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首页> 外文期刊>European Heart Journal: The Journal of the European Society of Cardiology >Epidermal fatty-acid-binding protein: a new circulating biomarker associated with cardio-metabolic risk factors and carotid atherosclerosis
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Epidermal fatty-acid-binding protein: a new circulating biomarker associated with cardio-metabolic risk factors and carotid atherosclerosis

机译:表皮脂肪酸结合蛋白:与心血管代谢危险因素和颈动脉粥样硬化相关的一种新的循环生物标志物

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AimsEpidermal fatty-acid-binding protein (E-FABP) is highly homologous to adipocyte FABP (A-FABP), which mediatesobesity-related metabolic syndrome (MetS), diabetes and atherosclerosis in animals. Combined deficiency of E-FABP and A-FABP protects against the MetS and atherosclerosis in mice. This study investigated the association of serum E-FABP with cardio-metabolic risk factors and carotid atherosclerosis in humans.MethodsThe presence of E-FABP in human plasma was detected by tandem mass spectrometry. Serum E-FABP levels, deter-and resultsmined by an enzyme-linked immunosorbent assay in 479 Chinese subjects (age: 55.4 + 13.5 years; M/F: 232/247),correlated positively (P < 0.05 to <0.001, age-adjusted) with parameters of adiposity, adverse lipid profiles, serum insulin, A-FABP, and C-reactive protein levels and were higher in subjects with the MetS (P < 0.001 vs. no MetS). The association of E-FABP with the MetS was independent of A-FABP. Furthermore, serum E-FABP correlated with carotid intima-media thickness (IMT; P< 0.001) and was independently associated with carotid IMT in men (adjusted P = 0.03).ConclusionE-FABP is a new circulating biomarker associated with increased cardio-metabolic risk. It may contribute to the devel-opment of the MetS and carotid atherosclerosis in humans, independent of the effect of A-FABP.
机译:目的表皮脂肪酸结合蛋白(E-FABP)与脂肪细胞FABP(A-FABP)高度同源,脂肪细胞FABP(A-FABP)介导肥胖相关的代谢综合症(MetS),糖尿病和动物动脉粥样硬化。 E-FABP和A-FABP的综合缺乏可预防小鼠的MetS和动脉粥样硬化。本研究探讨了血清E-FABP与人心血管代谢危险因素和颈动脉粥样硬化的关系。方法采用串联质谱法检测人血浆中E-FABP的存在。酶联免疫吸附测定法测定的479名中国受试者(年龄:55.4 + 13.5岁;男/女:232/247)中血清E-FABP的水平与结果呈正相关(P <0.05至<0.001,年龄-调整后)的参数,包括肥胖,不良脂质谱,血清胰岛素,A-FABP和C反应蛋白水平,并且在患有MetS的受试者中更高(P <0.001 vs.无MetS)。 E-FABP与MetS的关联独立于A-FABP。此外,血清E-FABP与男性颈动脉内膜中层厚度相关(IMT; P <0.001),并且与颈动脉IMT独立相关(校正后P = 0.03)。风险。不依赖于A-FABP的作用,它可能有助于人类MetS的发展和颈动脉粥样硬化。

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