Neurotransmitter abnormalities and response to supplementation in SPG11

Mol Genet Metab. 2012 Sep;107(1-2):229-33. doi: 10.1016/j.ymgme.2012.05.020. Epub 2012 Jun 1.

Abstract

Objective: To report the detection of secondary neurotransmitter abnormalities in a group of SPG11 patients and describe treatment with l-dopa/carbidopa and sapropterin.

Design: Case reports.

Setting: National Institutes of Health in the Undiagnosed Disease Program; Children's National Medical Center in the Myelin Disorders Bioregistry Program.

Patients: Four SPG11 patients with a clinical picture of progressive spastic paraparesis complicated by extrapyramidal symptoms and maculopathy.

Interventions: L-Dopa/carbidopa and sapropterin.

Results: 3/4 patients presented secondary neurotransmitter abnormalities; 4/4 partially responded to L-dopa as well as sapropterin.

Conclusions: In the SPG11 patient with extrapyramidal symptoms, a trial of L-dopa/carbidopa and sapropterin and/or evaluation of cerebrospinal fluid neurotransmitters should be considered.

Publication types

  • Case Reports
  • Research Support, N.I.H., Intramural

MeSH terms

  • Adult
  • Brain / pathology
  • Female
  • Humans
  • Magnetic Resonance Imaging
  • Male
  • Mutation
  • Neurotransmitter Agents / cerebrospinal fluid*
  • Proteins / genetics
  • Retina / pathology
  • Spastic Paraplegia, Hereditary / cerebrospinal fluid*
  • Spastic Paraplegia, Hereditary / diagnosis
  • Spastic Paraplegia, Hereditary / drug therapy*
  • Young Adult

Substances

  • Neurotransmitter Agents
  • Proteins
  • SPG11 protein, human

Supplementary concepts

  • Spastic paraplegia 11, autosomal recessive