Cargando…
Neuropsychiatric symptoms as a sign of small vessel disease progression in cognitive impairment
BACKGROUND: Neuropsychiatric symptoms associate cross-sectionally with cerebral small vessel disease but it is not clear whether these symptoms could act as early clinical markers of small vessel disease progression. We investigated whether longitudinal change in Neuropsychiatric Inventory (NPI) sco...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9616231/ https://www.ncbi.nlm.nih.gov/pubmed/36324402 http://dx.doi.org/10.1016/j.cccb.2022.100041 |
_version_ | 1784820604788015104 |
---|---|
author | Clancy, Una Ramirez, Joel Chappell, Francesca M. Doubal, Fergus N. Wardlaw, Joanna M. Black, Sandra E. |
author_facet | Clancy, Una Ramirez, Joel Chappell, Francesca M. Doubal, Fergus N. Wardlaw, Joanna M. Black, Sandra E. |
author_sort | Clancy, Una |
collection | PubMed |
description | BACKGROUND: Neuropsychiatric symptoms associate cross-sectionally with cerebral small vessel disease but it is not clear whether these symptoms could act as early clinical markers of small vessel disease progression. We investigated whether longitudinal change in Neuropsychiatric Inventory (NPI) scores associated with white matter hyperintensity (WMH) progression in a memory clinic population. MATERIAL AND METHODS: We included participants from the prospective Sunnybrook Dementia Study with Alzheimer's disease and vascular subtypes of mild cognitive impairment and dementia with two MRI and ≥ 1 NPI. We conducted linear mixed-effects analyses, adjusting for age, atrophy, vascular risk factors, cognition, function, and interscan interval. RESULTS: At baseline (n=124), greater atrophy, age, vascular risk factors and total NPI score were associated with higher baseline WMH volume, while longitudinally, all but vascular risk factors were associated. Change in total NPI score was associated with change in WMH volume, χ2 = 7.18, p = 0.007, whereby a one-point change in NPI score from baseline to follow-up was associated with a 0.0017 change in normalized WMH volume [expressed as cube root of (WMH volume cm³ as % intracranial volume)], after adjusting for age, atrophy, vascular risk factors and interscan interval. CONCLUSIONS: In memory clinic patients, WMH progression over 1–2 years associated with worsening neuropsychiatric symptoms, while WMH volume remained unchanged in those with stable NPI scores in this population with low background WMH burden. |
format | Online Article Text |
id | pubmed-9616231 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-96162312022-11-01 Neuropsychiatric symptoms as a sign of small vessel disease progression in cognitive impairment Clancy, Una Ramirez, Joel Chappell, Francesca M. Doubal, Fergus N. Wardlaw, Joanna M. Black, Sandra E. Cereb Circ Cogn Behav Article BACKGROUND: Neuropsychiatric symptoms associate cross-sectionally with cerebral small vessel disease but it is not clear whether these symptoms could act as early clinical markers of small vessel disease progression. We investigated whether longitudinal change in Neuropsychiatric Inventory (NPI) scores associated with white matter hyperintensity (WMH) progression in a memory clinic population. MATERIAL AND METHODS: We included participants from the prospective Sunnybrook Dementia Study with Alzheimer's disease and vascular subtypes of mild cognitive impairment and dementia with two MRI and ≥ 1 NPI. We conducted linear mixed-effects analyses, adjusting for age, atrophy, vascular risk factors, cognition, function, and interscan interval. RESULTS: At baseline (n=124), greater atrophy, age, vascular risk factors and total NPI score were associated with higher baseline WMH volume, while longitudinally, all but vascular risk factors were associated. Change in total NPI score was associated with change in WMH volume, χ2 = 7.18, p = 0.007, whereby a one-point change in NPI score from baseline to follow-up was associated with a 0.0017 change in normalized WMH volume [expressed as cube root of (WMH volume cm³ as % intracranial volume)], after adjusting for age, atrophy, vascular risk factors and interscan interval. CONCLUSIONS: In memory clinic patients, WMH progression over 1–2 years associated with worsening neuropsychiatric symptoms, while WMH volume remained unchanged in those with stable NPI scores in this population with low background WMH burden. Elsevier 2022-01-19 /pmc/articles/PMC9616231/ /pubmed/36324402 http://dx.doi.org/10.1016/j.cccb.2022.100041 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Clancy, Una Ramirez, Joel Chappell, Francesca M. Doubal, Fergus N. Wardlaw, Joanna M. Black, Sandra E. Neuropsychiatric symptoms as a sign of small vessel disease progression in cognitive impairment |
title | Neuropsychiatric symptoms as a sign of small vessel disease progression in cognitive impairment |
title_full | Neuropsychiatric symptoms as a sign of small vessel disease progression in cognitive impairment |
title_fullStr | Neuropsychiatric symptoms as a sign of small vessel disease progression in cognitive impairment |
title_full_unstemmed | Neuropsychiatric symptoms as a sign of small vessel disease progression in cognitive impairment |
title_short | Neuropsychiatric symptoms as a sign of small vessel disease progression in cognitive impairment |
title_sort | neuropsychiatric symptoms as a sign of small vessel disease progression in cognitive impairment |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9616231/ https://www.ncbi.nlm.nih.gov/pubmed/36324402 http://dx.doi.org/10.1016/j.cccb.2022.100041 |
work_keys_str_mv | AT clancyuna neuropsychiatricsymptomsasasignofsmallvesseldiseaseprogressionincognitiveimpairment AT ramirezjoel neuropsychiatricsymptomsasasignofsmallvesseldiseaseprogressionincognitiveimpairment AT chappellfrancescam neuropsychiatricsymptomsasasignofsmallvesseldiseaseprogressionincognitiveimpairment AT doubalfergusn neuropsychiatricsymptomsasasignofsmallvesseldiseaseprogressionincognitiveimpairment AT wardlawjoannam neuropsychiatricsymptomsasasignofsmallvesseldiseaseprogressionincognitiveimpairment AT blacksandrae neuropsychiatricsymptomsasasignofsmallvesseldiseaseprogressionincognitiveimpairment |