Literature DB >> 23505323

Genomic study in Mexicans identifies a new locus for triglycerides and refines European lipid loci.

Daphna Weissglas-Volkov1, Carlos A Aguilar-Salinas, Elina Nikkola, Kerry A Deere, Ivette Cruz-Bautista, Olimpia Arellano-Campos, Linda Liliana Muñoz-Hernandez, Lizeth Gomez-Munguia, Maria Luisa Ordoñez-Sánchez, Prasad M V Linga Reddy, Aldons J Lusis, Niina Matikainen, Marja-Riitta Taskinen, Laura Riba, Rita M Cantor, Janet S Sinsheimer, Teresa Tusie-Luna, Päivi Pajukanta.   

Abstract

BACKGROUND: The Mexican population and others with Amerindian heritage exhibit a substantial predisposition to dyslipidemias and coronary heart disease. Yet, these populations remain underinvestigated by genomic studies, and to date, no genome-wide association (GWA) studies have been reported for lipids in these rapidly expanding populations. METHODS AND
FINDINGS: We performed a two-stage GWA study for hypertriglyceridemia and low high-density lipoprotein cholesterol (HDL-C) in Mexicans (n=4361), and identified a novel Mexican-specific genome-wide significant locus for serum triglycerides (TGs) near the Niemann-Pick type C1 protein gene (p=2.43×10(-08)). Furthermore, three European loci for TGs (APOA5, GCKR and LPL), and four loci for HDL-C (ABCA1, CETP, LIPC and LOC55908) reached genome-wide significance in Mexicans. We used cross-ethnic mapping to narrow three European TG GWA loci, APOA5, MLXIPL, and CILP2 that were wide and contained multiple candidate variants in the European scan. At the APOA5 locus, this reduced the most likely susceptibility variants to one, rs964184. Importantly, our functional analysis demonstrated a direct link between rs964184 and postprandial serum apoAV protein levels, supporting rs964184 as the causative variant underlying the European and Mexican GWA signal. Overall, 52 of the 100 reported associations from European lipid GWA meta-analysis generalised to Mexicans. However, in 82 of the 100 European GWA loci, a different variant other than the European lead/best-proxy variant had the strongest regional evidence of association in Mexicans.
CONCLUSIONS: This first Mexican GWA study of lipids identified a novel GWA locus for high TG levels; used the interpopulation heterogeneity to significantly restrict three previously known European GWA signals, and surveyed whether the European lipid GWA SNPs extend to the Mexican population.

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Year:  2013        PMID: 23505323      PMCID: PMC3917605          DOI: 10.1136/jmedgenet-2012-101461

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  51 in total

1.  PLINK: a tool set for whole-genome association and population-based linkage analyses.

Authors:  Shaun Purcell; Benjamin Neale; Kathe Todd-Brown; Lori Thomas; Manuel A R Ferreira; David Bender; Julian Maller; Pamela Sklar; Paul I W de Bakker; Mark J Daly; Pak C Sham
Journal:  Am J Hum Genet       Date:  2007-07-25       Impact factor: 11.025

2.  Identification of two common variants contributing to serum apolipoprotein B levels in Mexicans.

Authors:  Daphna Weissglas-Volkov; Christopher L Plaisier; Adriana Huertas-Vazquez; Ivette Cruz-Bautista; Daniela Riaño-Barros; Miguel Herrera-Hernandez; Laura Riba; Rita M Cantor; Janet S Sinsheimer; Carlos A Aguilar-Salinas; Teresa Tusie-Luna; Päivi Pajukanta
Journal:  Arterioscler Thromb Vasc Biol       Date:  2009-12-03       Impact factor: 8.311

3.  A high-resolution association mapping panel for the dissection of complex traits in mice.

Authors:  Brian J Bennett; Charles R Farber; Luz Orozco; Hyun Min Kang; Anatole Ghazalpour; Nathan Siemers; Michael Neubauer; Isaac Neuhaus; Roumyana Yordanova; Bo Guan; Amy Truong; Wen-pin Yang; Aiqing He; Paul Kayne; Peter Gargalovic; Todd Kirchgessner; Calvin Pan; Lawrence W Castellani; Emrah Kostem; Nicholas Furlotte; Thomas A Drake; Eleazar Eskin; Aldons J Lusis
Journal:  Genome Res       Date:  2010-01-06       Impact factor: 9.043

