Impact Factor 3.552

The 2nd most cited open-access journal in Clinical Neurology

Original Research ARTICLE

Front. Neurol., 21 December 2015 | https://doi.org/10.3389/fneur.2015.00264

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

  • Neonatal Brain Research Group, Department of Paediatrics and Child Health, Irish Centre for Fetal and Neonatal Translational Research, Cork University Maternity Hospital, Cork, Ireland

Brain-specific glial fibrillary acidic protein (GFAP) has been suggested as a potential biomarker for hypoxic ischemic encephalopathy (HIE) in newborns (1, 2). Previous studies have shown increased levels in post-natal blood samples. However, its ability to guide therapeutic intervention in HIE is unknown. Therapeutic hypothermia for HIE must be initiated within 6 h of birth, therefore a clinically useful marker of injury would have to be available immediately following delivery. The goal of our study was to examine the ability of GFAP to predict grade of encephalopathy and neurological outcome when measured in umbilical cord blood (UCB). Infants with suspected perinatal asphyxia (PA) and HIE were enrolled in a single, tertiary maternity hospital, where UCB was drawn, processed, and bio-banked at birth. Expression levels of GFAP were measured by ELISA. In total, 169 infants (83 controls, 56 PA, 30 HIE) were included in the study. GFAP levels were not increased in UCB of case infants (PA/HIE) when compared to healthy controls or when divided into specific grades of HIE. Additionally, no correlation was found between UCB levels of GFAP and outcome at 36 months.

Introduction

Perinatal asphyxia (PA) occurs when there is a disruption of oxygen delivery or blood supply to the fetus around time of birth. PA, when severe, leads to hypoxic–ischemic encephalopathy (HIE) in the neonatal period. HIE remains one of the leading clinical challenges faced in the neonatal period and the greatest cause of acquired brain injury in term infants. To optimize outcomes in neonatal HIE, early and accurate prediction of the degree of encephalopathy is vital. Neuroprotective therapies must be commenced prior to the development of secondary brain injury, giving a narrow therapeutic window of <6 h after delivery (3). Approximately 20 per 1000 live births will require significant resuscitation at birth, and 10% of these infants will go on to have moderate-to-severe encephalopathy. Using currently available assessment methods, it is estimated that 20% of infants with significant hypoxic injury are clinically misclassified in the first hours of life and do not receive hypothermia (4). Thus, there is a critical need for improved biomarkers for prediction of grade of HIE and outcome (5).

Glial fibrillary acidic protein (GFAP), a monomeric intermediate filament protein predominant in astrocytes is known to display increased expression following acute brain injury or CNS degeneration (6). Previous studies, primarily carried out in adults have reported elevated levels of GFAP in traumatic brain injury, specifically related to focal mass lesions (7). Its use as a biomarker of HIE has previously been suggested, but the ability to differentiate between PA and HIE at birth has not been examined (1). Furthermore, little work has been carried out to determine the use of GFAP as a marker of moderate/severe HIE specifically to guide therapeutic intervention. To improve our ability to identify infants who will benefit from therapeutic hypothermia in time for effective intervention, any clinically useful biomarker will need to be reliably altered at or soon after birth.

Therefore, our aim was to examine the use of GFAP as an early clinical marker of HIE severity in full-term neonates by determining expression in umbilical cord blood (UCB) samples from healthy control infants, infants with perinatal asphyxia, and infants with HIE. We also wished to examine correlation of UCB GFAP with neurological outcome at 36 months.

Materials and Methods

Study Population

The BiHIVE Study (Biomarkers of HIE), including all recruitment, consenting, and sample processing procedures, was approved by the Clinical Research Ethics Committee of the Cork Teaching Hospitals. Through this study, any infant with suspected perinatal asphyxia or HIE in Cork University Maternity Hospital (CUMH), Ireland born between May 2009 and June 2011, was recruited as previously described (8). Briefly, infants >36 weeks gestational age were identified under strict enrollment criteria: cord pH <7.1 and/or Apgar score ≤6 at 5 min of life and/or requiring intubation or CPR at birth. Once infants were stable, parents were approached and informed about the study and written consent was obtained for each infant. All clinical and demographic information deemed relevant to the study was then recorded prospectively. Healthy matched controls were recruited through the BASELINE Study (www.baselinestudy.net), a longitudinal birth cohort study based in Cork. Controls were matched for sex, gestation, birth-weight, and gender, and all had uncomplicated deliveries.

