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血清Lp-PLA_2含量对早期无症状糖尿病周围神经病变的筛查价值 被引量:10

The value of serum lipoprotein associated phospholipase A_2 levels in screening patients with early asymptomatic diabetic peripheral neuropathy
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摘要 目的:探讨血清脂蛋白相关磷脂酶A_2(Lp-PLA_2)浓度在早期无症状糖尿病周围神经病变(diabetic peripheral neuropathy,DPN)中的诊断和筛查价值。方法:选择病程小于12个月的早期2型糖尿病患者89例,以神经肌电图检查为标准,将其分为DPN组和单纯糖尿病组。分别检测其血清Lp-PLA_2等血脂含量。用ROC曲线分析方法,评价Lp-PLA_2的诊断价值,并找出合适的截断点。结果:DPN组血清Lp-PLA_2浓度显著低于单纯糖尿病组(t=-3.772,P=0.000),ROC曲线下面积为0.731(P=0.001),说明Lp-PLA_2对DPN的诊断有意义,且当Lp-PLA_2浓度为133.50 ng/m L时最具有DPN诊断意义。结论:血清Lp-PLA_2浓度可能预测DPN,但仍需大样本研究进一步验证。 Objective: To investigate the value of the serum lipoprotein associated phospholipase A2( Lp-PLA2) levels in the diagnosis and screening of early asymptomatic diabetic peripheral neuropathy( DPN). Methods: A total of 89 patients diagnosed with type 2 diabetes less than 12 months were divided into DPN group and non-DPN group according to neural electromyography. The diagnostic value of Lp-PLA2 by diagnostic test and ROC curve analysis were evaluated and the appropriate cut-off point were determined. Results: The level of serum Lp-PLA2 of DPN group was significantly lower than that of nonDPN group( t =-3. 772,P = 0. 000). The area under curve( AUC) of Lp-PLA2 was 0. 731( P =0. 001). The appropriate cut-off point was 133. 50 ng/m L. Conclusion: Serum Lp-PLA2 levels could predict DPN,but which still need further to be validated in larger sample research.
出处 《江苏大学学报(医学版)》 CAS 2017年第4期324-326,共3页 Journal of Jiangsu University:Medicine Edition
基金 镇江市社会发展项目(SH2013089 SH2015027)
关键词 脂蛋白相关磷脂酶A2 糖尿病周围神经病变 肌电图 lipoprotein associated phospholipase A2 diabetic peripheral neuropathy electromyography
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  • 1栾松,崔丽英.糖尿病性周围神经病发病机制和电生理研究进展[J].临床神经电生理学杂志,2005,14(1):44-47. 被引量:57
  • 2卢祖能,李竟,董红娟,周桂兰,胡胜,王真真.F波对糖尿病周围神经病的早期评估(英文)[J].中国临床康复,2005,9(17):202-204. 被引量:19
  • 3Candrilli SD, Davis KL, Kan HJ, et al. Prevalence and the associated burden of illness of symptoms of diabetic peripheral neuropathy and diabetic retinopathy[J]. J Diabetes Complications, 2007, 21: 306-314
  • 4Sasaki H, Schmelzer JD, Zollman PJ, et al. Neuropathology and blood flow of nerve, spinal roots and dorsal root ganglia in longstanding diabetic rats[J].Acta Neuropathol, 1997, 93:118-128
  • 5van Dam PS, van Asbeck BS, Bravenboer B, et al. Nerve function and oxidative stress in diabetic and vitamin E-deficient rats[J].Free Radic Biol Med, 1998, 24: 18-26
  • 6Fernyhough P, Huang TJ, Verkhratsky A. Mechanism of mitochondrial dysfunction in diabetic sensory neuropathy[J]. J Peripher Nerv Syst, 2003, 8:227-235
  • 7Schmeichel AM, Schmelzer JD, Low PA. Oxidative injury and apoptosis of dorsal root ganglion neurons in chronic experimental diabetic neuropathy[J]. Diabetes, 2003, 52: 165-171
  • 8Brownlee M. Biochemistry and molecular cell biology of diabetic complications[J]. Nature, 2001, 414:813-820
  • 9Oates PJ. Polyol pathway and diabetic peripheral neuropathy[J]. Int Rev Neurobiol, 2002, 50: 325-392
  • 10Deuther-Conrad W, Loske C, Schinzel R, et al. Advanced glycation end products change glutathione redos status in SH-SY5Y human neuroblastoma cells by a hydrogen peroxide dependent mechanism [J]. Neurosci Lett, 2001, 312:29-32

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