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  4. MRI-based brain volumetry and retinal optical coherence tomography as the biomarkers of outcome in acute methanol poisoning.
 
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Titre

MRI-based brain volumetry and retinal optical coherence tomography as the biomarkers of outcome in acute methanol poisoning.

Type
article
Institution
UNIL/CHUV/Unisanté + institutions partenaires
Périodique
NeuroToxicology  
Auteur(s)
Hlusicka, J.
Auteure/Auteur
Mana, J.
Auteure/Auteur
Vaneckova, M.
Auteure/Auteur
Kotikova, K.
Auteure/Auteur
Diblik, P.
Auteure/Auteur
Urban, P.
Auteure/Auteur
Navratil, T.
Auteure/Auteur
Marechal, B.
Auteure/Auteur
Kober, T.
Auteure/Auteur
Zakharov, S.
Auteure/Auteur
Liens vers les personnes
Maréchal, Bénédicte  
Liens vers les unités
Radiodiagnostic & radiol. Interven.  
ISSN
1872-9711
Statut éditorial
Publié
Date de publication
2020-09
Volume
80
Première page
12
Dernière page/numéro d’article
19
Peer-reviewed
Oui
Langue
anglais
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov't
Publication Status: ppublish
Résumé
Basal ganglia lesions are typical findings on magnetic resonance imaging (MRI) of the brain in survivors of acute methanol poisoning. However, no data are available on the association between the magnitude of damaged brain regions, serum concentrations of markers of acute methanol toxicity, oxidative stress, neuroinflammation, and the rate of retinal nerve ganglion cell loss.
To investigate the association between MRI-based volumetry of the basal ganglia, retinal nerve fibre layer (RNFL) thickness and prognostic laboratory markers of outcomes in acute methanol poisoning.
MRI-based volumetry of putamen, nucleus caudatus and globus pallidus was performed and compared with laboratory parameters of severity of poisoning and acute serum markers of oxidative damage of lipids (8-isoprostan, MDA, HHE, HNE), nucleic acids (8-OHdG, 8-OHG, 5-OHMU), proteins (o-Thyr, NO-Thyr, Cl-Thyr) and leukotrienes (LTC4, LTD4, LTE4, LTB4), as well as with the results of RNFL measurements by optic coherence tomography (OCT) in 16 patients with acute methanol poisoning (Group I) and in 28 survivors of poisoning two years after discharge with the same markers measured within the follow-up examination (Group II). The control group consisted of 28 healthy subjects without methanol poisoning.
The survivors of acute methanol poisoning had significantly lower volumes of basal ganglia than the controls. The patients with MRI signs of methanol-induced toxic brain damage had significantly lower volumes of basal ganglia than those without these signs. A positive correlation was found between the volume of putamen and arterial blood pH on admission (r = 0.45; p = 0.02 and r = 0.44; p = 0.02 for left and right putamen, correspondingly). A negative correlation was present between the volumes of putamen and acute serum lactate (r = -0.63; p < 0.001 and r = -0.59; p = 0.01), creatinine (r = -0.53; p = 0.01 and r = -0.47; p = 0.01) and glucose (r = -0.55; p < 0.001 and r = -0.50; p = 0.01) concentrations. The volume of basal ganglia positively correlated with acute concentrations of markers of lipoperoxidation (8-isoprostan: r = 0.61; p < 0.05 and r = 0.59; p < 0.05 for left and right putamen, correspondingly) and inflammation (leukotriene LTB4: r = 0.61; p < 0.05 and r = 0.61; p < 0.05 for left and right putamen, correspondingly). The higher the volume of the basal ganglia, the higher the thickness of the RNFL, with the strongest positive association between global RNFL and the volume of putamen bilaterally (all p < 0.01). In the follow-up markers of oxidative stress and inflammation, only o-Thyr concentration negatively correlated with the volume of putamen bilaterally (r = -0.39; p < 0.05 and r = -0.37; p < 0.05 for left and right putamen, correspondingly).
In survivors of acute methanol poisoning with signs of toxic brain damage, the magnitude of affected areas correlated with acute parameters of severity of poisoning, markers of oxidative stress and neuroinflammation. There was a positive association between the basal ganglia volume and the thickness of RNFL, making OCT an important screening test and MRI-based volumetry the confirmative diagnostic method for the detection of CNS sequelae of methanol poisoning.
Sujets

Adult

Basal Ganglia/diagnos...

Basal Ganglia/drug ef...

Basal Ganglia/metabol...

Biomarkers/blood

Case-Control Studies

Female

Humans

Inflammation Mediator...

Magnetic Resonance Im...

Male

Methanol/poisoning

Middle Aged

Nerve Fibers/drug eff...

Organ Size

Oxidative Stress

Poisoning/blood

Poisoning/diagnostic ...

Predictive Value of T...

Retina/diagnostic ima...

Retina/drug effects

Retina/metabolism

Severity of Illness I...

Tomography, Optical C...

Long-term CNS sequela...

Methanol toxicity

Prognostic parameters...

Toxic brain damage

PID Serval
serval:BIB_455F36653A53
DOI
10.1016/j.neuro.2020.06.006
PMID
32554081
WOS
000571495600002
Permalien
https://iris.unil.ch/handle/iris/36281
Date de création
2020-07-06T12:01:46.613Z
Date de création dans IRIS
2025-05-20T13:39:53Z
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