Hydrogen Gas Protects Skin from Radiation Damage During Cancer Treatment

Therapeutic Potential of Hydrogen as a Radioprotective Agent for the Prevention of Radiation Dermatitis

Research hubs: Skin & Dermatology System

Evidence type
Laboratory study (cells or tissue)
Authors
Deng-Yu Kuo, Yu-Chi Wang, Pei-Han Chou, Chen-Wei Lai, Fu-I Tung, Tse-Ying Liu
Journal
Antioxidants
Year
2024
DOI
10.3390/antiox13121475
Study Type
Cell Culture
Outcome
Positive
Peer Reviewed
Yes
Country
Taiwan
Health Condition
Radiation Dermatitis
Body System
Integumentary

This research was done on cells or tissue in a lab, not in people or animals.

TL;DR

Hydrogen gas can help protect the skin from damage and inflammation caused by radiation therapy.

Key Finding

Hydrogen gas and transdermal hydrogen application reduced radiation-induced skin damage in laboratory and animal models by decreasing DNA breaks, cell death, and inflammatory responses.

Summary

Radiation dermatitis is a common skin injury that occurs in cancer patients undergoing radiation therapy. This study tested whether hydrogen molecules could protect skin cells from radiation damage. Researchers found that hydrogen reduced DNA damage, cell death, and inflammation in both laboratory-grown skin cells and in animal skin exposed to radiation, suggesting it may help prevent or reduce radiation dermatitis.

Practical Takeaway

While these early laboratory and animal results are promising, this study does not yet demonstrate that hydrogen would work in human patients receiving radiation therapy. Human clinical trials would be needed to determine whether hydrogen gas or topical hydrogen treatments could actually prevent radiation dermatitis in cancer patients.

Abstract (excerpt)

Radiation dermatitis (RD) is a common side effect in patients receiving radiotherapy. Currently, clinical skincare approaches for acute RD vary widely among institutions and lack consensus. Hydrogen molecules, acting as radioprotective agents by selectively scavenging free radicals, have…

Read the full abstract via DOI