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Updated: May 12, 2026

High-resolution In Vivo Manual Segmentation Protocol for Human Hippocampal Subfields Using 3T Magnetic Resonance Imaging
Published on: November 10, 2015
Longitudinal MRI study of hippocampal subfields Morphometry in early Parkinson's disease
Tingyu Wu1, Samuel Yong-Ern Ng2, Thomas Wei Jun Teo2
1Duke-NUS Medical School, National University of Singapore, Singapore.
Background:
Parkinson's Disease (PD) is a neurodegenerative disorder characterised by motor and non-motor symptoms. Cognitive impairment is a prominent non-motor feature.
Objective:
This study investigated hippocampal subfield shape deformation and atrophy in early-stage PD using spherical harmonic-based shape analysis.
Methods:
Our cohort of early PD patients (n = 146; disease duration = 14.9 ± 9.5 months; 44% Female) and matched healthy controls (HC) (n = 59; 56% Female) underwent magnetic resonance imaging (MRI) and cognitive assessments at baseline and 2-year follow-up. Hippocampal subfields were segmented in FreeSurfer; shape analysed with SPHARM-PDM.
Results:
Baseline shape analysis identified morphological changes in Cornu Ammonis 1 (CA1), CA3, subiculum, and fimbria in early PD patients compared to HCs, despite no baseline volumetric differences. Longitudinally, volume decline/atrophy was observed in the right whole hippocampus, right CA1, and left fimbria. In the PD-Mild Cognitive Impairment (PD-MCI) subgroup, localised shape deformations in CA1, CA3, Granule Cell Layer and Molecular Layer of the Dentate Gyrus (GC-ML-DG), and fimbria were observed at baseline when compared to PD-Normal Cognition (PD-NC), with longitudinal left fimbria decline observed and associated with cognitive deterioration in this cohort, especially with visuospatial and executive function domains.
Conclusion:
These findings suggest that, in this cohort, shape analysis may capture baseline subfield differences that are not apparent using volumetric measures in early-stage PD. This study suggests hippocampal subfield shape analysis may help characterize early structural differences related to cognition in PD. The left fimbria warrants further study as a candidate imaging marker of cognitive vulnerability in PD.
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