Measuring Mitochondrial DNA Could Predict Severe COVID-19 Hospitalization
One of the most vexing aspects of the COVID-19 pandemic is doctors’ inability to predict which newly hospitalized patients will go on to develop severe disease.
Now, scientists at Washington University School of Medicine in St. Louis have shown that a relatively simple and rapid blood test can predict within a day of hospitalization which patients with COVID-19 are at the highest risk of severe complications or death.
There are surprises when younger, seemingly healthier patients suffer severe complications from COVID-19.
The researchers evaluated 97 patients with COVID-19 at Barnes-Jewish Hospital, measuring their mitochondrial DNA levels on the first day of their hospital stays. They found that mitochondrial DNA levels were much higher in patients who eventually were admitted to the ICU, intubated, or died.
The researchers found this association held independently of a patient’s age, sex, and underlying health conditions.
On average, mitochondrial DNA levels were about tenfold higher in patients with COVID-19 who developed severe lung dysfunction or eventually died.
Those with elevated levels were almost six times more likely to be intubated, three times more likely to be admitted to the ICU, and nearly twice as likely to die than those with lower levels.
Further, the test predicted outcomes and or better than existing markers of inflammation currently measured in patients hospitalized with COVID-19.
Most other markers of inflammation measured in patients with COVID-19, including those still under investigation, are general markers of systemic inflammation, rather than inflammation specific to cell death, according to the researchers.
This blood test measures mitochondrial DNA levels, a unique type of DNA molecule that usually resides inside the energy factories of cells. Mitochondrial DNA spilling out of cells and into the bloodstream is a sign that a particular type of violent cell death is taking place in the body.
“Doctors need better tools to evaluate the status of COVID-19 patients as early as possible because many of the treatments — such as monoclonal antibodies — are in short supply, and we know that some patients will get better without intensive treatments,” said co-senior author Andrew E. Gelman, Ph.D., the Jacqueline G. and William E. Maritz Endowed Chair in Immunology and Oncology in the Department of Surgery, in a press release.
“There’s so much we still don’t understand about this disease,” he added. “In particular, we need to understand why some patients, irrespective of their ages or underlying health in some cases, go into this hyperinflammatory death spiral.”
“Our study suggests that tissue damage may be one cause of this spiral since the mitochondrial DNA that is released is itself an inflammatory molecule.”
The researchers said the test could serve as a way to predict disease severity as well as a tool to better design clinical trials, identifying patients who might, for example, benefit from specific investigational treatments. They also said they would like to evaluate whether the test could serve as a way to monitor the effectiveness of new therapies.
Presumably, effective treatments would lower mitochondrial DNA levels.
“We will need larger trials to verify what we found in this study, but if we could determine in the first 24 hours of admission whether a patient is likely to need dialysis or intubation or medication to keep their blood pressure from dropping too low, that would change how we triage the patient, and it might change how we manage them much earlier in the disease course,” added co-senior author Hrishikesh S. Kulkarni, M.D., an assistant professor of medicine.
“Viruses can cause a type of tissue damage called necrosis that is a violent, inflammatory response to the infection,” Gelman said. “The cell breaks open, releasing the contents, including mitochondrial DNA, which itself drives inflammation.”
“In COVID-19 patients, there has been anecdotal evidence of this type of cell and tissue damage in the lung, heart, and kidney. We think it’s possible that measures of mitochondrial DNA in the blood may be an early sign of this type of cell death in vital organs.”
The researchers also emphasized that the test is quick and straightforward to perform in most hospital settings because it uses the same machinery that processes the standard PCR test for COVID-19.
The method they developed allows mitochondrial DNA levels to be quantified directly in the blood. Without requiring intermediate steps to extract the DNA from the blood, the technique returned results in less than an hour.
Before they can apply for approval from the Food and Drug Administration (FDA), the scientists will need to verify that the test is accurate in a larger multi-center trial. They have plans to expand the research to more sites.
The study was published on January 14, 2021, in JCI Insight.
The Barnes Jewish Hospital Foundation supported this work, the Children’s Discovery Institute, the National Institutes of Health, and the Washington University Institute of Clinical and Translational Sciences COVID-19 Research Program funded by the National Center for Advancing Translational Sciences of the NIH.
No industry conflicts of interest were disclosed.
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