Evidence map›Paper›PMID 41444290›Full record

ArticleScientific reports2025

Effects of bisphosphonates after denosumab discontinuation and treatment effect heterogeneity using causal machine learning.

Miryoung Kim, Nakyung Jeon, Hae Sun Suh

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

The trial behind it

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

3 authors.

Miryoung KimCollege of Pharmacy, Pusan National University, Busan, Republic of Korea.
Nakyung JeonCollege of Pharmacy, Pusan National University, Busan, Republic of Korea.
Hae Sun SuhCollege of Pharmacy, Kyung Hee University, Seoul, Republic of Korea. haesun.suh@khu.ac.kr.ORCID 0000-0003-3445-6607

Funding

Ministry of Food and Drug Safety 21153MFDS601National Research Foundation of Korea RS-2024-00331719 and RS-2024-00345981
6 · The paper itself

Abstract

Discontinuation of denosumab is associated with a rebound increase in osteoporotic fracture (OF) risk, and bisphosphonates (BPs) are commonly recommended as sequential therapy to mitigate this risk. However, their real-world effectiveness-and whether certain patients benefit more than others-remains unclear. To address this question, we employed a causal machine learning approach capable of estimating heterogeneous treatment effects. We conducted a nationwide retrospective cohort study using Korean health insurance claims data and applied the causal survival forest model to evaluate the effect of BPs on recurrent OFs and explore treatment effect heterogeneity. Patients were followed for up to one year after the index date to ascertain fracture outcomes. BPs significantly reduced the risk of recurrent OFs (fracture-free probability difference: 0.032; 95% CI 0.022-0.042). Treatment effects varied by age, prior BP use, diabetes without complications, peptic ulcer disease, steroid use, and type of treatment institution. The model incorporated doubly robust adjustment for treatment assignment and time-to-event outcomes, while correcting for censoring in survival time estimation, resulting in conservative but robust effect estimates. Sensitivity analyses using traditional statistical methods supported the findings. This study provides causally informed, real-world evidence for the effectiveness of BPs after denosumab discontinuation and highlights the potential of causal machine learning to support personalized fracture prevention by identifying patient subgroups most likely to benefit.

Indexed as

Bone Density Conservation AgentsDenosumabDiphosphonatesMachine LearningOsteoporotic FracturesAgedAged, 80 and overFemaleHumansMaleMiddle AgedOsteoporosisRepublic of KoreaRetrospective StudiesTreatment Effect HeterogeneityTreatment OutcomeBone Density Conservation AgentsDenosumabDiphosphonatesBisphosphonatesCausal effectMachine learningOsteoporotic fracturesTreatment effect heterogeneity

Identifiers

PMID41444290
PMCPMC12738746

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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.