Evidence map›Paper›PMID 42377735›Full record

ReviewMetabolic brain disease2026

The interplay between gut microbiota and Alzheimer's disease: mechanistic insights from dysbiosis to disease modulation.

Kakali Das, Rupjan Khatun, Sanjana Begum, Koushik Bhattacharyya, Madhushree Datta, Dipankar Saha, Anupam Sarma, Prachi Mehta, Bhrigu Kumar Das

Abstract readReview
PubMed Publisher
In one paragraph

Review in Metabolic brain disease, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Kakali DasDepartment of Pharmacology, School of Pharmaceutical Sciences, Girijananda Chowdhury University, Azara, 781017, Guwahati, Assam, India.
Rupjan KhatunDepartment of Pharmacology, School of Pharmaceutical Sciences, Girijananda Chowdhury University, Azara, 781017, Guwahati, Assam, India.
Sanjana BegumDepartment of Pharmacology, School of Pharmaceutical Sciences, Girijananda Chowdhury University, Azara, 781017, Guwahati, Assam, India.
Koushik BhattacharyyaDepartment of Pharmacology, School of Pharmaceutical Sciences, Girijananda Chowdhury University, Azara, 781017, Guwahati, Assam, India.
Madhushree DattaDepartment of Pharmacology, School of Pharmaceutical Sciences, Girijananda Chowdhury University, Azara, 781017, Guwahati, Assam, India.
Dipankar SahaDepartment of Pharmacology, School of Pharmaceutical Sciences, Girijananda Chowdhury University, Azara, 781017, Guwahati, Assam, India.
Anupam SarmaAdvanced Drug Delivery Laboratory, Department of Pharmaceutics, School of Pharmaceutical Sciences, Girijananda Chowdhury University, Guwahati, 781017, Assam, India.
Prachi MehtaDepartment of Pharmacology, School of Pharmaceutical Sciences, Girijananda Chowdhury University, Azara, 781017, Guwahati, Assam, India.
Bhrigu Kumar DasDepartment of Pharmacology, School of Pharmaceutical Sciences, Girijananda Chowdhury University, Azara, 781017, Guwahati, Assam, India. bhrigu.mon@gmail.com.ORCID 0000-0002-2367-2382

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alzheimer's disease (AD) is a chronic, progressive, neurodegenerative condition marked by memory loss and cognitive decline. It is characterized by neuropathological features such as amyloid plaque accumulation, neurofibrillary tangles of tau protein, and inflammatory changes in the brain. Recent research emphasizes how gut microbes influence the onset and progression of AD primarily through the gut-brain connection, a bidirectional communication system. The human gastrointestinal tract (GI) contains trillions of bacteria, primarily Bacteroidetes, Firmicutes, and Actinobacteria, which play vital roles in digestion, metabolic regulation, and immune modulation. However, factors such as diet, lifestyle, and environmental exposure can disrupt microbial balance, weaken intestinal barrier function, and initiate systemic inflammation. Such dysbiosis has been linked to defective regulation of the amyloid precursor protein (APP), leading to increased deposition of amyloidogenic peptides (Aβ). Moreover, the enteric nervous system, which expresses APP, may serve as an initial site of amyloid deposition, affecting gastrointestinal motility and inflammatory susceptibility. The gut microbiota also produces key bioactive compounds, including neurotransmitters such as serotonin, dopamine, acetylcholine, histamine, and gamma-aminobutyric acid (GABA), which influence the central nervous system (CNS) through neural, immune, and endocrine pathways. An imbalance in these neuroactive molecules may disrupt synaptic signaling and contribute to Alzheimer's-related cognitive dysfunction. Therefore, improving our understanding of gut-brain communication may advance knowledge of AD development and support the creation of new therapies. This review highlights the strong association between intestinal microbes and Alzheimer's pathogenesis, emphasizing microbiota modulation through probiotics, prebiotics, postbiotics, synbiotics, and antibiotics as potential therapeutic approaches, supported by emerging clinical trial evidence.

Indexed as

Alzheimer DiseaseDysbiosisGastrointestinal MicrobiomeAmyloid beta-PeptidesAnimalsBrainHumansAmyloid beta-PeptidesAmyloid-betaGut-brain axisGut microbiomeLipopolysaccharideNeurodegeneration

Identifiers

PMID42377735

What OpenQuestion holds

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Registered trials

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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 OpenQuestion graph.