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首页> 外文期刊>Journal of the European Academy of Dermatology and Venereology: JEADV >Brain-derived neurotrophic factor gene polymorphisms and serum levels in Chinese atopic dermatitis patients.
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Brain-derived neurotrophic factor gene polymorphisms and serum levels in Chinese atopic dermatitis patients.

机译:中国特应性皮炎患者脑源性神经营养因子基因多态性和血清水平。

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摘要

BACKGROUND: Brain-derived neurotrophic factor (BDNF) plays an important role in the pathogenesis of atopic dermatitis (AD). Whether BDNF gene polymorphisms are associated with Chinese AD remains totally unknown. OBJECTIVE: The aim is to determine if BDNF gene C270T and G196A polymorphisms are associated with Chinese AD, and analyse the clinical relevance of BDNF gene polymorphisms and BDNF serum levels. Methods We conducted a case-control association analysis (160 patients and 169 controls) in Northern Chinese subjects. Genotyping was performed by restriction fragment length polymorphism, and serum levels of BDNF were measured using enzyme-linked immunosorbent assay. RESULTS: For C270T, there were significant differences in C/T genotype distribution (P = 0.003) and T allele frequencies (P = 0.004) between AD patients and controls in the whole dataset. Higher C/T genotype frequencies were found in male AD (10.6% vs. 1.1%, P = 0.018) and in intrinsic AD (IAD; 15.79% vs. 2.91%, P = 0.008). No association between G196A polymorphism and AD was observed in the whole cohort, while A allele was much more frequent in AD patients with atopy in first-degree relatives (65.8% vs. 34.2%, P = 0.038). Serum BDNF levels were correlated with IAD severity as measured by Scoring Atopic Dermatitis index (r = 0.576, P < 0.001). CONCLUSION: T allele in C270T may be a risk factor for AD, especially in IAD and male AD. A allele in G196A may be a risk factor in AD patients with atopy in first-degree relatives. Serum BDNF levels were correlated with the severity of IAD.
机译:背景:脑源性神经营养因子(BDNF)在特应性皮炎(AD)的发病机理中起着重要作用。 BDNF基因多态性是否与中国AD相关尚不清楚。目的:确定BDNF基因C270T和G196A多态性是否与中国AD相关,并分析BDNF基因多态性与BDNF血清水平的临床相关性。方法我们对中国北方受试者进行了病例对照关联分析(160例患者和169例对照)。通过限制性片段长度多态性进行基因分型,并使用酶联免疫吸附测定法测量血清BDNF水平。结果:对于C270T,在整个数据集中,AD患者和对照组之间的C / T基因型分布(P = 0.003)和T等位基因频率(P = 0.004)存在显着差异。男性AD(10.6%vs. 1.1%,P = 0.018)和内在AD(IAD; 15.79%vs. 2.91%,P = 0.008)发现较高的C / T基因型频率。在整个队列中均未观察到G196A基因多态性与AD之间的关联,而一级亲属中患有特应性遗传病的AD患者中A等位基因更为频繁(65.8%vs. 34.2%,P = 0.038)。血清BDNF水平与IAD严重程度相关,如通过特应性皮炎评分(r = 0.576,P <0.001)来衡量。结论:C270T中的T等位基因可能是AD的危险因素,尤其是在IAD和男性AD中。 G196A中的等位基因可能是一级亲属特应性过敏的AD患者的危险因素。血清BDNF水平与IAD的严重程度相关。

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