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All neurology briefings

The edition · Neurology

A blood test moves Alzheimer's diagnosis forward, and thrombectomy earns its place past 80

Phosphorylated tau 217 blood testing is entering routine Alzheimer's diagnosis, plasma biomarkers shift in complex ways on lecanemab, skin nerve loss tracks cognition in Parkinson's, and endovascular therapy helps even the oldest patients with large strokes.

The edition in brief

Today's neurology edition leads with a review of fluid biomarkers in Alzheimer's disease, where blood phosphorylated tau 217 for Alzheimer's and neurofilament light for frontotemporal dementia and ALS are now moving into clinical practice, timely as amyloid-targeting drugs arrive, though several markers are needed to capture copathology. A longitudinal cohort of 197 patients on lecanemab found plasma biomarkers move in four distinct directions, with p-tau217, MAPT and GFAP partially normalising while inflammatory markers such as TREM2 behave abnormally, suggesting different markers may suit monitoring versus prognosis. A cross-sectional study links lower intraepidermal nerve fibre density to worse cognition and frontal-insular atrophy in Parkinson's disease, pointing to a peripheral-central axis. A clinic pearl warns against abruptly stopping dopaminergic therapy. The edition closes on a pooled analysis of 270 patients aged 80 or older with large ischaemic stroke, where endovascular treatment improved 90-day function (common odds ratio 2.83) and lowered mortality despite more intracranial haemorrhage, with no attenuation by age.

In this edition

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