Hydrogenology
Hydrogenology editorial study record

Effect of hydrogen-rich water on oxidative stress, liver function, and viral load in patients with chronic hepatitis B

Xia C, Liu W, Zeng D, Zhu L, Sun X, Sun X. · Clinical and Translational Science. 2013;6(5):372–375.

HumanH₂-rich waterPublished 2013
Study record, not medical adviceThis page reports one source and Hydrogenology’s source-text extraction. It does not establish that molecular hydrogen is effective, safe or appropriate for any person. Human, animal and laboratory evidence must not be treated as equivalent.
Source and classification

What kind of evidence is this?

Evidence stream

Human

Reported design

Randomized controlled adjunctive-treatment study with healthy reference participants

Research topic

Liver health

Administration classification

H₂-rich water

Study result signal

Not reported in this record.

Outcome type

Not reported in this record.

Reported in the source

Methods at a glance

Population or model

Adults with chronic hepatitis B receiving routine treatment; a separate group of 30 healthy participants provided reference measurements.

Sample

185 patients were recruited, 101 met eligibility criteria and 84 were randomized to routine treatment n=41 or routine treatment plus hydrogen-rich water n=43. Only 30 participants in each randomized group were included in the final analysis.

Duration

Six consecutive weeks. The Methods describe consumption three times daily, while the abstract says twice daily; the source does not reconcile this discrepancy.

Intervention

Routine hepatitis-B treatment plus 1,200–1,800 mL/day of hydrogen-rich drinking water for six weeks.

Hydrogen form

H₂ dissolved in drinking water — H₂ only, not Brown's gas.

H₂ specification

Hydrogen-rich water was made with a metallic magnesium stick; the reported final dissolved-H₂ concentration was 0.55–0.65 mmol/L.

H₂ flow

Not applicable — drinking water, not gas inhalation.

O₂ delivered with H₂

No O₂ was co-delivered as part of the intervention.

Comparator

Routine hepatitis-B treatment without added hydrogen-rich water; the healthy group was a non-randomized reference group.

Reported, not endorsed

Outcomes and reported result

Outcomes measured

Serum superoxide dismutase, glutathione S-transferase, xanthine oxidase and malondialdehyde, liver-function tests and HBV DNA.

Reported result

Oxidative-stress markers improved more with hydrogen-rich water than with routine treatment alone. Liver-function measures and HBV DNA improved within both patient groups, but did not differ significantly between the randomized groups after treatment.

Results-extraction completeness

The complete open-access article, recruitment and attrition, randomization, water preparation, concentration and volume, positive and null results and reporting inconsistencies were checked.

A reported association, difference or mechanism is not automatically a clinical benefit. Null findings, outcome type, study design and precision all matter.

Interpretation limits

Cautions and applicability

Design and reporting cautions

Short trial with major post-randomization attrition: 24 of 84 randomized participants were excluded from the final analysis. The article's abstract says 60 patients were randomized although the Results show 84 randomized and 60 analyzed, and twice-daily dosing in the abstract conflicts with three-times-daily dosing in Methods. Masking and allocation procedures are sparsely described. No dedicated funding or conflict-of-interest statement was identified in the checked article, so absence of funding or conflicts is not inferred.

Applies directly to

Adults with chronic hepatitis B receiving the study's routine background treatment; the trial did not show an added liver-function or viral-load benefit.

Preliminary appraisal framework

Not reported in this record.

Preliminary risk-of-bias status

Not reported in this record.

Appraisal rationale

Not reported in this record.

No single-study GRADE certainty rating is assigned. Certainty is assessed by important outcome across a complete eligible evidence set, not by attaching a final grade to one source.

Provenance

Sources and record status

Identifiers

PMID: 24127924 · DOI: 10.1111/cts.12076

Publisher access

Open-access PubMed Central article.

Extraction basis

Complete PubMed Central article and PubMed metadata; full-text extraction checked 9 August 2026.

Record revision

2026-08-10