Citations 182

[P4–531]: TDP‐43 DRIVES FASTER RATES OF HIPPOCAMPAL ATROPHY IN ALZHEIMER's DISEASE STARTING AT LEAST 10 YEARS PRIOR TO DEATH

Alzheimer's & Dementia | October 20, 2017 | Volume: 13 | Issue: 7S_Part_32 | Pages: No page available

10.1016/j.jalz.2017.07.693

[S5–01–01]: C9RAN PROTEINS AS A HALLMARK FOR C9ORF72‐LINKED FTD AND ALS (C9FTD/ALS)

Alzheimer's & Dementia | October 20, 2017 | Volume: 13 | Issue: 7S_Part_30 | Pages: No page available

10.1016/j.jalz.2017.07.473

ARHGEF28 p.Lys280Metfs40Ter in an amyotrophic lateral sclerosis family with a C9orf72 expansion

Neurology Genetics | September 22, 2017 | Volume: 3 | Issue: 5 | Pages: No page available

10.1212/nxg.0000000000000190 | PMID 28971145

C9orf72 poly GA RAN-translated protein plays a key role in amyotrophic lateral sclerosis via aggregation and toxicity

Human Molecular Genetics | September 11, 2017 | Volume: 26 | Issue: 24 | Pages: 4765-4777

10.1093/hmg/ddx350 | PMID 28973350

Loss of clusterin shifts amyloid deposition to the cerebrovasculature via disruption of perivascular drainage pathways

Proceedings of the National Academy of Sciences | July 12, 2017 | Volume: 114 | Issue: 33 | Pages: No page available

10.1073/pnas.1701137114 | PMID 28701379

Significance Deposition of amyloid-β (Aβ) peptide in the form of parenchymal plaques and Aβ accumulation in the walls of cerebral vessels as cerebral amyloid angiopathy (CAA) are pathological hallmarks of Alzheimer’s disease (AD). The clusterin ( CLU ) gene, which confers AD risk, is associated with amyloid deposition. Here we show that loss of CLU promotes cerebrovascular CAA, yet significantly reduces the amount of parenchymal plaques by altering perivascular drainage of Aβ in the APP/PS1 mouse model of AD. The absence of CLU in these mice is associated with a lower number of hemorrhages and a decrease in inflammation. These results suggest that CLU functions as a major Aβ chaperone to maintain Aβ solubility along interstitial fluid drainage pathways and prevent CAA formation.
Phosphorylated neurofilament heavy chain: A biomarker of survival for C9ORF72‐associated amyotrophic lateral sclerosis

Annals of Neurology | June 19, 2017 | Volume: 82 | Issue: 1 | Pages: 139-146

10.1002/ana.24980 | PMID 28628244

As potential treatments for C9ORF72‐associated amyotrophic lateral sclerosis (c9ALS) approach clinical trials, the identification of prognostic biomarkers for c9ALS becomes a priority. We show that levels of phosphorylated neurofilament heavy chain (pNFH) in cerebrospinal fluid (CSF) predict disease status and survival in c9ALS patients, and are largely stable over time. Moreover, c9ALS patients exhibit higher pNFH levels, more rapid disease progression, and shorter survival after disease onset than ALS patients without C9ORF72 expansions. These data support the use of CSF pNFH as a prognostic biomarker for clinical trials, which will increase the likelihood of successfully developing a treatment for c9ALS. Ann Neurol 2017;82:139–146
Repetitive element transcripts are elevated in the brain of C9orf72 ALS/FTLD patients

Human Molecular Genetics | June 14, 2017 | Volume: 26 | Issue: 17 | Pages: 3421-3431

10.1093/hmg/ddx233 | PMID 28637276

Abnormal expression of homeobox genes and transthyretin in C9ORF72 expansion carriers

Neurology Genetics | June 8, 2017 | Volume: 3 | Issue: 4 | Pages: No page available

10.1212/nxg.0000000000000161 | PMID 28660252

Poly(GP) proteins are a useful pharmacodynamic marker for C9ORF72 -associated amyotrophic lateral sclerosis

Science Translational Medicine | March 29, 2017 | Volume: 9 | Issue: 383 | Pages: No page available

10.1126/scitranslmed.aai7866 | PMID 28356511

Poly(GP) proteins are a promising pharmacodynamic marker for developing and testing therapeutics for treating C9ORF72 -associated amyotrophic lateral sclerosis.
IC‐01‐05: Neuropathologic Features of AV1451 TAU Pet Autoradiography in Dementia

Alzheimer's & Dementia | October 17, 2016 | Volume: 12 | Issue: 7S_Part_1 | Pages: No page available

10.1016/j.jalz.2016.06.065