Zinc Finger 259 Gene Polymorphism rs964184 is Associated with Serum Triglyceride Levels and Metabolic Syndrome

被引:0
作者
Mirhafez, Seyed Reza [1 ,2 ,3 ]
Avan, Amir [2 ,3 ]
Pasdar, Alireza [2 ,3 ,4 ]
Khatamianfar, Sara [2 ,3 ]
Hosseinzadeh, Leila [2 ,3 ]
Ganjali, Shiva [2 ,3 ]
Movahedi, Ali [1 ]
Pirhoushiaran, Maryam [5 ]
Mellado, Valentina Gomez [6 ]
Rosace, Domenico [7 ]
van Krieken, Anne [8 ]
Nohtani, Mahdi [2 ,3 ]
Ferns, Gordon A. [9 ]
Ghayour-Mobarhan, Majid [2 ,3 ]
机构
[1] Neyshabur Univ Med Sci, Dept Basic Med Sci, Neyshabur, Iran
[2] Mashhad Univ Med Sci, Sch Med, Dept Modern Sci & Technol, Mashhad, Iran
[3] Mashhad Univ Med Sci, Sch Med, Biochem Nutr Res Ctr, Mashhad, Iran
[4] Univ Aberdeen, Sch Med, Div Appl Med, Foresterhill, Aberdeen AB25 2ZD, Scotland
[5] Mashhad Univ Med Sci, Fac Med, Dept Med Genet, Mashhad, Iran
[6] Vrije Univ Amsterdam, Med Ctr, De Boelelaan 1117, NL-1081 HV Amsterdam, Netherlands
[7] Univ Bologna, Bologna, Italy
[8] Peter MacCallum Ctr, St Andrews Pl, Melbourne, Vic, Australia
[9] Brighton & Sussex Med Sch, Div Med Educ, Brighton BN1 9PH, Sussex, England
关键词
Metabolic syndrome; gene polymorphisms; lipid pathway;
D O I
暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Metabolic syndrome (MetS) is characterized by a cluster of cardiovascular risk factors that include: abdominal obesity, dyslipidaemia, hypertension, insulin resistance and impaired glucose tolerance. Recent genome wide association studies have identified several susceptibility regions involved in lipid metabolism that are also associated with MetS. We have explored the association of 9 genetic polymorphisms involved in lipid metabolism and hypertension, including: MTHFR C677T, SELE L554F, FGB - 455G>A, GNB3 C825T, ZNF259 C>G, PSRC-1 A>G, CETP I405V, LPL S447X and LPA C>T in 97 subjects with MetS and 96 individuals without MetS who were recruited randomly from Mashhad stroke and heart atherosclerotic disorder (MASHAD) study using a stratified cluster random sampling technique. Anthropometric parameters and biochemical measurements were determined in all the subjects. Genotyping was carried out followed by univariate and multivariate analyses. The subjects with MetS had a higher triglyceride and lower HDL-C. CG+ GG genotypes of ZNF259 polymorphism (rs964184 C>G) and TT+ CT genotypes of MTHFR C677T (rs1801133) were associated with MetS, and individuals carrying the G allele for ZNF259 or the T allele for MTHFR polymorphisms were associated with MetS (e.g, odds ratio (OR) for CG+ GG genotypes vs. CC wild type: 2.52, CI=1.33-4.77; P=0.005). However, after multiple comparison adjustment, this relationship remained significant only for CG+ GG genotypes of ZNF259 polymorphism. Moreover, the ZNF259 CG+ GG genotypes were associated with increased serum concentrations of triglycerides and LDL-C, compared to the wild type. These data support the necessity for further studies in larger multicenter settings.
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页码:8 / 18
页数:11
相关论文
共 43 条
  • [1] Candidate genetic variants in the fibrinogen, methylenetetrahydrofolate reductase, and intercellular adhesion molecule-1 genes and plasma levels of fibrinogen, homocysteine, and intercellular adhesion molecule-1 among various race/ethnic groups: Data from the Women's Genome Health Study
    Albert, Michelle A.
    Pare, Guillaume
    Morris, Alanna
    Rose, Lynda
    Buring, Julie
    Ridker, Paul M.
    Zee, Robert Y. L.
