Your browser doesn't support javascript.
loading
High proton pump inhibitor exposure increases risk of calcinosis in systemic sclerosis.
Host, Lauren V; Campochiaro, Corrado; Afonso, Ana; Nihtyanova, Svetlana I; Denton, Christopher P; Ong, Voon H.
Afiliação
  • Host LV; Centre for Rheumatology and Connective Tissue Diseases, UCL Medical School, Royal Free Campus, London, UK.
  • Campochiaro C; Centre for Rheumatology and Connective Tissue Diseases, UCL Medical School, Royal Free Campus, London, UK.
  • Afonso A; Unit of Immunology, Rheumatology, Allergy and Rare Diseases (UniRAR), San Raffaele Scientific Institute, Milan, Italy.
  • Nihtyanova SI; Centre for Rheumatology and Connective Tissue Diseases, UCL Medical School, Royal Free Campus, London, UK.
  • Denton CP; Internal Medicine Department, Hospital Pedro Hispano, Matosinhos, Portugal.
  • Ong VH; Centre for Rheumatology and Connective Tissue Diseases, UCL Medical School, Royal Free Campus, London, UK.
Rheumatology (Oxford) ; 60(2): 849-854, 2021 02 01.
Article em En | MEDLINE | ID: mdl-32829395
ABSTRACT

OBJECTIVE:

To investigate the association between proton pump inhibitor (PPI) use and the presence and severity of calcinosis in SSc.

METHODS:

We analysed data from two SSc cohorts from a single centre. Cohort 1 included 199 patients reviewed over 10 years, for whom retrospective data on PPI use and calcinosis were available. Cohort 2 was recruited prospectively and included 215 consecutive patients, who underwent clinical assessment. Outcomes of interest were presence of current calcinosis (CC) or calcinosis at any time (CAT).

RESULTS:

The cohort 1 data analysis showed that among patients on standard dose PPI 20% had calcinosis, while in those on high doses of PPI calcinosis was present in 39% (P = 0.003). Analysis of the data from cohort 2 confirmed these findings, demonstrating that the odds of CAT increased significantly with longer PPI exposure [odds ratio (OR) 1.04, 95% CI 1.02, 1.06; P < 0.001], longer disease duration (OR 1.08, 95% CI 1.05, 1.12; P < 0.001) and greater age (OR 1.03, CI 1.01, 1.05; P = 0.010). Multivariable logistic regression showed that higher exposure to PPI remained a significant predictor of calcinosis, with PPI exposure >10 years increasing the risk of CAT >6-fold, compared with no PPI (OR 6.37, 95% CI 1.92, 21.17; P = 0.003) after adjusting for disease duration and antibodies.

CONCLUSION:

We confirm a significant association between high PPI exposure with severity of calcinosis in SSc. Given the clinical impact of calcinosis and reflux in SSc, PPI exposure as a potentially modifiable risk factor for calcinosis requires further evaluation.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Escleroderma Sistêmico / Calcinose / Refluxo Gastroesofágico / Inibidores da Bomba de Prótons / Efeitos Adversos de Longa Duração Tipo de estudo: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Revista: Rheumatology (Oxford) Assunto da revista: REUMATOLOGIA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Escleroderma Sistêmico / Calcinose / Refluxo Gastroesofágico / Inibidores da Bomba de Prótons / Efeitos Adversos de Longa Duração Tipo de estudo: Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Revista: Rheumatology (Oxford) Assunto da revista: REUMATOLOGIA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Reino Unido