WCN25-1928 Clustering patients with chronic kidney disease based on routinely measured laboratory biomarkers and its association with disease progression; findings from a population level feasibility study from British Columbia, Canada

the study period.Nephrotic syndrome is defined in children by 24hour proteinuria greater than or equal to 50 mg/kg/24 hours, hypoalbuminemia less than 25-30 g/l and hypoproteinemia less than 50-55 g/l.Results: A total of 26 patients had fulfilled the inclusion criteria, with a hospital prevalence of 0.69%.The males predominated with male to female ratio of 1.3.Most children were aged 5 to 10 years (57.69%).The mean age at diagnosis was 8 AE 2.9 years.In the majority of cases (61.54%) the delay between the onset of symptoms and the first consultation was more than 14 days.Edema was found in all patients at the time of consultation.The 24-hour proteinuria was between 50 to 100 mg / kg / day in 65% of cases with an average of 100.16AE 47.64 mg / kg / d.Mean serum protein and albumin were respectively 41.19 AE 12.41g / L and 18.46 AE 5.97g / L. The NS was pure in 15 patients or in 57.69% of cases and impure in 11 patients or in 42.31% of cases.Treatment was based on oral corticosteroid therapy (prednisolone) at a dosage of 2 mg/kg/day.Steroid sensitivity was observed in 22 patients, i.e. 84.61%, one child was steroid dependent (3.85%) and two children were steroid resistance, i.e. 7.69%.One child died due to severe renal impairment (mortality of 3.85%).Only one patient had benefited from a renal biopsy.Conclusions: NS remains common in children at the HNZ.The improvement of the technical platform for PBR and anatomopathological examinations as well as the establishment of social security prove necessary for a better management of SN in children at the HNZ.I have no potential conflict of interest to disclose.I did not use generative AI and AI-assisted technologies in the writing process.

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Journal
Kidney International Reports
Published
2025-01-27
DOI
https://doi.org/10.1016/j.ekir.2024.11.298
Primary Topic
Systemic Sclerosis and Related Diseases
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article
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article

WCN25-1928 Clustering patients with chronic kidney disease based on routinely measured laboratory biomarkers and its association with disease progression; findings from a population level feasibility study from British Columbia, Canada

Mohammad Atiquzzaman, Jennifer Susan Lees, Adeera Levin, Lee Er et al.
Kidney International Reports
Systemic Sclerosis and Related Diseases
article

WCN25-1928 Clustering patients with chronic kidney disease based on routinely measured laboratory biomarkers and its association with disease progression; findings from a population level feasibility study from British Columbia, Canada

Mohammad Atiquzzaman, Jennifer Susan Lees, Adeera Levin, Lee Er, Ognjenka Djurdjev
article en

Abstract

the study period.Nephrotic syndrome is defined in children by 24hour proteinuria greater than or equal to 50 mg/kg/24 hours, hypoalbuminemia less than 25-30 g/l and hypoproteinemia less than 50-55 g/l.Results: A total of 26 patients had fulfilled the inclusion criteria, with a hospital prevalence of 0.69%.The males predominated with male to female ratio of 1.3.Most children were aged 5 to 10 years (57.69%).The mean age at diagnosis was 8 AE 2.9 years.In the majority of cases (61.54%) the delay between the onset of symptoms and the first consultation was more than 14 days.Edema was found in all patients at the time of consultation.The 24-hour proteinuria was between 50 to 100 mg / kg / day in 65% of cases with an average of 100.16AE 47.64 mg / kg / d.Mean serum protein and albumin were respectively 41.19 AE 12.41g / L and 18.46 AE 5.97g / L. The NS was pure in 15 patients or in 57.69% of cases and impure in 11 patients or in 42.31% of cases.Treatment was based on oral corticosteroid therapy (prednisolone) at a dosage of 2 mg/kg/day.Steroid sensitivity was observed in 22 patients, i.e. 84.61%, one child was steroid dependent (3.85%) and two children were steroid resistance, i.e. 7.69%.One child died due to severe renal impairment (mortality of 3.85%).Only one patient had benefited from a renal biopsy.Conclusions: NS remains common in children at the HNZ.The improvement of the technical platform for PBR and anatomopathological examinations as well as the establishment of social security prove necessary for a better management of SN in children at the HNZ.I have no potential conflict of interest to disclose.I did not use generative AI and AI-assisted technologies in the writing process.

Kidney International ReportsVol. 10(2)
Vancouver Coastal Health (CA), University of British Columbia (CA), University of Glasgow (GB)
Good health and well-being
Openalex Percentile: Top 98%
Systemic Sclerosis and Related Diseases
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