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Sex influence on outcomes of patients with systemic sclerosis-associated interstitial lung disease: a EUSTAR database analysis.
Campochiaro, Corrado; Hoffmann-Vold, Anna-Maria; Avouac, Jerome; Henes, Jörg; de Vries-Bouwstra, Jeska; Smith, Vanessa; Siegert, Elise; Airò, Paolo; Oksel, Fahrettin; Pellerito, Raffaele; Vanthuyne, Marie; Pozzi, Maria Rosa; Inanc, Murat; Sibilia, Jean; Gabrielli, Armando; Distler, Oliver; Allanore, Yannick.
Afiliação
  • Campochiaro C; Unit of Immunology, Rheumatology, Allergy and Rare Diseases, IRCCS San Raffaele Hospital, Vita-Salute San Raffaele University, Milan, Italy.
  • Hoffmann-Vold AM; Department of Rheumatology, Oslo University Hospital, Oslo, Norway.
  • Avouac J; Service de Rheumatologie, Cochin Hospital, APHP, Universite Paris Descartes, Paris, France.
  • Henes J; Centre for Interdisciplinary Clinical Immunology, Rheumatology and Auto-Inflammatory Diseases and Department of Internal Medicine II (Haematology, Oncology, Immunology and Rheumatology), University Hospital Tuebingen, Tuebingen, Germany.
  • de Vries-Bouwstra J; Department of Rheumatology, Leiden University Medical Center, Leiden, The Netherlands.
  • Smith V; Department of Rheumatology, Ghent University Hospital, Ghent, Belgium.
  • Siegert E; Department of Rheumatology and Clinical Immunology, Charité-Universitatsmedizin Berlin, Berlin, Germany.
  • Airò P; Rheumatology and Clinical Immunology Department, Spedali Civili, Brescia, Italy.
  • Oksel F; Department of Internal Medicine, Division of Rheumatology, Ege University, Faculty of Medicine, Izmir, Turkey.
  • Pellerito R; Rheumatology Unit, Ospedale Mauriziano, Torino, Italy.
  • Vanthuyne M; Department of Rheumatology, Cliniques Universitaires Saint-Luc, Université Catholique de Louvain, Louvain-la-Neuve, Belgium.
  • Pozzi MR; Rheumatology Unit, S. Gerardo Hospital, Monza, Italy.
  • Inanc M; Division of Rheumatology, Department of Internal Medicine, Istanbul Faculty of Medicine, Istanbul, Turkey.
  • Sibilia J; Service de Rheumatologie, RESO: Centre de Reference des Maladies Autoimmunes Systémiques Rares Est Sud-Ouest, Hôpital De Hautepierre, Strasbourg, France.
  • Gabrielli A; Department of Clinical and Molecular Sciences, Universita' Politecnica Delle Marche, Ancona, Italy.
  • Distler O; Department of Rheumatology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.
  • Allanore Y; Service de Rheumatologie, Cochin Hospital, APHP, Universite Paris Descartes, Paris, France.
Rheumatology (Oxford) ; 62(7): 2483-2491, 2023 07 05.
Article em En | MEDLINE | ID: mdl-36413079
ABSTRACT

OBJECTIVE:

Interstitial lung disease (ILD) is the leading cause of morbidity and mortality in systemic sclerosis (SSc) patients. We aimed to investigate the impact of sex on SSc-ILD.

METHODS:

EUSTAR SSc patients with radiologically confirmed ILD and available percentage predicted forced vital capacity (%pFVC) were included. Demographics and disease features were recorded. A change in %pFVC over 12 months (s.d. 6) (cohort 1) was classified into stable (≤4%), mild (5-9%) and large progression (≥10%). In those with 2-year longitudinal %pFVC (cohort 2), the %pFVC change at each 12-month (s.d. 6) interval was calculated. Logistic regression analyses [odds ratio (OR) and 95% CI] and Cox proportional hazards models adjusted for age and %pFVC were applied.

RESULTS:

A total of 1136 male and 5253 female SSc-ILD patients were identified. Males were significantly younger, had a shorter disease duration, had a higher prevalence of CRP elevation and frequently had diffuse cutaneous involvement. In cohort 1 (1655 females and 390 males), a higher percentage of males had stable ILD (74.4% vs 69.4%, P = 0.056). In multivariable analysis, disease duration and %pFVC [OR 0.99 (95% CI 0.98, 0.99) and OR 0.97 (95% CI 0.95, 0.99), respectively] in males and age, %pFVC and anti-centromere [OR 1.02 (95% CI 1.00, 1.04), OR 0.97 (95% CI 0.96, 0.98) and OR 0.39 (95% CI 0.245, 0.63), respectively] in females were associated with large progression. The 1-year mortality rate was higher in males (5.1% vs 2.5%, P = 0.013). In cohort 2 (849 females and 209 males), a higher percentage of females showed periods of large progression (11.7% vs 7.7%, P = 0.023), the percentage of patients with none, one or two periods of worsening was not different. The overall death rate was 30.9% for males and 20.4% in females (P < 0.001). In the survival analysis, male sex was a predictor of mortality [OR 1.95 (95% CI 1.66, 2.28)].

CONCLUSIONS:

Male SSc-ILD patients have a poorer prognosis and sex-specific predictors exist in SSc-ILD.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Escleroderma Sistêmico / Doenças Pulmonares Intersticiais Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male Idioma: En Revista: Rheumatology (Oxford) Assunto da revista: REUMATOLOGIA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Itália

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Escleroderma Sistêmico / Doenças Pulmonares Intersticiais Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male Idioma: En Revista: Rheumatology (Oxford) Assunto da revista: REUMATOLOGIA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Itália