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Disease activity in rheumatoid arthritis and the risk of cardiovascular events.
Solomon, D H; Reed, G W; Kremer, J M; Curtis, J R; Farkouh, M E; Harrold, L R; Hochberg, M C; Tsao, P; Greenberg, J D.
Afiliação
  • Solomon DH; Brigham and Women's Hospital, Boston, Massachusetts.
  • Reed GW; University of Massachusetts Medical School, Worcester and the Consortium of Rheumatology Researchers of North America (CORRONA), Southborough, Massachusetts.
  • Kremer JM; Albany Medical College and Center for Rheumatology, Albany, New York and CORRONA, Southborough, Massachusetts.
  • Curtis JR; University of Alabama at Birmingham.
  • Farkouh ME; Mount Sinai School of Medicine, New York, New York.
  • Harrold LR; University of Massachusetts Medical School, Worcester and the Consortium of Rheumatology Researchers of North America (CORRONA), Southborough, Massachusetts.
  • Hochberg MC; University of Maryland School of Medicine, Baltimore.
  • Tsao P; Brigham and Women's Hospital, Boston, Massachusetts.
  • Greenberg JD; New York University School of Medicine and New York University Hospital for Joint Diseases, New York, New York, and CORRONA, Southborough, Massachusetts.
Arthritis Rheumatol ; 67(6): 1449-55, 2015 Jun.
Article em En | MEDLINE | ID: mdl-25776112
ABSTRACT

OBJECTIVE:

Use of several immunomodulatory agents has been associated with reduced numbers of cardiovascular (CV) events in epidemiologic studies of rheumatoid arthritis (RA). However, it is unknown whether time-averaged disease activity in RA correlates with CV events.

METHODS:

We studied patients with RA whose cases were followed in a longitudinal US-based registry. Time-averaged disease activity was assessed during followup using the area under the curve of the Clinical Disease Activity Index (CDAI), a validated measure of RA disease activity. Age, sex, presence of diabetes mellitus, hypertension, or hyperlipidemia, body mass index, family history of myocardial infarction (MI), use of aspirin or nonsteroidal antiinflammatory drugs (NSAIDs), presence of CV disease, and baseline use of an immunomodulator were assessed at baseline. Cox proportional hazards regression models were examined to determine the risk of a composite CV end point that included MI, stroke, and death from CV causes.

RESULTS:

A total of 24,989 patients who had been followed up for a median of 2.7 years were included in these analyses. During followup, we observed 534 confirmed CV end points, for an incidence rate of 7.8 per 1,000 person-years (95% confidence interval [95% CI] 6.7-8.9). In models adjusted for variables noted above, a 10-point reduction in the time-averaged CDAI was associated with a 21% reduction in CV risk (95% CI 13-29). These results were robust in subgroup analyses stratified by the presence of CV disease, use of corticosteroids, use of NSAIDs or selective cyclooxygenase 2 inhibitors, and change in RA treatment, as well as when restricted to events adjudicated as definite or probable.

CONCLUSION:

Our findings showed that reduced time-averaged disease activity in RA is associated with fewer CV events.
Assuntos

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 6_ODS3_enfermedades_notrasmisibles Base de dados: MEDLINE Assunto principal: Artrite Reumatoide / Acidente Vascular Cerebral / Infarto do Miocárdio Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged País/Região como assunto: America do norte Idioma: En Revista: Arthritis Rheumatol Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 6_ODS3_enfermedades_notrasmisibles Base de dados: MEDLINE Assunto principal: Artrite Reumatoide / Acidente Vascular Cerebral / Infarto do Miocárdio Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged País/Região como assunto: America do norte Idioma: En Revista: Arthritis Rheumatol Ano de publicação: 2015 Tipo de documento: Article