<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Wang S</submitter><funding>Space Utilization Project of China Manned Space Program</funding><funding>Shenzhen Science and Technology Innovation Program</funding><funding>Space Medical Experiment Project of China Manned Space Program</funding><funding>Chongming Project of the Heye Health Technology Co., Ltd</funding><funding>National Natural Science Foundation of China</funding><pagination>e0314199</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12040201</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>20(4)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Postmenopausal osteoporosis (PMOP) is the most common type of osteoporosis. Numerous studies have shown that static magnetic fields (SMFs) can inhibit bone loss by regulating bone remodeling. However, there are currently no clinical studies on the treatment of osteoporosis with SMFs. This study aims to investigate the clinical therapeutic effects of moderate static magnetic fields (MMFs) on PMOP.&lt;h4>Methods&lt;/h4>In this paper, we constructed MMF device using neodymium-iron-boron (NdFeB) materials. At the animal level, the effect of MMF exposure for 8 weeks on estrogen deficiency-induced bone loss was investigated by evaluating bone microstructure, mechanical properties, and bone conversion using ovariectomized (OVX) mice. Clinically, a single-blind randomized controlled s</pubmed_abstract><journal>PloS one</journal><pubmed_title>Moderate static magnetic fields prevent estrogen deficiency-induced bone loss: Evidence from ovariectomized mouse model and small sample size randomized controlled clinical trial.</pubmed_title><pmcid>PMC12040201</pmcid><funding_grant_id>HY-I-202101</funding_grant_id><funding_grant_id>HYZHXM01008</funding_grant_id><funding_grant_id>YYWT-0901-EXP-04</funding_grant_id><funding_grant_id>JCYJ20230807144159004</funding_grant_id><funding_grant_id>52037007</funding_grant_id><pubmed_authors>Yang J</pubmed_authors><pubmed_authors>Duan L</pubmed_authors><pubmed_authors>Hu Y</pubmed_authors><pubmed_authors>Guo Z</pubmed_authors><pubmed_authors>Zhang H</pubmed_authors><pubmed_authors>Luo C</pubmed_authors><pubmed_authors>Wei Y</pubmed_authors><pubmed_authors>Bai X</pubmed_authors><pubmed_authors>Sun L</pubmed_authors><pubmed_authors>Zhang W</pubmed_authors><pubmed_authors>Liao J</pubmed_authors><pubmed_authors>Fang Y</pubmed_authors><pubmed_authors>Li X</pubmed_authors><pubmed_authors>Wei M</pubmed_authors><pubmed_authors>Yang Z</pubmed_authors><pubmed_authors>Shang P</pubmed_authors><pubmed_authors>Cai C</pubmed_authors><pubmed_authors>Huyan T</pubmed_authors><pubmed_authors>Wang S</pubmed_authors><pubmed_authors>Gong M</pubmed_authors><pubmed_authors>Luo X</pubmed_authors><pubmed_authors>Chen S</pubmed_authors><pubmed_authors>Wu Y</pubmed_authors><pubmed_authors>Zhou J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Moderate static magnetic fields prevent estrogen deficiency-induced bone loss: Evidence from ovariectomized mouse model and small sample size randomized controlled clinical trial.</name><description>&lt;h4>Background&lt;/h4>Postmenopausal osteoporosis (PMOP) is the most common type of osteoporosis. Numerous studies have shown that static magnetic fields (SMFs) can inhibit bone loss by regulating bone remodeling. However, there are currently no clinical studies on the treatment of osteoporosis with SMFs. This study aims to investigate the clinical therapeutic effects of moderate static magnetic fields (MMFs) on PMOP.&lt;h4>Methods&lt;/h4>In this paper, we constructed MMF device using neodymium-iron-boron (NdFeB) materials. At the animal level, the effect of MMF exposure for 8 weeks on estrogen deficiency-induced bone loss was investigated by evaluating bone microstructure, mechanical properties, and bone conversion using ovariectomized (OVX) mice. Clinically, a single-blind randomized controlled s</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025</publication><modification>2025-07-04T03:06:05.479Z</modification><creation>2025-07-04T03:06:05.479Z</creation></dates><accession>S-EPMC12040201</accession><cross_references><pubmed>40299942</pubmed><doi>10.1371/journal.pone.0314199</doi></cross_references></HashMap>