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Causal association pathways between fetuin-A and kidney function: a mediation analysis

OBJECTIVE: Body mass index (BMI), uric acid, diabetes mellitus, and hypertension are risk factors for reduced kidney function and are associated with fetuin-A levels, but their causal pathways remain unclear. The objective of this study was to investigate this knowledge gap. METHODS: A repeated cros...

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Autores principales: Bassey, Philip Etabee, Numthavaj, Pawin, Rattanasiri, Sasivimol, Sritara, Piyamitr, McEvoy, Mark, Ongphiphadhanakul, Boonsong, Thakkinstian, Ammarin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9019358/
https://www.ncbi.nlm.nih.gov/pubmed/35435033
http://dx.doi.org/10.1177/03000605221082874
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author Bassey, Philip Etabee
Numthavaj, Pawin
Rattanasiri, Sasivimol
Sritara, Piyamitr
McEvoy, Mark
Ongphiphadhanakul, Boonsong
Thakkinstian, Ammarin
author_facet Bassey, Philip Etabee
Numthavaj, Pawin
Rattanasiri, Sasivimol
Sritara, Piyamitr
McEvoy, Mark
Ongphiphadhanakul, Boonsong
Thakkinstian, Ammarin
author_sort Bassey, Philip Etabee
collection PubMed
description OBJECTIVE: Body mass index (BMI), uric acid, diabetes mellitus, and hypertension are risk factors for reduced kidney function and are associated with fetuin-A levels, but their causal pathways remain unclear. The objective of this study was to investigate this knowledge gap. METHODS: A repeated cross-sectional design was used to assess causal pathway effects of fetuin-A on the estimated glomerular filtration rate (eGFR), which is mediated through BMI, uric acid, diabetes mellitus, and hypertension. RESULTS: Among 2305 participants, the mean eGFR at baseline decreased from 98.7 ± 23.6 mL/minute/1.73 m(2) in 2009 to 92.4 ± 22.9 mL/minute/1.73 m(2) in 2014. Fetuin-A was significantly associated with eGFR , suggesting that increasing fetuin-A levels predict a decrease in eGFR. Additionally, the indirect effect of fetuin-A on eGFR, as assessed through BMI, was also significant. The effects of fetuin-A on eGFR through other mediation pathways showed variable results. CONCLUSIONS: Our study revealed a possible role of fetuin-A in the etiology of declining renal function through mediating body mass index, uric acid, diabetes mellitus, and hypertension via complex causal pathways. Further studies to clarify these mediated effects are recommended.
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spelling pubmed-90193582022-04-21 Causal association pathways between fetuin-A and kidney function: a mediation analysis Bassey, Philip Etabee Numthavaj, Pawin Rattanasiri, Sasivimol Sritara, Piyamitr McEvoy, Mark Ongphiphadhanakul, Boonsong Thakkinstian, Ammarin J Int Med Res Retrospective Clinical Research Report OBJECTIVE: Body mass index (BMI), uric acid, diabetes mellitus, and hypertension are risk factors for reduced kidney function and are associated with fetuin-A levels, but their causal pathways remain unclear. The objective of this study was to investigate this knowledge gap. METHODS: A repeated cross-sectional design was used to assess causal pathway effects of fetuin-A on the estimated glomerular filtration rate (eGFR), which is mediated through BMI, uric acid, diabetes mellitus, and hypertension. RESULTS: Among 2305 participants, the mean eGFR at baseline decreased from 98.7 ± 23.6 mL/minute/1.73 m(2) in 2009 to 92.4 ± 22.9 mL/minute/1.73 m(2) in 2014. Fetuin-A was significantly associated with eGFR , suggesting that increasing fetuin-A levels predict a decrease in eGFR. Additionally, the indirect effect of fetuin-A on eGFR, as assessed through BMI, was also significant. The effects of fetuin-A on eGFR through other mediation pathways showed variable results. CONCLUSIONS: Our study revealed a possible role of fetuin-A in the etiology of declining renal function through mediating body mass index, uric acid, diabetes mellitus, and hypertension via complex causal pathways. Further studies to clarify these mediated effects are recommended. SAGE Publications 2022-04-17 /pmc/articles/PMC9019358/ /pubmed/35435033 http://dx.doi.org/10.1177/03000605221082874 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by-nc/4.0/Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Retrospective Clinical Research Report
Bassey, Philip Etabee
Numthavaj, Pawin
Rattanasiri, Sasivimol
Sritara, Piyamitr
McEvoy, Mark
Ongphiphadhanakul, Boonsong
Thakkinstian, Ammarin
Causal association pathways between fetuin-A and kidney function: a mediation analysis
title Causal association pathways between fetuin-A and kidney function: a mediation analysis
title_full Causal association pathways between fetuin-A and kidney function: a mediation analysis
title_fullStr Causal association pathways between fetuin-A and kidney function: a mediation analysis
title_full_unstemmed Causal association pathways between fetuin-A and kidney function: a mediation analysis
title_short Causal association pathways between fetuin-A and kidney function: a mediation analysis
title_sort causal association pathways between fetuin-a and kidney function: a mediation analysis
topic Retrospective Clinical Research Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9019358/
https://www.ncbi.nlm.nih.gov/pubmed/35435033
http://dx.doi.org/10.1177/03000605221082874
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