Abnormal pain perception is associated with thalamo-cortico-striatal atrophy in C9orf72 expansion carriers in the GENFI cohort. Issue 12 (5th August 2020)
- Record Type:
- Journal Article
- Title:
- Abnormal pain perception is associated with thalamo-cortico-striatal atrophy in C9orf72 expansion carriers in the GENFI cohort. Issue 12 (5th August 2020)
- Main Title:
- Abnormal pain perception is associated with thalamo-cortico-striatal atrophy in C9orf72 expansion carriers in the GENFI cohort
- Authors:
- Convery, Rhian S
Bocchetta, Martina
Greaves, Caroline V
Moore, Katrina M
Cash, David M
Van Swieten, John
Moreno, Fermin
Sánchez-Valle, Raquel
Borroni, Barbara
Laforce Jr, Robert
Masellis, Mario
Tartaglia, Maria Carmela
Graff, Caroline
Galimberti, Daniela
Rowe, James B
Finger, Elizabeth
Synofzik, Matthis
Vandenberghe, Rik
de Mendonca, Alexandre
Tagliavini, Fabrizio
Santana, Isabel
Ducharme, Simon
Butler, Christopher
Gerhard, Alex
Levin, Johannes
Danek, Adrian
Otto, Markus
Warren, Jason D
Rohrer, Jonathan D - Other Names:
- author non-byline.
Rossor M N author non-byline.
Fox N C author non-byline.
Woollacott I O C author non-byline.
Shafei R author non-byline.
Heller C author non-byline.
Peakman G author non-byline.
Swift I author non-byline.
Todd E author non-byline.
Guerreiro R author non-byline.
Bras J author non-byline.
Thomas D L author non-byline.
Nicholas J author non-byline.
Mead S author non-byline.
Jiskoot L author non-byline.
Meeter L author non-byline.
Panman J author non-byline.
Papma J author non-byline.
van Minkelen R author non-byline.
Pijnenburg Y author non-byline.
Barandiara M author non-byline.
Indakoetxea B author non-byline.
Gabilondo A author non-byline.
Tainta M author non-byline.
de Arriba M author non-byline.
Gorostidi A author non-byline.
Zulaica M author non-byline.
Villanua J author non-byline.
Diaz Z author non-byline.
Borrego-Ecija S author non-byline.
Olives J author non-byline.
Lladó A author non-byline.
Balasa M author non-byline.
Antonell A author non-byline.
Bargallo N author non-byline.
Premi E author non-byline.
Cosseddu M author non-byline.
Gazzina S author non-byline.
Padovani A author non-byline.
Gasparotti R author non-byline.
Archetti S author non-byline.
Black S author non-byline.
Mitchell S author non-byline.
Rogaeva E author non-byline.
Freedman M author non-byline.
Keren R author non-byline.
Tang-Wai D author non-byline.
Öijerstedt L author non-byline.
Andersson C author non-byline.
Jelic V author non-byline.
Thonberg H author non-byline.
Arighi A author non-byline.
Fenoglio C author non-byline.
Scarpini E author non-byline.
Fumagalli G author non-byline.
Cope T author non-byline.
Timberlake C author non-byline.
Rittman T author non-byline.
Shoesmith C author non-byline.
Bartha R author non-byline.
Rademakers R author non-byline.
Wilke C author non-byline.
Karnarth H-O author non-byline.
Bender B author non-byline.
Bruffaerts R author non-byline.
Vandamme P author non-byline.
Vandenbulcke M author non-byline.
Ferreira C B author non-byline.
Miltenberger G author non-byline.
Maruta C author non-byline.
Verdelho A author non-byline.
Afonso S author non-byline.
Taipa R author non-byline.
Caroppo P author non-byline.
Di Fede G author non-byline.
Giaccone G author non-byline.
Prioni S author non-byline.
Redaelli V author non-byline.
Rossi G author non-byline.
Tiraboschi P author non-byline.
Duro D author non-byline.
Almeida M R author non-byline.
Branco M C author non-byline.
Leitão M J author non-byline.
Tabuas-Pereira M author non-byline.
Santiago B author non-byline.
Gauthier S author non-byline.
Rosa-Neto P author non-byline.
Veldsman M author non-byline.
Flanagan T author non-byline.
Prix C author non-byline.
