# Systematic review of lung function assessment among youth and young adults e-cigarette users: Current tools and emerging methods

**Authors:** Nirul Isamuddin Nasir, Mohd Hasni Ja’afar, Norfazilah Ahmad

PMC · DOI: 10.1371/journal.pone.0342500 · PLOS One · 2026-02-06

## TL;DR

This systematic review examines lung function assessment tools for young e-cigarette users, highlighting the limitations of spirometry and the potential of emerging methods.

## Contribution

The study systematically evaluates current and emerging lung function assessment methods specifically for young e-cigarette users.

## Key findings

- Spirometry fails to detect subclinical lung changes, while FeNO, EBT, and MRI reveal acute and chronic effects of e-cigarette use.
- Chronic e-cigarette exposure reduces key spirometric parameters and increases Carboxyhaemoglobin levels.
- Multimodal assessments may improve early detection of lung dysfunction in young e-cigarette users.

## Abstract

This review focuses on the need to identify the lung function assessment tools used for young EC users. The objectives are to examine the current and emerging methods used in assessing lung function among young EC users, besides identifying the alterations in lung function following EC exposure measured by those tools.

This systematic review was conducted according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) 2020 flow checklist. Six databases (Web of Science, PubMed, Scopus, Taylor & Francis, SAGE, and ScienceDirect) were searched in April 2025 for original articles published between 2016 and 2025. Quality appraisal of the eligible articles was conducted using the Joanna Briggs Institute (JBI) Critical Appraisal Tools. Findings were synthesized using Narrative analysis.

A total of 7 studies were included. Spirometry was used in all included studies; however, it is unable to detect subclinical lung alterations, as observed through ventilation-perfusion (V/Q) MRI and fractional exhaled nitric oxide (FeNO). Acute exposure to EC results in a decrease of FEV₁, FVC, PEF, and MEF₇₅ spirometric parameters, as well as reducing FeNO levels, while concurrently increasing exhaled breath temperature (EBT). Besides, an increase in V/Q mismatch and heterogeneity in ventilation is observed, with a reduction in perfusion heterogeneity. Chronic EC exposure causes a reduction in FEV1, PEF, FEV1/FVC, and FEF25–75%, besides an increment of Carboxyhaemoglobin (HbCO) level. The assessment of the lung function post-EVALI in association with EC cessation revealed lung function improvement and increased diffusing capacity of the lung for carbon monoxide (DLCO).

Spirometry remains the first-line tool for assessing the lung function of young EC users; however, it often misses early lung dysfunction. Emerging methods (FeNO, DLCO, EBT, MRI, HbCO) increasingly complement this limitation. Tailoring multimodal assessment to exposure context, alongside screening and monitoring programs, may assist in early disease detection and prevent long-term respiratory effects.

## Full-text entities

- **Genes:** NOS2 (nitric oxide synthase 2) [NCBI Gene 4843] {aka HEP-NOS, INOS, NOS, NOS2A}, SRCIN1 (SRC kinase signaling inhibitor 1) [NCBI Gene 80725] {aka P140, SNIP}, ABCC1 (ATP binding cassette subfamily C member 1 (ABCC1 blood group)) [NCBI Gene 4363] {aka ABC29, ABCC, DFNA77, GS-X, MRP, MRP1}
- **Diseases:** pathologies (MESH:D005598), impaired lung functions (MESH:D003072), airway obstruction (MESH:D000402), asthmatic (MESH:D013224), COPD (MESH:D029424), respiratory disease (MESH:D012140), inflammatory lung (MESH:D016726), allergic (MESH:D004342), multiple sclerosis (MESH:D009103), lung abnormalities (MESH:D008171), cigarette addiction (OMIM:188890), airway inflammation (MESH:D007249), interstitial lung disease (MESH:D017563), Associated Lung Injury (MESH:D055370), reduced PEF (MESH:D001523), Respiratory (MESH:D012131), Use (MESH:D019966), lung impairments (MESH:D009422), diffuse cutaneous systemic sclerosis (MESH:D045743), asthma (MESH:D001249)
- **Chemicals:** carbon (MESH:D002244), e (MESH:D004540), oxygen (MESH:D010100), CO (MESH:D002248), propylene glycol (MESH:D019946), PAH (MESH:D011084), DLCO (-), NO (MESH:D009569), nicotine (MESH:D009538), iron (MESH:D007501)
- **Species:** Nicotiana tabacum (American tobacco, species) [taxon 4097], Homo sapiens (human, species) [taxon 9606]

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## References

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Source: https://tomesphere.com/paper/PMC12880674