Angiopoietin-like protein 3: a novel potential biomarker for nephrotic syndrome in children.

angiopoietin-like protein 3 biomarker children nephrotic syndrome proteinuria

Journal

Frontiers in pediatrics
ISSN: 2296-2360
Titre abrégé: Front Pediatr
Pays: Switzerland
ID NLM: 101615492

Informations de publication

Date de publication:
2023
Historique:
received: 01 12 2022
accepted: 03 05 2023
medline: 2 6 2023
pubmed: 2 6 2023
entrez: 2 6 2023
Statut: epublish

Résumé

Angiopoietin-like 3 (ANGPTL3) is a secretory glycoprotein. It has been demonstrated that ANGPTL3 level was upregulated in minimal change nephrotic syndrome (MCNS) kidney tissues. Subsequently, our group found that ANGPTL3 level was closely correlated with nephropathy A total of 200 NS patients and 80 healthy controls (age, 1-18 years) were admitted to our institution between 2021 and 2022. The etiology of NS included primary nephrotic syndrome (PNS, Serum ANGPTL3 and urinary ANGPTL3/Cre were remarkably elevated in NS patients compared with those in healthy controls. Furthermore, serum ANGPTL3 and urinary ANGPTL3/Cre were significantly correlated with proteinuria level. Additionally, multivariate linear regression analysis demonstrated that serum ALB was independently correlated with serum ANGPTL3 and PRO/CR was independently correlated with urinary ANGPTL3/Cre in NS patients. Serum ANGPTL3 and urinary ANGPTL3/Cre showed a promising performance in the diagnosis of NS, and served as novel potential noninvasive biomarkers to assess disease severity of NS. Further exploration of the role of ANGPTL3 level may shed a new light on the treatment of NS.

Sections du résumé

Background UNASSIGNED
Angiopoietin-like 3 (ANGPTL3) is a secretory glycoprotein. It has been demonstrated that ANGPTL3 level was upregulated in minimal change nephrotic syndrome (MCNS) kidney tissues. Subsequently, our group found that ANGPTL3 level was closely correlated with nephropathy
Methods UNASSIGNED
A total of 200 NS patients and 80 healthy controls (age, 1-18 years) were admitted to our institution between 2021 and 2022. The etiology of NS included primary nephrotic syndrome (PNS,
Results UNASSIGNED
Serum ANGPTL3 and urinary ANGPTL3/Cre were remarkably elevated in NS patients compared with those in healthy controls. Furthermore, serum ANGPTL3 and urinary ANGPTL3/Cre were significantly correlated with proteinuria level. Additionally, multivariate linear regression analysis demonstrated that serum ALB was independently correlated with serum ANGPTL3 and PRO/CR was independently correlated with urinary ANGPTL3/Cre in NS patients.
Conclusion UNASSIGNED
Serum ANGPTL3 and urinary ANGPTL3/Cre showed a promising performance in the diagnosis of NS, and served as novel potential noninvasive biomarkers to assess disease severity of NS. Further exploration of the role of ANGPTL3 level may shed a new light on the treatment of NS.

Identifiants

pubmed: 37266537
doi: 10.3389/fped.2023.1113484
pmc: PMC10229790
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1113484

Informations de copyright

© 2023 Wen, Liu, Dai, Hong, Ji, Liu, Zhang, Han, Lv, Liu, Shen and Xu.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Fujie Wen (F)

Department of Nephrology, Children's Hospital of Fudan University, Shanghai, China.

Junchao Liu (J)

Department of Traditional Chinese Medicine, Children's Hospital of Fudan University, Shanghai, China.

Rufeng Dai (R)

Department of Nephrology, Children's Hospital of Fudan University, Shanghai, China.

Sha Hong (S)

Department of Nephrology, Children's Hospital of Fudan University, Shanghai, China.

Baowei Ji (B)

Department of Nephrology, Children's Hospital of Fudan University, Shanghai, China.

Jiaojiao Liu (J)

Department of Nephrology, Children's Hospital of Fudan University, Shanghai, China.

Jun Zhang (J)

Department of Nephrology, Children's Hospital of Fudan University, Shanghai, China.

Xinli Han (X)

Department of Nephrology, Children's Hospital of Fudan University, Shanghai, China.

Qianying Lv (Q)

Department of Rheumatology, Children's Hospital of Fudan University, Shanghai, China.

Jialu Liu (J)

Department of Nephrology, Children's Hospital of Fudan University, Shanghai, China.

Qian Shen (Q)

Department of Nephrology, Children's Hospital of Fudan University, Shanghai, China.

Hong Xu (H)

Department of Nephrology, Children's Hospital of Fudan University, Shanghai, China.

Classifications MeSH