Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci.

نویسندگان

  • Folkert W Asselbergs
  • Yiran Guo
  • Erik P A van Iperen
  • Suthesh Sivapalaratnam
  • Vinicius Tragante
  • Matthew B Lanktree
  • Leslie A Lange
  • Berta Almoguera
  • Yolande E Appelman
  • John Barnard
  • Jens Baumert
  • Amber L Beitelshees
  • Tushar R Bhangale
  • Yii-Der Ida Chen
  • Tom R Gaunt
  • Yan Gong
  • Jemma C Hopewell
  • Toby Johnson
  • Marcus E Kleber
  • Taimour Y Langaee
  • Mingyao Li
  • Yun R Li
  • Kiang Liu
  • Caitrin W McDonough
  • Matthijs F L Meijs
  • Rita P S Middelberg
  • Kiran Musunuru
  • Christopher P Nelson
  • Jeffery R O'Connell
  • Sandosh Padmanabhan
  • James S Pankow
  • Nathan Pankratz
  • Suzanne Rafelt
  • Ramakrishnan Rajagopalan
  • Simon P R Romaine
  • Nicholas J Schork
  • Jonathan Shaffer
  • Haiqing Shen
  • Erin N Smith
  • Sam E Tischfield
  • Peter J van der Most
  • Jana V van Vliet-Ostaptchouk
  • Niek Verweij
  • Kelly A Volcik
  • Li Zhang
  • Kent R Bailey
  • Kristian M Bailey
  • Florianne Bauer
  • Jolanda M A Boer
  • Peter S Braund
  • Amber Burt
  • Paul R Burton
  • Sarah G Buxbaum
  • Wei Chen
  • Rhonda M Cooper-Dehoff
  • L Adrienne Cupples
  • Jonas S deJong
  • Christian Delles
  • David Duggan
  • Myriam Fornage
  • Clement E Furlong
  • Nicole Glazer
  • John G Gums
  • Claire Hastie
  • Michael V Holmes
  • Thomas Illig
  • Susan A Kirkland
  • Mika Kivimaki
  • Ronald Klein
  • Barbara E Klein
  • Charles Kooperberg
  • Kandice Kottke-Marchant
  • Meena Kumari
  • Andrea Z LaCroix
  • Laya Mallela
  • Gurunathan Murugesan
  • Jose Ordovas
  • Willem H Ouwehand
  • Wendy S Post
  • Richa Saxena
  • Hubert Scharnagl
  • Pamela J Schreiner
  • Tina Shah
  • Denis C Shields
  • Daichi Shimbo
  • Sathanur R Srinivasan
  • Ronald P Stolk
  • Daniel I Swerdlow
  • Herman A Taylor
  • Eric J Topol
  • Elina Toskala
  • Joost L van Pelt
  • Jessica van Setten
  • Salim Yusuf
  • John C Whittaker
  • A H Zwinderman
  • Sonia S Anand
  • Anthony J Balmforth
  • Gerald S Berenson
  • Connie R Bezzina
  • Bernhard O Boehm
  • Eric Boerwinkle
  • Juan P Casas
  • Mark J Caulfield
  • Robert Clarke
  • John M Connell
  • Karen J Cruickshanks
  • Karina W Davidson
  • Ian N M Day
  • Paul I W de Bakker
  • Pieter A Doevendans
  • Anna F Dominiczak
  • Alistair S Hall
  • Catharina A Hartman
  • Christian Hengstenberg
  • Hans L Hillege
  • Marten H Hofker
  • Steve E Humphries
  • Gail P Jarvik
  • Julie A Johnson
  • Bernhard M Kaess
  • Sekar Kathiresan
  • Wolfgang Koenig
  • Debbie A Lawlor
  • Winfried März
  • Olle Melander
  • Braxton D Mitchell
  • Grant W Montgomery
  • Patricia B Munroe
  • Sarah S Murray
  • Stephen J Newhouse
  • N Charlotte Onland-Moret
  • Neil Poulter
  • Bruce Psaty
  • Susan Redline
  • Stephen S Rich
  • Jerome I Rotter
  • Heribert Schunkert
  • Peter Sever
  • Alan R Shuldiner
  • Roy L Silverstein
  • Alice Stanton
  • Barbara Thorand
  • Mieke D Trip
  • Michael Y Tsai
  • Pim van der Harst
  • Ellen van der Schoot
  • Yvonne T van der Schouw
  • W M Monique Verschuren
  • Hugh Watkins
  • Arthur A M Wilde
  • Bruce H R Wolffenbuttel
  • John B Whitfield
  • G Kees Hovingh
  • Christie M Ballantyne
  • Cisca Wijmenga
  • Muredach P Reilly
  • Nicholas G Martin
  • James G Wilson
  • Daniel J Rader
  • Nilesh J Samani
  • Alex P Reiner
  • Robert A Hegele
  • John J P Kastelein
  • Aroon D Hingorani
  • Philippa J Talmud
  • Hakon Hakonarson
  • Clara C Elbers
  • Brendan J Keating
  • Fotios Drenos
چکیده

Genome-wide association studies (GWASs) have identified many SNPs underlying variations in plasma-lipid levels. We explore whether additional loci associated with plasma-lipid phenotypes, such as high-density lipoprotein cholesterol (HDL-C), low-density lipoprotein cholesterol (LDL-C), total cholesterol (TC), and triglycerides (TGs), can be identified by a dense gene-centric approach. Our meta-analysis of 32 studies in 66,240 individuals of European ancestry was based on the custom ∼50,000 SNP genotyping array (the ITMAT-Broad-CARe array) covering ∼2,000 candidate genes. SNP-lipid associations were replicated either in a cohort comprising an additional 24,736 samples or within the Global Lipid Genetic Consortium. We identified four, six, ten, and four unreported SNPs in established lipid genes for HDL-C, LDL-C, TC, and TGs, respectively. We also identified several lipid-related SNPs in previously unreported genes: DGAT2, HCAR2, GPIHBP1, PPARG, and FTO for HDL-C; SOCS3, APOH, SPTY2D1, BRCA2, and VLDLR for LDL-C; SOCS3, UGT1A1, BRCA2, UBE3B, FCGR2A, CHUK, and INSIG2 for TC; and SERPINF2, C4B, GCK, GATA4, INSR, and LPAL2 for TGs. The proportion of explained phenotypic variance in the subset of studies providing individual-level data was 9.9% for HDL-C, 9.5% for LDL-C, 10.3% for TC, and 8.0% for TGs. This large meta-analysis of lipid phenotypes with the use of a dense gene-centric approach identified multiple SNPs not previously described in established lipid genes and several previously unknown loci. The explained phenotypic variance from this approach was comparable to that from a meta-analysis of GWAS data, suggesting that a focused genotyping approach can further increase the understanding of heritability of plasma lipids.

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عنوان ژورنال:
  • American journal of human genetics

دوره 91 5  شماره 

صفحات  -

تاریخ انتشار 2012