Department of Psychiatry and Behavioral Sciences, University of California, Davis Medical Center, Sacramento, USA.
J Clin Psychiatry. 2011 Feb;72(2):175-82. doi: 10.4088/JCP.09m05407blu. Epub 2010 Aug 24.
The authors studied the lifetime prevalence of DSM-IV-TR psychiatric disorders in a population of adults with the fragile X premutation.
The Structured Clinical Interview for DSM-IV was conducted, from 2007-2008, in 85 individuals with the fragile X premutation, 47 with the fragile X-associated tremor/ataxia syndrome (FXTAS; 33 male, 14 female; mean age = 66 years) and 38 without FXTAS (16 male, 22 female; mean age = 52 years). Lifetime prevalence for mood and anxiety disorders among carriers with and without FXTAS was compared to available age-specific population estimates from the National Comorbidity Survey Replication (NCS-R).
Among participants with FXTAS, 30 (65%) met lifetime DSM-IV-TR criteria for a mood disorder; 24 (52%) met lifetime DSM-IV-TR criteria for an anxiety disorder. Among the non-FXTAS participants, there were 15 instances of lifetime mood disorder (42%) and 18 of lifetime anxiety disorder (47%). When compared to age-specific NCS-R data, the lifetime prevalences of any mood disorder (P < .0001), major depressive disorder (P < .0001), any anxiety disorder (P < .0001), panic disorder (P = .006), specific phobia (P = .0003), and posttraumatic stress disorder (P = .004) were significantly higher in participants with FXTAS. The lifetime rates of social phobia in individuals with the premutation without FXTAS were significantly higher than NCS-R data (P = .001).
This sample of carriers of the fragile X premutation had a notably high lifetime risk of mood and anxiety disorders. Mood and anxiety disorders may be part of the clinical phenotype of the fragile X premutation conditions, especially in carriers with FXTAS. Clinicians encountering these patients are advised to consider FXTAS as a neuropsychiatric syndrome as well as a neurologic disorder.
本研究旨在调查脆性 X 前突变携带者一生中出现 DSM-IV-TR 精神障碍的患病率。
2007-2008 年,研究人员使用 DSM-IV 结构临床访谈对 85 名脆性 X 前突变携带者进行了评估,其中 47 名患有脆性 X 相关震颤/共济失调综合征(FXTAS;33 名男性,14 名女性;平均年龄=66 岁),38 名无 FXTAS(16 名男性,22 名女性;平均年龄=52 岁)。研究比较了 FXTAS 携带者和非 FXTAS 携带者的心境和焦虑障碍的终生患病率与来自国家共病调查-复制(NCS-R)的年龄特异性人群估计值。
在 FXTAS 患者中,30 名(65%)符合 DSM-IV-TR 心境障碍的终生诊断标准;24 名(52%)符合 DSM-IV-TR 焦虑障碍的终生诊断标准。在非 FXTAS 患者中,有 15 例(42%)出现了终生心境障碍,18 例(47%)出现了终生焦虑障碍。与年龄特异性 NCS-R 数据相比,FXTAS 患者的任何心境障碍终生患病率(P<0.0001)、重性抑郁障碍终生患病率(P<0.0001)、任何焦虑障碍终生患病率(P<0.0001)、惊恐障碍终生患病率(P=0.006)、特定恐惧症终生患病率(P=0.0003)和创伤后应激障碍终生患病率(P=0.004)均显著更高。非 FXTAS 脆性 X 前突变携带者的社交恐怖症终生发生率明显高于 NCS-R 数据(P=0.001)。
本脆性 X 前突变携带者样本的一生中出现心境和焦虑障碍的风险明显较高。心境和焦虑障碍可能是脆性 X 前突变疾病的临床表型的一部分,尤其是在 FXTAS 携带者中。遇到这些患者的临床医生建议将 FXTAS 视为一种神经精神综合征以及一种神经障碍。