Skip to main content
Top
Published in: BMC Neurology 1/2014

Open Access 01-12-2014 | Research article

The GC + CC genotype at position -418 in TIMP-2 promoter and the -1575GA/-1306CC genotype in MMP-2is genetic predisposing factors for prevalence of moyamoya disease

Authors: Young Seok Park, Young Joo Jeon, Hyun Seok Kim, In Bo Han, Seung-Hun Oh, Dong-Seok Kim, Nam Keun Kim

Published in: BMC Neurology | Issue 1/2014

Login to get access

Abstract

Background

To investigate the association of single-nucleotide polymorphisms (SNPs) in matrix metalloproteinases (MMPs)-2, -3, and -9 and tissue inhibitor of metalloproteinase (TIMP)-2 with moyamoya disease (MMD). We conducted a case-control study of MMD patients by assessing the prevalence of six SNPs of MMP-2 -1575G > A [rs243866], MMP-2 -1306C > T [rs243865], MMP-3 -1171 5a/6a [rs3025058], MMP-9 -1562C > T [rs3918242], MMP-9 Q279R [rs17576], and TIMP-2 -418G > C [rs8179090].

Methods

Korean patients with MMD (n = 107, mean age, 20.9 ± 15.9 years; 66.4% female) and 243 healthy control subjects (mean age, 23.0 ± 16.1 years; 56.8% female) were included. The subjects were divided into pediatric and adult groups. The genotyping of six well-known SNPs (MMP-2 -1575G > A, MMP-2 -1306C > T, MMP-3 -1171 5a/6a, MMP-9 -1562C > T, MMP-9 Q279R, and TIMP-2 -418G > C) in MMP and TIMP genes was performed by polymerase chain reaction-restriction fragment length polymorphism assays.

Results

A significantly higher frequency of the GC genotype for TIMP-2 -418 G > C was found in MMD patients. The MMP-9 Q279R GA + AA genotype showed a protective effect for MMD. The GA/CC MMP-2 -1575/-1306 genotype was significantly more prevalent in MMD patients.

