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Causal association of metformin and osteoporosis: A 2-sample Mendelian randomization study
To investigate the causal relationship between metformin use and osteoporosis and different subtypes of osteoporosis using a 2-sample Mendelian randomization method. Data from genome-wide association studies were analyzed, with the exposure factor being metformin and the outcome variables being oste...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10615397/ https://www.ncbi.nlm.nih.gov/pubmed/37904346 http://dx.doi.org/10.1097/MD.0000000000035191 |
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author | Wei, Yong-Kang Chen, Ping-Bo Ju, Ling-Ling Deng, Guang-Hua |
author_facet | Wei, Yong-Kang Chen, Ping-Bo Ju, Ling-Ling Deng, Guang-Hua |
author_sort | Wei, Yong-Kang |
collection | PubMed |
description | To investigate the causal relationship between metformin use and osteoporosis and different subtypes of osteoporosis using a 2-sample Mendelian randomization method. Data from genome-wide association studies were analyzed, with the exposure factor being metformin and the outcome variables being osteoporosis and different subtypes. Mendelian randomization was performed using Inverse Variance Weighted (IVW), MR-Egger, and weight median (WM) methods, and heterogeneity tests, horizontal multivariate analyses, and sensitivity analyses were performed. The IVW method analysis with metformin and osteoporosis showed P = 1.53E-04, OR (95%CI) = 1.81E-02 (2.27E-02-1.44E-01); the IVW method analysis with metformin and postmenopausal osteoporosis with pathologic fracture showed P = 2.22E-01, OR (95%CI) = 4.89E-02 (3. 83E-04-6.23E + 00); the IVW method using metformin with osteoporosis with pathological fracture showed that P = 2.14E-01, OR (95%CI) = 1.64E + 00(5.78E-02-6.44E-04); the IVW method using metformin with pharmacological osteoporosis with pathological fracture showed that P = 9. 83E- 01, OR (95%CI) = 1.11E + 00 (3.99E-05-3.11E + 04); IVW method of metformin use and pharmacological osteoporosis showed that P = 5.99E-01, OR (95%CI) = 2.27E + 01 (2.00E-04-2.57E + 06); there is a causal relationship between metformin use and osteoporosis, but there is no causal relationship between metformin use and postmenopausal osteoporosis with pathological fracture, osteoporosis with pathological fracture, pharmacological osteoporosis, and pharmacological osteoporosis with pathological fracture, and metformin use is a protective factor for osteoporosis. |
format | Online Article Text |
id | pubmed-10615397 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-106153972023-10-31 Causal association of metformin and osteoporosis: A 2-sample Mendelian randomization study Wei, Yong-Kang Chen, Ping-Bo Ju, Ling-Ling Deng, Guang-Hua Medicine (Baltimore) 4300 To investigate the causal relationship between metformin use and osteoporosis and different subtypes of osteoporosis using a 2-sample Mendelian randomization method. Data from genome-wide association studies were analyzed, with the exposure factor being metformin and the outcome variables being osteoporosis and different subtypes. Mendelian randomization was performed using Inverse Variance Weighted (IVW), MR-Egger, and weight median (WM) methods, and heterogeneity tests, horizontal multivariate analyses, and sensitivity analyses were performed. The IVW method analysis with metformin and osteoporosis showed P = 1.53E-04, OR (95%CI) = 1.81E-02 (2.27E-02-1.44E-01); the IVW method analysis with metformin and postmenopausal osteoporosis with pathologic fracture showed P = 2.22E-01, OR (95%CI) = 4.89E-02 (3. 83E-04-6.23E + 00); the IVW method using metformin with osteoporosis with pathological fracture showed that P = 2.14E-01, OR (95%CI) = 1.64E + 00(5.78E-02-6.44E-04); the IVW method using metformin with pharmacological osteoporosis with pathological fracture showed that P = 9. 83E- 01, OR (95%CI) = 1.11E + 00 (3.99E-05-3.11E + 04); IVW method of metformin use and pharmacological osteoporosis showed that P = 5.99E-01, OR (95%CI) = 2.27E + 01 (2.00E-04-2.57E + 06); there is a causal relationship between metformin use and osteoporosis, but there is no causal relationship between metformin use and postmenopausal osteoporosis with pathological fracture, osteoporosis with pathological fracture, pharmacological osteoporosis, and pharmacological osteoporosis with pathological fracture, and metformin use is a protective factor for osteoporosis. Lippincott Williams & Wilkins 2023-10-27 /pmc/articles/PMC10615397/ /pubmed/37904346 http://dx.doi.org/10.1097/MD.0000000000035191 Text en Copyright © 2023 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY) (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | 4300 Wei, Yong-Kang Chen, Ping-Bo Ju, Ling-Ling Deng, Guang-Hua Causal association of metformin and osteoporosis: A 2-sample Mendelian randomization study |
title | Causal association of metformin and osteoporosis: A 2-sample Mendelian randomization study |
title_full | Causal association of metformin and osteoporosis: A 2-sample Mendelian randomization study |
title_fullStr | Causal association of metformin and osteoporosis: A 2-sample Mendelian randomization study |
title_full_unstemmed | Causal association of metformin and osteoporosis: A 2-sample Mendelian randomization study |
title_short | Causal association of metformin and osteoporosis: A 2-sample Mendelian randomization study |
title_sort | causal association of metformin and osteoporosis: a 2-sample mendelian randomization study |
topic | 4300 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10615397/ https://www.ncbi.nlm.nih.gov/pubmed/37904346 http://dx.doi.org/10.1097/MD.0000000000035191 |
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