Zusammenfassung
Veränderungen des zentralen Nervensystems nach einem Verlust des Riechvermögens wurden bisher vor allem für den Bulbus olfactorius (OB) beschrieben. Wir stellen eine Studie zu voxelbasierter Morphometrie (VBM) vor, die Hirnveränderungen bei Patienten mit Anosmie in dem OB übergeordneten Arealen darstellt. Datensätze von 17 Patienten mit Anosmie sowie von 17 normosmischen Kontrollpersonen wurden auf einem 3-T-Magnetresonanztomographen aufgezeichnet. Die Datenverarbeitung und Auswertung erfolgte mit der SPM5-Software (Wellcome Department of Imaging Neuroscience Group, London, UK) und der hierin implementierten VBM5-Toolbox. Die Patientengruppe zeigte eine signifikante Volumenabnahme der grauen Hirnsubstanz sowohl im primären olfaktorischen Kortex als auch in sekundären olfaktorischen Arealen (Insula, orbitofrontaler Kortex, Cingulum, Hippokampus). Auch wurden größere Volumenabnahmen im Nucleus accumbens mit dem angrenzenden Gyrus subcallosus sowie im dorsolateralen präfrontalen Kortex gefunden. Eine längere Erkrankungsdauer war mit ausgeprägteren Gehirnveränderungen verbunden. VBM ist somit geeignet, Hirnveränderungen bei Patienten mit Riechstörungen darzustellen.
Abstract
Alterations in the central nervous system in patients with a loss of sense of smell are well documented for the olfactory bulb (OB). Here we present a voxel-based morphometry (VBM) study on cerebral alterations in the gray matter of patients with anosmia above the OB. 3-Tesla MRI datasets were obtained from 17 patients with anosmia as well as from 17 normosmic controls. Data processing and evaluation was performed using the SPM5 software package (Wellcome Department of Imaging Neuroscience Group, London, UK) and the implemented VBM5 toolbox. Patients with anosmia showed a significant volume decrease in the gray matter in the primary olfactory cortex as well as in secondary olfactory areas (insular cortex, orbitofrontal cortex, cingulate cortex and hippocampus). Furthermore, volume decreases in areas like the nucleus accumbens with adjacent subcallosal gyrus and the dorsolateral prefrontal cortex were found. Longer disease duration was associated with more profound alterations in the gray matter. VBM is appropriate to document brain alterations in patients with olfactory disorders.
Literatur
Alexander GE, Delong MR, Strick PL (1986) Parallel organization of functionally segregated circuits linking basal ganglia and cortex. Annu Rev Neurosci 9:357–381
Ashburner J, Friston KJ (2000) Voxel-based morphometry – the methods. Neuroimage 11:805–821
Baldo BA, Kelley AE (2007) Discrete neurochemical coding of distinguishable motivational processes: insights from nucleus accumbens control of feeding. Psychopharmacology (Berl) 191:439–459
Bitter T, Bruderle J, Gudziol H et al (2010) Gray and white matter reduction in hyposmic subjects – A voxel-based morphometry study. Brain Res 1347:42–47
Bitter T, Gudziol H, Burmeister HP et al (2010) Anosmia leads to a loss of gray matter in cortical brain areas. Chem Senses 35:407–415
Bitter T, Josiger M, Mentzel HJ et al (2011) Detection of olfactory areas in functional MRI – how many repetitions are necessary? Laryngorhinootologie. DOI:10.1055/s-0030-1267216
Bitter T, Siegert F, Gudziol H et al (2011) Gray matter alterations in parosmia. Neuroscience. DOI:10.1016/j.neuroscience.2011.01.016
Burmeister HP, Baltzer PAT, Möslein C et al (2011) Visual grading characteristics (VGC) analysis of diagnostic image quality for high resolution 3 tesla MRI volumetry of the olfactory bulb. Acad Radiol: in press
Cerf-Ducastel B, Murphy C (2006) Neural substrates of cross-modal olfactory recognition memory: an fMRI study. Neuroimage 31:386–396
Cummings DM, Henning HE, Brunjes PC (1997) Olfactory bulb recovery after early sensory deprivation. J Neurosci 17:7433–7440
Curtis MA, Kam M, Nannmark U et al (2007) Human neuroblasts migrate to the olfactory bulb via a lateral ventricular extension. Science 315:1243–1249
Dade LA, Zatorre RJ, Evans AC et al (2001) Working memory in another dimension: functional imaging of human olfactory working memory. Neuroimage 14:650–660
Frasnelli J, Lundstrom JN, Boyle JA et al (2010) Neuroanatomical correlates of olfactory performance. Exp Brain Res 201:1–11
Gottfried JA (2006) Smell: central nervous processing. Adv Otorhinolaryngol 63:44–69
Gottfried JA, Deichmann R, Winston JS et al (2002) Functional heterogeneity in human olfactory cortex: an event-related functional magnetic resonance imaging study. J Neurosci 22:10819–10828
