Effect of urine alkalization on urinary inflammatory markers in cystinuric patients.

cystinuria inflammation nephrolithiasis urine proteomics

Journal

Clinical kidney journal
ISSN: 2048-8505
Titre abrégé: Clin Kidney J
Pays: England
ID NLM: 101579321

Informations de publication

Date de publication:
Mar 2024
Historique:
received: 22 11 2023
medline: 21 3 2024
pubmed: 21 3 2024
entrez: 21 3 2024
Statut: epublish

Résumé

Cystinuria is associated with a high prevalence of chronic kidney disease (CKD). We previously described a urinary inflammatory-protein signature (UIS), including 38 upregulated proteins, in cystinuric patients (Cys-patients), compared with healthy controls (HC). This UIS was higher in Cys-patients with CKD. In the present observational study, we aimed to investigate the UIS in Cys-patients without CKD and patients with calcium nephrolithiasis (Lith-patients), versus HC and the effect of urine alkalization on the UIS of Cys-patients. UIS was evaluated by nano-liquid chromatography coupled to high-resolution mass spectrometry in adult HC, Lith-patients and non-treated Cys-patients with an estimated glomerular filtration rate >60 mL/min/1.73 m Twenty-one Cys-patients [12 men, median age (interquartile range) 30.0 (25.0-44.0) years], 12 Lith-patients [8 men, 46.2 (39.5-54.2) years] and 7 HC [2 men, 43.1 (31.0-53.9) years] were included. Among the 38 proteins upregulated in our previous work, 11 proteins were also upregulated in Cys-patients compared with HC in this study (5 circulating inflammatory proteins and 6 neutrophil-derived proteins). This UIS was also found in some Lith-patients. Using this UIS, we identified two subclusters of Cys-patients (5 with a very high/high UIS and 16 with a moderate/low UIS). In the Cys-patients with very high/high UIS, urine alkalization induced a significant decrease in urinary neutrophil-derived proteins. A high UIS is present in some Cys-patients without CKD and decreases under alkalizing treatment. This UIS could be a prognostic marker to predict the evolution towards CKD in cystinuria.

Sections du résumé

Background UNASSIGNED
Cystinuria is associated with a high prevalence of chronic kidney disease (CKD). We previously described a urinary inflammatory-protein signature (UIS), including 38 upregulated proteins, in cystinuric patients (Cys-patients), compared with healthy controls (HC). This UIS was higher in Cys-patients with CKD. In the present observational study, we aimed to investigate the UIS in Cys-patients without CKD and patients with calcium nephrolithiasis (Lith-patients), versus HC and the effect of urine alkalization on the UIS of Cys-patients.
Methods UNASSIGNED
UIS was evaluated by nano-liquid chromatography coupled to high-resolution mass spectrometry in adult HC, Lith-patients and non-treated Cys-patients with an estimated glomerular filtration rate >60 mL/min/1.73 m
Results UNASSIGNED
Twenty-one Cys-patients [12 men, median age (interquartile range) 30.0 (25.0-44.0) years], 12 Lith-patients [8 men, 46.2 (39.5-54.2) years] and 7 HC [2 men, 43.1 (31.0-53.9) years] were included. Among the 38 proteins upregulated in our previous work, 11 proteins were also upregulated in Cys-patients compared with HC in this study (5 circulating inflammatory proteins and 6 neutrophil-derived proteins). This UIS was also found in some Lith-patients. Using this UIS, we identified two subclusters of Cys-patients (5 with a very high/high UIS and 16 with a moderate/low UIS). In the Cys-patients with very high/high UIS, urine alkalization induced a significant decrease in urinary neutrophil-derived proteins.
Conclusion UNASSIGNED
A high UIS is present in some Cys-patients without CKD and decreases under alkalizing treatment. This UIS could be a prognostic marker to predict the evolution towards CKD in cystinuria.

Identifiants

pubmed: 38510798
doi: 10.1093/ckj/sfae040
pii: sfae040
pmc: PMC10953617
doi:

Types de publication

Journal Article

Langues

eng

Pagination

sfae040

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of the ERA.

