Diffusion tensor–based imaging reveals occult abnormalities in adrenomyeloneuropathy

“Pure” adrenomyeloneuropathy (AMN) is the noninflammatory myeloneuropathic variant of X‐linked adrenoleukodystrophy, where the disease process appears to be restricted to spinal cord tracts and peripheral nerves. The absence of obvious brain involvement makes it distinct from the inflammatory cerebral phenotypes of X‐linked adrenoleukodystrophy. However, some pure AMN patients later experience development of cerebral demyelination, but little is known about the extent of brain involvement in pure AMN patients who have normal brain magnetic resonance imaging. We used diffusion tensor imaging to investigate possible occult cerebral abnormalities in such pure AMN patients. Fractional anisotropy and trace were studied in three‐dimensional reconstructions of white matter tracts commonly involved in cerebral phenotypes of X‐linked adrenoleukodystrophy. Results demonstrated reduced fractional anisotropy and increased trace in bilateral corticospinal tracts and genu of corpus callosum (p < 0.05). Diffusion tensor imaging–based three‐dimensional fiber tracking showed occult tract‐specific cerebral microstructural abnormalities in pure AMN patients who had a normal conventional brain magnetic resonance image. Corticospinal tract abnormalities could reflect a centripetal extension of spinal cord long‐tract distal axonopathy. Accompanying abnormalities in genu of corpus callosum indicate that the disease pathology in pure AMN may not be limited to spinal cord long tracts alone, although the involvement of the latter is most prominent and severe. Ann Neurol 2005;58:758–766

[1]  H. Moser,et al.  Magnetization transfer MRI demonstrates spinal cord abnormalities in adrenomyeloneuropathy , 2005, Neurology.

[2]  H. Moser,et al.  Spectroscopic evidence of cerebral axonopathy in patients with “pure” adrenomyeloneuropathy , 2005, Neurology.

[3]  David Eidelberg,et al.  Microstructural white matter changes in carriers of the DYT1 gene mutation , 2004 .

[4]  H. Moser,et al.  Progress in X-linked adrenoleukodystrophy , 2004, Current opinion in neurology.

[5]  C. Scriver,et al.  The Metabolic and Molecular Bases of Inherited Disease, 8th Edition 2001 , 2001, Journal of Inherited Metabolic Disease.

[6]  William,et al.  The Metabolic and Molecular Bases of Inherited Disease (Scriver, C. R., Beaudet, A. L., Sly, W. S., Valle, D., Childs, B., Kinzler, K. W., and Vogelstein, B., eds., 8th ed., McGraw-Hill, New-York, 2001, 7012 p., $550.00) , 2004, Biochemistry (Moscow).

[7]  S. Wakana,et al.  Fiber tract-based atlas of human white matter anatomy. , 2004, Radiology.

[8]  H. Moser,et al.  Analysis of MRI patterns aids prediction of progression in X-linked adrenoleukodystrophy , 2003, Neurology.

[9]  H. Moser,et al.  MRI and proton MRSI in women heterozygous for X-linked adrenoleukodystrophy , 2003, Neurology.

[10]  Susumu Mori,et al.  Fiber tracking: principles and strategies – a technical review , 2002, NMR in biomedicine.

[11]  Susumu Mori,et al.  Proton MR spectroscopic and diffusion tensor brain MR imaging in X-linked adrenoleukodystrophy: initial experience. , 2002, Radiology.

[12]  Roland Bammer,et al.  Diffusion tensor imaging using single‐shot SENSE‐EPI , 2002, Magnetic resonance in medicine.

[13]  H. Moser,et al.  ABCD1 mutations and the X‐linked adrenoleukodystrophy mutation database: Role in diagnosis and clinical correlations , 2001, Human mutation.

[14]  G. Pearlson,et al.  Diffusion Tensor Imaging and Axonal Tracking in the Human Brainstem , 2001, NeuroImage.

[15]  H. Moser,et al.  Evolution of phenotypes in adult male patients with X‐linked adrenoleukodystrophy , 2001, Annals of neurology.

[16]  H. Moser,et al.  Adrenomyeloneuropathy: A Neuropathologic Review Featuring Its Noninflammatory Myelopathy , 2000, Journal of neuropathology and experimental neurology.

[17]  P. Boesiger,et al.  SENSE: Sensitivity encoding for fast MRI , 1999, Magnetic resonance in medicine.

[18]  M. Horsfield,et al.  Optimal strategies for measuring diffusion in anisotropic systems by magnetic resonance imaging , 1999, Magnetic resonance in medicine.

[19]  M. Raichle,et al.  Tracking neuronal fiber pathways in the living human brain. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[20]  P. V. van Zijl,et al.  Three‐dimensional tracking of axonal projections in the brain by magnetic resonance imaging , 1999, Annals of neurology.

[21]  H. Moser,et al.  Plasma very long chain fatty acids in 3,000 peroxisome disease patients and 29,000 controls , 1999, Annals of neurology.

[22]  E. Ralston,et al.  Expression of the Adrenoleukodystrophy Protein in the Human and Mouse Central Nervous System , 1997, Neurobiology of Disease.

[23]  H. Moser,et al.  Cognitive and brain magnetic resonance imaging findings in adrenomyeloneuropathy , 1996, Annals of neurology.

[24]  P. Basser,et al.  Microstructural and physiological features of tissues elucidated by quantitative-diffusion-tensor MRI. , 1996, Journal of magnetic resonance. Series B.

[25]  H. Moser,et al.  Interactions of a very long chain fatty acid with model membranes and serum albumin. Implications for the pathogenesis of adrenoleukodystrophy. , 1995, The Journal of clinical investigation.

[26]  A. J. Kumar,et al.  MR findings in adult-onset adrenoleukodystrophy. , 1995, AJNR. American journal of neuroradiology.

[27]  H. Moser,et al.  Adrenoleukodystrophy: a scoring method for brain MR observations. , 1994, AJNR. American journal of neuroradiology.

[28]  J. Mosser,et al.  The gene responsible for adrenoleukodystrophy encodes a peroxisomal membrane protein. , 1994, Human molecular genetics.

[29]  Jean Mosser,et al.  Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transporters , 1993, Nature.

[30]  Powers Jm Adreno-leukodystrophy (adreno-testiculo-leukomyelo-neuropathic-complex). , 1985 .

[31]  J. Powers,et al.  Adreno-leukodystrophy (adreno-testiculo-leukomyelo-neuropathic-complex). , 1985, Clinical neuropathology.

[32]  J. Kurtzke Rating neurologic impairment in multiple sclerosis , 1983, Neurology.

[33]  J. Dave,et al.  Membrane microviscosity is increased in the erythrocytes of patients with adrenoleukodystrophy and adrenomyeloneuropathy. , 1983, The Journal of clinical investigation.

[34]  K. Suzuki,et al.  FATTY ACID ABNORMALITY IN ADRENOLEUKODYSTROPHY , 1976, Journal of neurochemistry.