Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility

全基因组关联研究 遗传建筑学 生物 遗传关联 遗传学 单核苷酸多态性 遗传谱系 等位基因 1000基因组计划 特质 进化生物学 基因 荟萃分析 数量性状位点 基因型 人口 医学 环境卫生 计算机科学 程序设计语言 内科学
作者
Anubha Mahajan,Min Jin Go,Weihua Zhang,Jennifer E. Below,Kyle J. Gaulton,Teresa Ferreira,Momoko Horikoshi,Andrew D. Johnson,Maggie C. Y. Ng,Inga Prokopenko,Danish Saleheen,Xu Wang,Eleftheria Zeggini,Gonçalo R. Abecasis,Linda S. Adair,Peter Almgren,Mustafa Atalay,Tin Aung,Damiano Baldassarre,Beverley Balkau,Yuqian Bao,Anthony Barnett,Inês Barroso,Abdul Basit,Latonya Been,John Beilby,Graeme I. Bell,Rafn Benediktsson,Richard N. Bergman,Bernhard O. Boehm,Eric Boerwinkle,Lori L. Bonnycastle,Noël P. Burtt,Qiuyin Cai,Harry Campbell,Jason Carey,Stéphane Cauchi,Mark Caulfield,Juliana C.N. Chan,Li-Ching Chang,Tien-Jyun Chang,Yi–Cheng Chang,G. Charpentier,Chien-Hsiun Chen,Han Chen,Yuan-Tsong Chen,Kee‐Seng Chia,Manickam Chidambaram,Peter S. Chines,Nam H. Cho,Young Min Cho,Lee‐Ming Chuang,Francis S. Collins,Marilyn C. Cornelis,David Couper,Andrew Crenshaw,Rob M. van Dam,John Danesh,Debashish Das,Ulf dé Fairé,George Dedoussis,Panos Deloukas,Antigone S. Dimas,Christian Dina,Alex S. F. Doney,Peter Donnelly,Mozhgan Dorkhan,Cornelia M. van Duijn,Josée Dupuis,Sarah Edkins,Paul Elliott,Valur Emilsson,Raimund Erbel,Johan G. Eriksson,Jorge Escobedo,Tõnu Esko,Elodie Eury,José C. Florez,Pierre Fontanillas,Nita G. Forouhi,Tom Forsén,Caroline S. Fox,Ross M. Fraser,Timothy M. Frayling,Philippe Froguel,Philippe Frossard,Yu‐Tang Gao,Karl Gertow,Christian Gieger,Bruna Gigante,Harald Grallert,George Grant,Leif Groop,Christopher J. Groves,Elin Grundberg,Candace Guiducci,Anders Hamsten,Bok‐Ghee Han,Kazuo Hara,Neelam Hassanali,Andrew T. Hattersley,Caroline Hayward,Åsa K. Hedman,Christian Herder,Albert Hofman,Oddgeir L. Holmen,Kees Hovingh,Ástráður B. Hreiðarsson,Cheng Hu,Frank B. Hu,Jennie Hui,Steve E. Humphries,Sarah Hunt,David J. Hunter,Kristian Hveem,Zafar I Hydrie,Hiroshi Ikegami,Thomas Illig,Erik Ingelsson,Muhammed Islam,Bo Isomaa,Anne Jackson,Tazeen H. Jafar,Alan James,Weiping Jia,Karl‐Heinz Jöckel,Anna Jonsson,Jeremy B. M. Jowett,Takashi Kadowaki,Hyun Min Kang,Stavroula Kanoni,W. H. Linda Kao,Sekar Kathiresan,Norihiro Kato,Prasad Katulanda,Sirkka Keinänen‐Kiukaanniemi,Ann Marie Kelly,Hassan Khan,Kay-Tee Khaw,Chiea‐Chuen Khor,Hyung-Lae Kim,Sang Soo Kim,Young Jin Kim,Leena Kinnunen,Norman Klopp,Augustine Kong,Eeva Korpi-Hyövälti,Sudhir Kowlessur,Peter Kraft,Jasmina Kravić,Malene M Kristensen,S. Krithika,Ashish Kumar,J Kumate,Johanna Kuusisto,Soo Heon Kwak,Markku Laakso,Vasiliki Lagou,Timo A. Lakka,Claudia Langenberg,Cordelia Langford,Robert Lawrence,Karin Leander,Jen-Mai Lee,Nanette R. Lee,Man Li,Xinzhong Li,Yun Li,Junbin Liang,Samuel Liju,Wei‐Yen Lim,Lars Lind,Cecilia M. Lindgren,Eero Lindholm,Ching‐Ti Liu,Jing Liu,Stéphane Lobbens,Jirong Long,Ruth J. F. Loos,Wei Lü,Jian’an Luan,Valeriya Lyssenko,C. Ronald,Shiro Maeda,Reedik Mägi,Satu Männistö,David R. Matthews,James B. Meigs,Olle Melander,Andres Metspalu,Julia Meyer,Ghazala Mirza,Evelin Mihailov,Susanne Moebus,Viswanathan Mohan,Karen L. Mohlke,Andrew D. Morris,Thomas W. Mühleisen,Martina Müller‐Nurasyid,Bill Musk,Jiro Nakamura,Eitaro Nakashima,Pau Navarro,Peng-Keat Ng,Alexandra C. Nica,Peter