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特发性 REM 行为障碍家族史:一项多中心病例对照研究。

Family history of idiopathic REM behavior disorder: a multicenter case-control study.

机构信息

Department of Neurology, Hôpital Gui de Chauliac, INSERM U1061, Montpellier, France.

出版信息

Neurology. 2013 Jun 11;80(24):2233-5. doi: 10.1212/WNL.0b013e318296e967. Epub 2013 May 8.

Abstract

OBJECTIVE

To compare the frequency of proxy-reported REM sleep behavior disorder (RBD) among relatives of patients with polysomnogram-diagnosed idiopathic RBD (iRBD) in comparison to controls using a large multicenter clinic-based cohort.

METHODS

A total of 316 patients with polysomnography-confirmed iRBD were recruited from 12 RBD study group centers, along with 316 controls matched on sex and age group. All subjects completed a self-administered questionnaire that collected proxy-reported information on family history of tremor, gait trouble, balance trouble, Parkinson disease, memory loss, and Alzheimer disease. The questionnaire also included a single question that asked about possible symptoms of RBD among first-degree relatives (siblings, parents, and children).

RESULTS

A positive family history of dream enactment was reported in 13.8% of iRBD cases compared to 4.8% of controls (odds ratio [OR] = 3.9, 95% confidence interval [CI] 2.0-7.7). ORs were increased for both siblings (OR = 6.1, 95% CI 2.1-18.1) and parents (OR = 3.2, 95% CI 1.4-7.8). We found no significant difference in sex, current age (65.3 ± 10.2 vs 66.9 ± 10.2 years), or age at self-reported RBD onset (55.2 ± 11.7 vs 56.6 ± 15.1 years) in possible familial vs sporadic iRBD. No differences were found in family history of tremor, walking and balance troubles, Parkinson disease, memory loss, or Alzheimer disease.

CONCLUSION

We found increased odds of proxy-reported family history of presumed RBD among individuals with confirmed iRBD. This suggests the possibility of a genetic contribution to RBD.

摘要

目的

通过一项大型多中心基于诊所的队列研究,比较多导睡眠图诊断的特发性 REM 睡眠行为障碍(iRBD)患者亲属与对照组中,由代理人报告的 REM 睡眠行为障碍(RBD)的频率。

方法

从 12 个 RBD 研究组中心招募了 316 名经多导睡眠图证实的 iRBD 患者,以及 316 名按性别和年龄组匹配的对照者。所有受试者均完成了一份自我管理问卷,该问卷收集了关于亲属震颤、步态障碍、平衡障碍、帕金森病、记忆力减退和阿尔茨海默病家族史的代理报告信息。该问卷还包括一个问题,询问一级亲属(兄弟姐妹、父母和子女)中是否存在 RBD 的可能症状。

结果

与对照组(4.8%)相比,iRBD 病例中报告有梦境行为阳性家族史的比例为 13.8%(比值比 [OR] = 3.9,95%置信区间 [CI] 2.0-7.7)。兄弟姐妹(OR = 6.1,95% CI 2.1-18.1)和父母(OR = 3.2,95% CI 1.4-7.8)的 OR 均升高。在可能的家族性和散发性 iRBD 中,我们未发现性别、当前年龄(65.3 ± 10.2 岁比 66.9 ± 10.2 岁)或自报告 RBD 发病年龄(55.2 ± 11.7 岁比 56.6 ± 15.1 岁)存在显著差异。在震颤、行走和平衡障碍、帕金森病、记忆力减退或阿尔茨海默病家族史方面也未发现差异。

结论

我们发现,在确诊的 iRBD 患者中,代理人报告的家族史中有 RBD 的可能性增加。这表明 RBD 可能存在遗传因素。

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