Headache and sleep quality in mitochondrial diseases

Author:

Martin Alejandro Herrero San1234,Gonzalez Cristina Dominguez1256,Conejo Montserrat Morales78,Salas Maria Elena Hernández9,Gallego Jesús Hernández19

Affiliation:

1. Department of Neurology, Hospital Universitario 12 de Octubre, Madrid, Spain

2. Biomedical Research Networking Center in Neurodegenerative Diseases (CIBERNED), Madrid, Spain

3. Group of Neurodegenerative Diseases, Investigation Institute, Hospital 12 de Octubre (I+12), Madrid, Spain

4. Multidisciplinary Sleep Unit, Hospital Universitario 12 de Octubre, Madrid, Spain

5. Neuromuscular Unit, Hospital Universitario 12 de Octubre, Madrid, Spain

6. CSUR - National Reference Unit in Rare Neuromuscular Diseases, Hospital Universitario 12 de Octubre, Madrid, Spain

7. Department of Internal Medicine, Hospital Universitario 12 de Octubre, Madrid, Spain

8. Reference Center for Inherited Metabolic Disease – MetabERN, Hospital Universitario 12 de Octubre, Madrid, Spain

9. Facultad de Medicina, Universidad Complutense de Madrid, Madrid, Spain

Abstract

Objective: Describe the characteristics and prevalence of headache in patients with mitochondrial diseases (MDs), as well as sleep quality, trying to observe possible associations. To assess whether these patients are more likely to suffer headaches in relation to poorer quality of sleep. Background: Sleep disorders and headache are considered to be common in MDs. We present the largest sample analyzed to date. Methods: Observational, descriptive, cross-sectional study that analyzed a database of 232 patients with MDs, including age, sex, genotype, phenotype, presence and characteristics of headache. All patients fulfilled the Epworth Sleepiness Scale (ESS), the Pittsburgh Sleep Quality Index (PSQI) and, in migraine, the Migraine Disability Assessment questionnaire (MIDAS). Headache was divided into two groups: migraine headache, according to criteria of the International Classification of Headache Disorders (ICHD-III beta), and non-migraine headache. Results: A total of 203 cases were analyzed, 124 women (61%) and 79 men (39%). Average age was 46 years. Most frequent DNA mutation was m.3243 A > G in MITL1 gene (33%). Most frequent phenotype was MELAS syndrome: 28 patients (13.8%). Ninety-two patients (45.3%), reported headache, 44 fulfilling migraine criteria (21.7%). Headache was more frequent in MELAS syndrome ( p < 0.01). Statistically significant differences were found in the number of disabling episodes per month in patients with migraine ( p < 0.001). Patients with headache scored higher in Epworth ( p = 0.01) and Pittsburgh scales ( p < 0.001). Conclusions: A higher prevalence of migraine is observed in patients with mitochondrial diseases, independent of genotype and phenotype. MD-associated migraine tends to be chronic and more disabling. A higher frequency of headache, not specifically migraine, has also been observed in patients with MELAS syndrome. Mitochondrial dysfunction could be one of the pathophysiological mechanisms of migraine and a factor of chronification and severity. Poor sleep quality could also be associated with headache in patients with MDs. Assessment of headache and sleep disturbances should be part of the routine workup of patients with mitochondrial disease. Trial registration: N/A.

Publisher

SAGE Publications

Subject

Neurology (clinical)

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