Article Text

PDF
The epidemiology of progressive intellectual and neurological deterioration in childhood
  1. Christopher Verity1,
  2. Anne Marie Winstone1,
  3. Lesley Stellitano1,
  4. Robert Will2,
  5. Angus Nicoll3
  1. 1PIND Surveillance Group, Addenbrooke's Hospital, Cambridge, UK
  2. 2National Creutzfeldt–Jakob Disease Surveillance Unit, Western General Hospital, Edinburgh, Scotland, UK
  3. 3European Centre for Disease Prevention and Control, Stockholm, Sweden
  1. Correspondence to Dr C M Verity, Child Development Centre, Box 107, Addenbrooke's Hospital, Hills Road, Cambridge CB2 0QQ, UK; christopher.verity{at}addenbrookes.nhs.uk

Abstract

Objective To study the epidemiology of diseases that cause progressive intellectual and neurological deterioration (PIND) in UK children.

Design Since May 1997, the authors have performed active surveillance to search for variant Creutzfeldt–Jakob Disease (vCJD) among the many diseases that cause neurological deterioration in children, using the monthly surveillance card sent to all UK consultant paediatricians by the British Paediatric Surveillance Unit. The authors obtain clinical details from reporting paediatricians by questionnaire or site visit, and an Expert Group then independently classifies the cases.

Results After 12 years, 2636 patients less than 16 years old with suspected PIND had been reported, of whom 1114 had a confirmed diagnosis to explain their deterioration: in these children, there were 147 different diseases. These were the six commonest diagnostic groups: leukoencephalopathies (183 cases), neuronal ceroid lipofuscinoses (141 cases), mitochondrial diseases (122 cases), mucopolysaccharidoses (102 cases), gangliosidoses (100 cases) and peroxisomal disorders (69 cases). Relatively large numbers of PIND children were reported from parts of the UK where there are high rates of consanguinity. Only six children with vCJD (four definite, two probable) had been identified.

Conclusions Although this study does not ascertain all UK cases, it provides a novel insight into the epidemiology of the neurodegenerative diseases that cause PIND in children. It is reassuring that in general these children are carefully investigated and that active surveillance has found only six children with vCJD. However, there is concern that more childhood vCJD cases may appear, possibly with a different genotype from those identified so far.

Statistics from Altmetric.com

Footnotes

  • Funding This is independent research funded by the Department of Health, UK (grant reference: 121/6443). The views expressed in the publication are those of the authors and not necessarily those of the Department of Health.

  • Competing interests None.

  • Ethics approval Ethics approval was provided by the Cambridgeshire 2 Research Ethics Committee.

  • Provenance and peer review Not commissioned; externally peer reviewed.

  • Patient consent The Patient Information Advisory Group, now the National Information Governance Board, gave the study approval to obtain clinical information about cases without prior approval from carers or patients.

Request permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.