Evidence map›Paper›PMID 42942739›Full record

ReviewPharmaceutics2026

Beyond Creatinine: D-Amino Acids as Emerging Indicators of Kidney Function and Disease.

Alina Uifălean, Maria Iacobescu, Ximena Maria Mureșan, Simona Codruța Hegheş, Liana Claudia Salanță, Radu-Cristian Moldovan, Cristina-Adela Iuga

Abstract readReview
In one paragraph

Review in Pharmaceutics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the 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.

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

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

7 authors.

Alina UifăleanDepartment of Pharmaceutical Analysis, Faculty of Pharmacy, "Iuliu Hațieganu" University of Medicine and Pharmacy, Louis Pasteur Street 6, 400349 Cluj-Napoca, Romania.ORCID 0000-0003-1297-6345
Maria IacobescuDepartment of Personalized Medicine and Rare Diseases, MEDFUTURE-Institute for Biomedical Research, "Iuliu Hațieganu" University of Medicine and Pharmacy, Louis Pasteur Street 6, 400349 Cluj-Napoca, Romania.ORCID 0000-0002-0659-8926
Ximena Maria MureșanDepartment of Personalized Medicine and Rare Diseases, MEDFUTURE-Institute for Biomedical Research, "Iuliu Hațieganu" University of Medicine and Pharmacy, Louis Pasteur Street 6, 400349 Cluj-Napoca, Romania.
Simona Codruța HegheşDepartment of Pharmaceutical Analysis, Faculty of Pharmacy, "Iuliu Hațieganu" University of Medicine and Pharmacy, Louis Pasteur Street 6, 400349 Cluj-Napoca, Romania.ORCID 0000-0001-7823-4390
Liana Claudia SalanțăDepartment of Food Science, Faculty of Food Science and Technology, University of Agricultural Sciences and Veterinary Medicine Cluj-Napoca, 400372 Cluj-Napoca, Romania.ORCID 0000-0003-2435-405X
Radu-Cristian MoldovanDepartment of Personalized Medicine and Rare Diseases, MEDFUTURE-Institute for Biomedical Research, "Iuliu Hațieganu" University of Medicine and Pharmacy, Louis Pasteur Street 6, 400349 Cluj-Napoca, Romania.ORCID 0000-0002-2847-1301
Cristina-Adela IugaDepartment of Pharmaceutical Analysis, Faculty of Pharmacy, "Iuliu Hațieganu" University of Medicine and Pharmacy, Louis Pasteur Street 6, 400349 Cluj-Napoca, Romania.ORCID 0000-0002-0345-0993

Funding

Iuliu Hațieganu University of Medicine and Pharmacy 32154/4/16.12.2024
6 · The paper itself

Abstract

Despite decades of clinical use, serum creatinine and cystatin C remain imperfect indicators of kidney function, being influenced by muscle mass, age, sex, and inflammation and often showing limited sensitivity to early renal injury. D-amino acids (D-AAs), once largely regarded as by-products of microbial metabolism, have emerged as biologically active chiral metabolites with promising potential for improving the assessment of renal function and disease. This review synthesizes current mechanistic, analytical, and clinical evidence on D-AAs in chronic kidney disease, tracing their origins in diet, gut microbiota, and endogenous racemization through their stereoselective renal transport, tubular handling, and urinary excretion. Among these molecules, D-serine and D-asparagine have emerged as particularly promising biomarkers, showing strong associations with measured glomerular filtration rate and, in early studies, performance comparable or superior to conventional markers, though evidence remains limited to small or selected cohorts, while appearing less dependent on body composition across adult and pediatric populations. Beyond their biomarker potential, D-AAs participate in signaling and metabolic processes linking the gut, kidney, and brain, with altered D-AA homeostasis implicated in both renal injury and uremic neurological dysfunction. We critically examine the biological and clinical confounders, analytical challenges, and validation gaps that currently limit their translation into clinical practice and discuss how chiral metabolomics could contribute to a more precise assessment of kidney function and disease.

Indexed as

biomarkerschiral metabolomicschronic kidney diseaseD-amino acidsD-asparagineD-serinegut–kidney axis

Identifiers

PMID42942739
PMCPMC13708084

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Registered trials

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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.