SERPINE1, serpin family E member 1, 5054

N. diseases: 770; N. variants: 23
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.300 Biomarker disease BEFREE Independent predictors of death were PAI-1 rise and final Thrombolysis in Myocardial Infarction flow. 29972733 2018
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.300 AlteredExpression disease BEFREE The present study demonstrates that patients with AMI exhibit decreased miR-30b expression and elevated PAI-1 expression in the peripheral blood. miR-30b may therefore inhibit the damage to myocardial cells that occurs following AMI and protect myocardial cell function by targeting PAI-1 expression. 29805539 2018
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.300 GeneticVariation disease BEFREE Our results showed that carriers of PAI-1 4G/5G genotype with myocardial infarction have increased odds of coronary artery occlusion more than 1.6 times in comparison to the carriers of homozygous genotypes. 26273123 2015
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.300 Biomarker disease BEFREE We aimed to investigate the association of plasminogen activator inhibitor-1 (PAI-1) and tissue plasminogen activator (TPA) genes polymorphisms with myocardial infarction and its outcomes in Egyptian patients. 25113642 2015
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.300 GeneticVariation disease BEFREE The Mendelian randomization meta-analysis confirmed previous knowledge that the PAI-1 4G allele slightly increases the risk for MI. 24695040 2014
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.300 GeneticVariation disease BEFREE Polymorphisms in plasminogen activator inhibitor-1 (PAI-1, SERPINE1) and tissue plasminogen activator (tPA, PLAT), such as PAI-1 (-675 4G/5G deletion/insertion) and tPA (Alu insertion/deletion [I/D]), are associated with strokes, myocardial infarctions, bacterial infections and septic shock severity, and trauma. 23570848 2013
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.300 GeneticVariation disease BEFREE MTHFRA1298C and PAI-1 deletions were most frequent genetic variants in risk groups for MI in patients with diabetes mellitus (value of odds ratio sequentially [OR] = 3.79, p = 0.06 and [OR] = 5 × 10(8), p = 0.000). 22752805 2012
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.300 GeneticVariation disease BEFREE Two are associated with thrombophilia (765 4G/5G and -844 A>G, in the promoter), risk of myocardial infarction and postoperative deep venous thrombosis related to higher than normal levels of PAI-1. 21663586 2011
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.300 GeneticVariation disease BEFREE In conclusion the PAI-1 gene polymorphism was found to have a gender specific role in the female MI patients. 21082259 2011
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.300 AlteredExpression disease BEFREE The aim of this study was to investigate the association between PAI-1-844G/A and 4G/5G polymorphisms and changes in PAI-1 and tissue plasminogen activator (tPA) levels in MI in a Tunisian population. 19929406 2010
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.300 GeneticVariation disease BEFREE Plasminogen activator inhibitor type-1 (PAI-1) has already been associated with atherosclerosis; myocardial infarction; and cardiovascular disease risk factors such as obesity, insulin resistance, and dyslipidemia. 20127289 2010
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.300 GeneticVariation disease BEFREE The 4G allele of the PAI-1 -675(4G/5G) insertion/deletion promoter polymorphism has been associated with elevated plasma levels of PAI-1 and an increased risk of myocardial infarction. 20806116 2010
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.300 GeneticVariation disease BEFREE We explored whether 4G/5G polymorphism of the PAI-1 gene is associated with the development of MI <or= 35 years of age. 19844663 2010
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.300 GeneticVariation disease BEFREE In essence, tagging polymorphisms, including the 4G/5G polymorphism, and common haplotypes of the SERPINE1 gene region were not associated with MI in a German sample, and no compelling evidence was obtained for a relationship of the 4G/5G polymorphism to MI and coronary atherosclerosis in a meta-analysis. 20352162 2010
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.300 Biomarker disease BEFREE Myocardial infarction occurs with a similar 24 h pattern in the 4G/5G versions of plasminogen activator inhibitor-1. 19444746 2009
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.300 AlteredExpression disease BEFREE The PAI-1 HindIII polymorphism has been associated with high PAI-1 plasma levels in myocardial infarction patients and control populations. 19238514 2009
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.300 GeneticVariation disease BEFREE PAI-1 4G/4G genotype was the only independent variable (OR 2.67, 95%CI 1.43-4.96, P = 0.002) associated with MI in this regression model. 17721742 2008
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.300 GeneticVariation disease LHGDN PAI-1 4G/4G genotype was the only independent variable (OR 2.67, 95%CI 1.43-4.96, P = 0.002) associated with MI in this regression model. 17721742 2008
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.300 GeneticVariation disease BEFREE AMI is associated with polymorphisms in the NOS3 and FGB but not in PAI-1 genes in young adults. 17126309 2007
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.300 GeneticVariation disease BEFREE Multivariable logistic regression analyses and stepwise forward selection procedures revealed that seven different polymorphisms were significantly (P<0.005) associated with MI in individuals with low or high serum concentrations of HDL- or LDL-cholesterol or of TG: the 190T --> C (Trp64Arg) polymorphism of ADRB3 in individuals with low HDL-cholesterol; the 1018C --> T (Thr145Met) polymorphism of GP1BA, the A --> G (Ile646Val) polymorphism of AKAP10, and the -55C --> T polymorphism of UCP3 in individuals with high HDL-cholesterol; the -603A --> G polymorphism of F3 and the -11377C --> G polymorphism of ADIPOQ in individuals with low LDL-cholesterol; the 1018C --> T polymorphism of GP1BA in individuals with low TG; and the 4G --> 5G polymorphism of PAI1 in individuals with high TG. 17786291 2007
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.300 GeneticVariation disease LHGDN SERPINE1 haplotypes are mildly associated with plasma levels of PAI-1 and with the risk of MI in nonsmokers. 17656673 2007
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.300 GeneticVariation disease BEFREE SERPINE1 haplotypes are mildly associated with plasma levels of PAI-1 and with the risk of MI in nonsmokers. 17656673 2007
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.300 GeneticVariation disease BEFREE GJA4 1019 C > T, MMP3 -1171delA, and SERPINE1 -668delG genotypes have been associated with the risk of incident myocardial infarction. 17719307 2007
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.300 GeneticVariation disease BEFREE The 4G allele is associated with higher PAI-1 levels, but this study does not support an association of the PAI gene polymorphisms with the risk of either myocardial infarction or stroke. 17161063 2006
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.300 Biomarker disease BEFREE Polymorphisms of GJA4 and CYBA and of PAI1 and MMP3 are associated with myocardial infarction (MI) in men and women, respectively. 16998253 2006