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Cognition and gray and white matter characteristics of presymptomatic C9orf72 repeat expansion.
Papma, Janne M; Jiskoot, Lize C; Panman, Jessica L; Dopper, Elise G; den Heijer, Tom; Donker Kaat, Laura; Pijnenburg, Yolande A L; Meeter, Lieke H; van Minkelen, Rick; Rombouts, Serge A R B; van Swieten, John C.
Affiliation
  • Papma JM; From the Departments of Neurology (J.M.P., L.C.J., J.L.P., E.G.D., L.D.K., L.H.M., J.C.v.S.), Epidemiology (T.d.H.), and Clinical Genetics (R.v.M.), Erasmus Medical Center, Rotterdam; Departments of Radiology (L.C.J., J.L.P., E.G.D., S.A.R.B.R.) and Clinical Genetics (L.D.K.), Leiden University Medi
  • Jiskoot LC; From the Departments of Neurology (J.M.P., L.C.J., J.L.P., E.G.D., L.D.K., L.H.M., J.C.v.S.), Epidemiology (T.d.H.), and Clinical Genetics (R.v.M.), Erasmus Medical Center, Rotterdam; Departments of Radiology (L.C.J., J.L.P., E.G.D., S.A.R.B.R.) and Clinical Genetics (L.D.K.), Leiden University Medi
  • Panman JL; From the Departments of Neurology (J.M.P., L.C.J., J.L.P., E.G.D., L.D.K., L.H.M., J.C.v.S.), Epidemiology (T.d.H.), and Clinical Genetics (R.v.M.), Erasmus Medical Center, Rotterdam; Departments of Radiology (L.C.J., J.L.P., E.G.D., S.A.R.B.R.) and Clinical Genetics (L.D.K.), Leiden University Medi
  • Dopper EG; From the Departments of Neurology (J.M.P., L.C.J., J.L.P., E.G.D., L.D.K., L.H.M., J.C.v.S.), Epidemiology (T.d.H.), and Clinical Genetics (R.v.M.), Erasmus Medical Center, Rotterdam; Departments of Radiology (L.C.J., J.L.P., E.G.D., S.A.R.B.R.) and Clinical Genetics (L.D.K.), Leiden University Medi
  • den Heijer T; From the Departments of Neurology (J.M.P., L.C.J., J.L.P., E.G.D., L.D.K., L.H.M., J.C.v.S.), Epidemiology (T.d.H.), and Clinical Genetics (R.v.M.), Erasmus Medical Center, Rotterdam; Departments of Radiology (L.C.J., J.L.P., E.G.D., S.A.R.B.R.) and Clinical Genetics (L.D.K.), Leiden University Medi
  • Donker Kaat L; From the Departments of Neurology (J.M.P., L.C.J., J.L.P., E.G.D., L.D.K., L.H.M., J.C.v.S.), Epidemiology (T.d.H.), and Clinical Genetics (R.v.M.), Erasmus Medical Center, Rotterdam; Departments of Radiology (L.C.J., J.L.P., E.G.D., S.A.R.B.R.) and Clinical Genetics (L.D.K.), Leiden University Medi
  • Pijnenburg YAL; From the Departments of Neurology (J.M.P., L.C.J., J.L.P., E.G.D., L.D.K., L.H.M., J.C.v.S.), Epidemiology (T.d.H.), and Clinical Genetics (R.v.M.), Erasmus Medical Center, Rotterdam; Departments of Radiology (L.C.J., J.L.P., E.G.D., S.A.R.B.R.) and Clinical Genetics (L.D.K.), Leiden University Medi
  • Meeter LH; From the Departments of Neurology (J.M.P., L.C.J., J.L.P., E.G.D., L.D.K., L.H.M., J.C.v.S.), Epidemiology (T.d.H.), and Clinical Genetics (R.v.M.), Erasmus Medical Center, Rotterdam; Departments of Radiology (L.C.J., J.L.P., E.G.D., S.A.R.B.R.) and Clinical Genetics (L.D.K.), Leiden University Medi
  • van Minkelen R; From the Departments of Neurology (J.M.P., L.C.J., J.L.P., E.G.D., L.D.K., L.H.M., J.C.v.S.), Epidemiology (T.d.H.), and Clinical Genetics (R.v.M.), Erasmus Medical Center, Rotterdam; Departments of Radiology (L.C.J., J.L.P., E.G.D., S.A.R.B.R.) and Clinical Genetics (L.D.K.), Leiden University Medi
