Zusammenfassung
Die Bedeutung der molekularen bildgebenden Techniken zum besseren Verständnis der pathophysiologischen Krankheitszustände steigt. Heutzutage kann die Positronenemissionstomographie (PET) als die Methode der Wahl zum nichtinvasiven Studium der biochemischen und molekularen Prozesse in Mensch und Tier in vivo bezeichnet werden. Aufgrund der rasanten Entwicklung in der Radiochemie und der Tracer-Technologie können verschiedenste endogen exprimierte und exogen eingeführte Gene mittels PET dargestellt werden. Diese Möglichkeiten öffnen das Fenster zum bedeutenden und rasch wachsenden Feld der molekularen Bildgebung, die auf die visuelle Lokalisation biologisch interessanter Prozesse in normalen und pathologischen Zellen in Tiermodellen und beim Menschen hinzielen. Neben der Bedeutung für die Grundlagenforschung ist PET den konventionellen diagnostischen Methoden in mehreren klinischen Indikationen deutlich überlegen. Dies wird illustriert durch die Visualisierung von biologischen und anatomischen Veränderungen, die nicht mittels Computertomographie oder Magnetresonanzstudien dargestellt werden können, bevor erste Symptome auftreten. Die vorliegende Übersichtsarbeit fasst den klinischen Gebrauch der PET im Gebiet der Neurowissenschaften zusammen und versucht die Untersuchung des pathophysiologischen Hintergrunds einer Anzahl an Krankheiten zu beleuchten und—aufgrund der mittels molekularen Bildgebung gewonnenen Erkennntnisse—neue Strategien in der Behandlung dieser Patienten aufzuzeigen.
Abstract
The role of molecular neuroimaging techniques is increasing in the understanding of pathophysiological mechanism of diseases. To date, positron emission tomography is the most powerful tool for the non-invasive study of biochemical and molecular processes in humans and animals in vivo. With the development in radiochemistry and tracer technology, a variety of endogenously expressed and exogenously introduced genes can be analyzed by PET. This opens up the exciting and rapidly field of molecular imaging, aiming at the non-invasive localisation of a biological process of interest in normal and diseased cells in animal models and humans in vivo. Besides its usefulness for basic research positron emission tomography has been proven to be superior to conventional diagnostic methods in several clinical indications. This is illustrated by detection of biological or anatomic changes that cannot be demonstrated by computed tomography or magnetic resonance imaging, as well as even before symptoms are expressed. The present review summarizes the clinical use of positron emission tomography in neuroscience that has helped elucidate the pathophysiology of a number of diseases and has suggested strategies in the treatment of these patients. Special reference is given to the neurovascular, neurodegenerative and neurooncological disease.
Literatur
Krause T (2002) Nuklearmedizin: PET—eine bezahlbare Innovation? Schweiz Med Forum 2:1233–1235
Davis MR, Votaw JR, Bremner JD et al. (2003) Initial Human PET Imaging studies with the dopamine transporter ligand 18F-FECNT. J Nucl Med 44:855–861
Heiss WD, Pawlik G, Herholz K et al. (1984) Regional kinetic constants and cerebral metabolic rate for glucose in normal human volunteers determined by dynamic positron emission tomography of [18F]-2-fluoro-2-deoxy-D-glucose. J Cereb Blood Flow Metab 4:212–223
Heiss WD, Podreka I (1993) Role of PET and SPECT in the assessment of ischemic cerebrovascular disease. Cerebrovasc Brain Metab Rev 5:235–263
Fazekas F, Payer F (2002) F-18-Fluorodeoxy-Glucose-Positroenemissionstomogrpahie in der Neurologie. Wien Med Wochenschr 152:293–297
Roelcke U, Leenders KL (2001) PET in neuro-oncology. J Cancer Res Clin Oncol 127:2–8
Schaller B, Graf R, Sanada Y et al. (2003) Hemodynamic changes after occlusion of the posterior superior sagittal sinus. An experimental PET-study in cats. Am J Neuroradiol 24:1876–1880
Schaller B, Graf R, Sanada Y et al. (2003) Hemodynamic and metabolic effects of decompressive hemicraniectomy in normal brain. An experimental PET-study in cats. Brain Res 982:31–37
Gambhir SS (2002) Molecular imaging of cancer with positron emission tomography. Nat Rev Cancer 2:683–693
Jacobs AH, Li H, Winkeler A et al. (2003) PET-based molecular imaging in neuroscience. Eur J Nucl Med Mol Imaging 30:1051–1065
