Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2020 Feb 27:7:63.
doi: 10.3389/fmed.2020.00063. eCollection 2020.

Urate-Lowering Therapy May Prevent the Development of Coronary Artery Disease in Patients With Gout

Affiliations

Urate-Lowering Therapy May Prevent the Development of Coronary Artery Disease in Patients With Gout

Fu-Shun Yen et al. Front Med (Lausanne). .

Abstract

Substantial evidence has demonstrated a close relationship between hyperuricemia and cardiovascular (CV) diseases, but few studies have explored the possibility of using urate-lowering therapy (ULT) to attenuate the development of CV diseases. To compare the risks of incident coronary artery disease (CAD), stroke, and heart failure (HF) between ULT users and non-users in patients with gout, we conducted a retrospective cohort study from the population-based National Health Insurance Research Database in Taiwan. In total, 4,072 patients with gout were included between 2000 and 2012. The overall incident rates of CAD, stroke, and HF were compared between 2,036 ULT users and 2,036 matched non-users. The incident rates of incident CAD were 1.3 and 1.7 per 100 person-years for ULT users and non-users. ULT users had a lower adjusted hazard ratio (aHR) for CAD [aHR: 0.7, 95% confidence interval (CI): 0.55-0.89] compared with non-users. ULT users also had a lower aHR for incident stroke (aHR: 0.68, 95% CI: 0.5-0.92) compared with non-users. ULT had a neutral effect on the risk of incident HF (aHR: 0.92, 95% CI: 0.58-1.45). Among the urate-lowering therapy, subgroup analyses indicated that uricosuric agents had a significant effect on the prevention of CAD and stroke development; and the protection against the development of CAD by uricosuric agents appeared to have a dose-response trend. Our study demonstrated that ULT associated with lower risks of incident CAD and stroke. We recommend that patients with gout receive ULT to lower the burden of CV diseases.

Keywords: coronary artery disease; gout; heart failure; stroke; urate-lowering therapy.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Flow chart of the process for deriving the urate-lowering therapy cohort and the control cohort from the National Health Insurance Research Database.
Figure 2
Figure 2
Cumulative incidences of new-onset coronary artery disease (A), stroke (B), and heart failure (C) in patients receiving and not receiving urate-lowering therapy.

Similar articles

Cited by

References

    1. Sacco RL, Roth GA, Reddy KS, Arnett DK, Bonita R, Gaziano TA, et al. . The heart of 25 by 25: achieving the goal of reducing global and regional premature deaths from cardiovascular diseases and stroke: a modeling study from the American Heart Association and World Heart Federation. Circulation. (2016) 133:e674–90. 10.1161/CIR.0000000000000395 - DOI - PubMed
    1. Institute for Health Metrics and Evaluation . GBD 2017 data (2017). Available online at: https://vizhub.healthdata.org/gbd-compare/ (accessed October 18, 2019).
    1. GBD 2016 Stroke Collaborators. Global, regional, and national burden of stroke, 1990–2016: a systematic analysis for the Global Burden of Disease Study 2016. Lancet Neurol. (2019) 18:439–58. 10.1016/S1474-4422(19)30034-1 - DOI - PMC - PubMed
    1. Rajsic S, Gothe H, Borba HH, Sroczynski G, Vujicic J, Toell T, et al. . Economic burden of stroke: a systematic review on post-stroke care. Eur J Health Econ. (2019) 20:107–34. 10.1007/s10198-018-0984-0 - DOI - PubMed
    1. Lebovitz HE. Type 2 diabetes mellitus–current therapies and the emergence of surgical options. Nat Rev Endocrinol. (2011) 7:408–19. 10.1038/nrendo.2011.10 - DOI - PubMed