# Development of Robust Brain Measurement Tools Informed by Ultrahigh Field 7T MRI

> **NIH NIH R01** · UNIV OF NORTH CAROLINA CHAPEL HILL · 2020 · $438,169

## Abstract

Development of Robust Brain Measurement Tools Informed by
 Ultrahigh Field 7T MRI
Abstract:
Summary. Neuroimaging can provide safe, non-invasive, and whole-brain measurements for large clinical and
research studies of brain disorders. However, many disorders such as Alzheimer's Disease (AD) cause
complex spatiotemporal patterns of brain alterations, which are often difficult to tease out due to limited image
quality afforded by the popular 3T MRI scanners (with 20,000+ units available worldwide). Although 7T MRI
scanners provide better image quality, these ultrahigh field scanners are not widely available (with only 40+
units available worldwide) and are also not used clinically. Thus, tools for reconstructing 7T-like high-quality
MRI from 3T MRI scan are highly desirable. A means for achieving this is by learning the relationship between
3T and 7T MRI scans from training samples. This renewal project is dedicated to developing a set of novel
learning-based methods to transfer image contrast and tissue/anatomical labels of 7T MRI of training subjects
to 3T MRI of new subjects for 1) image quality enhancement, 2) high-precision tissue segmentation, 3) accurate
anatomical ROI (region of interest) labeling, and eventually 4) early detection of brain disorders such as AD.
Specifically, (Aim 1) to enhance the image quality of 3T MRI, we will develop a novel deep learning
architecture to learn a complex multi-layer 3T-to-7T mapping from training subjects, each with coupled 3T and
7T MRI scans. This mapping will then be applied to reconstruct quality-enhanced 7T-like MRI scans from new
3T MRI scans. (Aim 2) For brain structural measurement (e.g., brain atrophies, and hippocampal volume
shrinkage), a crucial step is brain tissue segmentation. We will thus develop a robust and accurate random
forest tissue segmentation method, which maps 7T label information to 3T scans. The mapping function is
trained using tissue labels generated for 7T scans, instead of 3T scans which often have limited image contrast.
(Aim 3) To further quantify local atrophies in ROIs or even sub-ROIs (i.e., hippocampal subfields), we will
develop a deformable multi-ROI segmentation method by employing (a) random forest to predict
deformation from each image location to the target boundary by adaptive integration of multimodal (anatomical,
structural & functional connectivity) information and (b) auto-context model to iteratively refine ROI
segmentation results. Note that the adaptive integration of multimodal MRI data, especially resting-state fMRI
(rs-fMRI), is critical to the segmentation of sub-ROIs such as hippocampal subfields, since local functional
connectivity patterns can help distinguish boundaries between neighboring subfields that often have different
cortico-cortical connections. (Aim 4) Finally, by integrating anatomical features from all accurately segmented
ROIs/sub-ROIs and also structural & functional connectivity features between those segmented ROIs/sub-ROIs,
we ...

## Key facts

- **NIH application ID:** 9977173
- **Project number:** 5R01EB006733-11
- **Recipient organization:** UNIV OF NORTH CAROLINA CHAPEL HILL
- **Principal Investigator:** Pew-Thian Yap
- **Activity code:** R01 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2020
- **Award amount:** $438,169
- **Award type:** 5
- **Project period:** 2008-09-17 → 2023-05-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/9977173

## Citation

> US National Institutes of Health, RePORTER application 9977173, Development of Robust Brain Measurement Tools Informed by Ultrahigh Field 7T MRI (5R01EB006733-11). Retrieved via AI Analytics 2026-05-27 from https://api.ai-analytics.org/grant/nih/9977173. Licensed CC0.

---

*[NIH grants dataset](/datasets/nih-grants) · CC0 1.0*
