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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">Front. Neurosci.</journal-id>
<journal-title>Frontiers in Neuroscience</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Neurosci.</abbrev-journal-title>
<issn pub-type="epub">1662-453X</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.3389/fnins.2025.1644236</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Neuroscience</subject>
<subj-group>
<subject>Original Research</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Assessing the impact of posture on brain volume in healthy subjects with a rotatable cryogen-free 1.5T superconducting MRI</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Ke</surname>
<given-names>Shiying</given-names>
</name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
<uri xlink:href="https://loop.frontiersin.org/people/3074260/overview"/>
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<role content-type="https://credit.niso.org/contributor-roles/data-curation/"/>
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<role content-type="https://credit.niso.org/contributor-roles/software/"/>
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<role content-type="https://credit.niso.org/contributor-roles/visualization/"/>
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</contrib>
<contrib contrib-type="author">
<name>
<surname>Wang</surname>
<given-names>Yulin</given-names>
</name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<role content-type="https://credit.niso.org/contributor-roles/data-curation/"/>
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</contrib>
<contrib contrib-type="author">
<name>
<surname>Zhang</surname>
<given-names>Jichang</given-names>
</name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<xref ref-type="aff" rid="aff3"><sup>3</sup></xref>
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</contrib>
<contrib contrib-type="author">
<name>
<surname>Zeng</surname>
<given-names>Jie</given-names>
</name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
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<contrib contrib-type="author">
<name>
<surname>Niu</surname>
<given-names>Shengyang</given-names>
</name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
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<contrib contrib-type="author">
<name>
<surname>Zheng</surname>
<given-names>Jianjun</given-names>
</name>
<xref ref-type="aff" rid="aff4"><sup>4</sup></xref>
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<contrib contrib-type="author">
<name>
<surname>Meersmann</surname>
<given-names>Thomas</given-names>
</name>
<xref ref-type="aff" rid="aff5"><sup>5</sup></xref>
<xref ref-type="aff" rid="aff6"><sup>6</sup></xref>
<xref ref-type="aff" rid="aff7"><sup>7</sup></xref>
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<contrib contrib-type="author" corresp="yes">
<name>
<surname>Wang</surname>
<given-names>Chengbo</given-names>
</name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<xref ref-type="corresp" rid="c001"><sup>&#x002A;</sup></xref>
<uri xlink:href="https://loop.frontiersin.org/people/1862955/overview"/>
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<aff id="aff1"><sup>1</sup><institution>Department of Electrical and Electronic Engineering, Faculty of Science and Engineering, University of Nottingham Ningbo China</institution>, <addr-line>Ningbo</addr-line>, <country>China</country></aff>
<aff id="aff2"><sup>2</sup><institution>Department of Medical Imaging, Quanzhou Medical College</institution>, <addr-line>Quanzhou</addr-line>, <country>China</country></aff>
<aff id="aff3"><sup>3</sup><institution>Xingaoyi Medical Equipment Company, Ltd.</institution>, <addr-line>Ningbo</addr-line>, <country>China</country></aff>
<aff id="aff4"><sup>4</sup><institution>Department of Radiology, Ningbo No. 2 Hospital</institution>, <addr-line>Ningbo</addr-line>, <country>China</country></aff>
<aff id="aff5"><sup>5</sup><institution>School of Medicine, Sir Peter Mansfield Imaging Centre, Translational Medical Sciences, University of Nottingham</institution>, <addr-line>Nottingham</addr-line>, <country>United Kingdom</country></aff>
<aff id="aff6"><sup>6</sup><institution>NIHR Nottingham Biomedical Research Centre, Nottingham University Hospitals NHS Trust, Queen&#x2019;s Medical Centre</institution>, <addr-line>Nottingham</addr-line>, <country>United Kingdom</country></aff>
<aff id="aff7"><sup>7</sup><institution>Department for Strategic Development of Health Science and Technology, University of Nottingham Ningbo China, Ningbo</institution>, <addr-line>Zhejiang</addr-line>, <country>China</country></aff>
<author-notes>
<fn fn-type="edited-by" id="fn0002">
<p>Edited by: <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/408178/overview">Yi Zhang</ext-link>, Zhejiang University, China</p>
</fn>
<fn fn-type="edited-by" id="fn0003">
<p>Reviewed by: <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/3101268/overview">Cong Chu</ext-link>, University of Pittsburgh, United States</p>
<p><ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/3101818/overview">Shubham Gupta</ext-link>, Parul University, India</p>
<p><ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/3102966/overview">Haoze Zhu</ext-link>, Indiana University, Purdue University Indianapolis, United States</p>
</fn>
<corresp id="c001">&#x002A;Correspondence: Chengbo Wang, <email>chengbo.wang@nottingham.edu.cn</email></corresp>
</author-notes>
<pub-date pub-type="epub">
<day>02</day>
<month>09</month>
<year>2025</year>
</pub-date>
<pub-date pub-type="collection">
<year>2025</year>
</pub-date>
<volume>19</volume>
<elocation-id>1644236</elocation-id>
<history>
<date date-type="received">
<day>10</day>
<month>06</month>
<year>2025</year>
</date>
<date date-type="accepted">
<day>28</day>
<month>07</month>
<year>2025</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#x00A9; 2025 Ke, Wang, Zhang, Zeng, Niu, Zheng, Meersmann and Wang.</copyright-statement>
<copyright-year>2025</copyright-year>
<copyright-holder>Ke, Wang, Zhang, Zeng, Niu, Zheng, Meersmann and Wang</copyright-holder>
<license xlink:href="http://creativecommons.org/licenses/by/4.0/">
<p>This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.</p>
</license>
</permissions>
<abstract>
<sec id="sec1">
<title>Background</title>
<p>Magnetic Resonance Imaging (MRI) is crucial for detailed visualization of brain structure and function. However, conventional supine imaging limits the exploration of how posture impacts brain morphology. While recent advancements in upright MRI systems have enabled studies of postural effects on various body systems, investigations into posture&#x2019;s impact on brain anatomy remain limited.</p>
</sec>
<sec id="sec2">
<title>Method</title>
