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The effect of anti-TNF on renal function in patients with ankylosing spondylitis: a prospective cohort study.
Swart, I A P; Visman, I M; Heslinga, M; van der Horst-Bruinsma, I E; van Denderen, J C; Nurmohamed, M T.
Afiliación
  • Swart IAP; Amsterdam Rheumatology and Immunology Center, Amsterdam UMC, Vrije Universiteit, Amsterdam, The Netherlands.
  • Visman IM; Department of Rheumatology, Amsterdam Rheumatology and Immunology Center, Jan van Breemenstraat 2, Reade, Amsterdam, 1056 AB, The Netherlands. i.visman@reade.nl.
  • Heslinga M; Department of Rheumatology, Amsterdam Rheumatology and Immunology Center, Jan van Breemenstraat 2, Reade, Amsterdam, 1056 AB, The Netherlands.
  • van der Horst-Bruinsma IE; Department of Rheumatology, Amsterdam Rheumatology and Immunology Center, Jan van Breemenstraat 2, Reade, Amsterdam, 1056 AB, The Netherlands.
  • van Denderen JC; Department of Rheumatology, Amsterdam Rheumatology and Immunology Center, Jan van Breemenstraat 2, Reade, Amsterdam, 1056 AB, The Netherlands.
  • Nurmohamed MT; Amsterdam Rheumatology and Immunology Center, Amsterdam UMC, Vrije Universiteit, Amsterdam, The Netherlands.
Clin Rheumatol ; 41(12): 3747-3752, 2022 Dec.
Article en En | MEDLINE | ID: mdl-35962246
ABSTRACT

BACKGROUND:

Biologicals, such as anti-tumor necrosis factor (anti-TNF), reduce cardiovascular disease (CVD) in patients with inflammatory rheumatic diseases. Impaired renal function is a known predictor of CVD and elevated in ankylosing spondylitis (AS).

OBJECTIVE:

To assess the effect of anti-TNF on renal function in patients with AS and whether anti-TNF use is safe in AS patients with pre-existing risk factors for renal decline.

METHOD:

Biological-naïve consecutive AS patients treated with etanercept or adalimumab were prospectively followed from 2005 to 2014. Renal function was determined by calculation of the estimated glomerular filtration rate (eGFR), estimated with the abbreviated modification of diet in renal disease (MDRD) formula. The effect of anti-TNF on eGFR was analyzed using mixed model analysis.

RESULTS:

211 AS patients were followed for a median of 156 (36-286) weeks. Overall mixed model analyses showed a significant decrease of eGFR over time (ß = - 0.040, p = 0.000), although this association did not remain significant after adjustment for responding to anti-TNF, alcohol use, disease duration, body mass index (BMI), C-reactive protein (CRP), and disease activity (ß = - 0.018, p = 0.094). However, patients with pre-existing risk factors for renal decline did have a significant change in eGFR over time (ß = - 0.029, p = 0.006).

CONCLUSIONS:

We found a significant change in eGFR over time, although this small decrease was not clinically relevant. This study further demonstrates that anti-TNF does not affect renal function in AS patients with and without existing risk factors for renal decline, which means that use of anti-TNF is safe concerning renal function in patients with AS. Key Points • Previous studies showed that biologicals, such as anti-tumor necrosis factor (anti-TNF), reduce cardiovascular disease (CVD) in patients with inflammatory rheumatic diseases, such as ankylosing spondylitis (AS). • Impaired renal function is a known predictor of CVD, and also a known concern for many AS patients. • Use of anti-TNF is safe with regard to renal function in patients with AS. • The effect of anti-TNF on CVD in AS patients does not seem to be mediated by changes in renal function.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Espondilitis Anquilosante / Enfermedades Cardiovasculares / Enfermedades Reumáticas / Antirreumáticos Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Clin Rheumatol Año: 2022 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Espondilitis Anquilosante / Enfermedades Cardiovasculares / Enfermedades Reumáticas / Antirreumáticos Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Clin Rheumatol Año: 2022 Tipo del documento: Article