Detailed examination of the relationship between CD34+CD133+ (log-transformed) and the risk of AD/dementia risk
CD34+CD133+ cells plus covariates | AD | All-cause dementia | ||
---|---|---|---|---|
HR (95% CI) | P value | HR (95% CI) | P value | |
Model 1: no covariates | 0.57 (0.40, 0.81)n = 1,617 | 0.002* | 0.57 (0.42, 0.77)n = 1,640 | 0.003* |
Model 2: age, sex, years of education | 0.64 (0.45, 0.93)n = 1,617 | 0.02* | 0.64 (0.47, 0.87)n = 1,640 | 0.005* |
Model 3: Model 2 + APOE ɛ4 + vascular diseases | 0.64 (0.44, 0.94)n = 1,340 | 0.02* | 0.63 (0.45, 0.87)n = 1,362 | 0.006* |
Model 3 after stratification | ||||
No vascular diseasesa | 1.23 (0.15, 10.18)n = 256 | 0.85 | 1.12 (0.19, 6.56)n = 257 | 0.90 |
Peripheral vascular diseasesb only | 0.62 (0.40, 0.94)n = 832 | 0.02* | 0.61 (0.43, 0.88)n = 850 | 0.008* |
Cerebrovascular diseasesc only | 0.58 (0.35, 0.96)n = 628 | 0.03* | 0.53 (0.35, 0.81)n = 641 | 0.003* |
Cox proportional hazards regression models were used to study the relationship between log-transformed CD34+CD133+ cell frequency (%) and the risk of AD or all-cause dementia after adjusting for the covariates. HR with 95% CI with P values is shown. Model 1: simple association without confounders; Model 2: adjusting for age, sex, and education; Model 3: Model 2 + APOE ɛ4 + vascular diseases. a Model 3 after the stratification as no vascular diseases for those with no CHD, no HTN, no stroke, no silent infarct, no CMB, and low level of WMHI; b Model 3 after the stratification as peripheral vascular diseases for those with CHD or HTN; c Model 3 after the stratification as cerebrovascular diseases for those with stroke, silent infarct, CMB, or high level of WMHI; * P value significant < 0.05
The supplementary materials for this article are available at: https://www.explorationpub.com/uploads/Article/file/1001216_sup_1.pdf
We want to express our thanks to the FHS participants for their decades of dedication and to the FHS staff for their hard work in collecting and preparing the data.
YW and J Huang: Data curation, Investigation, Formal analysis, Writing—original draft. TFAA: Data curation, Investigation, Formal analysis, Writing—review & editing. YZ and QT: Data curation, Investigation. JM, MA, GVD, AB, AG, MR, BG, J Han, KLL, and TDS: Formal analysis, Writing—review & editing. RA and LAF: Supervision, Formal analysis, Writing—review & editing. XZ and WQQ: Conceptualization, Writing—review & editing, Methodology, Supervision.
Lindsay A. Farrer who is the Editor-in-Chief of Exploration of Medicine had no involvement in the decision-making or the review process of this manuscript.
The FHS was approved by the Institutional Review Board of Boston University, and all participants provided written informed consent. The ROS and MAP studies were approved by the Institutional Review Board of Rush University Medical Center. All participants signed an informed consent, an Anatomic Gift Act for brain donation, and a repository consent to allow their data and biospecimens to be shared.
Informed consent to participate in the study was obtained from all participants.
Not applicable.
The FHS data is available at dbGaP (https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs000007.v33.p14) upon reasonable request/application. The ROSMAP data is available at the AD Knowledge Portal (https://adknowledgeportal.org). The other datasets that support the findings of this study are available from the corresponding author upon reasonable request.
This study was supported by National Institute on Aging grants [U19-AG068753, RF1-AG057519, and R01-AG048927]. The FHS data collection was supported by the National Heart, Lung, and Blood Institute contract [N01-HC-25195]. The sponsor institutes did not play any role in design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review, or approval of the manuscript; and decision to submit the manuscript for publication.
© The Author(s) 2024.