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Publication Detail

Title: Altered Bioenergetics in Primary Dermal Fibroblasts from Adult Carriers of the FMR1 Premutation Before the Onset of the Neurodegenerative Disease Fragile X-Associated Tremor/Ataxia Syndrome.

Authors: Napoli, Eleonora; Song, Gyu; Wong, Sarah; Hagerman, Randi; Giulivi, Cecilia

Published In Cerebellum, (2016 Oct)

Abstract: Fragile X-associated tremor/ataxia syndrome (FXTAS) is a late onset neurodegenerative disorder, characterized by tremors, ataxia, impaired coordination, and cognitive decline. While all FXTAS individuals are carriers of a 55-200 CGG expansion at the 5'-UTR of the fragile X mental retardation gene (FMR1), also known as premutation, not all carriers develop FXTAS symptoms and some display other types of psychological/emotional disorders (e.g., autism, anxiety). The goal of this study was to investigate whether the mitochondrial dysfunction previously observed in fibroblasts from older premutation individuals (>60 years) was already present in younger (17-48 years), non-FXTAS-affected carriers and to identify the type and severity of the bioenergetic deficit. Since FXTAS affects mostly males, while females account for a small part of the FXTAS-affected population displaying less severe symptoms, only fibroblasts from males were evaluated in this study. Based on polarographic and enzymatic measurements, a generalized OXPHOS deficit was noted accompanied by increases in the matrix biomarker citrate synthase, oxidative stress (as increased mtDNA copy number and deletions), and mitochondrial network disruption/disorganization. Some of the outcomes (ATP-linked oxygen uptake, coupling, citrate synthase activity, and mitochondrial network organization) strongly correlated with the extent of the CGG expansion, with more severe deficits observed in cell lines carrying higher CGG number. Furthermore, mitochondrial outcomes can identify endophenotypes among carriers and are robust predictors of the premutation diagnosis before the onset of FXTAS, with the potential to be used as markers of prognosis and/or as readouts of pharmacological interventions.

PubMed ID: 27089882 Exiting the NIEHS site

MeSH Terms: Adenosine Triphosphate/metabolism; Adolescent; Adult; Ataxia/metabolism*; Ataxia/pathology; Biomarkers/metabolism; Cells, Cultured; Child; Citrate (si)-Synthase/metabolism; Dermis/metabolism; Dermis/pathology; Endophenotypes/metabolism; Fibroblasts/metabolism*; Fibroblasts/pathology; Fragile X Mental Retardation Protein/genetics*; Fragile X Mental Retardation Protein/metabolism; Fragile X Syndrome/metabolism*; Fragile X Syndrome/pathology; Heterozygote*; Humans; Male; Middle Aged; Mitochondria/metabolism; Mitochondria/pathology; Oxidative Stress/physiology; Oxygen/metabolism; Prodromal Symptoms; Tremor/metabolism*; Tremor/pathology; Trinucleotide Repeat Expansion; Young Adult

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