Blood phosphorylated tau elevation as a biomarker in immunoglobulin light chain and transthyretin amyloidosis
Summary
Elevated blood levels of phosphorylated tau (p-tau) are diagnostic of Alzheimer disease and are associated with the deposition of amyloid-β in the cerebral neuropil. Elevated p-tau levels have also been associated with cerebral deposition of Danish amyloid and prion protein amyloid. Here we analyzed p-tau in serum from four different cohorts of people with the most common types of systemic amyloidosis, transthyretin (ATTR) amyloidosis and immunoglobulin light chain (AL) amyloidosis. We fou
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# Blood phosphorylated tau elevation as a biomarker in immunoglobulin light chain and transthyretin amyloidosis
*Published: 2026 May*
Elevated blood levels of phosphorylated tau (p-tau) are diagnostic of Alzheimer
disease and are associated with the deposition of amyloid-β in the cerebral
neuropil. Elevated p-tau levels have also been associated with cerebral
deposition of Danish amyloid and prion protein amyloid. Here we analyzed p-tau
in serum from four different cohorts of people with the most common types of
systemic amyloidosis, transthyretin (ATTR) amyloidosis and immunoglobulin light
chain (AL) amyloidosis. We found higher levels of serum p-tau181 in the AL and
ATTR groups than in controls. Subsequent analyses revealed that these effects
were more pronounced in the presence of polyneuropathy (PNP) and in AL compared
to ATTR amyloidosis. Individuals with different forms of PNP that were not due
to amyloidosis did not exhibit elevated p-tau181 levels. In cases of
presymptomatic (genetic) ATTR, p-tau181 levels increased as a function of
predicted years from symptom onset. Additional measurement of p-tau217 in one
cohort revealed similar increases, and discriminated people with AL and those
with ATTR from controls equally as well as p-tau181. These findings suggest that
elevated serum p-tau levels are not specific to Alzheimer disease and may also
serve as a diagnostic tool of ATTR and AL amyloidosis, with potential utility in
distinguishing amyloidosis-related PNP from PNP of other etiologies.
DOI: 10.1038/s41591-026-04272-2