DOI: 10.1210/clinem/dgag250 ISSN: 0021-972X

Reversible Mitochondrial Iron Toxicity in Wolfram Syndrome Type 2 Monogenic Diabetes

Amitay Cohen, Ola Karmi, Ulla Najwa Abdulhag, Tehila Klopstock, Yang-Sung Sohn, Orit Lobel, Abdulsalam Abu Libdeh, Eran Lavi, Michael Wilchansky, Muntaser Abbasi, Maha Abdulhadi-Atwan, Gil Leibowitz, Ariella Weinberg-Shukron, Paul Renbaum, Ioav Z Cabantchik, Ephrat Levy-Lahad, Ron Mittler, Rachel Nechushtai, David Zangen

Abstract

Context

Wolfram syndrome type 2 (WS2) is a rare monogenic diabetes syndrome caused by CISD2 mutations. Its cellular pathophysiology remains poorly understood, and no targeted therapies exist.

Objective

To characterize the clinical phenotype and cellular pathophysiology of the largest WS2 cohort to date, and to evaluate a novel, mechanistically targeted pharmacological intervention.

Design

Observational cohort study paired with ex vivo functional cellular assays and a proof-of-concept pilot clinical intervention.

Setting

Multicenter academic and clinical institutions in Israel and the Palestinian territories.

Patients

Twenty-two patients from 11 unrelated Palestinian families presenting with atypical juvenile-onset diabetes and gastrointestinal bleeding. Patient-derived fibroblasts (n = 4) were utilized for functional assays.

Intervention(s)

Fibroblasts and two patients were treated with a combination of the iron chelator deferiprone (DFP) and the antioxidant N-acetylcysteine (NAC).

Main Outcome Measure(s)

Clinical phenotype, CISD2 genetic analysis, mitochondrial labile iron (mLI) and reactive oxygen species (ROS) levels, organelle morphology, and preliminary clinical response (HbA1c, platelet aggregation).

Results

Patients were homozygous for a CISD2 c.109G > C founder mutation (carrier rate 1:40). The clinical phenotype was expanded to include prevalent psychiatric morbidity and congenital heart defects. Patient fibroblasts exhibited profound mitochondrial and endoplasmic reticulum damage, with increased mLI (+25%, p < 0.0001) and mROS (+28%, p < 0.0001). In vitro DFP/NAC treatment fully reversed these cellular anomalies. In a preliminary pilot study, two patients receiving DFP/NAC demonstrated improved reported glycemic control and corrected platelet aggregation.

Conclusions

WS2 is an underdiagnosed monogenic diabetes driven by mitochondrial iron dysregulation and oxidative stress. Repurposing DFP/NAC reverses this toxicity, offering a strong mechanistic rationale for future clinical trials.

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