Imperial College London

ProfessorAbbasDehghan

Faculty of MedicineSchool of Public Health

Professor in Molecular Epidemiology
 
 
 
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Contact

 

+44 (0)20 7594 3347a.dehghan CV

 
 
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Location

 

Sir Michael Uren HubWhite City Campus

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Summary

 

Publications

Citation

BibTex format

@article{Huan:2015:10.1371/journal.pgen.1005035,
author = {Huan, T and Esko, T and Peters, MJ and Pilling, LC and Schramm, K and Schurmann, C and Chen, BH and Liu, C and Joehanes, R and Johnson, AD and Yao, C and Ying, S-X and Courchesne, P and Milani, L and Raghavachari, N and Wang, R and Liu, P and Reinmaa, E and Dehghan, A and Hofman, A and Uitterlinden, AG and Hernandez, DG and Bandinelli, S and Singleton, A and Melzer, D and Metspalu, A and Carstensen, M and Grallert, H and Herder, C and Meitinger, T and Peters, A and Roden, M and Waldenberger, M and Doerr, M and Felix, SB and Zeller, T and Vasan, R and O'Donnell, CJ and Munson, PJ and Yang, X and Prokisch, H and Voelker, U and van, Meurs JBJ and Ferrucci, L and Levy, D},
doi = {10.1371/journal.pgen.1005035},
journal = {PLoS Genetics},
title = {A meta-analysis of gene expression signatures of blood pressure and hypertension},
url = {http://dx.doi.org/10.1371/journal.pgen.1005035},
volume = {11},
year = {2015}
}

RIS format (EndNote, RefMan)

TY  - JOUR
AB - Genome-wide association studies (GWAS) have uncovered numerous genetic variants (SNPs) that are associated with blood pressure (BP). Genetic variants may lead to BP changes by acting on intermediate molecular phenotypes such as coded protein sequence or gene expression, which in turn affect BP variability. Therefore, characterizing genes whose expression is associated with BP may reveal cellular processes involved in BP regulation and uncover how transcripts mediate genetic and environmental effects on BP variability. A meta-analysis of results from six studies of global gene expression profiles of BP and hypertension in whole blood was performed in 7017 individuals who were not receiving antihypertensive drug treatment. We identified 34 genes that were differentially expressed in relation to BP (Bonferroni-corrected p<0.05). Among these genes, FOS and PTGS2 have been previously reported to be involved in BP-related processes; the others are novel. The top BP signature genes in aggregate explain 5%–9% of inter-individual variance in BP. Of note, rs3184504 in SH2B3, which was also reported in GWAS to be associated with BP, was found to be a trans regulator of the expression of 6 of the transcripts we found to be associated with BP (FOS, MYADM, PP1R15A, TAGAP, S100A10, and FGBP2). Gene set enrichment analysis suggested that the BP-related global gene expression changes include genes involved in inflammatory response and apoptosis pathways. Our study provides new insights into molecular mechanisms underlying BP regulation, and suggests novel transcriptomic markers for the treatment and prevention of hypertension.
AU - Huan,T
AU - Esko,T
AU - Peters,MJ
AU - Pilling,LC
AU - Schramm,K
AU - Schurmann,C
AU - Chen,BH
AU - Liu,C
AU - Joehanes,R
AU - Johnson,AD
AU - Yao,C
AU - Ying,S-X
AU - Courchesne,P
AU - Milani,L
AU - Raghavachari,N
AU - Wang,R
AU - Liu,P
AU - Reinmaa,E
AU - Dehghan,A
AU - Hofman,A
AU - Uitterlinden,AG
AU - Hernandez,DG
AU - Bandinelli,S
AU - Singleton,A
AU - Melzer,D
AU - Metspalu,A
AU - Carstensen,M
AU - Grallert,H
AU - Herder,C
AU - Meitinger,T
AU - Peters,A
AU - Roden,M
AU - Waldenberger,M
AU - Doerr,M
AU - Felix,SB
AU - Zeller,T
AU - Vasan,R
AU - O'Donnell,CJ
AU - Munson,PJ
AU - Yang,X
AU - Prokisch,H
AU - Voelker,U
AU - van,Meurs JBJ
AU - Ferrucci,L
AU - Levy,D
DO - 10.1371/journal.pgen.1005035
PY - 2015///
SN - 1553-7390
TI - A meta-analysis of gene expression signatures of blood pressure and hypertension
T2 - PLoS Genetics
UR - http://dx.doi.org/10.1371/journal.pgen.1005035
UR - http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000352197100027&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=1ba7043ffcc86c417c072aa74d649202
UR - http://hdl.handle.net/10044/1/65848
VL - 11
ER -