Hyperuricaemia, gout and related adverse events associated with antihypertensive drugs: A real-world analysis using the FDA adverse event reporting system

Background: The role of antihypertensive drugs in inducing hyperuricaemia and gout has been a long-term concern in clinical practice. However, clinical studies regarding this issue are limited in number and have yielded inconsistent results. We comprehensively evaluated the association between vario...

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Main Authors: Xue-Feng Jiao (Author), Kunpeng Song (Author), Xueyan Jiao (Author), Hailong Li (Author), Linan Zeng (Author), Kun Zou (Author), Wei Zhang (Author), Huiqing Wang (Author), Lingli Zhang (Author)
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Published: Frontiers Media S.A., 2023-01-01T00:00:00Z.
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100 1 0 |a Xue-Feng Jiao  |e author 
700 1 0 |a Xue-Feng Jiao  |e author 
700 1 0 |a Xue-Feng Jiao  |e author 
700 1 0 |a Xue-Feng Jiao  |e author 
700 1 0 |a Kunpeng Song  |e author 
700 1 0 |a Xueyan Jiao  |e author 
700 1 0 |a Hailong Li  |e author 
700 1 0 |a Hailong Li  |e author 
700 1 0 |a Hailong Li  |e author 
700 1 0 |a Hailong Li  |e author 
700 1 0 |a Linan Zeng  |e author 
700 1 0 |a Linan Zeng  |e author 
700 1 0 |a Linan Zeng  |e author 
700 1 0 |a Linan Zeng  |e author 
700 1 0 |a Kun Zou  |e author 
700 1 0 |a Kun Zou  |e author 
700 1 0 |a Kun Zou  |e author 
700 1 0 |a Kun Zou  |e author 
700 1 0 |a Wei Zhang  |e author 
700 1 0 |a Wei Zhang  |e author 
700 1 0 |a Huiqing Wang  |e author 
700 1 0 |a Lingli Zhang  |e author 
700 1 0 |a Lingli Zhang  |e author 
700 1 0 |a Lingli Zhang  |e author 
700 1 0 |a Lingli Zhang  |e author 
700 1 0 |a Lingli Zhang  |e author 
245 0 0 |a Hyperuricaemia, gout and related adverse events associated with antihypertensive drugs: A real-world analysis using the FDA adverse event reporting system 
260 |b Frontiers Media S.A.,   |c 2023-01-01T00:00:00Z. 
500 |a 1663-9812 
500 |a 10.3389/fphar.2022.1045561 
520 |a Background: The role of antihypertensive drugs in inducing hyperuricaemia and gout has been a long-term concern in clinical practice. However, clinical studies regarding this issue are limited in number and have yielded inconsistent results. We comprehensively evaluated the association between various antihypertensive drugs and the occurrences of hyperuricaemia, gout and related adverse events (AEs) using the FDA Adverse Event Reporting System (FAERS), aiming to guide the selection of antihypertensive drugs with a goal of minimizing the risk of hyperuricaemia, gout and related AEs.Methods: We used OpenVigil 2.1 to query the FAERS database. Hyperuricaemia, gout and related AEs were defined by 5 Preferred Terms: hyperuricaemia, gout, gouty arthritis, gouty tophus and urate nephropathy. Disproportionality analysis was performed, and a positive signal indicated an association between AEs and antihypertensive drugs.Results: The numbers of antihypertensive drugs with positive signals for hyperuricaemia, gout, gouty arthritis, gouty tophus and urate nephropathy were 46, 66, 27, 8 and 6, respectively. These drugs included diuretics, antihypertensive drugs with central action, α blockers, β blockers, α and β blockers, calcium channel blockers, angiotensin converting enzyme inhibitors, angiotensin II receptor blockers, renin inhibitors, vasodilators, and compound preparations. Furthermore, 42 antihypertensive drugs had positive signal for more than one AEs.Conclusion: Our study suggests that some potassium-sparing diuretics, calcium channel blockers and losartan may be associated with increased risk of hyperuricaemia, gout or related AEs, which is inconsistent with most previous studies. Moreover, Our study also suggests that some antihypertensive drugs with central action, α and β blockers, renin inhibitors and vasodilators may be associated with increased risk of hyperuricaemia, gout or related AEs, which has not been reported in previous studies. These findings complement real-world evidence on the potential risks of hyperuricaemia, gout and related AEs associated with antihypertensive drugs. 
546 |a EN 
690 |a antihypertensive drugs 
690 |a hyperuricaemia 
690 |a gout 
690 |a adverse events 
690 |a the FDA adverse event reporting system 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
655 7 |a article  |2 local 
786 0 |n Frontiers in Pharmacology, Vol 13 (2023) 
787 0 |n https://www.frontiersin.org/articles/10.3389/fphar.2022.1045561/full 
787 0 |n https://doaj.org/toc/1663-9812 
856 4 1 |u https://doaj.org/article/9e72e78d56a341e7a62e7fe57737d7d6  |z Connect to this object online.