Evidence map›Paper›PMID 30710167›Full record

ArticleJournal of neurology2019

Muscle pain in mitochondrial diseases: a picture from the Italian network.

Massimiliano Filosto, Stefano Cotti Piccinelli, Costanza Lamperti, Tiziana Mongini, Serenella Servidei, Olimpia Musumeci, Paola Tonin, Filippo Maria Santorelli, Costanza Simoncini, Guido Primiano and 10 more

Open access · greenAbstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in Journal of neurology, 2019. 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
0.7field-weighted citation impact, top 32% 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, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Chronic pain is common in mitochondrial disease.Neuromuscular disorders : NMD · 2020
    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

20 authors at 12 institutions in 1 country.

Massimiliano FilostoCenter for Neuromuscular Diseases, Unit of Neurology, ASST Spedali Civili and University of Brescia, Brescia, Italy. massimiliano.filosto@unibs.it.ORCID http://orcid.org/0000-0002-2852-7512
Stefano Cotti PiccinelliCenter for Neuromuscular Diseases, Unit of Neurology, ASST Spedali Civili and University of Brescia, Brescia, Italy.
Costanza LampertiUnit of Medical Genetics and Neurogenetics, Fondazione IRCCS Istituto Neurologico 'Carlo Besta', Milan, Italy.
Tiziana MonginiDepartment of Neurosciences Rita Levi Montalcini, University of Torino, Torino, Italy.
Serenella ServideiUOC Neurofisiopatologia Fondazione Policlinico Universitario A. Gemelli IRCCS, Istituto di Neurologia Università Cattolica del Sacro Cuore, Roma, Italy.
Olimpia MusumeciDepartment of Clinical and Experimental Medicine, UOC di Neurologia e Malattie Neuromuscolari, University of Messina, Messina, Italy.
Paola ToninNeurological Clinic, University of Verona, Verona, Italy.
Filippo Maria SantorelliUnit of Molecular Medicine, IRCCS Foundation Stella Maris, Pisa, Italy.
Costanza SimonciniNeurological Clinic, University of Pisa, Pisa, Italy.
Guido PrimianoUOC Neurofisiopatologia Fondazione Policlinico Universitario A. Gemelli IRCCS, Istituto di Neurologia Università Cattolica del Sacro Cuore, Roma, Italy.
Liliana VercelliDepartment of Neurosciences Rita Levi Montalcini, University of Torino, Torino, Italy.
Anna RubegniUnit of Molecular Medicine, IRCCS Foundation Stella Maris, Pisa, Italy.
Anna GalvagniCenter for Neuromuscular Diseases, Unit of Neurology, ASST Spedali Civili and University of Brescia, Brescia, Italy.
Maurizio MoggioNeuromuscular and Rare Diseases Unit, Department of Neuroscience, Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico, Milan, Italy.
Giacomo Pietro ComiNeurology Unit, Neuroscience Section, Department of Pathophysiology and Transplantation, Dino Ferrari Centre, IRCCS Foundation Ca' Granda Ospedale Maggiore Policlinico, University of Milan, Milan, Italy.
Valerio CarelliIRCCS Institute of Neurological Sciences of Bologna, Bellaria Hospital, Bologna, Italy.
Antonio ToscanoDepartment of Clinical and Experimental Medicine, UOC di Neurologia e Malattie Neuromuscolari, University of Messina, Messina, Italy.
Alessandro PadovaniCenter for Neuromuscular Diseases, Unit of Neurology, ASST Spedali Civili and University of Brescia, Brescia, Italy.
Gabriele SicilianoNeurological Clinic, University of Pisa, Pisa, Italy.
Michelangelo MancusoNeurological Clinic, University of Pisa, Pisa, Italy.
University of Brescia · ITUniversity of Pisa · ITFondazione Stella Maris · ITUniversità Cattolica del Sacro Cuore · ITUniversity of Messina · ITUniversity of Turin · ITAzienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia · ITFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico · ITFondazione IRCCS Istituto Neurologico Carlo Besta · ITInstitute of Neurological Sciences · ITUniversity of Milan · ITUniversity of Verona · IT

Funding

Fondazione Telethon GSP16001Fondazione Telethon GUP09004
6 · The paper itself

Abstract

Muscle pain may be part of many neuromuscular disorders including myopathies, peripheral neuropathies and lower motor neuron diseases. Although it has been reported also in mitochondrial diseases (MD), no extensive studies in this group of diseases have been performed so far. We reviewed clinical data from 1398 patients affected with mitochondrial diseases listed in the database of the "Nation-wide Italian Collaborative Network of Mitochondrial Diseases", to assess muscle pain and its features. Muscle pain was present in 164 patients (11.7%). It was commonly observed in subjects with chronic progressive external ophthalmoplegia (cPEO) and with primary myopathy without cPEO, but also-although less frequently-in multisystem phenotypes such as MELAS, MERFF, Kearns Sayre syndrome, NARP, MNGIE and Leigh syndrome. Patients mainly complain of diffuse exercise-related muscle pain, but focal/multifocal and at rest myalgia were often also reported. Muscle pain was more commonly detected in patients with mitochondrial DNA mutations (67.8%) than with nuclear DNA changes (32.2%). Only 34% of the patients showed a good response to drug therapy. Interestingly, patients with nuclear DNA mutations tend to have a better therapeutic response than patients with mtDNA mutations. Muscle pain is present in a significant number of patients with MD, being one of the most common symptoms. Although patients with a myopathic phenotype are more prone to develop muscle pain, this is also observed in patients with a multi system involvement, representing an important and disabling symptom having poor response to current therapy.

Indexed as

AdolescentAdultAgedAged, 80 and overChildChild, PreschoolFemaleHumansItalyMaleMiddle AgedMitochondrial DiseasesMyalgiaPhenotypePrevalenceRetrospective StudiescPEOMitochondrial diseasesMitochondrial myopathyMuscle painMyalgia

Identifiers

PMID30710167
OpenAlexW2914636212

What Socratic 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 Socratic graph.