Conclusions

Our findings demonstrate that TIMP-2 -418 GC + CC and MMP-2 -1575GA/-1306CC genotypes could be genetic predisposing factors for MMD development.
Appendix
Available only for authorised users
Literature
1.
go back to reference Kang HS, Kim SK, Cho BK, Kim YY, Hwang YS, Wang KC: Single nucleotide polymorphisms of tissue inhibitor of metalloproteinase genes in familial moyamoya disease. Neurosurgery. 2006, 58: 1074-1080. 10.1227/01.NEU.0000215854.66011.4F. discussion 1074-1080CrossRefPubMed Kang HS, Kim SK, Cho BK, Kim YY, Hwang YS, Wang KC: Single nucleotide polymorphisms of tissue inhibitor of metalloproteinase genes in familial moyamoya disease. Neurosurgery. 2006, 58: 1074-1080. 10.1227/01.NEU.0000215854.66011.4F. discussion 1074-1080CrossRefPubMed
2.
go back to reference Andreone V, Scala S, Tucci C, Di Napoli D, Linfante I, Tessitore A, Faiella A: Single nucleotide polymorphisms of tissue inhibitors of metalloproteinase genes in familial moyamoya disease.Neurosurgery 2008, 62:E1384. author reply E1384., Andreone V, Scala S, Tucci C, Di Napoli D, Linfante I, Tessitore A, Faiella A: Single nucleotide polymorphisms of tissue inhibitors of metalloproteinase genes in familial moyamoya disease.Neurosurgery 2008, 62:E1384. author reply E1384.,
3.
go back to reference Yilmaz EY, Pritz MB, Bruno A, Lopez-Yunez A, Biller J: Moyamoya: Indiana University Medical Center experience. Arch Neurol. 2001, 58: 1274-1278. 10.1001/archneur.58.8.1274.CrossRefPubMed Yilmaz EY, Pritz MB, Bruno A, Lopez-Yunez A, Biller J: Moyamoya: Indiana University Medical Center experience. Arch Neurol. 2001, 58: 1274-1278. 10.1001/archneur.58.8.1274.CrossRefPubMed
4.
go back to reference Ikeda H, Sasaki T, Yoshimoto T, Fukui M, Arinami T: Mapping of a familial moyamoya disease gene to chromosome 3p24.2-p26. Am J Hum Genet. 1999, 64: 533-537. 10.1086/302243.CrossRefPubMedPubMedCentral Ikeda H, Sasaki T, Yoshimoto T, Fukui M, Arinami T: Mapping of a familial moyamoya disease gene to chromosome 3p24.2-p26. Am J Hum Genet. 1999, 64: 533-537. 10.1086/302243.CrossRefPubMedPubMedCentral
5.
go back to reference Inoue TK, Ikezaki K, Sasazuki T, Matsushima T, Fukui M: Linkage analysis of moyamoya disease on chromosome 6. J Child Neurol. 2000, 15: 179-182. 10.1177/088307380001500307.CrossRefPubMed Inoue TK, Ikezaki K, Sasazuki T, Matsushima T, Fukui M: Linkage analysis of moyamoya disease on chromosome 6. J Child Neurol. 2000, 15: 179-182. 10.1177/088307380001500307.CrossRefPubMed
6.
go back to reference Sakurai K, Horiuchi Y, Ikeda H, Ikezaki K, Yoshimoto T, Fukui M, Arinami T: A novel susceptibility locus for moyamoya disease on chromosome 8q23. J Hum Genet. 2004, 49: 278-281. 10.1007/s10038-004-0143-6.CrossRefPubMed Sakurai K, Horiuchi Y, Ikeda H, Ikezaki K, Yoshimoto T, Fukui M, Arinami T: A novel susceptibility locus for moyamoya disease on chromosome 8q23. J Hum Genet. 2004, 49: 278-281. 10.1007/s10038-004-0143-6.CrossRefPubMed
7.
go back to reference Yamauchi T, Tada M, Houkin K, Tanaka T, Nakamura Y, Kuroda S, Abe H, Inoue T, Ikezaki K, Matsushima T, Fukui M: Linkage of familial moyamoya disease (spontaneous occlusion of the circle of Willis) to chromosome 17q25. Stroke. 2000, 31: 930-935. 10.1161/01.STR.31.4.930.CrossRefPubMed Yamauchi T, Tada M, Houkin K, Tanaka T, Nakamura Y, Kuroda S, Abe H, Inoue T, Ikezaki K, Matsushima T, Fukui M: Linkage of familial moyamoya disease (spontaneous occlusion of the circle of Willis) to chromosome 17q25. Stroke. 2000, 31: 930-935. 10.1161/01.STR.31.4.930.CrossRefPubMed
8.
go back to reference Kang HS, Kim JH, Phi JH, Kim YY, Kim JE, Wang KC, Cho BK, Kim SK: Plasma matrix metalloproteinases, cytokines and angiogenic factors in moyamoya disease. J Neurol Neurosurg Psychiatry. 2010, 81: 673-678. 10.1136/jnnp.2009.191817.CrossRefPubMed Kang HS, Kim JH, Phi JH, Kim YY, Kim JE, Wang KC, Cho BK, Kim SK: Plasma matrix metalloproteinases, cytokines and angiogenic factors in moyamoya disease. J Neurol Neurosurg Psychiatry. 2010, 81: 673-678. 10.1136/jnnp.2009.191817.CrossRefPubMed
9.