4.  Orphan nuclear receptor Nur77 participates in human apolipoprotein A5 gene expression.

Authors:  Kwang-Hoon Song
Journal:  Biochem Biophys Res Commun       Date:  2010-01-07       Impact factor: 3.575

5.  Proper analysis of secondary phenotype data in case-control association studies.

Authors:  D Y Lin; D Zeng
Journal:  Genet Epidemiol       Date:  2009-04       Impact factor: 2.135

6.  Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations.

Authors:  David Meyre; Jérôme Delplanque; Jean-Claude Chèvre; Cécile Lecoeur; Stéphane Lobbens; Sophie Gallina; Emmanuelle Durand; Vincent Vatin; Franck Degraeve; Christine Proença; Stefan Gaget; Antje Körner; Peter Kovacs; Wieland Kiess; Jean Tichet; Michel Marre; Anna-Liisa Hartikainen; Fritz Horber; Natascha Potoczna; Serge Hercberg; Claire Levy-Marchal; François Pattou; Barbara Heude; Maithé Tauber; Mark I McCarthy; Alexandra I F Blakemore; Alexandre Montpetit; Constantin Polychronakos; Jacques Weill; Lachlan J M Coin; Julian Asher; Paul Elliott; Marjo-Riitta Järvelin; Sophie Visvikis-Siest; Beverley Balkau; Rob Sladek; David Balding; Andrew Walley; Christian Dina; Philippe Froguel
Journal:  Nat Genet       Date:  2009-01-18       Impact factor: 38.330

7.  The National Niemann-Pick Type C1 Disease Database: correlation of lipid profiles, mutations, and biochemical phenotypes.

Authors:  William S Garver; David Jelinek; F John Meaney; James Flynn; Kathleen M Pettit; Glen Shepherd; Randall A Heidenreich; Cate M Walsh Vockley; Graciela Castro; Gordon A Francis
Journal:  J Lipid Res       Date:  2009-09-09       Impact factor: 5.922

8.  Common missense variant in the glucokinase regulatory protein gene is associated with increased plasma triglyceride and C-reactive protein but lower fasting glucose concentrations.

Authors:  Marju Orho-Melander; Olle Melander; Candace Guiducci; Pablo Perez-Martinez; Dolores Corella; Charlotta Roos; Ryan Tewhey; Mark J Rieder; Jennifer Hall; Goncalo Abecasis; E Shyong Tai; Cullan Welch; Donna K Arnett; Valeriya Lyssenko; Eero Lindholm; Richa Saxena; Paul I W de Bakker; Noel Burtt; Benjamin F Voight; Joel N Hirschhorn; Katherine L Tucker; Thomas Hedner; Tiinamaija Tuomi; Bo Isomaa; Karl-Fredrik Eriksson; Marja-Riitta Taskinen; Björn Wahlstrand; Thomas E Hughes; Laurence D Parnell; Chao-Qiang Lai; Göran Berglund; Leena Peltonen; Erkki Vartiainen; Pekka Jousilahti; Aki S Havulinna; Veikko Salomaa; Peter Nilsson; Leif Groop; David Altshuler; Jose M Ordovas; Sekar Kathiresan
Journal:  Diabetes       Date:  2008-08-04       Impact factor: 9.461

9.  A polygenic basis for four classical Fredrickson hyperlipoproteinemia phenotypes that are characterized by hypertriglyceridemia.

