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Increased Risk of Invasive Meningococcal Disease Associated with Primary and Secondary Immunodeficiency

BACKGROUND: Risk of invasive meningococcal disease (IMD) is increased for persistent complement deficiency and HIV infection. However, risk associated with other primary and secondary immunodeficiency is unknown. METHODS: Nationwide case–control study of adults aged >18 years. Cases and matched c...

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Autores principales: Lundbo, Lene Fogt, Harboe, Zitta Barrella, Smith-Hansen, Lars, Benfield, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5631989/
http://dx.doi.org/10.1093/ofid/ofx162.018
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author Lundbo, Lene Fogt
Harboe, Zitta Barrella
Smith-Hansen, Lars
Benfield, Thomas
author_facet Lundbo, Lene Fogt
Harboe, Zitta Barrella
Smith-Hansen, Lars
Benfield, Thomas
author_sort Lundbo, Lene Fogt
collection PubMed
description BACKGROUND: Risk of invasive meningococcal disease (IMD) is increased for persistent complement deficiency and HIV infection. However, risk associated with other primary and secondary immunodeficiency is unknown. METHODS: Nationwide case–control study of adults aged >18 years. Cases and matched controls were identified by registry linkage. Primary and secondary immunodeficiencies diagnosed prior to IMD were based on International Classification of Disease (ICD), eight or tenth revision. Odds ratios (OR) with 95% confidence intervals (CI) were estimated by conditional logistic regression after adjustment for sex, age, and the year of IMD. RESULTS: We identified 2,179 IMD cases (46% male) with a median age of 44 years (interquartile range: 24–63 years). Increased risk of IMD was associated with HIV infection (OR 10.03 [95% confidence interval (CI), 2.91–34.66]), splenectomy/splenic resection (OR 6.88 [95% CI, 3.9–14.82]), solid organ transplantation (SOT) (OR 20.00 [95% CI, 5.00–79.96]), hemolytic anemia (OR 7.78 [95% CI, 2.90–20.90]), antibody deficiency (OR 6.67 [1.11–39.90]) and autoimmune diseases (OR 1.80 [95% CI, 1.44–2.14]). Primary immunodeficiency overall was not associated with an increased risk (OR 1.43 (95% CI, 0.61–3.36)). CONCLUSION: This large study of Danish adults with IMD over four decades showed an increased risk of IMD associated with HIV infection, SOT, asplenia, hemolytic anemia, antibody deficiency, and autoimmune disease ranging from 2- to a 20-fold increased risk. Vaccination may be warranted in these populations. DISCLOSURES: Z. Barrella Harboe, Pfizer: independent physician, Travel grants.
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spelling pubmed-56319892017-11-07 Increased Risk of Invasive Meningococcal Disease Associated with Primary and Secondary Immunodeficiency Lundbo, Lene Fogt Harboe, Zitta Barrella Smith-Hansen, Lars Benfield, Thomas Open Forum Infect Dis Abstracts BACKGROUND: Risk of invasive meningococcal disease (IMD) is increased for persistent complement deficiency and HIV infection. However, risk associated with other primary and secondary immunodeficiency is unknown. METHODS: Nationwide case–control study of adults aged >18 years. Cases and matched controls were identified by registry linkage. Primary and secondary immunodeficiencies diagnosed prior to IMD were based on International Classification of Disease (ICD), eight or tenth revision. Odds ratios (OR) with 95% confidence intervals (CI) were estimated by conditional logistic regression after adjustment for sex, age, and the year of IMD. RESULTS: We identified 2,179 IMD cases (46% male) with a median age of 44 years (interquartile range: 24–63 years). Increased risk of IMD was associated with HIV infection (OR 10.03 [95% confidence interval (CI), 2.91–34.66]), splenectomy/splenic resection (OR 6.88 [95% CI, 3.9–14.82]), solid organ transplantation (SOT) (OR 20.00 [95% CI, 5.00–79.96]), hemolytic anemia (OR 7.78 [95% CI, 2.90–20.90]), antibody deficiency (OR 6.67 [1.11–39.90]) and autoimmune diseases (OR 1.80 [95% CI, 1.44–2.14]). Primary immunodeficiency overall was not associated with an increased risk (OR 1.43 (95% CI, 0.61–3.36)). CONCLUSION: This large study of Danish adults with IMD over four decades showed an increased risk of IMD associated with HIV infection, SOT, asplenia, hemolytic anemia, antibody deficiency, and autoimmune disease ranging from 2- to a 20-fold increased risk. Vaccination may be warranted in these populations. DISCLOSURES: Z. Barrella Harboe, Pfizer: independent physician, Travel grants. Oxford University Press 2017-10-04 /pmc/articles/PMC5631989/ http://dx.doi.org/10.1093/ofid/ofx162.018 Text en © The Author 2017. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Abstracts
Lundbo, Lene Fogt
Harboe, Zitta Barrella
Smith-Hansen, Lars
Benfield, Thomas
Increased Risk of Invasive Meningococcal Disease Associated with Primary and Secondary Immunodeficiency
title Increased Risk of Invasive Meningococcal Disease Associated with Primary and Secondary Immunodeficiency
title_full Increased Risk of Invasive Meningococcal Disease Associated with Primary and Secondary Immunodeficiency
title_fullStr Increased Risk of Invasive Meningococcal Disease Associated with Primary and Secondary Immunodeficiency
title_full_unstemmed Increased Risk of Invasive Meningococcal Disease Associated with Primary and Secondary Immunodeficiency
title_short Increased Risk of Invasive Meningococcal Disease Associated with Primary and Secondary Immunodeficiency
title_sort increased risk of invasive meningococcal disease associated with primary and secondary immunodeficiency
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5631989/
http://dx.doi.org/10.1093/ofid/ofx162.018
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