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Authors
Swanson, C. M. https://orcid.org/0000-0003-1554-0862
Blatchford, P. J.
Stone, K. L.
Cauley, J. A.
Lane, N. E.
Rogers-Soeder, T. S.
Redline, S.
Bauer, D. C.
Wright, K. P. Jr
Wierman, M. E.
Kohrt, W. M.
Orwoll, E. S.
,
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Funding
Funding for this research was provided by:
National Institute of Arthritis and Musculoskeletal and Skin Diseases (K23AR070275, U01 AR066160)
U.S. Department of Veterans Affairs (Eastern Colorado VA Geriatric, Research, Education and Clinical Center (GRECC))
National Center for Advancing Translational Sciences (UL1 TR002535)
National Heart, Lung, and Blood Institute (R01HL071194, R01HL070848, R01 HL070847, R01HL070842, R01 HL070841, R01 HL 070837, R01 HL070838, R01HL070839, R35 HL 135818, R01 HL131458, U01 HL150596)
National Institute of Diabetes and Digestive and Kidney Diseases (T32 DK007674, T32 DK007446, R01 DK114272, R01 DK115502)
National Institute on Aging (U01 AG027810, U01 AG042124, U01 AG042139, U01 AG042140, U01 AG042143, U01 AG042145, U01 AG042168, R01 AG030089)
National Heart, Lung, and Blood Institute (R01 HL135598)
Eunice Kennedy Shriver National Institute of Child Health and Human Development (R01 HD087707)
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Article History
Received: 12 May 2020
Accepted: 1 September 2020
First Online: 15 September 2020
Compliance with ethical standards
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: In the interest of full disclosure, we report the following; however, we do not believe any of these pertain to the current work. CMS, PJB, JAC, NEL, TSRS, DCB, MEW, WMK have nothing to disclose. KLS has received grant funding from Merck. SR has received consulting fees from Jazz Pharma, Respircardia and Eisa Inc and grant support from Jazz Pharma (unrelated to this paper). KPW reports research support from the NIH, Office of Naval Research, Pac-12; Financial relationships: consulting fees Circadian Therapeutics, LTD., Circadian Biotherapies, Philips Respironics. Board of Directors: Sleep Research Society. ESO has received research support from or consulting for Amgen, Mereo and Bayer.
: All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. The Institutional Review Board at each clinical site approved the study, and all participants provided written consent. The current analysis used de-identified serum and data and was deemed non-human subject research by the Colorado Multiple Institution Review Board.
: The SAS Code used to generate these results are not publicly available but are available from the corresponding author on reasonable request.
