An in vivo PET/CT investigation of mitochondrial complex 1, sigma 1, and synaptic vesicle 2 A in patients with amyotrophic lateral sclerosis

Our findings reveal loss of MC1 and S1R in ALS, suggesting mitochondrial dysfunction associated with disease progression. This work provides initial insights of mitochondrial and receptor pathology in ALS, potentially guiding future biomarker development and therapeutic interventions.

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Publication Details

Journal
Neurobiology of Disease
Published
2025-10-09
DOI
https://doi.org/10.1016/j.nbd.2025.107138
Primary Topic
Amyotrophic Lateral Sclerosis Research
Type
article
Field-Weighted Citation Impact
0.00
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article

An in vivo PET/CT investigation of mitochondrial complex 1, sigma 1, and synaptic vesicle 2 A in patients with amyotrophic lateral sclerosis

Pegah Khosropanah, Heather Wilson, Eugenii A. Rabiner, Graham Searle et al.
Neurobiology of Disease
Amyotrophic Lateral Sclerosis Research
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An in vivo PET/CT investigation of mitochondrial complex 1, sigma 1, and synaptic vesicle 2 A in patients with amyotrophic lateral sclerosis

Pegah Khosropanah, Heather Wilson, Eugenii A. Rabiner, Graham Searle, Marios Politis, Edoardo Rosario de Natale, Robert A. Comley, Alana Terry, Luca Passamonti, Hideo Tsukada, Jan Passchier, Alex Whittington, Joji Philip Verghese, Roger N. Gunn, Holly Wright, Karleyton C. Evans, Ekaterina Pererva
article en

Abstract

Our findings reveal loss of MC1 and S1R in ALS, suggesting mitochondrial dysfunction associated with disease progression. This work provides initial insights of mitochondrial and receptor pathology in ALS, potentially guiding future biomarker development and therapeutic interventions.

Neurobiology of DiseaseVol. 216
Biogen (United States) (US), Hamamatsu Photonics (Japan) (JP), University of Exeter (GB), Hammersmith Hospital (GB), AbbVie (United States) (US), MRC Brain Network Dynamics Unit (GB)
Openalex Percentile: Top 59%
Amyotrophic Lateral Sclerosis Research
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