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Authors
Stottlemyer, Britney A.
Abebe, Kaleab Z.
Palevsky, Paul M.
Fried, Linda
Schulman, Ivonne H.
Parikh, Chirag R.
Poggio, Emilio
Siew, Edward D.
Gutierrez, Orlando M.
Horwitz, Edward
Weir, Matthew R.
Wilson, F. Perry
Kane-Gill, Sandra L. https://orcid.org/0000-0001-7523-4846
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Funding
Funding for this research was provided by:
National Institute of Diabetes and Digestive and Kidney Diseases (U01DK130010)
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Article History
Accepted: 18 April 2023
First Online: 24 May 2023
Declarations
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: Ivonne H. Schulman contributed to this manuscript in her personal capacity. The opinions expressed in this article are the author’s own and do not reflect the view of the National Institutes of Health, the Department of Health and Human Services, or the United States Government.
: This study was funded by U01DK130010.
: The author(s) declared the following potential conflicts of interest with respect to the research, authorship, and/or publication of this article: KZA has received support from AKI grant U01DK130010. LF has served as a consultant for Bayer and is a member of the DSMB for Novo Nordisk and CSL Behring. ES serves on the Editorial Board of CJASN and has received royalties as an author for UpToDate. FPW has received support from AKI grants R01DK113191, P30DK079310, and R01HS027626. MRW has served as a scientific advisor for Bayer, AstraZeneca, Boehringer-Ingelheim, Janssen, Merck, and Novo Nordisk. SKG has received support from AKI grants U01DK130010 and R01DK121730-01. Authors BAS, PMP, IHS, CRP, EP, OMG, EH declare that they have no conflicts of interest.
: This study was reviewed by the University of Pittsburgh International Review Board (STUDY21070204) and designated as exempt for minimal risk before study commencement.
: Recruitment materials explained that completion of the survey constituted consent to have the respondent’s de-identified results included in the study, but that the respondent could opt out at any time.
: Recruitment materials explained that completion of the survey constituted consent to have the respondent’s anonymous results included in the study, but that the respondent could opt out at any time.
: Available upon request to the corresponding author.
: Not applicable.
: BS was responsible for concept generation, materials creation, ethics approval, data analysis, manuscript drafting, and revision; KA for concept generation, material review, and manuscript review; PMP for concept generation, material review, manuscript review. LF: concept generation, material review, manuscript review; IS, CP, EP, ES, JF, OMG, EH, MW, and FPW for concept generation and manuscript review; and SKG for concept generation and material review and distribution, manuscript drafting, and revision. All authors read and approved the final version.
