Association of five common polymorphisms in the plasminogen activator inhibitor-1 gene with primary ovarian insufficiency

Objective To investigate the association between potentially functional plasminogen activator inhibitor-1 (PAI-1) genetic polymorphisms and primary ovarian insufficiency (POI). Design Case–control study. Setting Urban university-based hospital. Patient(s) A cohort of 137 POI patients and 227 control...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Fertility and sterility 2014-03, Vol.101 (3), p.825-832.e1
Hauptverfasser: Jeon, Young Joo, M.S, Kim, Young Ran, M.D, Lee, Bo Eun, M.S, Cha, Sun Hee, M.D., Ph.D, Moon, Myoung-Jin, M.D., Ph.D, Oh, Doyeun, M.D., Ph.D, Lee, Woo Sik, M.D., Ph.D, Kim, Nam Keun, Ph.D
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Objective To investigate the association between potentially functional plasminogen activator inhibitor-1 (PAI-1) genetic polymorphisms and primary ovarian insufficiency (POI). Design Case–control study. Setting Urban university-based hospital. Patient(s) A cohort of 137 POI patients and 227 controls. Intervention(s) None. Main Outcome Measure(s) Genotyping of five PAI-1 polymorphisms (−844G>A [rs2227631], −675 4G/5G [rs1799889], 43G>A (Ala>Thr) [rs6092], 9785G>A [rs2227694], and 11053T>G [rs7242]) was assessed by polymerase chain reaction–restriction fragment length polymorphism assay. Result(s) PAI-1 polymorphisms 9785GA+AA, −844A/9785A, 4G/9785A, and 9785A/11053G were associated with POI occurrence. Moreover, −844GA+AA and 11053TG+GG were associated with lower serum E2 levels in controls. Conclusion(s) We have identified an association between five PAI-1 polymorphisms and POI occurrence. However, the mechanism underlying the function of these polymorphisms in POI remains to be determined. Further studies are needed to improve understanding of the roles of PAI-1 polymorphisms and genes in related pathways, using a larger and more heterogeneous cohort.
ISSN:0015-0282
1556-5653
DOI:10.1016/j.fertnstert.2013.11.015