Serum tyrosine associates with increased CSF Aβ42, reduced Aβ deposition, and cognitive improvement in MCI: modulation by confounding factors.
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| Title: | Serum tyrosine associates with increased CSF Aβ42, reduced Aβ deposition, and cognitive improvement in MCI: modulation by confounding factors. |
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| Authors: | Dhiaa Younis, Shahad Mohammed (AUTHOR), Shareef, Abdulkareem (AUTHOR), Kumar Bishoyi, Ashok (AUTHOR), Roopashree, R. (AUTHOR), Kashyap, Aditya (AUTHOR), Pramanik, Atreyi (AUTHOR), Ray, Subhashree (AUTHOR), Mavlyanova, Zilola (AUTHOR), Naji Sameer, Hayder (AUTHOR), Yaseen, Ahmed (AUTHOR), H. Athab, Zainab (AUTHOR), Adil, Mohaned (AUTHOR) |
| Source: | International Journal of Neuroscience. Mar2026, Vol. 136 Issue 3, p343-358. 16p. |
| Subjects: | Mild cognitive impairment, Amyloid beta-protein, Cognition disorders, Amyloid plaque, Tyrosine, Cerebrospinal fluid, Cognitive ability |
| Abstract: | Background: Tyrosine, a precursor to dopamine, norepinephrine, and epinephrine, has shown mixed results in cognitive impairment studies, suggesting a complex role in mild cognitive impairment (MCI). This study is the first to explore its relationship with CSF amyloid-beta (Aβ) 42, Aβ accumulation, and cognitive function in MCI (n = 251). Method: Cognitive function was assessed using ADAS-Cog, serum tyrosine by UPLC-MS/MS, Aβ42 by ELISA, and Aβ accumulation via florbetapir PET with SUVr, all validated with quality control. Two analysis models were used: Model 1 (unadjusted) and Model 2 (adjusted for age, gender, education, handedness, and ApoE status). Results: The study found a significant positive link between serum tyrosine levels and CSF Aβ42, with higher tyrosine levels associated with increased Aβ42, independent of demographic and genetic factors. Mediation analysis revealed that in Model 1, higher serum tyrosine was associated with improved cognitive function, potentially through increased CSF Aβ42 levels. However, this association was not present after adjusting for confounders in Model 2. Further investigation of Aβ accumulation in specific brain regions (global, frontal, temporal, and parietal lobes) found that, in Model 1, higher serum tyrosine was linked to reduced Aβ accumulation in the frontal and temporal lobes, wich in turn correlated with better cognitive function. Yet, after adjusting for confounders in Model 2, these effects were no longer significant. Conclusion: Overall, the findings suggest that while serum tyrosine may influence cognitive improvement in MCI through its relationship with CSF Aβ42 and Aβ accumulation, these effects are strongly influenced by demographic and genetic factors. [ABSTRACT FROM AUTHOR] |
| Copyright of International Journal of Neuroscience is the property of Taylor & Francis Ltd 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 |
| FullText | Text: Availability: 0 |
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| Header | DbId: pbh DbLabel: Psychology and Behavioral Sciences Collection An: 191948379 AccessLevel: 6 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Serum tyrosine associates with increased CSF Aβ42, reduced Aβ deposition, and cognitive improvement in MCI: modulation by confounding factors. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Dhiaa+Younis%2C+Shahad+Mohammed%22">Dhiaa Younis, Shahad Mohammed</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Shareef%2C+Abdulkareem%22">Shareef, Abdulkareem</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Kumar+Bishoyi%2C+Ashok%22">Kumar Bishoyi, Ashok</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Roopashree%2C+R%2E%22">Roopashree, R.</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Kashyap%2C+Aditya%22">Kashyap, Aditya</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Pramanik%2C+Atreyi%22">Pramanik, Atreyi</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Ray%2C+Subhashree%22">Ray, Subhashree</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Mavlyanova%2C+Zilola%22">Mavlyanova, Zilola</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Naji+Sameer%2C+Hayder%22">Naji Sameer, Hayder</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Yaseen%2C+Ahmed%22">Yaseen, Ahmed</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22H%2E+Athab%2C+Zainab%22">H. Athab, Zainab</searchLink> (AUTHOR)<br /><searchLink fieldCode="AR" term="%22Adil%2C+Mohaned%22">Adil, Mohaned</searchLink> (AUTHOR) – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22International+Journal+of+Neuroscience%22">International Journal of Neuroscience</searchLink>. Mar2026, Vol. 136 Issue 3, p343-358. 