Cord Blood Sampling

Umbilical cord blood samples were collected immediately after delivery of all infants in this study and processed within 3 h following strict laboratory SOPs by a dedicated research team who were available 24 h a day. Samples were stored at −80°C in a monitored storage facility until analysis.

Neonatal Assessment

All infants with suspected HIE received continuous multi-channel EEG monitoring. Our protocol for EEG monitoring has been previously described (9). Clinical grade of encephalopathy was assigned by a dedicated research fellow (BW) using the modified Sarnat score. Additionally, grade was further confirmed using EEG analysis with an experienced neonatal electroencephalographer (GB) who reviewed all EEG data. Therapeutic hypothermia was commenced at the discretion of clinicians blinded to the study data in all infants deemed to have moderate or severe encephalopathy using the TOBY registry treatment criteria and protocol (3).

GFAP Analysis

Glial fibrillary acidic protein analysis was carried out by Banyan Biomarkers Inc., Alachua, FL, USA, on UCB serum samples using Banyan Biomarker’s proprietary sandwich Enzyme-Linked Immunosorbent Assays (ELISA) specific to GFAP. Detection levels for the Banyan Assay range from 0.03 to 50 ng/ml. All samples were run in duplicate and inter/intra assay variabilities of <10% were reported.

Neurodevelopment Outcome

Where possible, developmental outcome was assessed at 36 months of age using the Bayley Scales of Infant and Toddler Development (Ed. III) (BSID-III) or the Ages and Stages Questionnaire (Ed. III) Ages and Stages Questionnaire (ASQ3) when the BSID-III was not possible due to reasons such as family relocation, etc. The Ages and Stages Questionnaire (ASQ3) is a parent-completed developmental screening questionnaire. It consists of 30 developmental items organized into five areas: Communication, Gross Motor, Fine Motor, Problem-Solving, and Personal–Social. Questionnaires for each child’s appropriate age interval were administered.

All BSID-III assessments were performed by a dedicated research fellow blinded to the clinical history of the patients (CA). For infants who underwent the assessment using the BSID-III, outcome was determined using the composite scores of the three subscales; cognitive, language, and motor. Infants were deemed to have an abnormal outcome if they scored ≤85 in two or more subscales or suffered neonatal death, cerebral palsy or autism. For infants who were assessed with ASQ3 only, results were considered abnormal if scores indicated the need for further assessment, falling >2 SD below the standardized mean, was advised in more than one area.

Statistical Analysis

Statistical analysis was performed using IBM SPSS Statistics 22 (SPSS Inc., USA). Results were calculated using Student t-tests, Mann–Whitney, and Kruskal–Wallis tests, as appropriate.

Results

Study Population

In total, 169 infants were included in this study; 83 controls and 86 HIE cases. Of the 86 cases, 56 were classified as perinatal asphyxia without HIE, 21 with mild HIE, 5 with moderate HIE, and 4 with severe HIE, according to both the modified Sarnat assessment and EEG classification. Population demographics for the entire cohort are shown in Table 1.

TABLE 1
www.frontiersin.org

Table 1. Comparison of population demographics for entire study cohort (n = 169).

GFAP Expression

On analysis of ELISA results, there was no statistically significant difference in serum GFAP levels between case and control infants within this study (p = 0.287). Similarly, when case infants were grouped as PA without HIE (n = 56) and infants with HIE (n = 30), no difference was observed (p = 0.566, Figure 1). Additionally, when grade of HIE was specifically analyzed, no difference was observed between UCB levels of GFAP in mild, moderate or severe HIE (0.199 ± 0.095 ng/ml vs. 0.216 ± 0.087 ng/ml vs. 0.168 ± 0.258 ng/ml, p = 0.931). Finally, when grouped as infants who would be deemed eligible for therapeutic hypothermia (n = 9) vs. those who would not (n = 160), again no increase was observed (p = 0.919, Figure 2).

FIGURE 1
www.frontiersin.org

Figure 1. Boxplot representing umbilical cord blood (UCB) levels of GFAP (ng/ml) following commercial ELISA analysis. Infants grouped as healthy controls (n = 83), infants with perinatal asphyxia (PA) without HIE (n = 56), and infants with clinical and electrographically confirmed HIE (n = 30). No significant alteration was detected between groups (p = 0.566).

