| Literature DB >> 33349633 |
Lei-Ke Zhang1, Yuan Sun1, Haolong Zeng2, Qingxing Wang1, Xiaming Jiang1, Wei-Juan Shang1, Yan Wu1, Shufen Li1, Yu-Lan Zhang1, Zhao-Nian Hao3, Hongbo Chen4, Runming Jin4, Wei Liu5, Hao Li6, Ke Peng7, Gengfu Xiao8.
Abstract
The coronavirus disease (COVID-19) caused by the novel severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has now spread to >200 countries posing a global public health concern. Patients with comorbidity, such as hypertension suffer more severe infection with elevated mortality. The development of effective antiviral drugs is in urgent need to treat COVID-19 patients. Here, we report that calcium channel blockers (CCBs), a type of antihypertensive drug that is widely used in clinics, inhibited the post-entry replication events of SARS-CoV-2 in vitro, while no in vitro anti-SARS-CoV-2 effect was observed for the two other major types of antihypertensive drugs, namely, angiotensin-converting enzyme inhibitors and angiotensin II receptor blockers. CCB combined with chloroquine showed a significantly enhanced anti-SARS-CoV-2 efficacy. A retrospective clinical investigation on hospitalized COVID-19 patients with hypertension as the only comorbidity revealed that the CCB amlodipine besylate therapy was associated with a decreased case fatality rate. The results from this study suggest that CCB administration to COVID-19 patients with hypertension as the comorbidity might improve the disease outcome.Entities:
Year: 2020 PMID: 33349633 PMCID: PMC7752915 DOI: 10.1038/s41421-020-00235-0
Source DB: PubMed Journal: Cell Discov ISSN: 2056-5968 Impact factor: 10.849