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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2022
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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. |
format | Online Article Text |
id | pubmed-9019358 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
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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