Evidence map›Paper›PMID 41089430›Full record

ArticlePCN reports : psychiatry and clinical neurosciences2025

Corticosteroids with low glucocorticoid activity as a potential therapeutic strategy for post-COVID-19 myalgic encephalomyelitis/chronic fatigue syndrome in patients with bipolar affective disorder: A case report.

Kan Nakajima, Nobutaka Ayani, Teruyuki Matsuoka, Kenya Kasahara, Yoshiyuki Nakajima, Haruki Ikawa, Riki Kitaoka, Tatsuhiko Akimoto, Jin Narumoto

Abstract read
In one paragraph

Article in PCN reports : psychiatry and clinical neurosciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
–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

3 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. 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

9 authors.

Kan NakajimaDepartment of Psychiatry NHO Maizuru Medical Center Maizuru-shi Kyoto Japan.
Nobutaka AyaniDepartment of Psychiatry NHO Maizuru Medical Center Maizuru-shi Kyoto Japan.ORCID https://orcid.org/0000-0003-1130-052X
Teruyuki MatsuokaDepartment of Psychiatry NHO Maizuru Medical Center Maizuru-shi Kyoto Japan.ORCID https://orcid.org/0000-0001-7683-7825
Kenya KasaharaDepartment of Endocrinology and Metabolism Graduate School of Medical Science Kyoto Prefectural University of Medicine Kamigyo-ku Kyoto Japan.
Yoshiyuki NakajimaDepartment of Psychiatry Higashikouri Hospital Hirakata-shi Osaka Japan.
Haruki IkawaDepartment of Psychiatry Graduate School of Medical Science Kyoto Prefectural University of Medicine Kamigyo-ku Kyoto Japan.
Riki KitaokaDepartment of Psychiatry Graduate School of Medical Science Kyoto Prefectural University of Medicine Kamigyo-ku Kyoto Japan.
Tatsuhiko AkimotoDepartment of Psychiatry Kitayama Hospital Sakyo-ku Kyoto Japan.
Jin NarumotoDepartment of Psychiatry Graduate School of Medical Science Kyoto Prefectural University of Medicine Kamigyo-ku Kyoto Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The COVID-19 pandemic has led to an increase in post-acute sequelae, including myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS), potentially mediated by dysfunction of the hypothalamic-pituitary-adrenal (HPA) axis. Corticosteroids are occasionally administered to ameliorate fatigue symptoms in ME/CFS; however, their psychiatric adverse effects, particularly in individuals with preexisting mood disorders, necessitate careful consideration. Case Presentation: We report the case of a 32-year-old woman with bipolar disorder who developed ME/CFS following COVID-19 infection. Initial corticosteroid therapy with betamethasone and prednisolone, agents with potent glucocorticoid receptor (GR) activity, resulted in a manic episode with psychotic features, necessitating psychiatric hospitalization. Although mood stabilization was achieved with olanzapine and valproate, corticosteroid withdrawal subsequently led to metabolic alkalosis and hypoxemia, secondary to hypothalamic hypoadrenalism. Following a comprehensive endocrinological assessment, physiological replacement therapy with hydrocortisone, characterized by relatively higher mineralocorticoid receptor (MR) activity and lower GR potency, was initiated, resulting in the resolution of physical symptoms without destabilization of psychiatric status. Conclusion: The clinical course suggests that GR-dominant corticosteroids may exacerbate psychiatric instability in patients with mood disorders. Simultaneously, MR-favoring agents, such as hydrocortisone, may offer a safer therapeutic alternative for managing HPA axis dysfunction. This case underscores the critical role of receptor selectivity in corticosteroid therapy, particularly in patients with comorbid psychiatric conditions, and highlights the necessity for individualized treatment strategies that integrate both endocrine and neuropsychiatric considerations.

Indexed as

antipsychoticsbipolar affective disordermyalgic encephalomyelitis/chronic fatigue syndromepost‐COVIDsteroid switch

Identifiers

PMID41089430
PMCPMC12515714

What Socratic 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 Socratic graph.