Evidence map›Paper›PMID 35058480›Full record

ArticleScientific reports2022

Arrhythmogenic mechanisms of interleukin-6 combination with hydroxychloroquine and azithromycin in inflammatory diseases.

Xiaojia Zhu, Yuwei Wang, Yujie Xiao, Qianwen Gao, Li Gao, Wenhui Zhang, Xiaofeng Xin, Kesu Chen, Ujala Srivastava, Vamsi Krishna Murthy Ginjupalli and 5 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.4field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
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  8. Obesity Arrhythmias: Role of IL-6 Trans-Signaling.International journal of molecular sciences · 2024
    Review
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  11. Observational
  12. Article
  13. Review
  14. Article
  15. Effects of COVID-19 on Arrhythmia.Journal of cardiovascular development and disease · 2022
    Review
  16. Review
  17. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors at 7 institutions in 3 countries.

Xiaojia Zhu *National Standard Laboratory of Pharmacology for Chinese Materia Medica, School of Pharmacy, Nanjing University of Chinese Medicine, Nanjing, 210036, China.
Yuwei Wang *National Standard Laboratory of Pharmacology for Chinese Materia Medica, School of Pharmacy, Nanjing University of Chinese Medicine, Nanjing, 210036, China.
Yujie Xiao *National Standard Laboratory of Pharmacology for Chinese Materia Medica, School of Pharmacy, Nanjing University of Chinese Medicine, Nanjing, 210036, China.
Qianwen Gao *National Standard Laboratory of Pharmacology for Chinese Materia Medica, School of Pharmacy, Nanjing University of Chinese Medicine, Nanjing, 210036, China.
Li GaoNational Standard Laboratory of Pharmacology for Chinese Materia Medica, School of Pharmacy, Nanjing University of Chinese Medicine, Nanjing, 210036, China.
Wenhui ZhangNational Standard Laboratory of Pharmacology for Chinese Materia Medica, School of Pharmacy, Nanjing University of Chinese Medicine, Nanjing, 210036, China.
Xiaofeng XinDepartment of Respiration, Affiliated Jinling Hospital School of Medicine, Nanjing University, Nanjing, 210002, China.
Kesu ChenDepartment of Respiration, Affiliated Jinling Hospital School of Medicine, Nanjing University, Nanjing, 210002, China.
Ujala SrivastavaResearch and Development (151), Cardiovascular Research Program, Departments of Medicine, Cell Biology and Pharmacology, VA New York Harbor Healthcare System, State University of New York Downstate Health Sciences University, Brooklyn, NY, 11209, USA.
Vamsi Krishna Murthy GinjupalliResearch and Development (151), Cardiovascular Research Program, Departments of Medicine, Cell Biology and Pharmacology, VA New York Harbor Healthcare System, State University of New York Downstate Health Sciences University, Brooklyn, NY, 11209, USA.
Michael CupelliResearch and Development (151), Cardiovascular Research Program, Departments of Medicine, Cell Biology and Pharmacology, VA New York Harbor Healthcare System, State University of New York Downstate Health Sciences University, Brooklyn, NY, 11209, USA.
Pietro Enea Lazzerini *Department of Medical Sciences, Surgery and Neurosciences, University of Siena, Siena, Italy.
Pier Leopoldo Capecchi *Department of Medical Sciences, Surgery and Neurosciences, University of Siena, Siena, Italy.
Long Chen *National Standard Laboratory of Pharmacology for Chinese Materia Medica, School of Pharmacy, Nanjing University of Chinese Medicine, Nanjing, 210036, China. longchen@njucm.edu.cn.
Mohamed Boutjdir *Research and Development (151), Cardiovascular Research Program, Departments of Medicine, Cell Biology and Pharmacology, VA New York Harbor Healthcare System, State University of New York Downstate Health Sciences University, Brooklyn, NY, 11209, USA. mohamed.boutjdir@va.gov.
Nanjing University of Chinese Medicine · CNState University of New York · USUniversity of Siena · ITNanjing General Hospital of Nanjing Military Command · CNNanjing University · CNNew York University · USVA NY Harbor Healthcare System · US

Funding

fourth-round-high-level innovation-program in Taizhou China Medical City and high-level innovative-talent-team of Jiangsu Province 2016024 and TD-SWYY-069
6 · The paper itself

Abstract

Inflammatory diseases including COVID-19 are associated with a cytokine storm characterized by high interleukin-6 (IL-6) titers. In particular, while recent studies examined COVID-19 associated arrhythmic risks from cardiac injury and/or from pharmacotherapy such as the combination of azithromycin (AZM) and hydroxychloroquine (HCQ), the role of IL-6 per se in increasing the arrhythmic risk remains poorly understood. The objective is to elucidate the electrophysiological basis of inflammation-associated arrhythmic risk in the presence of AZM and HCQ. IL-6, AZM and HCQ were concomitantly administered to guinea pigs in-vivo and in-vitro. Electrocardiograms, action potentials and ion-currents were analyzed. IL-6 alone or the combination AZM + HCQ induced mild to moderate reduction in heart rate, PR-interval and corrected QT (QTc) in-vivo and in-vitro. Notably, IL-6 alone was more potent than the combination of the two drugs in reducing heart rate, increasing PR-interval and QTc. In addition, the in-vivo or in-vitro combination of IL-6 + AZM + HCQ caused severe bradycardia, conduction abnormalities, QTc prolongation and asystole. These electrocardiographic abnormalities were attenuated in-vivo by tocilizumab (TCZ), a monoclonal antibody against IL-6 receptor, and are due in part to the prolongation of action potential duration and selective inhibition of Na

Indexed as

Arrhythmias, CardiacCOVID-19COVID-19 Drug TreatmentAnimalsAntibodies, Monoclonal, HumanizedAzithromycinFemaleGuinea PigsHumansHydroxychloroquineInflammationInterleukin-6Interleukin-6 InhibitorsMaleSARS-CoV-2Antibodies, Monoclonal, HumanizedAzithromycinHydroxychloroquineInterleukin-6Interleukin-6 Inhibitorstocilizumab

Identifiers

PMID35058480
PMCPMC8776801
OpenAlexW4206827747

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.