  • Rombouts SARB; From the Departments of Neurology (J.M.P., L.C.J., J.L.P., E.G.D., L.D.K., L.H.M., J.C.v.S.), Epidemiology (T.d.H.), and Clinical Genetics (R.v.M.), Erasmus Medical Center, Rotterdam; Departments of Radiology (L.C.J., J.L.P., E.G.D., S.A.R.B.R.) and Clinical Genetics (L.D.K.), Leiden University Medi
  • van Swieten JC; From the Departments of Neurology (J.M.P., L.C.J., J.L.P., E.G.D., L.D.K., L.H.M., J.C.v.S.), Epidemiology (T.d.H.), and Clinical Genetics (R.v.M.), Erasmus Medical Center, Rotterdam; Departments of Radiology (L.C.J., J.L.P., E.G.D., S.A.R.B.R.) and Clinical Genetics (L.D.K.), Leiden University Medi
Neurology ; 89(12): 1256-1264, 2017 Sep 19.
Article de En | MEDLINE | ID: mdl-28855404
OBJECTIVE: To investigate cognitive function, gray matter volume, and white matter integrity in the presymptomatic stage of chromosome 9 open reading frame 72 repeat expansion (C9orf72RE). METHODS: Presymptomatic C9orf72RE carriers (n = 18) and first-degree family members without a pathogenic expansion (healthy controls [HC], n = 15) underwent a standardized protocol of neuropsychological tests, T1-weighted MRI, and diffusion tensor imaging within our cohort study of autosomal dominant frontotemporal dementia (FTD). We investigated group differences in cognitive function, gray matter volume through voxel-based morphometry, and white matter integrity by means of tract-based spatial statistics. We correlated cognitive change with underlying gray or white matter. RESULTS: Our data demonstrate lower scores on letter fluency, Stroop card I, and Stroop card III, accompanied by white matter integrity loss in tracts connecting the frontal lobe, the thalamic radiation, and tracts associated with motor functioning in presymptomatic C9orf72RE compared with HC. In a subgroup of C9orf72RE carriers above 40 years of age, we found gray matter volume loss in the thalamus, cerebellum, and parietal and temporal cortex. We found no significant relationship between subtle cognitive decline and underlying gray or white matter. CONCLUSIONS: This study demonstrates that a decline in cognitive functioning, white matter integrity, and gray matter volumes are present in presymptomatic C9orf72RE carriers. These findings suggest that neuropsychological assessment, T1-weighted MRI, and diffusion tensor imaging might be useful to identify early biomarkers in the presymptomatic stage of FTD or amyotrophic lateral sclerosis.
Sujet(s)

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Protéines / Expansion de séquence répétée de l'ADN / Démence frontotemporale / Dysfonctionnement cognitif / Substance grise / Substance blanche Type d'étude: Observational_studies / Prognostic_studies / Risk_factors_studies Limites: Adult / Female / Humans / Male / Middle aged Langue: En Journal: Neurology Année: 2017 Type de document: Article Pays de publication: États-Unis d'Amérique

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Protéines / Expansion de séquence répétée de l'ADN / Démence frontotemporale / Dysfonctionnement cognitif / Substance grise / Substance blanche Type d'étude: Observational_studies / Prognostic_studies / Risk_factors_studies Limites: Adult / Female / Humans / Male / Middle aged Langue: En Journal: Neurology Année: 2017 Type de document: Article Pays de publication: États-Unis d'Amérique