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Can we predict kidney involvement in patients with systemic lupus erythematosus? A retrospective cohort study with independent validation.
Katechis, Spyridon; Nikolopoulos, Dionysis; Flouda, Sofia; Adamichou, Christina; Chavatza, Katerina; Kapsala, Noemin; Katsimbri, Pelagia; Bertsias, George; Boumpas, Dimitrios T; Fanouriakis, Antonis.
Afiliação
  • Katechis S; Department of Rheumatology, "Asklepieion" General Hospital, Athens, Greece.
  • Nikolopoulos D; Rheumatology and Clinical Immunology Unit, 4th Department of Internal Medicine, Attikon University Hospital, Athens, Greece.
  • Flouda S; Rheumatology and Clinical Immunology Unit, 4th Department of Internal Medicine, Attikon University Hospital, Athens, Greece.
  • Adamichou C; Rheumatology and Clinical Immunology, University of Crete Medical School, Heraklion, Greece.
  • Chavatza K; Rheumatology and Clinical Immunology Unit, 4th Department of Internal Medicine, Attikon University Hospital, Athens, Greece.
  • Kapsala N; Rheumatology and Clinical Immunology Unit, 4th Department of Internal Medicine, Attikon University Hospital, Athens, Greece.
  • Katsimbri P; Rheumatology and Clinical Immunology Unit, 4th Department of Internal Medicine, Attikon University Hospital, Athens, Greece.
  • Bertsias G; Rheumatology and Clinical Immunology, University of Crete Medical School, Heraklion, Greece.
  • Boumpas DT; Rheumatology and Clinical Immunology Unit, 4th Department of Internal Medicine, Attikon University Hospital, Athens, Greece.
  • Fanouriakis A; Rheumatology and Clinical Immunology Unit, 4th Department of Internal Medicine, Attikon University Hospital, Athens, Greece.
Article em En | MEDLINE | ID: mdl-38745434
ABSTRACT

OBJECTIVES:

To discern predictive factors for incident kidney involvement in patients with systemic lupus erythematosus (SLE).

METHODS:

Patients with SLE from the 'Attikon' Lupus cohort were monitored for lupus nephritis (LN), defined by kidney histology and/or classification criteria. Demographic and clinical characteristics at baseline were compared against patients who did not develop LN. LN-free survival curves were generated by Kaplan-Meier. A multivariate Cox proportional hazards model was used to identify independent predictors of LN. Independent validation was performed in the University of Crete Lupus registry.

RESULTS:

Among the 570 patients in the derivation cohort, 59 exhibited LN as their initial presentation, while an additional 66 developed LN during the follow-up period (collectively, 21.9% incidence). In the latter group, baseline factors predictive of subsequent kidney involvement were male sex (multivariable-adjusted [a]HR 4.31, 95% CI 1.82-10.2), age of SLE diagnosis below 26 years (aHR 3.71, 95% CI 1.84-7.48), high anti-dsDNA titre (aHR 2.48, 95% CI 1.03-5.97) and low C3 and/or C4 (although not statistically significant, aHR 2.24, 95% CI 0.83-6.05, p= 0.11). A combination of these factors at time of diagnosis conferred an almost 90-fold risk compared with serologically inactive, older, female patients (aHR 88.77, 95% CI 18.75-420.41), signifying a very high-risk group. Independent validation in the Crete Lupus registry showed concordant results with the original cohort.

CONCLUSION:

Male sex, younger age and serologic activity at SLE diagnosis are strongly associated with subsequent kidney involvement. Vigilant surveillance and consideration of early use of disease-modifying drugs is warranted in these subsets of patients.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article