<p>This study investigated volumetric differences between upright and supine positions to establish a baseline for future investigations into how posture influenced brain structure. Thirty-one healthy volunteers underwent scans using a rotatable cryogen-free 1.5T MRI scanner in supine and upright postures. The 3D T1-weighted MP-RAGE brain images were segmented into 109 regions, and volume changes across these regions were analyzed.</p>
</sec>
<sec id="sec3">
<title>Result</title>
<p>Volumetric analysis across 109 brain regions in both supine and upright postures shows minimal changes, with most regions displaying variations within a &#x00B1;5% range. The coefficient of variation (COV) indicated that posture-induced volume changes are even smaller than the measurement precision of the method. These findings provide a solid groundwork for future studies on the effects of posture on brain structure.</p>
</sec>
<sec id="sec4">
<title>Conclusion</title>
<p>The majority of brain regions exhibited no significant volumetric differences between supine and upright positions, suggesting that brain structure remains consistent and stable across different postures. These findings offer valuable insights for future research on the postural influences on brain morphology.</p>
</sec>
</abstract>
<kwd-group>
<kwd>MRI</kwd>
<kwd>brain structures</kwd>
<kwd>volumetric differences</kwd>
<kwd>postural effects</kwd>
<kwd>MP-RAGE</kwd>
</kwd-group>
<counts>
<fig-count count="6"/>
<table-count count="1"/>
<equation-count count="0"/>
<ref-count count="32"/>
<page-count count="11"/>
<word-count count="6279"/>
</counts>
<custom-meta-wrap>
<custom-meta>
<meta-name>section-at-acceptance</meta-name>
<meta-value>Brain Imaging Methods</meta-value>
</custom-meta>
</custom-meta-wrap>
</article-meta>
</front>
<body>
<sec sec-type="intro" id="sec5">
<label>1</label>
<title>Introduction</title>
<p>Magnetic Resonance Imaging (MRI) has emerged as a crucial tool for visualizing brain structures and functions due to its non-invasive nature, high spatial resolution, and ability to provide detailed anatomical and functional insights (<xref ref-type="bibr" rid="ref27">Thompson et al., 2005</xref>).</p>
<p>Traditionally, most MRI scans are conducted with subjects in a supine position, a practice necessitated by the design constraints of conventional MRI scanners (<xref ref-type="bibr" rid="ref9">E&#x015F;er et al., 2007</xref>). Although effective for many diagnostic purposes, this fixed, non-physiological posture may not fully represent how brain structures and functions operate, as human bodies are typically more dynamic and engage in various postures in daily life (<xref ref-type="bibr" rid="ref2">Alperin et al., 2005a</xref>). Posture is known to significantly influence physiological and anatomical characteristics across the body. For example, shifting from lying down standing can alter spinal alignment, change lung capacity, and modify cardiovascular dynamics, among other effects (<xref ref-type="bibr" rid="ref22">Rossberg and Pe&#x0148;az, 1988</xref>; <xref ref-type="bibr" rid="ref10">Fawcett et al., 2021</xref>). These observations underscore the importance of incorporating different postures in studies of body systems and their functions. However, traditional MRI systems are limited in their ability to assess posture-related structural differences, highlighting the need for innovative multi-positional MRI technologies.</p>
<p>To overcome these limitations, researchers have introduced various MRI systems capable for upright or weight-bearing imaging, including Fonar&#x2019;s 0.6T system (<xref ref-type="bibr" rid="ref21">Nicholson et al., 2023</xref>), Siemens&#x2019; 1.0T system (<xref ref-type="bibr" rid="ref11">Gufler et al., 2004</xref>), and G-Scan&#x2019;s 0.25T system (<xref ref-type="bibr" rid="ref13">Lee et al., 2015b</xref>), et al. Although these systems operate at relatively low magnetic field strengths, which may reduce image resolution and signal-to-noise ratio (SNR) during scanning (<xref ref-type="bibr" rid="ref17">Marques et al., 2019</xref>), they have proven the research value in the effects of specific postures on body structures (<xref ref-type="bibr" rid="ref26">Shymon et al., 2014</xref>; <xref ref-type="bibr" rid="ref12">Hansen et al., 2019</xref>). The 1.5T MRI system provides higher SNR and spatial resolution, allowing for clearer visualization of small lesions and anatomical structures, thus enhancing the quantitative analysis capabilities of the images and assisting clinicians in making more accurate diagnostic and treatment decisions (<xref ref-type="bibr" rid="ref16">Magee et al., 2003</xref>; <xref ref-type="bibr" rid="ref5">Arnold et al., 2023</xref>; <xref ref-type="bibr" rid="ref24">Schmid et al., 1999</xref>). For instance, upright MRI has proven notably effective in detecting spinal stenosis (<xref ref-type="bibr" rid="ref10">Fawcett et al., 2021</xref>) and in visualizing medial meniscus extrusion in the knee under weight-bearing conditions (<xref ref-type="bibr" rid="ref7">Draper et al., 2011</xref>). Additionally, these systems offer significant benefits in the early diagnosis of pelvic organ prolapse (<xref ref-type="bibr" rid="ref25">Shaikh et al., 2021</xref>), thereby facilitating more prompt and effective treatment. Despite significant technological advancements, most existing studies have focused on other body systems, leaving research on the impact of posture on brain morphology relatively underexplored. Regions of the brain, such as the pituitary gland, cerebellum, and choroid plexus, which are more susceptible to gravitational effects, are particularly affected. A previous study has shown that the choroid plexus undergoes morphological changes under the influence of gravity (<xref ref-type="bibr" rid="ref28">Wang et al., 2025</xref>). These findings highlight the gap in our understanding of how posture affects brain structure and emphasize the pressing need for innovative MRI systems specifically designed for brain research.</p>
<p>While traditional MRI systems and some newly developed upright MRI systems have significantly advanced our understanding of postural effects on other body systems, research in the brain domain remains limited due to technical and methodological challenges. In prior studies, the evaluation of brain regions in the upright posture was typically done through visual assessment by two blinded clinicians, without image segmentation. This approach likely arose from the lack of automatic segmentation technology available in 2001, and the image quality at that time may not have met the requirements for accurate segmentation (<xref ref-type="bibr" rid="ref19">Nakada and Tasaka, 2001</xref>). Additionally, there was relatively limited research on upright head imaging. To address these challenges, we have developed a cryogen-free 1.5T superconductive MRI system that can operate with an active magnetic field during scanner rotation (<xref ref-type="bibr" rid="ref29">Wang et al., 2023</xref>). This system offers a unique opportunity to study the impact of different postures on brain morphology under conditions that closely mimic everyday physiological activities. This innovative design allows for high-resolution imaging in both supine and upright positions without compromising image quality.</p>
