Evidence map›Paper›PMID 40806495›Full record

ReviewInternational journal of molecular sciences2025

Salivary α-Amylase as a Metabolic Biomarker: Analytical Tools, Challenges, and Clinical Perspectives.

Gita Erta, Gita Gersone, Antra Jurka, Peteris Tretjakovs

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

4 authors.

Gita ErtaDepartment of Human Physiology and Biochemistry, Riga Stradins University, LV-1007 Riga, Latvia.ORCID 0000-0002-6425-5956
Gita GersoneDepartment of Human Physiology and Biochemistry, Riga Stradins University, LV-1007 Riga, Latvia.ORCID 0000-0003-2228-4713
Antra JurkaDepartment of Human Physiology and Biochemistry, Riga Stradins University, LV-1007 Riga, Latvia.
Peteris TretjakovsDepartment of Human Physiology and Biochemistry, Riga Stradins University, LV-1007 Riga, Latvia.ORCID 0000-0001-9446-0558

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Salivary α-amylase, primarily encoded by the AMY1 gene, initiates the enzymatic digestion of dietary starch in the oral cavity and has recently emerged as a potential biomarker in metabolic research. Variability in salivary amylase activity (SAA), driven largely by copy number variation of AMY1, has been associated with postprandial glycemic responses, insulin secretion dynamics, and susceptibility to obesity. This review critically examines current analytical approaches for quantifying SAA, including enzymatic assays, colorimetric techniques, immunoassays, and emerging biosensor technologies. The methodological limitations related to sample handling, intra-individual variability, assay standardization, and specificity are highlighted in the context of metabolic and clinical studies. Furthermore, the review explores the physiological relevance of SAA in energy homeostasis and its associations with visceral adiposity and insulin resistance. We discuss the potential integration of SAA measurements into obesity risk stratification and personalized dietary interventions, particularly in individuals with altered starch metabolism. Finally, the review identifies key research gaps and future directions necessary to validate SAA as a reliable metabolic biomarker in clinical practice. Understanding the diagnostic and prognostic value of salivary amylase may offer new insights into the prevention and management of obesity and related metabolic disorders.

Indexed as

BiomarkersSalivaSalivary alpha-AmylasesAnimalsHumansInsulin ResistanceObesityBiomarkersSalivary alpha-AmylasesAMY1 genebiomarker standardizationenzymatic assayglucose homeostasismetabolic biomarkerpersonalized nutritionsalivary α-amylasestarch metabolismvisceral adiposity

Identifiers

PMID40806495
PMCPMC12347534

What OpenQuestion holds

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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.