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Contrast agents in magnetic resonance imaging: the new challenges regarding toxicity and increased safety

2019-09Conference object Open access
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dc.contributor.authorRibeiro, Margarida
dc.contributor.authorCoelho, André
dc.date.accessioned2019-11-27T15:13:22Z
dc.date.available2019-11-27T15:13:22Z
dc.date.issued2019-09
dc.description.abstractMagnetic Resonance Imaging (MRI) provides images of any part of the body with a multiplanar spatial location and is currently a widely used imaging method in the clinical diagnostic routine. Indeed, MRI provides better soft tissue contrast than the other imaging methods and can better differentiate fat, water, muscle, and other soft tissues. The first MRI contrast agent to be used as ferric chloride in 1981. Over the past 3 decades, many contrast agents have been developed for use in clinical practice and some of them were withdrawn due to safety conditions. The justified use of gadolinium-based contrast agents (GBCAs) carries some risks, including side effects such as allergic reactions and nephrogenic systemic fibrosis (NSF). The Gadolinium related toxicity has been documented for at least 10 years, with potentially life-threatening diseases recognized in 1997 in 15 dialyzed patients. The MRI contrast agents include T1-weighted (T1W) and T2-weighted contrast agents. Since its image signal increases the positive contrast, gadolinium (Gd) chelates as (T1W) contrast agents, dominate the current market of MRI. The current scientific evidence, from the last 4 years, recognizes a concentration-dependent deposition of gadolinium in the brain of the post-mortem human or animal mainly through the high signal intensities in the globus pallidus and dentate nucleus on T1Wimages, demonstrating roundly the residual deposition of gadolinium T1-hyperintensity in anatomical areas, raising new concerns on the safety of GBCAs. Since 2017 the International Society of Magnetic Resonance in Medicine (ISMRM) Safety Committee, the US Food and Drug Administration (FDA) and The Pharmacovigilance Risk Assessment Committee (PRAC) produced many recommendations and some restrictions on the use of linear gadolinium agents, giving preference to these contrast agents only for liver scans in low concentrations. From this recommendation, some types of linear agents were suspended and replaced by more stable and appropriate gadolinium agents known as macrocyclic agents, like gadoteric acid, gadobutrol, and gadoteridol. Regarding that problem, with the focus on the research of new contrast agents, new-typed nano-scaled T1W MRI contrast agents have been designed to overcome the draw-back of clinical gadolinium agents. So, due to the better biocompatibility compared with the Gd-chelates, magnetic iron oxide nanoparticles (MIONs) have been increasing attention as MRI contrast agents. So, due to the better biocompatibility compared with the Gd-chelates, MIONs have attracted increased attention as MRI contrast agents.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationRibeiro MM, Coelho A. Contrast agents in magnetic resonance imaging: the new challenges regarding toxicity and increased safety. In: ICEH 2019 – International Congress on Environmental Health, ESTeSL, Lisbon (Portugal), September 25-27, 2019.pt_PT
dc.identifier.urihttp://hdl.handle.net/10400.21/10759
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.relation.publisherversionhttps://iceh2019.estesl.ipl.pt/pt_PT
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/pt_PT
dc.subjectRadiologypt_PT
dc.subjectMagnetic resonance imagingpt_PT
dc.subjectClinical diagnosticpt_PT
dc.subjectContrast agentpt_PT
dc.titleContrast agents in magnetic resonance imaging: the new challenges regarding toxicity and increased safetypt_PT
dc.typeconference object
dspace.entity.typePublication
oaire.citation.conferencePlaceLisboapt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typeconferenceObjectpt_PT

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