<p>The objective of this study is to investigate and validate whether significant volumetric changes occur in various brain regions between upright and supine positions in healthy individuals. By identifying and quantifying these differences, we aim to elucidate the potential clinical implications of postural effects on brain structure. These findings could offer valuable insights for advancing clinical brain research, especially in conditions where postural influences may play a significant role.</p>
</sec>
<sec sec-type="methods" id="sec6">
<label>2</label>
<title>Method</title>
<p>All imaging was conducted using a state-of-the-art, rotatable, cryogen-free superconductive 1.5T MRI scanner (XGY-Spin MRI-R001, XGY, Ningbo, China), which served as the primary imaging platform (<xref ref-type="fig" rid="fig1">Figure 1</xref>). This prospective study was carried out between August to September 2024, with ethical approval granted by the institutional ethics committees of both the University of Nottingham Ningbo China, and Ningbo No. 2 Hospital. Written informed consent was obtained from all participants, ensuring compliance with established guidelines for human research. Additionally, participant confidentiality was meticulously maintained by anonymizing data prior to analysis.</p>
<fig position="float" id="fig1">
<label>Figure 1</label>
<caption>
<p>Design and configuration of the 1.5T superconductive cryogen-free spin MRI system: <bold>(a)</bold> at 0&#x00B0; angle for supine scanning, <bold>(b)</bold> at 45&#x00B0; angle for an oblique view, and <bold>(c)</bold> at 90&#x00B0; angle for upright scanning.</p>
</caption>
<graphic xlink:href="fnins-19-1644236-g001.tif" mimetype="image" mime-subtype="tiff">
<alt-text content-type="machine-generated">Three MRI machines are displayed in the image, labeled a, b, and c. Machine a shows a patient lying on a table entering a scanner. Machine b is similar but without a patient, featuring a circular opening and a touchscreen panel on the side. Machine c is a different model, showing a mannequin positioned vertically inside a scanner.</alt-text>
</graphic>
</fig>
<p>The inclusion criteria for eligible participants were aged 20&#x2013;35&#x202F;years, without any history of neurological or psychiatric disorders, and met all MRI scanning safety requirements. The exclusion criteria included significant brain abnormalities, a history of brain surgery, systemic diseases affecting brain structure (e.g., hypertension or diabetes), or pregnancy. Initially, 33 individuals were enrolled; however, one was excluded due to the presence of a cerebral lipoma. Additionally, due to a computer system error, data from one individual was corrupted, leading to exclusion. As a result, the final cohort consisted of 31 healthy volunteers (mean age: 26.5&#x202F;&#x00B1;&#x202F;3.7&#x202F;years; comprising 16 males and 15 females). Each subject underwent an MRI scan using a 3D T1-weighted MPRAGE sequence, with the following settings: Repetition Time (TR)&#x202F;=&#x202F;10.0&#x202F;ms, Echo Time (TE)&#x202F;=&#x202F;3.4&#x202F;ms, Field of View (FOV)&#x202F;=&#x202F;230&#x202F;mm&#x202F;&#x00D7;&#x202F;230&#x202F;mm&#x202F;&#x00D7;&#x202F;187.2&#x202F;mm, Sampling Matrix&#x202F;=&#x202F;192&#x202F;&#x00D7;&#x202F;192&#x202F;&#x00D7;&#x202F;156, Reconstruction Matrix&#x202F;=&#x202F;480&#x202F;&#x00D7;&#x202F;480&#x202F;&#x00D7;&#x202F;156, Spatial Resolution&#x202F;=&#x202F;0.48&#x202F;mm&#x202F;&#x00D7;&#x202F;0.48&#x202F;mm&#x202F;&#x00D7;&#x202F;1.20&#x202F;mm, Slice Thickness&#x202F;=&#x202F;1.20&#x202F;mm, and Flip Angle&#x202F;=&#x202F;12&#x00B0;. The scan time for the 3D MP-RAGE sequence was 4&#x202F;min and 15&#x202F;s. Scans were performed in two different postures&#x2014;supine (0 degrees) and upright (90 degrees). For supine scans, participants&#x2019; heads were supported by foam pads to minimize motion. In the upright posture, restraint straps and additional foam pads were used to secure and align the head, effectively reducing motion artifacts.</p>
<p>A comprehensive volumetric analysis of 109 brain regions was performed using the United Imaging analysis system to assess structural changes between the two postures. The automated whole-brain segmentation from 3D T1-weighted MPRAGE images was conducted via the uAI Research Portal (United Imaging Intelligence, China) (<xref ref-type="bibr" rid="ref31">Wu et al., 2023</xref>), a clinical research platform developed using Python (version 3.7.3). This process utilized the PyRadiomics package<xref ref-type="fn" rid="fn0001"><sup>1</sup></xref> (<xref ref-type="bibr" rid="ref15">Liu et al., 2022</xref>), enabling precise segmentation of the whole brain into 109 distinct regions and providing volumetric measurements for each region to assess structural changes between the two postures (<xref ref-type="fig" rid="fig2">Figure 2</xref>).</p>
<fig position="float" id="fig2">
<label>Figure 2</label>
<caption>
<p>Sagittal 3D T1-weighted MPRAGE MRI images of the brain from a 29-year-old male in upright <bold>(a,b)</bold> and supine <bold>(c,d)</bold> positions. Anatomical images are shown in <bold>(a,c)</bold>, <bold>(b,d)</bold> corresponding regional brain segmentations.</p>
</caption>
<graphic xlink:href="fnins-19-1644236-g002.tif" mimetype="image" mime-subtype="tiff">
<alt-text content-type="machine-generated">Four MRI brain scans in sagittal view. Panel a and c show grayscale images with the person upright and supine respectively. Panel b and d display colored overlays indicating different brain regions, corresponding to the upright and supine positions of panels a and c.</alt-text>
</graphic>
</fig>
<p>To assess both the reproducibility and repeatability of this analysis method, an experiment was conducted with three selected subjects. Measurements of brain volume in the supine posture were performed for each subject at three time points: Day 1 (first scan), Day 30 (second scan, initial scan), and Day 30 (third scan, taken 30&#x202F;min after the second scan). This approach aimed to determine the stability of measurements over time and the reliability of the method. The coefficient of variation (COV) (<xref ref-type="bibr" rid="ref6">Bland and Altman, 2010</xref>) was calculated using the formula: COV&#x202F;=&#x202F;(Standard deviation/Mean)&#x202F;&#x00D7;&#x202F;100% (<xref ref-type="bibr" rid="ref1">Abdi, 2010</xref>). And the average COV was calculated across the three subjects. In this study, the COV was expressed as a percentage, providing a depiction of measurement variability and aiding in the assessment of the precision and consistency of the measurements.</p>
