Citation

BibTex format

@article{Gjesing:2010:10.1371/journal.pone.0010084,
author = {Gjesing, AP and Larsen, LH and Torekov, SS and Hainerova, IA and Kapur, R and Johansen, A and Albrechtsen, A and Boj, S and Holst, B and Harper, A and Urhammer, SA and Borch-Johnsen, K and Pisinger, C and Echwald, SM and Eiberg, H and Astrup, A and Lebl, J and Ferrer, J and Schwartz, TW and Hansen, T and Pedersen, O},
doi = {10.1371/journal.pone.0010084},
journal = {PLoS ONE},
title = {Family and population-based studies of variation within the Ghrelin receptor locus in relation to measures of obesity},
url = {http://dx.doi.org/10.1371/journal.pone.0010084},
volume = {5},
year = {2010}
}

RIS format (EndNote, RefMan)

TY  - JOUR
AB - BackgroundThe growth hormone secretagogue receptor (GHSR) is mediating hunger sensation when stimulated by its natural ligand ghrelin. In the present study, we tested the hypothesis that common and rare variation in the GHSR locus are related to increased prevalence of obesity and overweight among Whites.Methodology/Principal FindingsIn a population-based study sample of 15,854 unrelated, middle-aged Danes, seven variants were genotyped to capture common variation in an 11 kbp region including GHSR. These were investigated for their individual and haplotypic association with obesity. None of these analyses revealed consistent association with measures of obesity. A -151C/T promoter mutation in the GHSR was found in two unrelated obese patients. One family presented with complete co-segregation, but the other with incomplete co-segregation. The mutation resulted in an increased transcriptional activity (p<0.02) and introduction of a specific binding for Sp-1-like nuclear extracts relative to the wild type. The -151C/T mutation was genotyped in the 15,854 Danes with a minor allele frequency of 0.01%. No association with obesity in carriers (mean BMI: 27±4 kg/m2) versus non-carriers (mean BMI: 28±5 kg/m2) (p>0.05) could be shown.Conclusions/SignificanceIn a population-based study sample of 15,854 Danes no association between GHSR genotypes and measures of obesity and overweight was found. Also, analyses of GHSR haplotypes lack consistent associations with obesity related traits. A rare functional GHSR promoter mutation variant was identified, yet there was no consistent relationship with obesity in neither family- nor population-based studies.
AU - Gjesing,AP
AU - Larsen,LH
AU - Torekov,SS
AU - Hainerova,IA
AU - Kapur,R
AU - Johansen,A
AU - Albrechtsen,A
AU - Boj,S
AU - Holst,B
AU - Harper,A
AU - Urhammer,SA
AU - Borch-Johnsen,K
AU - Pisinger,C
AU - Echwald,SM
AU - Eiberg,H
AU - Astrup,A
AU - Lebl,J
AU - Ferrer,J
AU - Schwartz,TW
AU - Hansen,T
AU - Pedersen,O
DO - 10.1371/journal.pone.0010084
PY - 2010///
SN - 1932-6203
TI - Family and population-based studies of variation within the Ghrelin receptor locus in relation to measures of obesity
T2 - PLoS ONE
UR - http://dx.doi.org/10.1371/journal.pone.0010084
UR - http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000276482100010&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=1ba7043ffcc86c417c072aa74d649202
UR - http://hdl.handle.net/10044/1/60892
VL - 5
ER -
Faculty of MedicineDepartment of Metabolism, Digestion and Reproduction

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