Answers are grounded in this paper and cite their sources.
The past decades have witnessed an enormous expansion of the literature on cerebrospinal fluid (CSF) biomarkers for Alzheimer's disease (AD). It is now clear that a triplet of CSF biomarkers (total-tau, phospho-tau, and the 42 amino acid fragment of amyloid-β) reflects core neuropathological features of AD and contributes diagnostically relevant information if measured in a proper manner. Here, we discuss what is needed for these biomarkers to become generally implemented in the clinical routine. We also discuss novel CSF biomarkers, the challenge of differential diagnosis-making in diseases with shared pathologies, and if CSF biomarkers will survive in the long run, given the advancements in molecular neuroimaging and ultra-sensitive blood tests.
No takes yet. Share an insight, caveat, or question.
Zetterberg et al. (2012) studied this question.
Synapse has enriched 5 related papers. Consider them for comparative context: