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患有脆性X染色体扩展和脆性X染色体相关震颤共济失调综合征(FXTAS)的女性的免疫介导疾病。

Immune mediated disorders in women with a fragile X expansion and FXTAS.

作者信息

Jalnapurkar Isha, Rafika Nuva, Tassone Flora, Hagerman Randi

机构信息

Medical Investigation of Neurodevelopmental Disorders (MIND) Institute, University of California, Davis Medical Center, Sacramento, California.

出版信息

Am J Med Genet A. 2015 Jan;167A(1):190-7. doi: 10.1002/ajmg.a.36748. Epub 2014 Nov 14.

Abstract

Premutation alleles in fragile X mental retardation 1 (FMR1) can cause the late-onset neurodegenerative disorder, fragile X-associated tremor ataxia syndrome (FXTAS) and/or the fragile X-associated primary ovarian insufficiency in approximately 20% of heterozygotes. Heterozygotes of the FMR1 premutation have a higher incidence of immune mediated disorders such as autoimmune thyroid disorder, especially when accompanied by FXTAS motor signs. We describe the time course of symptoms of immune mediated disorders and the subsequent development of FXTAS in four women with an FMR1 CGG expansion, including three with the premutation and one with a gray zone expansion. These patients developed an immune mediated disorder followed by neurological symptoms that become consistent with FXTAS. In all patients we observed a pattern involving an initial appearance of disease symptoms-often after a period of heightened stress (depression, anxiety, divorce, general surgery) followed by the onset of tremor and/or ataxia. Immune mediated diseases are associated with the manifestations of FXTAS temporally, although further studies are needed to clarify this association. If a cause and effect relationship can be established, treatment of pre-existing immune mediated disorders may benefit patients with pathogenic FMR1 mutations.

摘要

脆性X智力低下1(FMR1)基因的前突变等位基因可导致迟发性神经退行性疾病——脆性X相关震颤共济失调综合征(FXTAS)和/或脆性X相关原发性卵巢功能不全,约20%的杂合子会出现这种情况。FMR1基因前突变的杂合子发生免疫介导疾病的几率更高,如自身免疫性甲状腺疾病,尤其是伴有FXTAS运动症状时。我们描述了4名FMR1基因CGG扩增女性免疫介导疾病的症状发展过程以及随后FXTAS的发生情况,其中3名是前突变携带者,1名是灰色区域扩增携带者。这些患者先出现免疫介导疾病,随后出现符合FXTAS的神经症状。在所有患者中,我们观察到一种模式,即疾病症状通常在一段压力增大时期(抑郁、焦虑、离婚、普通外科手术)后首次出现,随后出现震颤和/或共济失调。免疫介导疾病在时间上与FXTAS的表现相关,不过还需要进一步研究来阐明这种关联。如果能建立因果关系,治疗已有的免疫介导疾病可能会使携带致病性FMR1突变的患者受益。

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