Cited by 20Metabolism and Genetic DisordersLysosomal Storage Disorders ResearchHereditary Neurological Disorders

Cognitive impairment in adult-onset adrenoleukodystrophy

Edwin, David, Speedie, Lynn, Naidu, Sakkubai, Moser, Hugo·1990·Molecular and Chemical Neuropathology

Abstract

Adrenoleukodystrophy (ALD) is a progressive X-linked disorder that produces pathological changes, mainly in the adrenal cortex and the white matter of the central nervous system. The main biochemical abnormality is the accumulation of saturated unbranched fatty acids with a chain length of 24 or more, referred to as very-long-chain fatty acids (VLCFA). Affected children develop large zones of demyelination associated with perivascular lymphoctyic infiltrations resembling those seen in multiple sclerosis. Adults show a more chronic form of the disease, referred to as adrenomyeloneuropathy (AMN). AMN mainly involves the spinal cord ad peripheral nerves, although the cerebral hemispheres may also be affected. Approximately 15% of female carriers have nervous-system involvement that resembles AMN. It is well known that ALD may initially appear as a psychiatric disorder. In the present study, we have assessed the prevalence of cognitive impairment in a group of AMN patients and neurologically symptomatic ALD heterozygotes initially presenting primarily physical complaints. Sixty percent of these patients demonstrated significant neuropsychological impairment, most commonly a pattern of spared and impaired functions typical of a subcortical dementia. We suggest that this progressive cognitive impairment may underlie other behavioral deficits, affirming the significance of the psychological features of this genetically determined disorder.

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Crossref · 10.1007/bf03159942

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  • Cognitive decline and psychiatric manifestations in cALD are often misdiagnosed.

    “The cognitive decline [39] and psychiatric manifestations are often misdiagnosed [40,41,42].”

    From Revisiting the Pathogenesis of X-Linked Adrenoleukodystrophy (2025) · cites this paper as [39]

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Authors
Edwin, D., Speedie, L., Naidu, S., & Moser, H.
Affiliations
  • Johns Hopkins University (US)
  • Kennedy Krieger Institute (US)
Venue
Molecular and Chemical Neuropathology
Published
1990-06
Volume
12
Issue
3
Pages
167-176
ISSN
1044-7393 (ISSN-L)
OpenAlex
W1970011811
Cited by
20
References
0
Citations by year
2026: 1 · 2025: 2 · 2022: 2 · 2021: 1 · 2018: 1 · 2016: 1 · 2013: 1 · 2012: 1
FWCI
0.47
Type
journal article
Language
en
Open access
closed
Locations
  • Molecular and Chemical Neuropathology (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • National Center for Research Resources (M01RR000722, M01RR000035, 5MO1 RR000722, 5MO1 RR0035)
  • Eunice Kennedy Shriver National Institute of Child Health and Human Development (5P3O HD24061)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Clinical Biochemistry › Metabolism and Genetic Disorders
  • Health Sciences › Medicine › Physiology › Lysosomal Storage Disorders Research
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Hereditary Neurological Disorders
Keywords
adrenomyeloneuropathy, cognitive impairment, very long chain fatty acids, X-linked disorders, subcortical dementia, neuropsychological assessment, heterozygous carriers, demyelination, behavioral deficits
MeSH terms
Adrenoleukodystrophy, Adult, Cognition Disorders, Education, Female, Humans, Intelligence, Male, Middle Aged, Neuropsychological Tests

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