Hydrogenology
Hydrogenology editorial study record

Effects of hydrogen-rich water prepared by alternating-current-electrolysis on antioxidant activity, DNA oxidative injuries, and diabetes-related markers

Asada R, Tazawa K, Sato S, Miwa N. · Medical Gas Research. 2020;10(3):114–121.

HumanH₂-rich waterPublished 2020
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

Open-label single-arm clinical study accompanied by laboratory characterization of the prepared water

Research topic

Metabolic and lipid 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

Japanese adults with fasting blood glucose above 6.1 mmol/L and below approximately 7.8 mmol/L who were not taking glucose-lowering medication.

Sample

Ten enrolled; one withdrew for clinical reasons and nine completed (five men, four women; age 39–63 years).

Duration

Eight weeks, with measurements at baseline, four weeks and eight weeks.

Intervention

Participants drank 1,500 mL/day of freshly prepared AC-electrolyzed H₂-rich water for eight weeks.

Hydrogen form

H₂ dissolved in drinking water — not Brown's gas and not inhalation.

H₂ specification

Dissolved H₂ reached 1.55 mg/L after 30 minutes of AC electrolysis; the same preparation had pH 7.7–7.8, dissolved O₂ 14.6 mg/L and ORP −270 mV.

H₂ flow

Not applicable — oral water administration; 1,500 mL/day at a reported preparation concentration of 1.55 mg/L H₂.

O₂ delivered with H₂

No O₂ gas was administered. Dissolved O₂ in the prepared water was reported as 14.6 mg/L.

Comparator

Baseline values in the same participants; there was no randomized, blinded or concurrent control group.

Reported, not endorsed

Outcomes and reported result

Outcomes measured

Urinary 8-OHdG measures, fasting glucose, HbA1c, fructosamine, 1,5-anhydro-D-glucitol, routine blood/urine tests and adverse findings.

Reported result

Urinary 8-OHdG decreased at eight weeks (P=0.028) and fructosamine at four weeks (P=0.008). The 8-OHdG formation-rate change, 1,5-AG changes and eight-week HbA1c change were not statistically significant. The article calls the fasting-glucose change significant while reporting P=0.051, which is above the conventional P<0.05 threshold. No treatment-related abnormality was reported among completers.

Results-extraction completeness

The complete free PMC article, methods, figures and disclosure section were checked for water preparation/concentration, participant flow, time points, positive and null findings, the internally problematic P=0.051 wording, safety, funding and conflicts.

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

Very small uncontrolled open-label study, one dropout, selected borderline-hyperglycemic participants, multiple outcomes and no control for diet, exercise or regression to the mean. The apparatus used a patented commercial method. A Japanese anti-aging research grant partly funded the study; authors declared no conflicts.

Applies directly to

Exploratory biomarker observations in nine adults; it does not establish prevention or treatment of diabetes.

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: 33004708 · DOI: 10.4103/2045-9912.296041

Publisher access

Free full article in PubMed Central.

Extraction basis

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

Record revision

2026-08-10