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(WFRF:(Scott Laura J.)) pers:(Thorsteinsdottir Unnur)
 

Sökning: (WFRF:(Scott Laura J.)) pers:(Thorsteinsdottir Unnur) > (2010-2014) > Genetic evidence th...

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FältnamnIndikatorerMetadata
00005974naa a2200985 4500
001oai:lup.lub.lu.se:4eb8830c-976a-4e8d-b426-9faa9b2dba1f
003SwePub
008160401s2010 | |||||||||||000 ||eng|
024a https://lup.lub.lu.se/record/15336892 URI
024a https://doi.org/10.1093/hmg/ddp5222 DOI
040 a (SwePub)lu
041 a engb eng
042 9 SwePub
072 7a art2 swepub-publicationtype
072 7a ref2 swepub-contenttype
100a Perry, John R. B.4 aut
2451 0a Genetic evidence that raised sex hormone binding globulin (SHBG) levels reduce the risk of type 2 diabetes
264 c 2009-11-18
264 1b Oxford University Press (OUP),c 2010
520 a Epidemiological studies consistently show that circulating sex hormone binding globulin (SHBG) levels are lower in type 2 diabetes patients than non-diabetic individuals, but the causal nature of this association is controversial. Genetic studies can help dissect causal directions of epidemiological associations because genotypes are much less likely to be confounded, biased or influenced by disease processes. Using this Mendelian randomization principle, we selected a common single nucleotide polymorphism (SNP) near the SHBG gene, rs1799941, that is strongly associated with SHBG levels. We used data from this SNP, or closely correlated SNPs, in 27 657 type 2 diabetes patients and 58 481 controls from 15 studies. We then used data from additional studies to estimate the difference in SHBG levels between type 2 diabetes patients and controls. The SHBG SNP rs1799941 was associated with type 2 diabetes [odds ratio (OR) 0.94, 95% CI: 0.91, 0.97; P = 2 x 10(-5)], with the SHBG raising allele associated with reduced risk of type 2 diabetes. This effect was very similar to that expected (OR 0.92, 95% CI: 0.88, 0.96), given the SHBG-SNP versus SHBG levels association (SHBG levels are 0.2 standard deviations higher per copy of the A allele) and the SHBG levels versus type 2 diabetes association (SHBG levels are 0.23 standard deviations lower in type 2 diabetic patients compared to controls). Results were very similar in men and women. There was no evidence that this variant is associated with diabetes-related intermediate traits, including several measures of insulin secretion and resistance. Our results, together with those from another recent genetic study, strengthen evidence that SHBG and sex hormones are involved in the aetiology of type 2 diabetes.
650 7a MEDICIN OCH HÄLSOVETENSKAPx Medicinska och farmaceutiska grundvetenskaperx Medicinsk genetik0 (SwePub)301072 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Basic Medicinex Medical Genetics0 (SwePub)301072 hsv//eng
700a Weedon, Michael N.4 aut
700a Langenberg, Claudia4 aut
700a Jackson, Anne U.4 aut
700a Lyssenko, Valeriya4 aut
700a Sparso, Thomas4 aut
700a Thorleifsson, Gudmar4 aut
700a Grallert, Harald4 aut
700a Ferrucci, Luigi4 aut
700a Maggio, Marcello4 aut
700a Paolisso, Giuseppe4 aut
700a Walker, Mark4 aut
700a Palmer, Colin N. A.4 aut
700a Payne, Felicity4 aut
700a Young, Elizabeth4 aut
700a Herder, Christian4 aut
700a Narisu, Narisu4 aut
700a Morken, Mario A.4 aut
700a Bonnycastle, Lori L.4 aut
700a Owen, Katharine R.4 aut
700a Shields, Beverley4 aut
700a Knight, Beatrice4 aut
700a Bennett, Amanda4 aut
700a Groves, Christopher J.4 aut
700a Ruokonen, Aimo4 aut
700a Jarvelin, Marjo Riitta4 aut
700a Pearson, Ewan4 aut
700a Pascoe, Laura4 aut
700a Ferrannini, Ele4 aut
700a Bornstein, Stefan R.4 aut
700a Stringham, Heather M.4 aut
700a Scott, Laura J.4 aut
700a Kuusisto, Johanna4 aut
700a Nilsson, Peteru Lund University,Lunds universitet,Internmedicin - epidemiologi,Forskargrupper vid Lunds universitet,Internal Medicine - Epidemiology,Lund University Research Groups4 aut0 (Swepub:lu)medf-pni
700a Neptin, Malinu Lund University,Lunds universitet,Genomik, diabetes och endokrinologi,Forskargrupper vid Lunds universitet,Genomics, Diabetes and Endocrinology,Lund University Research Groups4 aut0 (Swepub:lu)infl-mne
700a Gjesing, Anette P.4 aut
700a Pisinger, Charlotta4 aut
700a Lauritzen, Torsten4 aut
700a Sandbaek, Annelli4 aut
700a Sampson, Mike4 aut
700a Magic, Ele Zeggini4 aut
700a Lindgren, Cecilia M.4 aut
700a Steinthorsdottir, Valgerdur4 aut
700a Thorsteinsdottir, Unnur4 aut
700a Hansen, Torben4 aut
700a Schwarz, Peter4 aut
700a Illig, Thomas4 aut
700a Laakso, Markku4 aut
700a Stefansson, Kari4 aut
700a Morris, Andrew D.4 aut
700a Groop, Leifu Lund University,Lunds universitet,Genomik, diabetes och endokrinologi,Forskargrupper vid Lunds universitet,Genomics, Diabetes and Endocrinology,Lund University Research Groups4 aut0 (Swepub:lu)endo-lgr
700a Pedersen, Oluf4 aut
700a Boehnke, Michael4 aut
700a Barroso, Ines4 aut
700a Wareham, Nicholas J.4 aut
700a Hattersley, Andrew T.4 aut
700a McCarthy, Mark I.4 aut
700a Frayling, Timothy M.4 aut
710a Internmedicin - epidemiologib Forskargrupper vid Lunds universitet4 org
773t Human Molecular Geneticsd : Oxford University Press (OUP)g 19:3, s. 535-544q 19:3<535-544x 0964-6906x 1460-2083
856u http://dx.doi.org/10.1093/hmg/ddp522y FULLTEXT
856u https://academic.oup.com/hmg/article-pdf/19/3/535/17251164/ddp522.pdf
8564 8u https://lup.lub.lu.se/record/1533689
8564 8u https://doi.org/10.1093/hmg/ddp522

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