High Concordance of E-Nose-Derived Breathprints in a Healthy Population: A Cross-Sectional Observational Study

Exhaled breath analysis using electronic noses (e-noses) is a promising non-invasive diagnostic tool. However, a lack of standardized protocols limits clinical implementation. This study evaluates the consistency of breathprints in healthy subjects using the Cyranose 320 e-nose to support standardiz...

Full description

Saved in:
Bibliographic Details
Published inSensors (Basel, Switzerland) Vol. 25; no. 8; p. 2610
Main Authors Dragonieri, Silvano, Quaranta, Vitaliano Nicola, Portacci, Andrea, Ranieri, Teresa, Carpagnano, Giovanna Elisiana
Format Journal Article
LanguageEnglish
Published Switzerland MDPI AG 20.04.2025
MDPI
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Exhaled breath analysis using electronic noses (e-noses) is a promising non-invasive diagnostic tool. However, a lack of standardized protocols limits clinical implementation. This study evaluates the consistency of breathprints in healthy subjects using the Cyranose 320 e-nose to support standardization efforts. Breath samples from 139 healthy non-smoking subjects (age range 18–65 years) were collected using a standardized protocol. Participants exhaled into a Tedlar bag for immediate analysis with the Cyranose 320. Principal Component Analysis (PCA) was used to reduce data dimensionality, and K-means clustering grouped subjects based on breathprints. PCA identified four principal components explaining 97.15% of variance. K-means clustering revealed two clusters: 1 outlier and 138 subjects with highly similar breathprints. The median distance from the cluster center was 0.21 (IQR: 0.18–0.24), indicating low variability. Box plots confirmed breathprint consistency across subjects. The high consistency of breathprints in healthy subjects supports the feasibility of standardizing e-nose protocols. These findings highlight the potential of e-noses for clinical diagnostics, warranting further research in diverse populations and disease cohorts.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
ObjectType-Undefined-3
ISSN:1424-8220
1424-8220
DOI:10.3390/s25082610