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参与音猬因子信号传导的基因突变患者的海马体不完全反转。

Incomplete hippocampal inversion in patients with mutations in genes involved in sonic hedgehog signaling.

作者信息

Higashijima Takefumi, Shirozu Hiroshi, Saitsu Hirotomo, Sonoda Masaki, Fujita Atsushi, Masuda Hiroshi, Yamamoto Tetsuya, Matsumoto Naomichi, Kameyama Shigeki

机构信息

Department of Neurosurgery, Yokohama City University Medical Center, 4-57 Urafune, Minami, Yokohama, 2320024, Japan.

Department of Functional Neurosurgery, National Hospital Organization Nishiniigata Chuo Hospital, 1-14-1 Masago, Nishi Ward, Niigata, 950-2085, Japan.

出版信息

Heliyon. 2023 Mar 21;9(4):e14712. doi: 10.1016/j.heliyon.2023.e14712. eCollection 2023 Apr.

Abstract

Sonic hedgehog (Shh) signaling pathways are known to play an important role in the morphological development of the hippocampus in vivo, but their actual roles in humans have not been clarified. Hypothalamic hamartoma (HH) is known to be associated with germline or somatic gene mutations of Shh signaling. We hypothesized that patients with HH and mutations of Shh-related genes also show hippocampal maldevelopment and an abnormal hippocampal infolding angle (HIA). We analyzed 45 patients (age: 1-37 years) with HH who underwent stereotactic radiofrequency thermocoagulation and found Shh-related gene mutations in 20 patients. In addition, 44 pediatric patients without HH (age: 2-25 years) who underwent magnetic resonance imaging (MRI) examinations under the same conditions during the same period were included in this study as a control group. HIA evaluated on MRI was compared between patients with gene mutations and the control group. The median HIA at the cerebral peduncle slice in patients with the gene mutation was 74.36° on the left and 76.11° on the right, and these values were significantly smaller than the corresponding values in the control group (80.46° and 80.56°, respectively, p < 0.01). Thus, mutations of Shh-related genes were correlated to incomplete hippocampal inversion. The HIA, particularly at the cerebral peduncle slice, is a potential indicator of abnormalities of the Shh-signaling pathway.

摘要

已知音猬因子(Shh)信号通路在体内海马体的形态发育中起重要作用,但其在人类中的实际作用尚未阐明。已知下丘脑错构瘤(HH)与Shh信号的种系或体细胞基因突变有关。我们推测,患有HH且Shh相关基因突变的患者也会出现海马体发育异常和海马体折叠角(HIA)异常。我们分析了45例接受立体定向射频热凝治疗的HH患者(年龄1至37岁),发现20例患者存在Shh相关基因突变。此外,本研究纳入了同期44例在相同条件下接受磁共振成像(MRI)检查的非HH儿科患者(年龄2至25岁)作为对照组。比较了基因突变患者与对照组在MRI上评估的HIA。基因突变患者大脑脚层面的HIA中位数,左侧为74.36°,右侧为76.11°,这些值显著低于对照组相应的值(分别为80.46°和80.56°,p < 0.01)。因此,Shh相关基因突变与海马体反转不完全相关。HIA,尤其是大脑脚层面的HIA,是Shh信号通路异常的潜在指标。

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Epilepsy Res. 2021 Sep;175:106692. doi: 10.1016/j.eplepsyres.2021.106692. Epub 2021 Jun 24.
3
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Brain Sci. 2021 Apr 5;11(4):463. doi: 10.3390/brainsci11040463.
6
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Neurol Genet. 2020 Dec 8;7(1):e540. doi: 10.1212/NXG.0000000000000540. eCollection 2021 Feb.
7
The Ciliary Protein Arl13b Functions Outside of the Primary Cilium in Shh-Mediated Axon Guidance.
Cell Rep. 2019 Dec 10;29(11):3356-3366.e3. doi: 10.1016/j.celrep.2019.11.015.
8
Pathogenic variants of , , and associated with hypothalamic hamartoma.
Neurology. 2019 Jul 16;93(3):e237-e251. doi: 10.1212/WNL.0000000000007774. Epub 2019 Jun 13.
10
Developmental and Repairing Production of Myelin: The Role of Hedgehog Signaling.
Front Cell Neurosci. 2018 Sep 6;12:305. doi: 10.3389/fncel.2018.00305. eCollection 2018.

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