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Billings, L.K.* ; Hsu, Y.H.* ; Ackerman, R.J.* ; Dupuis, J.* ; Voight, B.F.* ; Rasmussen-Torvik, L.J.* ; Hercberg, S.* ; Lathrop, M* ; Barnes, D.* ; Langenberg, C.* ; Hui, J.* ; Fu, M.* ; Bouatia-Naji, N.* ; Lecoeur, C.* ; An, P.* ; Magnusson, P.K.* ; Surakka, I.* ; Ripatti, S.* ; Christiansen, L.* ; Dalgård, C.* ; Folkersen, L.* ; Grundberg, E.* ; MAGIC Investigators (Gieger, C. ; Grallert, H. ; Meisinger, C. ; Wichmann, H.-E. ; Thorand, B. ; Illig, T.) ; DIAGRAM Consortium (Huth, C. ; Klopp, N. ; Meitinger, T. ; Thorand, B. ; Grallert, H. ; Gieger, C. ; Wichmann, H.-E. ; Illig, T. ; Petersen, A.-K.) ; MuTHER Consortium (*) ; ASCOT Investigators (*) ; GEFOS Consortium (*) ; Eriksson, P.* ; Kaprio, J.* ; Ohm Kyvik, K.* ; Pedersen, N.L.* ; Borecki, I.B.* ; Province, M.A.* ; Balkau, B.* ; Froguel, P.* ; Shuldiner, A.R.* ; Palmer, L.J.* ; Wareham, N.J.* ; Meneton, P.* ; Johnson, T.* ; Pankow, J.S.* ; Karasik, D.* ; Meigs, J.B.* ; Kiel, D.P.* ; Florez, J.C*

Impact of common variation in bone-related genes on type 2 diabetes and related traits.

Diabetes 61, 2176-2186 (2012)
DOI PMC
Open Access Green möglich sobald Postprint bei der ZB eingereicht worden ist.
Exploring genetic pleiotropy can provide clues to a mechanism underlying the observed epidemiological association between type 2 diabetes and heightened fracture risk. We examined genetic variants associated with bone mineral density (BMD) for association with type 2 diabetes and glycemic traits in large well-phenotyped and -genotyped consortia. We undertook follow-up analysis in ∼19,000 individuals and assessed gene expression. We queried single nucleotide polymorphisms (SNPs) associated with BMD at levels of genome-wide significance, variants in linkage disequilibrium (r(2) > 0.5), and BMD candidate genes. SNP rs6867040, at the ITGA1 locus, was associated with a 0.0166 mmol/L (0.004) increase in fasting glucose per C allele in the combined analysis. Genetic variants in the ITGA1 locus were associated with its expression in the liver but not in adipose tissue. ITGA1 variants appeared among the top loci associated with type 2 diabetes, fasting insulin, β-cell function by homeostasis model assessment, and 2-h post-oral glucose tolerance test glucose and insulin levels. ITGA1 has demonstrated genetic pleiotropy in prior studies, and its suggested role in liver fibrosis, insulin secretion, and bone healing lends credence to its contribution to both osteoporosis and type 2 diabetes. These findings further underscore the link between skeletal and glucose metabolism and highlight a locus to direct future investigations.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Korrespondenzautor
Schlagwörter GENOME-WIDE ASSOCIATION; BODY-MASS INDEX; MINERAL DENSITY; FRACTURE RISK; OSTEOPOROTIC FRACTURES; INSULIN-RESISTANCE; ENERGY-METABOLISM; FASTING GLUCOSE; LOCI; METAANALYSIS
ISSN (print) / ISBN 0012-1797
e-ISSN 1939-327X
Zeitschrift Diabetes
Quellenangaben Band: 61, Heft: 8, Seiten: 2176-2186 Artikelnummer: , Supplement: ,
Verlag American Diabetes Association
Verlagsort Alexandria, VA.
Nichtpatentliteratur Publikationen
Begutachtungsstatus Peer reviewed
Institut(e) Research Unit Molecular Epidemiology (AME)
Institute of Genetic Epidemiology (IGE)
Institute of Epidemiology II (EPI2)
Institute of Epidemiology (EPI)