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Cited 3 time in webofscience Cited 3 time in scopus
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Independent effect of body mass index variation on amyloid-beta positivityopen access

Authors
Kang, Sung HoonKim, Jong HyukChang, YoosooCheon, Bo KyoungChoe, Yeong SimJang, HyeminKim, Hee JinKoh, Seong-BeomNa, Duk L.Kim, KyungaSeo, Sang Won
Issue Date
Jul-2022
Publisher
Frontiers Media S.A.
Keywords
amyloid-beta (A beta); body mass index (BMI); BMI change; BMI variability; Alzheimer's disease
Citation
Frontiers in Aging Neuroscience, v.14
Indexed
SCIE
SCOPUS
Journal Title
Frontiers in Aging Neuroscience
Volume
14
URI
https://scholarworks.korea.ac.kr/kumedicine/handle/2021.sw.kumedicine/61391
DOI
10.3389/fnagi.2022.924550
ISSN
1663-4365
1663-4365
Abstract
Objectives: The relationship of body mass index (BMI) changes and variability with amyloid-β (Aβ) deposition remained unclear, although there were growing evidence that BMI is associated with the risk of developing cognitive impairment or AD dementia. To determine whether BMI changes and BMI variability affected Aβ positivity, we investigated the association of BMI changes and BMI variability with Aβ positivity, as assessed by PET in a non-demented population. Methods: We retrospectively recruited 1,035 non-demented participants ≥50 years of age who underwent Aβ PET and had at least three BMI measurements in the memory clinic at Samsung Medical Center. To investigate the association between BMI change and variability with Aβ deposition, we performed multivariable logistic regression. Further distinctive underlying features of BMI subgroups were examined by employing a cluster analysis model. Results: Decreased (odds ratio [OR] = 1.68, 95% confidence interval [CI] 1.16–2.42) or increased BMI (OR = 1.60, 95% CI 1.11–2.32) was associated with a greater risk of Aβ positivity after controlling for age, sex, APOE e4 genotype, years of education, hypertension, diabetes, baseline BMI, and BMI variability. A greater BMI variability (OR = 1.73, 95% CI 1.07–2.80) was associated with a greater risk of Aβ positivity after controlling for age, sex, APOE e4 genotype, years of education, hypertension, diabetes, baseline BMI, and BMI change. We also identified BMI subgroups showing a greater risk of Aβ positivity. Conclusion: Our findings suggest that participants with BMI change, especially those with greater BMI variability, are more vulnerable to Aβ deposition regardless of baseline BMI. Furthermore, our results may contribute to the design of strategies to prevent Aβ deposition with respect to weight control.
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Koh, Seong Beom
Guro Hospital (Department of Neurology, Guro Hospital)
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