Intact working memory in non-manifesting LRRK2 carriers -- an fMRI study.
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| Title: | Intact working memory in non-manifesting LRRK2 carriers -- an fMRI study. |
|---|---|
| Authors: | Thaler, Avner, Helmich, Rick C., Or‐Borichev, Ayelet, Nuenen, Bart F.L., Shapira‐Lichter, Irit, Gurevich, Tanya, Orr‐Urtreger, Avi, Marder, Karen, Bressman, Susan, Bloem, Bastiaan R., Giladi, Nir, Hendler, Talma, Mirelman, Anat, Munoz, Doug |
| Source: | European Journal of Neuroscience. Jan2016, Vol. 43 Issue 1, p106-112. 7p. 1 Color Photograph, 4 Charts. |
| Subjects: | Parkinson's disease, Mild cognitive impairment, Disease prevalence, Short-term memory, Functional magnetic resonance imaging, Brain imaging, Genetic mutation, Executive function |
| Abstract: | Cognitive impairments are prevalent in patients with Parkinson's disease. Mutations in the leucine-rich repeat kinase 2 (LRRK2) gene are the most common cause of genetic Parkinsonism. Non-manifesting carriers of the G2019S mutation in the LRRK2 gene were found to have lower executive functions as measured by the Stroop task. This exploratory study aimed to assess whether the cognitive impairment in non-manifesting carriers is specific for executive functions or includes other cognitive domains such as working memory. We recruited 77 non-manifesting first-degree relatives of Parkinson's disease patients (38 carriers). A blockdesign fMRI N-back task, with 0-back, 2-back and 3-back conditions, was used in order to assess working memory. Participants were well matched on the Montreal Cognitive Assessment, University of Pennsylvania Smell Identification Test, Unified Parkinson's Disease Rating Scale part III, digit span, age, gender and Beck Depression Inventory. The task achieved the overall expected effect in both groups with longer reaction times and lower accuracy rates with increasing task demands. However, no whole-brain or region-of-interest between-groups differences were found on any of the task conditions. These results indicate that non-manifesting carriers of the G2019S mutation in the LRRK2 gene have a specific cognitive profile with executive functions, as assessed by the Stroop task, demonstrating significant impairment but with working memory, as assessed with the N-back task, remaining relatively intact. These finding shed light on the pre-motor cognitive changes in this unique 'at risk' population and should enable more focused cognitive assessments of these cohorts. [ABSTRACT FROM AUTHOR] |
| Copyright of European Journal of Neuroscience is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.) | |
| Database: | Psychology and Behavioral Sciences Collection |
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| Header | DbId: pbh DbLabel: Psychology and Behavioral Sciences Collection An: 112198656 AccessLevel: 6 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Intact working memory in non-manifesting LRRK2 carriers -- an fMRI study. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Thaler%2C+Avner%22">Thaler, Avner</searchLink><br /><searchLink fieldCode="AR" term="%22Helmich%2C+Rick+C%2E%22">Helmich, Rick C.</searchLink><br /><searchLink fieldCode="AR" term="%22Or‐Borichev%2C+Ayelet%22">Or‐Borichev, Ayelet</searchLink><br /><searchLink fieldCode="AR" term="%22Nuenen%2C+Bart+F%2EL%2E%22">Nuenen, Bart F.L.</searchLink><br /><searchLink fieldCode="AR" term="%22Shapira‐Lichter%2C+Irit%22">Shapira‐Lichter, Irit</searchLink><br /><searchLink fieldCode="AR" term="%22Gurevich%2C+Tanya%22">Gurevich, Tanya</searchLink><br /><searchLink fieldCode="AR" term="%22Orr‐Urtreger%2C+Avi%22">Orr‐Urtreger, Avi</searchLink><br /><searchLink fieldCode="AR" term="%22Marder%2C+Karen%22">Marder, Karen</searchLink><br /><searchLink fieldCode="AR" term="%22Bressman%2C+Susan%22">Bressman, Susan</searchLink><br /><searchLink fieldCode="AR" term="%22Bloem%2C+Bastiaan+R%2E%22">Bloem, Bastiaan R.</searchLink><br /><searchLink fieldCode="AR" term="%22Giladi%2C+Nir%22">Giladi, Nir</searchLink><br /><searchLink fieldCode="AR" term="%22Hendler%2C+Talma%22">Hendler, Talma</searchLink><br /><searchLink fieldCode="AR" term="%22Mirelman%2C+Anat%22">Mirelman, Anat</searchLink><br /><searchLink fieldCode="AR" term="%22Munoz%2C+Doug%22">Munoz, Doug</searchLink> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22European+Journal+of+Neuroscience%22">European Journal of Neuroscience</searchLink>. Jan2016, Vol. 43 Issue 1, p106-112. 