Falkai Peter, Honer William G, Kamer Thomas, Dustert Simone, Vogeley Kai, Schneider-Axmann Thomas, Dani Indra, Wagner Michael, Rietschel Marcella, Müller Daniel J, Schulze Thomas G, Gaebel Wolfgang, Cordes Joachim, Schönell Helmut, Schild Hans H, Block Wolfgang, Träber Frank, Steinmetz Helmuth, Maier Wolfgang, Tepest Ralf
Department of Psychiatry and Psychotherapy, University of Göttingen, Von-Siebold-Str. 5, 37075 Göttingen, Germany.
J Psychiatr Res. 2007 Nov;41(10):805-13. doi: 10.1016/j.jpsychires.2006.07.018. Epub 2006 Oct 30.
Recently, in a post-mortem and a subsequent structural MR study, a significantly increased gyrification index (GI) was demonstrated in the frontal lobe in individuals with schizophrenia. To examine whether frontal lobe hypergyria is region-specific and whether this might be a suitable endophenotype in the search for the genetic basis of schizophrenia, the frontal as well as parieto-occipital GI were determined in MRI scans of families affected with schizophrenia.
In the MRI scans of 48 subjects suffering from schizophrenia, in 82 of their first-degree relatives and in 41 control subjects, the GI was determined in three sections anterior to the genu of the corpus callosum and three sections posterior to the splenium, thus allowing for a selective determination of this measure in the frontal as well as the parietal lobe. Outer and inner contours constituting the GI was determined in each section by manual tracing. Statistical analysis was performed using MANOVA with factors diagnostic group and intervening factors from preliminary analyses.
The frontal, but not parieto-occipital GI was significantly higher in schizophrenic patients as well as unaffected relatives compared with control subjects (right: 7%, F=13.24, df=3, 155, p<0.0005, left: 6%, F=8.92, df=3, 155, p<0.0005). There was no overall difference between affected and unaffected family members. On the left side however, there was a significant interaction between diagnostic group and genetic loading (F=4.68, df=2, 101, p=0.01): significantly higher GI was found in affected compared with unaffected family members only in uniaffected and not multiaffected families.
These results support our primary finding of hypergyria in the frontal lobe in schizophrenic patients. Compared to the parietal lobe, hypergyria seems to affect the frontal lobe selectively and serves as a suitable neurodevelopmental, possibly even an endophenotypic marker.
最近,在一项尸检及后续的结构磁共振成像(MR)研究中,精神分裂症患者额叶的脑回化指数(GI)显著升高。为了研究额叶脑回过度发育是否具有区域特异性,以及这是否可能是寻找精神分裂症遗传基础的合适内表型,我们在精神分裂症患者家系的MRI扫描中测定了额叶以及顶枕叶的GI。
在48例精神分裂症患者、82例其一级亲属以及41例对照者的MRI扫描中,在胼胝体膝部前方的三个层面和压部后方的三个层面测定GI,从而能够分别在额叶和顶叶选择性地测定该指标。通过手动描绘确定每个层面构成GI的内外轮廓。使用多因素方差分析(MANOVA)进行统计分析,分析因素包括诊断组以及初步分析中的干预因素。
与对照者相比,精神分裂症患者及其未患病亲属的额叶而非顶枕叶GI显著更高(右侧:7%,F = 13.24,自由度 = 3, 155,p < 0.0005;左侧:6%,F = 8.92,自由度 = 3, 155,p < 0.0005)。患病和未患病家庭成员之间没有总体差异。然而,在左侧,诊断组与遗传负荷之间存在显著交互作用(F = 4.68,自由度 = 2, 101,p = 0.01):仅在未患多种疾病的家庭中,患病家庭成员的GI显著高于未患病家庭成员。
这些结果支持了我们最初关于精神分裂症患者额叶脑回过度发育的发现。与顶叶相比,脑回过度发育似乎选择性地影响额叶,并可作为一个合适的神经发育标记,甚至可能是一个内表型标记。