Journals / Alpha psychiatry (Online) / 2021 / Cilt: 22 - Sayı: 5

Association of Temporolimbic Volumes with TreatmentResponse to Antipsychotic Medication for Delusion inPatients with Alzheimer’s Disease

Pages
244–249
Publication Date
2022-10-12
DOI
—
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Conclusion: Our findings suggest that specific gray matter volumes, including those ofthe temporal region and the limbic system, may affect treatment response to antipsy chotic medication in terms of delusional symptoms in patients with AD.

📌 3 Key Takeaways

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Objective & Hypothesis:Objective: This study investigated the association between gray matter volume and thetreatment response to antipsychotic medication in patients with Alzheimer’s disease (AD).
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Key Findings & Data:Methods: We included 26 AD patients with delusions from the Memory Impairment Centerof the Pusan National University Hospital in South Korea.
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Conclusion & Impact:Conclusion: Our findings suggest that specific gray matter volumes, including those ofthe temporal region and the limbic system, may affect treatment response to antipsy chotic medication in terms of delusional symptoms in patients with AD.
🔬Design:Modeling & Simulation
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Objective: This study investigated the association between gray matter volume and thetreatment response to antipsychotic medication in patients with Alzheimer’s disease (AD). Methods: We included 26 AD patients with delusions from the Memory Impairment Centerof the Pusan National University Hospital in South Korea. All participants underwent base line brain magnetic resonance imaging and took risperidone as an antipsychotic medica tion for 6 weeks. Gray matter volumes were measured using voxel-based morphometryat baseline. Treatment response with respect to delusional symptoms was defined as thechange in delusion item scores in the Korean version of the Neuropsychiatry Inventory(K-NPI), from baseline to 6 weeks later. A voxel-based multiple linear regression modelintegrated with statistical parametric mapping was used to investigate the associationbetween gray matter volume and treatment response after controlling for covariates. Results: The treatment response was significantly positively correlated with gray mattervolume in the temporal lobe (both the fusiform gyri and the left superior and inferior tem poral gyri) and the limbic system (the left parahippocampal gyrus and left amygdala) aftercontrolling for age, sex, education level, total intracranial volume, risperidone dosage,baseline Korean version of the Mini-Mental Status Examination scores, and baseline K-NPIscores for the delusion and non-delusion domains (P 100 voxels). Conclusion: Our findings suggest that specific gray matter volumes, including those ofthe temporal region and the limbic system, may affect treatment response to antipsy chotic medication in terms of delusional symptoms in patients with AD.

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Cite This Article

JEONG, H., SUH, H., LEE, Y., PARK, H. K., KİM, H., PAK, K., CHOİ, K., CHUNG, Y. (2022). Association of Temporolimbic Volumes with TreatmentResponse to Antipsychotic Medication for Delusion inPatients with Alzheimer’s Disease. Alpha psychiatry (Online), Cilt: 22 - Sayı: 5, 244–249. https://ajindex.com/articles/435197

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References (13)

  1. Ahn HJ, Chin J, Park A, et al. Seoul Neuropsychological Screening Batterydementia version (SNSB-D): a useful tool for assessing and monitoring cognitive impairments in dementia patients. J Korean Med Sci. 2010
  2. 25(7):1071-1076. [CrossRef] 2. Schneider LS, Pollock VE, Lyness SA. A metaanalysis of controlled trials of neuroleptic treatment in dementia. J Am Geriatr Soc. 1990
  3. 38(5):553- 563. [CrossRef] 3. Hsu WT, Esmaily-Fard A, Lai CC, et al. Antipsychotics and the risk of cerebrovascular accident: a systematic review and meta-analysis of observational studies. J Am Med Dir Assoc. 2017
  4. 18(8):692-699. [CrossRef] 4. Yang C, Hao Z, Tian J, et al. Does antipsychotic drug use increase the risk of long term mortality? A systematic review and meta-analysis of observational studies. Oncotarget. 2018
  5. 9(19):15101-15110. [CrossRef] 5. Bruen PD, McGeown WJ, Shanks MF, Venneri A. Neuroanatomical correlates of neuropsychiatric symptoms in Alzheimer’s disease. Brain. 2008
  6. 131(9):2455-2463. [CrossRef] 6. Prasad KM, Patel AR, Muddasani S, Sweeney J, Keshavan MS. The entorhinal cortex in first-episode psychotic disorders: a structural magnetic resonance imaging study. Am J Psychiatry. 2004
  7. 161(9):1612-1619. [CrossRef] 7. Murray PS, Kumar S, Demichele-Sweet MA, Sweet RA. Psychosis in Alzheimer’s disease. Biol Psychiatry. 2014
  8. 75(7):542-552. [CrossRef] 8. Murray PS, Kirkwood CM, Gray MC, et al. β-amyloid 42/40 ratio and kalirin expression in Alzheimer disease with psychosis. Neurobiol Aging. 2012
  9. 33(12):2807-2816. [CrossRef] 9. Farber NB, Rubin EH, Newcomer JW, et al. Increased neocortical neurofibrillary tangle density in subjects with Alzheimer disease and psychosis. Arch Gen Psychiatry. 2000
  10. 57(12):1165-1173. [CrossRef] 10. Fung G, Cheung C, Chen E, et al. MRI predicts remission at 1 year in firstepisode schizophrenia in females with larger striato-thalamic volumes. Neuropsychobiology. 2014
  11. 69(4):243-248. [CrossRef] 11. Bodnar M, Malla AK, Joober R, et al. Neural markers of early remission in first-episode schizophrenia: a volumetric neuroimaging study of the parahippocampus. Psychiatry Res. 2012
  12. 201(1):40-47. [CrossRef] 12. Prasad KM, Sahni SD, Rohm BR, Keshavan MS. Dorsolateral prefrontal cortex morphology and short-term outcome in first-episode schizophrenia. Psychiatry Res. 2005
  13. 140(2):147-155. [CrossRef] 13. Bodnar M, Harvey PO, Malla AK, Joober R, Lepage M. The parahippocampal gyrus as a neural marker of early remission in first-episode psychosis: a voxel-ba