Gudden (1870) Experimentaluntersuchungen über das peripherische und centrale Nervensystem. Eur Arch Psychiatry Clin Neurosci 2:693–723
Gudziol V, Buschhuter D, Abolmaali N et al (2009) Increasing olfactory bulb volume due to treatment of chronic rhinosinusitis – a longitudinal study. Brain 132:3096–3101
Lerch JP, Evans AC (2005) Cortical thickness analysis examined through power analysis and a population simulation. Neuroimage 24:163–173
Lledo PM, Saghatelyan A, Lemasson M (2004) Inhibitory interneurons in the olfactory bulb: from development to function. Neuroscientist 10:292–303
Martin JH (2003) The Basal Ganglia. In: Martin JH (Hrsg) Neuroanatomy - text and atlas. The McGraw-Hill Companies Inc, New York, S 326–349
Maruniak JA, Taylor JA, Henegar JR et al (1989) Unilateral naris closure in adult mice: atrophy of the deprived-side olfactory bulbs. Brain Res Dev Brain Res 47:27–33
Mueller A, Rodewald A, Reden J et al (2005) Reduced olfactory bulb volume in post-traumatic and post-infectious olfactory dysfunction. Neuroreport 16:475–478
Nicola SM (2007) The nucleus accumbens as part of a basal ganglia action selection circuit. Psychopharmacology (Berl) 191:521–550
Noppeney U, Friston KJ, Ashburner J et al (2005) Early visual deprivation induces structural plasticity in gray and white matter. Curr Biol 15:R488–R490
Nordin S, Bramerson A (2008) Complaints of olfactory disorders: epidemiology, assessment and clinical implications. Curr Opin Allergy Clin Immunol 8:10–15
Oldfield RC (1971) The assessment and analysis of handedness: the Edinburgh inventory. Neuropsychologia 9:97–113
Penhune VB, Cismaru R, Dorsaint-Pierre R et al (2003) The morphometry of auditory cortex in the congenitally deaf measured using MRI. Neuroimage 20:1215–1225
Qureshy A, Kawashima R, Imran MB et al (2000) Functional mapping of human brain in olfactory processing: a PET study. J Neurophysiol 84:1656–1666
Ramirez-Lugo L, Nunez-Jaramillo L, Bermudez-Rattoni F (2007) Taste memory formation: role of nucleus accumbens. Chem Senses 32:93–97
Rombaux P, Mouraux A, Bertrand B et al (2006) Olfactory function and olfactory bulb volume in patients with postinfectious olfactory loss. Laryngoscope 116:436–439
Rombaux P, Mouraux A, Bertrand B et al (2006) Retronasal and orthonasal olfactory function in relation to olfactory bulb volume in patients with posttraumatic loss of smell. Laryngoscope 116:901–905
Rombaux P, Potier H, Bertrand B et al (2008) Olfactory bulb volume in patients with sinonasal disease. Am J Rhinol 22:598–601
Rombaux P, Potier H, Markessis E et al (2010) Olfactory bulb volume and depth of olfactory sulcus in patients with idiopathic olfactory loss. Eur Arch Otorhinolaryngol
Rombaux P, Weitz H, Mouraux A et al (2006) Olfactory function assessed with orthonasal and retronasal testing, olfactory bulb volume, and chemosensory event-related potentials. Arch Otolaryngol Head Neck Surg 132:1346–1351
Shepherd GM (2006) Smell images and the flavour system in the human brain. Nature 444:316–321
Stathis P, Panourias IG, Themistocleous MS et al (2007) Connections of the basal ganglia with the limbic system: implications for neuromodulation therapies of anxiety and affective disorders. Acta Neurochir Suppl 97:575–586
Varney NR, Pinkston JB, Wu JC (2001) Quantitative PET findings in patients with posttraumatic anosmia. J Head Trauma Rehabil 16:253–259
Vennemann MM, Hummel T, Berger K (2008) The association between smoking and smell and taste impairment in the general population. J Neurol 255:1121–1126
Yousem DM, Geckle RJ, Bilker WB et al (1999) Posttraumatic smell loss: relationship of psychophysical tests and volumes of the olfactory bulbs and tracts and the temporal lobes. Acad Radiol 6:264–272
Zahm DS (2000) An integrative neuroanatomical perspective on some subcortical substrates of adaptive responding with emphasis on the nucleus accumbens. Neurosci Biobehav Rev 24:85–105
Zatorre RJ, Jones-Gotman M, Evans AC et al (1992) Functional localization and lateralization of human olfactory cortex. Nature 360:339–340
Interessenkonflikt
Der korrespondierende Autor gibt an, dass kein Interessenkonflikt besteht.
Author information
Authors and Affiliations
Corresponding author
Additional information
Daten aus der hier vorgestellten Studie wurden bereits andernorts publiziert [5].
Rights and permissions
About this article
Cite this article
Bitter, T., Gudziol, H., Burmeister, H. et al. Volumenänderungen der grauen Hirnsubstanz bei Anosmikern. HNO 59, 248–254 (2011). https://doi.org/10.1007/s00106-011-2267-2
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00106-011-2267-2