# Health Implications of Radon Exposure Among Children: A Systematic Review

**Authors:** Rasaq Yusuf, Phoka C. Rathebe

PMC · DOI: 10.3390/children13020208 · 2026-01-31

## TL;DR

Childhood exposure to radon increases lung cancer risk later in life and causes early biological changes that can be measured.

## Contribution

This study systematically reviews evidence linking childhood radon exposure to lung cancer and identifies early biological indicators of exposure.

## Key findings

- Childhood radon exposure is projected to increase lung cancer risk by 10–20%.
- Early biological changes like IL-5 and epigenetic reprogramming are linked to radon exposure in children.
- Radon exposure in childhood acts as a latent trigger in the progression of lung cancer.

## Abstract

What are the main findings?
Childhood radon exposure is linked to lung cancer, as evidenced by adult dose–response cohorts indicating a projected risk increase of 10–20%.Some measurable inflammatory markers, cytogenetic changes, and epigenetic reprogramming were identified as early indicators of radon-induced biological stress in children.

Childhood radon exposure is linked to lung cancer, as evidenced by adult dose–response cohorts indicating a projected risk increase of 10–20%.

Some measurable inflammatory markers, cytogenetic changes, and epigenetic reprogramming were identified as early indicators of radon-induced biological stress in children.

What are the implication of the main findings?
Early exposure functions as a latent trigger within the multistage carcinogenic progression of lung cancer, consistent with radiation epidemiology models where the incidence rate correlates with the early cumulative dose.Biological responses to radon exposure occur significantly prior to the clinical manifestation of malignancy, indicating that alpha-particle radiation induces a continuum of molecular injury that bridges disease onset. This highlights the importance of incorporating molecular biomarkers into radon exposure risk assessment frameworks.

Early exposure functions as a latent trigger within the multistage carcinogenic progression of lung cancer, consistent with radiation epidemiology models where the incidence rate correlates with the early cumulative dose.

Biological responses to radon exposure occur significantly prior to the clinical manifestation of malignancy, indicating that alpha-particle radiation induces a continuum of molecular injury that bridges disease onset. This highlights the importance of incorporating molecular biomarkers into radon exposure risk assessment frameworks.

Background: Radon exposure has been recognised as a risk factor for developing lung cancer and other health issues. The mutagenic changes associated with long-term radon exposure take 10–30 years to manifest, which may lead to a lower observed incidence of lung cancer in children. Children are more vulnerable to radon exposure and its effects due to their smaller lung capacity and faster breathing rates, resulting in greater radon inhalation. Objective: The aim of the study is to present current evidence on the association between radon exposure and health effects among children. Methodology: We conducted a systematic review of the available literature on radon exposure and its health impacts, focusing on children. A preliminary literature scoping was conducted in CINAHL, PubMed, Google Scholar, and ScienceDirect. Some of the search terms included: “children” OR “health” OR “implications” OR “radon” OR “exposure”. Subsequently, a comprehensive search was conducted, covering quantitative studies in EBSCOhost across all selected databases. The review adhered to the 27-item PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) checklist. The quality of the evidence gathered was assessed using the Grading of Recommendations Assessment, Development and Evaluation (GRADE) tool. The study was registered with PROSPERO under the ID: CRD420251269394. The review analysed 26 studies, all published between 1994 and 2025. Results: The incidence of lung cancer was projected to increase with childhood radon exposure, with statistical significance (OR per radon 100 Bq/m3 = 1.16; 1.05–1.31). Certain biological markers were associated with childhood long-term radon exposure: IL-5 (13.4%; 95% CI: 0.4–2.8; p = 0.044). Conclusions: Childhood radon exposure, although rarely enough to cause overt malignancy, contributes cumulatively to lifetime lung cancer risk and causes detectable biological markers.

## Linked entities

- **Chemicals:** radon (PubChem CID 24857)
- **Diseases:** lung cancer (MONDO:0005138)

## Full-text entities

- **Genes:** IL5 (interleukin 5) [NCBI Gene 3567] {aka EDF, IL-5, TRF}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}
- **Diseases:** Leukaemia (MESH:D015458), lymphoma (MESH:D008223), hoarseness (MESH:D006685), cough (MESH:D003371), carcinogenic (MESH:D011230), chest pain (MESH:D002637), asthma (MESH:D001249), Lung Cancer (MESH:D008175), breathlessness (MESH:D004417), Cancer (MESH:D009369), chromosomal aberrations (MESH:D002869), asthmatics (MESH:D013224), LRR (MESH:D000080822), respiratory disease (MESH:D012140), Inflammatory (MESH:D007249), injury to (MESH:D014947)
- **Chemicals:** lead (MESH:D007854), Radon (MESH:D011886), 238U (MESH:D014501), thorium (MESH:D013910), radium (MESH:D011883), bismuth (MESH:D001729), CR-39 alpha (-), polonium (MESH:D011059), 222Rn (MESH:C000615148)
- **Species:** Homo sapiens (human, species) [taxon 9606], Nicotiana tabacum (American tobacco, species) [taxon 4097]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12939725/full.md

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Source: https://tomesphere.com/paper/PMC12939725