FIGURE 2
www.frontiersin.org

Figure 2. Boxplot representing further analysis of umbilical cord blood (UCB) levels of GFAP (ng/ml) in infants which would be deemed eligible for therapeutic hypothermia (TH; moderate and severe hypoxic–ischemic encephalopathy, n = 9) and infants who would not meet the eligible criteria (Non-TH; controls, perinatal asphyxia, and mild hypoxic–ischemic encephalopathy, n = 160). No significant elevation in GFAP levels was observed (p = 0.919).

Outcome at 36 Months of Age

In the total study population, outcome at 36 months was available in 116/169 (69%) infants [61 (73%) controls, 32 PA (57%), and 23 (77%) HIE]. Of these, 70 infants underwent outcome assessment using the Bayley Scales of Infant and Toddler Development (Ed. III). The remaining 46 infants underwent assessment using the Ages and Stages Questionnaire (Ed. III-ASQ3). Further breakdown of grade of HIE and outcome is available in Table 2. When classed as infants with a normal outcome vs. infants with an abnormal outcome at 36 months, no discernable elevation in UCB GFAP levels was observed Figure 3.

TABLE 2
www.frontiersin.org

Table 2. Comparison of neurodevelopmental follow-up at 36 months of age, primarily using the Bayley Scales of Infant and Toddler Development (Ed. III) (n = 70) or the Ages and Stages Questionnaire (Ed. III) (n = 46).

FIGURE 3
www.frontiersin.org

Figure 3. Comparison of umbilical cord blood (UCB) levels of GFAP (nanogram per milliliter) from infants with a normal outcome at 24–36 months (n = 103) compared to those with an abnormal outcome (n = 13), presented as a box plot. A significant difference was not detected between groups (p = 0.919).

Discussion

Increased levels of GFAP have been shown to be useful biomarkers of adult brain pathology (6, 1015). In spite of this, investigations into its use in the neonatal field have been somewhat limited, with only a small number of publications suggesting GFAP as a biomarker in HIE with the ability to distinguish between grades of HIE (1, 2, 1618). While these studies provided promising results, they also cited major limitations with regard to sample size and sample availability throughout. Post-natal blood samples were predominately used, with few studies determining levels in UCB, which is arguably the earliest possible source for a biomarker of HIE. However, as HIE is known to encompass a two stage evolving mechanism of injury, the time at which GFAP levels most represent degree of injury must be established.

In this study, our goal was to add to the current knowledge available for this promising biomarker specifically in relation to HIE. We aimed to validate the use of GFAP as a marker of HIE severity specifically and to overcome the previously cited limitations, mainly through the use of a larger, carefully defined population cohort and through the use of UCB as our sample source. All our samples are collected and processed in an operational biobank following strict SOPs. Additionally, UCB represents the earliest possible blood sample available after delivery. Although it is not taken directly from the infant, it provides a snapshot of an infant’s circulation at the time of delivery and can therefore offer a unique insight into the neonatal condition. This sample is relatively easy to obtain, does not involve an invasive procedure to an already stressed newborn and could potentially classify infants depending on degree of injury, contributing to rapid and reliable therapeutic decision-making.

A large collection of previously published research focused on GFAP and CNS damage in general is available; however, a recent review of neonatal biomarkers by Bersani et al. (19) called for further work to investigate the validity of this protein with a particular focus on outcome. We discovered no significant alterations in GFAP expression between our case and control groups or between different grades of HIE. Additionally, we found no correlation of GFAP levels with outcome at 36 months of age.

Our findings initially seem to contradict previously published research regarding the potential use of GFAP as an early biomarker of moderate/severe HIE. However, most studies to date have focused on post-natal samples, with significant elevation seen after 6–12 h (1, 18). More recently, a study focused on mixed cord samples in a historical cohort has shown no difference in serum GFAP levels between controls and infants with moderate-severe HIE (20). This is in keeping with previous work in adult TBI where peak levels occur at 12 h post-injury.

While there is good evidence that GFAP may be a useful marker of HIE severity in samples taken after six post-natal hours, we have not shown altered levels in UCB samples. This is the first prospective, carefully defined cohort study to focus on GFAP in UCB. This may limit the usefulness of GFAP as a biomarker to guide therapeutic intervention.

