Abstract

ObjectiveWe previously showed that MELAS patients have decreased cerebrovascular reactivity (CVR) (p≤ 0.002) and increased cerebral blood flow (CBF) (p<0.0026); changes correlated with disease severity and % mutant mtDNA (inversely for CVR; directly for CBF). We ran a prospective pilot in 3 MELAS sibs (m.3243A>G tRNALeu(UUR)) with variable % mutant blood mtDNA to assess effects of L-Arginine (L-Arg) (single dose and 6-wk steady-state trial) on regional CBF, arterial CVR and neurovascular coupling.MethodsPatients were studied with 3T MRI using arterial spin labeling (ASL) to measure CBF and changes in % Blood Oxygen Level Dependent (BOLD) signal to changes in arterial partial pressure of CO2 to measure CVR. Task fMRI consisted of an alternating black and white checkerboard to evaluate visual cortex response in MELAS and controls.ResultsFollowing L-Arg, there was restoration of serum Arg (76–230 μM) in MELAS sibs and a trend towards increasing CVR in frontal and corresponding decrease in occipital cortex; CVR was unchanged globally. There was a 29–37% reduction in baseline CBF in one patient following 6 wks of L-Arg. Pre-treatment fMRI activation in response to visual cortex stimulus was markedly decreased in the same patient compared to controls in primary visual striate cortex V1 and extrastriate regions V2 to V5 with a marked increase toward control values following a single dose and 6 wks of L-Arg.ConclusionProposed “healing” effect may be due to more efficient utilization of energy substrates with increased cellular energy balances and ensuing reduction in signalling pathways that augment flow in the untreated state.Classification of evidenceThis prospective pilot study provides Class III evidence that oral L-Arginine (100 mg/kg single dose or 100 mg/kg three times daily po X 6 weeks) normalizes resting blood flow from elevated pre-treatment levels in patients with MELAS syndrome, selectively increases their CVR from reduced pre-treatment levels in regions most impaired at the expense of less abnormal regions, and normalizes reduced BOLD fMRI activation in response to visual cortex stimulus.Clinical trials.gov (NIH)NCT01603446.

Highlights

  • Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome (m.3243A>G tRNALeu (UUR) in MT-TL1 gene) (OMIM # 590050) [1] is associated with failure to thrive, lactic acidosis, neuromyopathy, epilepsy, migraine-like headaches and recurrent stroke-like episodes (SLEs) resembling vaso-occlusive strokes [2]

  • Patients were studied with 3T MRI using arterial spin labeling (ASL) to measure cerebral blood flow (CBF) and changes in % Blood Oxygen Level Dependent (BOLD) signal to changes in arterial partial pressure of CO2 to measure cerebrovascular reactivity (CVR)

  • We have previously demonstrated that a family of MELAS siblings had lower serum Arg (53 ± 11 μM; controls 94 ± 18; p = 0.001) with decreased CVR (p 0.002) and increased CBF (p 0.0026) compared to controls

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Summary

Introduction

Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome (m.3243A>G tRNALeu (UUR) in MT-TL1 gene) (OMIM # 590050) [1] is associated with failure to thrive, lactic acidosis, neuromyopathy, epilepsy, migraine-like headaches and recurrent stroke-like episodes (SLEs) resembling vaso-occlusive strokes [2]. These SLEs have a predilection for occipital, posterior parietal and temporal cortices [3]. SLEs are not restricted to vascular territories, unlike vaso-occlusive strokes [3]. Demonstrated increases in mitochondrial size and number in cerebral vascular endothelial and smooth muscle cells support cerebral angiopathy [10,11,12], but cerebrovascular reactivity studies have had contradictory results [13,14,15,16]

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