Neuropsychiatric symptoms and white matter hyperintensities in older adults without dementia
- PMID: 38639110
- PMCID: PMC11489321
- DOI: 10.1017/S1041610224000607
Neuropsychiatric symptoms and white matter hyperintensities in older adults without dementia
Abstract
Objective: We aimed to examine associations between neuropsychiatric symptoms (NPS) and white matter hyperintensities (WMH) status in older adults without dementia under the hypothesis that WMH increased the odds of having NPS.
Design: Longitudinal analysis of data acquired from the National Alzheimer's Coordinating Center Uniform Data Set.
Settings: Data were derived from 46 National Institute on Aging - funded Alzheimer's Disease Research Centers.
Participants: NACC participants aged ≥50 years with available data on WMH severity with a diagnosis of mild cognitive impairment (MCI) or who were cognitively unimpaired (CU) were studied. Among 4617 CU participants, 376 had moderate and 54 extensive WMH. Among 3170 participants with MCI, 471 had moderate and 88 had extensive WMH.
Measurements: Using Cardiovascular Health Study (CHS) scores, WMH were coded as no to mild (CHS score: 0-4), moderate (score: 5-6) or extensive (score: 7-8). NPS were quantified on the Neuropsychiatric Inventory Questionnaire. Binary logistic regression models estimated the odds of reporting each of 12 NPS by WMH status separately for individuals with MCI or who were CU.
Results: Compared to CU individuals with no to mild WMH, the odds of having elation [9.87, (2.63-37.10)], disinhibition [4.42, (1.28-15.32)], agitation [3.51, (1.29-9.54)] or anxiety [2.74, (1.28-5.88)] were higher for the extensive WMH group, whereas the odds of having disinhibition were higher for the moderate WMH group [1.94, (1.05-3.61)]. In the MCI group, he odds of NPS did not vary by WMH status.
Conclusions: Extensive WMH were associated with higher odds of NPS in CU older adults but not in those with MCI.
Keywords: agitation; anxiety; disinhibition; elation.
Conflict of interest statement
Conflict of interest
The authors declare that they have no conflict of interest.
Figures
Similar articles
-
Neuropsychiatric Symptoms and White Matter Hyperintensities in Older Cognitively Unimpaired Men Versus Women.Int J Geriatr Psychiatry. 2025 Jun;40(6):e70107. doi: 10.1002/gps.70107. Int J Geriatr Psychiatry. 2025. PMID: 40495289 Free PMC article.
-
Independent effects of white matter hyperintensities on cognitive, neuropsychiatric, and functional decline: a longitudinal investigation using the National Alzheimer's Coordinating Center Uniform Data Set.Alzheimers Res Ther. 2019 Jul 27;11(1):64. doi: 10.1186/s13195-019-0521-0. Alzheimers Res Ther. 2019. PMID: 31351489 Free PMC article.
-
The Longitudinal Assessment of Neuropsychiatric Symptoms in Mild Cognitive Impairment and Alzheimer's Disease and Their Association With White Matter Hyperintensities in the National Alzheimer's Coordinating Center's Uniform Data Set.Biol Psychiatry Cogn Neurosci Neuroimaging. 2021 Jan;6(1):70-78. doi: 10.1016/j.bpsc.2020.03.006. Epub 2020 Apr 2. Biol Psychiatry Cogn Neurosci Neuroimaging. 2021. PMID: 32389747 Free PMC article.
-
The burden of white matter hyperintensities is a predictor of progressive mild cognitive impairment in patients with Parkinson's disease.Eur J Neurol. 2014 Jun;21(6):922-e50. doi: 10.1111/ene.12412. Epub 2014 Mar 24. Eur J Neurol. 2014. PMID: 24661277
-
Sex differences in the development of mild cognitive impairment and probable Alzheimer's disease as predicted by hippocampal volume or white matter hyperintensities.J Women Aging. 2019 Mar-Apr;31(2):140-164. doi: 10.1080/08952841.2018.1419476. Epub 2018 Jan 10. J Women Aging. 2019. PMID: 29319430 Free PMC article.
