2021
DOI: 10.1007/s12035-021-02562-z
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Serum Neurofilament Light: a Potential Diagnostic and Prognostic Biomarker in Obstetric Posterior Reversible Encephalopathy Syndrome

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Cited by 4 publications
(4 citation statements)
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“…NfL is a marker of neuroaxonal damage in primary and non-primary neurological diseases [32]. To date, only one study has investigated and demonstrated an increase in serum NfL in patients with PRES [33]. Our case report supports these observations, but we cannot exclude the significant confounding effects of cerebral haemorrhage and neurosurgical treatment on NfL concentrations as described previously [13,34].…”
Section: Discussionsupporting
confidence: 77%
“…NfL is a marker of neuroaxonal damage in primary and non-primary neurological diseases [32]. To date, only one study has investigated and demonstrated an increase in serum NfL in patients with PRES [33]. Our case report supports these observations, but we cannot exclude the significant confounding effects of cerebral haemorrhage and neurosurgical treatment on NfL concentrations as described previously [13,34].…”
Section: Discussionsupporting
confidence: 77%
“…Regarding biomarkers and therapeutic studies in PRES, there is no preclinical data and little clinical data, leaving a large field of research requiring suitable animal models. Indeed, with the exception of 2 studies on serum neurofilaments light, a marker of neuroaxonal injury, 42 4 In this sense, experimental animal models could help meet diagnostic challenges by studying biological and radiological biomarkers. The mixed PRES model of Kimura et al 35 highlights the importance of the fractional anisotropy increase as a marker for the reversibility of brain edema.…”
Section: Perspectivesmentioning
confidence: 99%
“…Regarding biomarkers and therapeutic studies in PRES, there is no preclinical data and little clinical data, leaving a large field of research requiring suitable animal models. Indeed, with the exception of 2 studies on serum neurofilaments light, a marker of neuroaxonal injury, 42 or copeptin, a precursor of AVP, 43 the assessment of clinical biomarkers in PRES is poorly studied. Most available studies have focused on nonspecific biomarkers (eg, transaminases, albumin, lactate dehydrogenase), which do not specifically access pharmacological targets.…”
Section: Perspectivesmentioning
confidence: 99%
“…MRI can be used as a gold standard for the diagnosis of PRES. 17,18 Fang et al 19 found that the serum neurofilament light (NFL) level of patients with PRES increased, which may provide an important research direction for the diagnosis and prognosis of PRES.…”
Section: Diagnosismentioning
confidence: 99%