Postmortem study of ataxia with retinitis pigmentosa by mutation of the α-tocopherol transfer protein gene

T. Yokota, R. Okeda, H. Mizusawa, T. Uchihara, J. Kumagai, T. Shiojiri, J. J. Pang, M. Arita, H. Arai, M. Hayashi, M. Kiyosawa

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59 Citations (Scopus)

Abstract

A new syndrome of ataxia and retinitis pigmentosa with vitamin E deficiency caused by the missense mutation of α-tocopherol transfer protein (α-TTP) gene was recently proposed. After studying the first postmortem case with this mutation pathologically and biochemically, whether the symptoms can be treated by supplementation of vitamin E or not is discussed. The major pathological findings were retinal atrophy; severe dying back-type degeneration of the posterior column; and massive accumulation of lipofuscin in neurons including dorsal root ganglion (DRG) cells, which were almost identical to those in vitamin E deficient animals and patients with fat malabsorption. Also, mild loss of Purkinje cells was noted. Because robust expression of α-TTP was detected in the cerebellum as well as in the liver and the tissue concentration of vitamin E in the cerebellum was still low even after oral supplementation, the mild Purkinje cell loss might be related to the mutant α-TTP in the cerebellum. By contrast, in the DRG, thought to be mainly responsible for ataxia, no expression of α-TTP was detected, and the tissue concentration of vitamin E increased to normal after supplementation. It is therefore considered that oral supplementation of vitamin E should effectively counteract the progression of ataxia.

Original languageEnglish
Pages (from-to)521-525
Number of pages5
JournalJournal of Neurology Neurosurgery and Psychiatry
Volume68
Issue number4
DOIs
Publication statusPublished - 2000 Apr
Externally publishedYes

Keywords

  • Ataxia
  • Retinitis pigmentosa
  • Vitamin E
  • α-tocopherol transfer protein

ASJC Scopus subject areas

  • Surgery
  • Clinical Neurology
  • Psychiatry and Mental health

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    Yokota, T., Okeda, R., Mizusawa, H., Uchihara, T., Kumagai, J., Shiojiri, T., Pang, J. J., Arita, M., Arai, H., Hayashi, M., & Kiyosawa, M. (2000). Postmortem study of ataxia with retinitis pigmentosa by mutation of the α-tocopherol transfer protein gene. Journal of Neurology Neurosurgery and Psychiatry, 68(4), 521-525. https://doi.org/10.1136/jnnp.68.4.521