Age-Specific Biometric Ratios of the Posterior Fossa in Pediatric Neuroimaging: Establishing Normative Reference Values.

IF 1 Q4 CLINICAL NEUROLOGY
Sam Mirfendereski, Shahin Fesharaki, Mohadeseh Zadehmir
{"title":"Age-Specific Biometric Ratios of the Posterior Fossa in Pediatric Neuroimaging: Establishing Normative Reference Values.","authors":"Sam Mirfendereski, Shahin Fesharaki, Mohadeseh Zadehmir","doi":"10.22037/ijcn.v20i1.48884","DOIUrl":null,"url":null,"abstract":"<p><strong>Objectives: </strong>Understanding normative biometric data of the posterior fossa is imperative to elucidate pathological alterations. Consequently, a reference for normative biometric data on posterior fossa structures in pediatric populations is essential for diagnosing cerebellar hypoplasia and other associated anomalies. However, a comprehensive set of objective, age-stratified biometric ratios for key posterior fossa structures is lacking, limiting diagnostic precision. To the best of our knowledge, only one study has evaluated the biometric data of the posterior fossa components in children.</p><p><strong>Materials & methods: </strong>The current study is a cross-sectional study conducted among children hospitalized at Imam Hossein Children's Hospital in Isfahan, Iran, in 2022-2023. All magnetic resonance imaging (MRI) examinations, including midline sagittal sections, performed in children ≤ 15 years of age, were included. Patients with a clinical history of posterior fossa involvement or MRI abnormalities were excluded from this study. Two-dimensional (2D) parameters, including the height of the vermian (H-V), anterior-posterior diameter of the vermis (APD-V), anterior-posterior diameter of the midbrain-pons junction (APD-MP), and anterior-posterior diameter of the midpons, were all measured. Four biometric ratios were calculated to normalize posterior fossa morphology across age groups, accounting for individual size variability and providing objective criteria.</p><p><strong>Results: </strong>Four hundred twenty patients, with a mean age of 5.79 ± 4.02 years, were investigated, of whome 222 (52.9%) were boys. All parameters, except APD-V, were significantly higher in boys than in girls. Although boys had a higher mean APD-V than girls, this difference was not statistically significant. In addition, all studied parameters had the fastest growth rates in the first year and continued to grow more slowly until the end of the 15th year. Key findings reveal a mean APD-P/APD-V ratio of 0.77 ± 0.09. The ratio was generally higher in older children, indicating that pontine growth outpaces vermian expansion during development-values near or above 1.00 may suggest pontocerebellar hypoplasia. The H-V/APD-V ratio (mean 1.72 ± 0.18) shows a dip in early childhood, particularly at 1-3 years, suggestingtransient vermian flattening. The H-V/APD-P ratio declines from ~2.30 in infancy to ~2.11 in adolescence, reflecting posterior fossa maturation. Meanwhile, the APD-P/APD-MP ratio remains consistently around 1.91-1.95, aligning with the expected 2:1 anatomical norm, and serving as a reliable reference across age and sex groups.</p><p><strong>Conclusion: </strong>The present study showed that all posterior fossa parameters, except APD-V, were significantly higher in boys. This study establishes normative reference values for key posterior fossa ratios. The APD-P/APD-V ratio (mean 0.77 ± 0.09) increases with age, while the H-V/APD-P ratio declines from ~2.30 to ~2.11. The APD-P/APD-MP ratio remains stable at ~1.91, consistent with the 2:1 anatomical norm. These objective criteria provide quantifiable thresholds for detecting anomalies like pontocerebellar hypoplasia.</p>","PeriodicalId":14537,"journal":{"name":"Iranian Journal of Child Neurology","volume":"20 1","pages":"9-16"},"PeriodicalIF":1.0000,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12904298/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Iranian Journal of Child Neurology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.22037/ijcn.v20i1.48884","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Objectives: Understanding normative biometric data of the posterior fossa is imperative to elucidate pathological alterations. Consequently, a reference for normative biometric data on posterior fossa structures in pediatric populations is essential for diagnosing cerebellar hypoplasia and other associated anomalies. However, a comprehensive set of objective, age-stratified biometric ratios for key posterior fossa structures is lacking, limiting diagnostic precision. To the best of our knowledge, only one study has evaluated the biometric data of the posterior fossa components in children.

