Literature DB >> 14551155

Linkage and association between distinct variants of the APOA1/C3/A4/A5 gene cluster and familial combined hyperlipidemia.

Sophie Eichenbaum-Voline1, Michael Olivier, Emma L Jones, Rossitza P Naoumova, Bethan Jones, Brian Gau, Hetal N Patel, Mary Seed, D John Betteridge, David J Galton, Edward M Rubin, James Scott, Carol C Shoulders, Len A Pennacchio.   

Abstract

OBJECTIVE: Combined hyperlipidemia is a common disorder, characterized by a highly atherogenic lipoprotein profile and a substantially increased risk of coronary heart disease. The purpose of this study was to establish whether variations of apolipoprotein A5 (APOA5), a newly discovered gene of lipid metabolism located 30 kbp downstream of the APOA1/C3/A4 gene cluster, contributes to the transmission of familial combined hyperlipidemia (FCHL). METHODS AND
RESULTS: We performed linkage and association tests on 128 families. Two independent alleles, APOA5c.56G and APOC3c.386G, of the APOA1/C3/A4/A5 gene cluster were overtransmitted in FCHL (P=0.004 and 0.007, respectively). This was paired with reduced transmission of the common APOA1/C3/A4/A5 haplotype (frequency 0.4461) to affected subjects (P=0.012). The APOA5c.56G genotype accounted for 7.3% to 13.8% of the variance in plasma triglyceride levels in probands (P<0.004). The APOC3c.386G genotypes accounted for 4.4% to 5.1% of the variance in triglyceride levels in FCHL spouses (P<0.007), suggesting that this allele marks a FCHL quantitative trait as well as representing a susceptibility locus for the condition.
CONCLUSIONS: A combined linkage and association analysis establishes that variation at the APOA1/C3/A4/A5 gene cluster contributes to FCHL transmission in a substantial proportion of northern European families.

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Year:  2003        PMID: 14551155      PMCID: PMC2773540          DOI: 10.1161/01.ATV.0000099881.83261.D4

Source DB:  PubMed          Journal:  Arterioscler Thromb Vasc Biol        ISSN: 1079-5642            Impact factor:   8.311


  46 in total

1.  Genomewide scan for familial combined hyperlipidemia genes in finnish families, suggesting multiple susceptibility loci influencing triglyceride, cholesterol, and apolipoprotein B levels.

Authors:  P Pajukanta; J D Terwilliger; M Perola; T Hiekkalinna; I Nuotio; P Ellonen; M Parkkonen; J Hartiala; K Ylitalo; J Pihlajamäki; K Porkka; M Laakso; J Viikari; C Ehnholm; M R Taskinen; L Peltonen
Journal:  Am J Hum Genet       Date:  1999-05       Impact factor: 11.025

2.  Phenotype expression in familial combined hyperlipidemia.

Authors:  K V Porkka; I Nuotio; P Pajukanta; C Ehnholm; L Suurinkeroinen; M Syvänne; T Lehtimäki; A T Lahdenkari; S Lahdenperä; K Ylitalo; M Antikainen; M Perola; O T Raitakari; P Kovanen; J S Viikari; L Peltonen; M R Taskinen
Journal:  Atherosclerosis       Date:  1997-09       Impact factor: 5.162

3.  Linkage analysis of complex traits using affected sibpairs: effects of single-locus approximations on estimates of the required sample size.

Authors:  A A Todorov; I B Borecki; D C Rao
Journal:  Genet Epidemiol       Date:  1997       Impact factor: 2.135

4.  Evidence against linkage of familial combined hyperlipidemia to the apolipoprotein AI-CIII-AIV gene complex.

Authors:  E M Wijsman; J D Brunzell; G P Jarvik; M A Austin; A G Motulsky; S S Deeb
Journal:  Arterioscler Thromb Vasc Biol       Date:  1998-02       Impact factor: 8.311

5.  Clinical and molecular evidence of abnormal processing and trafficking of the vasopressin preprohormone in a large kindred with familial neurohypophyseal diabetes insipidus due to a signal peptide mutation.

Authors:  C Siggaard; S Rittig; T J Corydon; P H Andreasen; T G Jensen; B S Andresen; G L Robertson; N Gregersen; L Bolund; E B Pedersen
Journal:  J Clin Endocrinol Metab       Date:  1999-08       Impact factor: 5.958

6.  ApoCIII gene variants modulate postprandial response to both glucose and fat tolerance tests.

Authors:  D M Waterworth; J Ribalta; V Nicaud; J Dallongeville; S E Humphries; P Talmud
Journal:  Circulation       Date:  1999-04-13       Impact factor: 29.690

7.  A novel mutation of the signal peptide of the preproparathyroid hormone gene associated with autosomal recessive familial isolated hypoparathyroidism.

