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Human parechovirus meningitis and gross-motor neurodevelopment in young children

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Abstract

This multicenter prospective cohort study describes the impact of human parechovirus meningitis on gross-motor neurodevelopment of young children. Gross-motor function was measured using Alberta Infant Motor Scale. Of a total of 38 eligible children < 10 months of age at onset, nine cases had clinical evidence of meningitis and polymerase chain reaction positive for human parechovirus in cerebrospinal fluid; 11 had no meningitis and polymerase chain reaction positive for human parechovirus in nasopharyngeal aspirate, blood, urine, or feces; and in 18, no pathogen was identified (reference group).

The children with human parechovirus meningitis showed more frequent albeit not statistically significant suspect gross-motor function delay (mean Z-score (standard deviation) − 1.69 (1.05)) than children with human parechovirus infection-elsewhere (− 1.38 (1.51)). The reference group did not fall in the range of suspect gross-motor function delay (− 0.96 (1.07)). Adjustment for age at onset and maternal education did not alter the results.

Conclusion: Six months after infection, children with human parechovirus meningitis showed more frequent albeit not statistically significant suspect gross-motor function delay compared to the population norm and other two groups. Longitudinal studies in larger samples and longer follow-up periods are needed to confirm the impact and persistence of human parechovirus meningitis on neurodevelopment in young children.

What is Known:

• Human parechovirus is progressively becoming a major viral cause of meningitis in children.

• There is keen interest in the development of affected infants with human parechovirus meningitis.

What is New:

• This study describes prospectively gross-motor functional delay in children with both clinical evidence of meningitis and polymerase chain reaction positive for human parechovirus in cerebrospinal fluid.

• It shows the importance of screening young children for developmental delay in order to refer those with delay for early intervention to maximize their developmental potential.

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Abbreviations

AIMS:

Alberta Infant Motor Scale

CI:

Confidence interval

CNS:

Central nervous system

CP:

Cerebral palsy

CSF:

Cerebrospinal fluid

EV:

Enterovirus

GMF:

Gross-motor function

HPeV:

Human parechovirus

n :

Number

NPA:

Nasopharyngeal aspirate

RT-qPCR:

Reverse transcriptase real-time quantitative polymerase chain reaction

SD:

Standard deviation of the mean

T0:

Presenting at emergency or outpatient departments of the participating hospitals

T6:

Follow-up 6 months after visiting the emergency or outpatient departments of the participating hospitals

References

  1. Barnett A, Mercuri E, Rutherford M, Haataj L, Frisone MF, Henderson S, Cowan F, Dubowitz L (2002) Neurological and perceptual-motor outcome at 5 - 6 years of age in children with neonatal encephalopathy: relationship with neonatal brain MRI. Neuropediatrics 33:242–248. https://doi.org/10.1055/s-2002-36737

    Article  CAS  PubMed  Google Scholar 

  2. Belcastro V, Bini P, Barachetti R, Barbarini M (2014) Teaching neuroimages: neonatal parechovirus encephalitis: typical MRI findings. Neurology 82:e23. https://doi.org/10.1212/WNL.0000000000000040

    Article  PubMed  Google Scholar 

  3. Benschop KS, Schinkel J, Minnaar RP, Pajkrt D, Spanjerberg L, Kraakman HC, Berkhout B, Zaaijer HL, Beld MG, Wolthers KC (2006) Human parechovirus infections in Dutch children and the association between serotype and disease severity. Clin Infect Dis 42:204–210. https://doi.org/10.1086/498905

    Article  CAS  PubMed  Google Scholar 

  4. Berk MC, Bruning AHL, van Wassenaer-Leemhuis AG, Wolthers KC, Pajkrt D (2018) Human parechovirus meningitis with adverse neurodevelopmental outcome: a case report. Pediatr Infect Dis J 37:e256–e257. https://doi.org/10.1097/INF.0000000000001984

