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首页> 外文期刊>BMC Neuroscience >The neurodevelopmental basis of schizophrenia: clinical clues from craniofacial dysmorphology in northwest Ethiopia, 2020
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The neurodevelopmental basis of schizophrenia: clinical clues from craniofacial dysmorphology in northwest Ethiopia, 2020

机译:精神分裂症的神经发育基础:西北埃塞俄比亚颅面缺血性临床线索,2020

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The neurodevelopmental speculation of schizophrenia states that the pathogenesis of schizophrenia starts with early fetal or neonatal neurocraniofacial development rather than youthful adulthood when manic signs and symptoms are evident. However, there is no direct evidence of a pre-or peri-natal lesion associated with schizophrenia, rather indirect evidence of impaired development can be seen in macroscopic anatomical variations as well as microscopic immunohistochemical anomalies. One approach to studying neurodevelopmental disturbances among schizophrenic patients is somatic physical evidence or neurodevelopmental markers. Thus Our study aimed to assess the neurodevelopmental basis of schizophrenia clinical clues from anthropometric assessment of craniofacial dysmorphology among schizophrenic patients in North West Ethiopia 2019–2020. Institutional-based comparative cross-sectional study design was conducted in Debre Markos comprehensive specialized hospitals in 190 schizophrenic patients, 190 1st-degree relatives, and 190 healthy controls. Data were collected using standard methods, entered into EpiData version 3.1, and exports to SPSS version 24 for analysis. Descriptive data were analyzed using descriptive statistics.?Welch ANOVA and post hoc comparison, a Games-Howell test, were conducted. Significance was set at a p-value of α?=?0.05. Read back analysis was also conducted for the conclusion. Five hundred seventy study samples, male 375(65.8%), and female 195 (34.2%), were included in this study. The Games-Howell test revealed that the coronal arc length and sagittal arc length among schizophrenic patients were statistically significantly longer than the healthy controls (p??0.006; p??0.001, respectively). However, the difference between schizophrenic and healthy control regarding head circumference was marginally significant (p?=?0.056). Schizophrenic patients had a significantly shorter total facial height (p??0.001) and upper facial height (p??0.001) than healthy controls. Regarding facial depth, schizophrenic patients had significantly shallow upper facial depth (p??0.001), middle facial depth (p?=?0.046), and lower facial depth (p??0.001). our finding indicated indirect evidence for disturbed craniofacial development in schizophrenia patients, and close and read back analysis of the result supported the neurodevelopmental basis of disease.
机译:精神分裂症的神经开发爆发表明精神分裂症的发病机制从早期的胎儿或新生儿神经科学发展开始,而不是青春的成年,当躁狂症症状和症状是显而易见的。然而,没有直接证据表明与精神分裂症相关的预先或豚鼠病变,相当在宏观解剖学变化以及微观免疫组化异常中可以看到受损的发育的间接证据。学习精神分裂症患者神经发育紊乱的一种方法是体细胞体现或神经发育标记。因此,我们的研究旨在评估精神法缺血性评估西北埃塞俄比亚2019 - 2020年西北西北埃塞俄比亚精神分法缺血性评估的精神分病评估的神经发育基础。基于机构的比较横断面研究设计在190名精神分裂症患者,190名1度亲属和190名健康对照中在德布雷斯综合专业医院进行。使用标准方法收集数据,输入EPIDATA 3.1版本3.1,并导出到SPSS版本24进行分析。使用描述性统计分析描述性数据.?Welch Anova和Hoc比较,进行了一个游戏-Whell测试。在α的p值设置有意义?= 0.05。结论也进行了读取分析。本研究纳入五百七十七十研究样品,男性375(65.8%)和女性195(34.2%)。游戏 - 豪威尔的测试显示,精神分裂症患者中的冠状弧长和矢状弧长均明显长于健康对照(P 1 0.006; 0.006; 0.001分别)。然而,有关头周长的精神分裂症和健康对照的差异略微显着(P?= 0.056)。精神分裂症患者的总面高度显着较短(P?<0.001)和上部高度(p≤≤0.001),而不是健康的对照。关于面部深度,精神分裂症患者具有显着较浅的上面部深度(p≤≤0.001),中部面部深度(P?= 0.046),以及较低的面部深度(p≤≤0.001)。我们的发现表明了精神分裂症患者的干扰性颅面发育的间接证据,并关闭了并读出了结果的疾病神经开发基础。

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