Abstract
The most important feature of abdominal aortic aneurysm (AAA) pathogenesis is an enzymatic degradation of elastic lamellae and extracellular matrix proteins particularly with participation of matrix metalloproteinases. Plasmin, which is responsible for the dissolution of fibrin in blood vessels, plays also a key role in the cascade for activation of the metalloproteinases. The purpose of this study was to evaluate the influence of selected polymorphisms in genes coding for tissue plasminogen activator (−7351 C/T polymorphism), urokinase-type plasminogen activator (1788 C/T polymorphism) and plasminogen activator inhibitor 1 (−675 4G/5G and −844 G/A polymorphism) on the susceptibility to AAA. We performed a case–control study of 153 polish patients hospitalized due to AAA and compared them with matched healthy control subjects. The polymorphisms were ascertained through genotyping by polymerase chain reaction and restriction digestion of amplified fragments or through high-resolution melting analysis. In this study we have found lower frequency of wild-type GG genotype of the −844G/A PAI-1 polymorphism in cases than in controls, what may suggest the protective effect of this genotype for the risk of AAA development. None of the remaining polymorphisms tested were associated with AAA occurrence.
Similar content being viewed by others
![](https://media.springernature.com/w215h120/springer-static/image/art%3A10.1186%2Fs12881-019-0833-8/MediaObjects/12881_2019_833_Fig1_HTML.png)
Avoid common mistakes on your manuscript.
Introduction
Fibrinolytic system is a proteolytic cascade of activation events responsible for the enzymatic dissolution of fibrin blood clots. It is composed of plasminogen, its active form—plasmin, plasminogen activators—tissue-type (t-PA) and urokinase type (u-PA), inhibitors which regulate activation of plasminogen—plasminogen activator inhibitor type 1(PAI-1) and type 2 (PAI-2) and activity of plasmin—α2-antiplasmin. Plasmin, which is formed from plasminogen by t-PA or u-PA, is an enzyme responsible for the dissolution of fibrin in blood vessels, but also plays a key role in the cascade for activation of matrix metalloproteinases (MMPs) [1, 2]. MMPs could play an essential role in the destruction of extracellular matrix (ECM) in the aortic wall. Whereas an enzymatic degradation of elastic lamellae and ECM proteins, particularly with participation of MMPs, is the most important feature of abdominal aortic aneurysm (AAA) pathogenesis. AAA represents a degenerative life-threatening process of the abdominal aorta. Previous studies have found elevated levels of plasmin, as well as its activators in AAA tissue compared with controls [3–7]. It is also known that overexpression of PAI-1 may prevent the development of AAA [8].
Tissue type plasminogen activator is mainly involved in intravascular thrombolysis, while urokinase mediates pericellular proteolysis during cell migration, wound healing, and tissue remodeling under physiological and pathological conditions [9–11]. −7351 C/T single nucleotide polymorphism of the gene encoding t-PA (rs63020761) is located within the enhancer region and the substitution of cytosine for thymine at position −7351 reduces the Sp1/Sp3 binding affinity resulting in the inhibition of DNA transcription [12]. This polymorphism was found to be strongly correlated with reduced endothelial t-PA release [13] and associated with the occurrence of myocardial infarction and stroke [14, 15]. A genetic polymorphism of u-PA consisting in a transition of cytosine to thymine at position 1788 (rs2227564) causes a missense mutation (Pro141Leu) in the kringle domain of uPA protein, which has been shown to decrease the affinity for fibrin [16]. This polymorphism has been associated with asthma, Alzheimer’s disease, colorectal cancer and Helicobacter pylori infection [17–21].
