4.2 Article

Chronic pain is common in mitochondrial disease

期刊

NEUROMUSCULAR DISORDERS
卷 30, 期 5, 页码 413-419

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.nmd.2020.02.017

关键词

Mitochondrial disorders; Pain; Neuropathy; Mitochondria; Genetics

资金

  1. EMBO Long-term Fellowship [ALTF 1600_2014]
  2. Wellcome Trust Postdoctoral Training Fellowship for Clinicians [105839]
  3. Medical Research Council Clinician Scientist Fellowship [MR/S002065/1]
  4. Medical Research Council Mitochondrial Biology Unit [MC_UU_00015/9]
  5. Medical Research Council (MRC) International Centre for Genomic Medicine in Neuromuscular Disease
  6. Evelyn Trust
  7. National Institute for Health Research (NIHR) Biomedical Research Centre based at Cambridge University Hospitals NHS Foundation Trust
  8. UK NHS Highly Specialised Commissioners
  9. University of Cambridge
  10. MRC [MR/S002065/1, MC_UU_00015/9] Funding Source: UKRI

向作者/读者索取更多资源

In the absence of cure, the main objectives in the management of patients with mitochondrial disease are symptom control and prevention of complications. While pain is a complicating symptom in many chronic diseases and is known to have a clear impact on quality of life, its prevalence and severity in people with mitochondrial disease is unknown. We conducted a survey of pain symptoms in patients with genetically confirmed mitochondrial disease from two UK mitochondrial disease specialist centres. The majority (66.7%) of patients had chronic pain which was primarily of neuropathic nature. Presence of pain did not significantly impact overall quality of life. The m.3243A > G MTTL1 mutation was associated with higher pain severity and increased the likelihood of neuropathic pain compared to other causative nuclear and mitochondrial gene mutations. Although previously not considered a core symptom in people with mitochondrial disease, pain is a common clinical manifestation, frequently of neuropathic nature, and influenced by genotype. Therefore, pain-related symptoms should be carefully characterised and actively managed in this patient population. (C) 2020 The Author(s). Published by Elsevier B.V.

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