Dietary lithium intake, graft failure and mortality in kidney transplant recipients

ABSTRACT Background Long-term high-dose lithium therapy in bipolar disorder is known to adversely affect kidney function. However, recent animal studies have revealed that low amounts of lithium are beneficial for the kidney when it is damaged by exposure to nephrotoxic compounds, inflammation or ox...

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Veröffentlicht in:Nephrology, dialysis, transplantation dialysis, transplantation, 2023-07, Vol.38 (8), p.1867-1879
Hauptverfasser: Post, Adrian, Kremer, Daan, Groothof, Dion, Seidel, Ulrike, Huebbe, Patricia, Franssen, Casper F M, Kema, Ido P, Lüersen, Kai, Rimbach, Gerald, Bakker, Stephan J L
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Sprache:eng
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Zusammenfassung:ABSTRACT Background Long-term high-dose lithium therapy in bipolar disorder is known to adversely affect kidney function. However, recent animal studies have revealed that low amounts of lithium are beneficial for the kidney when it is damaged by exposure to nephrotoxic compounds, inflammation or oxidative stress. This study aimed to investigate whether urinary lithium excretion, reflecting dietary lithium intake, is associated with adverse long-term kidney graft outcomes and patient survival. Methods Urinary lithium concentration was measured using inductively coupled plasma mass spectrometry in 642 stable kidney transplant recipients (KTRs). Graft failure was defined as the start of dialysis or retransplantation and kidney function decline was defined as a doubling of serum creatinine. Results The median urinary lithium excretion was 3.03 μmol/24 h [interquartile range (IQR) 2.31–4.01]. Urinary lithium excretion was associated with energy, plant protein and water intake. During a median follow-up of 5.3 years (IQR 4.5–6.0), 79 (12%) KTRs developed graft failure and 127 (20%) KTRs developed kidney function decline. Higher urinary lithium excretion was associated with a lower risk of graft failure {hazard ratio [HR] per doubling 0.54 [95% confidence interval (CI) 0.38–0.79]} and kidney function decline [HR per doubling 0.73 (95% CI 0.54–0.99)]. These associations remained independent of adjustment for potential confounders and in sensitivity analyses. There was a significant effect modification with the use of proliferation inhibitors (P = .05) and baseline estimated glomerular filtration rate (eGFR; P 
ISSN:0931-0509
1460-2385
DOI:10.1093/ndt/gfac340