    Article  PubMed  Google Scholar 

  5. Britton PN, Dale RC, Nissen MD, Crawford N, Elliott E, Macartney K, Khandaker G, Booy R, Jones CA, PAEDS-ACE Investigators (2016) Parechovirus encephalitis and neurodevelopmental outcomes. Pediatrics 137:e20152848. https://doi.org/10.1542/peds.2015-2848

    Article  PubMed  Google Scholar 

  6. Britton PN, Khandaker G, Khatami A, Teutsch S, Francis S, McMullan BJ, Jones CA (2017) High prevalence of developmental concern amongst infants at 12 months following hospitalised parechovirus infection. J Paediatr Child Health 54:289–295. https://doi.org/10.1111/jpc.13728

    Article  PubMed  Google Scholar 

  7. Cabrerizo M, Díaz-Cerio M, Muñoz-Almagro C, Rabella N, Tarragó D, Romero MP, Pena MJ, Calvo C, Sonia R, Antonio M, Rienda IM, Otero A, Trallero G (2017) Molecular epidemiology of enterovirus and parechovirus infections according to patient age over a 4-year period in Spain. J Med Virol 89:435–442. https://doi.org/10.1002/jmv.24658

    Article  CAS  PubMed  Google Scholar 

  8. Chakrabarti P, Warren C, Vincent L, Kumar Y (2018) Outcome of routine cerebrospinal fluid screening for enterovirus and human parechovirus infection among infants with sepsis-like illness or meningitis in Cornwall, UK. Eur J Pediatr 177:1523–1529. https://doi.org/10.1007/s00431-018-3209-8

    Article  PubMed  Google Scholar 

  9. de Crom SC, Obihara CC, de Moor RA, Veldkamp EJ, van Furth AM, Rossen JW (2013) Prospective comparison of the detection rates of human enterovirus and parechovirus RT-qPCR and viral culture in different pediatric specimens. J Clin Virol 58:449–454. https://doi.org/10.1016/j.jcv.2013.07.017

    Article  CAS  PubMed  Google Scholar 

  10. de Crom SC, Rossen JW, de Moor RA, Veldkamp EJ, van Furth AM, Obihara CC (2016) Prospective assessment of clinical symptoms associated with enterovirus and parechovirus genotypes in a multicenter study in Dutch children. J Clin Virol 77:15–20. https://doi.org/10.1016/j.jcv.2016.01.014

    Article  PubMed  Google Scholar 

  11. Darrah J, Bartlett D, Maguire TOR, Avison WR, Lacaze-Masmonteil T (2014) Have infant gross motor abilities changed in 20 years? A re-evaluation of the Alberta Infant Motor Scale normative values. Dev Med Child Neurol 56:877–881. https://doi.org/10.1111/dmcn.12452

    Article  PubMed Central  PubMed  Google Scholar 

  12. Doyle LW, Anderson PJ, Battin M, Bowen JR, Brown N, Callanan C, Campbell C, Chandler S, Cheong J, Darlow B, Davis PG, DePaoli T, French N, McPhee A, Morris S, O’Callaghan M, Rieger I, RobertsG SAJ, Wolke D, Woodward LJ (2014) Long term follow up of high risk children: who, why and how? BMC Pediatr 14:279. https://doi.org/10.1186/1471-2431-14-279

    Article  PubMed Central  PubMed  Google Scholar 

  13. Fischer TK, Midgley S, Dalgaard C, Nielsen AY (2014) Human parechovirus infection, Denmark. Emerg Infect Dis 20:83–87. https://doi.org/10.3201/eid2001.130569

    Article  PubMed Central  PubMed  Google Scholar 

  14. Gupta S, Fernandez D, Siddiqui A, Tong WC, Pohl K, Jungbluth H (2010) Extensive white matter abnormalities associated with neonatal parechovirus (HPeV) infection. Eur J Paediatr Neurol 14:531–534. https://doi.org/10.1016/j.ejpn.2009

