Congenital Anomalies and Childhood Celiac Disease: A Swedish Register-based Study.
(2012) In Journal of Pediatric Gastroenterology and Nutrition - Jpgn 55(6). p.736-739- Abstract
- Previously, chromosomal anomalies, and to a lesser extent, other congenital anomalies have been associated with an increased risk of celiac disease (CD). We investigated these associations using a systematic approach. We identified all singleton children (792,401) born in Sweden between 1987 and 1993, and obtained cases of CD using the Swedish National Inpatient Registry. We applied COX regression models as well as sibling designs to study the association between congenital anomalies and childhood CD. We observed that anomalies of either face, neck, ear, heart, digestive tract or of chromosomes were associated with CD.
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/3047931
- author
- Wingren, Carl Johan LU ; Agardh, Daniel LU and Merlo, Juan LU
- organization
- publishing date
- 2012
- type
- Contribution to journal
- publication status
- published
- subject
- keywords
- child, celiac disease, congenital abnormalities, epidemiology, heart, diseases, risk factors
- in
- Journal of Pediatric Gastroenterology and Nutrition - Jpgn
- volume
- 55
- issue
- 6
- pages
- 736 - 739
- publisher
- Lippincott Williams & Wilkins
- external identifiers
-
- wos:000311702500028
- pmid:22847461
- scopus:84870940594
- pmid:22847461
- ISSN
- 1536-4801
- DOI
- 10.1097/MPG.0b013e318269f19d
- language
- English
- LU publication?
- yes
- id
- 6c70778b-1076-43f4-bb67-57601dbc9006 (old id 3047931)
- alternative location
- http://www.ncbi.nlm.nih.gov/pubmed/22847461?dopt=Abstract
- date added to LUP
- 2016-04-01 11:04:56
- date last changed
- 2022-02-17 23:53:29
@article{6c70778b-1076-43f4-bb67-57601dbc9006, abstract = {{Previously, chromosomal anomalies, and to a lesser extent, other congenital anomalies have been associated with an increased risk of celiac disease (CD). We investigated these associations using a systematic approach. We identified all singleton children (792,401) born in Sweden between 1987 and 1993, and obtained cases of CD using the Swedish National Inpatient Registry. We applied COX regression models as well as sibling designs to study the association between congenital anomalies and childhood CD. We observed that anomalies of either face, neck, ear, heart, digestive tract or of chromosomes were associated with CD.}}, author = {{Wingren, Carl Johan and Agardh, Daniel and Merlo, Juan}}, issn = {{1536-4801}}, keywords = {{child; celiac disease; congenital abnormalities; epidemiology; heart; diseases; risk factors}}, language = {{eng}}, number = {{6}}, pages = {{736--739}}, publisher = {{Lippincott Williams & Wilkins}}, series = {{Journal of Pediatric Gastroenterology and Nutrition - Jpgn}}, title = {{Congenital Anomalies and Childhood Celiac Disease: A Swedish Register-based Study.}}, url = {{http://dx.doi.org/10.1097/MPG.0b013e318269f19d}}, doi = {{10.1097/MPG.0b013e318269f19d}}, volume = {{55}}, year = {{2012}}, }