Back to Search Start Over

Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology.

Authors :
Ferreira MA
Vonk JM
Baurecht H
Marenholz I
Tian C
Hoffman JD
Helmer Q
Tillander A
Ullemar V
van Dongen J
Lu Y
Rüschendorf F
Esparza-Gordillo J
Medway CW
Mountjoy E
Burrows K
Hummel O
Grosche S
Brumpton BM
Witte JS
Hottenga JJ
Willemsen G
Zheng J
Rodríguez E
Hotze M
Franke A
Revez JA
Beesley J
Matheson MC
Dharmage SC
Bain LM
Fritsche LG
Gabrielsen ME
Balliu B
Nielsen JB
Zhou W
Hveem K
Langhammer A
Holmen OL
Løset M
Abecasis GR
Willer CJ
Arnold A
Homuth G
Schmidt CO
Thompson PJ
Martin NG
Duffy DL
Novak N
Schulz H
Karrasch S
Gieger C
Strauch K
Melles RB
Hinds DA
Hübner N
Weidinger S
Magnusson PKE
Jansen R
Jorgenson E
Lee YA
Boomsma DI
Almqvist C
Karlsson R
Koppelman GH
Paternoster L
Source :
Nature genetics [Nat Genet] 2017 Dec; Vol. 49 (12), pp. 1752-1757. Date of Electronic Publication: 2017 Oct 30.
Publication Year :
2017

Abstract

Asthma, hay fever (or allergic rhinitis) and eczema (or atopic dermatitis) often coexist in the same individuals, partly because of a shared genetic origin. To identify shared risk variants, we performed a genome-wide association study (GWAS; n = 360,838) of a broad allergic disease phenotype that considers the presence of any one of these three diseases. We identified 136 independent risk variants (P < 3 × 10 <superscript>-8</superscript> ), including 73 not previously reported, which implicate 132 nearby genes in allergic disease pathophysiology. Disease-specific effects were detected for only six variants, confirming that most represent shared risk factors. Tissue-specific heritability and biological process enrichment analyses suggest that shared risk variants influence lymphocyte-mediated immunity. Six target genes provide an opportunity for drug repositioning, while for 36 genes CpG methylation was found to influence transcription independently of genetic effects. Asthma, hay fever and eczema partly coexist because they share many genetic risk variants that dysregulate the expression of immune-related genes.

Details

Language :
English
ISSN :
1546-1718
Volume :
49
Issue :
12
Database :
MEDLINE
Journal :
Nature genetics
Publication Type :
Academic Journal
Accession number :
29083406
Full Text :
https://doi.org/10.1038/ng.3985