Kennedy C, Sakurada O, Shinohara M et al. (1978) Local cerebral glucose utilization in the normal conscious macaque monkey. Ann Neurol 4:293–301
Heiss WD, Grond M, Thiel A et al. (1997) Ischemic brain tissue salvaged from infarction with alteplase. Lancet 349:1599–1600
Lassen NA (1985) Normal average value of cerebral blood flow in younger adults is 50 ml/100 g/min. J Cereb Blood Flow Metab 5:347–349
Leenders KL, Perani D, Lammertsma AA et al. (1990) Cerebral blood flow, blood volume and oxygen utilization. Normal values and effect of age. Brain 113:27–47
Phelps ME, Huang SC, Hoffmann EJ et al. (1979) Validation of tomographic measurement of cerebral blood volume with C-11-labeled carboxyhemoglobin. J Nucl Med 20:328–34
Mintun MA, Raichle ME, Martin W et al. (1984) Brain oxygen utilization measured with O-15 radiotracers and positron emission tomography. J Nucl Med 25:177–187
Phelps ME, Huang SC, Hoffman EJ et al. (1979) Tomographic measurement of local cerebral glucose metabolic rate in humans with (F-18)2-fluoro-2-deoxy-D-glucose: validation of method. Ann Neurol 6:371–388
Herholz K, Heiss WD (1991) Positronemission-Tomographie zur Darstellung der Pathophysiologie der zerebralen Ischämie. Arzneimittelforschung 41:298–303
Powers WJ, Press GW, Grubb RL et al. (1987) The effect of hemodynamically significant carotid artery disease on the hemdoynamic status of the cerebral circulation. Ann Int Med 106:27–35
Heiss WD, Edmunds HG, Herholz K (1993) Cerebral glucose metabolism as a predictor of rehabilitation after ischemic stroke. Stroke 24:1784–1788
Suhonen-Polvi H, Kero P, Korvenranta H et al. (1993) Repeated fluorodeoxyglucose positron emission tomography on the brain in infarcts with suspected hypoxic-ischemic brain injury. Eur J Nucl Med 20:759–765
Feeney DM, Baron JC (1986) Diaschisis. Stroke 17:817–830
Schaller B (2002) Head trauma: new pathophysiological and therapeutic aspects. part 1: the treatment in the primary phase. Swiss Surg 8:123–137
Adams JH (1984) Head injury. In: Adams JH, Corsellis JAN, Duchen LW (eds) Greenfield’s Neuropathology, 4 th edn. Edward Arnold, London, pp 85–124
Henry TR, Engle J Jr, Mazziotta JC (1993) Clinical evaluation of interictal fluorine-18-fluordeoxyglucose PET in partial epilepsy. J Nucl Med 34:1892–1898
Gaillard WD, Bhatia S, Bookheimer SY et al. (1995) FDG-PET and volumetric MRI in the evalution of patients with partial epilepsy. Neurology 45.123–126
Juhasz C, Chugani D, Musik O et al. (2000) Relationsship between EEG and positron emission tomography abnormalities in clinical epilepsy. J Clin Neurophysiol 17:29–42
Engle J Jr, Henry TR, Swartz BE (1995) Positron emission tomography in frontal lobe epilepsy. Adv Neurol 66:223–238
Arnold S, Schlaug G, Niemann H et al. (1996) Topography of interictal glucose hypometabolism in unilateral mesiotemporal epilepsy. Neurology 46:1422–1430
Gaillard WD, Bhatia S, Bookheimer SY et al. (1995) FDG-PET and volumetric MRI in the evaluation of patients with partial epilepsy. Neurology 45:123–126
Peyron R, Cinotti L, LeBars D et al. (1994) Effects of GABAA receptors activation on brain glucose metabolism in normal subjects and temporal lobe epilepsy (TLE) patients. A positron emission tomography (PET) study. Part II: The focal hypometablism is reactive to GABA agonist administration in TLE. Epilepsy Res 19:55–62
Sperling MR, Alavi A, Reivich M et al. (1995) False lateralization of temporal lobe epilepsy with FDG positron emission tomography. Epilepsia 36:722–727
Radtke RA, Hanson MW, Hoffman JM et al. (1993) Temporal lobe hypometabolism on PET: prediction of seizure control after temporal lobectomy. Neurology 43:1088–1092
Schaller B, Rüegg SJ (2003) Brain tumor and seizures—pathophysiology and treatment revisited. Epilepsia 44:1223–1232
Savic I, Ingvar M, Stone-Elander S (1993) Comparison of 11C flumazenil and 18F FDG as PET markers of epileptic foci. J Neurol Neurosurg Psychiatry 56:615–621
Szelies B, Weber G, Mielke R et al. (2000) Interictal hippocampal benzodiazepine receptors in temporal lobe epilepsy: comparison with coregistered hippocampal metabolism and volumetry. Eur J Neurol 7:393–400
Burdette DE, Sakurai SY, Henry TR et al. (1995) Temporal lobe central benzodiazepine binding in unilateral mesial temporal lobe epilepsy. Neurology 45:934–941