<p>Subsequently, brain volume was measured in both the supine and upright positions for all 31 subjects to evaluate changes in brain region volumes between these two postures. Additionally, the percentage change in brain volume between the upright and supine measurements was calculated using the formula: (V<sub>upright</sub>&#x202F;&#x2212;&#x202F;V<sub>supine</sub>)/(V<sub>upright</sub>)&#x202F;&#x00D7;&#x202F;100%, where V<sub>supine</sub> and V<sub>upright</sub> represent the brain volume in the supine and upright postures, respectively. To ensure the validity of the parametric analysis, the Shapiro&#x2013;Wilk test was conducted for each brain region to assess whether the volume data conformed to a normal distribution. Only regions that satisfied the normality assumption were included in the subsequent two-tailed paired Student&#x2019;s t-test. For regions that did not meet the normality assumption, the non-parametric Wilcoxon signed-rank test was applied instead. These statistical tests were used to evaluate volume differences between the two positions. Multiple comparison corrections were also applied to control for Type 1 errors.</p>
</sec>
<sec sec-type="results" id="sec7">
<label>3</label>
<title>Results</title>
<p><xref ref-type="table" rid="tab1">Table 1</xref> presents the demographic characteristics of the participants, all of whom are young adults. This selection minimizes the influence of age-related brain volume decline. Additionally, the balanced gender ratio helps reduce the potential impact of sex differences on brain structure.</p>
<table-wrap position="float" id="tab1">
<label>Table 1</label>
<caption>
<p>Demographic characteristics of the study participants.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" valign="top">Normal volunteers</th>
<th align="center" valign="top">Pre-scan</th>
<th align="center" valign="top">Post-scan</th>
<th align="center" valign="top"><italic>p</italic> value</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" valign="middle">Age (years)</td>
<td align="center" valign="middle">26.5&#x202F;&#x00B1;&#x202F;3.7</td>
<td/>
<td/>
</tr>
<tr>
<td align="left" valign="middle">Gender (M/F)</td>
<td align="center" valign="middle">16/15</td>
<td/>
<td/>
</tr>
<tr>
<td align="left" valign="middle">Height (cm)</td>
<td align="center" valign="middle">168.8&#x202F;&#x00B1;&#x202F;6.6</td>
<td/>
<td/>
</tr>
<tr>
<td align="left" valign="middle">Weight (kg)</td>
<td align="center" valign="middle">64.8&#x202F;&#x00B1;&#x202F;11.7</td>
<td/>
<td/>
</tr>
<tr>
<td align="left" valign="middle">HR (beats/min)</td>
<td align="center" valign="middle">78.9&#x202F;&#x00B1;&#x202F;13.8</td>
<td align="center" valign="middle">76.7&#x202F;&#x00B1;&#x202F;11.6</td>
<td align="center" valign="middle">0.501</td>
</tr>
<tr>
<td align="left" valign="middle">Systolic BP (mmHg)</td>
<td align="center" valign="middle">115.2&#x202F;&#x00B1;&#x202F;12.6</td>
<td align="center" valign="middle">110.5&#x202F;&#x00B1;&#x202F;11.7</td>
<td align="center" valign="middle">0.148</td>
</tr>
<tr>
<td align="left" valign="middle">Diastolic BP (mmHg)</td>
<td align="center" valign="middle">74.1&#x202F;&#x00B1;&#x202F;7.2</td>
<td align="center" valign="middle">70.9&#x202F;&#x00B1;&#x202F;7.5</td>
<td align="center" valign="middle">0.101</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<p>HR, heart rate; BP, blood pressure.</p>
</table-wrap-foot>
</table-wrap>
<p>Imaging was conducted on all subjects using the spin MRI, with no adverse effects. <xref ref-type="fig" rid="fig2">Figure 2</xref> illustrates the segmentation of 109 distinct brain regions from 3D T1-weighted MPRAGE images of a sample subject in both upright and supine positions, performed using the uAI Research Portal. Volumetric measurements for each region were obtained to evaluate structural differences between the two positions.</p>
<p>As shown in <xref ref-type="fig" rid="fig3">Figure 3</xref>, the average COV across the three subjects was 4.61%&#x202F;&#x00B1;&#x202F;2.60%, indicating good measurement repeatability. The COV values remained consistent across the three time points: Day 1 (first scan), Day 30 (second scan, initial scan), and Day 30 (third scan, conducted 30&#x202F;min after the second scan). The absence of significant fluctuation further suggests that the scanning method provides reliable precision and temporal stability. Overall, the low mean COV reflects the high repeatability and low variability of the brain volume measurements in the supine posture.</p>
<fig position="float" id="fig3">
<label>Figure 3</label>
<caption>
<p>Box plot of mean coefficient of variation (COV) values for volume measurements across three time points: first scan on Day 1, second scan on Day 30 (initial scan), and third scan on Day 30 (30&#x202F;min after the second scan) for three selected subjects in the same supine posture. <bold>(a)</bold> COV values averaged across all three subjects. <bold>(b)</bold> COV values for each individual subject (Subject A, Subject B, and Subject C) with three repeated scans. The square markers represent the mean values. Data represent the COV values across all 109 brain regions.</p>
</caption>
<graphic xlink:href="fnins-19-1644236-g003.tif" mimetype="image" mime-subtype="tiff">
<alt-text content-type="machine-generated">Two box plots displaying CoV multiplied by one hundred in percentages. Plot a shows the average with a median around 5 and several outliers. Plot b compares subjects A, B, and C with median values around 5 for all, but varying spreads and outliers, particularly in subjects B and C.</alt-text>
</graphic>
</fig>
<p>To further assess the measurement precision of the scanning method, we calculated the coefficient of variation (COV) for brain volume measurements in three subjects across the three designated time points: Day 1 (first scan), Day 30 (second scan, initial scan), and Day 30 (third scan, conducted 30&#x202F;min after the second scan). For each subject, the COV was determined by dividing the standard deviation of the three volume measurements by their mean (<xref ref-type="fig" rid="fig3">Figure 3b</xref>). The final mean COV was obtained by averaging the individual COV values across the three subjects (<xref ref-type="fig" rid="fig3">Figure 3a</xref>).</p>
<p><xref ref-type="fig" rid="fig4">Figure 4</xref> shows the overlap of the coefficient of variation (COV) values with the percentage volume changes across 109 brain regions between upright and supine postures. The gray bars represent brain regions with volume changes within the &#x00B1;5% range, while the blue bars indicate regions with volume changes exceeding 5%. Most brain regions exhibit volume changes within the &#x00B1;5% range, with only a few regions exceeding this threshold, suggesting that the volume changes between the two postures are very stable for the majority of brain regions.</p>