Cited by
-
Neuropsychiatric Symptoms Associated With Frontotemporal Atrophy in Older Adults Without Dementia.Int J Geriatr Psychiatry. 2024 Dec;39(12):e70008. doi: 10.1002/gps.70008. Int J Geriatr Psychiatry. 2024. PMID: 39617744 Free PMC article.
-
Neurofilament Light Chain in Cerebrospinal Fluid and Blood in Multiple System Atrophy: A Systematic Review and Meta-Analysis.Brain Sci. 2025 Feb 25;15(3):241. doi: 10.3390/brainsci15030241. Brain Sci. 2025. PMID: 40149766 Free PMC article. Review.
-
Factors associated with motor manifestations in older adults with Alzheimer's dementia: a cross-sectional analysis.Eur Geriatr Med. 2025 Jul 21. doi: 10.1007/s41999-025-01259-z. Online ahead of print. Eur Geriatr Med. 2025. PMID: 40690190
-
Neuropsychiatric Symptoms and White Matter Hyperintensities in Older Cognitively Unimpaired Men Versus Women.Int J Geriatr Psychiatry. 2025 Jun;40(6):e70107. doi: 10.1002/gps.70107. Int J Geriatr Psychiatry. 2025. PMID: 40495289 Free PMC article.
-
The need for identifying neuropsychiatric symptoms and neural correlates among racially and ethnically minoritized older adults. Commentary on "Neuropsychiatric symptoms and white matter hyperintensities in older adults without dementia" by Liampas et al.Int Psychogeriatr. 2025 Jan;37(1):100022. doi: 10.1016/j.inpsyc.2024.100022. Epub 2024 Dec 4. Int Psychogeriatr. 2025. PMID: 39924265 No abstract available.
References
MeSH terms
Grants and funding
- P20 AG068053/AG/NIA NIH HHS/United States
- P30 AG066515/AG/NIA NIH HHS/United States
- P30 AG062421/AG/NIA NIH HHS/United States
- P30 AG066508/AG/NIA NIH HHS/United States
- P30 AG066519/AG/NIA NIH HHS/United States
- P30 AG072973/AG/NIA NIH HHS/United States
- P30 AG066462/AG/NIA NIH HHS/United States
- P30 AG066530/AG/NIA NIH HHS/United States
- P30 AG066509/AG/NIA NIH HHS/United States
- P20 AG068077/AG/NIA NIH HHS/United States
- P30 AG066546/AG/NIA NIH HHS/United States
- P30 AG072972/AG/NIA NIH HHS/United States
- P30 AG072979/AG/NIA NIH HHS/United States
- P20 AG068082/AG/NIA NIH HHS/United States
- P30 AG072975/AG/NIA NIH HHS/United States
- P30 AG066444/AG/NIA NIH HHS/United States
- P30 AG066507/AG/NIA NIH HHS/United States
- P30 AG072946/AG/NIA NIH HHS/United States
- P30 AG066518/AG/NIA NIH HHS/United States
- P30 AG066511/AG/NIA NIH HHS/United States
- U24 AG072122/AG/NIA NIH HHS/United States
- P30 AG066512/AG/NIA NIH HHS/United States
- P30 AG072978/AG/NIA NIH HHS/United States
- P30 AG062429/AG/NIA NIH HHS/United States
- P30 AG062422/AG/NIA NIH HHS/United States
- R01 AG079280/AG/NIA NIH HHS/United States
- P30 AG072977/AG/NIA NIH HHS/United States
- P30 AG062677/AG/NIA NIH HHS/United States
- P20 AG068024/AG/NIA NIH HHS/United States
- P30 AG072958/AG/NIA NIH HHS/United States
- P30 AG062715/AG/NIA NIH HHS/United States
- P30 AG066506/AG/NIA NIH HHS/United States
- P30 AG066468/AG/NIA NIH HHS/United States
- P30 AG072976/AG/NIA NIH HHS/United States
- P30 AG072947/AG/NIA NIH HHS/United States
- P30 AG072931/AG/NIA NIH HHS/United States
- P30 AG066514/AG/NIA NIH HHS/United States
- P30 AG072959/AG/NIA NIH HHS/United States
LinkOut - more resources
Full Text Sources
Medical