Materials & methods: The current study is a cross-sectional study conducted among children hospitalized at Imam Hossein Children's Hospital in Isfahan, Iran, in 2022-2023. All magnetic resonance imaging (MRI) examinations, including midline sagittal sections, performed in children ≤ 15 years of age, were included. Patients with a clinical history of posterior fossa involvement or MRI abnormalities were excluded from this study. Two-dimensional (2D) parameters, including the height of the vermian (H-V), anterior-posterior diameter of the vermis (APD-V), anterior-posterior diameter of the midbrain-pons junction (APD-MP), and anterior-posterior diameter of the midpons, were all measured. Four biometric ratios were calculated to normalize posterior fossa morphology across age groups, accounting for individual size variability and providing objective criteria.

Results: Four hundred twenty patients, with a mean age of 5.79 ± 4.02 years, were investigated, of whome 222 (52.9%) were boys. All parameters, except APD-V, were significantly higher in boys than in girls. Although boys had a higher mean APD-V than girls, this difference was not statistically significant. In addition, all studied parameters had the fastest growth rates in the first year and continued to grow more slowly until the end of the 15th year. Key findings reveal a mean APD-P/APD-V ratio of 0.77 ± 0.09. The ratio was generally higher in older children, indicating that pontine growth outpaces vermian expansion during development-values near or above 1.00 may suggest pontocerebellar hypoplasia. The H-V/APD-V ratio (mean 1.72 ± 0.18) shows a dip in early childhood, particularly at 1-3 years, suggestingtransient vermian flattening. The H-V/APD-P ratio declines from ~2.30 in infancy to ~2.11 in adolescence, reflecting posterior fossa maturation. Meanwhile, the APD-P/APD-MP ratio remains consistently around 1.91-1.95, aligning with the expected 2:1 anatomical norm, and serving as a reliable reference across age and sex groups.

Conclusion: The present study showed that all posterior fossa parameters, except APD-V, were significantly higher in boys. This study establishes normative reference values for key posterior fossa ratios. The APD-P/APD-V ratio (mean 0.77 ± 0.09) increases with age, while the H-V/APD-P ratio declines from ~2.30 to ~2.11. The APD-P/APD-MP ratio remains stable at ~1.91, consistent with the 2:1 anatomical norm. These objective criteria provide quantifiable thresholds for detecting anomalies like pontocerebellar hypoplasia.

Abstract Image

儿童神经影像学中后窝年龄特异性生物特征比值:建立规范参考值。
目的:了解后窝的规范生物特征数据对于阐明病理改变是必要的。因此,参考儿童人群后窝结构的规范生物特征数据对于诊断小脑发育不全和其他相关异常至关重要。然而,缺乏一套全面客观的,年龄分层的关键后窝结构的生物计量比率,限制了诊断的准确性。据我们所知,只有一项研究评估了儿童后窝成分的生物特征数据。材料与方法:本研究是一项横断面研究,对2022-2023年在伊朗伊斯法罕伊玛目侯赛因儿童医院住院的儿童进行研究。所有年龄≤15岁的儿童进行的MRI检查,包括中线矢状面切片。有后颅窝受累病史或MRI异常的患者被排除在本研究之外。测量蚓体高度(H-V)、蚓体前后径(APD-V)、中脑-脑桥连接处前后径(APD-MP)、中脑脑桥前后径等二维参数。计算了四种生物特征比率,以标准化不同年龄组的后窝形态,考虑到个体大小的可变性并提供客观标准。结果:共调查患者420例,平均年龄5.79±4.02岁,其中男孩222例,占52.9%。除APD-V外,男孩的所有参数均显著高于女孩。虽然男孩的平均APD-V高于女孩,但这种差异没有统计学意义。此外,所有研究的参数在第一年的增长率都是最快的,直到第15年结束时,增长速度一直较慢。主要结果显示APD-P/APD-V平均比值为0.77±0.09。在年龄较大的儿童中,这一比例普遍较高,表明在发育过程中,桥脑的生长速度超过了蠕虫的扩张速度——该值接近或高于1.00可能提示桥小脑发育不全。H-V/APD-V比值(平均1.72±0.18)在儿童早期,特别是在1-3岁时出现下降,提示短暂的蠕虫变平。H-V/APD-P比值从婴儿期的~2.30下降到青春期的~2.11,反映了后窝的成熟。同时,APD-P/APD-MP比值始终保持在1.91-1.95左右,符合预期的2:1解剖规范,可作为跨年龄和性别群体的可靠参考。结论:本研究显示,除APD-V外,所有后窝参数在男孩中均显著升高。本研究建立了关键后窝比率的规范性参考值。APD-P/APD-V比值(平均0.77±0.09)随年龄增大而增大,H-V/APD-P比值由~2.30降至~2.11。APD-P/APD-MP比值稳定在~1.91,符合2:1的解剖标准。这些客观标准为检测桥小脑发育不全等异常提供了可量化的阈值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
1.40
自引率
0.00%
发文量
35
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书