Prasad Konasale M, Sanders Richard, Sweeney John, Montrose Debra, Diwadkar Vaibhav, Dworakowski Diana, Miewald Jean, Keshavan Matcheri
University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
Schizophr Res. 2009 Mar;108(1-3):163-9. doi: 10.1016/j.schres.2008.11.019. Epub 2008 Dec 23.
Neurological Examination Abnormalities (NEA, often called "neurological soft signs") have been observed in early schizophrenia and may be heritable. We investigated the prevalence, and neurocognitive and psychopathological correlates of NEA among offspring of schizophrenia patients who are at increased genetic risk for this illness.
Neurological examinations were conducted on high risk (HR, n=74) and healthy comparison subjects (HS, n=86), using the Heinrichs-Buchanan scale. Cognitive-perceptual (CogPer) and repetitive motor (RepMot) subscores, and total NEA scores were computed. All HR and HS were assessed using K-SADS/SCID for diagnoses. Schizotypy was measured using the Magical Ideation and the Perceptual Aberration subscales (Chapman scale), attention using Continuous Performance Test (CPT-IP) and executive functions using the Wisconsin Card Sorting Test (WCST).
CogPer (F(1,160)=7.14, p=0.008) but not RepMot NEA scores were higher in HR subjects compared to HS after controlling for age and sex. CogPer NEA scores were higher in HR subjects with axis I psychopathology compared to those without (F(2,170)-6.41, p=0.002). HR subjects had higher schizotypy scores (composite of the magical ideation and perceptual aberration scales) (F(1,141)=23.25, p=0.000004). Schizotypy scores were negatively correlated with sustained attention and executive functions. In addition, schizotypy was positively correlated with CogPer NEA scores.
Young relatives at increased genetic risk for schizophrenia show more frequent NEA. CogPer but not RepMot NEA scores were elevated, consistent with our prior observation of CogPer NEA being relatively specific for schizophrenia. The observed relationships between NEA, cognitive impairments, schizotypy and axis I disorders suggest that NEA may characterize a subgroup of HR offspring at an elevated risk for psychopathology.
在早期精神分裂症患者中已观察到神经学检查异常(NEA,常被称为“神经学软体征”),且可能具有遗传性。我们调查了精神分裂症患者后代中NEA的患病率、神经认知及精神病理学相关性,这些后代患该疾病的遗传风险增加。
使用海因里希斯 - 布坎南量表对高风险组(HR,n = 74)和健康对照组(HS,n = 86)进行神经学检查。计算认知 - 感知(CogPer)和重复运动(RepMot)子分数以及总NEA分数。所有HR组和HS组均使用K-SADS/SCID进行诊断。使用神奇观念和感知偏差子量表(查普曼量表)测量分裂型人格特质,使用连续性能测试(CPT-IP)测量注意力,使用威斯康星卡片分类测试(WCST)测量执行功能。
在控制年龄和性别后,HR组受试者的CogPer(F(1,160)=7.14,p = 0.008)而非RepMot NEA分数高于HS组。与无轴I精神病理学的HR组受试者相比,有轴I精神病理学的HR组受试者的CogPer NEA分数更高(F(2,170)-6.41,p = 0.002)。HR组受试者的分裂型人格特质分数更高(神奇观念和感知偏差量表的综合分数)(F(1,141)=23.25,p = 0.000004)。分裂型人格特质分数与持续注意力和执行功能呈负相关。此外,分裂型人格特质与CogPer NEA分数呈正相关。
精神分裂症遗传风险增加的年轻亲属表现出更频繁的NEA。CogPer而非RepMot NEA分数升高,这与我们之前观察到的CogPer NEA相对特定于精神分裂症的结果一致。观察到的NEA、认知障碍、分裂型人格特质和轴I障碍之间的关系表明,NEA可能是HR后代中一个精神病理学风险升高的亚组的特征。