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The dose-response relationship between sex hormones and hyperuricemia in different gender: NHANES 2013-2016
OBJECTIVES: To access the dose-response relationship between sex hormones and hyperuricemia (HUA), and to find the cut-off value in different gender. METHODS: 9,685 participants were derived from the database of National Health and Nutrition Examination Survey (NHANES). Restricted cubic spline (RCS)...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9663851/ https://www.ncbi.nlm.nih.gov/pubmed/36387910 http://dx.doi.org/10.3389/fendo.2022.1035114 |
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author | Li, Guo-yun Qian, Xu-dong Ma, Chun-ming Yin, Fu-zai |
author_facet | Li, Guo-yun Qian, Xu-dong Ma, Chun-ming Yin, Fu-zai |
author_sort | Li, Guo-yun |
collection | PubMed |
description | OBJECTIVES: To access the dose-response relationship between sex hormones and hyperuricemia (HUA), and to find the cut-off value in different gender. METHODS: 9,685 participants were derived from the database of National Health and Nutrition Examination Survey (NHANES). Restricted cubic spline (RCS) analysis were applied to explore the relationship between sex hormones and HUA after adjusting for confounding factors by propensity score match (PSM). Logistic regression was used to estimate the odds ratio (OR) and 95% CI. RESULTS: The prevalence of HUA was 15.13% in female participants and 22.30% in male participants. Logistic regression analysis showed that estradiol (E2) was independently associated with HUA for a P value of 0.003 and 0.01in female and male participants, respectively. Testosterone (T) was only independently associated with HUA in male participants (P<0.001) but not in female participants (P = 0.59). RCS analysis showed a dose-response relationship between sex hormones and HUA. The risk of HUA increased as E2 lower than 29.6pg/mL in female participants and T lower than 389.1ng/dL in male participants. E2 higher than 23.6pg/ml was an independent risk factor for HUA in male participants. CONCLUSION: A dose-response relationship was found between sex hormones and HUA. The cut-off value of E2 in male and female participants was 29.6pg/mL and 23.6pg/mL, respectively, and the cut-off value of T in male participants was 389.1ng/dL. These results provide a reference for preventing HUA and hormone supplement therapy. |
format | Online Article Text |
id | pubmed-9663851 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-96638512022-11-15 The dose-response relationship between sex hormones and hyperuricemia in different gender: NHANES 2013-2016 Li, Guo-yun Qian, Xu-dong Ma, Chun-ming Yin, Fu-zai Front Endocrinol (Lausanne) Endocrinology OBJECTIVES: To access the dose-response relationship between sex hormones and hyperuricemia (HUA), and to find the cut-off value in different gender. METHODS: 9,685 participants were derived from the database of National Health and Nutrition Examination Survey (NHANES). Restricted cubic spline (RCS) analysis were applied to explore the relationship between sex hormones and HUA after adjusting for confounding factors by propensity score match (PSM). Logistic regression was used to estimate the odds ratio (OR) and 95% CI. RESULTS: The prevalence of HUA was 15.13% in female participants and 22.30% in male participants. Logistic regression analysis showed that estradiol (E2) was independently associated with HUA for a P value of 0.003 and 0.01in female and male participants, respectively. Testosterone (T) was only independently associated with HUA in male participants (P<0.001) but not in female participants (P = 0.59). RCS analysis showed a dose-response relationship between sex hormones and HUA. The risk of HUA increased as E2 lower than 29.6pg/mL in female participants and T lower than 389.1ng/dL in male participants. E2 higher than 23.6pg/ml was an independent risk factor for HUA in male participants. CONCLUSION: A dose-response relationship was found between sex hormones and HUA. The cut-off value of E2 in male and female participants was 29.6pg/mL and 23.6pg/mL, respectively, and the cut-off value of T in male participants was 389.1ng/dL. These results provide a reference for preventing HUA and hormone supplement therapy. Frontiers Media S.A. 2022-11-01 /pmc/articles/PMC9663851/ /pubmed/36387910 http://dx.doi.org/10.3389/fendo.2022.1035114 Text en Copyright © 2022 Li, Qian, Ma and Yin https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Endocrinology Li, Guo-yun Qian, Xu-dong Ma, Chun-ming Yin, Fu-zai The dose-response relationship between sex hormones and hyperuricemia in different gender: NHANES 2013-2016 |
title | The dose-response relationship between sex hormones and hyperuricemia in different gender: NHANES 2013-2016 |
title_full | The dose-response relationship between sex hormones and hyperuricemia in different gender: NHANES 2013-2016 |
title_fullStr | The dose-response relationship between sex hormones and hyperuricemia in different gender: NHANES 2013-2016 |
title_full_unstemmed | The dose-response relationship between sex hormones and hyperuricemia in different gender: NHANES 2013-2016 |
title_short | The dose-response relationship between sex hormones and hyperuricemia in different gender: NHANES 2013-2016 |
title_sort | dose-response relationship between sex hormones and hyperuricemia in different gender: nhanes 2013-2016 |
topic | Endocrinology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9663851/ https://www.ncbi.nlm.nih.gov/pubmed/36387910 http://dx.doi.org/10.3389/fendo.2022.1035114 |
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