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Estradiol and Hyperhomocysteinemia Are Linked Predominantly Through Part Renal Function Indicators

BACKGROUND: Previous studies have shown that estrogen, kidney function, and homocysteine (Hcy) or hyperhomocysteinemia (HHcy) are related to each other. However, the underlying biological mechanisms still remain unclear. We aimed to explore the association between estradiol (E2) and HHcy in the fema...

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Autores principales: Niu, Xiao Na, Wen, He, Sun, Nan, Yang, Yi, Du, Shi Hong, Xie, Rong, Zhang, Yan Nan, Li, Yan, Hong, Xiu Qin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9157416/
https://www.ncbi.nlm.nih.gov/pubmed/35663317
http://dx.doi.org/10.3389/fendo.2022.817579
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author Niu, Xiao Na
Wen, He
Sun, Nan
Yang, Yi
Du, Shi Hong
Xie, Rong
Zhang, Yan Nan
Li, Yan
Hong, Xiu Qin
author_facet Niu, Xiao Na
Wen, He
Sun, Nan
Yang, Yi
Du, Shi Hong
Xie, Rong
Zhang, Yan Nan
Li, Yan
Hong, Xiu Qin
author_sort Niu, Xiao Na
collection PubMed
description BACKGROUND: Previous studies have shown that estrogen, kidney function, and homocysteine (Hcy) or hyperhomocysteinemia (HHcy) are related to each other. However, the underlying biological mechanisms still remain unclear. We aimed to explore the association between estradiol (E2) and HHcy in the female population, and to further evaluate the mediating role of renal function indicators. METHODS: This unmatched case–control study consisted of 1,044 female participants who were 60.60 ± 12.46 years old. Data on general demographic characteristics, such as age, smoking and drinking status, menopause and so on were collected in a personal interview, and laboratory examinations were performed by well-trained personnel. The mediating effect model was applied to analyze the direct and indirect effects of E2 on Hcy. RESULTS: The average levels of Hcy and E2 of the participants were 12.6 μmol/L and 14.95 pg/ml. There were statistical differences in renal indexes blood urea nitrogen (BUN), serum creatinine (Scr), uric acid (UA), glomerular filtration rate (GFR) and E2 between HHcy group and non-HHcy group. The logistic regression models showed that UA was risk factor for HHcy (P <0.001), GFR and E2 were protective factors for HHcy after adjusting for confounding factors (P <0.001). The indirect effects of E2 on Hcy through UA and GFR accounted for 14.63 and 18.29% of the total impacts of E2 on Hcy. CONCLUSIONS: These data indicated that E2 was a protective factor of HHcy, and the effects of E2 on HHcy may be mediated by renal function indicators UA and GFR.
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spelling pubmed-91574162022-06-02 Estradiol and Hyperhomocysteinemia Are Linked Predominantly Through Part Renal Function Indicators Niu, Xiao Na Wen, He Sun, Nan Yang, Yi Du, Shi Hong Xie, Rong Zhang, Yan Nan Li, Yan Hong, Xiu Qin Front Endocrinol (Lausanne) Endocrinology BACKGROUND: Previous studies have shown that estrogen, kidney function, and homocysteine (Hcy) or hyperhomocysteinemia (HHcy) are related to each other. However, the underlying biological mechanisms still remain unclear. We aimed to explore the association between estradiol (E2) and HHcy in the female population, and to further evaluate the mediating role of renal function indicators. METHODS: This unmatched case–control study consisted of 1,044 female participants who were 60.60 ± 12.46 years old. Data on general demographic characteristics, such as age, smoking and drinking status, menopause and so on were collected in a personal interview, and laboratory examinations were performed by well-trained personnel. The mediating effect model was applied to analyze the direct and indirect effects of E2 on Hcy. RESULTS: The average levels of Hcy and E2 of the participants were 12.6 μmol/L and 14.95 pg/ml. There were statistical differences in renal indexes blood urea nitrogen (BUN), serum creatinine (Scr), uric acid (UA), glomerular filtration rate (GFR) and E2 between HHcy group and non-HHcy group. The logistic regression models showed that UA was risk factor for HHcy (P <0.001), GFR and E2 were protective factors for HHcy after adjusting for confounding factors (P <0.001). The indirect effects of E2 on Hcy through UA and GFR accounted for 14.63 and 18.29% of the total impacts of E2 on Hcy. CONCLUSIONS: These data indicated that E2 was a protective factor of HHcy, and the effects of E2 on HHcy may be mediated by renal function indicators UA and GFR. Frontiers Media S.A. 2022-05-18 /pmc/articles/PMC9157416/ /pubmed/35663317 http://dx.doi.org/10.3389/fendo.2022.817579 Text en Copyright © 2022 Niu, Wen, Sun, Yang, Du, Xie, Zhang, Li and Hong 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
Niu, Xiao Na
Wen, He
Sun, Nan
Yang, Yi
Du, Shi Hong
Xie, Rong
Zhang, Yan Nan
Li, Yan
Hong, Xiu Qin
Estradiol and Hyperhomocysteinemia Are Linked Predominantly Through Part Renal Function Indicators
title Estradiol and Hyperhomocysteinemia Are Linked Predominantly Through Part Renal Function Indicators
title_full Estradiol and Hyperhomocysteinemia Are Linked Predominantly Through Part Renal Function Indicators
title_fullStr Estradiol and Hyperhomocysteinemia Are Linked Predominantly Through Part Renal Function Indicators
title_full_unstemmed Estradiol and Hyperhomocysteinemia Are Linked Predominantly Through Part Renal Function Indicators
title_short Estradiol and Hyperhomocysteinemia Are Linked Predominantly Through Part Renal Function Indicators
title_sort estradiol and hyperhomocysteinemia are linked predominantly through part renal function indicators
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9157416/
https://www.ncbi.nlm.nih.gov/pubmed/35663317
http://dx.doi.org/10.3389/fendo.2022.817579
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