Evidence map›Paper›PMID 41961089›Full record

ArticleOsteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA2026

Romosozumab versus teriparatide and risk of all-cause mortality in patients with osteoporosis: a real-world propensity score-matched cohort study.

Sung Huang Laurent Tsai, Yu Hsuan Chen, Chi-Ya Yang, Ching-Yu Lee, Chia-Hsien Chen, Tsung-Jen Huang, Meng-Huang Wu, Hung-En Huang, Wei Cheng Chung James

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Article in Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Sung Huang Laurent TsaiDepartment of Orthopedics, Taipei Medical University Hospital, No. 252, Wu-Hsing St, Taipei, 11031, Taiwan. laurenttsai@gmail.com.ORCID http://orcid.org/0000-0002-6993-5416
Yu Hsuan ChenCathay General Hospital, Taipei, Taiwan.
Chi-Ya YangDepartment of Family Medicine, Taipei Medical University Hospital, Taipei, Taiwan.
Ching-Yu LeeDepartment of Orthopedics, Taipei Medical University Hospital, No. 252, Wu-Hsing St, Taipei, 11031, Taiwan.
Chia-Hsien ChenDepartment of Orthopedics, Taipei Medical University Hospital, No. 252, Wu-Hsing St, Taipei, 11031, Taiwan.
Tsung-Jen HuangDepartment of Orthopedics, Taipei Medical University Hospital, No. 252, Wu-Hsing St, Taipei, 11031, Taiwan.
Meng-Huang WuDepartment of Orthopedics, Taipei Medical University Hospital, No. 252, Wu-Hsing St, Taipei, 11031, Taiwan.
Hung-En HuangCenter for Health Data Science, Department of Medical Research, Chung Shan Medical University Hospital, Taichung, Taiwan.
Wei Cheng Chung JamesDepartment of Health Policy and Management, College of Health Care and Management, Chung Shan Medical University, No. 110, Sec. 1, Jianguo N. Rd., South District, Taichung, 40201, Taiwan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study compared romosozumab and teriparatide for osteoporosis treatment using real-world data. Romosozumab was linked to significantly lower mortality, especially in older adults, without added cardiovascular risk. These findings highlight romosozumab as a potentially safer and more effective option for reducing death risk in patients with osteoporosis.

backgroundOsteoporosis is a prevalent condition among older adults and significantly increases the risk of fragility fractures, particularly affecting the hip and vertebrae. Pharmacologic therapy remains central to osteoporosis management, with anabolic agents such as romosozumab and teriparatide demonstrating efficacy in increasing bone mineral density and reducing fracture risk. However, direct comparative evidence regarding their impact on mortality is limited. This study aimed to evaluate the differences in all-cause mortality between romosozumab and teriparatide in patients with osteoporosis, utilizing a large real-world dataset.

methodsWe conducted a retrospective cohort study using electronic medical records from the TriNetX US Collaborative Network, comprising data from over 120 healthcare organizations. Patients aged ≥ 20 years diagnosed with osteoporosis between January 1, 2016, and December 31, 2023, initiating either romosozumab or teriparatide were included. Individuals with malignancies, bone neoplasms, multiple myeloma, parathyroid disorders, or cerebrovascular accidents were excluded. Propensity score matching (1:1) balanced demographic, clinical, and laboratory characteristics between cohorts. The primary outcome was all-cause mortality, with subgroup analyses performed based on age, sex, comorbidities, and treatment settings.

resultsEach treatment group included 2470 matched patients. Over the follow-up period, romosozumab was associated with significantly lower all-cause mortality compared to teriparatide (hazard ratio [HR] 0.68, 95% CI 0.49-0.94). This survival advantage was particularly evident in patients aged ≥ 60 years (HR 0.65, 95% CI 0.47-0.88). Subgroup analyses consistently favored romosozumab across multiple comorbid conditions, including diabetes mellitus and chronic kidney disease, although these subgroup results did not reach statistical significance. Importantly, no increased mortality risk was observed in patients with hypertension or coronary heart disease, indicating a favorable cardiovascular safety profile in these populations.

conclusionIn this real-world analysis, romosozumab was associated with a significantly lower risk of all-cause mortality compared to teriparatide among patients with osteoporosis. These findings may support the preferential consideration of romosozumab, particularly for older adults and patients at elevated fracture risk, given the inherent limitations of the study design, while highlighting the necessity of careful cardiovascular risk assessment.

Indexed as

OsteoporosisReal World AnalysisRomosozumabTeriparatide

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.