# Intermittent ketogenic fasting with medium-chain triglycerides improves ataxia in COQ8A-related coenzyme Q10 deficiency: A case report

**Authors:** Wiebke Hahn, Karla Erffmeier, Maximilian Schulze, Felix Zahnert, Susanne Knake, Panagiota-Eleni Tsalouchidou

PMC · DOI: 10.1016/j.ymgmr.2026.101296 · Molecular Genetics and Metabolism Reports · 2026-02-12

## TL;DR

A 46-year-old woman with a rare genetic disorder showed improved ataxia after following a ketogenic intermittent fasting diet with MCTs.

## Contribution

This case report is the first to show that ketogenic intermittent fasting may improve ataxia in COQ8A-related coenzyme Q10 deficiency.

## Key findings

- The patient's ataxia score improved significantly from 8.5 to 6.0 during the intervention.
- MRI scans suggested a trend toward improved cerebellar microstructural integrity.
- Ketogenic intermittent fasting was well-tolerated and showed potential as an adjunct therapy.

## Abstract

Mutations in COQ8A cause primary coenzyme Q10 deficiency, which can present clinically heterogeneously: Symptoms range from cerebellar ataxia, epilepsy, encephalomyopathy, macular degeneration to nephropathy. High-dose coenzyme Q10 supplementation is widely used, yet there is little evidence on complementary strategies, particularly for non-epileptic features such as cerebellar ataxia.

We report a 46-year-old female with genetically confirmed COQ8A-related coenzyme Q10 (CoQ10) deficiency, presenting with ataxia and epilepsy characterized by myoclonic and bilateral tonic–clonic seizures, who participated in a clinical protocol of ketogenic intermittent fasting, a method of intermittent fasting combined with medium-chain triglycerides (MCT) primarily designed for seizure management. The patient followed a 16:8 intermittent fasting regime combined with MCT intake for three months, followed by three months of all-alone intermittent fasting. Routine blood markers and brain MRI, including diffusion imaging were obtained before and after ketogenic fasting.

During the study protocol, while no seizure reduction in myoclonic seizures could be observed, ataxia - quantified by the Scale for the Assessment and Rating of Ataxia (SARA) - improved significantly from 8.5 to 6.0 during the interventions. MRI showed a trend suggesting improved cerebellar microstructural integrity.

This case highlights the potential of ketogenic intermittent fasting as an adjunct therapy for mitochondrial ataxia. Ketogenic intermittent fasting was associated with clinically meaningful improvement of ataxia in a patient with COQ8A-related CoQ10 deficiency, suggesting that ketogenic dietary strategies may represent a promising adjunct therapeutic approach for mitochondrial ataxia. Future research should assess this intervention in larger patient cohorts to confirm its potential benefits.

## Linked entities

- **Genes:** COQ8A (coenzyme Q8A) [NCBI Gene 56997]
- **Chemicals:** coenzyme Q10 (PubChem CID 5281915), MCT (PubChem CID 9958)
- **Diseases:** ataxia (MONDO:0000437), epilepsy (MONDO:0005027), encephalomyopathy (MONDO:0012791), macular degeneration (MONDO:0003004)

## Full-text entities

- **Genes:** COQ9 (coenzyme Q9) [NCBI Gene 57017] {aka C16orf49, COQ10D5}, COQ6 (coenzyme Q6, monooxygenase) [NCBI Gene 51004] {aka CGI-10, CGI10, COQ10D6}, COQ4 (coenzyme Q4) [NCBI Gene 51117] {aka CGI-92, COQ10D7, SPAX10}, COQ8A (coenzyme Q8A) [NCBI Gene 56997] {aka ADCK3, ARCA2, CABC1, COQ10D4, COQ8, SCAR9}, PDSS2 (decaprenyl diphosphate synthase subunit 2) [NCBI Gene 57107] {aka C6orf210, COQ10D3, COQ1B, DLP1, bA59I9.3, hDLP1}, COQ2 (coenzyme Q2, polyprenyltransferase) [NCBI Gene 27235] {aka CL640, COQ10D1, MSA1, PHB:PPT}, PDSS1 (decaprenyl diphosphate synthase subunit 1) [NCBI Gene 23590] {aka COQ1, COQ10D2, COQ1A, DPS, SPS, TPRT}
- **Diseases:** nephropathy (MESH:D007674), extremities (MESH:C563475), ketosis (MESH:D007662), MCT (MESH:C536038), mitochondrial ataxia (MESH:C579922), Epilepsy (MESH:D004827), pyruvate dehydrogenase deficiency (MESH:D015325), cerebellar ataxia (MESH:D002524), encephalomyopathy (MESH:D017237), CoQ10 deficiency (MESH:C564403), tremor (MESH:D014202), myoclonus (MESH:D009207), -limb ataxia (MESH:D001259), MAD (MESH:C538195), primary coenzyme Q10 deficiency (OMIM:607426), retinitis pigmentosa (MESH:D012174), drug resistant epilepsy (MESH:D000069279), slowing of motor skills and coordination (MESH:D019957), cerebellar atrophy (MESH:D002526), Seizure (MESH:D012640), status epilepticus (MESH:D013226), dystonia (MESH:D004421), inflammatory (MESH:D007249), neurodegenerative diseases (MESH:D019636), mitochondrial disease (MESH:D028361), visual impairment (MESH:D014786), temporal lobe epilepsy (MESH:D004833), arteriosclerosis (MESH:D001161), macular degeneration (MESH:D008268)
- **Chemicals:** citric acid (MESH:D019343), stiripentol (MESH:C021092), MCT (MESH:C000709826), Ubiquinone (MESH:D014451), carbamazepine (MESH:D002220), lipid (MESH:D008055), CoQ10 deficiency (MESH:C564403), C8 (MESH:C037690), lacosamide (MESH:D000078334), IF-MCT (-), levocarnitine (MESH:D002331), vitamin B1 (MESH:D013831), fatty acid (MESH:D005227), carbohydrate (MESH:D002241), vitamin C (MESH:D001205), pyrimidine (MESH:C030986), cholesterol (MESH:D002784), ketone body (MESH:D007657), brivaracetam (MESH:C482793), beta-hydroxybutyrate (MESH:D020155), clobazam (MESH:D000078306), CoQ10 (MESH:C024989), triglycerides (MESH:D014280)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

23 references — full list in the complete paper: https://tomesphere.com/paper/PMC12914829/full.md

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Source: https://tomesphere.com/paper/PMC12914829