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A Study of Dyslipidemia and Its Clinical Implications in Childhood Nephrotic Syndrome

Background: Nephrotic syndrome in children is characterized by dyslipidemia, which is an indirect risk factor for cardiovascular diseases, progressive glomerulosclerosis, and related complications. The objective is to determine the range of lipid profile abnormalities in relation to onset, relapse,...

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Autores principales: Dowerah, Pritikar, Gogoi, Arpita, Shira, Caroline D, Sarkar, Bikash, Mazumdar, Sarada
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10590184/
https://www.ncbi.nlm.nih.gov/pubmed/37869045
http://dx.doi.org/10.7759/cureus.47434
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author Dowerah, Pritikar
Gogoi, Arpita
Shira, Caroline D
Sarkar, Bikash
Mazumdar, Sarada
author_facet Dowerah, Pritikar
Gogoi, Arpita
Shira, Caroline D
Sarkar, Bikash
Mazumdar, Sarada
author_sort Dowerah, Pritikar
collection PubMed
description Background: Nephrotic syndrome in children is characterized by dyslipidemia, which is an indirect risk factor for cardiovascular diseases, progressive glomerulosclerosis, and related complications. The objective is to determine the range of lipid profile abnormalities in relation to onset, relapse, and remission, as well as to determine if there is any relationship between dyslipidemia and the frequency of relapses. Methods: One hundred and two diagnosed cases of nephrotic syndrome in the age group of less than 12 years were included, out of which 64 patients belonged to the first episode of nephrotic syndrome and 38 patients were relapse cases. Steroid-resistant nephrotic syndrome cases or patients with a history of diabetes mellitus, hypothyroidism, familial hypercholesterolemia, children with chronic kidney disease, and edema due to other causes were excluded from the study. Results: There was a statistically significant increase in lipid parameters except for high-density lipoprotein (HDL) cholesterol at the disease onset when compared to remission in cases of the first episode as well as relapse cases of nephrotic syndrome. There was a positive correlation between relapse frequency and dyslipidemia. Dyslipidaemia was also associated with low serum albumin, with a p-value <0.001, which is statistically significant. Conclusion: Dyslipidemia is significantly higher in relapse cases of nephrotic syndrome and remains higher even during remission. Dyslipidemia is a directly associated risk factor for atherosclerosis and coronary heart disease (CAD), along with progressive glomerulosclerosis. Early identification and treatment of hyperlipidemia is therefore justified so that along with longevity, we can also improve the quality of life of children suffering from nephrotic syndrome.
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spelling pubmed-105901842023-10-22 A Study of Dyslipidemia and Its Clinical Implications in Childhood Nephrotic Syndrome Dowerah, Pritikar Gogoi, Arpita Shira, Caroline D Sarkar, Bikash Mazumdar, Sarada Cureus Pediatrics Background: Nephrotic syndrome in children is characterized by dyslipidemia, which is an indirect risk factor for cardiovascular diseases, progressive glomerulosclerosis, and related complications. The objective is to determine the range of lipid profile abnormalities in relation to onset, relapse, and remission, as well as to determine if there is any relationship between dyslipidemia and the frequency of relapses. Methods: One hundred and two diagnosed cases of nephrotic syndrome in the age group of less than 12 years were included, out of which 64 patients belonged to the first episode of nephrotic syndrome and 38 patients were relapse cases. Steroid-resistant nephrotic syndrome cases or patients with a history of diabetes mellitus, hypothyroidism, familial hypercholesterolemia, children with chronic kidney disease, and edema due to other causes were excluded from the study. Results: There was a statistically significant increase in lipid parameters except for high-density lipoprotein (HDL) cholesterol at the disease onset when compared to remission in cases of the first episode as well as relapse cases of nephrotic syndrome. There was a positive correlation between relapse frequency and dyslipidemia. Dyslipidaemia was also associated with low serum albumin, with a p-value <0.001, which is statistically significant. Conclusion: Dyslipidemia is significantly higher in relapse cases of nephrotic syndrome and remains higher even during remission. Dyslipidemia is a directly associated risk factor for atherosclerosis and coronary heart disease (CAD), along with progressive glomerulosclerosis. Early identification and treatment of hyperlipidemia is therefore justified so that along with longevity, we can also improve the quality of life of children suffering from nephrotic syndrome. Cureus 2023-10-21 /pmc/articles/PMC10590184/ /pubmed/37869045 http://dx.doi.org/10.7759/cureus.47434 Text en Copyright © 2023, Dowerah et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Pediatrics
Dowerah, Pritikar
Gogoi, Arpita
Shira, Caroline D
Sarkar, Bikash
Mazumdar, Sarada
A Study of Dyslipidemia and Its Clinical Implications in Childhood Nephrotic Syndrome
title A Study of Dyslipidemia and Its Clinical Implications in Childhood Nephrotic Syndrome
title_full A Study of Dyslipidemia and Its Clinical Implications in Childhood Nephrotic Syndrome
title_fullStr A Study of Dyslipidemia and Its Clinical Implications in Childhood Nephrotic Syndrome
title_full_unstemmed A Study of Dyslipidemia and Its Clinical Implications in Childhood Nephrotic Syndrome
title_short A Study of Dyslipidemia and Its Clinical Implications in Childhood Nephrotic Syndrome
title_sort study of dyslipidemia and its clinical implications in childhood nephrotic syndrome
topic Pediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10590184/
https://www.ncbi.nlm.nih.gov/pubmed/37869045
http://dx.doi.org/10.7759/cureus.47434
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