Literature DB >> 7784132

Glial fibrillary acidic protein in the cerebrospinal fluid: a possible indicator of prognosis in full-term asphyxiated newborn infants?

M Blennow1, H Hagberg, L Rosengren.   

Abstract

Glial fibrillary acidic protein (GFAP) is the structural protein of intermediate filaments in astroglia. GFAP has extensively been used as a marker of gliosis in neuropathology. It also appears in excessive amounts in the cerebrospinal fluid in various acute brain disorders. Hypoxic-ischemic encephalopathy after perinatal asphyxia is a condition in which levels of GFAP could be expected to be elevated if brain cell damage occurs. We examined levels of GFAP by a sensitive ELISA in the cerebrospinal fluid of full-term infants between 12 and 48 h after birth. Cerebrospinal fluid-GFAP increased 5-fold in infants after perinatal asphyxia compared with a reference group (675 versus 137 ng/L, p < 0.001). The levels of GFAP also increased gradually in accordance with the severity of the neurologic symptoms ranked as degree of hypoxic-ischemic encephalopathy. We conclude that the cerebrospinal fluid levels of GFAP might be an important adjunct in the neonatal assessment of infants subject to perinatal asphyxia, and together with other neuronal or glial proteins, it might also help in defining temporal relationships in asphyxia.

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Year:  1995        PMID: 7784132     DOI: 10.1203/00006450-199503000-00002

Source DB:  PubMed          Journal:  Pediatr Res        ISSN: 0031-3998            Impact factor:   3.756


  6 in total

1.  Plasma glial fibrillary acidic protein levels in a child with sickle cell disease and stroke.

Authors:  William J Savage; Allen D Everett; James F Casella
Journal:  Acta Haematol       Date:  2010-11-24       Impact factor: 2.195

Review 2.  Bedside and laboratory neuromonitoring in neonatal encephalopathy.

Authors:  L Chalak; L Hellstrom-Westas; S Bonifacio; T Tsuchida; V Chock; M El-Dib; An N Massaro; A Garcia-Alix
Journal:  Semin Fetal Neonatal Med       Date:  2021-07-28       Impact factor: 3.726

3.  Serum brain injury biomarkers are gestationally and post-natally regulated in non-brain injured neonates.

Authors:  Sandra Brooks; Barbara D Friedes; Frances Northington; Ernest Graham; Aylin Tekes; Vera J Burton; Gwendolyn Gerner; Jie Zhu; Raul Chavez-Valdez; Dhananjay Vaidya; Allen D Everett
Journal:  Pediatr Res       Date:  2021-12-18       Impact factor: 3.953

Review 4.  Current and Emerging Therapies in the Management of Hypoxic Ischemic Encephalopathy in Neonates.

Authors:  Jayasree Nair; Vasantha H S Kumar
Journal:  Children (Basel)       Date:  2018-07-19

5.  Serial blood cytokine and chemokine mRNA and microRNA over 48 h are insult specific in a piglet model of inflammation-sensitized hypoxia-ischaemia.

Authors:  Ingran Lingam; Adnan Avdic-Belltheus; Christopher Meehan; Kathryn Martinello; Sara Ragab; Donald Peebles; Melinda Barkhuizen; Cally J Tann; Ilias Tachtsidis; Tim G A M Wolfs; Henrik Hagberg; Nigel Klein; Bobbi Fleiss; Pierre Gressens; Xavier Golay; Boris W Kramer; Nicola J Robertson
Journal:  Pediatr Res       Date:  2020-06-10       Impact factor: 3.756

6.  Glial Fibrillary Acidic Protein Is Not an Early Marker of Injury in Perinatal Asphyxia and Hypoxic-Ischemic Encephalopathy.

Authors:  Ann-Marie Looney; Caroline Ahearne; Geraldine B Boylan; Deirdre M Murray
Journal:  Front Neurol       Date:  2015-12-21       Impact factor: 4.003

  6 in total

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