Evidence map›Paper›PMID 42185591›Full record

ReviewGeroScience2026

Transglutaminase and its role in Alzheimer's disease: focus on mitochondria, aging, defective mitophagy, synaptic degeneration, and metabolomics.

Samson Prince Hiruthyaswamy, Dinesh Rao, Sreeja Balakrishna, Nazarene Marylene Nicky Macarius, Yukesh Kumar Sakthivel, Kanagavel Deepankumar, Murali Vijayan

Abstract readReview
PubMed Publisher
In one paragraph

Review in GeroScience, 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

7 authors.

Samson Prince HiruthyaswamyDepartment of Biotechnology, School of Biosciences and Technology, VIT University, Vellore, Tamil Nadu, 632014, India.
Dinesh RaoDepartment of Biosciences, School of Biosciences and Technology, VIT University, Vellore, Tamil Nadu, 632014, India.
Sreeja BalakrishnaDepartment of Biosciences, School of Biosciences and Technology, VIT University, Vellore, Tamil Nadu, 632014, India.
Nazarene Marylene Nicky MacariusDepartment of Biosciences, School of Biosciences and Technology, VIT University, Vellore, Tamil Nadu, 632014, India.
Yukesh Kumar SakthivelDepartment of Biotechnology, School of Biosciences and Technology, VIT University, Vellore, Tamil Nadu, 632014, India.
Kanagavel DeepankumarDepartment of Biotechnology, School of Biosciences and Technology, VIT University, Vellore, Tamil Nadu, 632014, India. deepankumar.k@vit.ac.in.
Murali VijayanDepartment of Nutritional Sciences, College of Health and Human Sciences, Texas Tech University, Lubbock, TX, 79409, USA. murali.vijayan@ttu.edu.ORCID http://orcid.org/0000-0002-7426-3415

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alzheimer's disease (AD) is a multifactorial neurodegenerative disorder characterized by progressive cognitive decline driven by amyloid-β plaques, tau neurofibrillary tangles, and extensive neuronal loss. Emerging evidence highlights mitochondrial dysfunction, defective mitophagy, and disrupted proteostasis as pivotal events in disease progression. Transglutaminase TG2, a multifunctional calcium-dependent enzyme, has gained attention for its capacity to link these pathological processes. Beyond catalyzing ε-(γ-glutamyl)-lysine crosslinks that stabilize amyloid and tau aggregates, TG2 interacts with mitochondrial membranes, altering permeability and bioenergetic efficiency. In neurons, aberrant TG2 activity promotes oxidative stress, impairs mitophagy through crosslinking of PINK1 and Parkin, and exacerbates calcium dyshomeostasis via modification of VDAC and ANT1, culminating in energy failure and apoptosis. Aging-related increases in ROS and inflammatory cytokines further amplify TG2 activation, reinforcing proteostatic collapse and synaptic degeneration. Recent metabolomic studies reveal that TG2-mediated dysregulation extends to lipid and amino acid metabolism, affecting mitochondrial respiration and neuronal signaling. Therapeutically, selective TG2 inhibition restores autophagic flux, mitigates mitochondrial damage, and reduces aggregate burden in preclinical models. This integrative review underscores TG2 as a central orchestrator connecting mitochondrial dysfunction, aging, mitophagy failure, and metabolic imbalance in AD. Targeting TG2's transamidase activity while preserving its regulatory roles may offer a promising strategy for neuroprotection and disease modification.

Indexed as

Alzheimer’s disease (AD)MetabolomicsMitochondrial dysfunctionMitophagySynaptic degenerationTransglutaminase 2 (TG2)

Identifiers

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.