go back to reference Fujimura M, Watanabe M, Narisawa A, Shimizu H, Tominaga T: Increased expression of serum Matrix Metalloproteinase-9 in patients with moyamoya disease. Surg Neurol. 2009, 72: 476-480. 10.1016/j.surneu.2008.10.009. discussion 480CrossRefPubMed Fujimura M, Watanabe M, Narisawa A, Shimizu H, Tominaga T: Increased expression of serum Matrix Metalloproteinase-9 in patients with moyamoya disease. Surg Neurol. 2009, 72: 476-480. 10.1016/j.surneu.2008.10.009. discussion 480CrossRefPubMed
10.
go back to reference Johnson C, Galis ZS: Matrix metalloproteinase-2 and -9 differentially regulate smooth muscle cell migration and cell-mediated collagen organization. Arterioscler Thromb Vasc Biol. 2004, 24: 54-60. 10.1161/01.ATV.0000100402.69997.C3.CrossRefPubMed Johnson C, Galis ZS: Matrix metalloproteinase-2 and -9 differentially regulate smooth muscle cell migration and cell-mediated collagen organization. Arterioscler Thromb Vasc Biol. 2004, 24: 54-60. 10.1161/01.ATV.0000100402.69997.C3.CrossRefPubMed
11.
go back to reference Paszkowiak JJ, Dardik A: Arterial wall shear stress: observations from the bench to the bedside. Vasc Endovascular Surg. 2003, 37: 47-57. 10.1177/153857440303700107.CrossRefPubMed Paszkowiak JJ, Dardik A: Arterial wall shear stress: observations from the bench to the bedside. Vasc Endovascular Surg. 2003, 37: 47-57. 10.1177/153857440303700107.CrossRefPubMed
12.
go back to reference Roder C, Nayak NR, Khan N, Tatagiba M, Inoue I, Krischek B: Genetics of Moyamoya disease. J Hum Genet. 2010, 55: 711-716. 10.1038/jhg.2010.103.CrossRefPubMed Roder C, Nayak NR, Khan N, Tatagiba M, Inoue I, Krischek B: Genetics of Moyamoya disease. J Hum Genet. 2010, 55: 711-716. 10.1038/jhg.2010.103.CrossRefPubMed
13.
go back to reference Asahi M, Wang X, Mori T, Sumii T, Jung JC, Moskowitz MA, Fini ME, Lo EH: Effects of matrix metalloproteinase-9 gene knock-out on the proteolysis of blood-brain barrier and white matter components after cerebral ischemia. J Neurosci. 2001, 21: 7724-7732.PubMed Asahi M, Wang X, Mori T, Sumii T, Jung JC, Moskowitz MA, Fini ME, Lo EH: Effects of matrix metalloproteinase-9 gene knock-out on the proteolysis of blood-brain barrier and white matter components after cerebral ischemia. J Neurosci. 2001, 21: 7724-7732.PubMed
14.
go back to reference Li H, Zhang ZS, Liu W, Yang WZ, Dong ZN, Ma MJ, Han C, Yang H, Cao WC, Duan L: Association of a functional polymorphism in the MMP-3 gene with Moyamoya Disease in the Chinese Han population. Cerebrovasc Dis. 2010, 30: 618-625. 10.1159/000319893.CrossRefPubMed Li H, Zhang ZS, Liu W, Yang WZ, Dong ZN, Ma MJ, Han C, Yang H, Cao WC, Duan L: Association of a functional polymorphism in the MMP-3 gene with Moyamoya Disease in the Chinese Han population. Cerebrovasc Dis. 2010, 30: 618-625. 10.1159/000319893.CrossRefPubMed
15.
go back to reference Paez MT, Yamamoto T: Single nucleotide polymorphisms of tissue inhibitor of metalloproteinase genes in familial moyamoya disease.Neurosurgery 2007, 60:E582. author reply E582., Paez MT, Yamamoto T: Single nucleotide polymorphisms of tissue inhibitor of metalloproteinase genes in familial moyamoya disease.Neurosurgery 2007, 60:E582. author reply E582.,
16.
go back to reference Lo EH, Dalkara T, Moskowitz MA: Mechanisms, challenges and opportunities in stroke. Nat Rev Neurosci. 2003, 4: 399-415. 10.1038/nrn1106.CrossRefPubMed Lo EH, Dalkara T, Moskowitz MA: Mechanisms, challenges and opportunities in stroke. Nat Rev Neurosci. 2003, 4: 399-415. 10.1038/nrn1106.CrossRefPubMed
17.
go back to reference Lee SR, Lo EH: Induction of caspase-mediated cell death by matrix metalloproteinases in cerebral endothelial cells after hypoxia-reoxygenation. J Cereb Blood Flow Metab. 2004, 24: 720-727. 10.1097/01.WCB.0000122747.72175.47.CrossRefPubMed Lee SR, Lo EH: Induction of caspase-mediated cell death by matrix metalloproteinases in cerebral endothelial cells after hypoxia-reoxygenation. J Cereb Blood Flow Metab. 2004, 24: 720-727. 10.1097/01.WCB.0000122747.72175.47.CrossRefPubMed
18.
