Plasminogen activator inhibitor-1 5G/5G genotype is a protecting factor preventing posttransplant diabetes mellitus

التفاصيل البيبلوغرافية
العنوان: Plasminogen activator inhibitor-1 5G/5G genotype is a protecting factor preventing posttransplant diabetes mellitus
المؤلفون: Ming-Chia Hsieh, Tung-Wei Hung, Horng-Rong Chang, Jong-Da Lian, Shun-Fa Yang, Sheng-Wen Wu, Hui-Ching Tsai, Jen-Pi Tsai, Jun-Huang Huang
المصدر: Clinica Chimica Acta. 412:322-326
بيانات النشر: Elsevier BV, 2011.
سنة النشر: 2011
مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Genotype, Clinical Biochemistry, Biochemistry, Gastroenterology, Diabetes mellitus genetics, chemistry.chemical_compound, Postoperative Complications, Insulin resistance, Gene Frequency, Internal medicine, Plasminogen Activator Inhibitor 1, Diabetes Mellitus, medicine, Humans, Prospective Studies, Kidney transplantation, Polymorphism, Genetic, business.industry, Biochemistry (medical), General Medicine, Middle Aged, medicine.disease, Kidney Transplantation, Tacrolimus, Gestational diabetes, Endocrinology, chemistry, Plasminogen activator inhibitor-1, Regression Analysis, Female, Gene polymorphism, business
الوصف: Objective Plasminogen activator inhibitor 1 (PAI-1) is thought to play a role in the pathogenesis of obesity and insulin resistance. A connection between gestational diabetes mellitus and the functional -675 PAI-1 genotype has been reported. Therefore, we examined the role of the PAI-1 gene polymorphism in kidney transplant recipients. Methods A total of 376 kidney transplant recipients were prospectively screened for posttransplant diabetes mellitus (PTDM). Eighty-one (21.5%) patients were diagnosed with PTDM and the other 295 patients were non-diabetic following kidney transplantation. DNA samples were isolated from the sera and analyzed for the functional − 675 4G/5G promoter polymorphisms of the PAI-1 gene. Results Kidney transplant recipients with PTDM were significantly associated with tacrolimus use (p = 0.03), older age (p = 0.036), and higher body mass index (p = 0.001). The genotype distribution was significantly different between the patients with PTDM (genotype 4G/4G:4G/5G:5G/5G = 33.3%:60.5%:6.2%) and those without PTDM (genotype 4G/4G:4G/5G:5G/5G = 36.9%:44.1%:19.0%) (p = 0.018). Patients with homozygosity for 5G had a significantly lower rate of PTDM (aOR, 0.286, p = 0.022) and higher cumulative event-free probability of time to PTDM (log rank test, p = 0.0058). Conclusion Homozygosity for the 5G allele of the PAI-1 gene constitutes a protecting factor for the development of PTDM. Our findings are similar to a previous study on gestational diabetes mellitus, and strongly support a possible genetic role of PAI-1 in the development of PTDM.
تدمد: 0009-8981
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::338bcf7e54a03657a66c832ad4722171Test
https://doi.org/10.1016/j.cca.2010.10.029Test
حقوق: CLOSED
رقم الانضمام: edsair.doi.dedup.....338bcf7e54a03657a66c832ad4722171
قاعدة البيانات: OpenAIRE