# Progress in Machine Learning-Assisted Biosensors for Alzheimer’s Disease

**Authors:** Yan Feng, Changdong Chen

PMC · DOI: 10.3390/bios16030161 · Biosensors · 2026-03-13

## TL;DR

This paper reviews how machine learning helps detect Alzheimer’s disease biomarkers in bodily fluids, aiming to improve early diagnosis.

## Contribution

The paper provides a comprehensive overview of recent advances in machine learning-assisted biosensors for Alzheimer’s disease detection.

## Key findings

- Machine learning algorithms are being integrated with biosensors to detect AD biomarkers like microRNAs and Tau protein.
- Electrochemical and optical biosensors assisted by machine learning show promise for early Alzheimer’s diagnosis.
- Challenges remain in translating these technologies into reliable clinical tools for neurodegenerative disease management.

## Abstract

Alzheimer’s disease (AD) is the most common cause of dementia, affecting 55 million people worldwide. Its characteristics include the accumulation of senile plaques and neurofibrillary tangles. This disease is associated with changes in the concentration of AD biomarkers, such as microRNAs, amyloid peptides, Tau protein, and neurofilament light chains. Due to the fact that neuropathological processes begin decades before the onset of cognitive symptoms, accurate detection of AD biomarkers is crucial for its early diagnosis. The combination of analytical techniques and machine learning methods plays a crucial role in medical innovation. Recently, efforts have been made to develop machine learning-assisted biosensors for AD diagnosis. This article provides an overview of the progress in machine learning-assisted sensing of AD biomarkers in bodily fluids. It mainly includes three parts: machine learning algorithms, machine learning-assisted electrochemical and optical biosensors, and challenges and future perspectives. We believe that this work will contribute to the development of innovative analytical devices based on artificial intelligence for monitoring and managing neurodegenerative diseases.

## Linked entities

- **Diseases:** Alzheimer’s disease (MONDO:0004975)

## Full-text entities

- **Genes:** MIR193B (microRNA 193b) [NCBI Gene 574455] {aka MIRN193B, mir-193b}, SPRED1 (sprouty related EVH1 domain containing 1) [NCBI Gene 161742] {aka LGSS, NFLS, PPP1R147, hSpred1, spred-1}, TAS2R62P (taste 2 receptor member 62, pseudogene) [NCBI Gene 338399] {aka PS1, T2R62, TAS2R62}, NEFL (neurofilament light chain) [NCBI Gene 4747] {aka CMT1F, CMT2E, CMTDIG, NF-L, NF68, NFL}, MAPT (microtubule associated protein tau) [NCBI Gene 4137] {aka DDPAC, FTD1, FTDP-17, MAPTL, MSTD, MTBT1}, APP (amyloid beta precursor protein) [NCBI Gene 351] {aka AAA, ABETA, ABPP, AD1, APPI, CTFgamma}, BDNF (brain derived neurotrophic factor) [NCBI Gene 627] {aka ANON2, BULN2}, App (amyloid beta precursor protein) [NCBI Gene 11820] {aka Abeta, Abpp, Adap, Ag, Cvap, E030013M08Rik}
- **Diseases:** injury to (MESH:D014947), NFTs (MESH:D055956), dementia (MESH:D003704), brain atrophy (MESH:C566985), cognitive dysfunction (MESH:D003072), AD (MESH:D000544), neurodegenerative disease (MESH:D019636), neuronal death (MESH:D009410)
- **Chemicals:** CHA (-), phosphatidylcholine (MESH:D010713), luminol (MESH:D008165), triolein (MESH:D014304), polyamidoamine (MESH:C531249), hydrogen peroxide (MESH:D006861), dendrimers (MESH:D050091), metal (MESH:D008670), carbon nanotube (MESH:D037742), graphene oxide (MESH:C000628730), Fe (MESH:D007501), pyrene (MESH:C030984), graphene (MESH:D006108), Au (MESH:D006046), aluminum (MESH:D000535), dopamine (MESH:D004298)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Rattus norvegicus (brown rat, species) [taxon 10116], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

11 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13023455/full.md

## References

99 references — full list in the complete paper: https://tomesphere.com/paper/PMC13023455/full.md

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Source: https://tomesphere.com/paper/PMC13023455