go back to reference Lee CZ, Xu B, Hashimoto T, McCulloch CE, Yang GY, Young WL: Doxycycline suppresses cerebral matrix metalloproteinase-9 and angiogenesis induced by focal hyperstimulation of vascular endothelial growth factor in a mouse model. Stroke. 2004, 35: 1715-1719. 10.1161/01.STR.0000129334.05181.b6.CrossRefPubMed Lee CZ, Xu B, Hashimoto T, McCulloch CE, Yang GY, Young WL: Doxycycline suppresses cerebral matrix metalloproteinase-9 and angiogenesis induced by focal hyperstimulation of vascular endothelial growth factor in a mouse model. Stroke. 2004, 35: 1715-1719. 10.1161/01.STR.0000129334.05181.b6.CrossRefPubMed
19.
go back to reference Rosenberg GA, Navratil M: Metalloproteinase inhibition blocks edema in intracerebral hemorrhage in the rat. Neurology. 1997, 48: 921-926. 10.1212/WNL.48.4.921.CrossRefPubMed Rosenberg GA, Navratil M: Metalloproteinase inhibition blocks edema in intracerebral hemorrhage in the rat. Neurology. 1997, 48: 921-926. 10.1212/WNL.48.4.921.CrossRefPubMed
20.
go back to reference Hamann GF, del Zoppo GJ, von Kummer R: Hemorrhagic transformation of cerebral infarction-possible mechanisms. Thromb Haemost. 1999, 82 (Suppl 1): 92-94.PubMed Hamann GF, del Zoppo GJ, von Kummer R: Hemorrhagic transformation of cerebral infarction-possible mechanisms. Thromb Haemost. 1999, 82 (Suppl 1): 92-94.PubMed
21.
go back to reference Romanic AM, White RF, Arleth AJ, Ohlstein EH, Barone FC: Matrix metalloproteinase expression increases after cerebral focal ischemia in rats: inhibition of matrix metalloproteinase-9 reduces infarct size. Stroke. 1998, 29: 1020-1030. 10.1161/01.STR.29.5.1020.CrossRefPubMed Romanic AM, White RF, Arleth AJ, Ohlstein EH, Barone FC: Matrix metalloproteinase expression increases after cerebral focal ischemia in rats: inhibition of matrix metalloproteinase-9 reduces infarct size. Stroke. 1998, 29: 1020-1030. 10.1161/01.STR.29.5.1020.CrossRefPubMed
22.
go back to reference Wu G, Shi J, Wang F, Wang L, Feng A, Ren S: Effects of minimally invasive procedures for evacuation of intracerebral hematoma in early stages on MMP-9 and BBB permeability in rabbits.BMC Neurol 2014, 14:85., Wu G, Shi J, Wang F, Wang L, Feng A, Ren S: Effects of minimally invasive procedures for evacuation of intracerebral hematoma in early stages on MMP-9 and BBB permeability in rabbits.BMC Neurol 2014, 14:85.,
23.
go back to reference Price SJ, Greaves DR, Watkins H: Identification of novel, functional genetic variants in the human matrix metalloproteinase-2 gene: role of Sp1 in allele-specific transcriptional regulation. J Biol Chem. 2001, 276: 7549-7558. 10.1074/jbc.M010242200.CrossRefPubMed Price SJ, Greaves DR, Watkins H: Identification of novel, functional genetic variants in the human matrix metalloproteinase-2 gene: role of Sp1 in allele-specific transcriptional regulation. J Biol Chem. 2001, 276: 7549-7558. 10.1074/jbc.M010242200.CrossRefPubMed
24.
go back to reference Ye S: Polymorphism in matrix metalloproteinase gene promoters: implication in regulation of gene expression and susceptibility of various diseases. Matrix Biol. 2000, 19: 623-629. 10.1016/S0945-053X(00)00102-5.CrossRefPubMed Ye S: Polymorphism in matrix metalloproteinase gene promoters: implication in regulation of gene expression and susceptibility of various diseases. Matrix Biol. 2000, 19: 623-629. 10.1016/S0945-053X(00)00102-5.CrossRefPubMed
25.
go back to reference Ye S, Eriksson P, Hamsten A, Kurkinen M, Humphries SE, Henney AM: Progression of coronary atherosclerosis is associated with a common genetic variant of the human stromelysin-1 promoter which results in reduced gene expression. J Biol Chem. 1996, 271: 13055-13060. 10.1074/jbc.271.22.13055.CrossRefPubMed Ye S, Eriksson P, Hamsten A, Kurkinen M, Humphries SE, Henney AM: Progression of coronary atherosclerosis is associated with a common genetic variant of the human stromelysin-1 promoter which results in reduced gene expression. J Biol Chem. 1996, 271: 13055-13060. 10.1074/jbc.271.22.13055.CrossRefPubMed
26.
