British Society of Gastroenterology guidelines for diagnosis and management of autoimmune hepatitis DOI
Dermot Gleeson,

Rosemary Bornand,

Ann Brownlee

et al.

Gut, Journal Year: 2025, Volume and Issue: unknown, P. gutjnl - 333171

Published: April 1, 2025

Autoimmune hepatitis (AIH) is a chronic inflammatory liver disease which, if untreated, often leads to cirrhosis, failure and death. The last British Society of Gastroenterology (BSG) guideline for the management AIH was published in 2011. Since then, our understanding has advanced many areas. This update previous commissioned by BSG developed multidisciplinary group. aim this review summarise current evidence, order inform guide diagnosis patients with its variant syndromes. main focus on adults, but guidelines should also be relevant older children adolescents.

Language: Английский

Melatonin modulation of the chronic dexamethasone-induced adrenal insufficiency DOI

Banalata Mohanty,

Brijesh Kumar Mishra

Endocrine, Journal Year: 2025, Volume and Issue: unknown

Published: Jan. 29, 2025

Language: Английский

Citations

0

Glucocorticoid-Induced Adrenal Insufficiency in Sarcoidosis Patients with Long-term Glucocorticoid Therapy DOI

Roman Düvel,

Vanessa Marggraf,

Carmen Pizarro

et al.

Pneumologie, Journal Year: 2025, Volume and Issue: unknown

Published: Feb. 19, 2025

Sarcoidosis is a granulomatous multi-system disease of unknown aetiology [1]. 10–30 % the chronic subpopulations require prolonged treatment [1], most commonly in form systemic glucocorticoids (GC), which are considered first line for symptomatic sarcoidosis patients [2] [3] [4]. Symptoms often unspecific and include fatigue, arthralgia, muscle pain, general weakness, fever anorexia. Of all symptoms, fatigue poses prevalent clinical feature seen nearly 70 [1] [5]. However, may also be caused by suppression hypothalamic-pituitary-adrenal (HPA) axis as an inevitable effect exogenous glucocorticoid therapy [6]. This can manifest glucocorticoid-induced adrenal insufficiency (GI-AI), among common causes cortisol deficiency [7]. Clinical symptoms GI-AI [8] overlap with aforementioned sarcoidosis. To our knowledge, no data available on prevalence patients. Recently, current or recent history GC use presenting signs suggestive classified being at high risk should, if they currently receive dose 5 mg prednisolone equivalent, tested measuring early morning serum 24 hours after last GCs Therefore, between March 2022 May 2023 we prospectively evaluated 62 consecutive histologically proven receiving less equivalent development insufficiency. Study inclusion required informed written consent. The study was approved ethics committee University Bonn.

Language: Английский

Citations

0

A Review on the Treatment and Diagnosis of Systemic Lupus Erythematosus Using Nanoparticle Systems DOI

Amin Seddigh,

Zahra Salmasi, Fatemeh Kalalinia

et al.

Journal of Pharmaceutical Innovation, Journal Year: 2025, Volume and Issue: 20(2)

Published: March 12, 2025

Language: Английский

Citations

0

The Effect of Gradual Withdrawal Versus Maintenance of Low‐Dose Glucocorticoid in Clinically Quiescent Systemic Lupus Erythematosus, a Pilot Double‐Blind Randomised Controlled Trial DOI Open Access

Supasa Niyompanichakarn,

Sumapa Chaiamnuay, Pongthorn Narongroeknawin

et al.

Musculoskeletal Care, Journal Year: 2025, Volume and Issue: 23(2)

Published: March 27, 2025

ABSTRACT Introduction Abrupt discontinuation of low dose glucocorticoids (GCs) in systemic lupus erythematosus (SLE) patients with clinical quiescent disease increased the risk flares. This study aimed to evaluate effect a gradual GC withdrawal scheme on flare rate among SLE sustained remission. Methods who received prednisolone 5 mg/day for at least 4 weeks and had Disease Activity Index‐2000 (cSLEDAI‐2K) = 0 minimum 6 months were recruited. The participants randomly assigned 1:1 ratio either 16‐week (withdrawal group) or continuation 24 (maintenance planned enrolment 36. primary outcome was proportion experiencing flare, defined change cSLEDAI‐2K ≥ 4, SLE‐Disease Score 1.72 any treatment escalation over weeks. Results Twenty maintenance group (10 patients), patients). higher compared (3 vs. 1 patient; HR 3.57; 95% CI 0.37 34.51, p 0.24). All experienced serologically active clinically screening. Adverse events (AEs) occurred more (7 Two trial terminated early due occurrence flares AEs. Conclusion Gradual tapering showed non‐significant relapse AEs Clinical number registered ClinicalTrials.gov, NCT06234852.

Language: Английский

Citations

0

British Society of Gastroenterology guidelines for diagnosis and management of autoimmune hepatitis DOI
Dermot Gleeson,

Rosemary Bornand,

Ann Brownlee

et al.

Gut, Journal Year: 2025, Volume and Issue: unknown, P. gutjnl - 333171

Published: April 1, 2025

Autoimmune hepatitis (AIH) is a chronic inflammatory liver disease which, if untreated, often leads to cirrhosis, failure and death. The last British Society of Gastroenterology (BSG) guideline for the management AIH was published in 2011. Since then, our understanding has advanced many areas. This update previous commissioned by BSG developed multidisciplinary group. aim this review summarise current evidence, order inform guide diagnosis patients with its variant syndromes. main focus on adults, but guidelines should also be relevant older children adolescents.

Language: Английский

Citations

0