Hoegen T author non-byline.
Wlasich E author non-byline.
Loosli S author non-byline.
Schonecker S author non-byline.
Semler E author non-byline.
Anderl-Straub S author non-byline.
… (more) - Abstract:
- Abstract : Objective: Frontotemporal dementia (FTD) is typically associated with changes in behaviour, language and movement. However, recent studies have shown that patients can also develop an abnormal response to pain, either heightened or diminished. We aimed to investigate this symptom in mutation carriers within the Genetic FTD Initiative (GENFI). Methods: Abnormal responsiveness to pain was measured in 462 GENFI participants: 281 mutation carriers and 181 mutation-negative controls. Changes in responsiveness to pain were scored as absent (0), questionable or very mild (0.5), mild (1), moderate (2) or severe (3). Mutation carriers were classified into C9orf72 (104), GRN (128) and MAPT (49) groups, and into presymptomatic and symptomatic stages. An ordinal logistic regression model was used to compare groups, adjusting for age and sex. Voxel-based morphometry was performed to identify neuroanatomical correlates of abnormal pain perception. Results: Altered responsiveness to pain was present to a significantly greater extent in symptomatic C9orf72 expansion carriers than in controls: mean score 0.40 (SD 0.71) vs 0.00 (0.04), reported in 29% vs 1%. No significant differences were seen between the other symptomatic groups and controls, or any of the presymptomatic mutation carriers and controls. Neural correlates of altered pain perception in C9orf72 expansion carriers were the bilateral thalamus and striatum as well as a predominantly right-sided network of regionsAbstract : Objective: Frontotemporal dementia (FTD) is typically associated with changes in behaviour, language and movement. However, recent studies have shown that patients can also develop an abnormal response to pain, either heightened or diminished. We aimed to investigate this symptom in mutation carriers within the Genetic FTD Initiative (GENFI). Methods: Abnormal responsiveness to pain was measured in 462 GENFI participants: 281 mutation carriers and 181 mutation-negative controls. Changes in responsiveness to pain were scored as absent (0), questionable or very mild (0.5), mild (1), moderate (2) or severe (3). Mutation carriers were classified into C9orf72 (104), GRN (128) and MAPT (49) groups, and into presymptomatic and symptomatic stages. An ordinal logistic regression model was used to compare groups, adjusting for age and sex. Voxel-based morphometry was performed to identify neuroanatomical correlates of abnormal pain perception. Results: Altered responsiveness to pain was present to a significantly greater extent in symptomatic C9orf72 expansion carriers than in controls: mean score 0.40 (SD 0.71) vs 0.00 (0.04), reported in 29% vs 1%. No significant differences were seen between the other symptomatic groups and controls, or any of the presymptomatic mutation carriers and controls. Neural correlates of altered pain perception in C9orf72 expansion carriers were the bilateral thalamus and striatum as well as a predominantly right-sided network of regions involving the orbitofrontal cortex, inferomedial temporal lobe and cerebellum. Conclusion: Changes in pain perception are a feature of C9orf72 expansion carriers, likely representing a disruption in somatosensory, homeostatic and semantic processing, underpinned by atrophy in a thalamo-cortico-striatal network. … (more)
- Is Part Of:
- Journal of neurology, neurosurgery and psychiatry. Volume 91:Issue 12(2020)
- Journal:
- Journal of neurology, neurosurgery and psychiatry
- Issue:
- Volume 91:Issue 12(2020)
- Issue Display:
- Volume 91, Issue 12 (2020)
- Year:
- 2020
- Volume:
- 91
- Issue:
- 12
- Issue Sort Value:
- 2020-0091-0012-0000
- Page Start:
- 1325
- Page End:
- 1328
- Publication Date:
- 2020-08-05
- Subjects:
- frontotemporal dementia -- pain
Neurology -- Periodicals
Nervous system -- Surgery -- Periodicals
Psychiatry -- Periodicals
616.8 - Journal URLs:
- http://jnnp.bmjjournals.com/ ↗
http://www.pubmedcentral.nih.gov/tocrender.fcgi?action=archive&journal=192 ↗
http://www.bmj.com/archive ↗ - DOI:
- 10.1136/jnnp-2020-323279 ↗
- Languages:
- English
- ISSNs:
- 0022-3050
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
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