TY - JOUR
T1 - Sleep, cardiovascular risk factors, and kidney function
T2 - The Multi-Ethnic Study of Atherosclerosis (MESA)
AU - Chen, Jinsong
AU - Ricardo, Ana C.
AU - Reid, Kathryn J.
AU - Lash, James
AU - Chung, Joon
AU - Patel, Sanjay R.
AU - Daviglus, Martha L.
AU - Huang, Tianyi
AU - Liu, Lei
AU - Hernandez, Rosalba
AU - Li, Quefeng
AU - Redline, Susan
N1 - Funding Information:
MESA is conducted and supported by the National Heart, Lung, and Blood Institute (NHLBI) in collaboration with MESA investigators. Support for MESA is provided by contracts HHSN268201500003I, N01-HC-95159, N01-HC-95160, N01-HC-95161, N01-HC-95162, N01-HC-95163, N01-HC-95164, N01-HC-95165, N01-HC-95166, N01-HC-95167, N01-HC-95168, N01-HC-95169, UL1-TR-000040, UL1-TR-001079, UL1-TR-001881, and DK06349. Funding support for the MESA Sleep Exam was provided by grant HL56984. A full list of participating MESA investigators and institutions can be found at http://www.mesa-nhlbi.org. Dr Susan Redline is partly funded through the National Heart, Lung, and Blood Institute (1R35 HL135818-01).T.Huang is supported by K01 HL143034.
Funding Information:
Dr Patel reports grants and personal fees from Philips Respironics, grants and personal fees from Bayer Pharmaceuticals, personal fees from NovaResp Technologies, grants from Sommetrics, grants from Respicardia, outside the submitted work. Dr Martha Daviglus reports grants from National Institutes of Health (NIH), during the conduct of the study. Dr Susan Redline reports grants from NIH, during the conduct of the study; personal fees from Apnimed Inc, grants and personal fees from Jazz Pharma, personal fees from Eli Lilly, outside the submitted work.
Funding Information:
MESA is conducted and supported by the National Heart, Lung, and Blood Institute (NHLBI) in collaboration with MESA investigators. Support for MESA is provided by contracts HHSN268201500003I, N01-HC-95159, N01-HC-95160, N01-HC-95161, N01-HC-95162, N01-HC-95163, N01-HC-95164, N01-HC-95165, N01-HC-95166, N01-HC-95167, N01-HC-95168, N01-HC-95169, UL1-TR-000040, UL1-TR-001079, UL1-TR-001881, and DK06349 . Funding support for the MESA Sleep Exam was provided by grant HL56984 . A full list of participating MESA investigators and institutions can be found at http://www.mesa-nhlbi.org . Dr Susan Redline is partly funded through the National Heart, Lung, and Blood Institute ( 1R35 HL135818-01 ).T.Huang is supported by K01 HL143034 .
Publisher Copyright:
© 2022 National Sleep Foundation
PY - 2022
Y1 - 2022
N2 - Objectives: Examine the associations of sleep measures with kidney function changes over time among individuals from a community-based study. Methods: The sample includes 1657 participants (287 with chronic kidney disease [CKD]) in the Multi-Ethnic Study of Atherosclerosis Sleep Cohort (mean age: 57.7 years, male: 46.0%). We examined associations between a large set of sleep variables (polysomnography, actigraphy, and questionnaires) and cardiovascular disease risk factors and changes in estimated glomerular filtration rate (eGFR) and urinary albumin-to-creatinine ratio over approximately 5 years using high-dimensional regression. We investigated the modifying effect of sleep on the associations between cardiovascular disease risk factors and kidney function. Results: Sleep metrics predicted kidney function decline only among individuals with baseline CKD. Among this group, eGFR decline was associated with decreased stage N3 sleep (0.32 mL/min/1.73 m2/y per 10% decrease in N3, p < .001); increased actigraphy napping frequency (beta: -0.20 [-0.30, -0.07]); and actigraphy sleep midpoint trajectory in early morning (ref: midnight, beta: -0.84 [-1.19, -0.50]). Urinary albumin-to-creatinine ratio increase was associated with high wake bouts trajectory (ref: low, beta: 0.97 [0.28, 1.67]) and increased sleep-related hypoxemia (oxygen saturation %time<90 [≥5%], beta: 2.17 [1.26, 3.08]). Sleep metrics–N3 sleep, naps, and midpoint trajectory–significantly modified associations between hemoglobin A1C and eGFR decline. Conclusions: Reduced deep sleep, daytime napping, increased wake bouts, delayed sleep rhythms, and overnight hypoxemia are associated with longitudinal kidney function decline, with effects most apparent in individuals with CKD. Deep sleep, napping, and sleep timing modified the association between hemoglobin A1C and kidney function.
AB - Objectives: Examine the associations of sleep measures with kidney function changes over time among individuals from a community-based study. Methods: The sample includes 1657 participants (287 with chronic kidney disease [CKD]) in the Multi-Ethnic Study of Atherosclerosis Sleep Cohort (mean age: 57.7 years, male: 46.0%). We examined associations between a large set of sleep variables (polysomnography, actigraphy, and questionnaires) and cardiovascular disease risk factors and changes in estimated glomerular filtration rate (eGFR) and urinary albumin-to-creatinine ratio over approximately 5 years using high-dimensional regression. We investigated the modifying effect of sleep on the associations between cardiovascular disease risk factors and kidney function. Results: Sleep metrics predicted kidney function decline only among individuals with baseline CKD. Among this group, eGFR decline was associated with decreased stage N3 sleep (0.32 mL/min/1.73 m2/y per 10% decrease in N3, p < .001); increased actigraphy napping frequency (beta: -0.20 [-0.30, -0.07]); and actigraphy sleep midpoint trajectory in early morning (ref: midnight, beta: -0.84 [-1.19, -0.50]). Urinary albumin-to-creatinine ratio increase was associated with high wake bouts trajectory (ref: low, beta: 0.97 [0.28, 1.67]) and increased sleep-related hypoxemia (oxygen saturation %time<90 [≥5%], beta: 2.17 [1.26, 3.08]). Sleep metrics–N3 sleep, naps, and midpoint trajectory–significantly modified associations between hemoglobin A1C and eGFR decline. Conclusions: Reduced deep sleep, daytime napping, increased wake bouts, delayed sleep rhythms, and overnight hypoxemia are associated with longitudinal kidney function decline, with effects most apparent in individuals with CKD. Deep sleep, napping, and sleep timing modified the association between hemoglobin A1C and kidney function.
KW - Albuminuria
KW - Chronic kidney disease
KW - Diabetes
KW - Sleep apnea
KW - Sleep duration
KW - Sleep health
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U2 - 10.1016/j.sleh.2022.08.004
DO - 10.1016/j.sleh.2022.08.004
M3 - Article
C2 - 36216749
AN - SCOPUS:85139664165
SN - 2352-7218
JO - Sleep Health
JF - Sleep Health
ER -