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Functional imaging of the cerebral olfactory system in patients with Parkinson's disease
  1. B Westermann (birgit.westermann{at}unibas.ch)
  1. University Hospital Basel, Switzerland
    1. E Wattendorf (elise.wattendorf{at}unibas.ch)
    1. University Hospital Basel, Switzerland
      1. U Schwerdtfeger (u.schwerdtfeger{at}web.de)
      1. University Hospital Basel, Switzerland
        1. A Husner (ahusner{at}gmx.ch)
        1. University Hospital Basel, Switzerland
          1. P Fuhr (pfuhr{at}uhbs.ch)
          1. University Hospital Basel, Switzerland
            1. O Gratzl (ogratzl{at}uhbs.ch)
            1. University Hospital Basel, Switzerland
              1. T Hummel (thummel{at}rcs.urz.tu-dresden.de)
              1. University of Dresden Medical School, Germany
                1. D Bilecen (dbilecen{at}uhbs.ch)
                1. University Hospital Basel, Switzerland
                  1. A Welge-Luessen (awelge{at}uhbs.ch)
                  1. University Hospital Basel, Switzerland

                    Abstract

                    Background: Olfactory dysfunction is a frequent non-motor symptom in Parkinson’s disease (PD) and is considered an early manifestation of the disease. Objective: To establish the cortical basis of olfactory function in PD patients.

                    Method: Functional magnetic resonance imaging (fMRI) was used to investigate brain activity related to olfactory processing in hyposmic PD patients at mild to moderate stages of the disease (n=12, median Hoehn and Yahr stage 2.0) and in healthy, age-matched controls (n=16) while passively perceiving a positively valenced (rose-like) odorant.

                    Results: In both, PD patients and healthy controls, olfactory stimulation activated brain regions relevant for olfactory processing, i.e., the amygdaloid complex, lateral orbitofrontal cortex, striatum, thalamus, midbrain and the hippocampal formation. In controls, a bilateral activation of the amygdala and hippocampus was observed, whereas PD patients involved these structures in the left hemisphere only. Group comparison showed that regions of higher activation in PD patients were located bilaterally in the inferior frontal gyrus (BA 44/45) and anterior cingulate gyrus (BA 24/32), and the left dorsal and right ventral striatum.

                    Conclusions: In PD patients, results obtained under the specific conditions used suggest that neuronal activity in the amygdala and hippocampus is reduced. Assuming an impact on olfactory related regions early in PD, our finding supports the idea that selective impairment of these brain regions contributes to olfactory dysfunction. Further, neuronal activity in components of dopaminergic, cortico-striatal loops appears to be up-regulated indicating compensatory processes. This mechanism has not yet been demonstrated during olfactory processing in PD.

                    • Parkinson's disease
                    • functional magnetic resonance imaging (fMRI)
                    • laterality
                    • olfactory dysfunction

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