PAI-1 belongs to the serpin superfamily of proteins and is the main regulatory protein of the fibrinolytic system. In addition to its role as a regulator of haemostasis, PAI-1 also plays a significant role in several biological processes which include: wound healing, atherosclerosis, such metabolic disturbances as obesity and insulin resistance, tumor angiogenesis, chronic stress, bone remodeling, asthma, rheumatoid arthritis, fibrosis, glomerulonephritis, sepsis, and others [22, 23]. Both −675 4G/5G insertion/deletion and −844 G/A promoter polymorphisms of PAI-1 gene cause the elevated PAI-1 level [24, 25]. The deletion of one guanine nucleotide at position −675 in the PAI-1 promoter results in the disappearance of one binding site for a DNA-binding protein that acts as a transcriptional repressor [26, 27]. Thus, 4G allele has higher transcriptional activity than 5G allele. Whereas, an exchange from G to A at position −844 in the PAI-1 gene promoter includes a consensus sequence binding site for the Ets nuclear protein and can be implicated in the regulation of the PAI-1 gene expression [28, 29].
The purpose of our study was to examine the occurrence of selected polymorphisms in genes coding for t-PA (−7351 C/T), u-PA (1788 C/T) and PAI-1 (−675 4G/5G insertion/deletion and −844 G/A) in patients suffering from AAA.
Materials and methods
Patients
The study population was comprised of 153 Polish patients with AAA, who were hospitalized in the M. Pirogow Regional Specialist Hospital in Lodz. Control group consisted of 152 healthy volunteers who had no history or symptoms of aneurysms and other cardiovascular diseases. The study was approved by Ethics Committee of Medical University of Lodz (consent number: RNN/19/07/KE). All subjects gave written informed consent to participate.
DNA isolation and genotyping
Venous blood samples were taken from all study participants. Genomic DNA was isolated from leukocytes obtained from whole blood samples using phenol–chloroform extraction method or QIAamp DNA Blood Mini Kit (Qiagen, Hilden, Germany).
u-PA 1788 C/T, PAI-1 -844 G/A and PAI-1 -675 4G/5G polymorphisms were genotyped using polymerase chain reaction-restriction fragment length polymorphism sites (PCR–RFLP). t-PA −7351 C/T polymorphism was determined by melting curve analysis using Light Scanner™ HR I 96 (Idaho Technology, Inc.). The PCR primer pairs, annealing temperature, PCR product sizes and restriction enzymes are listed in Table 1.
PCR reactions for amplification of polymorphic segments were performed in reaction mixture containing 2 μl of 10× PCR buffer (with 15 mM MgCl2), 2 μl of 2.5 mM dNTPs, 100 pmol of each primer, 1 U of Taq DNA polymerase (Fermentas, Qiagen), 2 μl of genomic DNA and deionized water added to a final volume of 20 μl. Moreover, in the case of PAI-1 −844 G/A polymorphisms there were additional 4 μl of 25 mM MgCl2 used. Basically, the amplification reactions were carried out as follows: 94 °C for 5 min, followed by 35 cycles of 95 °C for 30 s for DNA denaturation, 56–63 °C (depending on the DNA fragment, see the Table 1) for 30 s for primers annealing, 72 °C for 30 s for DNA extension and 72 °C for 10 min for final extension. Besides, the PCR cycles for amplification of t-PA −7351 C/T polymorphic site were run in different way: 95 °C for 30, 45 s for primers annealing at temperature lowering by 0.5 °C per each cycle from 63 to 56 °C (14 cycles and the remaining at 56 °C), 72 °C for 1 min. Amplification and correct sizes of PCR products were confirmed on polyacrylamide gels in Tris/acetate/EDTA buffer in comparison with 100 bp or 1 kb DNA Ladder (Fermentas). After staining with ethidium bromide the gels were photographed under UV light using Image Master VDS system (Pharmacia Biotech).
10 μl of the appropriate PCR product (for u-PA and PAI polymorphisms) was then digested overnight with an excess of proper restriction enzyme (see Table 1) under conditions recommended by the supplier (Fermentas). The digestion products were separated by electrophoresis on polyacrylamide gels, stained and visualized as described above. Molecular sizes of the restriction fragments are shown in Table 2.
