Evidence map›Paper›PMID 40235627›Full record

ArticleClinical kidney journal2025

Defining normal serum creatinine in pregnancy-results from the AKID UK prospective cohort study.

Laura Skinner, Kate Birnie, Katie A Mettam, Judith P Standing, Amy E Howell, Erik Lenguerrand, Abigail Fraser, Alison J Armitage, Christy Burden, Dominic M Taylor

Abstract read
In one paragraph

Article in Clinical kidney journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Beyond cardiovascular risk: integrating kidney health into the life-course approach to hypertensive disorders of pregnancy.Hypertension research : official journal of the Japanese Society of Hypertension · 2026
    Article
  2. Article
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

10 authors.

Laura SkinnerRichard Bright Renal Service, North Bristol NHS Trust, Bristol, UK.
Kate BirnieMRC Integrative Epidemiology Unit at the University of Bristol, Bristol, UK.
Katie A MettamRichard Bright Renal Service, North Bristol NHS Trust, Bristol, UK.
Judith P StandingRichard Bright Renal Service, North Bristol NHS Trust, Bristol, UK.
Amy E HowellPopulation Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.
Erik LenguerrandPopulation Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.
Abigail FraserMRC Integrative Epidemiology Unit at the University of Bristol, Bristol, UK.ORCID https://orcid.org/0000-0002-7741-9470
Alison J ArmitageRichard Bright Renal Service, North Bristol NHS Trust, Bristol, UK.
Christy BurdenRichard Bright Renal Service, North Bristol NHS Trust, Bristol, UK.
Dominic M TaylorRichard Bright Renal Service, North Bristol NHS Trust, Bristol, UK.ORCID https://orcid.org/0000-0002-1362-2146

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Abnormal kidney function in pregnancy may represent chronic kidney disease or pregnancy-associated acute kidney injury, both associated with adverse outcomes during and after pregnancy. Serum creatinine remains the standard biomarker for kidney function in pregnancy, but normal levels change dynamically through pregnancy and at term. Existing gestation-specific reference ranges for serum creatinine and recommendations to investigate for abnormal kidney function in pregnancy are based on limited data. Data describing trajectories of serum creatinine through pregnancy and the normal, physiological increase in serum creatinine at term are also lacking. Methods: We recruited 476 healthy pregnant individuals aged 16 years or over, 2019-21, measuring serum creatinine in the first, second and third trimesters of pregnancy, at birth and postpartum. Clinical data were abstracted. Gestation-specific reference ranges for serum creatinine were defined as mean ± 1.96 × SD, after excluding those with adverse pregnancy outcomes. Trajectories of serum creatinine through pregnancy, and the change in serum creatinine at delivery were described. Results: 1875 creatinine measurements were recorded. Reference ranges for serum creatinine in the first, second and third trimesters of healthy pregnancy were 37-67 μmol/l (0.42-0.75 mg/dl), 34-63 μmol/l (0.38-0.71 mg/dl), and 34-66 μmol/l (0.39-0.75 mg/dl). Increasing serum creatinine in early pregnancy was more common in those with hypertensive disorders of pregnancy, prior to disease onset. In healthy participants, median serum creatinine increase from 36 weeks to birth was 6.8% (95% CI 4.5%, 9.1%). Conclusions: Investigation for abnormal kidney function in pregnancy should be considered at a lower creatinine threshold than currently recommended. Detecting abnormal creatinine trajectories may help early identification of high-risk pregnancies.

Indexed as

Creatininepre-eclampsiapregnancypregnancy-induced hypertensionreference range

Identifiers

PMID40235627
PMCPMC11997792

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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.