An increased frequency of the 5A allele in the promoter region of the MMP3 gene is associated with abdominal aortic aneurysms

被引:39
作者
Deguara, Jean
Burnand, Kevin G.
Berg, Jonathan
Green, Peter
Lewis, Cathryn M.
Chinien, Ganesh
Waltham, Matthew
Taylor, Peter
Stern, Rachel F.
Solomon, Ellen
Smith, Alberto [1 ]
机构
[1] Kings Coll London, St Thomas Hosp, Div Cardiovasc, Acad Dept Surg, London SE1 7EH, England
[2] Kings Coll London, Guys Hosp, Div Genet & Mol Med, London SE1 9RT, England
[3] Univ Dundee, Ninewells Hosp & Med Sch, Dept Pathol & Neurosci, Dundee DD1 9SY, Scotland
[4] St Thomas Hosp, Guys & St Thomas NHS Fdn Trust, Dept Surg, London SE1 7EH, England
关键词
D O I
10.1093/hmg/ddm258
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Matrix metalloproteinase 3 (MMP3), is over expressed in the wall of abdominal aortic aneurysms (AAA), while inactivation of the gene expressing this enzyme is associated with reduced aneurysm formation in an experimental model. The 5A allele of the 5A/6A polymorphism in the promoter region of the MMP3 gene is associated with enhanced MMP3 expression. This study aimed to determine whether the presence of the 5A allele in the MMP3 promoter is a risk factor for AAA, and if this allele is associated with an increased expression of MMP3 in the aneurysm wall. We compared the frequencies of the 5A and 6A alleles in AAA (n=405), aortic occlusive disease (AOD) (n=123) and controls (n=405). The 5A allele frequency was higher in AAA compared with controls (odds ratio - OR 1.32, P=0.005) and AOD (OR 1.684, P=0.0004), but was similar in AOD compared to controls (OR 0.78, P=0.1). The ORs of the 5A/6A and the 5A/5A genotypes were 1.35 and 1.79, compared with 6A homozygotes. Although wall from 5A homozygotes contained 17% more MMP3 mRNA than homozygotes (P=0.049) the significance of this was lost when adjusted for age and sex (P=0.069), and size (P=0.30). Wall from 5A homozygotes did however contain over 45% more MMP3 protein than heterozygotes (P=0.009 when corrected for age and sex and P=0.043 when corrected for aneurysm size). It appears that an abnormality in the MMP3 gene is part of the genetic profile that predisposes to aneurysmal disease.
引用
收藏
页码:3002 / 3007
页数:6
相关论文
共 41 条
  • [1] Differential regulation of matrix metalloproteinase activities in abdominal aortic aneurysms
    Annabi, B
    Shédid, D
    Ghosn, P
    Kenigsberg, RL
    Desrosiers, RR
    Bojanowski, MW
    Beaulieu, É
    Nassif, E
    Moumdjian, R
    Béliveau, R
    [J]. JOURNAL OF VASCULAR SURGERY, 2002, 35 (03) : 539 - 546
  • [2] Association between RANTES promoter polymorphism-401A and enhanced RANTES production in atopic dermatitis patients
    Bai, BX
    Tanaka, K
    Tazawa, T
    Yamamoto, N
    Sugiura, H
    [J]. JOURNAL OF DERMATOLOGICAL SCIENCE, 2005, 39 (03) : 189 - 191
  • [3] Metalloproteinase inhibitors: biological actions and therapeutic opportunities
    Baker, AH
    Edwards, DR
    Murphy, G
    [J]. JOURNAL OF CELL SCIENCE, 2002, 115 (19) : 3719 - 3727
  • [4] Blanchard JF, 2000, AM J EPIDEMIOL, V151, P575
  • [5] ELASTIN DEGRADATION IN ABDOMINAL AORTIC-ANEURYSMS
    CAMPA, JS
    GREENHALGH, RM
    POWELL, JT
    [J]. ATHEROSCLEROSIS, 1987, 65 (1-2) : 13 - 21
  • [6] Stromelysin-1 (matrix metalloproteinase-3) and tissue inhibitor of metalloproteinase-3 are overexpressed in the wall of abdominal aortic aneurysms
    Carrell, TWG
    Burnand, KG
    Wells, GMA
    Clements, JM
    Smith, A
    [J]. CIRCULATION, 2002, 105 (04) : 477 - 482
  • [7] Response of encapsulated rat pancreatic islets to hypoxia
    de Groot, M
    Schuurs, TA
    Keizer, PPM
    Fekken, S
    Leuvenink, HGD
    van Schilfgaarde, R
    [J]. CELL TRANSPLANTATION, 2003, 12 (08) : 867 - 875
  • [8] Aneurysmatic dilatation of ascending aorta in a patient with β-thalassemia and a pseudoxanthoma elasticum-like syndrome
    Farmakis, D
    Vesleme, V
    Papadogianni, A
    Tsaftaridis, P
    Kapralos, P
    Aessopos, A
    [J]. ANNALS OF HEMATOLOGY, 2004, 83 (09) : 596 - 599
  • [9] THE ORDER AND ORIENTATION OF A CLUSTER OF METALLOPROTEINASE GENES, STROMELYSIN-2, COLLAGENASE, AND STROMELYSIN, TOGETHER WITH D11S385, ON CHROMOSOME-11Q22-Q23
    FORMSTONE, CJ
    BYRD, PJ
    AMBROSE, HJ
    RILEY, JH
    HERNANDEZ, D
    MCCONVILLE, CM
    TAYLOR, AMR
    [J]. GENOMICS, 1993, 16 (01) : 289 - 291
  • [10] Guo DC, 2001, CIRCULATION, V103, P2461