Literature DB >> 23550114

The Medical Research Council prion disease rating scale: a new outcome measure for prion disease therapeutic trials developed and validated using systematic observational studies.

Andrew G B Thompson1, Jessica Lowe, Zoe Fox, Ana Lukic, Marie-Claire Porter, Liz Ford, Michele Gorham, Gosala S Gopalakrishnan, Peter Rudge, A Sarah Walker, John Collinge, Simon Mead.   

Abstract

Progress in therapeutics for rare disorders like prion disease is impeded by the lack of validated outcome measures and a paucity of natural history data derived from prospective observational studies. The first analysis of the U.K. National Prion Monitoring Cohort involved 1337 scheduled clinical assessments and 479 telephone assessments in 437 participants over 373 patient-years of follow-up. Scale development has included semi-quantitative and qualitative carer interviews, item response modelling (Rasch analysis), inter-rater reliability testing, construct analysis and correlation with several existing scales. The proposed 20-point Medical Research Council prion disease rating scale assesses domains of cognitive function, speech, mobility, personal care/feeding and continence, according to their relative importance documented by carer interviews. It is quick and simple to administer, and has been validated for use by doctors and nurses and for use over the telephone, allowing for frequent assessments that capture the rapid change typical of these diseases. The Medical Research Council Scale correlates highly with widely used cognitive and single item scales, but has substantial advantages over these including minimal floor effects. Three clear patterns of decline were observed using the scale: fast linear decline, slow linear decline (usually inherited prion disease) and in some patients, decline followed by a prolonged preterminal plateau at very low functional levels. Rates of decline and progress through milestones measured using the scale vary between sporadic, acquired and inherited prion diseases following clinical expectations. We have developed and validated a new functionally-oriented outcome measure and propose that future clinical trials in prion disease should collect data compatible with this scale, to allow for combined and comparative analyses. Such approaches may be advantageous in orphan conditions, where single studies of feasible duration will often struggle to achieve statistical power.

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Year:  2013        PMID: 23550114     DOI: 10.1093/brain/awt048

Source DB:  PubMed          Journal:  Brain        ISSN: 0006-8950            Impact factor:   13.501


  34 in total

1.  Clinical Trial Simulations Based on Genetic Stratification and the Natural History of a Functional Outcome Measure in Creutzfeldt-Jakob Disease.

Authors:  Simon Mead; Matthew Burnell; Jessica Lowe; Andrew Thompson; Ana Lukic; Marie-Claire Porter; Christopher Carswell; Diego Kaski; Janna Kenny; Tze How Mok; Nina Bjurstrom; Edit Franko; Michele Gorham; Ronald Druyeh; Jonathan D F Wadsworth; Zane Jaunmuktane; Sebastian Brandner; Harpreet Hyare; Peter Rudge; A Sarah Walker; John Collinge
Journal:  JAMA Neurol       Date:  2016-04       Impact factor: 18.302

Review 2.  Therapies for human prion diseases.

Authors:  Peter K Panegyres; Elizabeth Armari
Journal:  Am J Neurodegener Dis       Date:  2013-09-18

3.  The most problematic symptoms of prion disease - an analysis of carer experiences.

Authors:  Liz Ford; Peter Rudge; Kathy Robinson; John Collinge; Michele Gorham; Simon Mead
Journal:  Int Psychogeriatr       Date:  2019-08       Impact factor: 3.878

4.  Prion disease: a promising rating scale for prion disease clinical research.

Authors:  Pietro Tiraboschi; Fabrizio Tagliavini
Journal:  Nat Rev Neurol       Date:  2013-06-11       Impact factor: 42.937

5.  Genotype-phenotype analysis in inherited prion disease with eight octapeptide repeat insertional mutation.

Authors:  Martin Paucar; Fengqing Xiang; Richard Moore; Ruth Walker; Elisabeth Winnberg; Per Svenningsson
Journal:  Prion       Date:  2013-11-25       Impact factor: 3.931

6.  Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease: a genome-wide association study.

Authors:  Emma Jones; Holger Hummerich; Emmanuelle Viré; James Uphill; Athanasios Dimitriadis; Helen Speedy; Tracy Campbell; Penny Norsworthy; Liam Quinn; Jerome Whitfield; Jacqueline Linehan; Zane Jaunmuktane; Sebastian Brandner; Parmjit Jat; Akin Nihat; Tze How Mok; Parvin Ahmed; Steven Collins; Christiane Stehmann; Shannon Sarros; Gabor G Kovacs; Michael D Geschwind; Aili Golubjatnikov; Karl Frontzek; Herbert Budka; Adriano Aguzzi; Hata Karamujić-Čomić; Sven J van der Lee; Carla A Ibrahim-Verbaas; Cornelia M van Duijn; Beata Sikorska; Ewa Golanska; Pawel P Liberski; Miguel Calero; Olga Calero; Pascual Sanchez-Juan; Antonio Salas; Federico Martinón-Torres; Elodie Bouaziz-Amar; Stéphane Haïk; Jean-Louis Laplanche; Jean-Phillipe Brandel; Phillipe Amouyel; Jean-Charles Lambert; Piero Parchi; Anna Bartoletti-Stella; Sabina Capellari; Anna Poleggi; Anna Ladogana; Maurizio Pocchiari; Serena Aneli; Giuseppe Matullo; Richard Knight; Saima Zafar; Inga Zerr; Stephanie Booth; Michael B Coulthart; Gerard H Jansen; Katie Glisic; Janis Blevins; Pierluigi Gambetti; Jiri Safar; Brian Appleby; John Collinge; Simon Mead
Journal:  Lancet Neurol       Date:  2020-09-16       Impact factor: 44.182

7.  Bank vole prion protein extends the use of RT-QuIC assays to detect prions in a range of inherited prion diseases.

Authors:  Tze How Mok; Akin Nihat; Connie Luk; Danielle Sequeira; Mark Batchelor; Simon Mead; John Collinge; Graham S Jackson
Journal:  Sci Rep       Date:  2021-03-04       Impact factor: 4.379

8.  Genome-wide association study of behavioural and psychiatric features in human prion disease.

Authors:  A G B Thompson; J Uphill; J Lowe; M-C Porter; A Lukic; C Carswell; P Rudge; A MacKay; J Collinge; S Mead
Journal:  Transl Psychiatry       Date:  2015-04-21       Impact factor: 6.222

9.  Evolution of Diffusion-Weighted Magnetic Resonance Imaging Signal Abnormality in Sporadic Creutzfeldt-Jakob Disease, With Histopathological Correlation.

Authors:  Laura Eisenmenger; Marie-Claire Porter; Christopher J Carswell; Andrew Thompson; Simon Mead; Peter Rudge; John Collinge; Sebastian Brandner; Hans R Jäger; Harpreet Hyare
Journal:  JAMA Neurol       Date:  2016-01       Impact factor: 18.302

10.  Diagnosing Sporadic Creutzfeldt-Jakob Disease by the Detection of Abnormal Prion Protein in Patient Urine.

Authors:  Connie Luk; Samantha Jones; Claire Thomas; Nick C Fox; Tze H Mok; Simon Mead; John Collinge; Graham S Jackson
Journal:  JAMA Neurol       Date:  2016-12-01       Impact factor: 18.302

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