Identification of GFAP gene mutation in hereditary adult-onset Alexander's disease

Michito Namekawa, Yoshihisa Takiyama, Yoko Aoki, Norio Takayashiki, Kumi Sakoe, Haruo Shimazaki, Tomohiro Taguchi, Yasufumi Tanaka, Masatoyo Nishizawa, Ken Saito, Yoichi Matsubara, Imaharu Nakano

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65 Citations (Scopus)

Abstract

Alexander's disease, a leukodystrophy characterized by Rosenthal fibers (RFs) in the brain, is categorized into three subtypes: infantile, juvenile, and adult. Although most are sporadic, occasional familial Alexander's disease cases have been reported for each subtype. Hereditary adult-onset Alexander's disease shows progressive spastic paresis, bulbar or pseudobulbar palsy, palatal myoclonus symptomatologically, and prominent atrophy of the medulla oblongata and upper spinal cord on magnetic resonance imaging. Recent identification of GFAP gene mutations in the sporadic infantile- and juvenile-onset Alexander's disease prompted us to examine the GFAP gene in two Japanese hereditary adult-onset Alexander's disease brothers with autopsy in one case. Both had spastic paresis without palatal myoclonus, and magnetic resonance imaging showed marked atrophy of the medulla oblongata and cervicothoracic cord. The autopsy showed severely involved shrunken pyramids, but scarce Rosenthal fibers (RFs). Moderate numbers of Rosenthal fibers (RFs) were observed in the stratum subcallosum and hippocampal fimbria. In both cases, we found a novel missense mutation of a G-to-T transition at nucleotide 841 in the GFAP gene that results in the substitution of arginine for leucine at amino acid residue 276 (R276L). This is the first report of identification of the causative mutation of the GFAP gene for neuropathologically proven hereditary adult-onset Alexander's disease, suggesting a common molecular mechanism underlies the three Alexander's disease subtypes.

Original languageEnglish
Pages (from-to)779-785
Number of pages7
JournalAnnals of Neurology
Volume52
Issue number6
DOIs
Publication statusPublished - 2002 Dec 1

ASJC Scopus subject areas

  • Neurology
  • Clinical Neurology

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