Behavioral and neurodevelopmental outcome of children after maternal allopurinol administration during suspected fetal hypoxia: 5-year follow up of the ALLO-trial

Job Klumper, Joepe J Kaandorp, Ewoud Schuit, Floris Groenendaal, Corine Koopman-Esseboom, Eduard J H Mulder, Frank Van Bel, Manon J N L Benders, Ben W J Mol, Ruurd M van Elburg, Arend F Bos, Jan B Derks, ALLO-trial study group, Job Klumper, Joepe J Kaandorp, Ewoud Schuit, Floris Groenendaal, Corine Koopman-Esseboom, Eduard J H Mulder, Frank Van Bel, Manon J N L Benders, Ben W J Mol, Ruurd M van Elburg, Arend F Bos, Jan B Derks, ALLO-trial study group

Abstract

Objective: To evaluate the long-term neurodevelopmental and behavioral outcome of antenatal allopurinol treatment during suspected fetal hypoxia.

Study design: We studied children born from women who participated in a randomized double-blind placebo controlled multicenter study (ALLO-trial). Labouring women in whom the fetus was suspected to have fetal hypoxia were randomly allocated to receive allopurinol or placebo. At 5 years of age, the children were assessed with 2 parent reported questionnaires, the Ages and Stages Questionnaire (ASQ) and the Child Behavior Checklist (CBCL). A child was marked abnormal for ASQ if it scored below 2 standard deviation under the normative mean of a reference population in at least one domain. For CBCL, a score above the cut-off value (95th percentile for narrowband scale, 85th percentile for broadband scale) in at least one scale was marked as abnormal.

Results: We obtained data from 138 out of the original 222 mildly asphyxiated children included in the ALLO-trial (response rate 62%, allopurinol n = 73, placebo n = 65). At 5 years of age, the number of children that scored abnormal on the ASQ were 11 (15.1%) in the allopurinol group versus 11 (9.2%) in the placebo group (relative risk (RR) 1.64, 95% confidence interval (CI): 0.64 to 4.17, p = 0.30). On CBCL 21 children (30.4%) scored abnormal in de allopurinol group versus 12 children (20.0%) in the placebo group (RR 1.52, 95% CI: 0.82 to 2.83, p = 0.18).

Conclusion: We found no proof that allopurinol administered to labouring women with suspected fetal hypoxia improved long-term developmental and behavioral outcome. These findings are limited due to the fact that the study was potentially underpowered.

Trial registration: NCT00189007 Dutch Trial Register NTR1383.

Conflict of interest statement

The authors have declared that no competing interests exist.

Figures

Fig 1. CONSORT flow diagram of the…
Fig 1. CONSORT flow diagram of the ALLO-trial and its follow-up.
ALLO-trial: Antenatal allopurinol trial for reduction of birth asphyxia induced brain damage. ASQ: Ages and Stages Questionnaire, CBCL: Child Behavior Checklist.

