scholarly journals Perioperative Glial Fibrillary Acidic Protein Is Associated with Long-Term Neurodevelopment Outcome of Infants with Congenital Heart Disease

Children ◽  
2021 ◽  
Vol 8 (8) ◽  
pp. 655
Author(s):  
Michela Vergine ◽  
Luca Vedovelli ◽  
Manuela Simonato ◽  
Valentina Tonazzo ◽  
Alessio Correani ◽  
...  

Background: Brain injury, impaired brain maturation, and long-term neurodevelopmental disorders are common in infants with congenital heart diseases (CHD). We aimed to assess whether plasma glial fibrillary acidic protein (GFAP) can predict neurodevelopmental anomalies in CHD infants operated on cardiopulmonary bypass (CPB). Methods: We measured plasma GFAP in 38 infants at multiple CPB phases. Cognitive, neuropsychological, and psychopathological functioning were assessed 5.7 ± 2.2 years after surgery. We identified an impaired global neurodevelopmental index (NDI) when at least two domains were abnormal. The relationships between NDI, GFAP, and clinical variables were explored with non-supervised feature selection methods and modeled with a nested non-linear logistic regression. Results: Intelligence quotient scores were within the normal range in 84% of children, whereas 58% showed an abnormal NDI, with the greatest impairments in the psychopathological area. The plasma GFAP peak was 0.95 (0.44–1.57) ng/mL, and it was correlated with age, weight, duration of surgery phases, and CPB minimum temperature. In the regression model, the GFAP peak was associated with an impaired NDI with a possible flexible point toward NDI impairment at 0.49 ng/mL, keeping constant ICU stay, CPB duration, CHD anatomy, weight, and CPB minimum temperature. Conclusion: GFAP is a promising early marker of abnormal long-term neuropsychological development.

2018 ◽  
Vol 18 (4) ◽  
pp. 315-319 ◽  
Author(s):  
Angeliki Zarkali ◽  
Oliver Cousins ◽  
Dilan Athauda ◽  
Samuel Moses ◽  
Nicholas Moran ◽  
...  

Glial fibrillary acidic protein antibody-positive meningoencephalomyelitis is a newly described, possibly under-recognised, severe inflammatory condition of the nervous system. The clinical presentation is variable but most commonly is a combination of meningitis, encephalitis and myelitis; other manifestations may include seizures, psychiatric symptoms and tremor. There is a significant association with malignancies, often occult, and with other autoimmune conditions. Although the disease responds well to corticosteroids acutely, it typically relapses when these are tapered, and so patients need long-term immunosuppression. We report a young man presenting with subacute meningoencephalitis and subsequent myelitis, and discuss the typical presentation and management of this severe but treatable condition.


2015 ◽  
Vol 7 (4) ◽  
pp. 265
Author(s):  
Myriam Bensemlali ◽  
Meriem Mostefa Kara ◽  
Bettina Bessières ◽  
Fanny Bajolle ◽  
Laurent Fermont ◽  
...  

1995 ◽  
Vol 58 (SupplementIV) ◽  
pp. 1272-1276
Author(s):  
Munetaka Masuda ◽  
Shigeki Morita ◽  
Hiroyuki Kouno ◽  
Hisanori Mayumi ◽  
Ryuii Tominaga ◽  
...  

1996 ◽  
Vol 2 (2) ◽  
pp. 91-95 ◽  
Author(s):  
Mikio Ishikawa ◽  
Tetsuro Tsukamoto ◽  
Teiji Yamamoto

The chronic demyelinated plaque of multiple sclerosis (MS) is characterised by a loss of oligodendrocytes, astrogliosis, and incomplete or no remyelination which probably results in part from the suppressive effects of gliotic astrocytes on myelin formation. We explanted mouse cerebella on astrocyte cultures which had been maintained for 2 to 12 weeks and assessed the myelination in the cerebellar tissue at 18 days after explanation. Myelination occurred vigorously in the tissue explanted on 2-to 4-week-old astrocytes, but was poorer in the tissue explanted on astrocytes older than 4 weeks. No myelin sheath was formed on 12-week-old astrocytes, although axons developed equally as well as those in the tissues explanted on 2-week-old astrocytes. As astrocytes were maintained longer, they became fibrous and immunostained more deeply with anti-glial fibrillary acidic protein antibody, being analogous to astrogliosis. These findings imply that astrogliosis in chronic demyelinated lesions of MS may potentially block remyelination.


1981 ◽  
Vol 45 (2) ◽  
pp. 238-242 ◽  
Author(s):  
KOUICHI OGAWA ◽  
TAKAYUKI ITO ◽  
MASAAKI BAN ◽  
KEIJI MIZUTANI ◽  
MASAMI NAGASHIMA

2012 ◽  
Vol 34 (1) ◽  
pp. 64-69 ◽  
Author(s):  
Taiyu Hayashi ◽  
Ryo Inuzuka ◽  
Yusuke Shiozawa ◽  
Takahiro Shindo ◽  
Nobutaka Shimizu ◽  
...  

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