Evidence map›Paper›PMID 34159491›Full record

ArticleClinical rheumatology2021

Myositis-specific antibodies and clinical characteristics in patients with autoimmune inflammatory myopathies: reported by the Argentine Registry of Inflammatory Myopathies of the Argentine Society of Rheumatology.

Graciela N Gómez, Nicolás Pérez, Andrea Braillard Poccard, Ramiro A Gómez, Ana C Costi, Mercedes A García, Malena Viola, Alejandro Benitez, Mariana M Aciar, María Crespo Espíndola and 9 more

Abstract read
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In one paragraph

Article in Clinical rheumatology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 15% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Onset of amyopathic dermatomyositis following mRNA-based SARS-CoV-2 vaccination.Journal of the European Academy of Dermatology and Venereology : JEADV · 2022
    Article
  9. Article
  10. 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

19 authors at 9 institutions in 1 country.

Graciela N GómezDepartment of Immunology, Instituto de Investigaciones Médicas Alfredo Lanari, Buenos Aires University, Autonomous City of Buenos Aires, 3150 Combatientes de Malvinas Ave, 1431, PC, Argentina. gragomez@live.com.ar.ORCID http://orcid.org/0000-0003-4389-3083
Nicolás PérezDepartment of Immunology, Instituto de Investigaciones Médicas Alfredo Lanari, Buenos Aires University, Autonomous City of Buenos Aires, 3150 Combatientes de Malvinas Ave, 1431, PC, Argentina.
Andrea Braillard PoccardDepartment of Rheumatology, Hospital de Clínicas, José de San Martín, Buenos Aires University, Autonomous City of Buenos Aires, Argentina.
Ramiro A GómezDepartment of Rheumatology, Hospital de Clínicas, José de San Martín, Buenos Aires University, Autonomous City of Buenos Aires, Argentina.
Ana C CostiDepartment of Rheumatology, Province of Buenos Aires, H.I.G.A San Martín, La Plata City, Argentina.
Mercedes A GarcíaDepartment of Rheumatology, Province of Buenos Aires, H.I.G.A San Martín, La Plata City, Argentina.
Malena ViolaDepartment of Rheumatology, Hospital General de Agudos Dr. Cosme Argerich, Autonomous City of Buenos Aires, Argentina.
Alejandro BenitezDepartment of Rheumatology, Hospital General de Agudos Dr. Cosme Argerich, Autonomous City of Buenos Aires, Argentina.
Mariana M AciarDepartment of Rheumatology, Hospital Nuestro Señor del Milagro, Salta City, Province of Salta, Argentina.
María Crespo EspíndolaDepartment of Rheumatology, Hospital Nuestro Señor del Milagro, Salta City, Province of Salta, Argentina.
Demelza YucraDepartment of Rheumatology, Sanatorio Güemes, Autonomous City of Buenos Aires, Argentina.
Micaela A CosattiDepartment of Rheumatology, CEMIC, Autonomous City of Buenos Aires, Argentina.
Cecilia PisoniDepartment of Rheumatology, CEMIC, Autonomous City of Buenos Aires, Argentina.
Dafne CapelusnikDepartment of Rheumatology, Instituto de Rehabilitación Psicofsica (IREP), Autonomous City of Buenos Aires, Argentina.
María N LojoDepartment of Rheumatology, Hospital Rossi, La Plata City, Province of Buenos Aires, Argentina.
Belen I BarriosDepartment of Rheumatology, Hospital Enrique Tornú, Autonomous City of Buenos Aires, Argentina.
Mariano RiveroDepartment of Rheumatology, British Hospital, Autonomous City of Buenos Aires, Argentina.
Boris KislukDepartment of Rheumatology, Hospital Eva Perón, Granadero Baigorria City, Province of Santa Fe, Argentina.
Amelia GranelDepartment of Rheumatology, Hospital San Roque, La Plata City, Province of Buenos Aires, Argentina.
Argerich Hospital · ARCentro de Educación Médica e Investigaciones Clínicas Norberto Quirno · ARHospital de Clínicas "José de San Martín" · ARHospital Italiano La Plata · ARNational University of Salta · ARUniversidad de Buenos Aires · ARHospital Británico de Buenos Aires · ARHospital El Cruce · ARInstituto Nacional de Rehabilitación Psicofísica · AR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

INTRODUCTION/

objectivesTo describe clinical features in patients with inflammatory myopathies (IMs) from the Argentine Registry of Inflammatory Myopathies, and their relationship with myositis-specific antibodies (MSAs).

methodsThis cross-sectional study included 360 adult patients with dermatomyositis (DM), polymyositis (PM), and inclusion body myositis. Demographics, clinical, and serological characteristics were retrospectively recorded (2016-2019). MSAs were determined by immunoblotting. Patients who were positive for anti-Jo-1, Mi-2, and MDA5 were compared against a group of patients, taken as reference group, who were negative for all MSAs.

resultsWomen 72%, median age at diagnosis was 47.3 years (18-82). The most frequent subtypes were DM (43.9%) followed by PM (30%).The most frequent MSAs were anti-Jo-1 (51/317), 16.1%; MDA5 (12/111), 10.8%, and Mi-2 (23/226), 10.2%. Anti-Jo-1 was associated (p < 0.05) with a higher frequency of chronic disease course, interstitial lung disease (ILD), arthritis, and mechanic's hands. Anti-Mi-2 was found in patients who had higher frequency of skin manifestations and higher CK values (p < 0.001). Patients with anti-MDA5 had normal or low CK levels. Anti-MDA5 was associated (p < 0.05) with skin manifestations, arthritis, and ILD. The rest of MSAs had frequencies lower than 8%. Anti-TIF1ϒ was found in eight DM patients and one had cancer. Anti-SRP was found in seven patients who had PM and elevated CK.

conclusionAnti-Jo-1 was the most frequent MSA, and was associated with ILD; MDA5 was associated with CADM and ILD, and Mi-2, with classical DM. Despite the different prevalence with respect to other cohorts, the clinical characteristics for each MSA group were similar to the data reported in other studies. Key Points • This study describes the prevalence of MSAs in the Argentine Registry of IMs. • Anti-Jo-1 and anti-MDA5 were associated with ILD. • Anti-Mi-2 was the third most frequent MSA, associated with classical DM.

Indexed as

DermatomyositisMyositisRheumatologyAdultAutoantibodiesCross-Sectional StudiesFemaleHumansRegistriesRetrospective StudiesAutoantibodiesArgentine Registry of Inflammatory MyopathiesDermatomyositisIdiopathic inflammatory myopathyInflammatory myopathiesMyositis-specific antibodiesPolymyositis

Identifiers

PMID34159491
OpenAlexW3177477296

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.