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D2 receptor imaging in neonates using I-123 iodobenzamide brain SPECT.
F Tranquart1, E Saliba, L Barantin
1INSERM Unit 316, CHU Tours, France. tranquart@med.univ-tours.fr
Clinical Nuclear Medicine
|January 4, 2001
Summary
Iodine-123 iodobenzamide brain SPECT can assess D2 receptor viability in neonates after hypoxic-ischemic events. This imaging method shows early D2 receptor maturation and potential damage from perinatal injury.
Area of Science:
- Neonatal neurology
- Neuroimaging
- Biochemical markers
Background:
- Hypoxic-ischemic injury in neonates can lead to severe neurodevelopmental impairments, including cerebral palsy.
- Damage to the striatum is often associated with the dyskinetic form of cerebral palsy.
- Early detection of brain injury and its impact on neurochemistry is crucial for intervention.
Purpose of the Study:
- To evaluate the viability of dopamine D2 receptors in the perinatal period using I-123 iodobenzamide brain SPECT.
- To correlate D2 receptor viability with early neurologic status in neonates following hypoxic-ischemic events.
Main Methods:
- 12 full-term neonates with hypoxic-ischemic events underwent I-123 iodobenzamide brain SPECT one week after birth.
- SPECT imaging was performed one hour after intravenous injection of I-123 iodobenzamide.
- Brain magnetic resonance imaging (T2 weighted) was acquired on the same day for comparison.
Main Results:
- I-123 iodobenzamide concentrated in the striatum, with striatum:cerebellum activity ratios ranging from 1.28 to 2.25.
- A trend towards decreased striatum:cerebellum ratios was observed with increasing severity of hypoxic-ischemic events.
- Striatal hypersignal on MRI was noted in only two neonates, highlighting SPECT's potential for detecting biochemical changes.
Conclusions:
- I-123 iodobenzamide is a viable imaging agent for use in the neonatal period.
- The study demonstrates the biochemical maturation of D2 receptors as early as one week postpartum.
- Perinatal hypoxic-ischemic events appear to have a deleterious effect on D2 receptor function.