Brain tissue gadolinium retention in pediatric patients after contrast-enhanced magnetic resonance exams: pathological confirmation.

Background: Retained gadolinium from gadolinium-based contrast agents (GBCAs) used in MR exams has been inferred based on signal changes on serial brain MRI and subsequently demonstrated pathologically in adults. Retention has been similarly inferred in children but pathological demonstration in ped...

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Published in:Pediatric Radiology Vol. 50; no. 3; pp. 388 - 397
Main Authors: Stanescu, A. Luana, Shaw, Dennis W., Murata, Nozomu, Murata, Kiyoko, Rutledge, Joe C., Maloney, Ezekiel, Maravilla, Kenneth R.
Format: research Journal Article
Published: Springer Nature Mar2020
Online Access:View this record in EBSCOhost
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      pub: Springer Nature
      place: New York, New York
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        atl: Brain tissue gadolinium retention in pediatric patients after contrast-enhanced magnetic resonance exams: pathological confirmation.
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        au:
          Stanescu, A. Luana
          Shaw, Dennis W.
          Murata, Nozomu
          Murata, Kiyoko
          Rutledge, Joe C.
          Maloney, Ezekiel
          Maravilla, Kenneth R.
        affil: Department of Radiology, Seattle Children's Hospital, University of Washington, 4800 Sand Point Way NE, M/S MA 7.220, 98105, Seattle, WA, USA
      sug:
        subj:
          Contrast Media Pharmacokinetics
          Elements Pharmacokinetics
          Image Enhancement Methods
          Brain Metabolism
          Magnetic Resonance Imaging Methods
          Autopsy
          Brain Drug Effects
          Cadaver
          Child, Preschool
          Female
          Adolescence
          Retrospective Design
          Child
          Male
          Scales
          Child, Preschool: 2-5 years
          Adolescent: 13-18 years
          Child: 6-12 years
          Female
          Male
      ab: Background: Retained gadolinium from gadolinium-based contrast agents (GBCAs) used in MR exams has been inferred based on signal changes on serial brain MRI and subsequently demonstrated pathologically in adults. Retention has been similarly inferred in children but pathological demonstration in pediatric patients is limited. The long-term effects of retained gadolinium are unknown but are potentially of greater concern in children given their increased vulnerability from continuing development and their expected longer period of exposure. Several factors can influence gadolinium retention. In adults as well as in children, greater accumulation has been demonstrated based on MR signal changes with linear compared with macrocyclic gadolinium chelates, attributed to lower chelate affinity with linear agents. Effects of age at exposure on retention are unknown, while differences in GBCA washout rates are still under investigation and might affect gadolinium retention relative to time of GBCA administration.Objective: The purpose of this study was to confirm whether gadolinium brain deposits are present in pediatric patients who received GBCAs and to quantify the amounts present.Materials and Methods: Brain autopsy specimens from 10 pediatric patients between 1 year and 13 years of age who underwent at least one contrast-enhanced MR exam were analyzed for elemental gadolinium using inductively coupled plasma mass spectrometry. Brain samples included white matter, basal ganglia (putamen, globus pallidus), thalamus, dentate nucleus and tumor tissue as available. Type and dose of contrast agent, number and timing of contrast-enhanced MR exams and renal function (estimated glomerular filtration rate [eGFR]) were documented for each child.Results: Patient exposures ranged from 1 dose to 20 doses of GBCAs including both macrocyclic and linear ionic agents. Gadolinium was found to be present in brain tissue in all children and was generally highest in the globus pallidus. Those who received only macrocyclic agents showed lower levels of gadolinium retention.Conclusion: This study demonstrates pathological confirmation of gadolinium retention in brain tissue of a series of pediatric patients exposed to GBCAs including not only linear ionic agents but also macrocyclic agents with both nonionic and ionic compounds. The distribution and deposition levels in this small pediatric population are comparable with the findings in adults. While the clinical significance of these deposits remains unknown, at this point it would be prudent to exert caution and avoid unnecessary use of GBCAs in pediatric patients.
      pubtype: Academic Journal
      doctype:
        research
        Journal Article
      ougenre: Article
    language: English
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