In the case of t-PA −7351 C/T polymorphism, the 247 bp PCR product was then diluted 1:50 and used directly as DNA template for nested PCR with following primers: forward 5′ TAGGGCTTTGGCCGCTCTCCC 3′ and reverse 5′ GAGTCCCAGGCCATGGCTGTG 3′. The PCR reaction was performed in a DNA thermal cycler (Biometra) in 96-well plate coated with 20 μl of mineral oil. Each reaction mixture contained 4 μl of Light Scanner Master Mix (Idaho Technology, Inc.), 4 μl of water, 0.5 μl of each primer (100 pmol/μl) and 1 μl of DNA template. The conditions of the PCR were as follows: 94 °C for 5 min, followed by 20 cycles of 94 °C for 30 s for DNA denaturation, 60 °C for 30 s for primers annealing and 72 °C for 5 s for DNA extension. Amplified products of 60 base pairs were subjected to high-resolution melting analysis (HRM) in the same plate using the light scanner instrument.
To confirm the results obtained using PCR–RFLP and HRM technique, selected samples (every tenth) were subjected to DNA sequence analysis carried out by Genomed S.A. (Warsaw, Poland).
Statistical analysis
The results are reported as percentages (%) or means with standard deviations (±SD). Analysis of association between genotype/allele distribution and AAA risk was performed with the use of the χ2 square test and the 95 % confidence intervals (CI) for disease odds ratio (OR) calculated with the use of logistic regression. All the analyses were derived by means of Statistica v8.0 software. The level of significance was set at p < 0.05.
Results
The study group consisted of 51 females (33.3 %) and 102 males (66.6 %) with an age range from 44 to 73 years. The mean age in the study population was 59 years, SD = 7. The control group consisted of 152 healthy volunteers: 60 females (39.5 %) and 92 males (60.5 %) with their ages ranging from 37 to 70 (mean age 55, SD ±9). The control subjects had no history or symptoms of aneurysms and other cardiovascular diseases. The cases and controls were homogenous in gender and age distribution (p > 0.20).
We did not observe any statistical differences in the distribution of genotypes and alleles of t-PA −7351 C/T, u-PA 1788 C/T and PAI-1 −675 4G/5G polymorphisms between AAA patients and healthy controls (p = 0.499, p = 0.628, p = 0.836, respectively) (Tables 3, 4, 5). Regarding the −844 G/A polymorphism of the PAI-1 gene, we found significant differences in genotype frequency between cases and controls (χ2 = 7.88; df = 2; p = 0.020) (Table 6). The following genotype frequencies of the −844 G/A polymorphism were obtained in the study group: GG = 9.2 %, AG = 57.9 %, AA = 32.9 %, while these frequencies in the control group were 20.4, 47.6 and 32.0 %, respectively. However, the difference concerns only the frequency of GG genotype in AAA patients vs. controls (OR 0.40; 95 % CI 0.20–0.78) and the result achieved statistical significance (p = 0.008). Thus, it could be suggested that the GG wild-type genotype may have protective effect for the risk of AAA development.
Discussion
The pathogenesis of AAA has not yet been completely defined. The literature data show that proteolytic activity of fibrinolytic system may be one of the factors contributing to the development of aneurysms [4, 7]. Thus, the aim of the present study was an attempt of finding correlation between genetic polymorphisms of selected fibrinolysis genes and occurrence of AAA.
The TT genotype of −7351 C/T tissue-type plasminogen activator gene polymorphism has been reported to be associated with reduced t-PA release rates due to the decreased transcriptional activity [12, 13]. It has been documented that −7351 T allele confers an increased risk of such cardiovascular diseases as myocardial infarction [14] and lacunar stroke [15]. However, there are conflicting data concerning the contribution of −7351 C/T polymorphism and ischemic stroke. Tuttolomondo et al. [30] demonstrated a higher frequency of the CT genotype in cases but other researchers did not find any significant association of t-PA −7351C/T polymorphism with ischemic stroke [31, 32]. To our knowledge, there are no existing data concerning the occurrence of this polymorphism in individuals suffering from aneurysm. In this study we observed slightly higher frequency of CT genotypes in AAA individuals compared to controls but the difference did not achieve statistical significance (54.3 vs. 48.0 %, p = 0.28).