go back to reference Zhang B, Ye S, Herrmann SM, Eriksson P, de Maat M, Evans A, Arveiler D, Luc G, Cambien F, Hamsten A, Watkins H, Henney AM: Functional polymorphism in the regulatory region of gelatinase B gene in relation to severity of coronary atherosclerosis. Circulation. 1999, 99: 1788-1794. 10.1161/01.CIR.99.14.1788.CrossRefPubMed Zhang B, Ye S, Herrmann SM, Eriksson P, de Maat M, Evans A, Arveiler D, Luc G, Cambien F, Hamsten A, Watkins H, Henney AM: Functional polymorphism in the regulatory region of gelatinase B gene in relation to severity of coronary atherosclerosis. Circulation. 1999, 99: 1788-1794. 10.1161/01.CIR.99.14.1788.CrossRefPubMed
27.
go back to reference Yoon S, Kuivaniemi H, Gatalica Z, Olson JM, Buttice G, Ye S, Norris BA, Malcom GT, Strong JP, Tromp G: MMP13 promoter polymorphism is associated with atherosclerosis in the abdominal aorta of young black males. Matrix Biol. 2002, 21: 487-498. 10.1016/S0945-053X(02)00053-7.CrossRefPubMed Yoon S, Kuivaniemi H, Gatalica Z, Olson JM, Buttice G, Ye S, Norris BA, Malcom GT, Strong JP, Tromp G: MMP13 promoter polymorphism is associated with atherosclerosis in the abdominal aorta of young black males. Matrix Biol. 2002, 21: 487-498. 10.1016/S0945-053X(02)00053-7.CrossRefPubMed
28.
go back to reference Yu C, Zhou Y, Miao X, Xiong P, Tan W, Lin D: Functional haplotypes in the promoter of matrix metalloproteinase-2 predict risk of the occurrence and metastasis of esophageal cancer. Cancer Res. 2004, 64: 7622-7628. 10.1158/0008-5472.CAN-04-1521.CrossRefPubMed Yu C, Zhou Y, Miao X, Xiong P, Tan W, Lin D: Functional haplotypes in the promoter of matrix metalloproteinase-2 predict risk of the occurrence and metastasis of esophageal cancer. Cancer Res. 2004, 64: 7622-7628. 10.1158/0008-5472.CAN-04-1521.CrossRefPubMed
29.
go back to reference Rauramaa R, Vaisanen SB, Luong LA, Schmidt-Trucksass A, Penttila IM, Bouchard C, Toyry J, Humphries SE: Stromelysin-1 and interleukin-6 gene promoter polymorphisms are determinants of asymptomatic carotid artery atherosclerosis. Arterioscler Thromb Vasc Biol. 2000, 20: 2657-2662. 10.1161/01.ATV.20.12.2657.CrossRefPubMed Rauramaa R, Vaisanen SB, Luong LA, Schmidt-Trucksass A, Penttila IM, Bouchard C, Toyry J, Humphries SE: Stromelysin-1 and interleukin-6 gene promoter polymorphisms are determinants of asymptomatic carotid artery atherosclerosis. Arterioscler Thromb Vasc Biol. 2000, 20: 2657-2662. 10.1161/01.ATV.20.12.2657.CrossRefPubMed
30.
go back to reference Gnasso A, Motti C, Irace C, Carallo C, Liberatoscioli L, Bernardini S, Massoud R, Mattioli PL, Federici G, Cortese C: Genetic variation in human stromelysin gene promoter and common carotid geometry in healthy male subjects. Arterioscler Thromb Vasc Biol. 2000, 20: 1600-1605. 10.1161/01.ATV.20.6.1600.CrossRefPubMed Gnasso A, Motti C, Irace C, Carallo C, Liberatoscioli L, Bernardini S, Massoud R, Mattioli PL, Federici G, Cortese C: Genetic variation in human stromelysin gene promoter and common carotid geometry in healthy male subjects. Arterioscler Thromb Vasc Biol. 2000, 20: 1600-1605. 10.1161/01.ATV.20.6.1600.CrossRefPubMed
31.
go back to reference Reuter B, Bugert P, Stroick M, Bukow S, Griebe M, Hennerici MG, Fatar M: TIMP-2 gene polymorphism is associated with intracerebral hemorrhage. Cerebrovasc Dis. 2009, 28: 558-563. 10.1159/000247599.CrossRefPubMed Reuter B, Bugert P, Stroick M, Bukow S, Griebe M, Hennerici MG, Fatar M: TIMP-2 gene polymorphism is associated with intracerebral hemorrhage. Cerebrovasc Dis. 2009, 28: 558-563. 10.1159/000247599.CrossRefPubMed
Metadata
Title
The GC + CC genotype at position -418 in TIMP-2 promoter and the -1575GA/-1306CC genotype in MMP-2is genetic predisposing factors for prevalence of moyamoya disease
Authors
Young Seok Park
Young Joo Jeon
Hyun Seok Kim
In Bo Han
Seung-Hun Oh
Dong-Seok Kim
Nam Keun Kim
Publication date
01-12-2014
Publisher
BioMed Central
Published in
BMC Neurology / Issue 1/2014
Electronic ISSN: 1471-2377
DOI
https://doi.org/10.1186/s12883-014-0180-5

Other articles of this Issue 1/2014

BMC Neurology 1/2014 Go to the issue