Abstract
BackgroundClinical heart failure frequently coexists with CKD and may precipitate kidney function decline. However, whether earlier-stage myocardial dysfunction assessable by speckle-tracking echocardiography (STE) is a contributor to kidney function decline remains unknown.MethodsWe studied 2135 Cardiovascular Health Study participants who were free of clinical heart failure and had year 2 baseline 2D-STE and two measurements of eGFR (year 2 and year 9). "Archival" speckle tracking of digitized echocardiogram videotapes was used to measure left ventricular longitudinal strain (LVLS), LV early diastolic strain rate (EDSR), left atrial reservoir strain (LARS), right ventricular free wall strain (RVFWS), and mitral annular velocity (e′). Multivariable Poisson regression models that adjusted for demographics and cardiovascular risk factors (RFs) were used to investigate the independent associations of cardiac mechanics indices and decline in kidney function defined as a 30% decline in eGFR over 7 years.ResultsIn RF models, LVLS, EDSR, RVFWS, and e′ were all significantly associated with the prevalence of kidney disease. After multivariable adjustment, left atrial dysfunction (relative risk [RR], 1.18; 95% confidence interval [CI], 1.01 to 1.38 per SD lower LARS) and left ventricular diastolic dysfunction (RR, 1.21; 95% CI, 1.04 to 1.41 per SD lower EDSR) were each significantly associated with 30% decline in eGFR.ConclusionsSubclinical myocardial dysfunction suggesting abnormal diastolic function detected by 2D-STE was independently associated with decline in kidney function over time. Further studies are needed to understand the mechanisms of these associations and to test whether interventions that may improve subclinical myocardial dysfunction can prevent decline of kidney function.
Original language | English (US) |
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Pages (from-to) | 622-630 |
Number of pages | 9 |
Journal | Kidney360 |
Volume | 4 |
Issue number | 5 |
DOIs | |
State | Published - May 1 2023 |
Funding
This research was supported by contracts HHSN268201200036C, HHSN268200800007C, HHSN268201800001C, N01HC55222, N01HC85079, N01HC85080, N01HC85081, N01HC85082, N01HC85083, N01HC85086, 75N92021D00006, and grants U01HL080295 and U01HL130114 from the National Heart, Lung, and Blood Institute (NHLBI), with additional contribution from the National Institute of Neurological Disorders and Stroke (NINDS). Additional support was provided by R01AG023629 from the National Institute on Aging (NIA). A full list of principal CHS investigators and institutions can be found at CHS-NHLBI.org . This study was also supported by grants P30DK114857, K23HL150236 (RM), R01DK102438 (TI), U54 HL160273 (SJS), R01 HL107577 (SJS), R01 HL127028 (SJS), R01 HL140731 (S.J. Shah), and R01 HL149423 (S.J. Shah), American Heart Association #16SFRN28780016 (S.J. Shah) and #19TPA34890060 (S.S. Khan). Research reported in this publication was also supported, in part, by the National Institutes of Health's National Center for Advancing Translational Sciences, Grant Number KL2TR001424. Acknowledgments This research was supported by contracts HHSN268201200036C, HHSN268200800007C, HHSN268201800001C, N01HC55222, N01HC85079, N01HC85080, N01HC85081, N01HC85082, N01HC85083, N01HC85086, 75N92021D00006, and grants U01HL080295 and U01HL130114 from the National Heart, Lung, and Blood Institute (NHLBI), with additional contribution from the National Institute of Neurological Disorders and Stroke (NINDS). Additional support was provided by R01AG023629 from the National Institute on Aging (NIA). A full list of principal CHS investigators and institutions can be found at CHS-NHLBI.org. This study was also supported by grants P30DK114857, K23HL150236 (RM), R01DK102438 (TI), U54 HL160273 (SJS), R01 HL107577 (SJS), R01 HL127028 (SJS), R01 HL140731 (S.J. Shah), and R01 HL149423 (S.J. Shah), American Heart Association 16SFRN28780016 (S.J. Shah) and 19TPA34890060 (S.S. Khan). Research reported in this publication was also supported, in part, by the National Institutes of Health's National Center for Advancing Translational Sciences, Grant Number KL2TR001424.
Keywords
- cardiac mechanics
- diastolic dysfunction
- heart failure
- kidney disease
ASJC Scopus subject areas
- Nephrology
- Medicine (miscellaneous)
- General Medicine