| Literature DB >> 33671916 |
In-Jeong Cho1, Jeong-Hun Shin2, Mi-Hyang Jung3, Chae Young Kang4, Jinseub Hwang4, Chang Hee Kwon5, Woohyeun Kim2, Dae-Hee Kim6, Chan Joo Lee7, Si-Hyuck Kang8, Ju-Hee Lee9, Hack-Lyoung Kim10, Hyue Mee Kim11, Iksung Cho7, Hae-Young Lee12, Wook-Jin Chung13, Sang-Hyun Ihm14, Kwang Il Kim8, Eun Joo Cho15, Il-Suk Sohn16, Sungha Park7, Jinho Shin2, Sung Kee Ryu17, Jang Young Kim18, Seok-Min Kang7, Myeong-Chan Cho9, Wook Bum Pyun1, Ki-Chul Sung19.
Abstract
We sought to assess the association between common antihypertensive drugs and the risk of incident cancer in treated hypertensive patients. Using the Korean National Health Insurance Service database, the risk of cancer incidence was analyzed in patients with hypertension who were initially free of cancer and used the following antihypertensive drug classes: Angiotensin-converting enzyme inhibitors (ACEIs); angiotensin receptor blockers (ARBs); beta blockers (BBs); calcium channel blockers (CCBs); and diuretics. During a median follow-up of 8.6 years, there were 4513 (6.4%) overall cancer incidences from an initial 70,549 individuals taking antihypertensive drugs. ARB use was associated with a decreased risk for overall cancer in a crude model (hazard ratio (HR): 0.744, 95% confidence interval (CI): 0.696-0.794) and a fully adjusted model (HR: 0.833, 95% CI: 0.775-0.896) compared with individuals not taking ARBs. Other antihypertensive drugs, including ACEIs, CCBs, BBs, and diuretics, did not show significant associations with incident cancer overall. The long-term use of ARBs was significantly associated with a reduced risk of incident cancer over time. The users of common antihypertensive medications were not associated with an increased risk of cancer overall compared to users of other classes of antihypertensive drugs. ARB use was independently associated with a decreased risk of cancer overall compared to other antihypertensive drugs.Entities:
Keywords: antihypertensive agent; cohort study; neoplasms
Year: 2021 PMID: 33671916 DOI: 10.3390/jcm10040771
Source DB: PubMed Journal: J Clin Med ISSN: 2077-0383 Impact factor: 4.241