首页> 外文期刊>Autoimmunity >Gene polymorphisms of TNF-alpha-308 (G/A), IL-10(-1082) (G/A), IL-6(-174) (G/C) and IL-1Ra (VNTR) in Egyptian cases with type 1 diabetes mellitus.
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Gene polymorphisms of TNF-alpha-308 (G/A), IL-10(-1082) (G/A), IL-6(-174) (G/C) and IL-1Ra (VNTR) in Egyptian cases with type 1 diabetes mellitus.

机译:在埃及病例中,TNF-alpha-308(G / A),IL-10(-1082)(G / A),IL-6(-174)(G / C)和IL-1Ra(VNTR)的基因多态性。 1型糖尿病。

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BACKGROUND: Type 1 diabetes (T1D) is a genetically conditioned autoimmune disease in which cytokines play an important role. Objectives. To check for the association of polymorphisms of cytokine genes with type 1 diabetes. Subjects. This work included 50 cases with T1D and 98 healthy individuals from the Nile Delta region of Egypt. Cases included 20 males and 30 females with a median age of 25 and range of 15-50 years. METHODS: DNA was amplified using PCR with sequence-specific primers for detection of polymorphisms related to tumor necrosis factor (TNF)-alpha(- 308) (G/A), interleukin (IL)-10(- 1082) (G/A), IL-6(- 174) (G/C), and IL-1Ra (VNTR). RESULTS: Cases with T1D showed significant higher frequency of genotypes of TNF-alpha(- 308) AA (p < 0.001, odds ratio (OR) = 7.91), IL-6-17CC (p < 0.05, OR = 3.36) and IL-1Ra A1A1 (p < 0.05, OR = 3.68) with significant lower frequencies of TNF-alpha(- 308) GA, and IL-1Ra A1A2 genotypes (p < 0.001 and < 0.05, respectively). They also showed significant higher frequency of TNF-alpha(- 308) allele A (p < 0.05, OR = 2.0), IL-1Ra allele A1 (p < 0.05, OR = 2.98) with a significant lower frequency of TNF-alpha(- 308) G allele and IL-1Ra A2 allele (p < 0.05). No significant difference was detected among cases in relation to IL-10(- 1082) (G/A) genotypes or alleles nor in relation to age, sex, consanguinity or family history of the disease. CONCLUSIONS: Polymorphisms related to TNF-alpha and IL-1Ra genes may be considered genetic markers for T1D among Egyptians with a potential impact on family counseling and management.
机译:背景:1型糖尿病(T1D)是一种遗传性自身免疫疾病,其中细胞因子起着重要的作用。目标。要检查细胞因子基因多态性与1型糖尿病的关联。主题。这项工作包括50例T1D病例和98名来自埃及尼罗河三角洲地区的健康个体。病例包括20名男性和30名女性,中位年龄为25岁,年龄范围为15至50岁。方法:使用序列特异性引物通过PCR扩增DNA,以检测与肿瘤坏死因子(TNF)-α(-308)(G / A),白介素(IL)-10(-1082)(G / A)相关的多态性),IL-6(-174)(G / C)和IL-1Ra(VNTR)。结果:T1D患者的TNF-α(-308)AA基因型(p <0.001,优势比(OR)= 7.91),IL-6-17CC(p <0.05,OR = 3.36)和IL的基因型发生率明显更高-1Ra A1A1(p <0.05,OR = 3.68),其TNF-α(-308)GA和IL-1Ra A1A2基因型的频率明显较低(分别为p <0.001和<0.05)。他们还显示TNF-α(-308)等位基因A(p <0.05,OR = 2.0),IL-1Ra等位基因A1(p <0.05,OR = 2.98)的频率明显较高,而TNF-alpha(-308 -308)G等位基因和IL-1Ra A2等位基因(p <0.05)。在与IL-10(-1082)(G / A)基因型或等位基因相关的病例中,与与该疾病的年龄,性别,血缘关系或家族史无关的病例之间未发现显着差异。结论:与TNF-α和IL-1Ra基因相关的多态性可能被认为是埃及人T1D的遗传标记,可能会对家庭咨询和管理产生影响。

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