Risk factors of damage in early diagnosed systemic lupus erythematosus: results of the Italian multicentre Early Lupus Project inception cohort

Author:

Piga Matteo1ORCID,Floris Alberto1ORCID,Sebastiani Gian Domenico2,Prevete Imma2,Iannone Florenzo3ORCID,Coladonato Laura3,Govoni Marcello4,Bortoluzzi Alessandra4,Mosca Marta5,Tani Chiara5,Doria Andrea6ORCID,Iaccarino Luca6,Franceschini Franco7,Fredi Micaela7,Conti Fabrizio8,Spinelli Francesca Romana8ORCID,Galeazzi Mauro9,Bellisai Francesca9,Zanetti Anna1011,Carrara Greta10,Scirè Carlo Alberto10,Mathieu Alessandro1

Affiliation:

1. Rheumatology Unit, University of Cagliari and AOU University Clinic, Cagliari

2. UOC di Reumatologia, Azienda Ospedaliera San Camillo-Forlanini, Rome

3. Dipartimento dell’Emergenza e dei Trapianto di Organi – Sezione di Reumatologia, Università di Bari, Bari

4. UOC e Sezione di Reumatologia – Dipartimento di Scienze Mediche, Università degli Studi di Ferrara, Ferrara

5. UOC di Reumatologia, Dipartimento di Medicina Clinica e Sperimentale, Università di Pisa, Pisa

6. Rheumatology Unit, Department of Medicine, University of Padova, Padova

7. UOC di Reumatologia e Immunologia Clinica, Dipartimento di Scienze Cliniche e Sperimentali, Università degli Studi di Brescia, ASST Spedali Civili, Brescia, Italy

8. Reumatologia, Dipartimento di Medicina Interna e Specialità Mediche, Sapienza Università di Roma, Roma

9. UOC di Reumatologia, Azienda Ospedaliera Universitaria Senese, Siena

10. Società Italiana di Reumatologia, Unità Epidemiologica, Milano

11. Divisione di Biostatistica, Epidemiologia e Salute Pubblica, Dipartimento di Statistica e Metodi Quantitativi, Università degli Studi di Milano-Bicocca, Milano, Italy

Abstract

Abstract Objective To investigate risk factors for damage development in a prospective inception cohort of early diagnosed SLE patients. Methods The Early Lupus Project recruited an inception cohort of patients within 12 months of SLE classification (1997 ACR criteria). At enrolment and every 6 months thereafter, the SLICC/ACR Damage Index was recorded. The contribution of baseline and time-varying covariates to the development of damage, defined as any SLICC/ACR Damage Index increase from 0 to ≥1, was assessed using univariate analysis. Forward-backward Cox regression models were fitted with covariates with P < 0.05 to identify factors independently associated with the risk of damage development. Results Overall, 230 patients with a mean (s.d.) age of 36.5 (14.4) years were eligible for this study; the mean number of visits per patient was 5.3 (2.7). There were 51 (22.2%) patients with SLICC/ACR Damage Index ≥1 after 12 months, 59 (25.6%) after 24 months and 67 (29.1%) after 36 months. Dyslipidaemia [P = 0.001; hazard ratio (HR) 2.9; 95% CI 1.5, 5.6], older age (P = 0.001; HR 3.0; 95% CI 1.6, 5.5), number of organs/systems involved (P = 0.002; HR 1.4; 95% CI 1.1, 1.8) and cardiorespiratory involvement (P = 0.041; HR 1.9; 95% CI 1.0, 3.7) were independently associated with an increased risk of developing damage. Risk profiles for damage development differed for glucocorticoid-related and -unrelated damage. HCQ use (P = 0.005; HR 0.4; 95% CI 0.2, 0.8) reduced the risk of glucocorticoid-unrelated damage. Conclusion We identified risk factors of damage development, but little effect of glucocorticoids, in this early SLE cohort. Addressing modifiable risk factors from the time of SLE diagnosis might improve patient outcomes.

Funder

Gruppo LES Italiano – ONLUS

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Rheumatology

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