M. Nilsson,Inger Njølstad,Markus M. Nöthen,Keizo Ohnaka,Twee Hee Ong,Katharine R. Owen,Colin N. A. Palmer,James S. Pankow,Kyong Soo Park,Melissa Parkin,Sonali Pechlivanis,Nancy L. Pedersen,Leena Peltonen,John Perry,Annette Peters,Janani Pinidiyapathirage,Carl Platou,Simon Potter,Jackie F. Price,Lu Qi,Venkatesan Radha,Lοukianos S. Rallidis,Awais Rasheed,Wolfgang Rathmann,Rainer Rauramaa,Soumya Raychaudhuri,Nigel W. Rayner,Simon D. Rees,Emil Rehnberg,Samuli Ripatti,Neil Robertson,Michael Roden,Elizabeth J. Rossin,Igor Rudan,Denis Rybin,Timo Saaristo,Veikko Salomaa,Juha Saltevo,Maria Samuel,Dharambir K. Sanghera,Jouko Saramies,James A. Scott,Laura J. Scott,Robert A. Scott,Ayellet V. Segrè,Joban Sehmi,Bengt Sennblad,Nabi Shah,Sonia Shah,A. Samad Shera,Xiao Ou Shu,Alan R. Shuldiner,Gunnar Sigurðsson,Eric J.G. Sijbrands,Angela Silveira,Xueling Sim,Suthesh Sivapalaratnam,Kerrin S. Small,Wing Yee So,Alena Stančáková,Kāri Stefánsson,Gerald Steinbach,Valgerður Steinthórsdóttir,Kathleen Stirrups,Rona J. Strawbridge,Heather M. Stringham,Qi Sun,Chen Suo,Ann‐Christine Syvänen,Ryoichi Takayanagi,Fumihiko Takeuchi,Wan Ting Tay,Tanya M. Teslovich,Barbara Thorand,Guðmar Þorleifsson,Unnur Þorsteinsdóttir,Emmi Tikkanen,Joseph Trakalo,Elena Tremoli,Mieke D. Trip,Fuu Jen Tsai,Tiinamaija Tuomi,Jaakko Tuomilehto,André G. Uitterlinden,Adán Valladares–Salgado,Sailaja Vedantam,Fabrizio Veglia,Benjamin F. Voight,Congrong Wang,Nicholas J. Wareham,Roman Wennauer,Ananda R. Wickremasinghe,Tom Wilsgaard,James F. Wilson,Steven Wiltshire,Wendy Winckler,Tien Yin Wong,Andrew R. Wood,Jer‐Yuarn Wu,Ying Wu,Ken Yamamoto,Toshimasa Yamauchi,Mingyu Yang,Loïc Yengo,Mitsuhiro Yokota,Robin Young,Delilah Zabaneh,Fan Zhang,Rong Zhang,Zheng Wang,Paul Zimmet,David Altshuler,Donald W. Bowden,Yoon Shin Cho,Nancy J. Cox,Miguel Cruz,Craig L. Hanis,Jaspal S. Kooner,Jong‐Young Lee,Mark Seielstad,Yik Ying Teo,Michael Boehnke,Esteban J. Parra,John C. Chambers,E Shyong Tai,Mark McCarthy,Andrew P. Morris
出处
期刊:Nature Genetics [Springer Nature]
卷期号:46 (3): 234-244 被引量:944
标识
DOI:10.1038/ng.2897
摘要

To further understanding of the genetic basis of type 2 diabetes (T2D) susceptibility, we aggregated published meta-analyses of genome-wide association studies (GWAS), including 26,488 cases and 83,964 controls of European, east Asian, south Asian and Mexican and Mexican American ancestry. We observed a significant excess in the directional consistency of T2D risk alleles across ancestry groups, even at SNPs demonstrating only weak evidence of association. By following up the strongest signals of association from the trans-ethnic meta-analysis in an additional 21,491 cases and 55,647 controls of European ancestry, we identified seven new T2D susceptibility loci. Furthermore, we observed considerable improvements in the fine-mapping resolution of common variant association signals at several T2D susceptibility loci. These observations highlight the benefits of trans-ethnic GWAS for the discovery and characterization of complex trait loci and emphasize an exciting opportunity to extend insight into the genetic architecture and pathogenesis of human diseases across populations of diverse ancestry.
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