Currently, LATE can only be definitively diagnosed after death through an autopsy. But for people with symptoms, a diagnosis of LATE can be suggested through:
- Clinical history
- MRI or fluorodeoxyglucose (FDG)-positron emission tomography (PET) findings
- Ruling out other causes
Your health care provider may look for changes in the brain that can be caused by LATE. These can include signs of brain shrinkage (atrophy) and thinning of the parts of the brain responsible for memory formation. These changes can be seen on MRI examination and on autopsies. Thinning seems to be a stronger indicator of how severe the disease is compared with atrophy.
A buildup of the protein transactive response DNA-binding protein 43(TDP-43) may be another sign of LATE. This naturally occurring protein helps with nerve development. This buildup of TDP-43 is usually found in the part of the brain that supports memory, emotion, behavior and mood (limbic system). Right now, there isn't a simple test to see whether a person has an excessive amount of TDP-43. This would be discovered only with an autopsy.
Another sign that could suggest a diagnosis of LATE is hardening and thickening of the walls of the arteries (arteriolosclerosis), which is common in people with LATE.
If your health care provider suspects you might have LATE, they may suggest a mental status examination to find out how severe the cognitive impairment is.
Researchers are working to find a simpler way to diagnose LATE, and other forms of dementia, to quickly identify these diseases. Researchers are working to develop a simple blood screening test for dementia, including LATE, but that is still being studied.