The loss of smell and taste, which is among the most common symptoms associated with coronavirus infection, is writ large in the brain, says a study that scanned brain images from a group of volunteers to compare changes before and after COVID-19.
Other studies, on the effects of respiratory viruses on brain functioning, have argued that coronavirus-like agents have an affinity for specific regions in the brain connected to smell, test, memory and multi-tasking abilities, and could explain reported instances of cognitive decline following a coronavirus infection.
However, this latest study, which is yet to be peer-reviewed, was able to paint a picture of a distinct loss of grey matter, in regions of the brain associated with smell and taste in those who had tested positive for the coronavirus compared to those who hadn’t.
Whether it was the coronavirus directly causing this loss, or if it was only indirectly influencing this damage, couldn’t be established by the study alone.
The brain’s grey matter is the tissue in the central nervous system that consists of nerve cells, and cells that are responsible for generating sensation and motor control. The white matter makes up axons, which are the wiring connecting grey matter tissue.
“This [the grey matter loss] might represent a more deleterious impact of COVID-19, or be due to risk factors (as hospitalised patients were older, had higher Body Mass Index) and blood pressure, and higher risk of having diabetes, or an interaction of both. The loss of grey matter in memory-related regions of the brain may in turn increase the risk of these patients of developing dementia in the longer term,” say the authors who include scientists at the University of Oxford, the Imperial College London, in the U.K. and the National Institutes of Health, U.S.A.
The study compared brain imaging scans sourced as part of the UK Biobank initiative, that prior to the pandemic had collected a large set of brain-scan images from over 40,000 volunteers over 45. From these, 394, who had tested positive for the virus and 388 who had not (and used as comparator controls), and who had appeared for follow-up brain imaging, were studied to tease out how parts of their brains had changed over time, and whether there was something distinctive in the images of those who had been infected by the coronavirus and if time between infection, age, ethnicity, gender, etc could also explain differences.
An advantage of their approach, the authors say, was that in having pre-infection imaging data, they could adjust for changes in the brain that could be explained by pre-existing risk factors or clinical conditions being misinterpreted as disease effects.
“Since a possible entry point of the virus to the central nervous system might be via the olfactory mucosa and the olfactory bulb, these brain imaging results might be the in vivo hallmark of the spread of the disease (or the virus itself) via the olfactory and gustatory pathways,” they observe.
Apoorva Bhandari, cognitive neuroscientist, Brown University, United States said that the findings showed a “significant though subtle grey matter loss” linked to a positive COVID-19 test or diagnosis. “It’s harder to say that it was due to COVID and in particular due to the novel coronavirus attacking the neurons. It may be due to secondary effects of the loss of olfactory functioning, which itself is likely due to the virus impacting other non-neural support cells in olfactory epithelium. When you have a profound effect on a sensory system’s processing, you can see its effects in subsequent processing regions (including in the grey matter volume) even in normal subjects, which is temporary and reversible,” Mr. Bhandari, who wasn’t connected to the study, told The Hindu .
Going ahead, data from this set that could establish if over time the grey matter loss reversed, stayed stable or further deteriorated could provide “very strong clues” to not only the mechanism (causing the loss) but the potential significance of these findings, he added.
Published - June 23, 2021 09:25 pm IST
