Low Serum Phosphorus Correlates with Cerebral Aβ Deposition in Cognitively Impaired Subjects: Results from the KBASE Study
Alzheimer's disease (AD), characterized by progressive cognitive decline, is the most prevalent neurodegenerative disease in the elderly. Cerebral β-amyloid (Aβ) deposition is the major pathological hallmark of AD. Recent studies also have shown that the serum level of phosphorus correlates to...
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Published in | Frontiers in aging neuroscience Vol. 9; p. 362 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
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Abstract | Alzheimer's disease (AD), characterized by progressive cognitive decline, is the most prevalent neurodegenerative disease in the elderly. Cerebral β-amyloid (Aβ) deposition is the major pathological hallmark of AD. Recent studies also have shown that the serum level of phosphorus correlates to the risk of incident dementia. To date, the linkage between cerebral Aβ deposition and the serum phosphorus level remains unknown. In this study, we analyzed the levels of serum phosphorus in 109 mild cognitive impairment (MCI) and 73 AD dementia (ADD) subjects. All subjects underwent Pittsburgh compound B positron emission tomography (PiB-PET) imaging to measure cerebral Aβ deposition. The results with Aβ deposition was compared with the serum levels of phosphorus. The subjects with cerebral Aβ deposition showed lower levels of serum phosphorus than those without Aβ deposition. Furthermore, multiple regression analyses showed that a low level of serum phosphorus correlated with cerebral Aβ deposition, even when age, sex, apolipoprotein E ε4 genotype, and MMSE z-score were controlled for. Serum levels of other ions, including calcium, iron, zinc, and copper, showed no such correlation. In conclusion, our results suggest that the serum level of phosphorus may be used as an easily accessible blood biomarker for cerebral Aβ deposition in a cognitively impaired population. |
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AbstractList | Alzheimer’s disease (AD), characterized by progressive cognitive decline, is the most prevalent neurodegenerative disease in the elderly. Cerebral β-amyloid (Aβ) deposition is the major pathological hallmark of AD. Recent studies also have shown that the serum level of phosphorus correlates to the risk of incident dementia. To date, the linkage between cerebral Aβ deposition and the serum phosphorus level remains unknown. In this study, we analyzed the levels of serum phosphorus in 109 mild cognitive impairment (MCI) and 73 AD dementia (ADD) subjects. All subjects underwent Pittsburgh compound B positron emission tomography (PiB-PET) imaging to measure cerebral Aβ deposition. The results with Aβ deposition was compared with the serum levels of phosphorus. The subjects with cerebral Aβ deposition showed lower levels of serum phosphorus than those without Aβ deposition. Furthermore, multiple regression analyses showed that a low level of serum phosphorus correlated with cerebral Aβ deposition, even when age, sex, apolipoprotein E ε4 genotype, and MMSE z-score were controlled for. Serum levels of other ions, including calcium, iron, zinc, and copper, showed no such correlation. In conclusion, our results suggest that the serum level of phosphorus may be used as an easily accessible blood biomarker for cerebral Aβ deposition in a cognitively impaired population. Alzheimer's disease (AD), characterized by progressive cognitive decline, is the most prevalent neurodegenerative disease in the elderly. Cerebral β-amyloid (Aβ) deposition is the major pathological hallmark of AD. Recent studies also have shown that the serum level of phosphorus correlates to the risk of incident dementia. To date, the linkage between cerebral Aβ deposition and the serum phosphorus level remains unknown. In this study, we analyzed the levels of serum phosphorus in 109 mild cognitive impairment (MCI) and 73 AD dementia (ADD) subjects. All subjects underwent Pittsburgh compound B positron emission tomography (PiB-PET) imaging to measure cerebral Aβ deposition. The results with Aβ deposition was compared with the serum levels of phosphorus. The subjects with cerebral Aβ deposition showed lower levels of serum phosphorus than those without Aβ deposition. Furthermore, multiple regression analyses showed that a low level of serum phosphorus correlated with cerebral Aβ deposition, even when age, sex, apolipoprotein E ε4 genotype, and MMSE z-score were controlled for. Serum levels of other ions, including calcium, iron, zinc, and copper, showed no such correlation. In conclusion, our results suggest that the serum level of phosphorus may be used as an easily accessible blood biomarker for cerebral Aβ deposition in a cognitively impaired population.Alzheimer's disease (AD), characterized by progressive cognitive decline, is the most prevalent neurodegenerative disease in the elderly. Cerebral β-amyloid (Aβ) deposition is the major pathological hallmark of AD. Recent studies also have shown that the serum level of phosphorus correlates to the risk of incident dementia. To date, the linkage between cerebral Aβ deposition and the serum phosphorus level remains unknown. In this study, we analyzed the levels of serum phosphorus