Brain white matter oedema due to ClC-2 chloride channel deficiency: an observational analytical study

Christel Depienne*, Marianna Bugiani, Celine Dupuits, Damien Galanaud, Valerie Touitou, Nienke Postma, Carola van Berkel, Emiel Polder, Eleonore Tollard, Frederic Darios, Alexis Brice, Christine E. de Die-Smulders, Johannes S. Vles, Adeline Vanderver, Graziella Uziel, Cengiz Yalcinkaya, Suzanna G. Frints, Vera M. Kalscheuer, Jan Klooster, Maarten KamermansTruus E. M. Abbink, Nicole I. Wolf, Frederic Sedel, Marjo S. van der Knaap

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review


Background Mutant mouse models suggest that the chloride channel ClC-2 has functions in ion and water hornoeostasis, but this has not been confirmed in human beings. We aimed to define novel disorders characterised by distinct patterns of MR1 abnormalities in patients with leukoencephalopathies of unknown origin, and to identify the genes mutated in these disorders. We were specifically interested in leukoencephalopathies characterised by white matter oedema, suggesting a defect in ion and water homoeostasis. Methods In this observational analytical study, we recruited patients with leukoencephalopathies characterised by MRI signal abnormalities in the posterior limbs of the internal capsules, midbrain cerebral peduncles, and middle cerebellar peduncles from our databases of patients with leulcoencephalopathies of unknown origin. We used exome sequencing to identify the gene involved. We screened the candidate gene in additional patients by Sanger sequencing and mRNA analysis, and investigated the functional effects of the mutations. We assessed the localisation of ClC-2 with immunohistochemistry and electron microscopy in post-mortem human brains of individuals without neurological disorders. Findings Seven patients met our indusion criteria, three with adult-onset disease and four with childhood-onset disease. We identified homozygous or compound-heterozygous mutations in CLCN2 in three adult and three paediatric patients. We found evidence that the CLCN2 mutations result in loss of function of ClC-2. The remaining paediatric patient had an X-linked family history and a mutation in GJB1, encoding connexin 32. Clinical features were variable and included cerebellar ataxia, spasticity, chorioretinopathy with visual field defects, optic neuropathy, cognitive defects, and headaches. MM showed restricted diffusion suggesting myelin vacuolation that was confined to the specified white matter structures in adult patients, and more diffusely involved the brain white matter in paediatric patients. We detected ClC-2 in all components of the panglial syncytium, enriched in astrocytic endfeet at the perivascular basal lamina, in the glia limitans, and in ependymal cells. Interpretation Our observations substantiate the concept that ClC-2 is involved in brain ion and water homoeostasis. Autosomal-recessive CLCN2 mutations cause a leukoencephalopathy that belongs to an emerging group of disorders affecting brain ion and water homoeostasis and characterised by intramyelinic oedema.
Original languageEnglish
Pages (from-to)659-668
JournalLancet Neurology
Issue number7
Publication statusPublished - Jul 2013


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