Authors:  T Sunthornthepvarakul; S Churesigaew; S Ngowngarmratana
Journal:  J Clin Endocrinol Metab       Date:  1999-10       Impact factor: 5.958

8.  A genome scan for familial combined hyperlipidemia reveals evidence of linkage with a locus on chromosome 11.

Authors:  B E Aouizerat; H Allayee; R M Cantor; R C Davis; C D Lanning; P Z Wen; G M Dallinga-Thie; T W de Bruin; J I Rotter; A J Lusis
Journal:  Am J Hum Genet       Date:  1999-08       Impact factor: 11.025

9.  Retinoids increase human apo C-III expression at the transcriptional level via the retinoid X receptor. Contribution to the hypertriglyceridemic action of retinoids.

Authors:  N Vu-Dac; P Gervois; I P Torra; J C Fruchart; V Kosykh; T Kooistra; H M Princen; J Dallongeville; B Staels
Journal:  J Clin Invest       Date:  1998-08-01       Impact factor: 14.808

10.  Haplotypes of the ApoA-I/C-III/A-IV gene cluster and familial combined hyperlipidemia.

Authors:  E Tahvanainen; P Pajukanta; K Porkka; S Nieminen; L Ikävalko; I Nuotio; M R Taskinen; L Peltonen; C Ehnholm
Journal:  Arterioscler Thromb Vasc Biol       Date:  1998-11       Impact factor: 8.311

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  35 in total

Review 1.  The genetics of familial combined hyperlipidaemia.

Authors:  Martijn C G J Brouwers; Marleen M J van Greevenbroek; Coen D A Stehouwer; Jacqueline de Graaf; Anton F H Stalenhoef
Journal:  Nat Rev Endocrinol       Date:  2012-02-14       Impact factor: 43.330

2.  Plasma apolipoprotein A5 and triglycerides in type 2 diabetes.

Authors:  G M Dallinga-Thie; A van Tol; H Hattori; L C van Vark-van der Zee; H Jansen; E J G Sijbrands
Journal:  Diabetologia       Date:  2006-04-28       Impact factor: 10.122

Review 3.  Give me A5 for lipoprotein hydrolysis!

Authors:  Martin Merkel; Joerg Heeren
Journal:  J Clin Invest       Date:  2005-10       Impact factor: 14.808

Review 4.  New technologies for delineating and characterizing the lipid exome: prospects for understanding familial combined hyperlipidemia.

Authors:  Stuart D Horswell; Helen E Ringham; Carol C Shoulders
Journal:  J Lipid Res       Date:  2008-11-20       Impact factor: 5.922

5.  Apoa5 Q139X truncation predisposes to late-onset hyperchylomicronemia due to lipoprotein lipase impairment.

Authors:  Christophe Marçais; Bruno Verges; Sybil Charrière; Valérie Pruneta; Micheline Merlin; Stéphane Billon; Laurence Perrot; Jocelyne Drai; Agnès Sassolas; Len A Pennacchio; Jamila Fruchart-Najib; Jean-Charles Fruchart; Vincent Durlach; Philippe Moulin
Journal:  J Clin Invest       Date:  2005-10       Impact factor: 14.808

6.  FABP4 plasma levels are increased in familial combined hyperlipidemia.

Authors:  Anna Cabré; Iolanda Lázaro; Montserrat Cofán; Estibaliz Jarauta; Núria Plana; Angel L Garcia-Otín; Juan F Ascaso; Raimón Ferré; Fernando Civeira; Emilio Ros; Lluís Masana
Journal:  J Lipid Res       Date:  2010-05       Impact factor: 5.922

7.  Genetic variation in lean body mass, changes of appetite and weight loss in response to diet interventions: The POUNDS Lost trial.

Authors:  Xiang Li; Tao Zhou; Hao Ma; Yoriko Heianza; Catherine M Champagne; Donald A Williamson; George A Bray; Frank M Sacks; Lu Qi
Journal:  Diabetes Obes Metab       Date:  2020-08-20       Impact factor: 6.577

8.  Gene-gene interaction between APOA5 and USF1: two candidate genes for the metabolic syndrome.

Authors:  Paula Singmann; Jens Baumert; Christian Herder; Christa Meisinger; Christina Holzapfel; Norman Klopp; H-Erich Wichmann; Martin Klingenspor; Wolfgang Rathmann; Thomas Illig; Harald Grallert
Journal:  Obes Facts       Date:  2009-07-20       Impact factor: 3.942

9.  Pharmacogenetic association of the APOA1/C3/A4/A5 gene cluster and lipid responses to fenofibrate: the genetics of lipid-lowering drugs and diet network study.

Authors:  Yongjun Liu; Jose M Ordovas; Guimin Gao; Michael Province; Robert J Straka; Michael Y Tsai; Chao-Qiang Lai; Kui Zhang; Ingrid Borecki; James E Hixson; David B Allison; Donna K Arnett
Journal:  Pharmacogenet Genomics       Date:  2009-02       Impact factor: 2.089

10.  Apolipoprotein A1 gene polymorphisms as risk factors for hypertension and obesity.

Authors:  Elizabeth Suchi Chen; Diego Robles Mazzotti; Tatiane Katsue Furuya; Maysa Seabra Cendoroglo; Luiz Roberto Ramos; Lara Quirino Araujo; Rommel Rodriguez Burbano; Marília de Arruda Cardoso Smith
Journal:  Clin Exp Med       Date:  2009-05-01       Impact factor: 3.984

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