Hydrogen Research Study
← Back to Research Library
Human clinical evidenceHuman Clinical StudyOther or not reported

Predicting Therapeutic Response to Molecular Hydrogen in Autoimmune Diseases via Immunophenotyping.

Shan-Wen Lui, Ting-Yu Hsieh, Jeng-Wei Lu, Yi-Jung Ho, Feng-Cheng Liu · APMIS : acta pathologica, microbiologica, et immunologica Scandinavica · 2025

Research-use notice

Independent study record

Each H2HUBB study page organizes source-linked research details for educational use. Interpretation should remain proportional to the study design, population, controls, and limitations.

H2HUBB Research Library branded molecular hydrogen research image
Primary topic Inflammation and Immune Regulation
Evidence type Human clinical evidence
Publication type Human Clinical Study
Hydrogen method Other or not reported

H2HUBB TAKEAWAY

The study reports that HRPI shows potential as a predictive biomarker for MHAT efficacy and guides personalized autoimmune treatment.

What the Researchers Studied

Source-reported study description: 25 patients with autoimmune diseases; 15 untreated RA patients served as controls

What the Study Found

The authors reported: Among the 108 immune subsets analyzed, 15 exhibited significant changes, including 11 T cell and 4 B cell subsets.

The authors reported: Based on baseline immune profiles and the percent change in fatigue scores (assessed by the Brief Fatigue Inventory, BFI-T), a Hydrogen-assisted Treatment Response Prediction Index (HRPI) was developed, demonstrating strong predictive performance (ROC = 0.9375, p = 0.0118).

What the Findings Mean

The authors concluded/reported: HRPI shows potential as a predictive biomarker for MHAT efficacy and guides personalized autoimmune treatment.

Hydrogen Dose and Delivery

Normalized molecular-hydrogen equivalent: 8.50 mg H₂ from 170 mg hydrogen-enriched coral calcium using the H2HUBB 20:1 Ca-equivalent rule.

Study Details

Publication type: human_clinical_study

Evidence source level: B_ABSTRACT

Original scholarly source: https://pubmed.ncbi.nlm.nih.gov/40590161/