Real-world application of the pediatric Glucocorticoid Toxicity Index in childhood-onset lupus.

Drug-related side effects Glucocorticoids Lupus nephritis Outcome measurement Pediatric rheumatology Systemic lupus erythematosus

Journal

Seminars in arthritis and rheumatism
ISSN: 1532-866X
Titre abrégé: Semin Arthritis Rheum
Pays: United States
ID NLM: 1306053

Informations de publication

Date de publication:
15 Jul 2024
Historique:
received: 06 04 2024
revised: 01 07 2024
accepted: 03 07 2024
medline: 27 7 2024
pubmed: 27 7 2024
entrez: 26 7 2024
Statut: aheadofprint

Résumé

The pediatric Glucocorticoid Toxicity Index (pGTI) is a new, pediatric-specific tool to quantify glucocorticoid (GC)-related morbidity in children. We evaluated the feasibility and construct validity of retrospective pGTI scoring in patients with pediatric-onset systemic lupus erythematosus (pSLE) and identified risk factors for cumulative toxicity. We conducted a retrospective cohort study of patients with pSLE treated with GCs at two pediatric centers (1999-2023). GC exposure was estimated using interval-averaged oral prednisone-equivalent dose and cumulative prednisone-equivalent dose. We scored change in GC toxicity every 6 months (±2) using a modified pGTI including 7 of 10 domains. We calculated the Cumulative Worsening Score (CWS), a continuous summation of toxicity accrued. Mixed effects linear regression was used to identify factors associated with CWS. There were 126 patients with pSLE, including 88 with nephritis, with a median of 6 visits/patient. Nearly half (47 %) experienced toxicity in the Blood Pressure domain. Other common toxicities were mood disturbance (25 %), followed by increased body mass index (BMI), striae, and sleep disturbance (21 % each). Decreased growth velocity was observed in 18 %. There was modest correlation between cumulative GC dose and CWS (rho 0.3; p < 0.01). Greater cumulative toxicity was associated with younger age, elevated BMI, and rituximab use at the time of GC initiation, albeit indications for the latter were not captured. Patients with pSLE experience a high burden of GC toxicity, particularly related to blood pressure, BMI, sleep, and growth. Standardized, pediatric-specific GC toxicity assessment is feasible in real-world settings and can facilitate evaluation of strategies to reduce morbidity in children requiring chronic GC treatment.

Identifiants

pubmed: 39059156
pii: S0049-0172(24)00156-2
doi: 10.1016/j.semarthrit.2024.152516
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

152516

Informations de copyright

Copyright © 2024. Published by Elsevier Inc.

Déclaration de conflit d'intérêts

Declaration of competing interest J.C.C previously received grant funding from GSK for investigator-driven research outside the scope of this work. Professor Stone's hospital, the Massachusetts General Hospital, owns the intellectual property of the pGTI. The worldwide licensing rights to the pGTI are controlled by Steritas, LLC. Professor Stone co-founded Steritas and is the chair of the Scientific Advisory Board but has no fiduciary responsibility at the company. The remaining co-authors have no other relevant financial conflicts of interest to disclose.

Auteurs

Emily Zhang (E)

Division of Immunology, Boston Children's Hospital and Harvard Medical School, Boston, MA, USA.

Sarah Capponi (S)

Division of Rheumatology, Children's Hospital of Philadelphia and the University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.

Rebecca Scobell (R)

Division of Rheumatology, Children's Hospital of Philadelphia and the University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.

Gabrielle Alonzi (G)

Division of Immunology, Boston Children's Hospital and Harvard Medical School, Boston, MA, USA.

Madeline Hlobik (M)

Division of Immunology, Boston Children's Hospital and Harvard Medical School, Boston, MA, USA.

Ankana Daga (A)

Division of Nephrology, Boston Children's Hospital and Harvard Medical School, Boston, MA, USA.

Esra Meidan (E)

Division of Immunology, Boston Children's Hospital and Harvard Medical School, Boston, MA, USA.

Holly Wobma (H)

Division of Immunology, Boston Children's Hospital and Harvard Medical School, Boston, MA, USA.

Liyoung Kim (L)

Division of Immunology, Boston Children's Hospital and Harvard Medical School, Boston, MA, USA.

Lauren A Henderson (LA)

Division of Immunology, Boston Children's Hospital and Harvard Medical School, Boston, MA, USA.

Siobhan Case (S)

Division of Immunology, Boston Children's Hospital and Harvard Medical School, Boston, MA, USA; Division of Rheumatology, Inflammation and Immunity, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.

Peter A Nigrovic (PA)

Division of Immunology, Boston Children's Hospital and Harvard Medical School, Boston, MA, USA; Division of Rheumatology, Inflammation and Immunity, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.

John H Stone (JH)

Division of Rheumatology, Allergy, and Immunology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.

Karen H Costenbader (KH)

Division of Rheumatology, Inflammation and Immunity, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.

Mary Beth F Son (MBF)

Division of Immunology, Boston Children's Hospital and Harvard Medical School, Boston, MA, USA.

Joyce C Chang (JC)

Division of Immunology, Boston Children's Hospital and Harvard Medical School, Boston, MA, USA; Division of Rheumatology, Children's Hospital of Philadelphia and the University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA. Electronic address: Joyce.Chang@childrens.harvard.edu.

Classifications MeSH