RT Journal Article SR Electronic T1 Clinical spectrum of the pentanucleotide repeat expansion in the RFC1 gene in ataxia syndromes JF Neurology JO Neurology FD Lippincott Williams & Wilkins SP e2912 OP e2923 DO 10.1212/WNL.0000000000010744 VO 95 IS 21 A1 Gisatulin, Maria A1 Dobricic, Valerija A1 Zühlke, Christine A1 Hellenbroich, Yorck A1 Tadic, Vera A1 Münchau, Alexander A1 Isenhardt, Klaus A1 Bürk, Katrin A1 Bahlo, Melanie A1 Lockhart, Paul J. A1 Lohmann, Katja A1 Helmchen, Christoph A1 Brüggemann, Norbert YR 2020 UL http://n.neurology.org/content/95/21/e2912.abstract AB Objective To determine the clinical significance of an intronic biallelic pentanucleotide repeat expansion in the gene encoding replication factor C subunit 1 (RFC1) in patients with late-onset cerebellar ataxia, neuropathy, and vestibular areflexia syndrome (CANVAS), in patients with other ataxias, and in healthy controls by comprehensive genetic analyses.Methods In this case-control study, we included 457 individuals comprising 26 patients with complete or incomplete CANVAS, 70 patients with late-onset cerebellar ataxia, 208 healthy controls, and 153 individuals from 39 multigenerational families without ataxia to determine repeat stability. All 96 patients were screened for the repeat expansion by duplex PCR. To further characterize the repeat type and lengths, we used fragment length analysis, repeat-primed PCR, Sanger sequencing, and Southern blotting. Expression of RFC1 and the neighboring gene WDR19 were determined by quantitative PCR.Results Massive biallelic pentanucleotide expansions were found in 15/17 patients with complete CANVAS (88%), in 2/9 patients with incomplete CANVAS (22%), in 4/70 patients with unspecified, late-onset cerebellar ataxia (6%), but not in controls. In patients, the expansion comprised 800–1,000 mostly AAGGG repeats. Nonmassively expanded repeat numbers were in the range of 7–137 repeats and relatively stable during transmission. Expression of RFC1 and WDR19 were unchanged and RFC1 intron retention was not found.Conclusions A biallelic pentanucleotide repeat expansion is a frequent cause of CANVAS and found in a considerable number of patients with an incomplete clinical presentation or other forms of cerebellar ataxia. The mechanism by which the repeat expansions are causing disease remains unclear and warrants further investigations.BAFME=benign adult familial myoclonic epilepsy; CANVAS=cerebellar ataxia, neuropathy, and vestibular areflexia syndrome; HIT=head impulse test; MSA-C=multiple system atrophy of the cerebellar subtype; qPCR=quantitative PCR; RP-PCR=repeat primed PCR; SCA=spinocerebellar ataxia; SDS=sodium dodecyl sulfate; SSC=standard sodium citrate; vHIT=video head impulse test; VOR=vestibulo-ocular reflex