We have also studied, for the first time, the association between the 1788 C/T urokinase-type plasminogen activator gene polymorphism and risk of AAA. Since it is documented that elevated urokinase expression may participate in AAA formation and rapture [33–35], and that an exchange of cytosine to thymine at nucleotide 1788 decreases the urokinase activity, we expected to find a protective effect of the polymorphic T allele on the occurrence of the disease. But we did not find any significant correlation, although the frequency of T allele was slightly higher in controls than in cases (23.4 vs. 21.4 %).
Another fibrinolytic gene which we have studied regarding to its contribution to the aneurysm disease is plasminogen activator inhibitor 1. We have chosen two polymorphisms in the PAI-1 gene promoter (−675 4G/5G and −844 G/A), that increase the PAI-1 expression and plasma concentration. Elevated levels of PAI-1 decrease plasmin formation resulting in the inhibition of the proteolytic activity of MMPs, and thus could prevent the formation of aneurysm. Our study indicates a lower frequency of wild-type GG genotype of the −844 G/A PAI-1 polymorphism in cases than in controls, what may suggest the protective effect of this genotype for the risk of AAA development. Although the −844 G/A PAI-1 polymorphism influences the plasma PAI-1 level, there is at present a lack of studies regarding the association of this polymorphism and risk of AAA. However, there are some literature data on the relationship between this polymorphism and other vascular system diseases involving myocardial infarction [36], ischemic stroke [37] or deep vein thrombosis [28]. But all these studies have found no significant effect of individual genotypes on the risk of respective disease.
Our study revealed also the lack of correlation between −675 4G/5G PAI-1 promoter polymorphism and AAA occurrence in Polish population. Nevertheless, there are some data concerning the correlation of 4G/5G PAI-1 polymorphism with AAA. Jones et al. [38] noticed that this promoter polymorphism does not influence the development of AAA, although they observed faster AAA growth in patients with 5G/5G genotype. Similarly, Eriksson et al. [39] documented that patients with PAI-1 5G/5G genotype presented with AAAs of largest diameter. Whereas another report found the influence of 5G/5G genotype on the aneurysm development, but only in the case of typical familial AAA [40]. −675 4G/5G PAI-1 promoter polymorphism is also reported to be associated with other cardiovascular diseases, including thrombosis [41], myocardial infarction [27, 36, 42] or coronary artery disease [43, 44].
In conclusions, in this study no association was observed between −7351 C/T t-PA, 1788 C/T u-PA and −675 4G/5G PAI-1 polymorphisms and the risk of AAA development. Only in the case of −844 G/A PAI-1 polymorphism the study revealed a slight difference in the wild-type genotype frequency between AAA patients and healthy controls. This result should be confirmed in a larger population.
References
Kadoglou NP, Liapis CD (2004) Matrix metalloproteinases: contribution to pathogenesis, diagnosis, surveillance and treatment of abdominal aortic aneurysms. Curr Med Res Opin 20:419–432. doi:10.1185/030079904125003143
Carmeliet P, Moons L, Lijnen R, Baes M, Lemaître V, Tipping P, Drew A, Eeckhout Y, Shapiro S, Lupu F, Collen D (1997) Urokinase-generated plasmin activates matrix metalloproteinases during aneurysm formation. Nat Genet 17:439–444. doi:10.1038/ng1297-439
