Evidence map›Paper›PMID 40873766›Full record

ArticleFrontiers in digital health2025

Voice as a biomarker: exploratory analysis for benign and malignant vocal fold lesions.

Phillip Jenkins, Rylan Harrison, Steven Bedrick, Lisa Karstens, Bridge2AI-Voice Consortium, William Hersh

Abstract read
In one paragraph

Article in Frontiers in digital health, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
–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 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Review
  4. Article
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

6 authors.

Phillip JenkinsDivision of Informatics, Clinical Epidemiology, Oregon Health and Science University, Portland, OR, United States.
Rylan HarrisonFariborz Maseeh Department of Mathematics and Statistics, Portland State University, Portland, OR, United States.
Steven BedrickDivision of Informatics, Clinical Epidemiology, Oregon Health and Science University, Portland, OR, United States.
Lisa KarstensDivision of Informatics, Clinical Epidemiology, Oregon Health and Science University, Portland, OR, United States.
Bridge2AI-Voice Consortium
William HershDivision of Informatics, Clinical Epidemiology, Oregon Health and Science University, Portland, OR, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Benign and malignant vocal fold lesions can alter voice quality and lead to significant morbidity or, in the case of malignancy, mortality. Early, noninvasive identification of these lesions using voice as a biomarker may improve diagnostic access and outcomes. In this study, we analyzed data from the initial release of the Bridge2AI-Voice dataset to evaluate which acoustic features best distinguish laryngeal cancer and benign vocal fold lesions from other vocal pathologies and healthy voice function. Seven diagnostic cohorts were grouped into two analyses: the first included participants with laryngeal cancer, benign lesions, or no voice disorder; the second included those with laryngeal cancer or benign lesions without other voice disorders, as well as individuals with spasmodic dysphonia or vocal fold paralysis. Acoustic features including fundamental frequency, jitter, shimmer, and harmonic-to-noise ratio (HNR) were extracted from standardized speech recordings and compared using nonparametric statistical methods. Among the overall sample, significant differences were identified in HNR and fundamental frequency between benign lesions and both healthy controls and laryngeal cancer. In cisgender men, these distinctions were also observed, particularly in HNR and its variability. No statistically significant differences were observed among cisgender women, likely due to the limited sample size. These findings suggest that HNR, particularly its variability, may hold promise as a voice-based marker for early detection and monitoring of vocal fold lesions. Further research with larger, more diverse populations is needed to refine these features and validate their clinical utility.

Indexed as

Bridge2AIlaryngeal lesionsmachine learning (ML)voice 2 AIvoice biomarkers

Identifiers

PMID40873766
PMCPMC12378753

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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.