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    題名: 紅斑性狼瘡病患併腎病變Interleukin-10基因多型性之關連性;The Association of Interleukin-10 Gene Polymorphism in Systemic Lupus Erythematosus Patients with Renal Disease
    作者: 林博文;Po-Wen Lin
    貢獻者: 中國醫藥大學:醫學研究所碩士班
    關鍵詞: 紅斑性狼瘡;狼瘡性腎病變;Interleukin-10基因多型性;Systemic Lupus Erythematosus;lupus nephropathy;Interleukin-10 Gene Polymorphism
    日期: 2007-07-24
    上傳時間: 2009-08-13 14:50:23 (UTC+8)
    摘要: 背景:紅斑性狼瘡是一種會影響全身各種器官的自體免疫疾病,流行病學上已經有強烈的證據指出基因是導致許多常見疾病發生的危險因素。之前的研究已經顯示在罹患紅斑性狼瘡的白人身上interleukin-10 (IL-10)-1082G、IL-10-819C 和IL-10-592C haplotype 與腎臟病的侵犯有關連性﹔但在中國人,另一組不同的IL-10-1087*A /-824*T /-597*A haplotype 也和腎臟病的影響有相關。我们的研究將探討IL-10 promoter 基因多型性是否為易導
    致狼瘡性腎病變的一個標記。
    方法:我们納入119 位有紅斑性狼瘡的中國人為研究對象,另一組居住在中台灣的100 位無血緣關係的健康人當作控制組。在紅斑性狼瘡病患這組,不僅腎臟病變(定義為每日蛋白尿超過1g)也包括其他臨床症狀和血清學上的數據都納入分析中。每組基因DNA 是經由抽取受試者周邊血液進一步使用基因組DNA 分離kit 所取得的(Genomaker, Taiwan)。每一種基因的多型性是以polymerase chain reaction (PCR)為基礎的限制酶方法來分析及進一步
    去探討。我们將基因多型性的變化分成可切除的AA homozygote、不可切除的CC homozygote 同型合子和A/C heterozygote 異型合子。此外,IL-10基因多型性和紅斑性狼瘡臨床表現的關係亦納入評估。
    結果:我们在紅斑性狼瘡病患身上並未發現IL-10 基因型和腎臟病變有相關性。同時針對紅斑性狼瘡其他系統的表現包括顴骨疹、光致敏性、中樞神經系統和抗核抗體(ANA)在基因型上皆無達到顯著的發現(all p>0.05)。但更進一步在基因的genotype 以及allelic frequency 上正常控制組和紅斑性狼瘡病患組卻有統計學上的差異(分別p 值為0.007 和0.003)。
    結論:雖然我们不能夠在紅斑性狼瘡併腎病變病患與健康人之間發現IL-10基因型有顯著的差異性,然而罹患紅斑性狼瘡者其-627IL-10 基因型包括genotype 與allelic frequency 確實有明顯的關連性。這進一步顯示在紅斑性狼瘡病患身上,IL-10 基因多型性在未來的研究可當作一個基因的標記。

    Background: Systemic lupus erythematosus (SLE) is a prototype of autoimmune diseases that affects practically every organ in the body. There are strong epidemiological evidences that genes contribute to the risk of developing
    many common diseases. The previous study had shown that interleukin-10 (IL-10)-1082G, IL-10-819C, and IL-10-592C haplotype were associated with renal involvement in white patients with SLE. In Chinese patients, a different
    IL-10-1087*A /-824*T /-597*A haplotype was also associated with renal involvement. Our study will investigate whether IL-10 promoter polymorphism is a marker of susceptibility of lupus nephropathy.
    Methods: The study included 119 Chinese patients with SLE. One hundred unrelated, healthy individuals living in central Taiwan served as control subjects. In SLE patients, not only renal disease (defined as proteinuria >1g/day) but also other clinical and serological data were analyzed. The genomic DNA was prepared from peripheral blood by use of a genomic DNA isolation reagent kit
    (Genomaker, Taiwan). Each polymorphism was detected as a result of a polymerase chain reaction (PCR)-based restriction analysis. The polymorphism was divided into digestible (AA homozygote), indigestible (CC homozygote)
    and A/C heterozygote. The relationship between the IL-10 gene polymorphism and clinical manifestations of SLE was evaluated.
    Results: We did not detect any association of IL-10 genotype with renal disease involvement in the SLE patients. There were also no significant finding in other parameters, including malar rash, photosensitivity, entral nervous system involvement and ANA (all p>0.05). Furthermore, for the genotype and allelic frequency, there were statistically significant differences between the
    SLE patients and the normal control subjects (p=0.007, and 0.003, respectively).
    Conclusion: We were unable to find significant differences in IL-10 gene polymorphism between SLE patients with renal disease and the healthy control subjects. However, there were significant relation of -627 IL-10 genotype and
    allelic frequencies with SLE. It implies that the IL-10 gene polymorphism can serve as a candidate gene marker for further study in patients with SLE.
    顯示於類別:[醫學研究所] 博碩士論文

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