# Association of Phenylacetylglutamine and Cognitive Impairment in CKD

**Authors:** Hélène Levassort, Julie Boucquemont, Sophie Liabeuf, Solène M. Laville, Céline Lange, Luc Frimat, Christian Combe, Denis Fouque, Maurice Laville, Christian Jacquelinet, Yves-Edouard Herpe, Islam Amine Larabi, Jean-Claude Alvarez, Natalia Alencar de Pinho, Marion Pépin, Ziad A. Massy, Natalia Alencar de Pinho, Natalia Alencar de Pinho, Dorothée Cannet, Christian Combe, Denis Fouque, Luc Frimat, Aghilès Hamroun, Yves-Edouard Herpe, Christian Jacquelinet, Maurice Laville, Sophie Liabeuf, Ziad A. Massy, Pascal Morel, Christophe Pascal, Roberto Pecoits-Filho, Joost Schanstra, Bénédicte Stengel, Céline Lange, Oriane Lambert, Marie Metzger

PMC · DOI: 10.1016/j.ekir.2025.05.037 · 2025-05-29

## TL;DR

This study finds that higher levels of phenylacetylglutamine in CKD patients are linked to cognitive impairment, suggesting a new potential target for treatment.

## Contribution

The study identifies phenylacetylglutamine as a new uremic toxin associated with cognitive impairment in nondialysis-dependent CKD patients.

## Key findings

- A 2-fold increase in PAG levels was associated with cognitive impairment after adjusting for multiple factors.
- 908 out of 2590 patients (35%) had an MMSE score indicating cognitive impairment.
- The association remained significant even after accounting for other known uremic toxins and risk factors.

## Abstract

Chronic kidney disease (CKD) leads to the accumulation of uremic toxins (UTs). Studies have suggested that UTs are associated with cognitive impairment (CI) in patients with CKD. Recently, studies reported that phenylacetylglutamine (PAG) contributes to the association between CKD and CI. However, this association has not been investigated in nondialysis-dependent adults with CKD.

The CKD–Renal Epidemiology and Information Network (CKD-REIN) cohort study included 3033 patients with CKD stages 2 to 5. This cross-sectional analysis included those with a PAG measurement and a mini-mental state examination (MMSE) score within 3 months of each other. CI was defined as an MMSE score ≤ 26 out of 30. Logistic regression was used to assess the association between PAG and CI.

Of the 2590 patients included (mean [SD] age: 67 [13] years, mean [SD] estimated glomerular filtration rate [eGFR]: 34 [13] ml/min per 1.73 m2, median [interquartile range, IQR] PAG level: 2.1 [1.2–3.6] mg/l), 908 (35%) presented an MMSE score ≤ 26 out of 30. After adjustment for sociodemographic factors (age, male sex, and educational level), cardiovascular risk factors, cerebrovascular disease, current depression, eGFR, urinary albumin-to-creatinine ratio (uACR), and UTs known to be associated with CI risk, a 2-fold increase in the PAG level was associated with CI (odds ratio [OR] [95% confidence interval]: 1.12 [1.01–1.23]).

This study shows that a higher serum PAG level was associated with CI in nondialysis-dependent adults with CKD and highlight a new UT associated with CI in patients with CKD. Further studies are needed to confirm the causal nature of the association and to explore strategies for reducing serum PAG levels to protect cognition.

## Linked entities

- **Chemicals:** phenylacetylglutamine (PubChem CID 92258), uric acid (PubChem CID 1175), indoxyl sulfate (PubChem CID 10258), p-cresyl sulfate (PubChem CID 4615423)
- **Diseases:** chronic kidney disease (MONDO:0005300), cardiovascular disease (MONDO:0004995), cerebrovascular disease (MONDO:0011057), depression (MONDO:0002050)

## Full-text entities

- **Genes:** ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}
- **Diseases:** CI (MESH:D003072), depression (MESH:D003866), cerebrovascular disease (MESH:D002561), uremic (MESH:D006463), CKD (MESH:D051436)
- **Chemicals:** creatinine (MESH:D003404), PAG (MESH:C003089)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12348181/full.md

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Source: https://tomesphere.com/paper/PMC12348181