ZNF804a 对精神分裂症患者大脑结构体积和症状严重程度的影响。

Thomas H Wassink, Eric A Epping, Danielle Rudd, Michael Axelsen, Stephen Ziebell, Frank W Fleming, Eric Monson, Beng Choon Ho, Nancy C Andreasen
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摘要

背景 ZNF804a 基因中的单核苷酸多态性 rs1344706 与精神分裂症以及定量表型特征(包括脑结构体积和精神分裂症的核心症状)有关。目的 评估 rs1344706 与脑结构和精神分裂症核心症状的相关性。设计 病例对照协方差分析。设置 大学研究医院。参与者 志愿者样本,包括 335 名精神分裂症谱系障碍患者(306 名核心精神分裂症患者)和 198 名健康志愿者。主要结果测量 大脑皮层灰质和白质(WM)体积(总体积、额叶、顶叶、颞叶和枕叶)、侧脑室脑脊液体积,以及阴性症状评估量表和阳性症状评估量表的症状严重程度,分为 3 个领域:精神病性、阴性和混乱。结果 rs1344706 基因型对总体、额叶和顶叶 WM 容量产生了显著的主效应(分别为 F = 3.98,P = .02;F = 4.95,P = .007 和 F = 3.08,P = .05)。在精神分裂症组中,rs1344706 对总 WM 容量(F = 3.93,P = .02)和额叶 WM 容量(F = 7.16,P < .001)以及精神病症状严重程度(F = 6.07,P = .003)产生显著的简单效应;效应模式与风险等位基因携带者比非风险等位基因携带者具有更大的容量和更严重的疾病症状相一致。在健康志愿者组中,与非风险等位基因携带者相比,风险等位基因同卵双生者的 WM 总体积增大(F = 4.61,P = .03),这与之前报道的相关性相同。结论 越来越多的证据表明,rs1347706 的风险等位基因与健康志愿者和精神分裂症患者的一系列独特表型特征有关。我们的研究发现,该多态性的特定基因型与精神分裂症患者和健康志愿者的大脑结构体积以及精神分裂症的症状严重程度有关,从而支持了这一论断。
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Influence of ZNF804a on brain structure volumes and symptom severity in individuals with schizophrenia.

CONTEXT The single-nucleotide polymorphism rs1344706 in the gene ZNF804a has been associated with schizophrenia and with quantitative phenotypic features, including brain structure volume and the core symptoms of schizophrenia. OBJECTIVE To evaluate associations of rs1344706 with brain structure and the core symptoms of schizophrenia. DESIGN Case-control analysis of covariance. SETTING University-based research hospital. PARTICIPANTS Volunteer sample of 335 individuals with schizophrenia spectrum disorders (306 with core schizophrenia) and 198 healthy volunteers. MAIN OUTCOME MEASURES Cerebral cortical gray matter and white matter (WM) volumes (total and frontal, parietal, temporal, and occipital lobes), lateral ventricular cerebrospinal fluid volume, and symptom severity from the Scale for the Assessment of Negative Symptoms and the Scale for the Assessment of Positive Symptoms divided into 3 domains: psychotic, negative, and disorganized. RESULTS The rs1344706 genotype produced significant main effects on total, frontal, and parietal lobe WM volumes (F = 3.98, P = .02; F = 4.95, P = .007; and F = 3.08, P = .05, respectively). In the schizophrenia group, rs1344706 produced significant simple effects on total (F = 3.93, P = .02) and frontal WM volumes (F = 7.16, P < .001) and on psychotic symptom severity (F = 6.07, P = .003); the pattern of effects was concordant with risk allele carriers having larger volumes and more severe symptoms of disease than nonrisk homozygotes. In the healthy volunteer group, risk allele homozygotes had increased total WM volume compared with nonrisk allele carriers (F = 4.61, P = .03), replicating a previously reported association. CONCLUSIONS A growing body of evidence suggests that the risk allele of rs1347706 is associated with a distinctive set of phenotypic features in healthy volunteers and individuals with schizophrenia. Our study supports this assertion by finding that specific genotypes of the polymorphism are associated with brain structure volumes in individuals with schizophrenia and healthy volunteers and with symptom severity in schizophrenia.

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Archives of general psychiatry
Archives of general psychiatry 医学-精神病学
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