Amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) are adult-onset neurodegenerative disorders in which up to one-third of patients have overlapping clinical and pathological features. In 2011 a large hexanucleotide repeat expansion in the C9ORF72 gene was discovered that caused both ALS and FTD. The C9ORF72 expansion mutation is the commonest cause of familial ALS and familial FTD in the US and also accounts for a significant number of sporadic ALS cases. Despite the large number of patients identified from testing of stored samples, relatively little is known about the natural history of C9ORF72-related disease: how quickly the motor weakness and cognitive dysfunction progress, whether clinical presentation influences survival, and whether subtle motor or cognitive abnormalities are detectable prior to the onset of definite symptoms. Therefore, the first aim of this project is designed to fill this knowledge gap through a 3-year prospective longitudinal study of a cohort of symptomatic individuals carrying the C9ORF72 repeat expansion and asymptomatic carriers who are relatives of affected patients.
The second aim of the study is to explore candidate biomarkers of disease progression. Biomarkers that can signal improvement or decline in disease activity before clinically evident deterioration would be valuable to speed the cycle of clinical trials. This is a highly collaborative study. Studies of biospecimens are coordinated by Dr. Bryan Traynor, a collaborative investigator in the National Institute of Aging. All participants consent to sharing of de-identified data and specimens. Participants undergo a structured battery of clinical ratings, neuropsychological tests, and motor measurements over a 2-4 day visit at NIH at enrollment and follow-up to assess disease severity and progression. Physiological, imaging, and biofluid biomarkers are obtained to examine their correlations with the clinical measures of progression. Skin biopsies are obtained at one visit for extramural collaborators studying disease mechanisms. The first participant was enrolled in FY14. As FY16 ends, 34 C9ORF72 mutation carriers have been enrolled and 91 visits have been carried out. To date, transcranial magnetic stimulation studies found evidence of cortical hyperexcitability in patients exhibiting lower motor neuron signs. Analysis of longitudinal physiological and imaging data is underway. CSF and plasma specimens have been shared with investigators at Johns Hopkins University, the Mayo Clinic Jacksonville, and pharmaceutical companies for exploring markers of disease activity and mechanisms of disease.
| Floeter, Mary Kay; Danielian, Laura E; Braun, Laura E et al. (2018) Longitudinal diffusion imaging across the C9orf72 clinical spectrum. J Neurol Neurosurg Psychiatry 89:53-60 |
| Floeter, Mary K; Traynor, Bryan J; Farren, Jennifer et al. (2017) Disease progression in C9orf72 mutation carriers. Neurology 89:234-241 |
| Cardenas, Agustin M; Sarlls, Joelle E; Kwan, Justin Y et al. (2017) Pathology of callosal damage in ALS: An ex-vivo, 7 T diffusion tensor MRI study. Neuroimage Clin 15:200-208 |
| Gendron, Tania F; Chew, Jeannie; Stankowski, Jeannette N et al. (2017) Poly(GP) proteins are a useful pharmacodynamic marker for C9ORF72-associated amyotrophic lateral sclerosis. Sci Transl Med 9: |
| Gendron, Tania F; C9ORF72 Neurofilament Study Group; Daughrity, Lillian M et al. (2017) Phosphorylated neurofilament heavy chain: A biomarker of survival for C9ORF72-associated amyotrophic lateral sclerosis. Ann Neurol 82:139-146 |
| Floeter, Mary Kay; Bageac, Devin; Danielian, Laura E et al. (2016) Longitudinal imaging in C9orf72 mutation carriers: Relationship to phenotype. Neuroimage Clin 12:1035-1043 |
| Schanz, Olivia; Bageac, Devin; Braun, Laura et al. (2016) Cortical hyperexcitability in patients with C9ORF72 mutations: Relationship to phenotype. Muscle Nerve 54:264-9 |
| Su, Zhaoming; Zhang, Yongjie; Gendron, Tania F et al. (2014) Discovery of a biomarker and lead small molecules to target r(GGGGCC)-associated defects in c9FTD/ALS. Neuron 83:1043-50 |
