AI Article Synopsis

  • Neurodegeneration with brain iron accumulation (NBIA) is a rare group of inherited diseases affecting 1-3 patients per 1,000,000, with around 15,000-20,000 cases globally characterized by abnormal iron buildup in the brain.
  • Symptoms include progressive movement issues, neuropathy, cognitive decline, and various neuropsychiatric disorders, with eleven identified subtypes, including common forms like PKAN and PLAN.
  • The overview addresses cellular imbalances and metabolic changes in NBIA subtypes, particularly focusing on mitochondrial function and lipid metabolism to enhance understanding of the disease.

Article Abstract

Neurodegeneration with brain iron accumulation (NBIA) is a broad, heterogeneous group of rare inherited diseases (1-3 patients/1,000,000 people) characterized by progressive symptoms associated with excessive abnormal iron deposition in the brain. Approximately 15,000-20,000 individuals worldwide are estimated to be affected by NBIA. NBIA is usually associated with slowly progressive pyramidal and extrapyramidal symptoms, axonal motor neuropathy, optic nerve atrophy, cognitive impairment and neuropsychiatric disorders. To date, eleven subtypes of NBIA have been described and the most common ones include pantothenate kinase-associated neurodegeneration (PKAN), PLA2G6-associated neurodegeneration (PLAN), mitochondrial membrane protein-associated neurodegeneration (MPAN) and beta-propeller protein-associated neurodegeneration (BPAN). We present a comprehensive overview of the evidence for disturbed cellular homeostasis and metabolic alterations in NBIA variants, with a careful focus on mitochondrial bioenergetics and lipid metabolism which drives a new perspective in understanding the course of this infrequent malady.

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http://dx.doi.org/10.1016/j.bbabio.2024.149517DOI Listing

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