Evidence map›Paper›PMID 30739220›Full record

ReviewCurrent neurology and neuroscience reports2019

Sleep Complaints, Sleep and Breathing Disorders in Myotonic Dystrophy Type 2.

Andrea Romigi, Michelangelo Maestri, Carmine Nicoletta, Giuseppe Vitrani, Marco Caccamo, Gabriele Siciliano, Enrica Bonanni, Diego Centonze, Alessandro Sanduzzi

Abstract readReview
PubMed Publisher
In one paragraph

Review in Current neurology and neuroscience reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 33% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

  1. Guideline
  2. The novel (TCTG)Human genomics · 2026
    Article
  3. Article
  4. Review
  5. A Greek National Cross-Sectional Study on Myotonic Dystrophies.International journal of molecular sciences · 2022
    Article
  6. Myotonic dystrophy type 2: the 2020 update.Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology · 2020
    Review
  7. Review
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

9 authors at 3 institutions in 1 country.

Andrea RomigiIRCCS Neuromed, Sleep Medicine Center, Via Atinense, 18, Pozzilli, (IS), Italy. andrea.romigi@gmail.com.ORCID 0000-0002-4505-2600
Michelangelo MaestriDepartment of Clinical and Experimental Medicine, Neurology Unit, University of Pisa, Pisa, Italy.
Carmine NicolettaDepartment of Clinical Medicine and Surgery, Section of Respiratory Diseases, University of Naples Federico II, Naples, Italy.
Giuseppe VitraniIRCCS Neuromed, Sleep Medicine Center, Via Atinense, 18, Pozzilli, (IS), Italy.
Marco CaccamoIRCCS Neuromed, Sleep Medicine Center, Via Atinense, 18, Pozzilli, (IS), Italy.
Gabriele SicilianoDepartment of Clinical and Experimental Medicine, Neurology Unit, University of Pisa, Pisa, Italy.
Enrica BonanniDepartment of Clinical and Experimental Medicine, Neurology Unit, University of Pisa, Pisa, Italy.
Diego CentonzeIRCCS Neuromed, Sleep Medicine Center, Via Atinense, 18, Pozzilli, (IS), Italy.
Alessandro SanduzziDepartment of Clinical Medicine and Surgery, Section of Respiratory Diseases, University of Naples Federico II, Naples, Italy.
Istituto Neurologico Mediterraneo · ITUniversity of Pisa · ITUniversity of Naples Federico II · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purpose of reviewTo update the current knowledge concerning sleep complaints and breathing disorders in myotonic dystrophy type 2 (DM2) and to better understand if sleep and breathing symptoms may add a further clinical definition of DM2. RECENT

findingsAlthough DM2 has been poorly evaluated, the most relevant sleep disorders are sleep-disordered breathing (SDB) (37.5-66.7%) and restless legs syndrome (RLS) (50-60%). Excessive daytime somnolence (EDS) is not consistent with SDB, and a large percentage of patients with sleep complaints (58-69%) report pain. In addition, respiratory dysfunctions are reported in 6 to 15% of DM2 patients, albeit few data are available regarding pulmonary restriction, hypoventilation, and non-invasive ventilation (NIV). SDB, RLS, and pain may contribute to sleep fragmentation and EDS in DM2. In addition, few studies report hypoventilation and pulmonary restriction, although there are no studies at all on NIV, except for limited clinical experiences. These findings suggest performing a careful pulmonary examination and NIV when required. Furthermore, sleep studies and respiratory evaluation should be recommended if OSA or respiratory muscle dysfunctions are suspected. A large polysomnographic study should be performed to clarify the link between sleep disorders, pain, and sleep disruption in DM2.

Indexed as

Disorders of Excessive SomnolenceFemaleHumansMaleMyotonic DystrophyPainPolysomnographyRestless Legs SyndromeSleep Apnea SyndromesSleep Wake DisordersExcessive daytime somnolenceFatigueHypoventilationMyotonic dystrophy type 2PainSleepSleep-disordered breathing

Identifiers

PMID30739220
OpenAlexW2913332942

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.