Déclaration de conflit d'intérêts

C.P.-B., B.K., V.J., K.R., I.C.G. and M.C. report support for the present work by Biohealth. M.C. reports grants by Advicenne, and consulting fees by Alnylam, Viatris, Advicenne, Withings, Usense. C.P.-B. reports consulting fees by Withings. M.C. reports payment for educational events and support for attending meetings and/or travel by Alnylam. All the other authors declared no competing interests.

Auteurs

Caroline Prot-Bertoye (C)

Assistance Publique-Hôpitaux de Paris, Hôpital Européen Georges Pompidou, Service de Physiologie - Explorations fonctionnelles, Paris, France.
Centre de Recherche des Cordeliers, INSERM, Sorbonne Université, Université Paris Cité, Paris, France.
CNRS ERL 8228 - Laboratoire de Physiologie Rénale et Tubulopathies, Paris, France.
Centre de Référence des Maladies Rénales Héréditaires de l'Enfant et de l'Adulte (MARHEA), Paris, France.
Centre de Référence des Maladies Rares du Calcium et du Phosphate, Paris, France.
Association LUNNE Lithiases UriNaires Network, Paris, France.

Vincent Jung (V)

Proteomics Platform Necker, Université Paris Cité - Structure Fédérative de Recherche Necker, INSERM US24/CNRS UAR3633, Paris, France.

Isabelle Tostivint (I)

Centre de Référence des Maladies Rénales Héréditaires de l'Enfant et de l'Adulte (MARHEA), Paris, France.
Association LUNNE Lithiases UriNaires Network, Paris, France.
Assistance Publique-Hôpitaux de Paris, Hôpital de la Pitié Salpêtrière, Service de Néphrologie, Paris, France.
GRC 20 ARDELURO groupe de recherche clinique Analyse, Recherche, Développement et Evaluation en Endourologie et Lithiase Urinaire, Médecine Sorbonne Université, Paris, France.

Kevin Roger (K)

Proteomics Platform Necker, Université Paris Cité - Structure Fédérative de Recherche Necker, INSERM US24/CNRS UAR3633, Paris, France.

Jean-François Benoist (JF)

Faculté de pharmacie, Université Paris Saclay, Orsay, France.
Assistance Publique-Hôpitaux de Paris, Hôpital Necker, Service de Biochimie métabolique, Paris, France.

Anne-Sophie Jannot (AS)

Assistance Publique-Hôpitaux de Paris - Centre, Université Paris Cité, Hôpital Européen Georges Pompidou, Service d'informatique Médicale, Santé Publique et Biostatistiques, Paris, France. HeKA, Centre de recherche des Cordeliers, INSERM, INRIA, Paris, France.

Alexis Van Straaten (A)

Assistance Publique-Hôpitaux de Paris - Centre, Université Paris Cité, Hôpital Européen Georges Pompidou, Service d'informatique Médicale, Santé Publique et Biostatistiques, Paris, France. HeKA, Centre de recherche des Cordeliers, INSERM, INRIA, Paris, France.

Bertrand Knebelmann (B)

Faculté de médecine, Université Paris Cité, Paris, France.
Assistance Publique-Hôpitaux de Paris, Hôpital Necker, Service de Néphrologie, Paris, France.
INEM Unité Inserm U1151, Paris, France.

Ida Chiara Guerrera (IC)

Proteomics Platform Necker, Université Paris Cité - Structure Fédérative de Recherche Necker, INSERM US24/CNRS UAR3633, Paris, France.

Marie Courbebaisse (M)

Assistance Publique-Hôpitaux de Paris, Hôpital Européen Georges Pompidou, Service de Physiologie - Explorations fonctionnelles, Paris, France.
Centre de Référence des Maladies Rénales Héréditaires de l'Enfant et de l'Adulte (MARHEA), Paris, France.
Centre de Référence des Maladies Rares du Calcium et du Phosphate, Paris, France.
Association LUNNE Lithiases UriNaires Network, Paris, France.
Faculté de médecine, Université Paris Cité, Paris, France.
INEM Unité Inserm U1151, Paris, France.

Classifications MeSH