    [J]. AMERICAN HEART JOURNAL, 2009, 157 (04) : 777 - 783
  • [2] Metabolic syndrome - a new world-wide definition. A consensus statement from the international diabetes federation
    Alberti, KGMM
    Zimmet, P
    Shaw, J
    [J]. DIABETIC MEDICINE, 2006, 23 (05) : 469 - 480
  • [3] Association of the variants in the BUD13-ZNF259 genes and the risk of hyperlipidaemia
    Aung, Lynn Htet Htet
    Yin, Rui-Xing
    Wu, Dong-Feng
    Wang, Wei
    Liu, Cheng-Wu
    Pan, Shang-Ling
    [J]. JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2014, 18 (07) : 1417 - 1428
  • [4] Unique lipoprotein phenotype and genotype associated with exceptional longevity
    Barzilai, N
    Atzmon, G
    Schechter, C
    Schaefer, EJ
    Cupples, AL
    Lipton, R
    Cheng, S
    Shuldiner, AR
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2003, 290 (15): : 2030 - 2040
  • [5] A Replication Study of GWAS-Derived Lipid Genes in Asian Indians: The Chromosomal Region 11q23.3 Harbors Loci Contributing to Triglycerides
    Braun, Timothy R.
    Been, Latonya F.
    Singhal, Akhil
    Worsham, Jacob
    Ralhan, Sarju
    Wander, Gurpreet S.
    Chambers, John C.
    Kooner, Jaspal S.
    Aston, Christopher E.
    Sanghera, Dharambir K.
    [J]. PLOS ONE, 2012, 7 (05):
  • [6] Interaction between Fibrinogen and IL-6 Genetic Variants and Associations with Cardiovascular Disease Risk in the Cardiovascular Health Study
    Carty, Cara L.
    Heagerty, Patrick
    Heckbert, Susan R.
    Jarvik, Gail P.
    Lange, Leslie A.
    Cushman, Mary
    Tracy, Russell P.
    Reiner, Alexander P.
    [J]. ANNALS OF HUMAN GENETICS, 2010, 74 : 1 - 10
  • [7] Genetic Loci Associated With Plasma Concentration of Low-Density Lipoprotein Cholesterol, High-Density Lipoprotein Cholesterol, Triglycerides, Apolipoprotein A1, and Apolipoprotein B Among 6382 White Women in Genome-Wide Analysis With Replication
    Chasman, Daniel I.
    Pare, Guillaume
    Zee, Robert Y. L.
    Parker, Alex N.
    Cook, Nancy R.
    Buring, Julie E.
    Kwiatkowski, David J.
    Rose, Lynda M.
    Smith, Joshua D.
    Williams, Paul T.
    Rieder, Mark J.
    Rotter, Jerome I.
    Nickerson, Deborah A.
    Krauss, Ronald M.
    Miletich, Joseph P.
    Ridker, Paul M.
    [J]. CIRCULATION-CARDIOVASCULAR GENETICS, 2008, 1 (01) : 21 - U115
  • [8] Genetic Variants Associated with Lp(a) Lipoprotein Level and Coronary Disease
    Clarke, Robert
    Peden, John F.
    Hopewell, Jemma C.
    Kyriakou, Theodosios
    Goel, Anuj
    Heath, Simon C.
    Parish, Sarah
    Barlera, Simona
    Franzosi, Maria Grazia
    Rust, Stephan
    Bennett, Derrick
    Silveira, Angela
    Malarstig, Anders
    Green, Fiona R.
    Lathrop, Mark
    Gigante, Bruna
    Leander, Karin
    de Faire, Ulf
    Seedorf, Udo
    Hamsten, Anders
    Collins, Rory
    Watkins, Hugh
    Farrall, Martin
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2009, 361 (26) : 2518 - 2528
  • [9] The LPL S447X cSNP is associated with decreased blood pressure and plasma triglycerides, and reduced risk of coronary artery disease
    Clee, SM
    Loubser, O
    Collins, J
    Kastelein, JJP
    Hayden, MR
    [J]. CLINICAL GENETICS, 2001, 60 (04) : 293 - 300
  • [10] Follow-up of a major linkage peak on chromosome 1 reveals suggestive QTLs associated with essential hypertension: GenNet study
    Ehret, Georg B.
    O'Connor, Ashley A.
    Weder, Alan
    Cooper, Richard S.
    Chakravarti, Aravinda
    [J]. EUROPEAN JOURNAL OF HUMAN GENETICS, 2009, 17 (12) : 1650 - 1657