Evidence map›Paper›PMID 36168256›Full record

ArticleNeuropathology and applied neurobiology2023

Myostatin in idiopathic inflammatory myopathies: Serum assessment and disease activity.

Alexandrine Mahoudeau, Céline Anquetil, Nozomu Tawara, Hossein Khademian, Damien Amelin, Loïs Bolko, Marco Silvestro, Julian Dal Cin, Bérénice Tendrel, Virginie Tardif and 4 more

Open access · hybridAbstract read
In one paragraph

Article in Neuropathology and applied neurobiology, 2023. 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
1.1field-weighted citation impact, top 23% 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, 7 citations in OpenAlex.

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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

14 authors at 2 institutions in 1 country.

Alexandrine MahoudeauINSERM, Center of Research in Myology UMRS 974, Sorbonne Université, Paris, France.ORCID https://orcid.org/0000-0003-0027-5402
Céline AnquetilINSERM, Center of Research in Myology UMRS 974, Sorbonne Université, Paris, France.
Nozomu TawaraINSERM, Center of Research in Myology UMRS 974, Sorbonne Université, Paris, France.
Hossein KhademianINSERM, Center of Research in Myology UMRS 974, Sorbonne Université, Paris, France.
Damien AmelinINSERM, Association Institut de Myologie, Center of Research in Myology UMRS 974, Sorbonne Université, Paris, France.
Loïs BolkoDepartment of Internal Medicine and Clinical Immunology, Sorbonne Université, Pitié-Salpêtrière Hospital, Paris, France.
Marco SilvestroDepartment of Internal Medicine and Clinical Immunology, Sorbonne Université, Pitié-Salpêtrière Hospital, Paris, France.
Julian Dal CinINSERM, Center of Research in Myology UMRS 974, Sorbonne Université, Paris, France.
Bérénice TendrelINSERM, Center of Research in Myology UMRS 974, Sorbonne Université, Paris, France.
Virginie TardifINSERM, Center of Research in Myology UMRS 974, Sorbonne Université, Paris, France.
Kubéraka MariampillaiDepartment of Internal Medicine and Clinical Immunology, Sorbonne Université, Pitié-Salpêtrière Hospital, Paris, France.
Gillian Butler-BrowneINSERM, Center of Research in Myology UMRS 974, Sorbonne Université, Paris, France.
Olivier BenvenisteINSERM, Center of Research in Myology UMRS 974, Sorbonne Université, Paris, France.
Yves AllenbachINSERM, Center of Research in Myology UMRS 974, Sorbonne Université, Paris, France.
Inserm · FRSorbonne Université · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsIn idiopathic inflammatory myopathies (IIM), disease activity is difficult to assess, and IIM may induce severe muscle damage, especially in immune-mediated necrotising myopathies (IMNM) and inclusion body myositis (IBM). We hypothesise that myostatin, a negative regulator of muscle mass, could be a new biomarker of disease activity and/or muscle damage.

methodsProspective assessment of myostatin protein level in 447 IIM serum samples (dermatomyositis [DM], n = 157; IBM, n = 72; IMNM, n = 125; and antisynthetase syndrome [ASyS], n = 93) and 59 healthy donors (HD) was performed by ELISA. A gene transcript analysis was also carried out on 18 IIM muscle biopsies and six controls to analyse myostatin and myostatin pathway-related gene expression.

resultsIIM patients had lower myostatin circulating protein levels and gene expression compared to HD (2379 [1490; 3678] pg/ml vs 4281 [3169; 5787] pg/ml; p < 0.0001 and log2FC = -1.83; p = 0.0005, respectively). Myostatin-related gene expression varied accordingly. Based on the Physician Global Assessment, inactive IIM patients showed higher myostatin levels than active ones. This was the case for all IIM subgroups, except IMNM where low myostatin levels were maintained (2186 [1235; 3815] vs 2349 [1518; 3922] pg/ml; p = 0.4).

conclusionsMyostatin protein and RNA levels are decreased in all IIM patients, and protein levels correlate with disease activity. Inactive ASyS and DM patients have higher myostatin levels than active patients. Myostatin could be a marker of disease activity in these subgroups. However, IMNM patients do not have significant increase in myostatin levels after disease remission. This may highlight a new pathological disease mechanism in IMNM patients.

Indexed as

DermatomyositisMyositisMyositis, Inclusion BodyHumansMyostatinProspective StudiesMyostatinbiomarkerdisease activityidiopathic inflammatory myopathiesmusclemyostatin

Identifiers

PMID36168256
PMCPMC10092350
OpenAlexW4297458517

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.