Limbic changes detected by MRI involved in memory and emotional dysfunctions in Parkinson's disease.

• Autores: Naroa Ibarretxe Bilbao
• Directores de la Tesis: Pere Vendrell Gómez (dir. tes.), Carme Junqué i Plaja (dir. tes.)
• Lectura: En la Universitat de Barcelona ( España ) en 2009
• Idioma: inglés
• Tribunal Calificador de la Tesis: Isidro Ferrer Abizanda (presid.), Javier Pagonabarraga Mora (secret.), Mona K. Beyer (voc.)
• Materias:
  • Psicología
• Enlaces
  • Tesis en acceso abierto en:  TDX  Dipòsit Digital de la UB 
• Resumen

  • According neuropathological research limbic changes occur in Parkinson's disease with and without dementia. Structural MRI have reported atrophy of limbic structures including amygadala and hippocampus, in both demented and non-demented PD patients; and a progression of limbic atrophy over time. In addition, atrophy of paralimbic areas (i.e. paracingulate gyrus) and limbic association cortex (i.e orbitofrontal cortex) has also been reported in PD. Functional studies have also reported limbic dysfunctions in Parkinson's disease. PET studies reported that orbitofrontal and amygdalar presynaptic dopaminergic functions are altered in early PD and a significant decrease in the metabolism of the medial OFC in a follow-up study of patients with early PD. fMRI studies showed an abnormal amygdalar response in PD while recognizing fearful faces and lack of activation in the right hippocampus and amygdala while perceiving odorant stimuli inside the scanner. Neuropsychological studies pointed out that the functions that are known to depend on the integrity of limbic system are impaired in Parkinson's disease even in the early stages of the disease. Specifically, it has been reported and impairment in verbal memory, recognition of facial expressions of emotions, decision-making and olfactory function. However, the neuroanatomical and neurofunctional correlates of these dysfunctions are not known or are poorly investigated. For memory functions, hippocampal and amygdalar volumes have been reported to correlate with memory impairment. For decision making and recognition of emotions there are no studies of its correlates; and for olfactory dysfunctions one study reported a correlations between this impairment and a reduced fractional anisotropy in the cerebellum.The general aim of this thesis is to investigate the neuroanatomical and neurofunctional correlates of declarative memory, decision-making, recognition of emotions and olfactory dysfunctions in PD. We hypothesized that all these dysfunctions are due to the limbic degenerative changes associated with PD. We used structural MRI (T1-weighted MRI and DTI), functional MRI (fMRI) and neuropsychological testing to assess declarative memory, emotional processing and decision-making, and olfactory function. Firstly, we focused on the hippocampal atrophy putatively related to declarative memory dysfunctions and PD, and a possible neuroradiological marker for the evolution to dementia. This issue was investigated in papers I and II. Secondly, we aimed to investigate structural correlates of deficits in the recognition of emotions, decision-making and olfactory dysfunction reported early in the disease course by means of VBM and DTI (paper III and IV). Finally in paper V the functional correlates of recognition memory were assessed using fMRI.The main conclusions of this thesis, derived from the five studies, can be summarized as follows:1) The pattern of atrophy in non-demented PD patients affects the anterior region of the hippocampus and progresses to the posterior part in demented patients but preserves the middle part of this structure. This pattern and evolution is similar to that seen in Mild Cognitive Impairment of amnestic type and Alzheimer's disease.2) Declarative memory dysfunctions in PD depend on the atrophy of the head of the hippocampus. 3) Patients with visual hallucinations present progressive hippocampal atrophy and also show widespread atrophy involving the limbic, paralimbic and neocortical areas in agreement with the evolution towards dementia. In contrast, patients without VH only show gray matter loss in the motor regions and their cognitive functions remain spared.4) Early PD patients present gray matter loss in some limbic regions. We observed gray matter loss in the amygdala and orbitofrontal cortex but not in the anterior cingulate, enthorrinal cortex and accumbes nuclei. These results only partially support the stages proposed by Braak.5) Impairment in decision-making and recognition of facial expressions of emotions occurs at early stages of PD. These neuropsychological deficits are accompanied by degeneration of orbitofrontal cortex (OFC) and amygdala. Bilateral OFC reductions are associated with impaired recognition of emotions, and gray matter volume loss in left lateral OFC is related to decision-making impairment in PD.6) PD patients presented abnormal white matter microstructural changes in several brain regions including cortical and subcortical areas early in the disease course. However, only reduction of fractional anisotropy in the white matter of the central olfactory areas, specifically the white matter adjacent to the gyrus rectus, is associated with olfactory dysfunction in PD patients.7) There is a disruption of functional networks involved in memory and default mode in early PD.