Jean-Claude J, Newman KM, Li H, Gregory AK, Tilson MD (1994) Possible key role for plasmin in the pathogenesis of abdominal aortic aneurysms. Surgery 116:472–478
Schneiderman J, Bordin GM, Engelberg I et al (1995) Expression of fibrinolytic genes in atherosclerotic abdominal aortic aneurysm wall. A possible mechanism for aneurysm expansion. J Clin Invest 96:639–645. doi:10.1172/JCI118079
Wang YX, Martin-McNulty B, Freay AD et al (2001) Angiotensin II increases urokinase-type plasminogen activator expression and induces aneurysm in the abdominal aorta of apolipoprotein E-deficient mice. Am J Pathol 159:1455–1464. doi:10.1016/S0002-9440(10)62532-1
Wanhainen A, Nilsson TK, Bergqvist D, Boman K, Björck M (2007) Elevated tissue plasminogen activator in patients with screening-detected abdominal aortic aneurysm. J Vasc Surg 45:1109–1113. doi:10.1016/j.jvs.2007.02.001
Houard X, Rouzet F, Touat Z et al (2007) Topology of the fibrinolytic system within the mural thrombus of human abdominal aortic aneurysms. J Pathol 212:20–28. doi:10.1002/path.2148
Qian HS, Gu JM, Liu P et al (2008) Overexpression of PAI-1 prevents the development of abdominal aortic aneurysm in mice. Gene Ther 15:224–232. doi:10.1038/sj.gt.3303069
Stepanova V, Mukhina S, Kohler E, Resink TJ, Erne P, Tkachuk VA (1999) Urokinase plasminogen activator induces human smooth muscle cell migration and proliferation via distinct receptor-dependent and proteolysis-dependent mechanisms. Mol Cell Biochem 195:199–206. doi:10.1023/A:1006936623106
Li WY, Chong SS, Huang EY, Tuan TL (2003) Plasminogen activator/plasmin system: a major player in wound healing? Wound Repair Regen 11:239–247. doi:10.1046/j.1524-475X.2003.11402.x
Plekhanova O, Parfyonova Y, Bibilashvily R et al (2001) Urokinase plasminogen activator augments cell proliferation and neointima formation in injured arteries via proteolytic mechanisms. Atherosclerosis 159:297–306. doi:10.1016/S0021-9150(01)00511-1
Tjarnlund-Wolf AT, Medcalf RL, Jern C (2005) The t-PA −7351C>T enhancer polymorphism decreases Sp1 and Sp3 protein binding affinity and transcriptional responsiveness to retinoic acid. Blood 105:1060–1067. doi:10.1182/blood-2003-12-4383
Ladenvall P, Wall U, Jern S, Jern C (2000) Identification of eight novel single-nucleotide polymorphisms at human tissue-type plasminogen activator (t-PA) locus: association with vascular t-PA release in vivo. Thromb Haemost 84:150–155
Ladenvall P, Johansson L, Jansson JH et al (2002) Tissue-type plasminogen activator −7351C/T enhancer polymorphism is associated with a first myocardial infarction. Thromb Haemost 87:105–109
Jannes J, Hamilton-Bruce MA, Pilotto L, Smith BJ, Mullighan CG, Bardy PG, Koblar SA (2004) Tissue plasminogen activator −7351C/T enhancer polymorphism is a risk factor for lacunar stroke. Stroke 35:1090–1094. doi:10.1161/01.STR.0000124123.76658.6c
Yoshimoto M, Ushiyama Y, Sakai M et al (1996) Characterization of single chain urokinase-type plasminogen activator with a novel amino-acid substitution in the kringle structure. Biochim Biophys Acta 1293:83–89
Bégin P, Tremblay K, Daley D et al (2007) Association of urokinase-type plasminogen activator with asthma and atopy. Am J Respir Crit Care Med 175:1109–1116. doi:10.1164/rccm.200607-1012OC
Finckh U, van Hadeln K, Müller-Thomsen T et al (2003) Association of late-onset Alzheimer disease with a genotype of PLAU, the gene encoding urokinase-type plasminogen activator on chromosome 10q22.2. Neurogenetics 4:213–217. doi:10.1007/s10048-003-0157-9
