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Romosozumab, by inhibiting sclerostin activates the Wnt signaling pathway, leading to increased bone formation and decreased bone resorption. The pivotal ARCH and FRAME studies established romosozumab\u2019s fracture reduction efficacy. Romosozumab was superior to alendronate in fracture reduction and bone mineral density gain in the ARCH study. Romosozumab treatment should be followed sequentially with a potent antiresorptive agent. The antifracture efficacy gained from romosozumab is maintained or improved after transitioning to an antiresorptive agent. As one of the most potent osteoanabolic agents, the introduction of romosozumab has significantly increased our ability to treat osteoporosis. Studies have provided important information on using romosozumab with other osteoporosis medications to optimize osteoporosis treatment. Romosozumab used before antiresorptive medications is associated with more significant bone mineral density increases than when an antiresorptive agent is used before romosozumab. Romosozumab is recommended for osteoporosis treatment in patients at very high risk for fracture with low cardiovascular risk. Romosozumab is generally well tolerated, with 4%\u20135% of patients having injection site reactions. The ARCH trial showed a higher risk of cardiovascular events in patients receiving romosozumab. Romosozumab carries a black box warning that romosozumab should not be initiated in patients with myocardial infarction or stroke in the preceding year. However, the information on romosozumab and increased cardiovascular risk is conflicting. The risk of cardiovascular disease with romosozumab is unclear. While romosozumab has demonstrated significant osteoanabolic effect and antifracture efficacy and will benefit high fracture risk patients, further studies are needed to investigate the cardiovascular safety of romosozumab.<\/jats:p>","DOI":"10.1177\/17455057221125577","type":"journal-article","created":{"date-parts":[[2022,9,24]],"date-time":"2022-09-24T06:37:40Z","timestamp":1664001460000},"update-policy":"https:\/\/doi.org\/10.1177\/sage-journals-update-policy","source":"Crossref","is-referenced-by-count":26,"title":["Romosozumab for the treatment of osteoporosis in women: Efficacy, safety, and cardiovascular risk"],"prefix":"10.1177","volume":"18","author":[{"ORCID":"https:\/\/orcid.org\/0000-0003-4886-9007","authenticated-orcid":false,"given":"Sian Yik","family":"Lim","sequence":"first","affiliation":[{"name":"Hawaii Pacific Health Medical Group, Pali Momi Medical Center, Aiea, HI, USA"},{"name":"John A. Burns School of Medicine, University of Hawai\u2019i at M\u0101noa, Honolulu, HI, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"179","published-online":{"date-parts":[[2022,9,24]]},"reference":[{"key":"bibr1-17455057221125577","doi-asserted-by":"publisher","DOI":"10.1001\/jama.285.6.785"},{"key":"bibr2-17455057221125577","unstructured":"International Osteoporosis Foundation (IOF). 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