<fig position="float" id="fig4">
<label>Figure 4</label>
<caption>
<p>Percentage volume changes between upright and supine postures across 109 brain regions, illustrated in the gray and blue bars. The red box displays the mean COV values for volume measurements across three selected subjects at three time points.</p>
</caption>
<graphic xlink:href="fnins-19-1644236-g004.tif" mimetype="image" mime-subtype="tiff">
<alt-text content-type="machine-generated">Bar chart displaying percentage changes in various brain regions, with percentages on the x-axis ranging from -20 to 20. Brain regions are listed on the y-axis. Bars are gray, red, and blue, indicating different levels of change.</alt-text>
</graphic>
</fig>
<p><xref ref-type="fig" rid="fig4">Figure 4</xref> illustrates that most of the gray bars, representing the average postural volume changes across the 31 subjects, fall within the red box, which denotes the average COV across the three selected subjects for each segmented brain region. This suggests that most brain regions are highly stable, with their postural changes resembling those observed in the same supine posture across different time points.</p>
<p><xref ref-type="fig" rid="fig5">Figure 5</xref> presents a scatter plot illustrating the relationship between percentage volume changes and <italic>p</italic>-values. The majority of brain regions display minimal volume changes, with <italic>p</italic>-values approaching 1, whereas a few regions near the threshold of significance with <italic>p</italic>-values close to 0.05, further underscoring the overall stability of brain volumes. Multiple comparison corrections were also applied, and the results remained consistent, reinforcing the stability and robustness of the observed findings.</p>
<fig position="float" id="fig5">
<label>Figure 5</label>
<caption>
<p>Scatter plot of percentage volume change versus <italic>p</italic>-values for 109 segmented brain regions. The x-axis represents the percentage change, while the y-axis shows p-values. Red dashed lines mark &#x00B1;5% on the x-axis and a significance level of 0.05 on the y-axis, where each triangle represents a brain region.</p>
</caption>
<graphic xlink:href="fnins-19-1644236-g005.tif" mimetype="image" mime-subtype="tiff">
<alt-text content-type="machine-generated">Scatter plot depicting p-values against percentages, with data points as triangles. The plot includes red dashed vertical lines at approximately -5% and 5%, and a horizontal line at a p-value of 0.05. Triangles are mostly concentrated around 0% with outliers to the left.</alt-text>
</graphic>
</fig>
<p>Most brain regions exhibited minimal volume changes between upright and supine postures. Notably, there was no significant difference in intracranial volume (ICV) between the two positions: supine position ICV was 1407981.60&#x202F;&#x00B1;&#x202F;138923.61&#x202F;mm<sup>3</sup>, and upright position ICV was 1402848.68&#x202F;&#x00B1;&#x202F;135176.12&#x202F;mm<sup>3</sup> (<italic>p</italic>&#x202F;=&#x202F;0.89). <xref ref-type="fig" rid="fig6">Figure 6a</xref> demonstrates that the Inferior Lateral Ventricle showed the most substantial negative volume change (&#x2212;18.56%), which exceeded the &#x00B1;5% threshold; however, this difference was not statistically significant (<italic>p</italic>&#x202F;=&#x202F;0.27). In contrast, the hippocampus depicted in <xref ref-type="fig" rid="fig6">Figure 6b</xref> showed a negligible volume change of 0.01% (<italic>p</italic>&#x202F;=&#x202F;0.97), exemplifying the typical stability observed across most brain regions. <xref ref-type="fig" rid="fig6">Figure 6c</xref> highlights the Choroid Plexus, which showed the largest positive volume change at 3.19% (<italic>p</italic>&#x202F;=&#x202F;0.64), yet maintained a relatively stable distribution.</p>
<fig position="float" id="fig6">
<label>Figure 6</label>
<caption>
<p>Box plots comparing brain region volumes between supine (blue) and upright (orange) postures for the Right Inferior Lateral Ventricle <bold>(a)</bold>, Right Hippocampus <bold>(b)</bold>, and Right Choroid Plexus <bold>(c)</bold>. Panel <bold>(a)</bold> illustrates the largest negative percentage change in the Right Inferior Lateral Ventricle, panel <bold>(b)</bold> shows the volume change closest to zero in the Right Hippocampus, and panel <bold>(c)</bold> displays the largest positive percentage change in the Right Choroid Plexus. No significant volume differences are observed between postures for these regions, as indicated by the p-values in each panel.</p>
</caption>
<graphic xlink:href="fnins-19-1644236-g006.tif" mimetype="image" mime-subtype="tiff">
<alt-text content-type="machine-generated">Three box plots comparing volumes in cubic millimeters for supine and upright positions. Plot a: Ventricle Inf Lat R shows an 18.56% volume decrease, p=0.27. Plot b: Hippocampus R shows a 0.01% volume change, p=0.97. Plot c: Choroid Plexus R shows a 3.19% volume increase, p=0.64.</alt-text>
</graphic>
</fig>
</sec>
<sec sec-type="discussion" id="sec8">
<label>4</label>
<title>Discussion</title>
<p>To the best of our knowledge, this study is the first to employ a cryogen-free, rotatable superconductive MRI system in the investigation of brain volume changes. While the system is capable of maintaining a continuous magnetic field during scanner rotation, it is important to note that all scans in this study were conducted at fixed positions (either 0 or 90 degrees), rather than during continuous rotation. We investigated the effects of postural changes on brain volume in healthy individuals by comparing supine and upright positions using this innovative rotatable MRI scanner, quantifying the statistical differences between these two postures. Our results indicate that postural changes have a minimal impact on brain volume in healthy individuals, which supports existing knowledge about the high stability of brain structure.</p>