Riemenschneider M, Konta L, Friedrich P et al (2006) A functional polymorphism within plasminogen activator urokinase (PLAU) is associated with Alzheimer’s disease. Hum Mol Genet 15:2446–2456. doi:10.1093/hmg/ddl167
Przybyłowska K, Smolarczyk K, Kulig A et al (2002) Antigen levels of the urokinase-type plasminogen activator and its gene polymorphisms in colorectal cancer. Cancer Lett 181:23–30. doi:10.1016/S0304-3835(02)00038-1
Goto Y, Hagikura S, Katsuda N, Hamajima N (2011) A C to T polymorphism of urokinase plasminogen activator (P141L) is associated with Helicobacter pylori infection. Asian Pac J Cancer Prev 12:803–806
Lijnen HR (2005) Pleiotropic functions of plasminogen activator inhibitor-1. J Thromb Haemost 3:35–45. doi:10.1111/j.1538-7836.2004.00827.x
Cesari M, Pahor M, Incalzi RA (2010) Plasminogen activator inhibitor-1 (PAI-1): a key factor linking fibrinolysis and age-related subclinical and clinical conditions. Cardiovasc Ther 28:e72–e91. doi:10.1111/j.1755-5922.2010.00171.x
Kathiresan S, Gabriel SB, Yang Q et al (2005) Comprehensive survey of common genetic variation at the plasminogen activator inhibitor-1 locus and relations to circulating plasminogen activator inhibitor-1 levels. Circulation 112:1728–1735. doi:10.1161/CIRCULATIONAHA.105.547836
Ding J, Nicklas BJ, Fallin MD et al (2006) Plasminogen activator inhibitor type 1 gene polymorphisms and haplotypes are associated with plasma plasminogen activator inhibitor type 1 levels but not with myocardial infarction or stroke. Am Heart J 152:1109–1115. doi:10.1016/j.ahj.2006.06.021
Dawson SJ, Wiman B, Hamsten A, Green F, Humphries S, Henney AM (1993) The two allele sequences of a common polymorphism in the promoter of the plasminogen activator inhibitor-1 (PAI-1) gene respond differently to interleukin-1 in HepG2 cells. J Biol Chem 268:10739–10745
Eriksson P, Kallin B, van ‘t Hooft FM, Båvenholm P, Hamsten A (1995) Allele-specific increase in basal transcription of the plasminogen-activator inhibitor 1 gene is associated with myocardial infarction. Proc Natl Acad Sci USA 92:1851–1855
Grubic N, Stegnar M, Peternel P, Kaider A, Binder BR (1996) A novel G/A and the 4G/5G polymorphism within the promoter of the plasminogen activator inhibitor-1 gene in patients with deep vein thrombosis. Thromb Res 84:431–443. doi:10.1016/S0049-3848(96)00211-3
Henry M, Chomiki N, Scarabin PY et al (1997) Five frequent polymorphisms of the PAI-1 gene: lack of association between genotypes, PAI activity, and triglyceride levels in a healthy population. Arterioscler Thromb Vasc Biol 7:851–858. doi:10.1161/01.ATV.17.5.851
Tuttolomondo A, Di Raimondo D, Forte GI et al (2012) Single nucleotide polymorphisms (SNPs) of pro-inflammatory/anti-inflammatory and thrombotic/fibrinolytic genes in patients with acute ischemic stroke in relation to TOAST subtype. Cytokine 58:398–405. doi:10.1016/j.cyto.2012.02.012
Attia J, Thakkinstian A, Wang Y, Lincz L, Parsons M, Sturm J, McGettigan P, Scott R, Meldrum C, Levi C (2007) The PAI-1 4G/5G gene polymorphism and ischemic stroke: an association study and meta-analysis. J Stroke Cerebrovasc Dis 16:173–179. doi:10.1016/j.jstrokecerebrovasdis.2007.03.002
Babu MS, Prabha TS, Kaul S, Al-Hazzani A, Shafi G, Roy S, Balakrishna N, Jyothy A, Munshi A (2012) Association of genetic variants of fibrinolytic system with stroke and stroke subtypes. Gene 495:76–80. doi:10.1016/j.gene.2011.12.046
Shireman PK, McCarthy WJ, Pearce WH, Shively VP, Cipollone M, Kwaan HC (1997) Elevations of tissue-type plasminogen activator and differential expression of urokinase-type plasminogen activator in diseased aorta. J Vasc Surg 25:157–164
