Evidence map›Paper›PMID 25989902›Full record

ArticleBMC musculoskeletal disorders2015

Tamoxifen use reduces the risk of osteoporotic fractures in women with breast cancer in Asia: a nationwide population-based cohort study.

Huey-En Tzeng, Chih-Hsin Muo, Hsien-Te Chen, Wen-Li Hwang, Horng-Chang Hsu, Chun-Hao Tsai

Open access · goldAbstract read
In one paragraph

Article in BMC musculoskeletal disorders, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.9field-weighted citation impact, top 25% of its field
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

9 citing papers in PubMed, 13 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 1 country.

Huey-En TzengGraduate Institute of Clinical Medicine, China Medical University, #91 Hsueh-Shih Road, Taichung, 404, Taiwan. tzenghueyen@gmail.com.
Chih-Hsin MuoManagement Office for Health Data, China Medical University Hospital, Taichung, Taiwan. a17776@mail.cmuh.org.tw.
Hsien-Te ChenDepartment of Orthopedics, China Medical University Hospital, Taichung, Taiwan. bonekid1@gmail.com.
Wen-Li HwangDivision of Hematology/Oncology, Taichung Veterans General Hospital, Taichung, Taiwan. kevinhwl@gmail.com.
Horng-Chang HsuSchool of Medicine, China Medical University, Taichung, Taiwan. D4749@mail.cmuh.org.tw.
Chun-Hao TsaiGraduate Institute of Clinical Medicine, China Medical University, #91 Hsueh-Shih Road, Taichung, 404, Taiwan. ritsai8615@gmail.com.
China Medical University · TWNational Yang Ming Chiao Tung University · TWTaichung Veterans General Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeBone mineral density changes with tamoxifen treatment have been reported in pre- and post-menopausal women with breast cancer. However, there remains controversy as to whether tamoxifen significantly reduces fracture rates in different age groups. Breast cancer occurs at 10-20 years younger in Asian women compared with Western women. Therefore we conducted this population-based case-control study to determine whether or not tamoxifen use is associated with osteoporotic fractures. PATIENTS AND

methodsWe selected 75488 women with breast cancer with no prior history of fractures from the Longitudinal Health Insurance Database for Catastrophic Illness Patients in 2000-2011. They were followed from the date of the diagnosis of breast cancer to the date a hip, vertebral or wrist fracture occurred. Because the use of tamoxifen was a time-dependent variable, we used a Cox proportional hazard model with time-dependent exposure covariates to estimate the risk of a fracture.

resultsThere were 50257 and 25231 women with breast cancer who did and did not receive tamoxifen treatment, respectively. The tamoxifen users had lower risks for overall fractures with hazard ratios (HRs) of 0.52 and 0.59 in the crude and adjusted models (95 % CI = 0.45-0.61 and 0.51-0.69), respectively. They also had lower risks for hip (HR = 0.55, 95 % CI = 0.45-0.67) and vertebral (HR = 0.64, 95 % CI = 0.50-0.82) fractures in the adjusted model. The risk of fractures decreased with an increasing dosage of tamoxifen. Regardless of the age group, the tamoxifen users had a lower risk of fractures than the non-users.

conclusionIn this Asian population-based case-control study, tamoxifen use was associated with a reduction in osteoporotic fractures, especially in hip fractures.

Indexed as

AgedAge FactorsAntineoplastic Agents, HormonalBone DensityBone Density Conservation AgentsBreast NeoplasmsCase-Control StudiesChi-Square DistributionFemaleHip FracturesHumansLongitudinal StudiesMiddle AgedOsteoporotic FracturesProportional Hazards ModelsProtective FactorsAntineoplastic Agents, HormonalBone Density Conservation AgentsTamoxifen

Identifiers

PMID25989902
PMCPMC4438570
OpenAlexW1512924461

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.