<p>Specifically, the volume changes in most brain regions between the upright and supine positions were within a &#x00B1;5% range, with the majority of regions showing near-zero volume changes and <italic>p</italic>-values close to 1, further validity the stability and reliability of the brain structure. This is consistent with prior upright MRI studies, which have shown that gravity exerts a negligible effect on brain structure, even in conditions such as brain atrophy (<xref ref-type="bibr" rid="ref19">Nakada and Tasaka, 2001</xref>). However, as illustrated in <xref ref-type="fig" rid="fig6">Figure 6a</xref>, the inferior lateral ventricle, where CSF is contained and circulated through, showed a positive shift in volume from upright to supine, yet the overall variability remained low. This region, adjacent to cerebrospinal fluid (CSF)-filled areas, has been documented in prior research to experience a significant increase in CSF flow when supine, suggesting that these regions may be more susceptible to postural changes and may exhibit unique anatomical or hemodynamic characteristics (<xref ref-type="bibr" rid="ref18">Muccio et al., 2021</xref>; <xref ref-type="bibr" rid="ref3">Alperin et al., 2015</xref>). Previous studies have reported that CSF flow, velocity, and stroke volume decrease significantly in the upright posture, with these changes closely related to body position (<xref ref-type="bibr" rid="ref33">Yukun et al., 2025</xref>). Although our study did not include direct CSF flow measurements, the volumetric trend observed may reflect posture-dependent redistribution of CSF. These findings provide preliminary structural evidence that may contribute to understanding how posture influences CSF dynamics.</p>
<p>Further investigations integrating structural, functional, and flow-sensitive imaging modalities are warranted to elucidate the mechanisms by which posture influences CSF distribution and ventricular morphology.</p>
<p>Furthermore, previous studies have demonstrated that, compared to the supine position, the upright posture reduces CSF oscillatory volume by approximately 48%, significantly increases intracranial compliance (ICC), and decreases intracranial pressure (ICP) by approximately 2.4 times (<xref ref-type="bibr" rid="ref4">Alperin et al., 2005b</xref>). These findings highlights the dynamic role of CSF in regulating intracranial pressure across different postural orientations, effectively maintaining intracranial pressure equilibrium. Notably, prior research has also shown that, even in cases of cerebrospinal fluid leakage, brain imaging differences between the upright and supine positions remain insignificant (<xref ref-type="bibr" rid="ref23">Schievink and Tourje, 2007</xref>). This further underscores that, despite the significant effects of upright posture on CSF distribution and ICP, the brain&#x2019;s intrinsic regulatory mechanisms ensure the stability of volume and morphology across brain regions (<xref ref-type="bibr" rid="ref14">Lee et al., 2015a</xref>).</p>
<p>On the other hand, the hippocampus (<xref ref-type="fig" rid="fig6">Figure 6b</xref>) demonstrated the overall stability of most brain regions, with minimal variation between postures. Likewise, despite relatively larger volume changes in the choroid plexus, its low variability further highlights the consistency of measurements across different postural conditions.</p>
<p>The results depicted in <xref ref-type="fig" rid="fig3">Figure 3</xref> demonstrate the good precision and repeatability of the current method. Measurement values for all three subjects exhibited minimal fluctuation across different time points indicating that the method provides consistent volume measurements. By calculating COV, we found that the measurement consistency for the vast majority of brain regions is high, indicating that the current measurement method demonstrates good repeatability and stability. The volume changes in brain regions induced by posture shifts mostly fall within the measurement error range, making them undetectable by the current method.</p>
</sec>
<sec id="sec9">
<label>5</label>
<title>Limitation</title>
<p>A limitation of this study is that the COV measurements were derived from data obtained from only three subjects. Such a small sample size may not be sufficiently robust to provide a comprehensive evaluation of the precision and consistency of the method at this scale. Although the results indicate that the method operates effectively within a reasonable margin, the limited sample size could introduce variability in the accuracy of the measurements. To achieve a more reliable estimation of the COV, it would be ideal to conduct multiple scans with a larger cohort, each undergoing at least three separate measurements. However, implementing such a protocol would significantly extend the required scanning time and necessitate multiple visits from the volunteers, which presents considerable logistical challenges. Consequently, the COV values observed in this study may not fully reflect the true precision of the method, highlighting the need for further studies involving larger sample sizes and repeated scans to confirm the reliability and generalizability of the findings.</p>
<p>Another limitation of this study concerns the accuracy of choroid plexus segmentation. Although we utilized the PyRadiomics package for segmentation of 109 brain regions, the tool is based on FreeSurfer, which has shown limited performance in choroid plexus segmentation (<xref ref-type="bibr" rid="ref34">Zhao et al., 2020</xref>). As the choroid plexus is a critical structure influenced by body position and CSF flow, previous studies have demonstrated that deep learning-based approaches perform significantly better in this context (<xref ref-type="bibr" rid="ref32">Yazdan-Panah et al., 2023</xref>; <xref ref-type="bibr" rid="ref8">Eisma et al., 2024</xref>; <xref ref-type="bibr" rid="ref34">Zhao et al., 2020</xref>). However, due to the scope of this study, these advanced deep learning techniques were not implemented. It is worth noting that a parallel study using this rotatable MRI system has analyzed the choroid plexus and provides supplementary data (<xref ref-type="bibr" rid="ref28">Wang et al., 2025</xref>). We acknowledge that the segmentation method used in this study may not provide the same level of precision as newer techniques, which may affect the reliability of the volumetric findings related to the choroid plexus. In future work, we plan to explore these advanced deep learning techniques to improve segmentation accuracy.</p>
</sec>
<sec sec-type="conclusions" id="sec10">
<label>6</label>
<title>Conclusion</title>
<p>In conclusion, while most brain regions showed no significant differences between supine and upright positions, these findings deepen our understanding of the potential clinical implications of postural effects on brain structure and provide valuable insights for future studies in clinical brain research.</p>
</sec>
</body>
<back>
<sec id="sec11">
<title>Author&#x2019;s note</title>
<p>Parts of this work have been presented as a digital poster at the 33rd Annual Meeting of the International Society for Magnetic Resonance in Medicine (ISMRM), 2025.</p>
</sec>
<sec sec-type="data-availability" id="sec12">
<title>Data availability statement</title>
<p>The datasets presented in this article are not readily available because this prospective study was approved by the institutional ethics committees of both the University of Nottingham Ningbo China and Ningbo No. 2 Hospital. Participant confidentiality was carefully maintained by anonymizing the data prior to analysis. Due to sensitivity concerns, the data supporting the findings of this study are not openly available. Access to the data may require institutional or ethical approval due to privacy considerations. Further, the data are available from the corresponding author upon reasonable request. Requests to access the datasets should be directed to <email>chengbo.wang@nottingham.edu.cn</email>.</p>
