58 THE PREVALENCE OF 4G5G POLYMORPHISM OF THE PLASMINOGEN ACTIVATOR INHIBITOR-1 (PAI-1) GENE IN POLYCYSTIC OVARIAN SYNDROME AND ITS ASSOCIATION WITH PLASMINOGEN ACTIVATOR INHIBITOR ACTIVITY LEVELS. (1st March 2005)
- Record Type:
- Journal Article
- Title:
- 58 THE PREVALENCE OF 4G5G POLYMORPHISM OF THE PLASMINOGEN ACTIVATOR INHIBITOR-1 (PAI-1) GENE IN POLYCYSTIC OVARIAN SYNDROME AND ITS ASSOCIATION WITH PLASMINOGEN ACTIVATOR INHIBITOR ACTIVITY LEVELS. (1st March 2005)
- Main Title:
- 58 THE PREVALENCE OF 4G5G POLYMORPHISM OF THE PLASMINOGEN ACTIVATOR INHIBITOR-1 (PAI-1) GENE IN POLYCYSTIC OVARIAN SYNDROME AND ITS ASSOCIATION WITH PLASMINOGEN ACTIVATOR INHIBITOR ACTIVITY LEVELS
- Authors:
- Glueck, C. J.
Sieve, L.
Salehi, M.
Wang, P. - Abstract:
- Abstract : We assessed the mutant 4G allele of the plasminogen activator inhibitor-1 (PAI-1) gene in women with polycystic ovary syndrome (PCOS) and its relationship to hypofibrinolytic plasminogen activator inhibitor activity (PAI-Fx), an independent determinant of miscarriage in PCOS. We studied 913 women with PCOS who met the 2003 ESHRE/ASRM diagnostic consensus criteria and 126 healthy normal female controls. Of the 913 PCOS women, 78% had 4G4G or 4G5G genotypes vs 69% of controls (χ2 = 4.98, p = .026). The 4G allele frequency was 53% in PCOS women vs 46% in controls (χ2 = 4.06, p = .044). PCOS and normal women were both in Hardy-Weinberg equilibrium for the PAI-1 genotype distribution. By stepwise multiple regression, positive independent determinants of PAI-Fx included BMI (partial R2 = 10.8%, p<.0001), serum insulin (partial R2 = 2.7%, p<.0001), 4G4G-4G5G genotype (partial R2 = 1%, p = .0022), and triglyceride (partial R2 = 1%, p<.002); PAI-Fx was inversely associated with age (partial R2 = .5%, p = .02). Of the 913 women, 409 had previous pregnancies. By logistic regression with the dependent variable being live birth pregnancies only (n = 191), or miscarriages only (n= 69), and explanatory variables PAI-1 genotype, PAI-Fx, insulin, BMI, and triglyceride, PAI-Fx was positively associated with miscarriage, p = .017. The 4G polymorphism of the PAI-1 gene is more common in PCOS than normal women and contributes to hypofibrinolytic-miscarriage-promoting PAI-Fx levels inAbstract : We assessed the mutant 4G allele of the plasminogen activator inhibitor-1 (PAI-1) gene in women with polycystic ovary syndrome (PCOS) and its relationship to hypofibrinolytic plasminogen activator inhibitor activity (PAI-Fx), an independent determinant of miscarriage in PCOS. We studied 913 women with PCOS who met the 2003 ESHRE/ASRM diagnostic consensus criteria and 126 healthy normal female controls. Of the 913 PCOS women, 78% had 4G4G or 4G5G genotypes vs 69% of controls (χ2 = 4.98, p = .026). The 4G allele frequency was 53% in PCOS women vs 46% in controls (χ2 = 4.06, p = .044). PCOS and normal women were both in Hardy-Weinberg equilibrium for the PAI-1 genotype distribution. By stepwise multiple regression, positive independent determinants of PAI-Fx included BMI (partial R2 = 10.8%, p<.0001), serum insulin (partial R2 = 2.7%, p<.0001), 4G4G-4G5G genotype (partial R2 = 1%, p = .0022), and triglyceride (partial R2 = 1%, p<.002); PAI-Fx was inversely associated with age (partial R2 = .5%, p = .02). Of the 913 women, 409 had previous pregnancies. By logistic regression with the dependent variable being live birth pregnancies only (n = 191), or miscarriages only (n= 69), and explanatory variables PAI-1 genotype, PAI-Fx, insulin, BMI, and triglyceride, PAI-Fx was positively associated with miscarriage, p = .017. The 4G polymorphism of the PAI-1 gene is more common in PCOS than normal women and contributes to hypofibrinolytic-miscarriage-promoting PAI-Fx levels in concert with hyperinsulinemia and hypertriglyceridemia. The 4G polymorphism of the PAI-1 gene and high PAI-Fx are markers for PCOS and its endocrine-metabolic-reproductive correlates. … (more)
- Is Part Of:
- Journal of investigative medicine. Volume 53:Number 2(2005)
- Journal:
- Journal of investigative medicine
- Issue:
- Volume 53:Number 2(2005)
- Issue Display:
- Volume 53, Issue 2 (2005)
- Year:
- 2005
- Volume:
- 53
- Issue:
- 2
- Issue Sort Value:
- 2005-0053-0002-0000
- Page Start:
- S397
- Page End:
- S397
- Publication Date:
- 2005-03-01
- Subjects:
- Clinical medicine -- Periodicals
Medicine -- Research -- Periodicals
Medicine
Research -- United States
Clinical medicine
Medicine -- Research
Periodicals
616.075 - Journal URLs:
- http://journals.lww.com/jinvestigativemed/pages/default.aspx ↗
http://jim.bmj.com/ ↗
https://journals.sagepub.com/home/IMJ ↗
http://journals.lww.com ↗ - DOI:
- 10.2310/6650.2005.00205.57 ↗
- Languages:
- English
- ISSNs:
- 1081-5589
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5008.010000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 19782.xml