References

    1. Hagberg B, Hagberg G, Olow I. The changing panorama of cerebral palsy in Sweden. Prevalence and origin during the year period 1983–1986. Acta Paediatr 1993;82:387–393.
    1. Ferriero DM. Neonatal brain injury. N Eng J Med 2004;351:1985–1995.
    1. Low JA. Determining the contribution of asphyxia to brain damage in the neonate. J Obstet Gynaecol Res 2004;30:276–86. 10.1111/j.1447-0756.2004.00194.x
    1. Jacobs SE, Berg M, Hunt R, Tarnow-mordi WO, Inder TE, Davis PG. Cooling for newborns with hypoxic ischaemic encephalopathy. Cochrane Database Syst Rev. 2013;(1):CD003311 10.1002/14651858.CD003311.pub3
    1. Inder TE, Volpe JJ. Mechanisms of perinatal brain injury. Semin Neonatol. 2000;5(1):3–16. 10.1053/siny.1999.0112
    1. Pacher P, Nivorozhkin A, Szabo C. Therapeutic effects of xanthine oxidase inhibitors: renaissance half a century after the discovery of allopurinol. Pharmacological Reviews 2006;58:87–114. 10.1124/pr.58.1.6
    1. Palmer C, Vannucci RC, Towfighi J. Reduction of perinatal hypoxic-ischemic brain damage with allopurinol. Pediatr Res 1990;27(4 Pt 1):332–6. 10.1203/00006450-199004000-00003
    1. Kaandorp JJ, Derks JB, Oudijk MA, Torrance HL, Harmsen MG, Nikkels PGJ et al. Antenatal allopurinol reduces hippocampal brain damage after acute birth asphyxia in late gestation fetal sheep. Reprod Sci 2014;21(2):251–9. 10.1177/1933719113493516
    1. Derks JB, Oudijk MA, Torrance HL, Rademaker CM, Benders MJ, Rosen KG et al. Allopurinol reduces oxidative stress in the ovine fetal cardiovascular system after repeated episodes of ischemia-reperfusion. Pediatr Res 2010;68(5):374–80. 10.1203/PDR.0b013e3181ef7780
    1. Benders MJ, Bos AF, Rademaker CM, Rijken M, Torrance HL, Groenendaal F et al. Early postnatal allopurinol does not improve short term outcome after severe birth asphyxia. Arch Dis Child Fetal Neonatal Ed 2006;91:F163–5. 10.1136/adc.2005.086652
    1. Van Bel F, Shadid M, Moison RM, Dorrepaal CA, Fontijn J, Monteiro L et al. Effect of allopurinol on postasphyxial free radical formation, cerebral hemodynamics, and electrical brain activity. Pediatrics 1998;101:185–93.
    1. Gunes T, Ozturk MA, Koklu E, Kose K, Gunes I. Effect of allopurinol supplementation on nitric oxide levels in asphyxiated newborns. Pediatr Neurol 2007;36:17–24. 10.1016/j.pediatrneurol.2006.08.005
    1. Chaudhari T, Mcguire W. Allopurinol for preventing mortality and morbidity in newborn infants with hypoxic-ischaemic encephalopathy. Cochrane Database Syst Rev 2012;(7):CD006817 10.1002/14651858.CD006817.pub3
    1. Gluckman PD, Wyatt JS, Azzopardi D, Ballard R, Edwards AD, Ferriero DM et al. Selective head cooling with mild systemic hypothermia after neonatal encephalopathy: multicentre randomised trial. Lancet 2005;365:663–70. 10.1016/S0140-6736(05)17946-X
    1. Kaandorp JJ, Benders MJ, Schuit E, Rademaker CM, Oudijk MA, Porath MM et al. Maternal allopurinol administration during suspected fetal hypoxia: a novel neuroprotective intervention? A multicentre randomized placebo controlled trial. Arch Dis Child Fetal Neonatal Ed 2015;100: F216–F223. 10.1136/archdischild-2014-306769
    1. Volpe JJ (2008) Neurology of the newborn. 5th edition, WB Saunders, Philadelphia.
    1. Van Handel M, Swaab H, de Vries LS, Jongmans MJ. Long-term cognitive and behavioral consequences of neonatal encephalopathy following perinatal asphyxia: a review. Eur J Pediatr. 2007;166(7):645–54. 10.1007/s00431-007-0437-8