</sec>
<sec sec-type="ethics-statement" id="sec13">
<title>Ethics statement</title>
<p>The studies involving humans were approved by ethical approval granted by the institutional ethics committees of both the University of Nottingham Ningbo China, and Ningbo No. 2 Hospital. Written informed consent was obtained from all participants, ensuring compliance with established guidelines for human research. The studies were conducted in accordance with the local legislation and institutional requirements. The participants provided their written informed consent to participate in this study. Written informed consent was obtained from the individual(s) for the publication of any potentially identifiable images or data included in this article.</p>
</sec>
<sec sec-type="author-contributions" id="sec14">
<title>Author contributions</title>
<p>SK: Conceptualization, Data curation, Formal analysis, Methodology, Resources, Software, Validation, Visualization, Writing &#x2013; original draft, Writing &#x2013; review &#x0026; editing. YW: Data curation, Methodology, Software, Validation, Writing &#x2013; review &#x0026; editing. JicZ: Data curation, Methodology, Validation, Writing &#x2013; review &#x0026; editing. JieZ: Data curation, Writing &#x2013; review &#x0026; editing. SN: Data curation, Writing &#x2013; review &#x0026; editing. JiaZ: Investigation, Resources, Writing &#x2013; review &#x0026; editing. TM: Methodology, Project administration, Writing &#x2013; review &#x0026; editing. CW: Methodology, Project administration, Writing &#x2013; review &#x0026; editing.</p>
</sec>
<sec sec-type="funding-information" id="sec15">
<title>Funding</title>
<p>The author(s) declare that financial support was received for the research and/or publication of this article. This study was supported by the National Key R&#x0026;D Program of China: 2022YFC2408900, Ningbo &#x201C;S&#x0026;T Innovation 2035&#x201D; Major programs: 2022Z141 &#x0026; 2023Z182.</p>
</sec>
<sec sec-type="COI-statement" id="sec16">
<title>Conflict of interest</title>
<p>JZ was employed by Xingaoyi Medical Equipment Company, Ltd.</p>
<p>The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.</p>
</sec>
<sec sec-type="ai-statement" id="sec17">
<title>Generative AI statement</title>
<p>The authors declare that no Gen AI was used in the creation of this manuscript.</p>
<p>Any alternative text (alt text) provided alongside figures in this article has been generated by Frontiers with the support of artificial intelligence and reasonable efforts have been made to ensure accuracy, including review by the authors wherever possible. If you identify any issues, please contact us.</p>
</sec>
<sec sec-type="disclaimer" id="sec18">
<title>Publisher&#x2019;s note</title>
<p>All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.</p>
</sec>
<fn-group>
<fn id="fn0001"><p><sup>1</sup><ext-link xlink:href="https://pyradiomics.readthedocs.io" ext-link-type="uri">https://pyradiomics.readthedocs.io</ext-link></p></fn>
</fn-group>
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</ref-list>
<glossary>
<def-list>
<title>Glossary</title>
<def-item>
<term>Precentral_L</term>
<def>
<p>Left Precentral Gyrus</p>
</def>
</def-item>
<def-item>
<term>Precentral_R</term>
<def>
<p>Right Precentral Gyrus</p>
</def>
</def-item>
<def-item>
<term>Postcentral_L</term>
<def>
<p>Left Postcentral Gyrus</p>
</def>
</def-item>
<def-item>
<term>Postcentral_R</term>
<def>
<p>Right Postcentral Gyrus</p>
</def>
</def-item>
<def-item>
<term>Paracentral_L</term>
<def>
<p>Left Paracentral Lobule</p>
</def>
</def-item>
<def-item>
<term>Paracentral_R</term>
<def>
<p>Right Paracentral Lobule</p>
</def>
</def-item>
<def-item>
<term>Frontal_Sup_L</term>
<def>
<p>Left Superior Frontal Gyrus</p>
</def>
</def-item>
<def-item>
<term>Frontal_Sup_R</term>
<def>
<p>Right Superior Frontal Gyrus</p>
</def>
</def-item>
<def-item>
<term>Frontal_Mid_Rostral_L</term>
<def>
<p>Left Rostral part of the Middle Frontal Gyrus</p>
</def>
</def-item>
<def-item>
<term>Frontal_Mid_Rostral_R</term>
<def>
<p>Right Rostral part of the Middle Frontal Gyrus</p>
</def>
</def-item>
<def-item>
<term>Frontal_Mid_Caudal_L</term>
<def>
<p>Left Caudal part of the Middle Frontal Gyrus</p>
</def>
</def-item>
<def-item>
<term>Frontal_Mid_Caudal_R</term>
<def>
<p>Right Caudal part of the Middle Frontal Gyrus</p>
</def>
</def-item>
<def-item>
<term>Frontalpole_L</term>
<def>
<p>Left Frontal Pole</p>
</def>
</def-item>
<def-item>
<term>Frontalpole_R</term>
<def>
<p>Right Frontal Pole</p>
</def>
</def-item>
<def-item>
<term>Orbitofrontal_Lat_L</term>
<def>
<p>Left Lateral Orbitofrontal Cortex</p>
</def>
</def-item>
<def-item>
<term>Orbitofrontal_Lat_R</term>
<def>
<p>Right Lateral Orbitofrontal Cortex</p>
</def>
</def-item>
<def-item>
<term>Orbitofrontal_Med_L</term>
<def>
<p>Left Medial Orbitofrontal Cortex</p>
</def>
</def-item>
<def-item>
<term>Orbitofrontal_Med_R</term>
<def>
<p>Right Medial Orbitofrontal Cortex</p>
</def>
</def-item>
<def-item>
<term>Parsopercularis_L</term>
<def>
<p>Left Pars Opercularis</p>
</def>
</def-item>
<def-item>
<term>Parsopercularis_R</term>
<def>
<p>Right Pars Opercularis</p>
</def>
</def-item>
<def-item>
<term>Parsorbitalis_L</term>
<def>
<p>Left Pars Orbitalis</p>
</def>
</def-item>
<def-item>
<term>Parsorbitalis_R</term>
<def>
<p>Right Pars Orbitalis</p>
</def>
</def-item>
<def-item>
<term>Parstriangularis_L</term>
<def>
<p>Left Pars Triangularis</p>
</def>
</def-item>
<def-item>
<term>Parstriangularis_R</term>
<def>
<p>Right Pars Triangularis</p>
</def>
</def-item>
<def-item>
<term>Insula_L</term>
<def>
<p>Left Insula</p>
</def>
</def-item>
<def-item>
<term>Insula_R</term>
<def>
<p>Right Insula</p>
</def>
</def-item>
<def-item>
<term>Cingulum_Ant_L</term>
<def>
<p>Left Anterior Cingulum</p>
</def>
</def-item>
<def-item>
<term>Cingulum_Ant_R</term>
<def>
<p>Right Anterior Cingulum</p>
</def>
</def-item>
<def-item>
<term>Cingulum_Mid_L</term>
<def>
<p>Left Middle Cingulum</p>
</def>
</def-item>
<def-item>
<term>Cingulum_Mid_R</term>
<def>
<p>Right Middle Cingulum</p>
</def>
</def-item>
<def-item>
<term>Cingulum_Post_L</term>
<def>
<p>Left Posterior Cingulum</p>
</def>
</def-item>
<def-item>
<term>Cingulum_Post_R</term>
<def>
<p>Right Posterior Cingulum</p>
</def>
</def-item>
<def-item>
<term>Isthmuscingulate_L</term>
<def>
<p>Left Isthmus of Cingulate Cortex</p>
</def>
</def-item>
<def-item>
<term>Isthmuscingulate_R</term>
<def>
<p>Right Isthmus of Cingulate Cortex</p>
</def>
</def-item>
<def-item>
<term>Hippocampus_L</term>
<def>
<p>Left Hippocampus</p>
</def>
</def-item>
