Cognitive Neuroscience Laboratory, Harvard Medical School, McLean Hospital, 115 Mill Street, Belmont, MA 02478, USA.
Schizophr Bull. 2011 Jul;37(4):778-87. doi: 10.1093/schbul/sbp134. Epub 2009 Nov 27.
Reduced power and phase locking of the early auditory gamma-band response (EAGBR) have been reported in schizophrenia, but findings are equivocal. Further, little is known about genetic (heritability) and environmental influences on the EAGBR or its potential as an endophenotype of schizophrenia. The present study used a twin design to examine whether EAGBR power and phase locking are heritable and reduced in schizophrenic patients and their unaffected co-twins and thus putative endophenotypes of schizophrenia.
The study sample included a total of 194 individuals, consisting of 15 monozygotic [MZ] twin pairs concordant for schizophrenia, 9 MZ twin pairs discordant for schizophrenia, and 42 MZ and 31 dizygotic (DZ) control pairs. Evoked power and phase-locking factor of the EAGBR were computed on Morlet wavelet-transformed electroencephalogram responses to standard tones during an auditory oddball target detection task. Structural equation modeling was applied to estimate heritability and genetic and environmental correlations with schizophrenia for the EAGBR measures.
Both evoked power and phase-locking phenotypes were heritable traits (power: h(2) = 0.65; phase locking: h(2) = 0.63). Impaired EAGBR measures were significantly associated with schizophrenia. Patients with schizophrenia and their unaffected identical co-twins exhibited significantly reduced EAGBR power compared with control subjects. In each phenotype, shared genetic factors were likely the source of the observed associations with schizophrenia.
Our results support EAGBR measures as putative endophenotypes of schizophrenia, likely reflecting an ubiquitous local cortical circuit deficit.
研究报道精神分裂症患者的早期听觉γ 频段响应(EAGBR)的功率和相位锁定降低,但研究结果存在争议。此外,对于 EAGBR 或其作为精神分裂症内表型的遗传(遗传性)和环境影响知之甚少。本研究采用双胞胎设计,以检查 EAGBR 功率和相位锁定是否可遗传以及在精神分裂症患者及其未受影响的同卵双胞胎中降低,从而作为精神分裂症的内表型。
该研究样本包括总共 194 个人,包括 15 对同卵双胞胎(MZ),精神分裂症一致,9 对 MZ 双胞胎精神分裂症不一致,以及 42 对 MZ 和 31 对双生子(DZ)对照组。在听觉Oddball 目标检测任务中,使用 Morlet 小波变换脑电图响应计算 EAGBR 的诱发功率和相位锁定因子。结构方程模型用于估计 EAGBR 测量的遗传性以及与精神分裂症的遗传和环境相关性。
EAGBR 的诱发功率和相位锁定表型均为遗传特征(功率:h(2) = 0.65;相位锁定:h(2) = 0.63)。受损的 EAGBR 测量值与精神分裂症显著相关。精神分裂症患者及其未受影响的同卵双胞胎的 EAGBR 功率明显低于对照组。在每种表型中,共享遗传因素可能是观察到的与精神分裂症相关的原因。
我们的研究结果支持 EAGBR 作为精神分裂症的内表型,可能反映了普遍存在的局部皮质电路缺陷。