PMID- 35663317 OWN - NLM STAT- MEDLINE DCOM- 20220608 LR - 20220716 IS - 1664-2392 (Print) IS - 1664-2392 (Electronic) IS - 1664-2392 (Linking) VI - 13 DP - 2022 TI - Estradiol and Hyperhomocysteinemia Are Linked Predominantly Through Part Renal Function Indicators. PG - 817579 LID - 10.3389/fendo.2022.817579 [doi] LID - 817579 AB - 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 mumol/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. CI - Copyright (c) 2022 Niu, Wen, Sun, Yang, Du, Xie, Zhang, Li and Hong. FAU - Niu, Xiao Na AU - Niu XN AD - First Affiliated Hospital of Hunan Normal University, Hunan Provincial People's Hospital, Changsha, China. FAU - Wen, He AU - Wen H AD - Department of Cardiology, The Second Affiliated Hospital of Air Force Military Medical University, Tangdu Hospital, Xi An, China. FAU - Sun, Nan AU - Sun N AD - Department of Cardiology, The Second Affiliated Hospital of Air Force Military Medical University, Tangdu Hospital, Xi An, China. FAU - Yang, Yi AU - Yang Y AD - First Affiliated Hospital of Hunan Normal University, Hunan Provincial People's Hospital, Changsha, China. FAU - Du, Shi Hong AU - Du SH AD - First Affiliated Hospital of Hunan Normal University, Hunan Provincial People's Hospital, Changsha, China. FAU - Xie, Rong AU - Xie R AD - First Affiliated Hospital of Hunan Normal University, Hunan Provincial People's Hospital, Changsha, China. FAU - Zhang, Yan Nan AU - Zhang YN AD - First Affiliated Hospital of Hunan Normal University, Hunan Provincial People's Hospital, Changsha, China. FAU - Li, Yan AU - Li Y AD - Department of Cardiology, The Second Affiliated Hospital of Air Force Military Medical University, Tangdu Hospital, Xi An, China. FAU - Hong, Xiu Qin AU - Hong XQ AD - First Affiliated Hospital of Hunan Normal University, Hunan Provincial People's Hospital, Changsha, China. LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20220518 PL - Switzerland TA - Front Endocrinol (Lausanne) JT - Frontiers in endocrinology JID - 101555782 RN - 268B43MJ25 (Uric Acid) RN - 4TI98Z838E (Estradiol) SB - IM MH - Aged MH - Case-Control Studies MH - Estradiol MH - Female MH - Humans MH - *Hyperhomocysteinemia/complications/epidemiology MH - Kidney/physiology MH - Middle Aged MH - Uric Acid PMC - PMC9157416 OTO - NOTNLM OT - case-control study OT - estradiol (E2) OT - homocysteine (Hcy) OT - hyperhomocysteinemia (HHcy) OT - mediation effect COIS- The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. EDAT- 2022/06/07 06:00 MHDA- 2022/06/09 06:00 PMCR- 2022/01/01 CRDT- 2022/06/06 13:57 PHST- 2021/11/18 00:00 [received] PHST- 2022/01/31 00:00 [accepted] PHST- 2022/06/06 13:57 [entrez] PHST- 2022/06/07 06:00 [pubmed] PHST- 2022/06/09 06:00 [medline] PHST- 2022/01/01 00:00 [pmc-release] AID - 10.3389/fendo.2022.817579 [doi] PST - epublish SO - Front Endocrinol (Lausanne). 2022 May 18;13:817579. doi: 10.3389/fendo.2022.817579. eCollection 2022.