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Uric Acid as a Risk Factor for Chronic Kidney Disease and Cardiovascular Disease - Japanese Guideline on the Management of Asymptomatic Hyperuricemia -

Journal

CIRCULATION JOURNAL
Volume 85, Issue 2, Pages 130-138

Publisher

JAPANESE CIRCULATION SOC
DOI: 10.1253/circj.CJ-20-0406

Keywords

Cardio-renal continuum; CARES study; Urate-lowering agent; Uric acid transporter; Xanthine oxidase

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High uric acid levels can impair endothelial function and are associated with chronic kidney disease and cardiovascular disease. Whether hyperuricemia is causally related to these diseases has been debated. Guidelines from the US and Japan provide different recommendations for treating hyperuricemia, with studies in Japan suggesting certain medications may be effective for treating hyperuricemia patients.
Serum uric acid (UA) is taken up by endothelial cells and reduces the level of nitric oxide (NO) by inhibiting its production and accelerating its degradation. Cytosolic and plasma xanthine oxidase (XO) generates superoxide and also decreases the NO level. Thus, hyperuricemia is associated with impaired endothelial function. Hyperuricemia is often associated with vascular diseases such as chronic kidney disease (CKD) and cardiovascular disease (CVD). It has long been debated whether hyperuricemia is causally related to the development of these diseases. The 2020 American College of Rheumatology Guideline for the Management of Gout (ACR2020) does not recommend pharmacological treatment of hyperuricemia in patients with CKD/CVD. In contrast, the Japanese Guideline on Management of Hyperuricemia and Gout (JGMHG), 3rd edition, recommends pharmacological treatment of hyperuricemia in patients with CKD. In a FREED study on Japanese hyperuricemic patients with CVD, an XO inhibitor, febuxostat, improved the primary composite endpoint of cerebro-cardio-renovascular events, providing a rationale for the use of urate-lowering agents (ULAs). Since a CARES study on American gout patients with CVD treated with febuxostat revealed increased mortality, ACR2020 recommends switching to different ULAs. However, there was no difference in the mortality of Japanese patients between the febuxostat-treated group and the placebo or allopurinol-treated groups in either the FEATHER or FREED studies.

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