SLE-related disease [n = 44] was the most common underlying diagnosis associated with depressed complement levels and were compared to a cohort of primary complement deficient patients [n = 18]. SBI per 100 person-years and cohort demographics were described in parallel. Our logistic regression analysis of pediatric patients with SLE showed low C3 level was temporally associated with having an SBI event. Given equivalent immunosuppression, patients with an SBI had lower C3 levels at the beginning of the observation period relative to patients without SBI. CONCLUSION: Pediatric patients with the diagnosis of SLE can develop very low C3 levels that associate with risk of serious bacterial infection comparable to that of patients with primary complement deficiency. Patients prone to severe complement consumption may particularly be at risk.
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spelling pubmed-75134992020-09-25 Bacterial infections in a pediatric cohort of primary and acquired complement deficiencies Al-Shaikhly, Taha Hayward, Kristen Basiaga, Matthew L. Allenspach, Eric J. Pediatr Rheumatol Online J Research Article BACKGROUND: Acquired complement deficiency can occur in the setting of autoimmune syndromes, such as systemic lupus erythematosus (SLE), with very low or, occasionally, undetectable C3 levels. Based on inherited complement defects, patients with transiently low complement may be at similar risk for serious bacterial infection, but the degree of risk related to C3 level and temporal association is unknown. METHODS: We performed a retrospective study including pediatric patients with undetectable total complement activity or absent individual complement components measured at our institution from 2002 to 2018. We assessed annual rate of serious bacterial infection (SBI) defined as requiring hospitalization and/or parenteral antibiotics by manual chart review. Among included SLE patients, we assessed the 30-day probability of SBI for given C3 measurements using a logistic regression model to determine risk. Primary complement deficiency was analyzed for SBI rate as comparison. Covariates included age, level of immune suppression and history of lupus nephritis. RESULTS: Acquired complement deficiency secondary to SLE-related disease [n = 44] was the most common underlying diagnosis associated with depressed complement levels and were compared to a cohort of primary complement deficient patients [n = 18]. SBI per 100 person-years and cohort demographics were described in parallel. Our logistic regression analysis of pediatric patients with SLE showed low C3 level was temporally associated with having an SBI event. Given equivalent immunosuppression, patients with an SBI had lower C3 levels at the beginning of the observation period relative to patients without SBI. CONCLUSION: Pediatric patients with the diagnosis of SLE can develop very low C3 levels that associate with risk of serious bacterial infection comparable to that of patients with primary complement deficiency. Patients prone to severe complement consumption may particularly be at risk. BioMed Central 2020-09-24 /pmc/articles/PMC7513499/ /pubmed/32972440 http://dx.doi.org/10.1186/s12969-020-00467-0 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Al-Shaikhly, Taha
Hayward, Kristen
Basiaga, Matthew L.
Allenspach, Eric J.
Bacterial infections in a pediatric cohort of primary and acquired complement deficiencies
title Bacterial infections in a pediatric cohort of primary and acquired complement deficiencies
title_full Bacterial infections in a pediatric cohort of primary and acquired complement deficiencies
title_fullStr Bacterial infections in a pediatric cohort of primary and acquired complement deficiencies
title_full_unstemmed Bacterial infections in a pediatric cohort of primary and acquired complement deficiencies
title_short Bacterial infections in a pediatric cohort of primary and acquired complement deficiencies
title_sort bacterial infections in a pediatric cohort of primary and acquired complement deficiencies
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7513499/
https://www.ncbi.nlm.nih.gov/pubmed/32972440
http://dx.doi.org/10.1186/s12969-020-00467-0
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