Herholz K, Salamon E, Perani D et al. (2002) Discrimination between Alzheimer dementia and controls by automated analysis of multicenter FDG PET. NeuroImagine 17:302–316
Herholz K, Salmon E, Perani D et al. (2002) Discrimination between Alzheimer dementia and controls by automated analysis of multicenter FDG PET. NeuroImagine 17:302–316
Iyo M, Namba H, Fukushi K et al. (1997) Measurement of acetylcholinesterase by positron emission tomograph in the brains of healthy controls and patients with Alzheimer’s disease. Lancet 349:1805–1809
Golan H, Kremer J, Freedman M et al. (1996) Usefulness of follow-up regional cerebral blood flow measurements by single-photon emission computed tomography in the differential diagnosis of dementia. J Neuroimaging 6:23–28
Heiss WD, Kessler J, Mielke R et al. (1994) Long-term effects of phosphatidylserine, pyrtiniol, and cognitive training in Alzheimer’s disease. A neuropsychological, EEG, and PET investigation. Dementia 5:88–98
Heiss WD, Kessler J, Slansky I et al. (1993) Activation PET as an instrument to determine therapeutic efficacy in Alzheimer’s disease. Ann NY Acad Sci 695:327–331
Shoghi-Jadid K, Small GW, Agdeppa ED et al. (2002) Localization of neurofibrillary tangles and beta-amyloid plaques in the brains of living patients with Alzheimer disease. Am J Geriatr Psychiatry 10:24–35
Baxter LR Jr, Phelps ME, Mazziotta JC et al. (1985) Cerebral metabolic rates for glucose in mood disorders. Studies with positron emission tomography and fluorodesoxyglucose F18. Arch Gen Psychiatry 42:441–447
Baxter LR Jr, Schwartz JM, Phelps ME et al. (1989) Reduction of prefrontal cortex glucose metabolism common to three types of depression. Arch Gen Psychiatry 46:243–250
Catafau AM, Parellada E, Lemona FJ et al. (1994) Prefrontal and temporal blood flow in schizophrenia. J Nucl Med 35:935–941.
Lewis SW, Frod RA, Syed GM et al. (1992) A controlled study of 99mTc-HMPAO single-photon emission imaging in chronic schizophrenia. Psychol Med 22:27–35
Sedvall G (1992) The current status of PET scanning with respect to schizophrenia. Neuropsychopharmacology 7:41–54
Liddle PF, Friston KJ, Frith CD et al. (1992) Patterns of cerebral blood flow in schizophrenia. Br J Psychiatry 160:179–186
Gunther W, Petsch R, Steinberg R et al. (1991) Brain dysfunction during motor activation and corpus callosum alterations in schizophrenia measured by cerebral blood flow and magnetic resonance imaging. Biol Psychiatry 29:535–555
Musalek M, Poderka I, Walter H et al. (1989) Regional brain function in hallucinations: a study of regional cerebral blood flow with 99m-Tc-HM-PAO-SPECT in patients with auditory hallucinations, tactile hallucinations, and normal controls. Comp Psychiatry 30:99–108
McGuire PK, Shah GM, Muray RM (1993) Increased blood flow in Boca’s area during auditory hallucinations in schizophrenia. Lancet 342:703–706
Heinz A, Knäble MB, Weinberger DR. Dopamine D2 receptor imaging and neuroleptic drug response. J Clin Psychiatry 57 [Suppl 11]:84–93
Nyberg S, Farde L, Halldin C et al. (1995) D2 dopamine receptor occupancy during low-dose treatment with haloperidol decanoate. Am J Psychiatry 152:173–178
Ebadi M, Peiffer RF, Murrin LC (1990) Pathogenesis and treatment of NMS. Gen Pharmacol 21:367–386
Jauss M, Krack P, Franz M et al. (1996) Imaging of dopamine receptors with (123I) Idobenzoamide single-photon emission-computed tomography in neuroleptic malignant syndrome. Mov Disord 11:726–728
Kramer EL, Sanger JJ (1990)Brain imaging in acquired immunodeficiency syndrome dementia complex. Seminars Nucl Med 20:353–363
Meyer JH, Paur S, Houle S et al. (1999) Prefrontal Cortex 5-HT2 receptors in depression. An (18F) setoperone PET imaging study. Am J Psychiatry 156:1029–1034
Eidelberg D, Moeller JR, Ishikawa T et al. (1994) Early differential diagnosis of Parkinson’s disease with 18F-fluorodeoxyglucose and positron emission tomography. Neurology 14:783–801
Leenders KL, Palmer AJ, Quinn N et al. (1986) Brain dopamine metabolism in patients with Parkinson’s disease measured with positron emission tomography. J Neurol Neursurg Psychiatr 49:853–860
Brooks DJ (1997) Advances in imaging Parkinson’s disease. Curr Opin Neurol 10:327–331
