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Published on: December 4, 2016
Pediatric Patients Demonstrate Progressive T1-Weighted Hyperintensity in the Dentate Nucleus following Multiple Doses
D R Roberts1,2, A R Chatterjee3, M Yazdani3
1From the Departments of Radiology and Radiological Sciences (D.R.R., A.R.C., M.Y., B.M., T.B., H.C., G.B.) robertdr@musc.edu.
Insights
Pediatric patients receiving multiple gadolinium-based contrast agent (GBCA) doses show increased T1 signal in the dentate nucleus. This suggests gadolinium retention in the pediatric brain, warranting cautious use of these agents.
Area of Science:
- Neuroradiology
- Pediatric Imaging
- Magnetic Resonance Imaging
Background:
- Gadolinium retention in the adult brain after contrast administration is documented.
- Pediatric brain retention of gadolinium has not been previously reported.
- Gadolinium-based contrast agents (GBCAs) are widely used in pediatric MRI.
Purpose of the Study:
- To investigate the relationship between GBCA dose number and T1 signal intensity in the pediatric dentate nucleus.
- To determine if pediatric patients exhibit dose-dependent gadolinium retention.
- To assess potential gadolinium deposition in the developing brain.
Main Methods:
- Retrospective analysis of pediatric patients receiving multiple GBCA doses.
- ROI analysis of dentate nucleus and cerebellar white matter on unenhanced T1-weighted MRI.
- Comparison of dentate-to-cerebellar white matter and dentate-to-pons ratios with GBCA dose number.
Main Results:
- Significant correlation found between GBCA dose number and increased T1 signal in the dentate nucleus (r=0.77, P=.001).
- Automated ROI analysis confirmed significant correlation between GBCA doses and dentate hyperintensity (P<.0001).
- Dose-dependent T1 signal changes were observed in pediatric brains.
Conclusions:
- GBCA administration in pediatric patients is associated with progressive T1-weighted dentate hyperintensity.
- Potential clinical effects of gadolinium retention in the developing brain remain unknown.
- Recommend cautious GBCA use in children, favoring higher-stability agents and detailed dose tracking.
Background And Purpose:
While there have been recent reports of brain retention of gadolinium following gadolinium-based contrast agent administration in adults, a retrospective series of pediatric patients has not previously been reported, to our knowledge. We investigated the relationship between the number of prior gadolinium-based contrast agent doses and increasing T1 signal in the dentate nucleus on unenhanced T1-weighted MR imaging. We hypothesized that despite differences in pediatric physiology and the smaller gadolinium-based contrast agent doses that pediatric patients are typically administered based on weighted-adjusted dosing, the pediatric brain would also demonstrate dose-dependent increasing T1 signal in the dentate nucleus.
Materials And Methods:
We included children with multiple gadolinium-based contrast agent administrations at our institution. A blinded reader placed ROIs within the dentate nucleus and adjacent cerebellar white matter. To eliminate reader bias, we also performed automated ROI delineation of the dentate nucleus, cerebellar white matter, and pons. Dentate-to-cerebellar white matter and dentate-to pons ratios were compared with the number of gadolinium-based contrast agent administrations.
Results:
During 20 years at our institution, 280 patients received at least 5 gadolinium-based contrast agent doses, with 1 patient receiving 38 doses. Sixteen patients met the inclusion/exclusion criteria for ROI analysis. Blinded reader dentate-to-cerebellar white matter ratios were significantly associated with gadolinium-based contrast agent doses (rs = 0.77, P = .001). The dentate-to-pons ratio and dentate-to-cerebellar white matter ratios based on automated ROI placement were also significantly correlated with gadolinium-based contrast agent doses (t = 4.98, P < .0001 and t = 2.73, P < .02, respectively).
Conclusions:
In pediatric patients, the number of prior gadolinium-based contrast agent doses is significantly correlated with progressive T1-weighted dentate hyperintensity. Definitive confirmation of gadolinium deposition requires tissue analysis. Any potential clinical sequelae of gadolinium retention in the developing brain are unknown. Given this uncertainty, we suggest taking a cautious stance, including the use, in pediatric patients, of higher stability, macrocyclic agents, which in both human and animal studies have been shown to be associated with lower levels of gadolinium deposition, and detailed documentation of dosing. Most important, a patient should not be deprived of a well-indicated contrasted MR examination.
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