7p. 1 Color Photograph, 4 Charts. – Name: Subject Label: Subjects Group: Su Data: <searchLink fieldCode="DE" term="%22Parkinson's+disease%22">Parkinson's disease</searchLink><br /><searchLink fieldCode="DE" term="%22Mild+cognitive+impairment%22">Mild cognitive impairment</searchLink><br /><searchLink fieldCode="DE" term="%22Disease+prevalence%22">Disease prevalence</searchLink><br /><searchLink fieldCode="DE" term="%22Short-term+memory%22">Short-term memory</searchLink><br /><searchLink fieldCode="DE" term="%22Functional+magnetic+resonance+imaging%22">Functional magnetic resonance imaging</searchLink><br /><searchLink fieldCode="DE" term="%22Brain+imaging%22">Brain imaging</searchLink><br /><searchLink fieldCode="DE" term="%22Genetic+mutation%22">Genetic mutation</searchLink><br /><searchLink fieldCode="DE" term="%22Executive+function%22">Executive function</searchLink> – Name: Abstract Label: Abstract Group: Ab Data: Cognitive impairments are prevalent in patients with Parkinson's disease. Mutations in the leucine-rich repeat kinase 2 (LRRK2) gene are the most common cause of genetic Parkinsonism. Non-manifesting carriers of the G2019S mutation in the LRRK2 gene were found to have lower executive functions as measured by the Stroop task. This exploratory study aimed to assess whether the cognitive impairment in non-manifesting carriers is specific for executive functions or includes other cognitive domains such as working memory. We recruited 77 non-manifesting first-degree relatives of Parkinson's disease patients (38 carriers). A blockdesign fMRI N-back task, with 0-back, 2-back and 3-back conditions, was used in order to assess working memory. Participants were well matched on the Montreal Cognitive Assessment, University of Pennsylvania Smell Identification Test, Unified Parkinson's Disease Rating Scale part III, digit span, age, gender and Beck Depression Inventory. The task achieved the overall expected effect in both groups with longer reaction times and lower accuracy rates with increasing task demands. However, no whole-brain or region-of-interest between-groups differences were found on any of the task conditions. These results indicate that non-manifesting carriers of the G2019S mutation in the LRRK2 gene have a specific cognitive profile with executive functions, as assessed by the Stroop task, demonstrating significant impairment but with working memory, as assessed with the N-back task, remaining relatively intact. These finding shed light on the pre-motor cognitive changes in this unique 'at risk' population and should enable more focused cognitive assessments of these cohorts. [ABSTRACT FROM AUTHOR] – Name: AbstractSuppliedCopyright Label: Group: Ab Data: <i>Copyright of European Journal of Neuroscience is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.) |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=pbh&AN=112198656 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1111/ejn.13120 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 7 StartPage: 106 Subjects: – SubjectFull: Parkinson's disease Type: general – SubjectFull: Mild cognitive impairment Type: general – SubjectFull: Disease prevalence Type: general – SubjectFull: Short-term memory Type: general – SubjectFull: Functional magnetic resonance imaging Type: general – SubjectFull: Brain imaging Type: general – SubjectFull: Genetic mutation Type: general – SubjectFull: Executive function Type: general Titles: – TitleFull: Intact working memory in non-manifesting LRRK2 carriers -- an fMRI study. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Thaler, Avner – PersonEntity: Name: NameFull: Helmich, Rick C. – PersonEntity: Name: NameFull: Or‐Borichev, Ayelet – PersonEntity: Name: NameFull: Nuenen, Bart F.L. – PersonEntity: Name: NameFull: Shapira‐Lichter, Irit – PersonEntity: Name: NameFull: Gurevich, Tanya – PersonEntity: Name: NameFull: Orr‐Urtreger, Avi – PersonEntity: Name: NameFull: Marder, Karen – PersonEntity: Name: NameFull: Bressman, Susan – PersonEntity: Name: NameFull: Bloem, Bastiaan R. – PersonEntity: Name: NameFull: Giladi, Nir – PersonEntity: Name: NameFull: Hendler, Talma – PersonEntity: Name: NameFull: Mirelman, Anat – PersonEntity: Name: NameFull: Munoz, Doug IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 01 Text: Jan2016 Type: published Y: 2016 Identifiers: – Type: issn-print Value: 0953816X Numbering: – Type: volume Value: 43 – Type: issue Value: 1 Titles: – TitleFull: European Journal of Neuroscience Type: main |
| ResultId | 1 |