Hydrogenology
Hydrogenology editorial study record

Possible clinical effects of molecular hydrogen (H₂) delivery during hemodialysis in chronic dialysis patients: Interim analysis in a 12 month observation

Nakayama M, Itami N, Suzuki H, et al. · PLOS ONE. 2017;12(9):e0184535.

HumanOther formsPublished 2017
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

Prospective multicenter non-randomized observational comparison; prespecified 12-month interim analysis

Research topic

Kidney and urinary health

Administration classification

Other forms

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 receiving maintenance hemodialysis at seven Japanese dialysis centers.

Sample

308 were registered; 262 selected participants with complete 12-month data and no hospitalization, new cancer or death were analyzed: E-HD n=140 and conventional HD n=122.

Duration

12 months; this publication is an interim analysis of the longer registered cohort.

Intervention

Electrolyzed-water hemodialysis three times weekly, generally 4–5 hours/session, using dialysate containing dissolved molecular H₂.

Hydrogen form

H₂ dissolved in dialysate — not inhaled, not swallowed and not Brown's gas.

H₂ specification

Dialysate H₂ concentration varied from 30 to 80 ppb; reported blood flow was 200 mL/min and dialysate flow 500 mL/min.

H₂ flow

Not applicable — H₂ was dissolved in dialysate rather than delivered as inhaled gas.

O₂ delivered with H₂

No O₂ was co-delivered as a distinct intervention.

Comparator

Conventional hemodialysis at participating centers; treatment allocation was not randomized and treatment type was largely center-dependent.

Reported, not endorsed

Outcomes and reported result

Outcomes measured

Dialysis and laboratory parameters, antihypertensive drug dose, self-reported fatigue and pruritus and multivariable associations.

Reported result

No clinically relevant group differences were found for dialysis-related parameters. Antihypertensive use and severe fatigue/pruritus were less frequent in E-HD in adjusted observational analyses, but the design cannot establish that H₂ caused those differences.

Results-extraction completeness

The complete PLOS ONE/PMC article, protocol, cohort selection, laboratory and symptom tables, funding and competing-interest disclosure were checked; the broad null dialysis findings and favorable adjusted associations are both represented.

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

Non-randomized center-based comparison, important baseline differences, subjective outcomes and selection of only event-free participants with complete data create substantial selection and confounding risks. This interim cohort may overlap later E-HD publications and is not counted as an independent participant cohort without confirmation. Nihon Trim and the Electrolyzed Water-Hemodialysis Study Group funded the work; two authors were Nihon Trim employees.

Applies directly to

Maintenance-hemodialysis patients under this Japanese E-HD system; not evidence about drinking or inhaling H₂.

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: 28902900 · DOI: 10.1371/journal.pone.0184535

Publisher access

Free full article on PLOS ONE and PubMed Central.

Extraction basis

PLOS ONE and PMC full article, supporting protocol and PubMed metadata; full-text and article-status check completed 8 August 2026.

Record revision

2026-08-10