Sawle GV, Leenders KL, Brooks DJ et al. (1991) Dopa-responsive dystonia: 18Fdopa positron emission tomography. Ann Neurol 30:24–30
Takei Y, Mirra S (1973) Striatonigral degeneration: a form of multiple system atrophy with clinical parkinsonism. In: Zimmermann HM (ed) Progress in neuropathology. Grune & Stratton, New York, pp 217–251
Blin J, Baron JC, Dubois B et al. (1990) Positron emission tomography study in progressive supranuclear palsy. Arch Neurol 47:747–752
Wienhard K, Coenenen HH, Pawlik G et al. (1990) PET studies of dopamine receptor distribution using (18F)fluoroethylspiperone: findings in disorders related to the dopaminergic system. J Neurol Transm 81:195–213
Hilker R, Klein C, Ghaemi M et al. (2001) Positron emission tomography analysis of the nigrostriatal dopaminergic system in familial parkinsonism associated with mutations in the parkin gene. Ann Neurol 49:367–376
Herholz K, Bauer B, Wienhard K et al. (2000) In-vivo measurements of regional acetylcholine esterase activity in degenrative dementia: comparison with blood flow and glucose metabolism. J Neuronal Transm 107:1457–1468
Marie RM, Rioux P, Eustache F et al. (1995) Clues about the functional neuroanatomy of verbal working memory: a study of resting brain glucose metabolism in Parkinson’s disease. Eur J Neurol 2:83–94
Ito K, Nagano A, Kato T et al. (2002) Striatal and extrastriatal dysfunction in parkinson‘ disease with dementia: a 6-(18F)fluoro-L-dopa PET study. Brain 125:1358–1365
Asahina M, Suhara T, Shinotoh H et al. (1998) Brain muscarinic receptors in progressive supranuclear palsy and Parkinson’s disease: a positron emission tomographic study. J Neurol Neurosurg Psychiatry 65:155–163
Weber G (1977) Enzymology of cancer cells. N Engl J Med 296:541–551
Herholz K, Rudolf J, Heiss WD (1992) FDG transport and phosphorylation in human gliomas measured with dynamic PET. Neuro Oncol 12:159–165
Roelcke U, Leenders KL (2001) PET in neuro-oncology. J Cancer Res Clin Oncol 127:2–8
Holthoff VA, Herholz K, Berthold F et al. (1993) In vivo metabolism of childhood posterior fossa tumors and primitive neuroectodermial tumors before and after treatment. Cancer 72:1394–1403
Hölzer T, Herholz K, Jeske J et al. (1993) FDG-PET as a prognostic indicator in radiochemotherapy of glioblastoma. J Comput Assist Tomogr 17:681–687
Cremerius U, Striepecke E, Henn W et al. (1994) 18FDG-PET in intracranial meningiomas versus grading, proliferation index, cellular density and cytogenetic analysis. Nuklearmedizin 33:144–149
Bustany P, Chatel M, Derlon JM et al. (1986) Brain tumor protein synthesis and histological grades: a study by positron emission tomography (PET) with C-11-L-methionine. J Neuro Oncol 3:397–404
Derlon JM, Petit-Taboue MC, Chapon F et al. (1997) The in vivo metabolic pattern of low-grade brain gliomas: a positron emission tomographic study using 18F-fluorodeoxyglucse and 11C-L-methylmethionine. Neurosurgery 40:276–288
Freedman L, Slechen DH, Black SE et al. (1991) Posterior cortical dementia with alexia: neurobehavioural, MRI, and PET findings. J Neurol Neurosurg Psychiatry 54:443–448
Herholz K, Reulen HJ, Stockhausen HM et al. (1997) Preoperative activation and intraoperative activation and intraoperative stimulation of language-related areas in glioma patients. Neurosurgery 41:1253–1262
Goldman S, Levivier M, Pirotte B et al. (1996) Regional glucose metabolism and histopathology of gliomas. A study based on positron emission tomography-guided stereotactic biopsy. Cancer 78:1098–1106
Barker FG, Chang SM, Valk PE et al. (1997) 18-Fluorodeoxy-glucose uptake and survival of patients with suspected recurrent malignant glioma. Cancer 79:115–126
Kracht LW, Firese M, Herholz K et al. (2003) Methyl 11C Lmethionne uptake as measured by positron emission tomography correlates to micorvessel density in patients with glioma. Eur J Nucl Med 30:868–873
Bergstrom M, Muhr C, Lundgerg PO et al. (1991) PET as a tool in the clinical evaluation of pituitary adenomas. J Nucl Med 32:610–615
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Schaller, B. Positronenemissionstomographie in den Neurowissenschaften. Radiologe 45, 186–196 (2005). https://doi.org/10.1007/s00117-004-1158-x
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DOI: https://doi.org/10.1007/s00117-004-1158-x