Reduced brain oxygen metabolism in patients with multiple sclerosis: Evidence from dual-calibrated functional MRI

Author:

Chandler Hannah L1,Stickland Rachael C12ORCID,Patitucci Eleonora1,Germuska Michael1ORCID,Chiarelli Antonio M34ORCID,Foster Catherine15,Bhome-Dhaliwal Shona6,Lancaster Thomas M17,Saxena Neeraj18,Khot Sharmila16,Tomassini Valentina134910,Wise Richard G134

Affiliation:

1. CUBRIC, School of Psychology, Cardiff University, Cardiff, UK

2. Department of Physical Therapy and Human Movement Sciences, Northwestern University, Chicago, IL, USA

3. Institute for Advanced Biomedical Technologies, University “G. d'Annunzio” of Chieti-Pescara, Chieti, Italy

4. Department of Neurosciences, Imaging and Clinical Sciences, University “G. d'Annunzio” of Chieti-Pescara, Chieti, Italy

5. Wales Institute of Social and Economic Research and Data, Cardiff University, Cardiff, UK

6. Cardiff University School of Medicine, Cardiff, UK

7. Department of Psychology, University of Bath, Bath, UK

8. Department of Anaesthetics, Intensive Care and Pain Medicine, Cwm Taf Morgannwg University Health Board, Abercynon, UK

9. MS Centre, Neurology Unit, “SS. Annunziata” University Hospital, Chieti, Italy

10. Division of Psychological Medicine and Clinical Neurosciences, School of Medicine, Cardiff University, Cardiff, UK

Abstract

Cerebral energy deficiency is increasingly recognised as an important feature of multiple sclerosis (MS). Until now, we have lacked non-invasive imaging methods to quantify energy utilisation and mitochondrial function in the human brain. Here, we used novel dual-calibrated functional magnetic resonance imaging (dc-fMRI) to map grey-matter (GM) deoxy-haemoglobin sensitive cerebral blood volume (CBVdHb), cerebral blood flow (CBF), oxygen extraction fraction (OEF), and cerebral metabolic rate of oxygen consumption (CMRO2) in patients with MS (PwMS) and age/sex matched controls. By integrating a flow-diffusion model of oxygen transport, we evaluated the effective oxygen diffusivity of the capillary network (DC) and the partial pressure of oxygen at the mitochondria (PmO2). Significant between-group differences were observed as decreased CBF ( p = 0.010), CMRO2 ( p < 0.001) and DC ( p = 0.002), and increased PmO2 ( p = 0.043) in patients compared to controls. No significant differences were observed for CBVdHb ( p = 0.389), OEF ( p = 0.358), or GM volume ( p = 0.302). Regional analysis showed widespread reductions in CMRO2 and DC for PwMS. Our findings may be indicative of reduced oxygen demand or utilisation in the MS brain and mitochondrial dysfunction. Our results suggest changes in brain physiology may precede MRI-detectable GM loss and may contribute to disease progression and neurodegeneration.

Publisher

SAGE Publications

Subject

Cardiology and Cardiovascular Medicine,Neurology (clinical),Neurology

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