<def-item>
<term>Hippocampus_R</term>
<def>
<p>Right Hippocampus</p>
</def>
</def-item>
<def-item>
<term>Parahippocampal_L</term>
<def>
<p>Left Parahippocampal Gyrus</p>
</def>
</def-item>
<def-item>
<term>Parahippocampal_R</term>
<def>
<p>Right Parahippocampal Gyrus</p>
</def>
</def-item>
<def-item>
<term>Amygdala_L</term>
<def>
<p>Left Amygdala</p>
</def>
</def-item>
<def-item>
<term>Amygdala_R</term>
<def>
<p>Right Amygdala</p>
</def>
</def-item>
<def-item>
<term>Caudate_L</term>
<def>
<p>Left Caudate Nucleus</p>
</def>
</def-item>
<def-item>
<term>Caudate_R</term>
<def>
<p>Right Caudate Nucleus</p>
</def>
</def-item>
<def-item>
<term>Putamen_L</term>
<def>
<p>Left Putamen</p>
</def>
</def-item>
<def-item>
<term>Putamen_R</term>
<def>
<p>Right Putamen</p>
</def>
</def-item>
<def-item>
<term>Pallidum_L</term>
<def>
<p>Left Pallidum</p>
</def>
</def-item>
<def-item>
<term>Pallidum_R</term>
<def>
<p>Right Pallidum</p>
</def>
</def-item>
<def-item>
<term>Thalamus_L</term>
<def>
<p>Left Thalamus</p>
</def>
</def-item>
<def-item>
<term>Thalamus_R</term>
<def>
<p>Right Thalamus</p>
</def>
</def-item>
<def-item>
<term>Accumbens_Area_L</term>
<def>
<p>Left Nucleus Accumbens</p>
</def>
</def-item>
<def-item>
<term>Accumbens_Area_R</term>
<def>
<p>Right Nucleus Accumbens</p>
</def>
</def-item>
<def-item>
<term>VentralDC_L</term>
<def>
<p>Left Ventral Dorsal Cortex</p>
</def>
</def-item>
<def-item>
<term>VentralDC_R</term>
<def>
<p>Right Ventral Dorsal Cortex</p>
</def>
</def-item>
<def-item>
<term>Choroid_Plexus_L</term>
<def>
<p>Left Choroid Plexus</p>
</def>
</def-item>
<def-item>
<term>Choroid_Plexus_R</term>
<def>
<p>Right Choroid Plexus</p>
</def>
</def-item>
<def-item>
<term>Ventricle_Lat_L</term>
<def>
<p>Left Lateral Ventricle</p>
</def>
</def-item>
<def-item>
<term>Ventricle_Lat_R</term>
<def>
<p>Right Lateral Ventricle</p>
</def>
</def-item>
<def-item>
<term>Ventricle_Inf_Lat_L</term>
<def>
<p>Left Inferior Lateral Ventricle</p>
</def>
</def-item>
<def-item>
<term>Ventricle_Inf_Lat_R</term>
<def>
<p>Right Inferior Lateral Ventricle</p>
</def>
</def-item>
<def-item>
<term>Parietal_Sup_L</term>
<def>
<p>Left Superior Parietal Lobule</p>
</def>
</def-item>
<def-item>
<term>Parietal_Sup_R</term>
<def>
<p>Right Superior Parietal Lobule</p>
</def>
</def-item>
<def-item>
<term>Parietal_Inf_L</term>
<def>
<p>Left Inferior Parietal Lobule</p>
</def>
</def-item>
<def-item>
<term>Parietal_Inf_R</term>
<def>
<p>Right Inferior Parietal Lobule</p>
</def>
</def-item>
<def-item>
<term>Cuneus_L</term>
<def>
<p>Left Cuneus</p>
</def>
</def-item>
<def-item>
<term>Cuneus_R</term>
<def>
<p>Right Cuneus</p>
</def>
</def-item>
<def-item>
<term>Entorhinal_L</term>
<def>
<p>Left Entorhinal Cortex</p>
</def>
</def-item>
<def-item>
<term>Entorhinal_R</term>
<def>
<p>Right Entorhinal Cortex</p>
</def>
</def-item>
<def-item>
<term>Fusiform_L</term>
<def>
<p>Left Fusiform Gyrus</p>
</def>
</def-item>
<def-item>
<term>Fusiform_R</term>
<def>
<p>Right Fusiform Gyrus</p>
</def>
</def-item>
<def-item>
<term>Lingual_L</term>
<def>
<p>Left Lingual Gyrus</p>
</def>
</def-item>
<def-item>
<term>Lingual_R</term>
<def>
<p>Right Lingual Gyrus</p>
</def>
</def-item>
<def-item>
<term>Pericalcarine_L</term>
<def>
<p>Left Pericalcarine Cortex</p>
</def>
</def-item>
<def-item>
<term>Pericalcarine_R</term>
<def>
<p>Right Pericalcarine Cortex</p>
</def>
</def-item>
<def-item>
<term>Precuneus_L</term>
<def>
<p>Left Precuneus</p>
</def>
</def-item>
<def-item>
<term>Precuneus_R</term>
<def>
<p>Right Precuneus</p>
</def>
</def-item>
<def-item>
<term>Supramarginal_L</term>
<def>
<p>Left Supramarginal Gyrus</p>
</def>
</def-item>
<def-item>
<term>Supramarginal_R</term>
<def>
<p>Right Supramarginal Gyrus</p>
</def>
</def-item>
<def-item>
<term>Temporal_Sup_L</term>
<def>
<p>Left Superior Temporal Gyrus</p>
</def>
</def-item>
<def-item>
<term>Temporal_Sup_R</term>
<def>
<p>Right Superior Temporal Gyrus</p>
</def>
</def-item>
<def-item>
<term>Temporal_Mid_L</term>
<def>
<p>Left Middle Temporal Gyrus</p>
</def>
</def-item>
<def-item>
<term>Temporal_Mid_R</term>
<def>
<p>Right Middle Temporal Gyrus</p>
</def>
</def-item>
<def-item>
<term>Temporal_Inf_L</term>
<def>
<p>Left Inferior Temporal Gyrus</p>
</def>
</def-item>
<def-item>
<term>Temporal_Inf_R</term>
<def>
<p>Right Inferior Temporal Gyrus</p>
</def>
</def-item>
<def-item>
<term>Temporalpole_L</term>
<def>
<p>Left Temporal Pole</p>
</def>
</def-item>
<def-item>
<term>Temporalpole_R</term>
<def>
<p>Right Temporal Pole</p>
</def>
</def-item>
<def-item>
<term>Temporal_Sup_Banks_L</term>
<def>
<p>Left Superior Temporal Banks</p>
</def>
</def-item>
<def-item>
<term>Temporal_Sup_Banks_R</term>
<def>
<p>Right Superior Temporal Banks</p>
</def>
</def-item>
<def-item>
<term>Transversetemporal_L</term>
<def>
<p>Left Transverse Temporal Gyrus</p>
</def>
</def-item>
<def-item>
<term>Transversetemporal_R</term>
<def>
<p>Right Transverse Temporal Gyrus</p>
</def>
</def-item>
<def-item>
<term>Occipital_Lat_L</term>
<def>
<p>Left Lateral Occipital Cortex</p>
</def>
</def-item>
<def-item>
<term>Occipital_Lat_R</term>
<def>
<p>Right Lateral Occipital Cortex</p>
</def>
</def-item>
<def-item>
<term>Cerebral_WM_L</term>
<def>
<p>Left Cerebral White Matter</p>
</def>
</def-item>
<def-item>
<term>Cerebral_WM_R</term>
<def>
<p>Right Cerebral White Matter</p>
</def>
</def-item>
<def-item>
<term>Cerebellum_Cortex_L</term>
<def>
<p>Left Cerebellar Cortex</p>
</def>
</def-item>
<def-item>
<term>Cerebellum_Cortex_R</term>
<def>
<p>Right Cerebellar Cortex</p>
</def>
</def-item>
<def-item>
<term>Cerebellum_WM_L</term>
<def>
<p>Left Cerebellar White Matter</p>
</def>
</def-item>
<def-item>
<term>Cerebellum_WM_R</term>
<def>
<p>Right Cerebellar White Matter</p>
</def>
</def-item>
<def-item>
<term>Ventricle_3rd</term>
<def>
<p>Third Ventricle</p>
</def>
</def-item>
<def-item>
<term>Ventricle_4th</term>
<def>
<p>Fourth Ventricle</p>
</def>
</def-item>
<def-item>
<term>Pons</term>
<def>
<p>Pons</p>
</def>
</def-item>
<def-item>
<term>CSF</term>
<def>
<p>Cerebrospinal Fluid</p>
</def>
</def-item>
<def-item>
<term>Optic_Chiasm</term>
<def>
<p>Optic Chiasm</p>
</def>
</def-item>
<def-item>
<term>CC_Anterior</term>
<def>
<p>Anterior Corpus Callosum</p>
</def>
</def-item>
<def-item>
<term>CC_Mid_Anterior</term>
<def>
<p>Mid-Anterior Corpus Callosum</p>
</def>
</def-item>
<def-item>
<term>CC_Central</term>
<def>
<p>Central Corpus Callosum</p>
</def>
</def-item>
<def-item>
<term>CC_Mid_Posterior</term>
<def>
<p>Mid-Posterior Corpus Callosum</p>
</def>
</def-item>
<def-item>
<term>CC_Posterior</term>
<def>
<p>Posterior Corpus Callosum</p>
</def>
</def-item>
<def-item>
<term>Midbrain</term>
<def>
<p>Midbrain</p>
</def>
</def-item>
<def-item>
<term>Medulla</term>
<def>
<p>Medulla</p>
</def>
</def-item>
<def-item>
<term>SCP</term>
<def>
<p>Superior Cerebellar Peduncle</p>
</def>
</def-item>
</def-list>
</glossary>
</back>
</article>