Koskinen L L E, Korponay-Szabo I R, Viiri K, Juuti-Uusitalo K, Kaukinen K, Lindfors K, Mustalahti K, Kurppa K, Adány R, Pocsai Z, Széles G, Einarsdottir E, Wijmenga C, Mäki M, Partanen J, Kere J, Saavalainen P
Department of Medical Genetics, and Research Programo f Molecular Medicine, University of Helsinki, Finland.
J Med Genet. 2008 Apr;45(4):222-7. doi: 10.1136/jmg.2007.053991. Epub 2007 Dec 12.
Coeliac disease is caused by dietary gluten, which triggers chronic inflammation of the small intestine in genetically predisposed individuals. In one quarter of the patients the disease manifests in the skin as dermatitis herpetiformis. Recently, a novel candidate gene, myosin IXB on chromosome 19p13, was shown to be associated with coeliac disease in the Dutch and Spanish populations. The same gene has previously been associated with inflammatory bowel disease, systemic lupus erythematosus and rheumatoid arthritis risk, making myosin IXB a potential shared risk factor in these inflammatory disorders.
In this study, previously reported myosin IXB variants were tested for genetic linkage and association with coeliac disease in 495 Hungarian and Finnish families and in an additional 270 patients and controls.
The results show significant linkage (logarithm of odds (LOD) 3.76, p = 0.00002) to 19p13 which supports the presence of a genuine risk factor for coeliac disease in this locus. Myosin IXB variants were not associated with coeliac disease in this study; however, weak evidence of association with dermatitis herpetiformis was found. The association could not explain the strong linkage seen in both phenotypes, indicating that the role of other neighbouring genes in the region cannot be excluded. Therefore, more detailed genetic and functional studies are required to characterise the role of the myosin IXB gene in both coeliac disease and dermatitis herpetiformis.
乳糜泻由膳食麸质引起,在具有遗传易感性的个体中引发小肠慢性炎症。四分之一的患者疾病表现为疱疹样皮炎。最近,一个新的候选基因,位于19号染色体p13上的肌球蛋白IXB,在荷兰和西班牙人群中被证明与乳糜泻相关。该基因此前也与炎症性肠病、系统性红斑狼疮和类风湿关节炎风险相关,使得肌球蛋白IXB成为这些炎症性疾病潜在的共同风险因素。
在本研究中,对先前报道的肌球蛋白IXB变异体进行了基因连锁检测,并在495个匈牙利和芬兰家庭以及另外270名患者和对照中检测其与乳糜泻的关联。
结果显示与19p13存在显著连锁(优势对数(LOD)3.76,p = 0.00002),支持该位点存在乳糜泻真正的风险因素。本研究中肌球蛋白IXB变异体与乳糜泻无关;然而,发现了与疱疹样皮炎存在关联的微弱证据。该关联无法解释在两种表型中均观察到的强连锁,表明不能排除该区域其他相邻基因的作用。因此,需要更详细的遗传和功能研究来确定肌球蛋白IXB基因在乳糜泻和疱疹样皮炎中的作用。