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Sporadic Alzheimer's Disease Pathway

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Sporadic Alzheimer's Disease Pathway

Introduction

Sporadic Alzheimer's disease (SAD) accounts for over 95% of all AD cases, distinguishing itself from familial AD through its complex polygenic architecture and multifactorial etiology. Unlike familial AD caused by deterministic mutations in [APP](/entities/app-protein), [PSEN1](/entities/psen1), or [PSEN2](/entities/psen2), sporadic AD arises from the interplay of multiple genetic risk variants, age-related changes, and environmental factors. [Karch et al., Neuron (2014)](https://pubmed.ncbi.nlm.nih.gov/24991952/) [Bellenguez et al., Nat Genet (2022)](https://pubmed.ncbi.nlm.nih.gov/35027798/) The challenge of the second century in AD research continues to drive new therapeutic approaches. [Holtzman et al., Sci Transl Med (2011)](https://pubmed.ncbi.nlm.nih.gov/21471435/) New genetic insights have revealed the complex architecture underlying sporadic disease. [Bertram & Tanzi, Science (2010)](https://pubmed.ncbi.nlm.nih.gov/20448179/) [Ridge et al., Biomed Res Int (2013)](https://pubmed.ncbi.nlm.nih.gov/23984328/)

Overview


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