Authors:  Robert A Hegele; Matthew R Ban; Neil Hsueh; Brooke A Kennedy; Henian Cao; Guang Yong Zou; Sonia Anand; Salim Yusuf; Murray W Huff; Jian Wang
Journal:  Hum Mol Genet       Date:  2009-08-05       Impact factor: 6.150

10.  Common variants at 30 loci contribute to polygenic dyslipidemia.

Authors:  Sekar Kathiresan; Cristen J Willer; Gina M Peloso; Serkalem Demissie; Kiran Musunuru; Eric E Schadt; Lee Kaplan; Derrick Bennett; Yun Li; Toshiko Tanaka; Benjamin F Voight; Lori L Bonnycastle; Anne U Jackson; Gabriel Crawford; Aarti Surti; Candace Guiducci; Noel P Burtt; Sarah Parish; Robert Clarke; Diana Zelenika; Kari A Kubalanza; Mario A Morken; Laura J Scott; Heather M Stringham; Pilar Galan; Amy J Swift; Johanna Kuusisto; Richard N Bergman; Jouko Sundvall; Markku Laakso; Luigi Ferrucci; Paul Scheet; Serena Sanna; Manuela Uda; Qiong Yang; Kathryn L Lunetta; Josée Dupuis; Paul I W de Bakker; Christopher J O'Donnell; John C Chambers; Jaspal S Kooner; Serge Hercberg; Pierre Meneton; Edward G Lakatta; Angelo Scuteri; David Schlessinger; Jaakko Tuomilehto; Francis S Collins; Leif Groop; David Altshuler; Rory Collins; G Mark Lathrop; Olle Melander; Veikko Salomaa; Leena Peltonen; Marju Orho-Melander; Jose M Ordovas; Michael Boehnke; Gonçalo R Abecasis; Karen L Mohlke; L Adrienne Cupples
Journal:  Nat Genet       Date:  2008-12-07       Impact factor: 38.330

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  59 in total

1.  Associations of common SNPs in the SORT1, GCKR, LPL, APOA1, CETP, LDLR, APOE genes with lipid trait levels in an Algerian population sample.

Authors:  Djabaria Naïma Meroufel; Sounnia Mediene-Benchekor; Sarah Aïcha Lardjam-Hetraf; Hadjira Ouhaïbi-Djellouli; Houssam Boulenouar; Imane Hamani-Medjaoui; Xavier Hermant; Nadhira Saïdi-Mehtar; Philippe Amouyel; Leïla Houti; Aline Meirhaeghe; Louisa Goumidi
Journal:  Int J Clin Exp Pathol       Date:  2015-06-01

2.  Investigation of associations between ten polymorphisms and the risk of coronary artery disease in Southern Han Chinese.

Authors:  Er-Wen Huang; Long-Yun Peng; Jin-Xiang Zheng; Dan Wang; Xiao-Hong Tan; Zhong-Yi Yang; Xue-Mei Li; Qiu-Ping Wu; Shuang-Bo Tang; Bin Luo; Li Quan; Shui-Ping Liu; Xiao-Shan Liu; Zhao-Hui Li; He Shi; Guo-Li Lv; Jian Zhao; Chao Liu; Jian-Ding Cheng
Journal:  J Hum Genet       Date:  2016-01-07       Impact factor: 3.172

3.  THOC5: a novel gene involved in HDL-cholesterol metabolism.

Authors:  Maria Keller; Dorit Schleinitz; Julia Förster; Anke Tönjes; Yvonne Böttcher; Antje Fischer-Rosinsky; Jana Breitfeld; Kerstin Weidle; Nigel W Rayner; Ralph Burkhardt; Beate Enigk; Ines Müller; Jan Halbritter; Moritz Koriath; Andreas Pfeiffer; Knut Krohn; Leif Groop; Joachim Spranger; Michael Stumvoll; Peter Kovacs
Journal:  J Lipid Res       Date:  2013-09-10       Impact factor: 5.922

Review 4.  Genetic and environmental determinants of the susceptibility of Amerindian derived populations for having hypertriglyceridemia.

Authors:  Carlos A Aguilar-Salinas; Teresa Tusie-Luna; Päivi Pajukanta
Journal:  Metabolism       Date:  2014-03-30       Impact factor: 8.694

5.  Fine-mapping of lipid regions in global populations discovers ethnic-specific signals and refines previously identified lipid loci.

