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Impact and longevity of measles-associated immune suppression: a matched cohort study using data from the THIN general practice database in the UK
OBJECTIVE: To test the hypothesis that measles infection increases the incidence of non-measles infectious diseases over a prolonged period of time. DESIGN: A population-based matched cohort study. DATA SOURCES: This study examined children aged 1–15 years in The Health Improvement Network UK genera...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6231568/ https://www.ncbi.nlm.nih.gov/pubmed/30413497 http://dx.doi.org/10.1136/bmjopen-2017-021465 |
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author | Gadroen, Kartini Dodd, Caitlin N Masclee, Gwen M C de Ridder, Maria A J Weibel, Daniel Mina, Michael J Grenfell, Bryan T Sturkenboom, Miriam C J M van de Vijver, David A M C de Swart, Rik L |
author_facet | Gadroen, Kartini Dodd, Caitlin N Masclee, Gwen M C de Ridder, Maria A J Weibel, Daniel Mina, Michael J Grenfell, Bryan T Sturkenboom, Miriam C J M van de Vijver, David A M C de Swart, Rik L |
author_sort | Gadroen, Kartini |
collection | PubMed |
description | OBJECTIVE: To test the hypothesis that measles infection increases the incidence of non-measles infectious diseases over a prolonged period of time. DESIGN: A population-based matched cohort study. DATA SOURCES: This study examined children aged 1–15 years in The Health Improvement Network UK general practice medical records database. Participants included 2228 patients diagnosed with measles between 1990 and 2014, which were matched on age, sex, general practitioner practice and calendar year with 19 930 children without measles. All controls had received at least one measles vaccination. Children with a history of immune-compromising conditions or with immune-suppressive treatment were excluded. PRIMARY OUTCOME MEASURES: Incidence rate ratio (IRR) of infections, anti-infective prescriptions and all-cause hospitalisations following measles in predetermined periods using multivariate analysis to adjust for confounding variables. RESULTS: In children with measles, the incidence rate for non-measles infectious disease was significantly increased in each time period assessed up to 5 years postmeasles: 43% in the first month (IRR: 1.43; 95% CI 1.22 to 1.68), 22% from month one to the first year (IRR: 1.22; 95% CI 1.14 to 1.31), 10% from year 1 to 2.5 years (IRR: 1.10; 95% CI 1.02 to 1.19) and 15% (IRR: 1.15; 95% CI 1.06 to 1.25) in years 2.5 to 5 years of follow-up. Children with measles were more than three times as likely to receive an anti-infective prescription in the first month and 15%–24% more likely between the first month and 5 years. The rate of hospitalisation in children with measles was increased only in the month following diagnosis but not thereafter (IRR: 2.83; 95% CI 1.72 to 4.67). CONCLUSION: Following measles, children had increased rates of diagnosed infections, requiring increased prescribing of antimicrobial therapies. This population-based matched cohort study supports the hypothesis that measles has a prolonged impact on host resistance to non-measles infectious diseases. |
format | Online Article Text |
id | pubmed-6231568 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-62315682018-12-11 Impact and longevity of measles-associated immune suppression: a matched cohort study using data from the THIN general practice database in the UK Gadroen, Kartini Dodd, Caitlin N Masclee, Gwen M C de Ridder, Maria A J Weibel, Daniel Mina, Michael J Grenfell, Bryan T Sturkenboom, Miriam C J M van de Vijver, David A M C de Swart, Rik L BMJ Open Infectious Diseases OBJECTIVE: To test the hypothesis that measles infection increases the incidence of non-measles infectious diseases over a prolonged period of time. DESIGN: A population-based matched cohort study. DATA SOURCES: This study examined children aged 1–15 years in The Health Improvement Network UK general practice medical records database. Participants included 2228 patients diagnosed with measles between 1990 and 2014, which were matched on age, sex, general practitioner practice and calendar year with 19 930 children without measles. All controls had received at least one measles vaccination. Children with a history of immune-compromising conditions or with immune-suppressive treatment were excluded. PRIMARY OUTCOME MEASURES: Incidence rate ratio (IRR) of infections, anti-infective prescriptions and all-cause hospitalisations following measles in predetermined periods using multivariate analysis to adjust for confounding variables. RESULTS: In children with measles, the incidence rate for non-measles infectious disease was significantly increased in each time period assessed up to 5 years postmeasles: 43% in the first month (IRR: 1.43; 95% CI 1.22 to 1.68), 22% from month one to the first year (IRR: 1.22; 95% CI 1.14 to 1.31), 10% from year 1 to 2.5 years (IRR: 1.10; 95% CI 1.02 to 1.19) and 15% (IRR: 1.15; 95% CI 1.06 to 1.25) in years 2.5 to 5 years of follow-up. Children with measles were more than three times as likely to receive an anti-infective prescription in the first month and 15%–24% more likely between the first month and 5 years. The rate of hospitalisation in children with measles was increased only in the month following diagnosis but not thereafter (IRR: 2.83; 95% CI 1.72 to 4.67). CONCLUSION: Following measles, children had increased rates of diagnosed infections, requiring increased prescribing of antimicrobial therapies. This population-based matched cohort study supports the hypothesis that measles has a prolonged impact on host resistance to non-measles infectious diseases. BMJ Publishing Group 2018-11-08 /pmc/articles/PMC6231568/ /pubmed/30413497 http://dx.doi.org/10.1136/bmjopen-2017-021465 Text en © Author(s) (or their employer(s)) 2018. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Infectious Diseases Gadroen, Kartini Dodd, Caitlin N Masclee, Gwen M C de Ridder, Maria A J Weibel, Daniel Mina, Michael J Grenfell, Bryan T Sturkenboom, Miriam C J M van de Vijver, David A M C de Swart, Rik L Impact and longevity of measles-associated immune suppression: a matched cohort study using data from the THIN general practice database in the UK |
title | Impact and longevity of measles-associated immune suppression: a matched cohort study using data from the THIN general practice database in the UK |
title_full | Impact and longevity of measles-associated immune suppression: a matched cohort study using data from the THIN general practice database in the UK |
title_fullStr | Impact and longevity of measles-associated immune suppression: a matched cohort study using data from the THIN general practice database in the UK |
title_full_unstemmed | Impact and longevity of measles-associated immune suppression: a matched cohort study using data from the THIN general practice database in the UK |
title_short | Impact and longevity of measles-associated immune suppression: a matched cohort study using data from the THIN general practice database in the UK |
title_sort | impact and longevity of measles-associated immune suppression: a matched cohort study using data from the thin general practice database in the uk |
topic | Infectious Diseases |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6231568/ https://www.ncbi.nlm.nih.gov/pubmed/30413497 http://dx.doi.org/10.1136/bmjopen-2017-021465 |
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