Cargando…

Celiac disease and Down syndrome mortality: a nationwide cohort study

BACKGROUND: Individuals with Down syndrome (DS) have increased mortality and are also at increased risk of celiac disease (CD). It is unknown if CD influences mortality in DS. In this study we examined the risk of death in individuals with DS according to celiac status. METHODS: In this nationwide p...

Descripción completa

Detalles Bibliográficos
Autores principales: Ludvigsson, Jonas F., Lebwohl, Benjamin, Green, Peter H. R., Chung, Wendy K., Mårild, Karl
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5282819/
https://www.ncbi.nlm.nih.gov/pubmed/28143429
http://dx.doi.org/10.1186/s12887-017-0801-4
_version_ 1782503399809351680
author Ludvigsson, Jonas F.
Lebwohl, Benjamin
Green, Peter H. R.
Chung, Wendy K.
Mårild, Karl
author_facet Ludvigsson, Jonas F.
Lebwohl, Benjamin
Green, Peter H. R.
Chung, Wendy K.
Mårild, Karl
author_sort Ludvigsson, Jonas F.
collection PubMed
description BACKGROUND: Individuals with Down syndrome (DS) have increased mortality and are also at increased risk of celiac disease (CD). It is unknown if CD influences mortality in DS. In this study we examined the risk of death in individuals with DS according to celiac status. METHODS: In this nationwide population-based cohort study, we first identified individuals with CD (diagnosed 1969–2008) through small intestinal biopsy report data showing villous atrophy (Marsh stage III) from Sweden’s 28 pathology departments. Celiac individuals were then matched with up to five reference individuals from the general population. In these cohorts we identified individuals with DS using International Classification of Disease codes (ICD) registered in the Swedish Patient Register (includes inpatients and hospital-based outpatients), the Medical Birth Register, and the Register of Congenital Malformations. Of 29,096 individuals with CD, 201 (0.7%) had DS compared to 124 of the 144,522 reference individuals (0.09%). Data on mortality were obtained from the Swedish Cause of Death Registry. Hazard ratios (HRs) for death were calculated using Cox regression. RESULTS: During follow-up, there were seven deaths among individuals with DS and CD (7/201, 3.5%) as compared with 14 deaths among DS individuals without a record of CD (14/124, 11.3%). Adjusting for potential confounders, CD did not influence the risk of death in DS (HR = 1.36; 95%CI = 0.33–5.59). Cardiovascular death occurred in two individuals with CD and three individuals without CD, while death from malignancy occurred in one individual with CD and two individuals without CD. CONCLUSION: While both DS and CD have been linked to increased risk of death, this study found no excess mortality in DS patients with a concurrent diagnosis of CD, however confidence intervals were wide. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12887-017-0801-4) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-5282819
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-52828192017-02-03 Celiac disease and Down syndrome mortality: a nationwide cohort study Ludvigsson, Jonas F. Lebwohl, Benjamin Green, Peter H. R. Chung, Wendy K. Mårild, Karl BMC Pediatr Research Article BACKGROUND: Individuals with Down syndrome (DS) have increased mortality and are also at increased risk of celiac disease (CD). It is unknown if CD influences mortality in DS. In this study we examined the risk of death in individuals with DS according to celiac status. METHODS: In this nationwide population-based cohort study, we first identified individuals with CD (diagnosed 1969–2008) through small intestinal biopsy report data showing villous atrophy (Marsh stage III) from Sweden’s 28 pathology departments. Celiac individuals were then matched with up to five reference individuals from the general population. In these cohorts we identified individuals with DS using International Classification of Disease codes (ICD) registered in the Swedish Patient Register (includes inpatients and hospital-based outpatients), the Medical Birth Register, and the Register of Congenital Malformations. Of 29,096 individuals with CD, 201 (0.7%) had DS compared to 124 of the 144,522 reference individuals (0.09%). Data on mortality were obtained from the Swedish Cause of Death Registry. Hazard ratios (HRs) for death were calculated using Cox regression. RESULTS: During follow-up, there were seven deaths among individuals with DS and CD (7/201, 3.5%) as compared with 14 deaths among DS individuals without a record of CD (14/124, 11.3%). Adjusting for potential confounders, CD did not influence the risk of death in DS (HR = 1.36; 95%CI = 0.33–5.59). Cardiovascular death occurred in two individuals with CD and three individuals without CD, while death from malignancy occurred in one individual with CD and two individuals without CD. CONCLUSION: While both DS and CD have been linked to increased risk of death, this study found no excess mortality in DS patients with a concurrent diagnosis of CD, however confidence intervals were wide. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12887-017-0801-4) contains supplementary material, which is available to authorized users. BioMed Central 2017-01-31 /pmc/articles/PMC5282819/ /pubmed/28143429 http://dx.doi.org/10.1186/s12887-017-0801-4 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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.
spellingShingle Research Article
Ludvigsson, Jonas F.
Lebwohl, Benjamin
Green, Peter H. R.
Chung, Wendy K.
Mårild, Karl
Celiac disease and Down syndrome mortality: a nationwide cohort study
title Celiac disease and Down syndrome mortality: a nationwide cohort study
title_full Celiac disease and Down syndrome mortality: a nationwide cohort study
title_fullStr Celiac disease and Down syndrome mortality: a nationwide cohort study
title_full_unstemmed Celiac disease and Down syndrome mortality: a nationwide cohort study
title_short Celiac disease and Down syndrome mortality: a nationwide cohort study
title_sort celiac disease and down syndrome mortality: a nationwide cohort study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5282819/
https://www.ncbi.nlm.nih.gov/pubmed/28143429
http://dx.doi.org/10.1186/s12887-017-0801-4
work_keys_str_mv AT ludvigssonjonasf celiacdiseaseanddownsyndromemortalityanationwidecohortstudy
AT lebwohlbenjamin celiacdiseaseanddownsyndromemortalityanationwidecohortstudy
AT greenpeterhr celiacdiseaseanddownsyndromemortalityanationwidecohortstudy
AT chungwendyk celiacdiseaseanddownsyndromemortalityanationwidecohortstudy
AT marildkarl celiacdiseaseanddownsyndromemortalityanationwidecohortstudy