Evidence map›Paper›PMID 30382420›Full record

ReviewCurrent neurology and neuroscience reports2018

Comparative Sleep Disturbances in Myotonic Dystrophy Types 1 and 2.

Andrea Romigi, Valentina Franco, Fabio Placidi, Claudio Liguori, Emanuele Rastelli, Giuseppe Vitrani, Diego Centonze, Roberto Massa

Open access · greenAbstract readReview
PubMed Publisher
In one paragraph

Review in Current neurology and neuroscience reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 3 pooled it
1.4field-weighted citation impact, top 20% 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

10 citing papers in PubMed, 3 syntheses or guidelines pooled it, 24 citations in OpenAlex.

  1. A systematic review of the frequency of sleep evaluations, sleep disorders, and treatments among individuals with muscular dystrophy.Journal of clinical sleep medicine : JCSM : official publication of the American Academy of Sleep Medicine · 2026
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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 2 institutions in 1 country.

Andrea RomigiSleep Medicine Center, IRCCS Neuromed, Via Atinense 18, 86077, Pozzilli, IS, Italy. andrea.romigi@gmail.com.
Valentina FrancoIRCCS Mondino Foundation, Pavia, Italy.
Fabio PlacidiSystem Medicine Department, University of Rome Tor Vergata, Rome, Italy.
Claudio LiguoriSystem Medicine Department, University of Rome Tor Vergata, Rome, Italy.
Emanuele RastelliSystem Medicine Department, University of Rome Tor Vergata, Rome, Italy.
Giuseppe VitraniSleep Medicine Center, IRCCS Neuromed, Via Atinense 18, 86077, Pozzilli, IS, Italy.
Diego CentonzeSleep Medicine Center, IRCCS Neuromed, Via Atinense 18, 86077, Pozzilli, IS, Italy.
Roberto MassaSystem Medicine Department, University of Rome Tor Vergata, Rome, Italy.
University of Rome Tor Vergata · ITIstituto Neurologico Mediterraneo · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purpose of reviewTo update current knowledge regarding sleep disturbances and myotonic dystrophies so as to better understand if sleep symptoms may help in the early recognition of the two genetic subtypes: myotonic dystrophy type 1 (DM1) and myotonic dystrophy type 2 (DM2). RECENT

findingsSleep-disordered breathing (SDB), restless legs syndrome, periodic limb movements in sleep, hypersomnia, and REM sleep dysregulation are frequently described in DM1 patients. SDB does not always explain hypersomnia, but a central dysregulation of sleep-wake modulation is reported mainly in DM1. Sleep apnea, restless legs syndrome, and REM sleep without atonia have been reported in single case reports and small case series of DM2. DM2 is less prevalent and more recently described than DM1, with a milder phenotype than DM1. The most frequent sleep disorders in DM1 are hypersomnia, SDB, periodic limb movements, and a narcoleptic-like phenotype, whereas restless legs syndrome, SDB, and REM sleep without atonia seem to be the most frequent sleep disorders in DM2. Comparative sleep studies are strongly required to delineate the sleep phenotype of myotonic dystrophies.

Indexed as

HumansMyotonic DystrophySleep Apnea SyndromesSleep, REMSleep Wake DisordersExcessive daytime somnolenceFatigueMyotonic dystrophy type 1Myotonic dystrophy type 2SleepSleep-disordered breathing

Identifiers

PMID30382420
OpenAlexW2899144642

What OpenQuestion holds

Textmetadata
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.