Evidence map›Paper›PMID 29417209›Full record

ReviewRheumatology international2018

Rapidly progressive interstitial lung disease due to anti-MDA5 antibodies without skin involvement: a case report and literature review.

Juan González-Moreno, Manuel Raya-Cruz, Ines Losada-Lopez, Ana Paula Cacheda, Cristina Oliver, Bartomeu Colom

Open access · bronzeAbstract readCase ReportsReview
In one paragraph

Review in Rheumatology international, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
4.1field-weighted citation impact, top 6% 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

26 citing papers in PubMed, 1 synthesis or guideline pooled it, 48 citations in OpenAlex.

  1. Pooled it
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  10. Review
  11. Review
  12. Article
  13. World journal of clinical cases · 2022
    Article
  14. Acute interstitial pneumonia due to amyopathic dermatomyositis.Proceedings (Baylor University. Medical Center) · 2022
    Article
  15. The significance of myositis autoantibodies in idiopathic inflammatory myopathy concomitant with interstitial lung disease.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2021
    Article
  16. Review
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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

6 authors at 1 institution in 1 country.

Juan González-MorenoInternal Medicine Department, Hospital Son Llàtzer, Carretera de Manacor Km4, 07198, Palma, Baleares, Spain. juan.glzmr@gmail.com.ORCID http://orcid.org/0000-0001-8046-112X
Manuel Raya-CruzInternal Medicine Department, Hospital Son Llàtzer, Carretera de Manacor Km4, 07198, Palma, Baleares, Spain.
Ines Losada-LopezInternal Medicine Department, Hospital Son Llàtzer, Carretera de Manacor Km4, 07198, Palma, Baleares, Spain.ORCID http://orcid.org/0000-0002-4834-0843
Ana Paula CachedaRheumatology Department, Hospital Son Llàtzer, Carretera de Manacor Km4, 07198, Palma, Baleares, Spain.
Cristina OliverRespiratory Department, Hospital Son Llàtzer, Carretera de Manacor Km4, 07198, Palma, Baleares, Spain.
Bartomeu ColomPathology Department, Hospital Son Llàtzer, Carretera de Manacor Km4, 07198, Palma, Baleares, Spain.ORCID http://orcid.org/0000-0001-5147-5987
Hospital Son Llatzer · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Anti-MDA5 antibodies have been strongly associated with rapidly progressive interstitial lung disease (RP-ILD) in dermatomyositis (DM) patients, especially in the clinically amyopathic subset (CADM). We present a case of anti-MDA5 antibody-associated RP-ILD in a patient with arthritis but with no other clinical signs suggestive of DM or CADM successfully treated with a combination of cyclophosphamide, cyclosporine and corticoids. A review of the literature was also done. Despite its rarity, anti-MDA5 antibody-associated ILD should be suspected in cases of RP-ILD even without other signs of DM or CADM as prompt and aggressive treatment could improve prognosis.

Indexed as

Anti-Inflammatory AgentsAutoantibodiesCyclosporineDermatomyositisFemaleHumansInterferon-Induced Helicase, IFIH1Lung Diseases, InterstitialMethylprednisoloneMiddle AgedAnti-Inflammatory AgentsAutoantibodiesCyclosporineIFIH1 protein, humanInterferon-Induced Helicase, IFIH1MethylprednisoloneAnti-CADM-140 antibodiesAnti-MDA5 antibodiesClinically amyopathic dermatomyositisDermatomyositisDiffuse alveolar damageRapidly progressive interstitial lung disease

Identifiers

PMID29417209
PMCPMC7101732
OpenAlexW2786968638

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.