4.2 Article

Is Behcet's syndrome associated with an increased risk of ischemic heart disease? A real-world evidence in Taiwan

Journal

ARTHRITIS RESEARCH & THERAPY
Volume 23, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s13075-021-02543-6

Keywords

Behcet's syndrome; Ischemic heart disease; Long-term mortality

Categories

Funding

  1. National Cheng Kung University Hospital [NCKUH-10903023, NCKUH-10803032]
  2. Ministry of Science and Technology [MOST 108-2314-B-006-007-MY2]

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This study found that, unlike common chronic systemic autoimmune disorders, Behcet's syndrome does not appear to be associated with an excess risk of ischemic heart disease (IHD), but patients with Behcet's syndrome exhibit a significantly higher risk of mortality.
BackgroundA variety of chronic inflammatory diseases are linked to ischemic heart disease (IHD); however, this association is less well studied in patients with Behcet's syndrome (BS). The primary objective of this study was to examine the impact of BS on the risk of IHD. The secondary objective was to estimate the long-term mortality risk in patients with BS.MethodsUsing a retrospective cohort design based on the Taiwan National Health Insurance Database, patients diagnosed with BS between 2000 and 2013, without prior history of IHD, were compared to non-BS individuals. The BS and non-BS cohorts were matched with a 1:2 ratio by propensity score, accounting for the following confounders: age, sex, year of index date, comorbidities, and drug exposure. Cox proportional hazard regression was used to derive the hazard ratio (HR) for IHD and mortality. The long-term survival rate was estimated using the Kaplan-Meier method.ResultsAfter propensity score matching, a total of 1554 patients newly diagnosed with BS and 3108 control subjects were identified. The incidence rate of IHD in the BS and control groups was 2.7 and 2.9 per 1000 person-years, respectively. The risk of IHD was comparable between BS and control cohorts [adjusted HR, 1.03; 95% confidence interval (CI), 0.66 to 1.62]. The 5- and 10-year survival rate of BS patients was 96.8% and 95.0%, respectively. Patients with BS exhibited a significantly higher risk of mortality than the sex- and age-matched general population (adjusted HR, 1.73; 95% CI, 1.30 to 2.32).ConclusionUnlike other chronic systemic autoimmune disorders, BS does not appear to be associated with an excess risk of IHD.

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