Evidence map›Paper›PMID 24504123›Full record

ArticlePloS one2014

Assessment of sleep in children with mucopolysaccharidosis type III.

Louise Victoria Mahon, Michelle Lomax, Sheena Grant, Elaine Cross, Dougal Julian Hare, James Ed Wraith, Simon Jones, Brian Bigger, Kia Langford-Smith, Maria Canal

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 39 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Sanfilippo syndrome: consensus guidelines for clinical care.Orphanet journal of rare diseases · 2022
    Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Dream enactment behavior: review for the clinician.Journal of clinical sleep medicine : JCSM : official publication of the American Academy of Sleep Medicine · 2020
    Article
  12. Cerebellar tumour-like aggregate of glycosaminoglycans in a MPS IIIB patient: a case report.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2020
    Article
  13. Review
  14. Review
  15. Article
  16. Sleep Disorders in Childhood Neurogenetic Disorders.Children (Basel, Switzerland) · 2017
    Review
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

Louise Victoria MahonDivision of Clinical Psychology, University of Manchester, Manchester, United Kingdom.
Michelle LomaxDivision of Clinical Psychology, University of Manchester, Manchester, United Kingdom.
Sheena GrantDivision of Clinical Psychology, University of Manchester, Manchester, United Kingdom.
Elaine CrossDivision of Clinical Psychology, University of Manchester, Manchester, United Kingdom.
Dougal Julian HareDivision of Clinical Psychology, University of Manchester, Manchester, United Kingdom.
James Ed WraithGenetic Medicine, St. Mary's Hospital, Manchester, United Kingdom.
Simon JonesGenetic Medicine, St. Mary's Hospital, Manchester, United Kingdom.
Brian BiggerFaculty of Medical and Human Sciences, University of Manchester, Manchester, United Kingdom.
Kia Langford-SmithFaculty of Medical and Human Sciences, University of Manchester, Manchester, United Kingdom.
Maria CanalFaculty of Life Sciences, University of Manchester, Manchester, United Kingdom.
University of Manchester · GBSt. Mary's Hospital · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sleep disturbances are prevalent in mucopolysaccharidosis Type III (MPS III), yet there is a lack of objective, ecologically valid evidence detailing sleep quantity, quality or circadian system. Eight children with MPS III and eight age-matched typically developing children wore an actigraph for 7-10 days/nights. Saliva samples were collected at three time-points on two separate days, to permit analysis of endogenous melatonin levels. Parents completed a sleep questionnaire and a daily sleep diary. Actigraphic data revealed that children with MPS III had significantly longer sleep onset latencies and greater daytime sleep compared to controls, but night-time sleep duration did not differ between groups. In the MPS III group, sleep efficiency declined, and sleep onset latency increased, with age. Questionnaire responses showed that MPS III patients had significantly more sleep difficulties in all domains compared to controls. Melatonin concentrations showed an alteration in the circadian system in MPS III, which suggests that treatment for sleep problems should attempt to synchronise the sleep-wake cycle to a more regular pattern. Actigraphy was tolerated by children and this monitoring device can be recommended as a measure of treatment success in research and clinical practice.

Indexed as

ActigraphyAdolescentCase-Control StudiesChildChild, PreschoolFemaleHumansMaleMelatoninMucopolysaccharidosis IIISleepTime FactorsMelatonin

Identifiers

PMID24504123
PMCPMC3913580
OpenAlexW2072137814

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.