Authors:  Niha Zubair; Mariaelisa Graff; Jose Luis Ambite; William S Bush; Gleb Kichaev; Yingchang Lu; Ani Manichaikul; Wayne H-H Sheu; Devin Absher; Themistocles L Assimes; Suzette J Bielinski; Erwin P Bottinger; Petra Buzkova; Lee-Ming Chuang; Ren-Hua Chung; Barbara Cochran; Logan Dumitrescu; Omri Gottesman; Jeffrey W Haessler; Christopher Haiman; Gerardo Heiss; Chao A Hsiung; Yi-Jen Hung; Chii-Min Hwu; Jyh-Ming J Juang; Loic Le Marchand; I-Te Lee; Wen-Jane Lee; Li-An Lin; Danyu Lin; Shih-Yi Lin; Rachel H Mackey; Lisa W Martin; Bogdan Pasaniuc; Ulrike Peters; Irene Predazzi; Thomas Quertermous; Alex P Reiner; Jennifer Robinson; Jerome I Rotter; Kelli K Ryckman; Pamela J Schreiner; Eli Stahl; Ran Tao; Michael Y Tsai; Lindsay L Waite; Tzung-Dau Wang; Steven Buyske; Yii-Der Ida Chen; Iona Cheng; Dana C Crawford; Ruth J F Loos; Stephen S Rich; Myriam Fornage; Kari E North; Charles Kooperberg; Cara L Carty
Journal:  Hum Mol Genet       Date:  2016-12-15       Impact factor: 6.150

6.  Association between rs2278426 (C/T) and rs892066 (C/G) variants of ANGPTL8 (betatrophin) and susceptibility to type2 diabetes mellitus.

Authors:  Hassan Ghasemi; Jamshid Karimi; Iraj Khodadadi; Massoud Saidijam; Heidar Tavilani
Journal:  J Clin Lab Anal       Date:  2018-09-07       Impact factor: 2.352

7.  Identity-by-Descent Mapping Identifies Major Locus for Serum Triglycerides in Amerindians Largely Explained by an APOC3 Founder Mutation.

Authors:  Wen-Chi Hsueh; Anup K Nair; Sayuko Kobes; Peng Chen; Harald H H Göring; Toni I Pollin; Alka Malhotra; William C Knowler; Leslie J Baier; Robert L Hanson
Journal:  Circ Cardiovasc Genet       Date:  2017-12

8.  Variants for HDL-C, LDL-C, and triglycerides identified from admixture mapping and fine-mapping analysis in African American families.

Authors:  Priya B Shetty; Hua Tang; Tao Feng; Bamidele Tayo; Alanna C Morrison; Sharon L R Kardia; Craig L Hanis; Donna K Arnett; Steven C Hunt; Eric Boerwinkle; Dabeeru C Rao; Richard S Cooper; Neil Risch; Xiaofeng Zhu
Journal:  Circ Cardiovasc Genet       Date:  2014-12-31

9.  Molecular Characterization of the Lipid Genome-Wide Association Study Signal on Chromosome 18q11.2 Implicates HNF4A-Mediated Regulation of the TMEM241 Gene.

Authors:  Alejandra Rodríguez; Luis Gonzalez; Arthur Ko; Marcus Alvarez; Zong Miao; Yash Bhagat; Elina Nikkola; Ivette Cruz-Bautista; Olimpia Arellano-Campos; Linda L Muñoz-Hernández; Maria-Luisa Ordóñez-Sánchez; Rosario Rodriguez-Guillen; Karen L Mohlke; Markku Laakso; Teresa Tusie-Luna; Carlos A Aguilar-Salinas; Päivi Pajukanta
Journal:  Arterioscler Thromb Vasc Biol       Date:  2016-05-19       Impact factor: 8.311

10.  The Arg59Trp variant in ANGPTL8 (betatrophin) is associated with total and HDL-cholesterol in American Indians and Mexican Americans and differentially affects cleavage of ANGPTL3.

Authors:  Robert L Hanson; Fatjon Leti; Darwin Tsinajinnie; Sayuko Kobes; Sobha Puppala; Joanne E Curran; Laura Almasy; Donna M Lehman; John Blangero; Ravindranath Duggirala; Johanna K DiStefano
Journal:  Mol Genet Metab       Date:  2016-04-19       Impact factor: 4.797

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