Extending the phenotypic spectrum assessed by the CDR plus NACC FTLD in genetic frontotemporal dementia

Author:

Samra Kiran1ORCID,Peakman Georgia1,MacDougall Amy M.2,Bouzigues Arabella1,Greaves Caroline V.1,Convery Rhian S.1,van Swieten John C.3,Jiskoot Lize3,Seelaar Harro3,Moreno Fermin45,Sanchez‐Valle Raquel6,Laforce Robert7,Graff Caroline89,Masellis Mario10,Tartaglia Maria Carmela11,Rowe James B.12,Borroni Barbara13,Finger Elizabeth14,Synofzik Matthis1516,Galimberti Daniela1718,Vandenberghe Rik192021,de Mendonça Alexandre22,Butler Chris R.2324,Gerhard Alexander2526,Ducharme Simon2728,Ber Isabelle Le29303132,Tiraboschi Pietro33,Santana Isabel3435,Pasquier Florence363738,Levin Johannes394041,Otto Markus42,Sorbi Sandro4344,Rohrer Jonathan D.1ORCID,Russell Lucy L.1,

Affiliation:

1. Dementia Research Centre Department of Neurodegenerative Disease UCL Queen Square Institute of Neurology London UK

2. Department of Medical Statistics London School of Hygiene and Tropical Medicine London UK

3. Department of Neurology Erasmus Medical Centre Rotterdam the Netherlands

4. Cognitive Disorders Unit Department of Neurology Donostia Universitary Hospital Donostia Spain

5. Neuroscience Area Biodonostia Health Research Institute San Sebastián Spain

6. Alzheimer's Disease and Other Cognitive Disorders Unit Neurology Service Hospital Clínic Institut d'Investigacións Biomèdiques August Pi I Sunyer University of Barcelona Barcelona Spain

7. Clinique Interdisciplinaire de Mémoire Département des Sciences Neurologiques CHU de Québec, and Faculté de Médecine Université Laval, Québec City Québec Canada

8. Center for Alzheimer Research Division of Neurogeriatrics Department of Neurobiology Care Sciences and Society, Bioclinicum, Karolinska Institutet, Solnavägen Solna Sweden

9. Unit for Hereditary Dementias Theme Aging Karolinska University Hospital Hälsovägen Stockholm Sweden

10. Sunnybrook Health Sciences Centre Sunnybrook Research Institute University of Toronto Toronto Ontario Canada

11. Tanz Centre for Research in Neurodegenerative Diseases University of Toronto Toronto Ontario Canada

12. Department of Clinical Neurosciences University of Cambridge Cambridge UK

13. Neurology Unit Department of Clinical and Experimental Sciences University of Brescia Piazza del Mercato Brescia Italy

14. Department of Clinical Neurological Sciences University of Western Ontario London Ontario Canada

15. Department of Neurodegenerative Diseases Hertie‐Institute for Clinical Brain Research and Center of Neurology University of Tübingen Tübingen Germany

16. Center for Neurodegenerative Diseases (DZNE) Tübingen Germany

17. Fondazione Ca’ Granda IRCCS Ospedale Policlinico Milan Italy

18. University of Milan Centro Dino Ferrari Milan Italy

19. Laboratory for Cognitive Neurology Department of Neurosciences KU Leuven Leuven Belgium

20. Neurology Service University Hospitals Leuven Leuven Belgium

21. Leuven Brain Institute KU Leuven Leuven Belgium

22. Faculty of Medicine University of Lisbon Lisbon Portugal

23. Nuffield Department of Clinical Neurosciences Medical Sciences Division University of Oxford Oxford UK

24. Department of Brain Sciences Imperial College London London UK

25. Division of Neuroscience and Experimental Psychology Wolfson Molecular Imaging Centre University of Manchester Manchester UK

26. Departments of Geriatric Medicine and Nuclear Medicine University of Duisburg‐Essen Duisburg Germany

27. Department of Psychiatry McGill University Health Centre McGill University Montreal Québec Canada

28. McConnell Brain Imaging Centre Montreal Neurological Institute McGill University Montreal Québec Canada

29. Sorbonne Université Paris Brain Institute – Institut du Cerveau – ICM Inserm U1127, CNRS UMR 7225 AP‐HP ‐ Hôpital Pitié‐Salpêtrière Paris France

30. Centre de référence des démences rares ou précoces IM2A, Département de Neurologie AP‐HP ‐ Hôpital Pitié‐Salpêtrière Paris France

31. Département de Neurologie AP‐HP ‐ Hôpital Pitié‐Salpêtrière Paris France

32. Reference Network for Rare Neurological Diseases (ERN‐RND) University Hospital Tübingen Tübingen Germany

33. Fondazione IRCCS Istituto Neurologico Carlo Besta Milan Italy

34. University Hospital of Coimbra (HUC) Neurology Service, Faculty of Medicine University of Coimbra Coimbra Portugal

35. Center for Neuroscience and Cell Biology Faculty of Medicine University of Coimbra Coimbra Portugal

36. Univ Lille Lille France

37. Inserm 1172 Lille France

38. CHU, CNR‐MAJ, Labex Distalz, LiCEND Lille Lille France

39. Department of Neurology Ludwig‐Maximilians Universität München Munich Germany

40. German Center for Neurodegenerative Diseases (DZNE) Munich Germany

41. Munich Cluster of Systems Neurology (SyNergy) Munich Germany

42. Department of Neurology University of Ulm Ulm Germany

43. Department of Neurofarba University of Florence Firenze Florence Italy

44. IRCCS Fondazione Don Carlo Gnocchi Firenze Florence Italy

Abstract

AbstractINTRODUCTIONWe aimed to expand the range of the frontotemporal dementia (FTD) phenotypes assessed by the Clinical Dementia Rating Dementia Staging Instrument plus National Alzheimer's Coordinating Center Behavior and Language Domains (CDR plus NACC FTLD).METHODSNeuropsychiatric and motor domains were added to the standard CDR plus NACC FTLD generating a new CDR plus NACC FTLD‐NM scale. This was assessed in 522 mutation carriers and 310 mutation‐negative controls from the Genetic Frontotemporal dementia Initiative (GENFI).RESULTSThe new scale led to higher global severity scores than the CDR plus NACC FTLD: 1.4% of participants were now considered prodromal rather than asymptomatic, while 1.3% were now considered symptomatic rather than asymptomatic or prodromal. No participants with a clinical diagnosis of an FTD spectrum disorder were classified as asymptomatic using the new scales.DISCUSSIONAdding new domains to the CDR plus NACC FTLD leads to a scale that encompasses the wider phenotypic spectrum of FTD with further work needed to validate its use more widely.Highlights The new Clinical Dementia Rating Dementia Staging Instrument plus National Alzheimer's Coordinating Center Behavior and Language Domains neuropsychiatric and motor (CDR plus NACC FTLD‐NM) rating scale was significantly positively correlated with the original CDR plus NACC FTLD and negatively correlated with the FTD Rating Scale (FRS). No participants with a clinical diagnosis in the frontotemporal dementia spectrum were classified as asymptomatic with the new CDR plus NACC FTLD‐NM rating scale. Individuals had higher global severity scores with the addition of the neuropsychiatric and motor domains. A receiver operating characteristic analysis of symptomatic diagnosis showed nominally higher areas under the curve for the new scales.

Funder

Deutsche Forschungsgemeinschaft

Instituto de Salud Carlos III

National Brain Appeal

UK Dementia Research Institute

UCLH Biomedical Research Centre

Wellcome Trust

Publisher

Wiley

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