    Article  PubMed  Google Scholar 

  15. van Haastert IC, de Vries LS, Helders PJ, Jongmans MJ (2006) Early gross motor development of preterm infants according to the Alberta Infant Motor Scale. J Pediatr 149:617–622. https://doi.org/10.1016/j.jpeds.2006.07.025

    Article  PubMed  Google Scholar 

  16. Hadders- Algra M (2000) The neuronal group selection theory: a framework to explain variation in normal motor development. Dev Med Child Neurol 42:566–572

    Article  CAS  PubMed  Google Scholar 

  17. Harvala H, Calvert J, Van Nguyen D, Clasper L, Gadsby N, Molyneaux P, Templeton K, McWilliams Leitch C, Simmonds P (2014) Comparison of diagnostic clinical samples and environmental sampling for enterovirus and parechovirus surveillance in Scotland, 2010 to 2012. Euro Surveill 19:1–9. https://doi.org/10.2807/1560-7917.ES2014.19.15.20772

  18. Johnston MV, Ishida A, Ishida WN, Matsushita HB, Nishimura A, Tsuji M (2009) Plasticity and injury in the developing brain. Brain Dev 31:1–10. https://doi.org/10.1016/j.braindev.2008.03.014

    Article  PubMed  Google Scholar 

  19. de Jong EP, Holscher HC, Steggerda SJ, Van Klink JMM, van Elzakker EPM, Lopriore E, Walther FJ, Brus F (2017) Cerebral imaging and neurodevelopmental outcome after entero- and human parechovirus sepsis in young infants. Eur J Pediatr 176:1595–1602. https://doi.org/10.1007/s00431-017-2981-1

    Article  PubMed Central  PubMed  Google Scholar 

  20. Morgan C, Darrah J, Gordon AM, Harbourne R, Spittle A, Johnson R, Fetters L (2016) Effectiveness of motor interventions in infants with CP: a systematic review. Dev Med Child Neurol 58:900–909. https://doi.org/10.1111/dmcn.13105

    Article  PubMed  Google Scholar 

  21. Pariani E, Pellegrinelli L, Pugni L, Bini P, Perniciaro S, Bubba L, Primache V, Amendola A, Barbarini M, Mosca F, Binda S (2014) Two cases of neonatal human parechovirus 3 encephalitis. Pediatr Infect Dis J 33:1191–1193. https://doi.org/10.1097/INF.0000000000000412

    Article  PubMed  Google Scholar 

  22. Piper MC, Darrah J (1994) Motor assessment of the developing infant, 1rd edn. WB Saunders, Philadelphia

    Google Scholar 

  23. Rice D, Barone S (2000) Critical periods of vulnerability for the developing nervous system: evidence from humans and animal models. Environ Health Perspect 108(Suppl 3):511–533. https://doi.org/10.1289/ehp.00108s3511

    Article  PubMed Central  PubMed  Google Scholar 

  24. Skram MK, Skanke LH, Krokstad S, Nordbø SA, Nietsch L, Døllner H (2014) Severe parechovirus infection in Norwegian infants. Pediatr Infect Dis J 33:1222–1225. https://doi.org/10.1097/INF.0000000000000456

    Article  PubMed  Google Scholar 

  25. Speedtsberg MB, Christensen SB, Andersen KK, Bencke J, Jensen BR, Curtis DJ (2017) Impaired postural control in children with developmental coordination disorder is related to less efficient central as well as peripheral control. Gait Posture 51:1–6. https://doi.org/10.1016/j.gaitpost.2016.09.019

    Article  PubMed  Google Scholar 

  26. Tapiainen T, Prevots R, Izurieta HS, Abramson J, Bilynsky R, Bonhoeffer J, Bonnet MC, Center K, Galama J, Gillard P, Griot M, Hartmann K, Heininger U, Hudson H, Koller A, Khetsuriani N, Khuri-Bulos N, Marcy SM, Matulionyte R, Schöndorf I, Sejvar J, Steele R, The Brighton Collaboration Aseptic Meningitis Working Group (2007) Aseptic meningitis: case definition and guidelines for collection, analysis and presentation of immunization safety data. Vaccine 25:5793–5802. https://doi.org/10.1016/j.vaccine.2007.04.058

