# Prognostic impact of corticosteroid maintenance dose and re-escalation in patients with cardiac sarcoidosis

**Authors:** Takuya Nishimura, Kohei Ishibashi, Koshiro Kanaoka, Kenzaburo Nakajima, Takashi Ikee, Daiki Syako, Toshihiro Nakamura, Satoshi Oka, Akinori Wakamiya, Nobuhiko Ueda, Tsukasa Kamakura, Mitsuru Wada, Yuko Inoue, Koji Miyamoto, Takeshi Aiba, Kengo Kusano

PMC · DOI: 10.1136/openhrt-2026-004048 · Open Heart · 2026-03-06

## TL;DR

This study found that following the recommended corticosteroid dose improves survival in patients with cardiac sarcoidosis, while deviating from it increases mortality risk.

## Contribution

The study provides evidence on the prognostic impact of corticosteroid maintenance doses and re-escalation in cardiac sarcoidosis.

## Key findings

- Patients on the recommended corticosteroid dose had better survival compared to low- and high-dose groups.
- Re-escalation of corticosteroids after achieving maintenance dose was linked to higher mortality in the high-dose group.
- Maintaining the recommended dose appears critical for better clinical outcomes in cardiac sarcoidosis.

## Abstract

Japanese guidelines recommend a corticosteroid maintenance dose of 5–10 mg/day for cardiac sarcoidosis (CS); however, the optimal dose remains unclear. This study aimed to evaluate the impact of maintenance dose and corticosteroid re-escalation on prognosis in patients with CS.

This multicentre retrospective cohort study used data from a Japanese nationwide CS registry. A total of 352 patients diagnosed according to the Japanese Circulation Society 2016 guideline and treated with oral corticosteroids were included. Patients were grouped by maintenance dose: low (<5.0 mg/day), recommended (5.0–10.0 mg/day) and high (>10.0 mg/day). Clinical outcomes were analysed. The main outcome was all-cause mortality.

The low-dose, recommended-dose and high-dose groups comprised 11% (n=40), 78% (n=276) and 10% (n=36) of patients, with mean maintenance doses of 2.2 mg/day, 6.7 mg/day and 16.2 mg/day, respectively. During a median follow-up of 5.12 years, 39 patients (11%) died. Kaplan-Meier survival analysis showed statistically better survival in the recommended dose group, with the high-dose group showing statistically significantly worse outcomes (log-rank p=0.012). Corticosteroid re-escalation occurred in 19% of patients (9% before and 11% after achieving maintenance dose). All-cause mortality was 8% in the recommended-dose group versus 25% in the low-dose and 17% in the high-dose groups. In univariable analyses, re-escalation after achieving maintenance was associated with mortality in the high-dose group (HR 4.34, 95% CI 1.24 to 98.3), whereas re-escalation before achieving maintenance was associated with mortality in the low-dose group (HR 19.41, 95% CI 2.71 to 138.5).

A recommended maintenance dose of corticosteroids was associated with better prognosis in patients with CS. Achieving and maintaining this dose appears critically important in clinical management.

## Linked entities

- **Diseases:** cardiac sarcoidosis (MONDO:0001707)

## Full-text entities

- **Genes:** NPPB (natriuretic peptide B) [NCBI Gene 4879] {aka BNP, Iso-ANP}
- **Diseases:** Mobitz type II (MESH:D006938), myocardial involvement (MESH:C564676), AVB (MESH:D054537), CV death (MESH:D002318), Infection (MESH:D007239), CS (MESH:D012507), arrhythmic deaths (MESH:D003643), ventricular fibrillation (MESH:D014693), VT (MESH:D017180), Sarcoid granulomas (MESH:D006099), Cardiac involvement (MESH:D006331), amyloidosis (MESH:D000686), heart failure (MESH:D006333), VF (MESH:C537182), malignancy (MESH:D009369), LGE (MESH:C564835), inflammation (MESH:D007249), myocardial diseases (MESH:D004194), iCS (MESH:C535741), genetic cardiomyopathies (MESH:D009202), sudden cardiac death (MESH:D016757), stroke (MESH:D020521), Mobitz type I (MESH:D006969), giant cell myocarditis (MESH:D009205), granulomatous disease (MESH:D006105), cardiac arrhythmias (MESH:D001145)
- **Chemicals:** 18F-FDG (MESH:D019788), ACE-i (-), Steroid (MESH:D013256), 67Ga (MESH:C000615429), infliximab (MESH:D000069285), methotrexate (MESH:D008727)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

18 references — full list in the complete paper: https://tomesphere.com/paper/PMC12970080/full.md

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Source: https://tomesphere.com/paper/PMC12970080