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Is the C677T polymorphism in methylenetetrahydrofolate reductase gene or plasma homocysteine a risk factor for diabetic peripheral neuropathy in Chinese individuals? 被引量:1

Is the C677T polymorphism in methylenetetrahydrofolate reductase gene or plasma homocysteine a risk factor for diabetic peripheral neuropathy in Chinese individuals?
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摘要 The present study enrolled 251 diabetic patients, including 101 with neuropathy and 150 without neuropathy. Of the 150 patients, 100 had no complications, such as retinopathy, nephropathy, or neuropathy. Polymerase chain reaction-restriction fragment length polymorphism analysis was used to identify methylenetetrahydrofolate reductase gene variants. Plasma homocysteine levels were also measured. Homocysteine levels and the frequency of hyperhomocysteinemia were significantly higher in patients with diabetic peripheral neuropathy compared with diabetic patients without neuropathy (P 〈 0.05). In logistic regression analysis with neuropathy as the dependent variable, the frequency of C677T in methylenetetrahydrofolate reductase was significantly higher in patients with diabetic peripheral neuropathy compared with patients without diabetic complications. Homocysteine levels were significantly higher in patients with diabetic peripheral neuropathy carrying the 677T allele and low folic acid levels. In conclusion, hyperhomocysteinemia is an independent risk factor for diabetic neuropathy in Chinese patients with diabetes. The C677T polymorphism in methylenetetrahydrofolate reductase and low folic acid levels may be risk factors for diabetic peripheral neuropathy in Chinese patients with diabetes. The present study enrolled 251 diabetic patients, including 101 with neuropathy and 150 without neuropathy. Of the 150 patients, 100 had no complications, such as retinopathy, nephropathy, or neuropathy. Polymerase chain reaction-restriction fragment length polymorphism analysis was used to identify methylenetetrahydrofolate reductase gene variants. Plasma homocysteine levels were also measured. Homocysteine levels and the frequency of hyperhomocysteinemia were significantly higher in patients with diabetic peripheral neuropathy compared with diabetic patients without neuropathy (P 〈 0.05). In logistic regression analysis with neuropathy as the dependent variable, the frequency of C677T in methylenetetrahydrofolate reductase was significantly higher in patients with diabetic peripheral neuropathy compared with patients without diabetic complications. Homocysteine levels were significantly higher in patients with diabetic peripheral neuropathy carrying the 677T allele and low folic acid levels. In conclusion, hyperhomocysteinemia is an independent risk factor for diabetic neuropathy in Chinese patients with diabetes. The C677T polymorphism in methylenetetrahydrofolate reductase and low folic acid levels may be risk factors for diabetic peripheral neuropathy in Chinese patients with diabetes.
出处 《Neural Regeneration Research》 SCIE CAS CSCD 2012年第30期2384-2391,共8页 中国神经再生研究(英文版)
基金 supported by the Natural Science Foundation of Beijing, No. 7102161
关键词 HOMOCYSTEINE methylenetetrahydrofolate reductase type 2 diabetes mellitus diabetic peripheralneuropathy neural regeneration homocysteine methylenetetrahydrofolate reductase type 2 diabetes mellitus diabetic peripheralneuropathy neural regeneration
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  • 1Basol N, Inanir A, Yigit S, et al. High Association of IL-4 Gene Intron 3 VNTR Polymorphism with Diabetic Peripheral Neuropathy [ J ]. Journal of Molecular Neuroscience, 2013,51 : 437-441.
  • 2Zelman DC, Gore M, Dukes E, et al. Validation of a modified version of the brief pain inventory for painful diabetic peripheral neuropathy [ J ]. Journal of Pain and Symptom Management,2005,29:401-410.
  • 3Leonel ER, Jorge AF, Andrea AM, et al. NeuroinflanuTtion : implications for the pathogenesis and molecular diagnosis of Alzheimer' s disease [ J ]. Archives of Medical Research ,2008, ( 39 ) : 1-16.
  • 4Pan H, Zhang L, Guo M, et al. The oxidative stress status in diabetes mellitus and diabetic nephropathy [ J ]. Acta diabetologica, 2010,47 ( 1 ) : 71-76.
  • 5Koch M, Mostert J, Arutjunyan A, et al. Peripheral blood leukocyte NO production and oxidative stress in multiple sclerosis [ J ]. Multiple Sclerosis ,2008, ld (2) : 159-65.
  • 6GonsetteRE. Neurodegeneration in multiple sclerosis: the role of oxidative stress and excitotoxicity [ J ]. Journal of the Neurological Sciences ,2008,274( 1 ) :48-53.
  • 7Yang X, Yao W, Li Q, et al. Mechanism of Tang Luo Ning effect on attenuating of oxidative stress in sciatic nerve of STZ-induced diabetic rats [ J ]. Journal of Ethnopharmacology,2015,174 : 1-10.
  • 8Dreger H, Westphal K, Weller A, et al. Nrf2-dependent upregulation of antioxidative enzymes : a novel pathway for proteasome inhibitor-mediated cardioprotection [ J ]. Cardiovascular Research,2009,83 (2) : 354-361.
  • 9Abraham NG, Kappas A. Pharmacological and clinical aspects of heme oxygenase[ J]. Pharmacological Reviews, 2008,60( 1 ) :79-127.
  • 10蔡维霞,张军,胡大海.氧化和化学应激的防御性转导通路——Nrf2/ARE[J].中国生物化学与分子生物学报,2009,25(4):297-303. 被引量:36

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