Evidence map›Paper›PMID 40237941›Full record

ReviewClinical rheumatology2025

Anti-mitochondrial antibody-positive inflammatory myopathy with multiple arrhythmias resistant to high-dose glucocorticoids and intravenous cyclophosphamide: a case-based review.

Tomoyuki Mutoh, Mikihiro Takahashi, Hiroyuki Satake, Kensuke Daikoku, Hiroshi Fujii

Abstract readCase ReportsReview
PubMed Publisher
In one paragraph

Review in Clinical rheumatology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
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  5. Review
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

5 authors.

Tomoyuki MutohDepartment of Rheumatology, Osaki Citizen Hospital, 3-8-1 Furukawa Honami, Osaki, Miyagi, 989 - 6183, Japan. qma-kyo@hotmail.co.jp.ORCID http://orcid.org/0000-0001-5995-8609
Mikihiro TakahashiDepartment of Rheumatology, Tohoku University Hospital, Sendai, Miyagi, Japan.
Hiroyuki SatakeDepartment of Cardiovascular Medicine, Osaki Citizen Hospital, Osaki, Miyagi, Japan.
Kensuke DaikokuDepartment of Nephrology and Endocrinology, Osaki Citizen Hospital, Osaki, Miyagi, Japan.
Hiroshi FujiiDepartment of Rheumatology, Tohoku University Hospital, Sendai, Miyagi, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Idiopathic inflammatory myopathies (IIMs) are a heterogeneous group of autoimmune diseases characterized primarily by muscle inflammation. Anti-mitochondrial antibodies (AMA) are typically associated with primary biliary cholangitis; however, they have also been linked to a rare subgroup of IIMs, namely "AMA-positive myositis," marked by a chronic disease course and muscle weakness, particularly affecting the paravertebral muscles, alongside muscle atrophy and cardiopulmonary complications. We report the case of a 40-year-old woman diagnosed with AMA-positive myositis, predominantly involving axial myopathy complicated by multiple arrhythmias and biopsy-proven focal segmental glomerulosclerosis with mitochondrial abnormalities on electron microscopy. The patient presented with progressive back pain and palpitations over a 3-month period. Although high-dose glucocorticoids and intravenous cyclophosphamide improved the axial myopathy and proteinuria, the cardiac condition remained unstable, necessitating permanent pacemaker implantation for persistent sinus dysfunction and radiofrequency catheter ablation for worsening atrial fibrillation (Af). Our literature review focusing on cardiac involvement in AMA-positive myositis revealed tachyarrhythmia was the most common (87.7%), particularly Af (55.4%), followed by cardiomyopathy (74.2%), myocarditis (43.2%), and bradyarrhythmia (40.0%). Arrhythmias and/or cardiac function deteriorated in 41.7% of patients treated with immunosuppressants and in 66.7% of patients treated without immunosuppressants, respectively. Furthermore, in the treated group, more patients with worsened cardiac lesions required additional electronic devices compared to those without (53.3% vs. 4.8%). Early detection and adequate management of cardiac complications in AMA-positive myositis are critical to prevent irreversible myocardial damage and fatal outcomes. In addition to cardiac complications, concomitant renal involvement associated with AMA-positive myositis may be also considered.

Indexed as

Arrhythmias, CardiacAutoantibodiesCyclophosphamideGlucocorticoidsMitochondriaMyositisAdultFemaleGlomerulosclerosis, Focal SegmentalHumansImmunosuppressive AgentsAutoantibodiesCyclophosphamideGlucocorticoidsImmunosuppressive AgentsAnti-mitochondrial antibodyAxial myopathyCardiac involvementFocal segmental glomerulosclerosisIdiopathic inflammatory myopathiesMyositis

Identifiers

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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.