Beyond the hippocampus: Limbic white matter injury implicated in post-radiation memory performance in primary brain tumor patients.

IF 16.4 1区 医学 Q1 CLINICAL NEUROLOGY
Alexander S Qian, Roshan Karunamuni, Soumya Unnikrishnan, Mia A Salans, Austin Hopper, Suma Gudipati, Justin Yu, Michael Connor, Kathryn R Tringale, Michelle D Tibbs, Anny Reyes, Jiwandeep S Kohli, Alena Stasenko, Carrie R McDonald, Jona A Hattangadi-Gluth
{"title":"Beyond the hippocampus: Limbic white matter injury implicated in post-radiation memory performance in primary brain tumor patients.","authors":"Alexander S Qian, Roshan Karunamuni, Soumya Unnikrishnan, Mia A Salans, Austin Hopper, Suma Gudipati, Justin Yu, Michael Connor, Kathryn R Tringale, Michelle D Tibbs, Anny Reyes, Jiwandeep S Kohli, Alena Stasenko, Carrie R McDonald, Jona A Hattangadi-Gluth","doi":"10.1093/neuonc/noaf144","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Limbic white matter (WM) of the Papez circuit, including the fornix, dorsal cingulum, and parahippocampal cingulum (PHC), interplay with the hippocampus as key components of the memory network. We analyzed biomarkers of injury to these pathways to understand their impact on post-radiation therapy (RT) memory performance.</p><p><strong>Methods: </strong>Primary brain tumor patients on a prospective trial receiving fractionated brain RT (n=57) underwent volumetric MRI, diffusion tensor imaging, and memory assessments (Hopkins Verbal Learning Test-Revised [HVLT-R] Total and Delayed Recall and Brief Visuospatial Memory Test -Revised [BVMT-R] Total and Delayed Recall) at baseline and 3, 6, and 12 months post-RT. MRI biomarkers included volume, fractional anisotropy (FA), and mean diffusivity (MD). Linear mixed-effects models assessed associations between biomarkers and memory performance over time.</p><p><strong>Results: </strong>Smaller volumes in the right fornix was associated with lower BVMT-R-Total scores (p=0.019) and left PHC volume loss was associated with worse performance on BVMT-R-Delayed (p=0.039). Lower FA in the left (p=0.010) and right (p=0.019) fornix was associated with lower BVMT-R-Total performance. Lower FA in the left dorsal cingulum (p=0.038) and right PHC (p=0.039) were associated with lower HVLT-R-Total and HVLT-R-Delayed scores, respectively. Higher MD in bilateral fornix (p=0.01) and right PHC (p=0.011) correlated with lower BVMT-R-Total scores; higher MD in the right PHC (p=0.046) also correlated with lower HVLT-R-Total scores. Hippocampal volume was not associated with memory scores.</p><p><strong>Conclusion: </strong>Poorer microstructural integrity in limbic WM tracts of the Papez circuit predicted worse memory performance, while hippocampal injury did not. Dose avoidance in these tracts may preserve memory outcomes.</p>","PeriodicalId":19377,"journal":{"name":"Neuro-oncology","volume":" ","pages":""},"PeriodicalIF":16.4000,"publicationDate":"2025-06-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Neuro-oncology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1093/neuonc/noaf144","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Limbic white matter (WM) of the Papez circuit, including the fornix, dorsal cingulum, and parahippocampal cingulum (PHC), interplay with the hippocampus as key components of the memory network. We analyzed biomarkers of injury to these pathways to understand their impact on post-radiation therapy (RT) memory performance.

Methods: Primary brain tumor patients on a prospective trial receiving fractionated brain RT (n=57) underwent volumetric MRI, diffusion tensor imaging, and memory assessments (Hopkins Verbal Learning Test-Revised [HVLT-R] Total and Delayed Recall and Brief Visuospatial Memory Test -Revised [BVMT-R] Total and Delayed Recall) at baseline and 3, 6, and 12 months post-RT. MRI biomarkers included volume, fractional anisotropy (FA), and mean diffusivity (MD). Linear mixed-effects models assessed associations between biomarkers and memory performance over time.

Results: Smaller volumes in the right fornix was associated with lower BVMT-R-Total scores (p=0.019) and left PHC volume loss was associated with worse performance on BVMT-R-Delayed (p=0.039). Lower FA in the left (p=0.010) and right (p=0.019) fornix was associated with lower BVMT-R-Total performance. Lower FA in the left dorsal cingulum (p=0.038) and right PHC (p=0.039) were associated with lower HVLT-R-Total and HVLT-R-Delayed scores, respectively. Higher MD in bilateral fornix (p=0.01) and right PHC (p=0.011) correlated with lower BVMT-R-Total scores; higher MD in the right PHC (p=0.046) also correlated with lower HVLT-R-Total scores. Hippocampal volume was not associated with memory scores.

Conclusion: Poorer microstructural integrity in limbic WM tracts of the Papez circuit predicted worse memory performance, while hippocampal injury did not. Dose avoidance in these tracts may preserve memory outcomes.

在海马体之外:边缘白质损伤与原发性脑肿瘤患者放射后记忆表现有关。
背景:Papez回路的边缘白质(WM),包括穹窿、背扣带和海马旁扣带(PHC),作为记忆网络的关键组成部分与海马相互作用。我们分析了这些通路损伤的生物标志物,以了解它们对放射治疗后(RT)记忆表现的影响。方法:前瞻性试验中接受分割脑放疗的原发性脑肿瘤患者(n=57)在基线和放疗后3、6和12个月分别接受了体积MRI、弥散张量成像和记忆评估(霍普金斯语言学习测试-修订[HVLT-R]总和延迟回忆和简短视觉空间记忆测试-修订[BVMT-R]总和延迟回忆)。MRI生物标志物包括体积、分数各向异性(FA)和平均扩散率(MD)。线性混合效应模型评估了生物标志物与记忆表现之间随时间的关系。结果:右穹窿体积较小与较低的BVMT-R-Total评分相关(p=0.019),左侧PHC体积损失与较差的BVMT-R-Delayed表现相关(p=0.039)。较低的左穹窿FA (p=0.010)和较低的右穹窿FA (p=0.019)与较低的BVMT-R-Total性能相关。左侧背带FA较低(p=0.038)和右侧PHC较低(p=0.039)分别与HVLT-R-Total和HVLT-R-Delayed评分较低相关。双侧穹窿MD高(p=0.01)、右侧PHC高(p=0.011)与BVMT-R-Total评分低相关;右侧PHC较高的MD也与较低的HVLT-R-Total评分相关(p=0.046)。海马体积与记忆分数无关。结论:Papez回路边缘WM束微结构完整性较差预示着较差的记忆表现,而海马损伤与之无关。这些束的剂量避免可能保留记忆结果。
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
Neuro-oncology
Neuro-oncology 医学-临床神经学
CiteScore
27.20
自引率
6.30%
发文量
1434
审稿时长
3-8 weeks
期刊介绍: Neuro-Oncology, the official journal of the Society for Neuro-Oncology, has been published monthly since January 2010. Affiliated with the Japan Society for Neuro-Oncology and the European Association of Neuro-Oncology, it is a global leader in the field. The journal is committed to swiftly disseminating high-quality information across all areas of neuro-oncology. It features peer-reviewed articles, reviews, symposia on various topics, abstracts from annual meetings, and updates from neuro-oncology societies worldwide.
×
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