16p. – Name: Subject Label: Subjects Group: Su Data: <searchLink fieldCode="DE" term="%22Mild+cognitive+impairment%22">Mild cognitive impairment</searchLink><br /><searchLink fieldCode="DE" term="%22Amyloid+beta-protein%22">Amyloid beta-protein</searchLink><br /><searchLink fieldCode="DE" term="%22Cognition+disorders%22">Cognition disorders</searchLink><br /><searchLink fieldCode="DE" term="%22Amyloid+plaque%22">Amyloid plaque</searchLink><br /><searchLink fieldCode="DE" term="%22Tyrosine%22">Tyrosine</searchLink><br /><searchLink fieldCode="DE" term="%22Cerebrospinal+fluid%22">Cerebrospinal fluid</searchLink><br /><searchLink fieldCode="DE" term="%22Cognitive+ability%22">Cognitive ability</searchLink> – Name: Abstract Label: Abstract Group: Ab Data: Background: Tyrosine, a precursor to dopamine, norepinephrine, and epinephrine, has shown mixed results in cognitive impairment studies, suggesting a complex role in mild cognitive impairment (MCI). This study is the first to explore its relationship with CSF amyloid-beta (Aβ) 42, Aβ accumulation, and cognitive function in MCI (n = 251). Method: Cognitive function was assessed using ADAS-Cog, serum tyrosine by UPLC-MS/MS, Aβ42 by ELISA, and Aβ accumulation via florbetapir PET with SUVr, all validated with quality control. Two analysis models were used: Model 1 (unadjusted) and Model 2 (adjusted for age, gender, education, handedness, and ApoE status). Results: The study found a significant positive link between serum tyrosine levels and CSF Aβ42, with higher tyrosine levels associated with increased Aβ42, independent of demographic and genetic factors. Mediation analysis revealed that in Model 1, higher serum tyrosine was associated with improved cognitive function, potentially through increased CSF Aβ42 levels. However, this association was not present after adjusting for confounders in Model 2. Further investigation of Aβ accumulation in specific brain regions (global, frontal, temporal, and parietal lobes) found that, in Model 1, higher serum tyrosine was linked to reduced Aβ accumulation in the frontal and temporal lobes, wich in turn correlated with better cognitive function. Yet, after adjusting for confounders in Model 2, these effects were no longer significant. Conclusion: Overall, the findings suggest that while serum tyrosine may influence cognitive improvement in MCI through its relationship with CSF Aβ42 and Aβ accumulation, these effects are strongly influenced by demographic and genetic factors. [ABSTRACT FROM AUTHOR] – Name: AbstractSuppliedCopyright Label: Group: Ab Data: <i>Copyright of International Journal of Neuroscience is the property of Taylor & Francis Ltd 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.) |
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| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1080/00207454.2025.2544791 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 16 StartPage: 343 Subjects: – SubjectFull: Mild cognitive impairment Type: general – SubjectFull: Amyloid beta-protein Type: general – SubjectFull: Cognition disorders Type: general – SubjectFull: Amyloid plaque Type: general – SubjectFull: Tyrosine Type: general – SubjectFull: Cerebrospinal fluid Type: general – SubjectFull: Cognitive ability Type: general Titles: – TitleFull: Serum tyrosine associates with increased CSF Aβ42, reduced Aβ deposition, and cognitive improvement in MCI: modulation by confounding factors. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Dhiaa Younis, Shahad Mohammed – PersonEntity: Name: NameFull: Shareef, Abdulkareem – PersonEntity: Name: NameFull: Kumar Bishoyi, Ashok – PersonEntity: Name: NameFull: Roopashree, R. – PersonEntity: Name: NameFull: Kashyap, Aditya – PersonEntity: Name: NameFull: Pramanik, Atreyi – PersonEntity: Name: NameFull: Ray, Subhashree – PersonEntity: Name: NameFull: Mavlyanova, Zilola – PersonEntity: Name: NameFull: Naji Sameer, Hayder – PersonEntity: Name: NameFull: Yaseen, Ahmed – PersonEntity: Name: NameFull: H. Athab, Zainab – PersonEntity: Name: NameFull: Adil, Mohaned IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 03 Text: Mar2026 Type: published Y: 2026 Identifiers: – Type: issn-print Value: 00207454 Numbering: – Type: volume Value: 136 – Type: issue Value: 3 Titles: – TitleFull: International Journal of Neuroscience Type: main |
| ResultId | 1 |