Correlation of Neuropsychiatric Symptoms in Dementia with Brain Perfusion: A 99mTc-SPECT-HMPAO Study with Brodmann Areas Analysis

Author:

Valotassiou Varvara1,Sifakis Nikolaos2,Tzavara Chara1,Lykou Evi3,Tsinia Niki4,Kamtsadeli Vasiliki3,Sali Dimitra5,Angelidis George6,Psimadas Dimitrios1,Tsougos Ioannis7,Papageorgiou Sokratis G.8,Georgoulias Panagiotis1,Papatriantafyllou John9

Affiliation:

1. Nuclear Medicine Department, University Hospital of Larissa, Thessaly, Greece

2. Nuclear Medicine Department, “Alexandra” General Hospital, Athens, Greece

3. 3rd Age Day Care Center, IASIS, Athens, Greece

4. 1st University Psychiatric Department, Aeginition Hospital, Athens, Greece

5. Neurology Department, Evrokliniki, Athens, Greece

6. Nuclear Medicine Department, University Hospital of Larissa, Thessaly,Greece

7. Medical Physics Department, Medical School, University of Thessaly, Greece

8. 2nd University Department of Neurology, Attikon Hospital, Athens, Greece

9. 3rd Age Day Care Center, IASIS, Athens,Greece | Memory Disorders Clinic, Medical Center, Athens, Greece

Abstract

Background: Neuropsychiatric symptoms (NPSs) are common in dementia. Their evaluation is based on Neuropsychiatric Inventory (NPI). Neuroimaging studies have tried to elucidate the underlying neural circuits either in isolated NPSs or in specific forms of dementia. Objective: : The objective of this study is to evaluate the correlation of NPS in the NPI with Brodmann areas (BAs) perfusion, for revealing BAs involved in the pathogenesis of NPSs in dementia of various etiologies. Method: We studied 201 patients (82 with Alzheimer's disease, 75 with Frontotemporal dementia, 27 with Corticobasal Syndrome, 17 with Parkinson Disease/Lewy Body Dementia). Exploratory factor analysis was carried out to evaluate underlying groups of BAs, and Principal Component analysis was chosen as extraction method using Varimax rotation. Partial correlation coefficients were computed to explore the association of factors obtained from analysis and NPI items controlling for age, educational yeas, and ACE-R. Results: We found 6 BAs Factors(F); F1 (BAs 8,9,10,11,24,32,44,45,46,47, bilaterally), F2 (Bas 4,5,6,7,23,31, bilaterally), F3 (BAs 19,21,22,37,39,40, bilaterally), F4 (BAs 20,28,36,38, bilaterally), F5 (BAs 25, bilaterally) and F6 (BAs 17,18, bilaterally). Significant and negative correlation was found between NPI1 (delusions) and F3,F6, NPI2 (hallucinations) and F6, NPI7 (apathy) and F1,F4,F5, NPI3 (agitation) - NPI10 (aberrant motor behavior) - NPI12 (eating disorders) and F1. We did not find any significant correlation for NPI4,5,6,8,9,11 (depression, anxiety, euphoria, disinhibition, irritability, sleep disorders, respectively). Conclusion: Several NPSs share the same BAs among different types of dementia, while the manifestation of the rest may be attributed to different neural networks. These findings may have an impact on patients’ treatment.

Publisher

Bentham Science Publishers Ltd.

Subject

Neurology (clinical),Neurology

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