    Article  CAS  PubMed  Google Scholar 

  27. Van Balen LC, Dijkstra LJ, Bos AF, Van Den Heuvel ER, Hadders-Algra M (2015) Development of postural adjustments during reaching in infants at risk for CP from 4 to 18 months. Dev Med Child Neurol 57:668–676. https://doi.org/10.1111/dmcn.12699

    Article  PubMed  Google Scholar 

  28. Verboon-Maciolek MA, Groenendaal F, Hahn CD, Hellmann J, van Loon AM, Boivin G, de Vries LS (2008) Human parechovirus causes encephalitis with white matter injury in neonates. Ann Neurol 64:266–273. https://doi.org/10.1002/ana.21445

    Article  PubMed  Google Scholar 

  29. Vergnano S, Kadambari S, Whalley K, Menson EN, Martinez-Alier N, Cooper M, Sanchez E, Heath PT, Lyall H (2015) Characteristics and outcomes of human parechovirus infection in infants (2008-2012). Eur J Pediatr 174:919–924. https://doi.org/10.1007/s00431-014-2483-3

    Article  PubMed  Google Scholar 

  30. Westerhuis BM, Koen G, Wildenbeest JG, Pajkrt D, de Jong MD, Benschop KS, Wolthers KC (2012) Specific cell tropism and neutralization of human parechovirus types 1 and 3: implications for pathogenesis and therapy development. J Gen Virol 93:2363–2370. https://doi.org/10.1099/vir.0.043323-0

    Article  CAS  PubMed  Google Scholar 

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Acknowledgements

We thank all children and their parents/legal guardians; pediatricians; nurses in St. Elisabeth, Tweesteden, and Amphia Hospital for participating in this study; Mrs. C.A.M. Smid for her work as study-secretary; and Mrs. N. Hmimsa for her work as planning-secretary.

Definitions

HPeV-meningitis: children with clinical evidence of meningitis and RT-qPCR positive for HPeV in CSF

HPeV-infection-elsewhere: children with no clinical evidence of meningitis and RT-qPCR HPeV-positive in nasopharyngeal aspirate swab, blood, urine, or feces

Reference: children with no clinical evidence of meningitis and in whom no pathogen was identified

No show: did not show after 3× reminded

Lost to follow-up: moved to another address, changed telephone number, parents too busy to come

Author information

Authors and Affiliations

Authors

Contributions

Mrs. van Hinsbergh, MSc., conceptualized and designed the follow-up study. She was responsible for the data collection, carried out the initial statistical analyses, drafted the initial manuscript, revised the manuscript, and approved the final manuscript.

Dr. R. Lindeboom interpreted the statistical data, reviewed the manuscript, and approved the final manuscript.

Prof. Dr. van Furth, Dr. de Crom, and Dr. Obihara conceptualized and designed the study, interpreted the data, reviewed the manuscript, and approved the final manuscript.

Corresponding author

Correspondence to Ted M. T. van Hinsbergh.

Ethics declarations

Conflict of interest

The authors declare that they have no conflict of interest.

Informed consent

Informed consent was obtained from all individual participants included in the study.

Ethical approval

All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. This study was approved of by the medical ethics committee of each participating center (NL-21361.008.07). This article does not contain any studies with animals performed by any of the authors.

Additional information

Communicated by Mario Bianchetti

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van Hinsbergh, T.M.T., de Crom, S.C.M., Lindeboom, R. et al. Human parechovirus meningitis and gross-motor neurodevelopment in young children. Eur J Pediatr 178, 473–481 (2019). https://doi.org/10.1007/s00431-019-03319-6

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