Conclusion

Serum GFAP is not altered in the UCB samples of infants with perinatal asphyxia, with or without clinical and electrographic HIE, compared to normal controls. GFAP therefore may not be the ideal early biomarker to predict eligibility for therapeutic intervention.

Conflict of Interest Statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Funding

A-ML, Dr. CA, Dr. DM, and the BiHIVE study are funded by the Health Research Board (HRB) (CSA/2012/40). This research was also supported by a Science Foundation Ireland (SFI) Research Centre Award (INFANT – 12/RC/2272).

References

1. Chalak LF, Sánchez PJ, Adams-Huet B, Laptook AR, Heyne RJ, Rosenfeld CR. Biomarkers for severity of neonatal hypoxic-ischemic encephalopathy and outcomes in newborns receiving hypothermia therapy. J Pediatr (2014) 164(3):468.–474. doi:10.1016/j.jpeds.2013.10.067

PubMed Abstract | CrossRef Full Text | Google Scholar

2. Douglas-Escobar M, Yang C, Bennett J, Shuster J, Theriaque D, Leibovici A, et al. A pilot study of novel biomarkers in neonates with hypoxic-ischemic encephalopathy. Pediatr Res (2010) 68(6):531–6. doi:10.1203/PDR.0b013e3181f85a03

PubMed Abstract | CrossRef Full Text | Google Scholar

3. Azzopardi DV, Strohm B, Edwards AD, Dyet L, Halliday HL, Juszczak E, et al. Moderate hypothermia to treat perinatal asphyxial encephalopathy. N Engl J Med (2009) 361(14):1349–58. doi:10.1056/NEJMoa0900854

CrossRef Full Text | Google Scholar

4. DuPont TL, Chalak LF, Morriss MC, Burchfield PJ, Christie L, Sánchez PJ. Short-term outcomes of newborns with perinatal acidemia who are not eligible for systemic hypothermia therapy. J Pediatr (2013) 162(1):35–41. doi:10.1016/j.jpeds.2012.06.042

PubMed Abstract | CrossRef Full Text | Google Scholar

5. Ferriero DM, Bonifacio SL. The search continues for the elusive biomarkers of neonatal brain injury. J Pediatr (2014) 164(3):438–40. doi:10.1016/j.jpeds.2013.11.042

CrossRef Full Text | Google Scholar

6. Middeldorp J, Hol E. GFAP in health and disease. Prog Neurobiol (2011) 93(3):421–43. doi:10.1016/j.pneurobio.2011.01.005

CrossRef Full Text | Google Scholar

7. Mondello S, Papa L, Buki A, Bullock MR, Czeiter E, Tortella FC, et al. Neuronal and glial markers are differently associated with computed tomography findings and outcome in patients with severe traumatic brain injury: a case control study. Crit Care (2011) 15(3):R156. doi:10.1186/cc10286

PubMed Abstract | CrossRef Full Text | Google Scholar

8. Looney A-M, Walsh BH, Moloney G, Grenham S, Fagan A, O’Keeffe GW, et al. Downregulation of umbilical cord blood levels of miR-374a in neonatal hypoxic ischemic encephalopathy. J Pediatr (2015) 167(2):269.e–73.e. doi:10.1016/j.jpeds.2015.04.060

PubMed Abstract | CrossRef Full Text | Google Scholar

9. Walsh BH, Boylan GB, Livingstone V, Kenny LC, Dempsey EM, Murray DM. Cord blood proteins and multichannel-electroencephalography in hypoxic-ischemic encephalopathy*. Pediatr Crit Care Med (2013) 14(6):621–30. doi:10.1097/PCC.0b013e318291793f

CrossRef Full Text | Google Scholar

10. Brophy GM, Mondello S, Papa L, Robicsek SA, Gabrielli A, Tepas J III, et al. Biokinetic analysis of ubiquitin C-terminal hydrolase-L1 (UCH-L1) in severe traumatic brain injury patient biofluids. J Neurotrauma (2011) 28(6):861–70. doi:10.1089/neu.2010.1564

PubMed Abstract | CrossRef Full Text | Google Scholar

11. Kaneko T, Kasaoka S, Miyauchi T, Fujita M, Oda Y, Tsuruta R, et al. Serum glial fibrillary acidic protein as a predictive biomarker of neurological outcome after cardiac arrest. Resuscitation (2009) 80(7):790–4. doi:10.1016/j.resuscitation.2009.04.003

