BU researchers say they’re closer to diagnosing CTE during life, rather than after death

BOSTON — Researchers are closer to diagnosing chronic traumatic encephalopathy, or CTE, in people who are still alive, according to a new study from Boston University’s CTE Center.

The study connects cognitive and behavioral symptoms to protein buildup in the brain that marks the neurodegenerative disease, and the severity of cognitive and functional symptoms, including problems with memory and executive function, according to researchers.

Historically, CTE can only be formally diagnosed after a person dies, at autopsy, experts say.

Like similar brain diseases, the clinical symptoms in life of people diagnosed with CTE after death can vary and there has been robust debate as to what symptoms, if any, are caused by CTE pathology.

In the new study, researchers “provide the most definitive evidence to date that CTE p-tau pathology is primarily responsible for cognitive and functional symptoms, explaining up to 49% of the variation seen in individual patients,” researchers said. For context, studies of Alzheimer’s disease have suggested that all pathologies, including p-tau, explain about 50% of symptoms.

“For the first time, we were able to show a clear dose-response relationship between the amount of CTE pathology and the severity of cognitive and functional symptoms, including problems with memory and executive function. These findings provide a clear step forward toward diagnosing CTE in life,” Dr. Jesse Mez, corresponding author and co-director of clinical research at the CTE Center and associate professor of neurology at Boston University Chobanian & Avedisian School of Medicine, said in a statement.

Neuropathologists rated the amount of p-tau pathology across 11 brain regions commonly affected in CTE in 364 brain donors with autopsy-confirmed CTE, according to researchers. Family and friends of brain donors completed seven standardized scales assessing their loved one’s cognitive, functional, mood and behavioral symptoms.

The researchers then examined the relationship between global and regional p-tau pathology and scores on the multiple scales.

They found that the amount of p-tau pathology across the brain, but most predominantly in the frontal lobe, was associated with more cognitive and functional symptoms and that the amount of p-tau pathology in the frontal lobe was associated with more neurobehavioral symptoms. However, neurobehavioral symptoms were less correlated than cognitive symptoms, with p-tau pathology only explaining about 14% of the variation in neurobehavioral symptoms.

Memory and executive function symptoms are included as core features of the 2021 NINDS Traumatic Encephalopathy Syndrome criteria, proposed by a group of multidisciplinary experts, to diagnose CTE in life. Currently, the criteria are not yet approved for use outside of research. These findings help validate the criteria, with the hope that they can eventually be used on living patients to help provide a diagnosis and treatment plan.

According to the researchers, these findings provide crucial insights into diagnosing CTE in life.

“Diagnosis is crucial before we can test therapies. With validated in-life diagnostic criteria, we will be able to design clinical trials for therapies,” says Mez.

These findings appear online in Molecular Neurodegeneration.

This is a developing story. Check back for updates as more information becomes available.

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