    1. Kaandorp JJ, Benders MJ, Rademaker CM, Torrance HL, Oudijk MA, de Haan TR, et al. Antenatal allopurinol for reduction of birth asphyxia induced brain damage (ALLO-Trial); a randomized double blind placebo controlled multicenter study. BMC Pregnancy Childbirth 2010;10:8 10.1186/1471-2393-10-8
    1. Boda D, Németh P, Kiss P, et al. Treatment of mothers with allopurinol to produce therapeutic blood levels in newborns. Prenat Neonat Med 1999;4:130–2, 133,, 134
    1. Torrance HL, Benders MJ, Derks JB, Rademaker CM, Bos AF, Van den Berg P et al. Maternal allopurinol during fetal hypoxia lowers cord blood levels of the brain injury marker S-100B. Pediatrics 2009;124:350–7. 10.1542/peds.2008-2228
    1. Gazzolo D, Visser GH, Lituania M, et al. S100B protein cord blood levels and development of fetal behavioral states: A study in normal and small-for-dates fetuses. J Matern Fetal Neonatal Med 2002;11:378–84. 10.1080/jmf.11.6.378.384
    1. Michetti F, Corvino V, Geloso MC, et al. The S100B protein in biological fluids: More than a lifelong biomarker of brain distress. J Neurochem 2012;120:644–59. 10.1111/j.1471-4159.2011.07612.x
    1. Beharier O, Kahn J, Shusterman E, et al. S100B—a potential biomarker for early detection of neonatal brain damage following asphyxia. J Matern Fetal Neonatal Med 2012;25:1523–8. 10.3109/14767058.2012.664200
    1. Squires J, Potter L, Bricker D. The Ages and Stages Questionnaire user’s guide. 2nd ed Baltimore: Paul Brooks Publishing: 1999.
    1. Achenbach TM, Rescorla LA. Aseba preschool forms and profiles. Burlington, VT: University of Vermont, Research Center for Children, Youth and Families; 2000.
    1. Radecki L, Sand-Loud N, O'Connor KG, Sharp S, Olson LM et al. Trends in the use of standardized tools for developmental screening in early childhood: 2002–2009. Pediatrics 2011. July;128(1):14–9. 10.1542/peds.2010-2180
    1. Hornman J, Kerstjens JM, De winter AF, Bos AF, Reijneveld SA. Validity and internal consistency of the Ages and Stages Questionnaire 60-month version and the effect of three scoring methods. Early Hum Dev 2013;89(12):1011–5. 10.1016/j.earlhumdev.2013.08.016
    1. Kaandorp JJ, van Bel F, Veen S, Derks JB, Groenendaal F, Rijken M et al. Long-term neuroprotective effects of allopurinol after moderate perinatal asphyxia: Follow-up of two randomised controlled trials. Arch Dis Child Fetal Neonatal Ed 2012;97:F162–6. 10.1136/archdischild-2011-300356
    1. Hurn PD, Vannucci SJ, Hagberg H. Adult or perinatal brain injury: does sex matter? Stroke 2005;36:193–5. 10.1161/01.STR.0000153064.41332.f6
    1. Nijboer CH, Kavelaars A, van Bel F, Heijnen CJ, Groenendaal F. Gender-dependent pathways of hypoxia-ischemia-induced cell death and neuroprotection in the immature P3 rat. Dev Neurosci 2007;29:385–92. 10.1159/000105479
    1. Renolleau S, Fau S, Charriaut-Marlangue C. Gender-related differences in apoptotic pathways after neonatal cerebral ischemia. Neuroscientist 2008;14:46–52. 10.1177/1073858407308889
    1. Spence RD, Hamby ME, Umeda E, Itoh N, Du S, Wisdom AJ et al. Neuroprotection mediated through estrogen receptor-alpha in astrocytes. Proc Natl Acad Sci USA 2011; 108:8867–72. 10.1073/pnas.1103833108
    1. Wen Y, Yang S, Liu R, Perez E, Yi KD, Koulen P et al. Estrogen attenuates nuclear factor-kappa B activation induced by transient cerebral ischemia. Brain Res 2004;1008:147–54. 10.1016/j.brainres.2004.02.019
    1. Nilsen RM, Vollset SE, Gjessing HK, Skjaerven R, Melve KK, Schreuder P et al. Self-selection and bias in a large prospective pregnancy cohort in Norway. Paediatr Perinat Epidemiol 2009;23(6):597–608. 10.1111/j.1365-3016.2009.01062.x

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