Evidence map›Paper›PMID 29429070›Full record

ArticleJournal of neurology2018

A 34-year longitudinal study on long-term cardiac outcomes in DM1 patients with normal ECG at baseline at an Italian clinical centre.

Elisabetta Bucci, Marco Testa, Loretta Licchelli, Alessandra Frattari, Nadia Attalla El Halabieh, Erica Gabriele, Giulia Pignatelli, Tiziana De Santis, Laura Fionda, Fiammetta Vanoli and 6 more

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of neurology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
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, 19 citations in OpenAlex.

  1. Review
  2. Observational
  3. Review
  4. Article
  5. Cardiac Pathology in Myotonic Dystrophy Type 1.International journal of molecular sciences · 2021
    Review
  6. Article
  7. Predictors of prognosis in type 1 myotonic dystrophy (DM1): longitudinal 18-years experience from a single center.Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology · 2020
    Observational
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

16 authors at 4 institutions in 1 country.

Elisabetta BucciDepartment of Neuroscience, Mental Health and Sensory Organs (NESMOS), School of Medicine and Psychology, Sapienza University of Rome, Sant'Andrea Hospital, Via di Grottarossa 1035, 00189, Rome, Italy.
Marco TestaDepartment of Cardiology, School of Medicine and Psychology, Sapienza University of Rome, Sant'Andrea Hospital, Rome, Italy.
Loretta LicchelliDepartment of Neuroscience, Mental Health and Sensory Organs (NESMOS), School of Medicine and Psychology, Sapienza University of Rome, Sant'Andrea Hospital, Via di Grottarossa 1035, 00189, Rome, Italy.
Alessandra FrattariDepartment of Cardiology, School of Medicine and Psychology, Sapienza University of Rome, Sant'Andrea Hospital, Rome, Italy.
Nadia Attalla El HalabiehDepartment of Cardiology, School of Medicine and Psychology, Sapienza University of Rome, Sant'Andrea Hospital, Rome, Italy.
Erica GabrieleDepartment of Cardiology, School of Medicine and Psychology, Sapienza University of Rome, Sant'Andrea Hospital, Rome, Italy.
Giulia PignatelliDepartment of Cardiology, School of Medicine and Psychology, Sapienza University of Rome, Sant'Andrea Hospital, Rome, Italy.
Tiziana De SantisDepartment of Neuroscience, Mental Health and Sensory Organs (NESMOS), School of Medicine and Psychology, Sapienza University of Rome, Sant'Andrea Hospital, Via di Grottarossa 1035, 00189, Rome, Italy.
Laura FiondaDepartment of Neuroscience, Mental Health and Sensory Organs (NESMOS), School of Medicine and Psychology, Sapienza University of Rome, Sant'Andrea Hospital, Via di Grottarossa 1035, 00189, Rome, Italy.
Fiammetta VanoliDepartment of Neuroscience, Mental Health and Sensory Organs (NESMOS), School of Medicine and Psychology, Sapienza University of Rome, Sant'Andrea Hospital, Via di Grottarossa 1035, 00189, Rome, Italy.
Stefania MorinoDepartment of Neuroscience, Mental Health and Sensory Organs (NESMOS), School of Medicine and Psychology, Sapienza University of Rome, Sant'Andrea Hospital, Via di Grottarossa 1035, 00189, Rome, Italy.
Matteo GaribaldiDepartment of Neuroscience, Mental Health and Sensory Organs (NESMOS), School of Medicine and Psychology, Sapienza University of Rome, Sant'Andrea Hospital, Via di Grottarossa 1035, 00189, Rome, Italy.
Antonella Di PasqualeDepartment of Neuroscience, Mental Health and Sensory Organs (NESMOS), School of Medicine and Psychology, Sapienza University of Rome, Sant'Andrea Hospital, Via di Grottarossa 1035, 00189, Rome, Italy.
Nicola VanacoreNational Centre for Disease Prevention and Health Promotion, National Institute of Health, Rome, Italy.
Annalisa BottaMedical Genetic Section, Department of Biomedicine and Prevention, Tor Vergata University, Rome, Italy.
Giovanni AntoniniDepartment of Neuroscience, Mental Health and Sensory Organs (NESMOS), School of Medicine and Psychology, Sapienza University of Rome, Sant'Andrea Hospital, Via di Grottarossa 1035, 00189, Rome, Italy. giovanni.antonini@uniroma1.it.ORCID http://orcid.org/0000-0002-7519-7739
Azienda Ospedaliera Sant'Andrea · ITSapienza University of Rome · ITIstituto Superiore di Sanità · ITUniversity of Rome Tor Vergata · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cardiac conduction and/or rhythm abnormalities (CCRA) are the most frequent and life-threatening complications in DM1. In order to determine prevalence, incidence, characteristics, age of onset and predictors of CCRA, CCRA progression and sudden cardiac death (SCD) in DM1, we collected ECG/24hECG-Holter data from a yearly updated 34-year database of a cohort of 103 DM1 patients without cardiac abnormalities at baseline, followed for at least 1 year. Fifty-five patients developed CCRA [39 developed conduction abnormalities (CCA) and 16 rhythm abnormalities (CRA)], which progressed in 22. Nine had SCD. Risk and incidence of CCRA amounted to 53.4 and 6.83% person-years (CCA: 37.9 and 4.8%; CRA 15.5 and 2%), respectively; risk and incidence of SCD amounted to 8.74 and 0.67% person-years, respectively. CTG expansion represented a predictor of CCRA incidence (HR 1.10, p = 0.04), CCRA progression (HR 1.28, p = 0.001) and SCD (HR 1.39, p = 0.002). MIRS progression during follow-up was associated with CCRA prevalence (OR 5.82, p = 0.004); older age and larger CTG expansion to SCD prevalence (OR 2.67, p = 0.012; OR 1.54, p = 0.005). Age of CCRA onset and CCRA progression was significantly lower in patients with larger CTG expansion and in those with MIRS progression. Age when SCD occurred was significantly lower in patients with larger CTG expansion. Amongst recorded cardiac abnormalities, both atrial flutter (OR 8.70; p = 0.031) and paroxysmal supraventricular tachycardia (OR 8.67; p = 0.040) were associated with SCD. Although all DM1patients may develop cardiac abnormalities at any time in their life, patients older than 30 years with larger CTG expansion and MIRS progression in particular should be carefully monitored via periodical ECG.

Indexed as

AdolescentAdultArrhythmias, CardiacCardiac Conduction System DiseaseCohort StudiesElectrocardiographyFemaleHumansItalyMaleMiddle AgedMyotonic DystrophyPrevalenceProportional Hazards ModelsSeverity of Illness IndexYoung AdultCardiac conduction and/or rhythm abnormalitiesCTG expansionIncidenceMyotonic dystrophy type 1PrevalenceRisk factorsSudden cardiac death

Identifiers

PMID29429070
OpenAlexW2786161669

What OpenQuestion holds

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Registered trials

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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.