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胎儿后颅窝的多维分析:健康与疾病。

Multidimensional analysis of fetal posterior fossa in health and disease.

机构信息

Imaging Sciences Department, MRC Clinical Sciences Centre, Imperial College London, Hammersmith Hospital Campus, London, W12 0NN, UK.

出版信息

Cerebellum. 2013 Oct;12(5):632-44. doi: 10.1007/s12311-013-0470-2.

DOI:10.1007/s12311-013-0470-2
PMID:23553467
Abstract

Fetal magnetic resonance imaging (MRI) is now routinely used to further investigate cerebellar malformations detected with ultrasound. However, the lack of 2D and 3D biometrics in the current literature hinders the detailed characterisation and classification of cerebellar anomalies. The main objectives of this fetal neuroimaging study were to provide normal posterior fossa growth trajectories during the second and third trimesters of pregnancy via semi-automatic segmentation of reconstructed fetal brain MR images and to assess common cerebellar malformations in comparison with the reference data. Using a 1.5-T MRI scanner, 143 MR images were obtained from 79 normal control and 53 fetuses with posterior fossa abnormalities that were grouped according to the severity of diagnosis on visual MRI inspections. All quantifications were performed on volumetric datasets, and supplemental outcome information was collected from the surviving infants. Normal growth trajectories of total brain, cerebellar, vermis, pons and fourth ventricle volumes showed significant correlations with 2D measurements and increased in second-order polynomial trends across gestation (Pearson r, p < 0.05). Comparison of normal controls to five abnormal cerebellum subgroups depicted significant alterations in volumes that could not be detected exclusively with 2D analysis (MANCOVA, p < 0.05). There were 15 terminations of pregnancy, 8 neonatal deaths, and a spectrum of genetic and neurodevelopmental outcomes in the assessed 24 children with cerebellar abnormalities. The given posterior fossa biometrics enhance the delineation of normal and abnormal cerebellar phenotypes on fetal MRI and confirm the advantages of utilizing advanced neuroimaging tools in clinical fetal research.

摘要

胎儿磁共振成像(MRI)现在常用于进一步研究超声检测到的小脑畸形。然而,目前文献中缺乏 2D 和 3D 生物测量学数据,这阻碍了对小脑异常的详细特征描述和分类。本胎儿神经影像学研究的主要目的是通过对重建的胎儿脑 MRI 图像进行半自动分割,提供妊娠第二和第三个三个月期间后颅窝生长轨迹的正常参考值,并与参考数据比较评估常见的小脑畸形。使用 1.5T MRI 扫描仪,从 79 名正常对照胎儿和 53 名后颅窝异常胎儿中获得了 143 个 MR 图像,这些胎儿根据 MRI 检查的视觉诊断严重程度分组。所有定量分析均在容积数据集上进行,并从存活婴儿中收集补充结果信息。全脑、小脑、蚓部、脑桥和第四脑室体积的正常生长轨迹与 2D 测量值具有显著相关性,并随着妊娠呈二阶多项式趋势增加(Pearson r,p<0.05)。正常对照组与五个小脑异常亚组的比较显示,体积存在显著变化,这些变化仅通过 2D 分析无法检测到(MANCOVA,p<0.05)。在评估的 24 名小脑异常婴儿中,有 15 例终止妊娠,8 例新生儿死亡,以及一系列遗传和神经发育结局。提供的后颅窝生物测量学增强了胎儿 MRI 上正常和异常小脑表型的描绘,并证实了在临床胎儿研究中利用先进神经影像学工具的优势。

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本文引用的文献

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Cortical overgrowth in fetuses with isolated ventriculomegaly.孤立性脑室扩大胎儿的皮质过度生长。
Cereb Cortex. 2014 Aug;24(8):2141-50. doi: 10.1093/cercor/bht062. Epub 2013 Mar 18.
2
Posterior fossa anomalies diagnosed with fetal MRI: associated anomalies and neurodevelopmental outcomes.胎儿 MRI 诊断的后颅窝异常:相关异常和神经发育结局。
Prenat Diagn. 2012 Jan;32(1):75-82. doi: 10.1002/pd.2911.
3
3D morphometric analysis of human fetal cerebellar development.三维形态计量分析人类胎儿小脑发育。
Childs Nerv Syst. 2023 Oct;39(10):2899-2927. doi: 10.1007/s00381-023-06109-6. Epub 2023 Aug 22.
4
Brain structural changes in patients with cardio-facio-cutaneous syndrome: effects of BRAF gene mutation and epilepsy on brain development. A case-control study by quantitative magnetic resonance imaging.心面皮肤综合征患者的脑结构变化:BRAF 基因突变和癫痫对脑发育的影响。一项基于定量磁共振成像的病例对照研究。
Neuroradiology. 2022 Jan;64(1):185-195. doi: 10.1007/s00234-021-02769-w. Epub 2021 Jul 26.
5
Normal human brainstem development in vivo: a quantitative fetal MRI study.正常人体脑干发育的体内研究:一项胎儿磁共振成像的定量研究。
Ultrasound Obstet Gynecol. 2021 Aug;58(2):254-263. doi: 10.1002/uog.22162. Epub 2021 Jul 6.
6
Morphometric development of the human fetal cerebellum during the early second trimester.人类胎儿小脑在第二个妊娠早期的形态发育。
Neuroimage. 2020 Feb 15;207:116372. doi: 10.1016/j.neuroimage.2019.116372. Epub 2019 Nov 18.
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Neuroradiology. 2017 Oct;59(10):1031-1041. doi: 10.1007/s00234-017-1887-y. Epub 2017 Aug 17.
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Brain Struct Funct. 2017 Jul;222(5):2295-2307. doi: 10.1007/s00429-016-1342-6. Epub 2016 Nov 24.
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