PubMed Abstract | CrossRef Full Text | Google Scholar

12. Mondello S, Palmio J, Streeter J, Hayes RL, Peltola J, Jeromin A. Ubiquitin carboxy-terminal hydrolase L1 (UCH-L1) is increased in cerebrospinal fluid and plasma of patients after epileptic seizure. BMC Neurol (2012) 12(1):85. doi:10.1186/1471-2377-12-85

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Nylen K, Öst M, Csajbok LZ, Nilsson I, Blennow K, Nellgård B, et al. Increased serum-GFAP in patients with severe traumatic brain injury is related to outcome. J Neurol Sci (2006) 240(1):85–91. doi:10.1016/j.jns.2005.09.007

PubMed Abstract | CrossRef Full Text | Google Scholar

14. Papa L, Akinyi L, Liu MC, Pineda JA, Tepas JJ III, Oli MW, et al. Ubiquitin C-terminal hydrolase is a novel biomarker in humans for severe traumatic brain injury*. Crit Care Med (2010) 38(1):138. doi:10.1097/CCM.0b013e3181b788ab

CrossRef Full Text | Google Scholar

15. Setsuie R, Wada K. The functions of UCH-L1 and its relation to neurodegenerative diseases. Neurochem Int (2007) 51(2):105–11. doi:10.1016/j.neuint.2007.05.007

PubMed Abstract | CrossRef Full Text | Google Scholar

16. Blennow M, Hagberg H, Rosengren L. Glial fibrillary acidic protein in the cerebrospinal fluid: a possible indicator of prognosis in full-term asphyxiated newborn infants? Pediatr Res (1995) 37(3):260–4. doi:10.1203/00006450-199503000-00002

PubMed Abstract | CrossRef Full Text | Google Scholar

17. Burtrum D, Silverstein FS. Hypoxic-ischemic brain injury stimulates glial fibrillary acidic protein mRNA and protein expression in neonatal rats. Exp Neurol (1994) 126(1):112–8. doi:10.1006/exnr.1994.1047

PubMed Abstract | CrossRef Full Text | Google Scholar

18. Ennen CS, Huisman TA, Savage WJ, Northington FJ, Jennings JM, Everett AD, et al. Glial fibrillary acidic protein as a biomarker for neonatal hypoxic-ischemic encephalopathy treated with whole-body cooling. Am J Obstet Gynecol (2011) 205(3):e1–7. doi:10.1016/j.ajog.2011.06.025

PubMed Abstract | CrossRef Full Text | Google Scholar

19. Bersani I, Auriti C, Ronchetti MP, Prencipe G, Gazzolo D, Dotta A. Use of early biomarkers in neonatal brain damage and sepsis: state of the art and future perspectives. Biomed Res Int (2015) 2015:253520. doi:10.1155/2015/253520

CrossRef Full Text | Google Scholar

20. Zaigham M, Lundberg F, Hayes R, Undén J, Olofsson P. Umbilical cord blood concentrations of ubiquitin carboxy-terminal hydrolase L1 (UCH-L1) and glial fibrillary acidic protein (GFAP) in neonates developing hypoxic-ischemic encephalopathy. J Matern Fetal Neonatal Med (2015) 10:1–7. doi:10.3109/14767058.2015.1064108

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: GFAP, hypoxic–ischemic encephalopathy, early diagnosis, biomaker, umbilical cord blood, therapeutic interventions

Citation: Looney A-M, Ahearne C, Boylan GB and Murray DM (2015) Glial Fibrillary Acidic Protein Is Not an Early Marker of Injury in Perinatal Asphyxia and Hypoxic–Ischemic Encephalopathy. Front. Neurol. 6:264. doi: 10.3389/fneur.2015.00264

Received: 19 July 2015; Accepted: 07 December 2015;
Published: 21 December 2015

Edited by:

Pedro M. Pimentel-Coelho, Universidade Federal do Rio de Janeiro, Brazil

Reviewed by:

Gouri Rao Passi, Choithram Hospital and Research Centre, India
Susan Cohen, Medical College of Wisconsin, USA

Copyright: © 2015 Looney, Ahearne, Boylan and Murray. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Ann-Marie Looney, am.looney@ucc.ie