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MIS-C, a rare COVID-19-linked condition, presents unique biochemical indicators of cell injury and damage. AI-controlled molecular sequencing reveals biomarkers indicating multi-organ damage, blood vessel lining, and nervous system damage. This discovery could enable more accurate diagnostics and tailored treatments for inflammatory conditions.

Children with multisystem inflammatory syndrome (MIS-C), a rare condition linked with the virus that causes COVID-19 have biochemical indicators of cell injury and cell death that are distinct from other children with COVID-19, according to a study funded by the National Institutes of Health. Using high speed, artificial intelligence-controlled molecular sequencing of blood-and-plasma RNA and plasma DNA, researchers found that children with MIS-C have biomarkers indicating damage to multiple organs, the lining of blood vessels and the nervous system. MIS-C usually occurs two to six weeks after SARS-CoV-2 infection, resulting in inflammation of the heart, lungs, kidneys, brain, skin, eyes or gastrointestinal tract.

To conduct the study, researchers analysed 416 blood samples from 237 patients. Their analysis enabled them to distinguish between patients with MIS-C and COVID-19. They believe their findings could lead to the development of tests that allow clinicians to distinguish between MIS-C and other conditions involving widespread inflammation, such as Kawasaki disease, septic shock, and severe COVID-19, and to the development of more appropriate treatments for each.

The study was conducted by Charles Y. Chiu, M.D., of the University of California, San Francisco, and colleagues at several other institutions. It was funded by NIH’s Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) and appears in Cell Reports Medicine.

Source:EH News Bureau

InnoHEALTH magazine digital team

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