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DOI 10.1371/journal.pone.0159593

Медицинская библиотека · PloS one · 2016

Shared Genetic Factors Involved in Celiac Disease, Type 2 Diabetes and Anorexia Nervosa Suggest Common Molecular Pathways for Chronic Diseases.

Mostowy Joanna, Montén Caroline, Gudjonsdottir Audur H, Arnell Henrik, Browaldh Lars, Nilsson Staffan, Agardh Daniel, Torinsson Naluai Åsa

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Аннотация

BACKGROUND AND

OBJECTIVES

Genome-wide association studies (GWAS) have identified several genetic regions involved in immune-regulatory mechanisms to be associated with celiac disease. Previous GWAS also revealed an over-representation of genes involved in type 2 diabetes and anorexia nervosa associated with celiac disease, suggesting involvement of common metabolic pathways for development of these chronic diseases. The aim of this study was to extend these previous analyses to study the gene expression in the gut from children with active celiac disease.

MATERIAL AND

METHODS

Thirty six target genes involved in type 2 diabetes and four genes associated with anorexia nervosa were investigated for gene expression in small intestinal biopsies from 144 children with celiac disease at median (range) age of 7.4 years (1.6-17.8) and from 154 disease controls at a median (range) age 11.4.years (1.4-18.3).

RESULTS

A total of eleven of genes were differently expressed in celiac patients compared with disease controls of which CD36, CD38, FOXP1, SELL, PPARA, PPARG, AGT previously associated with type 2 diabetes and AKAP6, NTNG1 with anorexia nervosa remained significant after correction for multiple testing.

CONCLUSION

Shared genetic factors involved in celiac disease, type 2 diabetes and anorexia nervosa suggest common underlying molecular pathways for these diseases.

Для цитирования: Mostowy Joanna, Montén Caroline, Gudjonsdottir Audur H, Arnell Henrik, Browaldh Lars, Nilsson Staffan, Agardh Daniel, Torinsson Naluai Åsa. Shared Genetic Factors Involved in Celiac Disease, Type 2 Diabetes and Anorexia Nervosa Suggest Common Molecular Pathways for Chronic Diseases.. PloS one. 2016. DOI: 10.1371/journal.pone.0159593.

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