Evidence map›Paper›PMID 41808871›Full record

SynthesisFrontiers in pharmacology2026

Natural compounds as multitarget agents in Alzheimer's diseases: evidence from

Vicko Suswidiantoro, Kim San Tang, Khalid Rahman, Donna Maretta Ariestanti, Richard Johari James, Choo Chee Yan, Mitsuyasu Kato, Fadlina Chany Saputri

Abstract readSystematic Review
In one paragraph

Synthesis in Frontiers in pharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Vicko SuswidiantoroDoctoral Programme, Faculty of Pharmacy, Universitas Indonesia, Depok, West Java, Indonesia.
Kim San TangSchool of Pharmacy, Monash University Malaysia, Bandar Sunway, Selangor, Malaysia.
Khalid RahmanFaculty of Science, School of Pharmacy and Biomolecular Sciences, Liverpool John Moores University, Liverpool, United Kingdom.
Donna Maretta AriestantiFaculty of Pharmacy, Universitas Indonesia, Depok, West Java, Indonesia.
Richard Johari JamesIntegrative Pharmacogenomics Institute (iPROMISE), UiTM Selangor Branch, Bandar Puncak Alam, Selangor, Malaysia.
Choo Chee YanIntegrative Pharmacogenomics Institute (iPROMISE), UiTM Selangor Branch, Bandar Puncak Alam, Selangor, Malaysia.
Mitsuyasu KatoFaculty of Pharmacy, Universitas Indonesia, Depok, West Java, Indonesia.
Fadlina Chany SaputriLaboratory of Pharmacology and Toxicology, Faculty of Pharmacy, Universitas Indonesia, Depok, Indonesia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Alzheimer's disease (AD), the most common cause of dementia, is marked by a gradual decline in cognitive function driven by amyloid-β (Aβ) deposition, tau hyperphosphorylation, synaptic failure, neuroinflammatory responses, and mitochondrial dysfunction. Despite extensive research efforts, currently available pharmacological treatments provide only limited symptomatic relief and do not prevent disease progression. These shortcomings have fuelled growing interest in natural compounds, which possess pleiotropic biological properties and may more effectively target the multifaceted pathology of AD. Methods: This systematic review was performed in compliance with the PRISMA 2020 guidelines. Comprehensive literature searches were conducted across PubMed, Scopus, and ScienceDirect to identify preclinical and clinical studies examining the effects of natural compounds in Results: A total of 41 studies fulfilled the inclusion criteria, including 25 Conclusion: Overall, the available evidence suggests that natural compounds confer multitarget neuroprotective effects that directly engage with key pathological mechanisms underlying AD. Nonetheless, significant translational challenges remain, particularly with respect to bioavailability, compound standardisation, and clinical efficacy. Further robust, well-controlled clinical trials are essential to establish the therapeutic value of these agents as potential disease-modifying interventions for AD.

Indexed as

inflammationmultitarget mechanismsnatural productsneurodegenerationneuroprotection

Identifiers

PMID41808871
PMCPMC12968286

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.