Evidence map›Paper›PMID 41507830›Full record

Observational studyBMC nephrology2026

Renal clearance of endogenous lithium as a marker of proximal tubule function in sepsis and sepsis-associated acute kidney injury : A prospective single-centre study.

Kjellbjørn Jakobsen, Hendrik Backmann, Njål Gunnar Nicolaysen, Rasmus Zahn, Sandra Huber, Vegard Skogen, Anders Benjamin Kildal, Lars Marius Ytrebø

Registry-linked trialAbstract readObservational Study
In one paragraph

Observational study in BMC nephrology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05982340 (Endogenous Lithium Clearance in Acute Kidney Injury), which is not on this map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT05982340 completednot on this map

Endogenous Lithium Clearance in Acute Kidney Injury

TypeobservationalSponsorUniversity Hospital of North NorwayRan2023 to 2025Enrolled20ConditionsAcute Kidney Injury Due to Sepsis, Proximal Tubule Function, Lithium ClearanceArmsLithium clearance
3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Kjellbjørn JakobsenAnesthesia and Critical Care Research Group, UiT - The Arctic University of Norway, Tromsø, Norway. kjellbjorn.jakobsen@uit.no.
Hendrik BackmannAnesthesia and Critical Care Research Group, UiT - The Arctic University of Norway, Tromsø, Norway.
Njål Gunnar NicolaysenAnesthesia and Critical Care Research Group, UiT - The Arctic University of Norway, Tromsø, Norway.
Rasmus ZahnAnesthesia and Critical Care Research Group, UiT - The Arctic University of Norway, Tromsø, Norway.
Sandra HuberDepartment of Laboratory Medicine, Division of Diagnostic Services, University Hospital of North Norway, Tromsø, Norway.
Vegard SkogenDepartment of Infectious Diseases, Division of Internal Medicine, University Hospital of North Norway, Tromsø, Norway.
Anders Benjamin KildalAnesthesia and Critical Care Research Group, UiT - The Arctic University of Norway, Tromsø, Norway.
Lars Marius YtrebøAnesthesia and Critical Care Research Group, UiT - The Arctic University of Norway, Tromsø, Norway.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCritically ill patients are at high risk of developing acute kidney injury (AKI). Precise functional biomarkers may be useful for monitoring renal tubular function in patients at risk of sepsis-associated AKI (SA-AKI) and to study its pathophysiology in vivo in humans. Lithium is passively reabsorbed in parallel with, and in proportion to, the reabsorption of sodium and water in the proximal tubule. The unreabsorbed fraction is almost entirely excreted in urine, and the fractional excretion of lithium thus provides a semiquantitative estimate of proximal sodium reabsorption. We hypothesized that endogenous lithium reabsorption is impaired in the early stages of SA-AKI. The aim of study was to measure renal clearance of endogenous lithium in patients with SA-AKI and in patients with sepsis without AKI.

methodsTen patients with SA-AKI and eight patients with non-AKI sepsis were studied, all without premorbid chronic kidney disease. Blood and urine samples were obtained at 8 AM, 2 PM and 8 PM over the course of a single study day and within the first 48 h after admission to the intensive care unit. Fractional excretion of lithium (FELi) was calculated, and linear mixed-effects model statistics were applied to analyse data.

resultsFELi was higher in the SA-AKI group compared with the non-AKI group (estimated mean difference 8.26%, p = 0.008) with median (interquartile range) FELi 7.5 (4.6–14.8) % and 3.0 (1.3–4.5) %, respectively. Excluding patients receiving diuretics did not alter the estimated mean FELi difference (8.79%, p = 0.004). Baseline estimated glomerular filtration rate, mean arterial pressure, and peak values for C-reactive protein were similar between groups (p = 0.98, 0.43, and 0.52, respectively). SOFA score and peak creatinine concentration during the entire hospital stay were significantly higher in the SA-AKI group (p < 0.001).

conclusionsThe results indicate an efficient proximal tubular sodium reabsorption in the sepsis group without AKI, and significantly lower reabsorption in the SA-AKI group. Measurement of endogenous lithium clearance may become useful for studies of proximal tubule function in critically ill patients.

trial registrationThe study was registered at www.clinicaltrials.gov (NCT05982340). Date of registration: 31.7.2023.

Indexed as

Acute Kidney InjuryKidney Tubules, ProximalLithiumSepsisAgedBiomarkersFemaleHumansMaleMiddle AgedProspective StudiesBiomarkersLithiumAcute kidney injuryCritical illnessGlomerular filtration rateICUKidney tubules, proximalLithiumSepsis

Identifiers

PMID41507830
PMCPMC12874695

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.