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Variants associated with HHIP expression have sex-differential effects on lung function.

Authors :
Fawcett KA
Obeidat M
Melbourne C
Shrine N
Guyatt AL
John C
Luan J
Richmond A
Moksnes MR
Granell R
Weiss S
Imboden M
May-Wilson S
Hysi P
Boutin TS
Portas L
Flexeder C
Harris SE
Wang CA
Lyytikäinen LP
Palviainen T
Foong RE
Keidel D
Minelli C
Langenberg C
Bossé Y
Van den Berge M
Sin DD
Hao K
Campbell A
Porteous D
Padmanabhan S
Smith BH
Evans DM
Ring S
Langhammer A
Hveem K
Willer C
Ewert R
Stubbe B
Pirastu N
Klaric L
Joshi PK
Patasova K
Massimo M
Polasek O
Starr JM
Karrasch S
Strauch K
Meitinger T
Rudan I
Rantanen T
Pietiläinen K
Kähönen M
Raitakari OT
Hall GL
Sly PD
Pennell CE
Kaprio J
Lehtimäki T
Vitart V
Deary IJ
Jarvis D
Wilson JF
Spector T
Probst-Hensch N
Wareham NJ
Völzke H
Henderson J
Strachan DP
Brumpton BM
Hayward C
Hall IP
Tobin MD
Wain LV
Source :
Wellcome open research [Wellcome Open Res] 2021 May 24; Vol. 5, pp. 111. Date of Electronic Publication: 2021 May 24 (Print Publication: 2020).
Publication Year :
2021

Abstract

Background: Lung function is highly heritable and differs between the sexes throughout life. However, little is known about sex-differential genetic effects on lung function. We aimed to conduct the first genome-wide genotype-by-sex interaction study on lung function to identify genetic effects that differ between males and females. Methods: We tested for interactions between 7,745,864 variants and sex on spirometry-based measures of lung function in UK Biobank (N=303,612), and sought replication in 75,696 independent individuals from the SpiroMeta consortium. Results: Five independent single-nucleotide polymorphisms (SNPs) showed genome-wide significant (P<5x10 <superscript>-8</superscript> ) interactions with sex on lung function, and 21 showed suggestive interactions (P<1x10 <superscript>-6</superscript> ). The strongest signal, from rs7697189 (chr4:145436894) on forced expiratory volume in 1 second (FEV <subscript>1</subscript> ) (P=3.15x10 <superscript>-15</superscript> ), was replicated (P=0.016) in SpiroMeta. The C allele increased FEV <subscript>1</subscript> more in males (untransformed FEV <subscript>1</subscript> β=0.028 [SE 0.0022] litres) than females (β=0.009 [SE 0.0014] litres), and this effect was not accounted for by differential effects on height, smoking or pubertal age. rs7697189 resides upstream of the hedgehog-interacting protein ( HHIP ) gene and was previously associated with lung function and HHIP lung expression. We found HHIP expression was significantly different between the sexes (P=6.90x10 <superscript>-6</superscript> ), but we could not detect sex differential effects of rs7697189 on expression. Conclusions: We identified a novel genotype-by-sex interaction at a putative enhancer region upstream of the HHIP gene. Establishing the mechanism by which HHIP SNPs have different effects on lung function in males and females will be important for our understanding of lung health and diseases in both sexes.<br />Competing Interests: Competing interests: The following authors report potential competing interests: L.V.W.: Louise V. Wain has received grant support from GSK. M.D.T.: Martin D. Tobin has received grant support from GSK. I.P.H.: Ian P. Hall has received support from GSK and BI.<br /> (Copyright: © 2021 Fawcett KA et al.)

Details

Language :
English
ISSN :
2398-502X
Volume :
5
Database :
MEDLINE
Journal :
Wellcome open research
Publication Type :
Academic Journal
Accession number :
33728380.2
Full Text :
https://doi.org/10.12688/wellcomeopenres.15846.2