Altered Brain Glucose Consumption in Cogan’s Syndrome

Purpose. Prospective, controlled cohort study to investigate possible alterations in brain glucose metabolism (CMRglc) in patients with Cogan’s syndrome (CS). Patients and Methods. Functional mapping of the CMRglc was obtained by quantitative molecular imaging positron emission tomography, combined...

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Main Authors: Paolo Mora, Livia Ruffini, Caterina Ghetti, Stella Ghirardini, Maura Scarlattei, Giorgio Baldari, Carla Cidda, Pierangela Rubino, Stefano A. Gandolfi, Jelka G. Orsoni
Format: Article
Language:English
Published: Wiley 2016-01-01
Series:Journal of Ophthalmology
Online Access:http://dx.doi.org/10.1155/2016/3207150
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author Paolo Mora
Livia Ruffini
Caterina Ghetti
Stella Ghirardini
Maura Scarlattei
Giorgio Baldari
Carla Cidda
Pierangela Rubino
Stefano A. Gandolfi
Jelka G. Orsoni
author_facet Paolo Mora
Livia Ruffini
Caterina Ghetti
Stella Ghirardini
Maura Scarlattei
Giorgio Baldari
Carla Cidda
Pierangela Rubino
Stefano A. Gandolfi
Jelka G. Orsoni
author_sort Paolo Mora
collection DOAJ
description Purpose. Prospective, controlled cohort study to investigate possible alterations in brain glucose metabolism (CMRglc) in patients with Cogan’s syndrome (CS). Patients and Methods. Functional mapping of the CMRglc was obtained by quantitative molecular imaging positron emission tomography, combined with computed tomography (FDG-PET/CT). The patients were divided into three clinical groups: typical CS; atypical CS (ACS); autoimmune inner ear disease (AIED). The unmatched control group (CG) consisted of subjects requiring FDG-PET/CT for an extracranial pathology. Statistical mapping searched areas of significant glucose hypometabolism in all the affected patients (DG) and in each clinical subgroup. The results were compared with those of the CG. Results. 44 patients were enrolled (DG) and assigned to the three study groups: 8 patients to the CS group; 21 patients to the ACS group; and 15 to the AIED group. Sixteen subjects formed the CG group. Areas of significant brain glucose hypometabolism were identified in all the study groups, with the largest number and extension in the DG and CS. Conclusions. This study revealed areas of significantly altered CMRglc in patients with CS (any subform) without neurologic complains and normal conventional neuroimaging. Our results suggest that FDG-PET/CT may represent a very useful tool for the global assessment of patients with Cogan’s syndrome.
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issn 2090-004X
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spelling doaj-art-bb17aa572b3740a89a16ca6553122a822025-02-03T06:42:11ZengWileyJournal of Ophthalmology2090-004X2090-00582016-01-01201610.1155/2016/32071503207150Altered Brain Glucose Consumption in Cogan’s SyndromePaolo Mora0Livia Ruffini1Caterina Ghetti2Stella Ghirardini3Maura Scarlattei4Giorgio Baldari5Carla Cidda6Pierangela Rubino7Stefano A. Gandolfi8Jelka G. Orsoni9Institute of Ophthalmology, University Hospital of Parma, Parma, ItalyNuclear Medicine Unit, University Hospital of Parma, Parma, ItalyMedical Physic Department, University Hospital of Parma, Parma, ItalyInstitute of Ophthalmology, University Hospital of Parma, Parma, ItalyNuclear Medicine Unit, University Hospital of Parma, Parma, ItalyNuclear Medicine Unit, University Hospital of Parma, Parma, ItalyNuclear Medicine Unit, University Hospital of Parma, Parma, ItalyInstitute of Ophthalmology, University Hospital of Parma, Parma, ItalyInstitute of Ophthalmology, University Hospital of Parma, Parma, ItalyInstitute of Ophthalmology, University Hospital of Parma, Parma, ItalyPurpose. Prospective, controlled cohort study to investigate possible alterations in brain glucose metabolism (CMRglc) in patients with Cogan’s syndrome (CS). Patients and Methods. Functional mapping of the CMRglc was obtained by quantitative molecular imaging positron emission tomography, combined with computed tomography (FDG-PET/CT). The patients were divided into three clinical groups: typical CS; atypical CS (ACS); autoimmune inner ear disease (AIED). The unmatched control group (CG) consisted of subjects requiring FDG-PET/CT for an extracranial pathology. Statistical mapping searched areas of significant glucose hypometabolism in all the affected patients (DG) and in each clinical subgroup. The results were compared with those of the CG. Results. 44 patients were enrolled (DG) and assigned to the three study groups: 8 patients to the CS group; 21 patients to the ACS group; and 15 to the AIED group. Sixteen subjects formed the CG group. Areas of significant brain glucose hypometabolism were identified in all the study groups, with the largest number and extension in the DG and CS. Conclusions. This study revealed areas of significantly altered CMRglc in patients with CS (any subform) without neurologic complains and normal conventional neuroimaging. Our results suggest that FDG-PET/CT may represent a very useful tool for the global assessment of patients with Cogan’s syndrome.http://dx.doi.org/10.1155/2016/3207150
spellingShingle Paolo Mora
Livia Ruffini
Caterina Ghetti
Stella Ghirardini
Maura Scarlattei
Giorgio Baldari
Carla Cidda
Pierangela Rubino
Stefano A. Gandolfi
Jelka G. Orsoni
Altered Brain Glucose Consumption in Cogan’s Syndrome
Journal of Ophthalmology
title Altered Brain Glucose Consumption in Cogan’s Syndrome
title_full Altered Brain Glucose Consumption in Cogan’s Syndrome
title_fullStr Altered Brain Glucose Consumption in Cogan’s Syndrome
title_full_unstemmed Altered Brain Glucose Consumption in Cogan’s Syndrome
title_short Altered Brain Glucose Consumption in Cogan’s Syndrome
title_sort altered brain glucose consumption in cogan s syndrome
url http://dx.doi.org/10.1155/2016/3207150
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