Sheng, Zehu
Wang, Lanyang
Chen, Ming
Zhong, Fuxin
Wu, Shijing
Liang, Shuyu
Song, Jiaqi
Chen, Lihua
Chen, Yingxi
Chen, Shiyu
Yu, Weihua
Lü, Yang
Funding for this research was provided by:
Chongqing Talent Plan (cstc2022ycjh-bgzxm0184, cstc2022ycjh-bgzxm0184)
Key Project of Science and Technology Research Program of Chongqing Municipal Education Commission (KJZD-K202200405, KJZD-K202200405)
Science Innovation Programs Led by the Academicians in Chongqing under Project (2022YSZX-JSX0002CSTB, 2022YSZX-JSX0002CSTB)
STI2030-Major Projects (No. 2021ZD0201802, No. 2021ZD0201802)
Program for Youth Innovation in Future Medicine, Chongqing Medical University (W0166, W0166)
Article History
Received: 24 September 2024
Accepted: 23 December 2024
First Online: 2 January 2025
Declarations
:
: ADNI was approved by the Institutional Review Boards of all participating institutions. All participants provided written informed consent by the Declaration of Helsinki before study enrollment. All study participants, authorized representatives, and study partners have provided written informed consent, and each participating site of ADNI has obtained the necessary ethical permits. More details can be found at adni.loni.usc.edu.ADNI study is conducted in compliance with the protocol, by GCP guidelines, and in full conformity with Regulations for the Protection of Human Subjects of Research codified in 45 CFR Part 46—Protection of Human Subjects, 21 CFR Part 50—Protection of Human Subjects, 21 CFR Part 56—IRBs, and/or the ICH E6, HIPAA, State and Federal regulations and all other applicable local regulatory requirements and laws. Study personnel involved in conducting this study will be qualified by education, training, and experience to perform their respective task(s) by GCP. Informed consent will be obtained by US 21 CFR 50.25, the Tri-Council Policy Statement: Ethical Conduct of Research Involving Humans and the Health Canada and ICH Good Clinical Practice. Applicable HIPAA privacy notifications will be implemented, and HIPAA authorizations signed before protocol procedures are carried out. Information should be given in both oral and written form as deemed appropriate by the site’s IRB.All work complied with ethical regulations for working with human participants. Ethics approval was obtained from the institutional review boards of each institution involved: Oregon Health and Science University; University of Southern California; University of California—San Diego and so on.
: Not applicable.
: The authors declare no competing interests.