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Longitudinal neuropsychological trajectories in idiopathic normal pressure hydrocephalus: a population–based study
Umeå University, Faculty of Medicine, Department of Clinical Sciences, Neurosciences.
Umeå University, Faculty of Medicine, Department of Clinical Sciences, Psychiatry.ORCID iD: 0000-0001-7868-8894
Umeå University, Faculty of Medicine, Department of Clinical Sciences, Neurosciences.ORCID iD: 0000-0002-4686-0941
Umeå University, Faculty of Medicine, Department of Clinical Sciences, Neurosciences.ORCID iD: 0000-0002-4107-3818
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2023 (English)In: BMC Geriatrics, E-ISSN 1471-2318, Vol. 23, no 1, article id 29Article in journal (Refereed) Published
Abstract [en]

Background: Idiopathic normal pressure hydrocephalus (iNPH) is a progressive syndrome affecting gait, incontinence, and cognition in a significant number of older adults. Still, prospective studies on early development of symptoms are scarce.

Aim: To investigate how neuropsychological functions develop before and in already diagnosed iNPH over a two-year period in a population-based material.

Method: A sample of 104 participants (median [IQR] 75 [72–80] years old) from the general population underwent CT-imaging and clinical assessment at baseline and follow-up. We used the iNPH symptom scale covering four domains (Neuropsychology, Gait, Balance, Incontinence) and additional tests of executive functions. Morphological signs were rated with the iNPH Radscale. Non-parametric statistics with Bonferroni corrections and a significance-level of p < 0.05 were used.

Results: Median (IQR) time to follow-up was 25 (23–26) months. Effect size (ES) for individuals who developed iNPH (n = 8) showed a large (ES r = -0.55) decline in the Gait domain and on the Radscale (ES r = -0.60), with a medium deterioration in declarative memory (ES r = -0.37). Those having iNPH at baseline (n = 12) performed worse on one executive sub-function i.e., shifting (p = 0.045).

Conclusion: Besides deterioration in gait and radiology, our results suggest that a neuropsychological trajectory for those developing iNPH includes a reduction in declarative memory. Executive dysfunction was limited to those already having iNPH at baseline. These findings could suggest that memory impairments are included in the early development of iNPH.

Place, publisher, year, edition, pages
BioMed Central (BMC), 2023. Vol. 23, no 1, article id 29
Keywords [en]
Ageing, Cognition, Cognitive development, Idiopathic normal pressure hydrocephalus, Life-span, Neuropsychology, Older adults, Population-based
National Category
Neurology Geriatrics
Identifiers
URN: urn:nbn:se:umu:diva-204071DOI: 10.1186/s12877-023-03747-yISI: 000949186600003PubMedID: 36647004Scopus ID: 2-s2.0-85146308972OAI: oai:DiVA.org:umu-204071DiVA, id: diva2:1731510
Funder
Umeå UniversityRegion Jämtland HärjedalenKnut and Alice Wallenberg FoundationAvailable from: 2023-01-27 Created: 2023-01-27 Last updated: 2024-07-04Bibliographically approved

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Lilja-Lund, OttoMaripuu, MartinKockum, KarinAndersson, JohannaLindam, AnnaNyberg, Lars

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Lilja-Lund, OttoMaripuu, MartinKockum, KarinAndersson, JohannaLindam, AnnaNyberg, Lars
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NeurosciencesPsychiatryDepartment of Public Health and Clinical MedicineDepartment of Integrative Medical Biology (IMB)Umeå Centre for Functional Brain Imaging (UFBI)
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