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Cystic fibrosis gene mutations and gastrointestinal diseases

Bahmanyar, Shahram (author)
Karolinska Institutet
Ekbom, Anders (author)
Karolinska Institutet
Askling, Johan (author)
Karolinska Institutet
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Johannesson, Marie (author)
Department, Paediatrics and Child Health, University of Otago, Wellington, New Zealand
Montgomery, Scott M. (author)
Karolinska Institutet,Örebro universitet,Institutionen för hälsovetenskap och medicin,Clinical Epidemiology Unit, Department of Medicine, Karolinska Hospital, Stockholm, Sweden; Department of Primary Care and Social Medicine, Charing Cross Hospital, Imperial College, London, United Kingdom,Clinical Epidemiology and Biostatistics
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 (creator_code:org_t)
Elsevier BV, 2010
2010
English.
In: Journal of Cystic Fibrosis. - : Elsevier BV. - 1569-1993 .- 1873-5010. ; 9:4, s. 288-291
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Background: This study examined if CF mutation heterozygosity is associated with diseases of gastrointestinal epithelial barrier function. Design and methods: Swedish registers identified 865 patients with a diagnosis of CF between 1968 and 2003 and matched with 8101 individuals without CF. Gastrointestinal disease risk was examined among 1534 biological parents and 1396 siblings of CF patients, compared with 15,526 parents and 15,542 siblings of individuals without CF. Results: First-degree relatives of CF patients were not at lower risk of the gastrointestinal diseases, in contrast with a raised risk among CF patients. Conclusion: Heterozygosity for CF gene mutations does not protect against gastrointestinal diseases where impaired barrier function may be relevant. (C) 2010 European Cystic Fibrosis Society. Published by Elsevier B.V. All rights reserved.

Keyword

Cystic fibrosis
Gene mutation
Gastrointestinal diseases
Barrier function
Medicine
Medicin

Publication and Content Type

ref (subject category)
art (subject category)

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