Evidence map›Paper›PMID 27708934›Full record

ArticleEuropean journal of rheumatology2015

High-dose intravenous immunoglobulin therapy for rapidly progressive interstitial pneumonitis accompanied by anti-melanoma differentiation-associated gene 5 antibody-positive amyopathic dermatomyositis.

Kazu Hamada-Ode, Yoshinori Taniguchi, Takahito Kimata, Yasushi Kawaguchi, Yoshiko Shimamura, Masataka Kuwana, Shimpei Fujimoto, Yoshio Terada

Open access · diamondAbstract read
In one paragraph

Article in European journal of rheumatology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 24% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 27 citations in OpenAlex.

  1. Pooled it
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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

8 authors at 3 institutions in 1 country.

Kazu Hamada-OdeDepartment of Endocrinology, Metabolism, Nephrology and Rheumatology, Kochi University Medical School, Kochi, Japan.
Yoshinori TaniguchiDepartment of Endocrinology, Metabolism, Nephrology and Rheumatology, Kochi University Medical School, Kochi, Japan.
Takahito KimataDepartment of Rheumatology, Misato Bay Side Medical Center, Kochi, Japan.
Yasushi KawaguchiDepartment of Rheumatology, Tokyo Women's Medical University, Tokyo, Japan.
Yoshiko ShimamuraDepartment of Endocrinology, Metabolism, Nephrology and Rheumatology, Kochi University Medical School, Kochi, Japan.
Masataka KuwanaDepartment of Rheumatology, Nippon Medical School, Tokyo, Japan.
Shimpei FujimotoDepartment of Endocrinology, Metabolism, Nephrology and Rheumatology, Kochi University Medical School, Kochi, Japan.
Yoshio TeradaDepartment of Endocrinology, Metabolism, Nephrology and Rheumatology, Kochi University Medical School, Kochi, Japan.
Kōchi University · JPNippon Medical School · JPTokyo Women's Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Anti-melanoma differentiation-associated gene 5 (MDA5) antibody-positive amyopathic dermatomyositis (ADM) associated with rapidly progressive interstitial pneumonitis (RPIP) frequently has a poor prognosis and optimal treatment is not well defined. Here, we report a 62-year-old Japanese man with anti-MDA5 antibody-positive ADM associated with RPIP presented with progressive shortness of breath, Heliotrope rash, Gottron's papules, arthralgia, and fatigue but no sign of muscle weakness. Laboratory investigation revealed serum levels of the following biomarkers: ferritin, 1393 ng/mL; Krebs von der Lungen-6, 1880 U/mL; and creatine kinase, 85 U/L. Computed tomography (CT) images showed diffuse ground-glass opacity in both lung fields. Because anti-MDA5 was positive, we made a diagnosis of ADM associated with RPIP and initiated treatment. Following five courses of combination therapy with prednisolone, cyclosporine A, and intravenous cyclophosphamide (IVCY), IVCY treatment was switched to high-dose intravenous immunoglobulin therapy (IVIg) because of the reactivation of interstitial pneumonia with an increased serum ferritin level. Additional treatment with IVIg improved RPIP, with normalization of anti-ADM antibody levels. Therefore, IVIg mayt be a new candidate treatment for anti-MDA5 antibody-positive ADM associated with RPIP.

Indexed as

Amyopathicanti-MDA5 antibodydermatomyositisinterstitial pneumonitis

Identifiers

PMID27708934
PMCPMC5047270
OpenAlexW2150158642

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.