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Williamson, A.* ; Norris, D.M.* ; Yin, X.* ; Broadaway, K.A.* ; Moxley, A.H.* ; Vadlamudi, S.* ; Wilson, E.P.* ; Jackson, A.U.* ; Ahuja, V.* ; Andersen, M.K.* ; Arzumanyan, Z.* ; Bonnycastle, L.L.* ; Bornstein, S.R. ; Bretschneider, M.P. ; Buchanan, T.A.* ; Chang, Y.C.* ; Chuang, L.M.* ; Chung, R.H.* ; Clausen, T.D.* ; Damm, P.* ; Delgado, G.E.* ; de Mello, V.D.* ; Dupuis, J.* ; Dwivedi, O.P.* ; Erdos, M.R.* ; Fernandes Silva, L.* ; Frayling, T.M.* ; Gieger, C. ; Goodarzi, M.O.* ; Guo, X.* ; Gustafsson, S.* ; Hakaste, L.* ; Hammar, U.* ; Hatem, G.* ; Herrmann, S. ; Højlund, K.* ; Horn, K.* ; Hsueh, W.A.* ; Hung, Y.J.* ; Hwu, C.M.* ; Jonsson, A.* ; Kårhus, L.L.* ; Kleber, M.E.* ; Kovacs, P.* ; Lakka, T.A.* ; Lauzon, M.* ; Lee, I.T.* ; Lindgren, C.M.* ; Lindstrom, J.* ; Linneberg, A.* ; Liu, C.T.* ; Luan, J.* ; Aly, D.M.* ; Mathiesen, E.* ; Moissl, A.P.* ; Morris, A.P.* ; Narisu, N.* ; Perakakis, N. ; Peters, A. ; Prasad, R.B.* ; Rodionov, R.N.* ; Roll, K.* ; Rundsten, C.F.* ; Sarnowski, C.* ; Savonen, K.* ; Scholz, M.* ; Sharma, S. ; Stinson, S.E.* ; Suleman, S.* ; Tan, J.* ; Taylor, K.D.* ; Uusitupa, M.* ; Vistisen, D.* ; Witte, D.R.* ; Walther, R. ; Wu, P.* ; Xiang, A.H.* ; Zethelius, B.* ; Ahlqvist, E.* ; Bergman, R.N.* ; Chen, Y.I.* ; Collins, F.S.* ; Fall, T.* ; Florez, J.C.* ; Fritsche, A.* ; Grallert, H. ; Groop, L.* ; Hansen, T.* ; Koistinen, H.A.* ; Komulainen, P.* ; Laakso, M.* ; Lind, L.* ; Loeffler, M.* ; Marz, W.* ; Meigs, J.B.* ; Raffel, L.J.* ; Rauramaa, R.* ; Rotter, J.I.* ; Schwarz, P.E. ; Stumvoll, M.* ; Sundström, J.* ; Tönjes, A.* ; Tuomi, T.* ; Tuomilehto, J.* ; Wagner, R.* ; Barroso, I.* ; Walker, M.* ; Grarup, N.* ; Boehnke, M.* ; Wareham, N.J.* ; Mohlke, K.L.* ; Wheeler, E.* ; O'Rahilly, S.* ; Fazakerley, D.J.* ; Langenberg, C.*

Genome-wide association study and functional characterization identifies candidate genes for insulin-stimulated glucose uptake.

Nat. Genet. 55, 973-983 (2023)
DOI PMC
Open Access Green möglich sobald Postprint bei der ZB eingereicht worden ist.
Distinct tissue-specific mechanisms mediate insulin action in fasting and postprandial states. Previous genetic studies have largely focused on insulin resistance in the fasting state, where hepatic insulin action dominates. Here we studied genetic variants influencing insulin levels measured 2 h after a glucose challenge in >55,000 participants from three ancestry groups. We identified ten new loci (P < 5 × 10-8) not previously associated with postchallenge insulin resistance, eight of which were shown to share their genetic architecture with type 2 diabetes in colocalization analyses. We investigated candidate genes at a subset of associated loci in cultured cells and identified nine candidate genes newly implicated in the expression or trafficking of GLUT4, the key glucose transporter in postprandial glucose uptake in muscle and fat. By focusing on postprandial insulin resistance, we highlighted the mechanisms of action at type 2 diabetes loci that are not adequately captured by studies of fasting glycemic traits.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Korrespondenzautor
Schlagwörter Glut4 Translocation; Diabetes-mellitus; Tolerance Test; Resistance; Muscle; Sensitivity; Glucose-transporter-4; Phosphorylation; Expression; Complex
ISSN (print) / ISBN 1061-4036
e-ISSN 1546-1718
Zeitschrift Nature Genetics
Quellenangaben Band: 55, Heft: 6, Seiten: 973-983 Artikelnummer: , Supplement: ,
Verlag Nature Publishing Group
Verlagsort New York, NY
Nichtpatentliteratur Publikationen
Begutachtungsstatus Peer reviewed
Institut(e) Institute for Pancreatic Beta Cell Research (IPI)
Institute of Epidemiology II (EPI2)