Evidence map›Paper›PMID 36793650›Full record

ArticleActa myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology2022

The Performance of Upper Limb (PUL) module in limb-girdle muscular dystrophy.

Eleonora Diella, Antonella LoMauro, Morena Delle Fave, Rossella Cima, Maria Grazie D'Angelo

Open access · greenAbstract read
In one paragraph

Article in Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.3field-weighted citation impact, top 38% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

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

5 authors at 1 institution in 1 country.

Eleonora DiellaNeuro Rehabilitation of Rare Diseases of Central and Pheripheral Nervous System Unit Scientific Institute IRCCS E. Medea, Bosisio Parini (LC), Italy.
Antonella LoMauroDipartimento di Elettronica, Informazione e Bioingegneria, Politecnico di Milano, Milan, Italy.
Morena Delle FaveNeuro Rehabilitation of Rare Diseases of Central and Pheripheral Nervous System Unit Scientific Institute IRCCS E. Medea, Bosisio Parini (LC), Italy.
Rossella CimaNeuro Rehabilitation of Rare Diseases of Central and Pheripheral Nervous System Unit Scientific Institute IRCCS E. Medea, Bosisio Parini (LC), Italy.
Maria Grazie D'AngeloNeuro Rehabilitation of Rare Diseases of Central and Pheripheral Nervous System Unit Scientific Institute IRCCS E. Medea, Bosisio Parini (LC), Italy.
Politecnico di Milano · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Limb-girdle muscular dystrophy (LGMD) is a genetic muscle disorder causing weakness and wasting of the proximal limb musculature. When ambulation is lost, the attention must be shifted to the upper limb muscles' function. We studied the upper limb muscle strength and the corresponding function in 15 LGMDR1/LGMD2A and 13 LGMDR2/LGMD2B, through the Performance of Upper Limb scale and the MRC score of upper limbs. The proximal item K and the distal items N and R were lower in LGMD2B/R2. The mean MRC score of all the muscles involved linearly correlated (r2 = 0.922) for item K in LGMD2B/R2. The functional worsening paralleled the muscles weakness in LGMD2B/R2. By contrast, at proximal level the function of LGMD2A/R1 was preserved despite muscle weakness was present, presumably due to compensatory strategies. Sometimes the combination of parameters might be more informative than considering them separately. PUL scale and MRC might be interesting outcome measures in non-ambulant patients.

Indexed as

Muscular Dystrophies, Limb-GirdleHumansMuscle, SkeletalMuscle WeaknessUpper ExtremityLGMD2A/R1LGMD2B/R2limb-girdle muscular dystrophyMRC scorePerformance of Upper Limb (PUL version 1.2) scale

Identifiers

PMID36793650
PMCPMC9896594
OpenAlexW4321004442

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.