# 3T sodium-MRI as predictor of neurocognition in nondemented older adults: a cross sectional study

**Authors:** Elaine Lui, Vijay K Venkatraman, Sue Finch, Michelle Chua, Tie-Qiang Li, Bradley P Sutton, Christopher E Steward, Bradford Moffat, Elizabeth V Cyarto, Kathryn A Ellis, Christopher C Rowe, Colin L Masters, Nicola T Lautenschlager, Patricia M Desmond

PMC · DOI: 10.1093/braincomms/fcae307 · Brain Communications · 2024-09-11

## TL;DR

This study finds that sodium-MRI measurements in the hippocampus better predict cognitive scores in older adults than traditional brain volume measurements.

## Contribution

The study introduces sodium-MRI as a novel imaging biomarker for early cognitive assessment in older adults.

## Key findings

- Left hippocampal sodium-MRI (Na-SI) was a better predictor of MMSE and ADAS-Cog11 scores than volume.
- Right entorhinal Na-SI outperformed volume in predicting ADAS-Cog11 scores.
- Adding amyloid PET status improved model fit for all cognitive metrics.

## Abstract

Dementia is a burgeoning global problem. Novel magnetic resonance imaging (MRI) metrics beyond volumetry may bring new insight and aid clinical trial evaluation of interventions early in the Alzheimer’s disease course to complement existing imaging and clinical metrics. To determine whether: (i) normalized regional sodium-MRI values (Na-SI) are better predictors of neurocognitive status than volumetry (ii) cerebral amyloid PET status improves modelling. Nondemented older adult (>60 years) volunteers of known Alzheimer's Disease Assessment Scale (ADAS-Cog11), Mini-Mental State Examination (MMSE) and Consortium to Establish a Registry for Alzheimer's Disease (CERAD) neurocognitive test scores, ApolipoproteinE (APOE) e4 +/− cerebral amyloid PET status were prospectively recruited for 3T sodium-MRI brain scans. Left and right hippocampal, entorhinal and precuneus volumes and Na-SI (using the proportional intensity scaling normalization method with field inhomogeneity and partial volume corrections) were obtained after segmentation and co-registration of 3D-T1-weighted proton images. Descriptive statistics, correlation and best-subset regression analyses were performed. In our 76 nondemented participants (mean(standard deviation) age 75(5) years; woman 47(62%); cognitively unimpaired 54/76(71%), mildly cognitively impaired 22/76(29%)), left hippocampal Na-SI, not volume, was preferentially in the best models for predicting MMSE (Odds Ratio (OR) = 0.19(Confidence Interval (CI) = 0.07,0.53), P-value = 0.001) and ADAS-Cog11 (Beta(B) = 1.2(CI = 0.28,2.1), P-value = 0.01) scores. In the entorhinal analysis, right entorhinal Na-SI, not volume, was preferentially selected in the best model for predicting ADAS-Cog11 (B = 0.94(CI = 0.11,1.8), P-value = 0.03). While right entorhinal Na-SI and volume were both selected for MMSE modelling (Na-SI OR = 0.23(CI = 0.09,0.6), P-value = 0.003; volume OR = 2.6(CI = 1.0,6.6), P-value = 0.04), independently, Na-SI explained more of the variance (Na-SI R2 = 10.3; volume R2 = 7.5). No imaging variable was selected in the best CERAD models. Adding cerebral amyloid status improved model fit (Akaike Information Criterion increased 2.0 for all models, P-value < 0.001–0.045). Regional Na-SI were more predictive of MMSE and ADAS-Cog11 scores in our nondemented older adult cohort than volume, hippocampal more robust than entorhinal region of interest. Positive amyloid status slightly further improved model fit.

Lui & Venkatraman et al. report that normalized hippocampal sodium MRI signal were more predictive of Alzheimer's Disease Assessment Scale Cognitive subscale and Mini-Mental State Examination scores in a nondemented older adult cohort than hippocampal cortical volumes and conclude that sodium MRI may have applications as an imaging neurocognitive marker.

Graphical Abstract

## Linked entities

- **Genes:** APOE (apolipoprotein E) [NCBI Gene 348]
- **Diseases:** Alzheimer's disease (MONDO:0004975)

## Full-text entities

- **Diseases:** amyloid (MESH:C000718787), Dementia (MESH:D003704), cerebral amyloid (MESH:D016657), Alzheimer's Disease (MESH:D000544)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

46 references — full list in the complete paper: https://tomesphere.com/paper/PMC11420980/full.md

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Source: https://tomesphere.com/paper/PMC11420980