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Dopaminergic imaging separates normal pressure hydrocephalus from its mimics
Gilles Allali1,2,3, Valentina Garibotto4, Ismini C Mainta4
1Division of Neurology, Department of Clinical Neurosciences, Geneva University Hospitals and University of Geneva, Geneva, Switzerland. gilles.allali@hcuge.ch.
Journal of Neurology
|August 30, 2018
Summary
Semi-quantitative [123I]FP-CIT SPECT imaging reliably differentiates idiopathic normal pressure hydrocephalus (iNPH) from mimic conditions. This neuroimaging biomarker aids in selecting iNPH patients for shunt surgery.
Area of Science:
- Neurology
- Neuroimaging
- Nuclear Medicine
Background:
- Idiopathic normal pressure hydrocephalus (iNPH) shares clinical symptoms with mimic conditions like Parkinson's disease, leading to diagnostic challenges.
- Distinguishing iNPH from mimics often requires invasive and time-consuming investigations.
Purpose of the Study:
- To compare visual and semi-quantitative [123I]FP-CIT SPECT imaging in differentiating iNPH from iNPH mimics.
- To evaluate [123I]FP-CIT SPECT as a potential biomarker for iNPH diagnosis.
Main Methods:
- 56 patients with suspected iNPH were assessed, with 26 diagnosed with iNPH and 30 as mimics.
- Visual assessment and semi-quantitative striatal binding ratios (SBR) of [123I]FP-CIT SPECT were analyzed.
- Logistic regression was used to determine the association between SPECT findings and diagnosis.
Main Results:
- A normal SBR on [123I]FP-CIT SPECT was observed in 69.2% of iNPH patients versus 37.9% of mimics (p=0.020).
- Visual assessment of SPECT scans did not significantly differ between the groups.
- Normal SBR values were significantly associated with an iNPH diagnosis, even after adjusting for confounding factors (aOR=4.17).
Conclusions:
- Semi-quantitative [123I]FP-CIT SPECT analysis effectively discriminates iNPH from its mimics.
- Visual assessment of [123I]FP-CIT SPECT is insufficient for differentiation.
- [123I]FP-CIT SPECT shows promise as a neuroimaging biomarker to improve patient selection for iNPH interventions.

