Laboratory of Clinical Neurophysiology, Institute and Department of Psychiatry, University of São Paulo, São Paulo, SP, Brazil.
Epilepsia. 2013 May;54(5):866-70. doi: 10.1111/epi.12116.
Despite growing evidence on the occurrence of poor psychosocial adjustment, to the moment there is no formal assessment of social adjustment (SA) using a validated instrument developed and standardized for this purpose in patients with juvenile myoclonic epilepsy (JME). We aimed to: (1) verify social adjustment in patients with JME with an objective scale and; (2) identify whether clinical variables, impulsiveness, and neuropsychological profile are associated with worse social adjustment.
We prospectively evaluated 42 patients with an unequivocal diagnosis of JME and 42 controls. The inclusion criteria for patients and controls included age range from 16 to 40 years and an estimated intelligence quotient (IQ) ranging from 85 to 110. One trained neuropsychologist administered the scales and tests in a standard sequence. Social Adjustment was evaluated by The Self-Report Social Adjustment Scale (Weissman & Bothwell, 1976), a 42-item scale, measuring performance in seven major areas: work; social and leisure activities; relationship with extended family; marital role as a spouse; parental role; membership in the family unit; and economic adequacy. Impulsivity was assessed by using the Temperament and Character Inventory (Cloninger, 2000). Patients with JME and control subjects were evaluated with a comprehensive battery of neuropsychological tests evaluating executive and memory functions. We evaluated the age at onset; time from onset to seizure control with antiepileptic drugs (duration of epilepsy); seizure control; frequency of myoclonic seizures; frequency of generalized tonic-clonic GTC seizures; frequency of absence seizures; family history of epilepsy; family history of psychiatric disorders; and personal history of psychiatric disorders.
The score on Global Social Adjustment was worse than controls (p = 0.001), especially on the factors: Work (p = 0.032); Extended Family (p = 0.005). Higher Novelty Seeking (NS) scores were significantly correlated with worse on Global (p = 0.002); Work (p = 0.001) and Leisure (p = 0.003). There was no correlation between cognitive performance and Social Adjustment Scale (SAS) factors. Higher seizure frequency--myoclonic (p = 0.005) and GTC (p = 0.035)--were correlated with higher scores on factor Work of SAS.
Our findings suggest that patients with JME have worse social adjustment in two relevant aspects of their lives--work and familiar relationship. In this series of patients with JME, higher seizure frequency and impulsive traits, but not cognitive performance, were correlated with worse social adjustment.
尽管有越来越多的证据表明青少年肌阵挛癫痫(JME)患者存在较差的心理社会适应,但目前尚无针对 JME 患者使用经过验证和标准化的工具进行社会适应(SA)正式评估的方法。我们旨在:(1)使用客观量表来验证 JME 患者的社会适应情况;(2)确定临床变量、冲动性和神经心理学特征是否与较差的社会适应相关。
我们前瞻性地评估了 42 名明确诊断为 JME 的患者和 42 名对照组。患者和对照组的纳入标准包括年龄在 16 至 40 岁之间,估计智商(IQ)在 85 至 110 之间。一名经过培训的神经心理学家按照标准顺序进行量表和测试的评估。社会适应通过 Weissman 和 Bothwell(1976 年)的自我报告社会适应量表(Self-Report Social Adjustment Scale)进行评估,该量表由 42 个项目组成,用于测量七个主要领域的表现:工作;社会和休闲活动;与大家庭的关系;婚姻角色作为配偶;父母角色;家庭成员单位;经济状况。冲动性通过使用特质和性格问卷(Temperament and Character Inventory,Cloninger,2000)进行评估。JME 患者和对照组接受了一系列全面的神经心理学测试,评估执行和记忆功能。我们评估了发病年龄;从发病到癫痫药物控制的时间(癫痫持续时间);癫痫发作控制情况;肌阵挛发作频率;全面强直-阵挛性 GTC 发作频率;失神发作频率;癫痫家族史;精神疾病家族史;以及个人精神疾病史。
总体社会适应评分低于对照组(p=0.001),特别是在工作(p=0.032)和大家庭(p=0.005)方面。较高的新颖寻求(Novelty Seeking,NS)评分与全球(p=0.002)、工作(p=0.001)和休闲(p=0.003)的评分较差显著相关。认知表现与社会适应量表(SAS)因子之间没有相关性。较高的癫痫发作频率-肌阵挛(p=0.005)和 GTC(p=0.035)与 SAS 因子工作的较高评分相关。
我们的研究结果表明,JME 患者在工作和家庭关系这两个生活重要方面存在较差的社会适应能力。在这一系列 JME 患者中,较高的癫痫发作频率和冲动特质,但不是认知表现,与较差的社会适应相关。