Vergona R, Sullivan ME, Morser J, Dole WP, Deng GG (2001) Angiotensin II increases urokinase-type plasminogen activator expression and induces aneurysm in the abdominal aorta of apolipoprotein E-deficient mice. Am J Pathol 159:1455–1464
Deng GG, Martin-McNulty B, Sukovich DA, Freay A, Halks-Miller M, Thinnes T, Loskutoff DJ, Carmeliet P, Dole WP, Wang YX (2003) Urokinase-type plasminogen activator plays a critical role in angiotensin II-induced abdominal aortic aneurysm. Circ Res 92:510–517. doi:10.1161/01.RES.0000061571.49375.E1
Fu L, Jin H, Song K, Zhang C, Shen J, Huang Y (2001) Relationship between gene polymorphism of the PAI-1 promoter and myocardial infarction. Chin Med J (Engl) 114:266–269
Adamski MG, Turaj W, Slowik A, Wloch-Kopec D, Wolkow P, Szczudlik A (2009) A-G-4G haplotype of PAI-1 gene polymorphisms -844 G/A, HindIII G/C, and -675 4G/5G is associated with increased risk of ischemic stroke caused by small vessel disease. Acta Neurol Scand 120:94–100. doi:10.1111/j.1600-0404.2008.01127.x
Jones K, Powell J, Brown L, Greenhalgh R, Jormsjö S, Eriksson P (2002) The influence of 4G/5G polymorphism in the plasminogen activator inhibitor-1 gene promoter on the incidence, growth and operative risk of abdominal aortic aneurysm. Eur J Vasc Endovasc Surg 23:421–425. doi:10.1006/ejvs.2002.1633
Eriksson P, Jormsjö-Pettersson S, Brady AR, Deguchi H, Hamsten A, Powell JT (2005) Genotype-phenotype relationships in an investigation of the role of proteases in abdominal aortic aneurysm expansion. Br J Surg 92:1372–1376. doi:10.1002/bjs.5126
Rossaak JI, Van Rij AM, Jones GT, Harris EL (2000) Association of the 4G/5G polymorphism in the promoter region of plasminogen activator inhibitor-1 with abdominal aortic aneurysms. J Vasc Surg 31:1026–1032. doi:10.1067/mva.2000.104589
Tsantes AE, Nikolopoulos GK, Bagos PG, Bonovas S, Kopterides P, Vaiopoulos G (2008) The effect of the plasminogen activator inhibitor-1 4G/5G polymorphism on the thrombotic risk. Thromb Res 122:736–742. doi:10.1016/j.thromres.2007.09.005
Ossei-Gerning N, Mansfield MW, Stickland MH, Wilson IJ, Grant PJ (1997) Plasminogen activator inhibitor-1 promoter 4G/5G genotype and plasma levels in relation to a history of myocardial infarction in patients characterized by coronary angiography. Arterioscler Thromb Vasc Biol 17:33–37. doi:10.1161/01.ATV.17.1.33
Anvari A, Schuster E, Gottsauner-Wolf M, Wojta J, Huber K (2001) PAI-I 4G/5G polymorphism and sudden cardiac death in patients with coronary artery disease. Thromb Res 103:103–107. doi:10.1016/S0049-3848(01)00277-8
Margaglione M, Cappucci G, Colaizzo D, Giuliani N, Vecchione G, Grandone E, Pennelli O, Di Minno G (1998) PAI-1 gene locus 4G/5G polymorphism is associated with a family history of coronary artery disease. Arterioscler Thromb Vasc Biol 18:152–156. doi:10.1161/01.ATV.18.2.152
Acknowledgments
This work was financially supported by a research grant no. 502-03/6-086-01/502-64-001 from the Medical University of Lodz.
Author information
Authors and Affiliations
Corresponding author
Additional information
Katarzyna Oszajca and Konrad Wroński have contributed equally to this work.
Rights and permissions
Open Access This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
About this article
Cite this article
Oszajca, K., Wroński, K., Janiszewska, G. et al. The study of t-PA, u-PA and PAI-1 genes polymorphisms in patients with abdominal aortic aneurysm. Mol Biol Rep 41, 2859–2864 (2014). https://doi.org/10.1007/s11033-014-3141-6
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s11033-014-3141-6