PMID- 36225670 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20221014 IS - 2040-6223 (Print) IS - 2040-6231 (Electronic) IS - 2040-6223 (Linking) VI - 13 DP - 2022 TI - Efficacy and safety of bisphosphonates on childhood osteoporosis secondary to chronic illness or its treatment: a meta-analysis. PG - 20406223221129163 LID - 10.1177/20406223221129163 [doi] LID - 20406223221129163 AB - BACKGROUND: Bisphosphonates are a type of medication that prevents the loss of bone density. Secondary childhood osteoporosis reduces bone strength and results in an increased risk of fragility fracture. This meta-analysis aims to explore the efficacy and safety of bisphosphonates on secondary childhood osteoporosis. METHODS: We performed a systematic search of PubMed, Cochrane library, and Web of Science databases up to 31 July 2022 to screen for random clinical trials (RCTs) on bisphosphonate treatment for childhood secondary osteoporosis. Data from selected studies, mainly changes in lumbar spine (LS) bone mineral density (BMD), changes in LS BMD Z-scores, fracture events, and adverse events (AEs), were extracted and analyzed. RESULTS: Nine RCTs (n = 429 in total) were included in our meta-analysis. The meta-analysis indicated that bisphosphonates improved the changes in LS BMD [mean difference (MD) = 0.04, 95% confidence intervals (CIs) = 0.01-0.07, p < 0.01] and LS BMD Z-scores [MD = 0.52, 95% CI = 0.23-0.81, p < 0.01]. Use of bisphosphonates did not increase the risk of AEs [odds ratio (OR) = 1.61, 95% CI = 0.87-2.99, p = 0.13]. Subgroup analysis showed that routes of administration, but not causes of secondary osteoporosis, might influence the efficacy of bisphosphonates. IV bisphosphonates close to significantly improved the incidence of fracture (OR = 0.34, 95% CI: 0.11-1.08, p = 0.07). CONCLUSIONS: The use of bisphosphonates improves LS BMD without increasing AE rates, which supports the clinical use of bisphosphonates in secondary childhood osteoporosis. Further large RCTs are still warranted, especially for their long-term effects on fracture rates. CI - (c) The Author(s), 2022. FAU - Zhao, Huawei AU - Zhao H AD - Department of Pharmacy, The Children's Hospital, Zhejiang University School of Medicine and National Clinical Research Center for Child Health, Hangzhou, China. FAU - Ding, Yunfei AU - Ding Y AD - Laboratory of Rheumatology & Institute of TCM Clinical Basic Medicine, College of Basic Medical Science, Zhejiang Chinese Medical University, Hangzhou, China. FAU - Yang, Jufei AU - Yang J AD - Department of Pharmacy, The Children's Hospital, Zhejiang University School of Medicine and National Clinical Research Center for Child Health, Hangzhou, China. FAU - Luo, Yijun AU - Luo Y AD - Laboratory of Rheumatology & Institute of TCM Clinical Basic Medicine, College of Basic Medical Science, Zhejiang Chinese Medical University, Hangzhou, China. FAU - Xu, Zhenghao AU - Xu Z AUID- ORCID: 0000-0003-0033-525X AD - Laboratory of Rheumatology & Institute of TCM Clinical Basic Medicine, College of Basic Medical Science, Zhejiang Chinese Medical University, No. 548 Binwen Road, Hangzhou 310053, Zhejiang, China. AD - Laboratory of Rheumatology & Institute of TCM Clinical Basic Medicine, College of Basic Medical Science, Zhejiang Chinese Medical University, Hangzhou, China. FAU - Miao, Jing AU - Miao J AD - Department of Pharmacy, The Children's Hospital, Zhejiang University School of Medicine and National Clinical Research Center for Child Health, Hangzhou 310052, Zhejiang, China. AD - Department of Pharmacy, The Children's Hospital, Zhejiang University School of Medicine and National Clinical Research Center for Child Health, Hangzhou, China. LA - eng PT - Journal Article DEP - 20221006 PL - United States TA - Ther Adv Chronic Dis JT - Therapeutic advances in chronic disease JID - 101532140 PMC - PMC9549182 OTO - NOTNLM OT - bisphosphonate OT - bone mineral density OT - children OT - secondary osteoporosis COIS- The authors declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article. EDAT- 2022/10/14 06:00 MHDA- 2022/10/14 06:01 PMCR- 2022/10/06 CRDT- 2022/10/13 02:35 PHST- 2022/02/23 00:00 [received] PHST- 2022/09/07 00:00 [accepted] PHST- 2022/10/13 02:35 [entrez] PHST- 2022/10/14 06:00 [pubmed] PHST- 2022/10/14 06:01 [medline] PHST- 2022/10/06 00:00 [pmc-release] AID - 10.1177_20406223221129163 [pii] AID - 10.1177/20406223221129163 [doi] PST - epublish SO - Ther Adv Chronic Dis. 2022 Oct 6;13:20406223221129163. doi: 10.1177/20406223221129163. eCollection 2022.