Department of Experimental and Clinical Pharmacology, Medical University of Warsaw, Center for Preclinical Research and Technology CEPT, Warsaw, Poland.
Department of Experimental and Clinical Pharmacology, Medical University of Warsaw, Center for Preclinical Research and Technology CEPT, Warsaw, Poland.
Can J Diabetes. 2019 Feb;43(1):19-26. doi: 10.1016/j.jcjd.2018.01.014. Epub 2018 Feb 3.
The aim of this study was to investigate the association of serum brain-derived neurotrophic factor (BDNF) levels with platelet reactivity and antidiabetes treatment, as well as serum adipocytokine concentrations.
This observational, open-label study enrolled 149 patients. Serum BDNF, hematologic, biochemical parameters and platelet reactivity were measured. Blood samples were taken after the last acetylsalicylic acid dose.
Patients with high BDNF levels were younger (65.60±8.956 vs. 68.59±8.516) and smoked cigarettes more frequently (14.6% vs. 4.1%); they were more commonly being treated by metformin (77.3% vs. 54%); had higher platelet counts (245.81±68.85 10/mm vs. 206.61±44.48 10/mm); had shorter collagen-adenosine diphosphate closure time (CADP-CT) values (104.88±69.73 s vs. 140.93±86.63 s); had higher triglyceride concentrations (140.73±67.5 vs. 121.76±60.49) and had higher concentrations of serum thromboxane B2 (0.938±1.59 vs. 0.364±0.76). In univariate linear regression analyses, predictive factors for serum BDNF levels above the median were metformin treatment, current smoking, platelet count, triglyceride concentration, total cholesterol concentration and CADP-CT >74 s. In multivariate backward stepwise analysis CADP-CT >141 s; adiponectin concentration >4.22 µg/mL; total cholesterol and low-density lipoprotein levels were independently associated with serum BDNF levels above the median.
Our results suggest that BDNF may be associated with lipid metabolism and that increased production of BDNF may be related to metformin treatment. Moreover, we showed an association between BDNF levels and platelet reactivity; we found that serum BDNF levels in patients with type 2 diabetes who had high platelet reactivity were higher than in subjects with normal platelet reactivity despite antiplatelet therapy.
本研究旨在探讨血清脑源性神经营养因子(BDNF)水平与血小板反应性及抗糖尿病治疗的关系,并研究其与血清脂肪细胞因子浓度的关系。
这是一项观察性、开放性研究,共纳入 149 例患者。测量血清 BDNF、血液学和生化参数以及血小板反应性。在最后一次服用阿司匹林后采血。
高 BDNF 水平组患者更年轻(65.60±8.956 岁 vs. 68.59±8.516 岁),吸烟更频繁(14.6% vs. 4.1%);他们更常接受二甲双胍治疗(77.3% vs. 54%);血小板计数较高(245.81±68.85×10⁹/L vs. 206.61±44.48×10⁹/L);胶原-腺苷二磷酸(collagen-adenosine diphosphate,CADP)-ADP 闭合时间(closure time,CT)值较短(104.88±69.73 s vs. 140.93±86.63 s);三酰甘油(triglyceride,TG)浓度较高(140.73±67.5 mg/dL vs. 121.76±60.49 mg/dL);血清血栓素 B2(thromboxane B2,TXB2)浓度较高(0.938±1.59 pg/mL vs. 0.364±0.76 pg/mL)。在单因素线性回归分析中,血清 BDNF 水平高于中位数的预测因素是二甲双胍治疗、当前吸烟、血小板计数、TG 浓度、总胆固醇浓度和 CADP-ADP CT>74 s。在多因素逐步向后分析中,CADP-ADP CT>141 s;脂联素浓度>4.22 μg/mL;总胆固醇和低密度脂蛋白水平与血清 BDNF 水平高于中位数独立相关。
我们的研究结果表明,BDNF 可能与脂代谢有关,而 BDNF 的产生增加可能与二甲双胍治疗有关。此外,我们还发现 BDNF 水平与血小板反应性之间存在关联,我们发现,在接受抗血小板治疗的情况下,2 型糖尿病患者中血小板反应性高的患者的血清 BDNF 水平高于血小板反应性正常的患者。