4.4 Article

Effects of acute kidney injury and chronic hypoxemia on fibroblast growth factor 23 levels in pediatric cardiac surgery patients

Journal

PEDIATRIC NEPHROLOGY
Volume 31, Issue 4, Pages 661-669

Publisher

SPRINGER
DOI: 10.1007/s00467-015-3257-5

Keywords

Fibroblast growth factor 23; Acute kidney injury; Chronic hypoxemia; Pediatrics; Cardiac surgery

Funding

  1. USPHS [DK-67563, DK-35423, DK-80984]
  2. CTSI Grant [UL1 TR-000124]
  3. NIH K12 Child Health Research Career Development Award [K12-HD-034610]
  4. NIH Training Grant [T32-DK-07789]
  5. UCLA Children's Discovery and Innovation Institute
  6. American Society of Nephrology Norman Siegel Foundation

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Background Fibroblast growth factor-23 (FGF23) levels are elevated in cardiopulmonary bypass (CPB)-associated acute kidney injury (AKI); however, it is unknown how much of the circulating FGF23 is intact and bioactive. Hypoxia may induce FGF23 production, yet its impact in humans is unknown. Pediatric cardiac surgery patients have both a high incidence of CPB-associated AKI and a high prevalence of chronic hypoxemia. Methods We assessed the effects of hypoxemia and CPB-associated AKI on C-terminal FGF23 (cFGF23) and intact FGF23 (iFGF23) levels in 32 pediatric cardiac surgery patients with normal estimated glomerular filtration rate (eGFR). Plasma cFGF23 and iFGF23 were measured preoperatively and serially postoperatively. Results Despite normal renal and ventricular function, preoperative cFGF23 levels were high and elevated out of proportion to iFGF23 levels. Preoperative oxygen saturation measurements correlated inversely with FGF23 levels. Preoperative cFGF23 and oxygen saturation both predicted postoperative AKI. Postoperatively, cFGF23 and iFGF23 increased by 2 h postreperfusion; iFGF23 then returned to baseline, but cFGF23 remained elevated through 24 h postreperfusion. Group status (AKI vs. non-AKI) modified the effect of time on changes in iFGF23 levels but not cFGF23 levels. Conclusions Preoperative cFGF23 may predict CPBassociated kidney dysfunction. Changes over time in cFGF23 and iFGF23 levels post-CPB differ. Chronic hypoxemia may affect FGF23 production in humans.

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