Cited by 6Dementia and Cognitive Impairment ResearchAcute Myeloid Leukemia ResearchAlzheimer's disease research and treatments

Association Between Clonal Hematopoiesis of Indeterminate Potential and Brain β-Amyloid Deposition in Korean Patients With Cognitive Impairment

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Yun, Jiwon, Youn, Young Chul, Kim, Hye Ryoun·2024·Annals of Laboratory Medicine

Abstract

and the C:G>T:A single-nucleotide variants were identified as the primary characteristics, which reflect aged hematopoiesis in the study population. Multivariate logistic regression revealed that the presence of CHIP was not associated with brain Aβ deposition. As both CHIP and brain Aβ deposition are associated with aging, further research is required to elucidate their possible interplay.

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Crossref · 10.3343/alm.2024.0086

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  • Yun et al. reported no significant association between CHIP and brain β-amyloid deposition in a small underpowered cohort of 58 participants.

    “Yun et al., examining a small cohort of Korean patients with cognitive impairment using amyloid positron emission tomography imaging, reported no significant association between CHIP and brain β-amyloid deposition; however, this analysis was critically underpowered with only 58 participants [12].”

    From Clonal Hematopoiesis of Indeterminate Potential as an Emerging Interdisciplinary Risk Factor in Alzheimer’s Disease: Current Evidence and Future Directions (2026) · cites this paper as [12]

    The Abstract reports 58 Korean patients with cognitive impairment who underwent amyloid PET, and the analysis found no significant association between CHIP and brain Aβ deposition. The limitations passage calls the study preliminary and says statistical power may have been insufficient, but it reports no power calculation; it does not establish that the analysis was critically underpowered. (LLM, conf=0.87)

    Experimental — accuracy not yet measured
  • Smaller biomarker-focused cohorts and genotype-stratified sequencing projects report either neutral effects or an increased risk of AD pathology.

    “smaller, biomarker-focused cohorts (n < 100) and specific genotype-stratified sequencing projects (n ≈ 30,000) indicate a different trajectory, reporting either neutral effects or an increased risk of AD pathology [12,13].”

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Authors
Yun, J., Youn, Y. C., & Kim, H. R.
Affiliations
  • Korea University (KR)
  • Chung-Ang University Healthcare System (KR)
  • Chung-Ang University Hospital (KR)
Corresponding author
Kim, Hye Ryoun
Venue
Annals of Laboratory Medicine
Published
2024-05-28
Volume
44
Issue
6
Pages
576-580
ISSN
  • 2234-3806 (ISSN-L)
  • 2234-3814
OpenAlex
W4399100120
Cited by
6
References
17
Citations by year
2026: 2 · 2025: 4
FWCI
1.76
Type
journal article
Language
en
Open access
Locations
  • Annals of Laboratory Medicine (publishedVersion, cc-by-nc)
  • PubMed Central (publishedVersion, cc-by-nc)
  • PubMed (publishedVersion)
Funders
  • National Research Foundation of Korea (NRF-2017R1A2B4011631, 2021R1A2C2013359)
  • Ministry of Science and ICT, South Korea
Topics
  • Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
  • Health Sciences › Medicine › Hematology › Acute Myeloid Leukemia Research
  • Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
Keywords
clonal hematopoiesis of indeterminate potential, cognitive impairment, single nucleotide variants, aging, hematopoiesis, Alzheimer's disease, Korean patients
MeSH terms
Clonal Hematopoiesis, DNA Methyltransferase 3A, East Asian People, Aged, Aged, 80 and over, Alzheimer Disease, Brain, DNA (Cytosine-5-)-Methyltransferases, Female, Humans, Male, Middle Aged, Mutation, Logistic Models, Amyloid beta-Peptides, Polymorphism, Single Nucleotide, Asian People, Positron-Emission Tomography, Republic of Korea, High-Throughput Nucleotide Sequencing, Cognitive Dysfunction

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