Alu DNA Polymorphism of Human Tissue Plasminogen Activator (tPA) Gene in Diabetic Jordanian Patients
Iran Biomed J
; 23(6): 423-8, 2019 11.
Article
en En
| MEDLINE
| ID: mdl-31104419
ABSTRACT
Background:
Hypercoagulability and hypofibrinolysis are among the symptoms exhibited by diabetic patients. Our study aimed to address the polymorphic nature of Alu DNA fragment in the human tissue plasminogen activator gene within diabetes mellitus (DM) Jordanian patients.Methods:
Genomic DNA was isolated from 76 DM patients and 60 non-diabetic Jordanian individuals, and the Alu fragment was amplified using PCR.Results:
The results showed that 80% of the non-diabetic Jordanian subjects were homozygotes for the deletion of the Alu fragment (Alu-/-), 16.7% were homozygotes for its insertion (Alu+/+), and 3.3% were heterozygotes (Alu+/-). Besides, 36.8% of the diabetic patients exhibited the Alu-/- or Alu+/- genotype, and 26.3% were Alu+/+. The Alu-/- genotype occurred less frequently in the diabetic individuals.Conclusion:
The high frequency of the Alu-/- genotype constitutes a protective deletion with respect to DM within the normal subjects.Palabras clave
Texto completo:
1
Base de datos:
MEDLINE
Asunto principal:
Polimorfismo Genético
/
Activador de Tejido Plasminógeno
/
Elementos Alu
/
Diabetes Mellitus
País/Región como asunto:
Asia
Idioma:
En
Revista:
Iran Biomed J
Asunto de la revista:
BIOLOGIA
/
MEDICINA
Año:
2019
Tipo del documento:
Article