in 109 mild cognitive impairment (MCI) and 73 AD dementia (ADD) subjects. All subjects underwent Pittsburgh compound B positron emission tomography (PiB-PET) imaging to measure cerebral Aβ deposition. The results with Aβ deposition was compared with the serum levels of phosphorus. The subjects with cerebral Aβ deposition showed lower levels of serum phosphorus than those without Aβ deposition. Furthermore, multiple regression analyses showed that a low level of serum phosphorus correlated with cerebral Aβ deposition, even when age, sex, apolipoprotein E ε4 genotype, and MMSE z-score were controlled for. Serum levels of other ions, including calcium, iron, zinc, and copper, showed no such correlation. In conclusion, our results suggest that the serum level of phosphorus may be used as an easily accessible blood biomarker for cerebral Aβ deposition in a cognitively impaired population. |
Author | Mook-Jung, Inhee Park, Jong-Chan Park, Kyua Lee, Jun Ho Lee, Dong Young Byun, Min S. Yi, Dahyun Han, Sun-Ho |
AuthorAffiliation | 3 Institute of Human Behavioral Medicine, Medical Research Center Seoul National University , Seoul , South Korea 5 Department of Biology, College of Arts & Sciences, University of Pennsylvania , Pennsylvania, PA , United States 4 Department of Neuropsychiatry, Seoul National University Hospital , Seoul , South Korea 1 Department of Biochemistry and Biomedical Sciences, College of Medicine, Seoul National University , Seoul , South Korea 2 Neuroscience Research Institute, College of Medicine, Seoul National University , Seoul , South Korea 6 Department of Psychiatry, Seoul National University College of Medicine , Seoul , South Korea |
AuthorAffiliation_xml | – name: 3 Institute of Human Behavioral Medicine, Medical Research Center Seoul National University , Seoul , South Korea – name: 6 Department of Psychiatry, Seoul National University College of Medicine , Seoul , South Korea – name: 2 Neuroscience Research Institute, College of Medicine, Seoul National University , Seoul , South Korea – name: 4 Department of Neuropsychiatry, Seoul National University Hospital , Seoul , South Korea – name: 1 Department of Biochemistry and Biomedical Sciences, College of Medicine, Seoul National University , Seoul , South Korea – name: 5 Department of Biology, College of Arts & Sciences, University of Pennsylvania , Pennsylvania, PA , United States |
Author_xml | – sequence: 1 givenname: Jong-Chan surname: Park fullname: Park, Jong-Chan – sequence: 2 givenname: Sun-Ho surname: Han fullname: Han, Sun-Ho – sequence: 3 givenname: Min S. surname: Byun fullname: Byun, Min S. – sequence: 4 givenname: Dahyun surname: Yi fullname: Yi, Dahyun – sequence: 5 givenname: Jun Ho surname: Lee fullname: Lee, Jun Ho – sequence: 6 givenname: Kyua surname: Park fullname: Park, Kyua – sequence: 7 givenname: Dong Young surname: Lee fullname: Lee, Dong Young – sequence: 8 givenname: Inhee surname: Mook-Jung fullname: Mook-Jung, Inhee |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/29163142$$D View this record in MEDLINE/PubMed |
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ContentType | Journal Article |
Copyright | 2017. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. Copyright © 2017 Park, Han, Byun, Yi, Lee, Park, Lee and Mook-Jung for the KBASE Research Group. 2017 Park, Han, Byun, Yi, Lee, Park, Lee and Mook-Jung for the KBASE Research Group |
Copyright_xml | – notice: 2017. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. – notice: Copyright © 2017 Park, Han, Byun, Yi, Lee, Park, Lee and Mook-Jung for the KBASE Research Group. 2017 Park, Han, Byun, Yi, Lee, Park, Lee and Mook-Jung for the KBASE Research Group |
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Keywords | blood-based biomarker KBASE mild cognitive impairment PiB-PET Alzheimer's disease phosphorus β-amyloid |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 Edited by: Fatima Nasrallah, The University of Queensland, Australia Information on the KBASE Research Group is provided in the Appendix (in Supplementary materials). Reviewed by: Rolf Andreas Heckemann, University of Gothenburg, Sweden; Douglas Watt, Boston University School of Medicine, United States These authors have contributed equally to this work. |
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Snippet | Alzheimer's disease (AD), characterized by progressive cognitive decline, is the most prevalent neurodegenerative disease in the elderly. Cerebral β-amyloid... Alzheimer’s disease (AD), characterized by progressive cognitive decline, is the most prevalent neurodegenerative disease in the elderly. Cerebral β-amyloid... |
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SubjectTerms | Age Aluminum Alzheimer's disease Apolipoprotein E Biomarkers Brain research Calcium Cognitive ability Dementia Dementia disorders Genotypes Geriatrics KBASE Medicine Memory mild cognitive impairment Neurodegeneration Neurodegenerative diseases Neuroscience NMR Nuclear magnetic resonance Pathogenesis Peptides Phosphorus PiB-PET Positron emission tomography Serum levels β-Amyloid |
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Title | Low Serum Phosphorus Correlates with Cerebral Aβ Deposition in Cognitively Impaired Subjects: Results from the KBASE Study |
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