Structural equation modeling (SEM) of kidney function markers and longitudinal CVD risk assessment

Lower kidney function is known to enhance cardiovascular disease (CVD) risk. It is unclear which estimated glomerular filtration rate (eGFR) equation best predict an increased CVD risk and if prediction can be improved by integration of multiple kidney function markers. We performed structural equat...

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Main Authors: Ryosuke Fujii, Roberto Melotti, Martin Gögele, Laura Barin, Dariush Ghasemi-Semeskandeh, Giulia Barbieri, Peter P. Pramstaller, Cristian Pattaro
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2023-01-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10118200/?tool=EBI
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author Ryosuke Fujii
Roberto Melotti
Martin Gögele
Laura Barin
Dariush Ghasemi-Semeskandeh
Giulia Barbieri
Peter P. Pramstaller
Cristian Pattaro
author_facet Ryosuke Fujii
Roberto Melotti
Martin Gögele
Laura Barin
Dariush Ghasemi-Semeskandeh
Giulia Barbieri
Peter P. Pramstaller
Cristian Pattaro
author_sort Ryosuke Fujii
collection DOAJ
description Lower kidney function is known to enhance cardiovascular disease (CVD) risk. It is unclear which estimated glomerular filtration rate (eGFR) equation best predict an increased CVD risk and if prediction can be improved by integration of multiple kidney function markers. We performed structural equation modeling (SEM) of kidney markers and compared the performance of the resulting pooled indexes with established eGFR equations to predict CVD risk in a 10-year longitudinal population-based design. We split the study sample into a set of participants with only baseline data (n = 647; model-building set) and a set with longitudinal data (n = 670; longitudinal set). In the model-building set, we fitted five SEM models based on serum creatinine or creatinine-based eGFR (eGFRcre), cystatin C or cystatin-based eGFR (eGFRcys), uric acid (UA), and blood urea nitrogen (BUN). In the longitudinal set, 10-year incident CVD risk was defined as a Framingham risk score (FRS)>5% and a pooled cohort equation (PCE)>5%. Predictive performances of the different kidney function indexes were compared using the C-statistic and the DeLong test. In the longitudinal set, a SEM-based estimate of latent kidney function based on eGFRcre, eGFRcys, UA, and BUN showed better prediction performance for both FRS>5% (C-statistic: 0.70; 95% CI: 0.65–0.74) and PCE>5% (C-statistic: 0.75; 95%CI: 0.71–0.79) than other SEM models and different eGFR formulas (DeLong test p-values<3.21×10−6 for FRS>5% and <1.49×10−9 for PCE>5%, respectively). However, the new derived marker could not outperform eGFRcys (DeLong test p-values = 0.88 for FRS>5% and 0.20 for PCE>5%, respectively). SEM is a promising approach to identify latent kidney function signatures. However, for incident CVD risk prediction, eGFRcys could still be preferrable given its simpler derivation.
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spelling doaj.art-8d4670cbd35c4b009520af549a6e2e4a2023-04-23T05:31:35ZengPublic Library of Science (PLoS)PLoS ONE1932-62032023-01-01184Structural equation modeling (SEM) of kidney function markers and longitudinal CVD risk assessmentRyosuke FujiiRoberto MelottiMartin GögeleLaura BarinDariush Ghasemi-SemeskandehGiulia BarbieriPeter P. PramstallerCristian PattaroLower kidney function is known to enhance cardiovascular disease (CVD) risk. It is unclear which estimated glomerular filtration rate (eGFR) equation best predict an increased CVD risk and if prediction can be improved by integration of multiple kidney function markers. We performed structural equation modeling (SEM) of kidney markers and compared the performance of the resulting pooled indexes with established eGFR equations to predict CVD risk in a 10-year longitudinal population-based design. We split the study sample into a set of participants with only baseline data (n = 647; model-building set) and a set with longitudinal data (n = 670; longitudinal set). In the model-building set, we fitted five SEM models based on serum creatinine or creatinine-based eGFR (eGFRcre), cystatin C or cystatin-based eGFR (eGFRcys), uric acid (UA), and blood urea nitrogen (BUN). In the longitudinal set, 10-year incident CVD risk was defined as a Framingham risk score (FRS)>5% and a pooled cohort equation (PCE)>5%. Predictive performances of the different kidney function indexes were compared using the C-statistic and the DeLong test. In the longitudinal set, a SEM-based estimate of latent kidney function based on eGFRcre, eGFRcys, UA, and BUN showed better prediction performance for both FRS>5% (C-statistic: 0.70; 95% CI: 0.65–0.74) and PCE>5% (C-statistic: 0.75; 95%CI: 0.71–0.79) than other SEM models and different eGFR formulas (DeLong test p-values<3.21×10−6 for FRS>5% and <1.49×10−9 for PCE>5%, respectively). However, the new derived marker could not outperform eGFRcys (DeLong test p-values = 0.88 for FRS>5% and 0.20 for PCE>5%, respectively). SEM is a promising approach to identify latent kidney function signatures. However, for incident CVD risk prediction, eGFRcys could still be preferrable given its simpler derivation.https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10118200/?tool=EBI
spellingShingle Ryosuke Fujii
Roberto Melotti
Martin Gögele
Laura Barin
Dariush Ghasemi-Semeskandeh
Giulia Barbieri
Peter P. Pramstaller
Cristian Pattaro
Structural equation modeling (SEM) of kidney function markers and longitudinal CVD risk assessment
PLoS ONE
title Structural equation modeling (SEM) of kidney function markers and longitudinal CVD risk assessment
title_full Structural equation modeling (SEM) of kidney function markers and longitudinal CVD risk assessment
title_fullStr Structural equation modeling (SEM) of kidney function markers and longitudinal CVD risk assessment
title_full_unstemmed Structural equation modeling (SEM) of kidney function markers and longitudinal CVD risk assessment
title_short Structural equation modeling (SEM) of kidney function markers and longitudinal CVD risk assessment
title_sort structural equation modeling sem of kidney function markers and longitudinal cvd risk assessment
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10118200/?tool=EBI
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