Useless. You descried a problem, did nothing to specify how to counteract low vitamin D levels; supplements or food and the amounts needed! And then you lazily threw out the further research needed canard, knowing that with NO stroke leadership nothing will occur.
The Moderating Effect of Serum Vitamin D on the Relationship Between Beta-Amyloid Deposition and Neurodegeneration
1Department of Psychiatry, Seoul National University College of Medicine, Seoul, Republic of Korea , 2Department of Neuropsychiatry, Seoul National University Hospital, Seoul, Republic of Korea , 3Seoul National University Dementia Research Center, Seoul, Republic of Korea , 4Institute of Human Behavioral Medicine, Seoul National University Medical Research Center, Seoul, Republic of Korea, 5Interdisciplinary program of cognitive science, Seoul National University College of Humanities, Seoul, Republic of Korea, 6Department of Psychiatry, Chungbuk National University Hospital, Cheongju, Republic of Korea, 7Department of Psychiatry, Keimyung University Dongsan Medical Center, Daegu, Republic of Korea, 8Department of Neuropsychiatry, SMG-SNU Boramae Medical Center, Seoul, Republic of Korea, 9Department of Nuclear Medicine, SMG-SNU Boramae Medical Center, Seoul, Republic of Korea, 10Department of Nuclear Medicine, Seoul National University College of Medicine, Seoul, Republic of Korea , 11Department
of Radiology, Seoul National University Hospital and Seoul National
University College of Medicine, Seoul, Republic of Korea
Received: March 16, 2024; Revised: June 1, 2024; Accepted: June 9, 2024; Published online: June 9, 2024.
© The Korean College of Neuropsychopharmacology. All rights reserved.
Abstract
- Objective:
- Previous studies have reported that vitamin D deficiency increased the
risk of Alzheimer’s disease (AD) dementia in older adults. However,
little is known about how vitamin D is involved in the pathophysiology
of AD. Thus, this study aimed to examine the association and interaction
of serum vitamin D levels with in vivo AD pathologies including
cerebral beta-amyloid (Aβ) deposition and neurodegeneration in
nondemented older adults.
- Methods:
- 428 nondemented older adults were recruited from the Korean
Brain Aging Study for the Early Diagnosis and Prediction of Alzheimer’s
Disease, a prospective cohort that began in 2014. All participants
underwent comprehensive clinical assessments, measurement of serum
25-hydroxyvitamin D (25[OH]D), and multimodal brain imaging including
Pittsburgh compound-B (PiB) positron emission tomography and magnetic
resonance imaging. Global PiB deposition was measured for the Aβ
biomarker. Intracranial volume-adjusted hippocampal volume (HVa) was
used as a neurodegeneration biomarker.
- Results:
- Overall, serum 25(OH)D level was not associated with either Aβ
deposition or HVa after controlling for age, sex, apolipoprotein E ε4
positivity, and vascular risk factors. However, serum 25(OH)D level had a
significant moderation effect on the association between Aβ and
neurodegeneration, with lower serum 25(OH)D level significantly
exacerbating cerebral Aβ-associated hippocampal volume loss (β = 34.612,
p = 0.008).
- Discussion:
- Our findings indicate that lower serum vitamin D levels may contribute to AD by exacerbating Aβ-associated neurodegeneration in nondemented older adults. Further studies to explore the potential therapeutic effect of vitamin D supplementation on the progression of AD pathology will be necessary.
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