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在动脉粥样硬化血栓形成疾病临床表现出现之前,2型糖尿病合并代谢综合征患者的低纤溶状态加重。

Hypofibrinolytic State in Subjects with Type 2 Diabetes Mellitus Aggravated by the Metabolic Syndrome before Clinical Manifestations of Atherothrombotic Disease.

作者信息

Aburto-Mejía Elsa, Santiago-Germán David, Martínez-Marino Manuel, Almeida-Gutiérrez Eduardo, López-Alarcón Mardia, Hernández-Juárez Jesús, Alvarado-Moreno Antonio, Leaños-Miranda Alfredo, Majluf-Cruz Abraham, Isordia-Salas Irma

机构信息

Servicio de Medicina Interna, UMAE Hospital de Especialidades, CMN Siglo XXI, Instituto Mexicano del Seguro Social, Ciudad de México, Mexico.

Servicio de Urgencias, H.G.R. No. 1 "Dr. Carlos Mac Gregor Sánchez Navarro", Instituto Mexicano del Seguro Social, Ciudad de México, Mexico.

出版信息

Biomed Res Int. 2017;2017:6519704. doi: 10.1155/2017/6519704. Epub 2017 Feb 8.

Abstract

. Metabolic and genetic factors induce plasminogen activator inhibitor type-1 (PAI-1) overexpression; higher PAI-1 levels decrease fibrinolysis and promote atherothrombosis. . To assess PAI-1 antigen levels among subjects with type 2 diabetes mellitus (T2DM) plus Metabolic Syndrome (MetS) before clinical manifestations of atherothrombosis and the contribution of metabolic factors and 4G/5G polymorphism of PAI-1 gene on the variability of PAI-1. . We conducted an observational, cross-sectional assay in a hospital in Mexico City from May 2010 to September 2011. MetS was defined by the International Diabetes Federation criteria. PAI-1 levels and 4G/5G polymorphism were determined by ELISA and PCR-RFLP analysis. . We enrolled 215 subjects with T2DM plus MetS and 307 controls. Subjects with T2DM plus MetS had higher PAI-1 levels than the reference group (58.4 ± 21 versus 49.9 ± 16 ng/mL, = 0.026). A model with components of MetS explained only 12% of variability on PAI-1 levels ( = 0.12; = 0.001), with = 0.18 ( = 0.03) for hypertension, = -0.16 ( = 0.05) for NL HDL-c, and = 0.15 ( = 0.05) for NL triglycerides. . Subjects with T2DM plus MetS have elevated PAI-1 levels before clinical manifestations of atherothrombotic disease. Metabolic factors have a more important contribution than 4G/5G polymorphism on PAI-1 plasma variability.

摘要

代谢和遗传因素可诱导纤溶酶原激活物抑制剂-1(PAI-1)过度表达;较高的PAI-1水平会降低纤维蛋白溶解并促进动脉粥样硬化血栓形成。为了评估2型糖尿病(T2DM)合并代谢综合征(MetS)患者在动脉粥样硬化血栓形成临床表现出现之前的PAI-1抗原水平,以及代谢因素和PAI-1基因的4G/5G多态性对PAI-1变异性的影响。我们于2010年5月至2011年9月在墨西哥城的一家医院进行了一项观察性横断面分析。MetS由国际糖尿病联盟标准定义。PAI-1水平和4G/5G多态性通过酶联免疫吸附测定(ELISA)和聚合酶链反应-限制性片段长度多态性分析(PCR-RFLP)来确定。我们纳入了215例T2DM合并MetS患者和307例对照。T2DM合并MetS患者的PAI-1水平高于参照组(58.4±21对49.9±16 ng/mL,P = 0.026)。一个包含MetS各组分的模型仅解释了PAI-1水平变异性的12%(R² = 0.12;P = 0.001),其中高血压的R²为0.18(P = 0.03),非高密度脂蛋白胆固醇(NL HDL-c)的R²为 -0.16(P = 0.05),非甘油三酯(NL甘油三酯)的R²为0.15(P = 0.05)。T2DM合并MetS患者在动脉粥样硬化血栓形成疾病临床表现出现之前PAI-1水平升高。代谢因素对PAI-1血浆变异性的贡献比4G/5G多态性更重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0590/5320378/d1043a79089e/BMRI2017-6519704.001.jpg

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