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Variants in MTNR1B influence fasting glucose levels.


ABSTRACT: To identify previously unknown genetic loci associated with fasting glucose concentrations, we examined the leading association signals in ten genome-wide association scans involving a total of 36,610 individuals of European descent. Variants in the gene encoding melatonin receptor 1B (MTNR1B) were consistently associated with fasting glucose across all ten studies. The strongest signal was observed at rs10830963, where each G allele (frequency 0.30 in HapMap CEU) was associated with an increase of 0.07 (95% CI = 0.06-0.08) mmol/l in fasting glucose levels (P = 3.2 x 10(-50)) and reduced beta-cell function as measured by homeostasis model assessment (HOMA-B, P = 1.1 x 10(-15)). The same allele was associated with an increased risk of type 2 diabetes (odds ratio = 1.09 (1.05-1.12), per G allele P = 3.3 x 10(-7)) in a meta-analysis of 13 case-control studies totaling 18,236 cases and 64,453 controls. Our analyses also confirm previous associations of fasting glucose with variants at the G6PC2 (rs560887, P = 1.1 x 10(-57)) and GCK (rs4607517, P = 1.0 x 10(-25)) loci.

SUBMITTER: Prokopenko I 

PROVIDER: S-EPMC2682768 | biostudies-literature | 2009 Jan

REPOSITORIES: biostudies-literature

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Variants in MTNR1B influence fasting glucose levels.

Prokopenko Inga I   Langenberg Claudia C   Florez Jose C JC   Saxena Richa R   Soranzo Nicole N   Thorleifsson Gudmar G   Loos Ruth J F RJ   Manning Alisa K AK   Jackson Anne U AU   Aulchenko Yurii Y   Potter Simon C SC   Erdos Michael R MR   Sanna Serena S   Hottenga Jouke-Jan JJ   Wheeler Eleanor E   Kaakinen Marika M   Lyssenko Valeriya V   Chen Wei-Min WM   Ahmadi Kourosh K   Beckmann Jacques S JS   Bergman Richard N RN   Bochud Murielle M   Bonnycastle Lori L LL   Buchanan Thomas A TA   Cao Antonio A   Cervino Alessandra A   Coin Lachlan L   Collins Francis S FS   Crisponi Laura L   de Geus Eco J C EJ   Dehghan Abbas A   Deloukas Panos P   Doney Alex S F AS   Elliott Paul P   Freimer Nelson N   Gateva Vesela V   Herder Christian C   Hofman Albert A   Hughes Thomas E TE   Hunt Sarah S   Illig Thomas T   Inouye Michael M   Isomaa Bo B   Johnson Toby T   Kong Augustine A   Krestyaninova Maria M   Kuusisto Johanna J   Laakso Markku M   Lim Noha N   Lindblad Ulf U   Lindgren Cecilia M CM   McCann Owen T OT   Mohlke Karen L KL   Morris Andrew D AD   Naitza Silvia S   Orrù Marco M   Palmer Colin N A CN   Pouta Anneli A   Randall Joshua J   Rathmann Wolfgang W   Saramies Jouko J   Scheet Paul P   Scott Laura J LJ   Scuteri Angelo A   Sharp Stephen S   Sijbrands Eric E   Smit Jan H JH   Song Kijoung K   Steinthorsdottir Valgerdur V   Stringham Heather M HM   Tuomi Tiinamaija T   Tuomilehto Jaakko J   Uitterlinden André G AG   Voight Benjamin F BF   Waterworth Dawn D   Wichmann H-Erich HE   Willemsen Gonneke G   Witteman Jacqueline C M JC   Yuan Xin X   Zhao Jing Hua JH   Zeggini Eleftheria E   Schlessinger David D   Sandhu Manjinder M   Boomsma Dorret I DI   Uda Manuela M   Spector Tim D TD   Penninx Brenda Wjh BW   Altshuler David D   Vollenweider Peter P   Jarvelin Marjo Riitta MR   Lakatta Edward E   Waeber Gerard G   Fox Caroline S CS   Peltonen Leena L   Groop Leif C LC   Mooser Vincent V   Cupples L Adrienne LA   Thorsteinsdottir Unnur U   Boehnke Michael M   Barroso Inês I   Van Duijn Cornelia C   Dupuis Josée J   Watanabe Richard M RM   Stefansson Kari K   McCarthy Mark I MI   Wareham Nicholas J NJ   Meigs James B JB   Abecasis Gonçalo R GR  

Nature genetics 20081207 1


To identify previously unknown genetic loci associated with fasting glucose concentrations, we examined the leading association signals in ten genome-wide association scans involving a total of 36,610 individuals of European descent. Variants in the gene encoding melatonin receptor 1B (MTNR1B) were consistently associated with fasting glucose across all ten studies. The strongest signal was observed at rs10830963, where each G allele (frequency 0.30 in HapMap CEU) was associated with an increase  ...[more]

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