COVID-19 survival among elderly patients could be improved by arthritis drug, study finds
- Date:
- November 13, 2020
- Source:
- Imperial College London
- Summary:
- A type of arthritis drug may reduce the risk of dying for elderly patients with COVID-19, according to new research.
- Share:
A type of arthritis drug may reduce the risk of dying for elderly patients with COVID-19. This is the finding of a new international study, led by scientists at Imperial College London and the Karolinska Institutet, Sweden, published in the journal Science Advances.
In the early-stage study, 83 patients, with a median age of 81 and all suffering from moderate to severe COVID-19 infection, were given a drug called baricitinib. This medication is usually used to treat rheumatoid arthritis, and was initially identified by the Imperial team using artificial intelligence as a drug that could have anti-viral and anti-inflammatory effects.
In the study, the patients, who were in multiple hospitals across Italy and Spain, had a 71 per cent reduced risk of dying compared to patients who had not taken the drug. The study also found that 17 per cent of patients who were given the drug died or needed to go on a ventilator, compared to 35 per cent in the control group who were not given the medication.
The research team say the findings are being followed up with large-scale clinical trials.
Professor Justin Stebbing, co-lead author of the study from the Department of Surgery and Cancer at Imperial said: "We urgently need to find more effective treatments for COVID-19 while we wait for a vaccine to become widely available. This is one of the first COVID-19 treatments to go from computer to clinic and laboratory. It was first identified by an AI algorithm in February, which scanned thousands of potential drugs that could work against this virus.
"The study suggests this drug can aid recovery of patients with moderate to severe COVID-19, and may provide a new weapon in our arsenal against the virus. Large-scale clinical trials of this drug, to further investigate its potential, are now under way"
In the research, scientists from the Karolinska Institutet in Sweden together with the Imperial team grew miniature human organs in the lab, called organoids, to investigate how exactly the drug may combat COVID-19.
The findings revealed that the drug may help work in two ways: reduce organ damage caused by inflammation, and blocking the virus entering human cells.
When infected with the COVID-19 virus, called SARS-CoV-2, the body releases different types of inflammatory molecules, called chemokines and cytokines. These molecules act as the early warning system for the body, telling the immune system the body is under attack.
However, in the case of COVID-19, particular cytokine and chemokines, including those called interleukins and interferons, causes this warning system to spiral out of control, and trigger a so-called cytokine storm.
This cytokine storm not only causes significant damage to the body's organs, but the study revealed it also helps the virus gain access inside human cells.
The study showed a particular cytokine, called an interferon, increases the number of receptors, or docking points, for the virus. By doing this it, in effect, lowers the drawbridge and lets the virus into the cells of the body.
The researchers revealed the drug blocks this process occurring and so increases survival from COVID-19. The research also suggested COVID-19 increases the activity of genes related to platelets, which can make the blood sticky and more likely to form clots. The drug baricitinib was shown to reduce the activity of the genes.
Professor Volker Lauschke, co-lead author from Karolinska Institutet in Sweden, explained: "This study confirms what AI predicted, and what we were hearing from patient case reports. For instance one case involved an 87-year-old severely unwell patient from Foggia, Italy, who showed rapid improvement after being given the drug, whereas her husband and son, who did not receive baricitinib, died. This study has also shone a light on exactly how this drug may protect us at the cellular level. This helps us understand why other types of drugs are proving beneficial, or not beneficial, as we as help identify other treatments which may tackle COVID-19."
Professor Stebbing added: "We have seen the top line results of a randomized study called the Adaptive Covid Treatment Trial-2 announced recently, showing benefits of baricitinib plus remdesevir, compared to remdesvir alone in over one thousand patients. Other very large trials occurring now include COV-BARRIER, and this will help create a fuller picture of the benefits and side effects of the oral medication (a small number of the patients in our study needed to stop the treatment due to problems with liver function). Further trials comparing baricitinib to other drugs in COVID-19 patients would also be helpful in improving outcomes."
Story Source:
Materials provided by Imperial College London. Original written by Kate Wighton. Note: Content may be edited for style and length.
Journal Reference:
- Justin Stebbing, Ginés Sánchez Nievas, Marco Falcone, Sonia Youhanna, Peter Richardson, Silvia Ottaviani, Joanne X. Shen, Christian Sommerauer, Giusy Tiseo, Lorenzo Ghiadoni, Agostino Virdis, Fabio Monzani, Luis Romero Rizos, Francesco Forfori, Almudena Avendaño-Céspedes, Salvatore De Marco, Laura Carrozzi, Fabio Lena, Pedro Manuel Sánchez-Jurado, Leonardo Gianluca Lacerenza, Nencioni Cesira, David Caldevilla-Bernardo, Antonio Perrella, Laura Niccoli, Lourdes Sáez Méndez, Daniela Matarrese, Delia Goletti, Yee-Joo Tan, Vanessa Monteil, George Dranitsaris, Fabrizio Cantini, Alessio Farcomeni, Shuchismita Dutta, Stephen K. Burley, Haibo Zhang, Mauro Pistello, William Li, Marta Mas Romero, Fernando Andrés Pretel, Rafaela Sánchez Simón-Talero, Rafael García-Molina, Claudia Kutter, James H. Felce, Zehra F. Nizami, Andras G. Miklosi, Josef M. Penninger, Francesco Menichetti, Ali Mirazimi, Pedro Abizanda, Volker M. Lauschke. JAK inhibition reduces SARS-CoV-2 liver infectivity and modulates inflammatory responses to reduce morbidity and mortality. Science Advances, 2020; eabe4724 DOI: 10.1126/sciadv.abe4724
Cite This Page: