Evidence map›Paper›PMID 35996993›Full record

ArticleMolecular genetics & genomic medicine2022

Sleep and Phelan-McDermid Syndrome: Lessons from the International Registry and the scientific literature.

Bridgette A Moffitt, Sara M Sarasua, Linda Ward, Diana Ivankovic, Kathleen Valentine, Curtis Rogers, Katy Phelan, Luigi Boccuto

Open access · goldAbstract read
In one paragraph

Article in Molecular genetics & genomic medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.3field-weighted citation impact, top 18% 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

6 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Updated consensus guidelines on the management of Phelan-McDermid syndrome.American journal of medical genetics. Part A · 2023
    Review
  6. 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

8 authors at 3 institutions in 1 country.

Bridgette A MoffittSchool of Nursing, Healthcare Genetics Doctoral Program, Clemson University, Clemson, South Carolina, USA.ORCID 0000-0002-5906-2391
Sara M SarasuaSchool of Nursing, Healthcare Genetics Doctoral Program, Clemson University, Clemson, South Carolina, USA.
Linda WardSchool of Nursing, Healthcare Genetics Doctoral Program, Clemson University, Clemson, South Carolina, USA.
Diana IvankovicSchool of Nursing, Healthcare Genetics Doctoral Program, Clemson University, Clemson, South Carolina, USA.
Kathleen ValentineSchool of Nursing, Healthcare Genetics Doctoral Program, Clemson University, Clemson, South Carolina, USA.
Curtis RogersGreenwood Genetics Center, Greenwood, South Carolina, USA.
Katy PhelanGenetics Laboratory, Florida Cancer Specialists and Research Institute, Fort Myers, Florida, USA.
Luigi BoccutoSchool of Nursing, Healthcare Genetics Doctoral Program, Clemson University, Clemson, South Carolina, USA.ORCID 0000-0003-2017-4270
Clemson University · USGreenwood Genetic Center · USFlorida Cancer Specialists & Research Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSleep is essential to maintaining a healthy life. Sleep disturbances among individuals with neurodevelopmental disorders are not well studied, affecting their early detection and treatment. Sleep disturbances in individuals with Phelan-McDermid Syndrome (PMS) are among the primary concerns reported by parents. However, little research has been aimed at addressing their concern.

methodsThe purpose of this investigation was to identify and quantify specific sleep disturbances in people with PMS by analyzing data collected by the PMS Foundation International Registry.

resultsThe registry shows that 284 out of 384 (73.4%) individuals with confirmed chromosome 22q13 deletions or SHANK3 pathogenic variants have a sleep disturbance. The prevalence of sleep disturbances increases with age with 56% reporting a sleep disturbance in the 0-3 year age group and 90% reporting these disturbances in those over age 18 years old. The primary sleep disturbances were circadian rhythm sleep disorders that included difficulty falling asleep, frequent nighttime awakenings, difficulty returning to sleep after a nighttime awakening event, and hypersomnia and parasomnias including enuresis, night terrors, sleepwalking, and sleep apnea. Sleep disturbances were similarly frequent among individuals with SHANK3 pathogenic variants (84.8%) and those with deletions (71.9%), supporting the role of haploinsufficiency of SHANK3 in sleep.

conclusionSleep disturbances are a common feature of PMS and should be considered in clinical evaluation and management because of the effect they have on the quality of life of the patients and their families.

Indexed as

Chromosome DisordersQuality of LifeChild, PreschoolChromosome DeletionChromosomes, Human, Pair 22HumansInfantInfant, NewbornRegistriesSleep22q13 deletion syndromePhelan-McDermid SyndromePMSSHANK3sleep disturbance

Identifiers

PMID35996993
PMCPMC9544216
OpenAlexW4292707662

What OpenQuestion holds

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LicenceCC BY-NC
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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.