Evidence map›Paper›PMID 39600735›Full record

ArticleCureus2024

Evaluation of Sarcopenia by Psoas Muscle Measurements in Bullous Pemphigoid: A Single-Institution Survey in Japan.

Yu Matsui, Teruhiko Makino, Tadamichi Shimizu

Abstract read
In one paragraph

Article in Cureus, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Yu MatsuiDepartment of Dermatology, University of Toyama, Toyama, JPN.
Teruhiko MakinoDepartment of Dermatology, University of Toyama, Toyama, JPN.
Tadamichi ShimizuDepartment of Dermatology, University of Toyama, Toyama, JPN.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bullous pemphigoid (BP) is a rare autoimmune blistering disease that primarily affects elderly individuals. Based on the Bullous Pemphigoid Disease Area Index (BPDAI) severity assessment, immunosuppressive drugs are recommended for severe cases that fall within the more than moderate classes. Sarcopenia, which is characterized by decreased skeletal muscle mass and function in elderly patients, is a progressive and widespread skeletal muscle disease. We retrospectively surveyed patients who received treatment for BP at our hospital between 2012 and 2024 to evaluate the relevance of sarcopenia, as assessed using the psoas muscle mass index (PMI), and to investigate the benefit of relapse-free survival (RFS). A total of 59 patients with BP were included in this study. A total of 57.6% (34 of 59 patients) of the BP patients had sarcopenia, as measured by PMI. Kaplan-Meier analysis showed that the sarcopenia group (n = 34) had a median RFS of 394 days, which was not longer than that of the non-sarcopenia group (n = 25, 275 days) (p = 0.894). No significant difference in RFS was observed in the subgroup analysis based on the severity of BPDAI. Our real-world data confirmed the high prevalence of sarcopenia in the BP population and the efficacy of standard treatment centered on immunosuppressive therapy based on the severity of BPDAI. There is little basis for reducing oral corticosteroids below 0.5 mg/kg based solely on the patient's perceived frailty, regardless of the severity of the BPDAI. Limited evidence is available to assess the association between sarcopenia and autoimmune diseases in terms of their etiology. As populations continue to age globally, it is important for clinicians to prioritize addressing diseases while considering whether patients experience frailty in daily practice.

Indexed as

bullous pemphigoid (bp)frailty syndromepsoas muscle indexretrospective researchsarcopenia

Identifiers

PMID39600735
PMCPMC11589168

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