Evidence map›Paper›PMID 20044785›Full record

ArticleRheumatology international2012

Treatment of inclusion body myositis: is low-dose intravenous immunoglobulin the solution?

Mike Recher, Ulrike Sahrbacher, Juliane Bremer, Börge Arndt, Urs Steiner, Adriano Fontana

Open access · greenAbstract readCase Reports
PubMed Publisher
In one paragraph

Article in Rheumatology international, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.6field-weighted citation impact, top 28% 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

8 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Emerging therapeutic options for sporadic inclusion body myositis.Therapeutics and clinical risk management · 2015
    Review
  5. Novel approaches in the treatment of myositis and myopathies.Therapeutic advances in musculoskeletal disease · 2012
    Article
  6. Review
  7. Review
  8. 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

6 authors at 1 institution in 1 country.

Mike RecherClinic for Immunology, Department of Internal Medicine, University Hospital Zürich, Haeldeliweg 4, 8044 Zurich, Switzerland. mike.recher@usz.ch
Ulrike Sahrbacher
Juliane Bremer
Börge Arndt
Urs Steiner
Adriano Fontana
University Hospital of Zurich · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inclusion body myositis (IBM), the most common inflammatory myopathy in the elderly, is often resistant to various forms of therapy. Placebo-controlled treatment trials with high dose intravenous immunoglobulins (IVIG) have shown disease amelioration in some but not all patients. Here, we present the informative case of a 70-year-old woman with diagnosed inclusion body myositis that showed progressive muscle weakness without treatment and following immuno-suppressive treatment with corticosteroids and azathioprine. A trial with low-dose intravenous immunoglobulins was started at that time. The patient responded rapidly to low dose IVIG treatment with amelioration of muscle strength and normalization of CK serum activities. Our results demonstrate that IBM patients may respond to low-dose IVIG treatment which has important clinical and economic consequences.

Indexed as

Adrenal Cortex HormonesAgedAzathioprineDrug ResistanceFemaleHumansImmunoglobulins, IntravenousMuscle, SkeletalMyositis, Inclusion BodyTreatment OutcomeAdrenal Cortex HormonesAzathioprineImmunoglobulins, Intravenous

Identifiers

PMID20044785
OpenAlexW2086575353

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.