Evidence map›Paper›PMID 32725307›Full record

ReviewDrugs2020

Assessment of Cardiovascular Safety of Anti-Osteoporosis Drugs.

N R Fuggle, C Cooper, N C Harvey, N Al-Daghri, M-L Brandi, O Bruyere, A Cano, E M Dennison, A Diez-Perez, J-M Kaufman and 8 more

Open access · hybridAbstract readReview
In one paragraph

Review in Drugs, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 5 pooled it
7.0field-weighted citation impact, top 2% 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

40 citing papers in PubMed, 5 syntheses or guidelines pooled it, 63 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Association between bisphosphonate use and stroke risk: a meta-analysis.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2023
    Pooled it
  4. Pooled it
  5. Pooled it
  6. Postmenopausal Osteoporosis, Endothelial Dysfunction, and Cardiovascular Risk.Journal of clinical rheumatology : practical reports on rheumatic & musculoskeletal diseases · 2026
    Article
  7. Article
  8. Observational
  9. Article
  10. Article
  11. Review
  12. Review
  13. Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Effect of Oral Bisphosphonate Drug Holiday on Mortality Following Hip Fracture.The Journal of clinical endocrinology and metabolism · 2024
    Article
  19. Review
  20. Review
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

18 authors at 14 institutions in 9 countries.

N R FuggleMRC Lifecourse Epidemiology Unit, University of Southampton, Tremona Road, Southampton, SO16 6YD, UK.
C CooperMRC Lifecourse Epidemiology Unit, University of Southampton, Tremona Road, Southampton, SO16 6YD, UK. cc@mrc.soton.ac.uk.
N C HarveyMRC Lifecourse Epidemiology Unit, University of Southampton, Tremona Road, Southampton, SO16 6YD, UK.
N Al-DaghriChair for Biomarkers of Chronic Diseases, Biochemistry Department, College of Science, King Saud University, Riyadh, Kingdom of Saudi Arabia.
M-L BrandiUnit of Bone and Mineral Diseases, Department of Surgery and Translational Medicine, University Hospital of Florence, University of Florence, 50139, Florence, Italy.
O BruyereWHO Collaborating Centre for Public Health Aspects of Musculoskeletal Health and Aging, Liège, Belgium.
A CanoDepartment of Obstetrics and Gynecology, University of Valencia and INCLIVA Health Research Institute, Valencia, Spain.
E M DennisonMRC Lifecourse Epidemiology Unit, University of Southampton, Tremona Road, Southampton, SO16 6YD, UK.
A Diez-PerezHospital del Mar Research Institute (IMIM), Centro de Investigación Biomédica en Red de Fragilidad y Envejecimiento Saludable (CIBERFES), Barcelona, Spain.
J-M KaufmanDepartment of Endocrinology, Ghent University Hospital, 9000, Ghent, Belgium.
S PalaciosThe Palacios Institute of Women's Health, Madrid, Spain.
D Prieto-AlhambraNuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences (NDORMS), University of Oxford, Oxford, UK.
S RozenbergDepartment of Obstetrics and Gynecology, CHU St Pierre, Laboratoire de Santé Génésique Université Libre de Bruxelles, Brussels, Belgium.
T ThomasDepartment of Rheumatology, Hôpital Nord, CHU de Saint-Etienne, and INSERM U1059, Université de Lyon, Saint-Etienne, France.
F TremollieresMenopause Centre, Hôpital Paule de Viguier, University Hospital of Toulouse and INSERM U1048-I2MC, Equipe 9, Toulouse, France.
R RizzoliService of Bone Diseases, Geneva University Hospitals and Faculty of Medicine, 1211, Geneva 14, Switzerland.
J A KanisMary McKillop Institute for Health Research, Australian Catholic University, Melbourne, Australia.
J Y ReginsterChair for Biomarkers of Chronic Diseases, Biochemistry Department, College of Science, King Saud University, Riyadh, Kingdom of Saudi Arabia.
Inserm · FRKing Saud University · SAMRC Lifecourse Epidemiology Unit · GBUniversity of Southampton · GBCentro de Investigación Biomédica en Red de Fragilidad y Envejecimiento Saludable · ESGhent University Hospital · BEInstituto Palacios · ESNuffield Orthopaedic Centre · GBUniversitat de València · ESUniversité Libre de Bruxelles · BEUniversity Hospital of Geneva · CHUniversity of Florence · ITUniversity of Liège · BEUniversity of Sheffield · GB

Funding

Medical Research Council MC_ST_U13058Medical Research Council MC_UU_12011/1
6 · The paper itself

Abstract

The incidence of osteoporosis and cardiovascular disease increases with age, and there are potentially shared mechanistic associations between the two conditions. It is therefore highly relevant to understand the cardiovascular implications of osteoporosis medications. These are presented in this narrative review. Calcium supplementation could theoretically cause atheroma formation via calcium deposition, and in one study was found to be associated with myocardial infarction, but this has not been replicated. Vitamin D supplementation has been extensively investigated for cardiac benefit, but no consistent effect has been found. Despite findings in the early 21st century that menopausal hormone therapy was associated with coronary artery disease and venous thromboembolism (VTE), this therapy is now thought to be potentially safe (from a cardiac perspective) if started within the first 10 years of the menopause. Selective estrogen receptor modulators (SERMs) are associated with increased risk of VTE and may be related to fatal strokes (a subset of total strokes). Bisphosphonates could theoretically provide protection against atheroma. However, data from randomised trials and observational studies have neither robustly supported this nor consistently demonstrated the potential association with atrial fibrillation. Denosumab does not appear to be associated with cardiovascular disease and, although parathyroid hormone analogues are associated with palpitations and dizziness, no association with a defined cardiovascular pathology has been demonstrated. Finally, romosozumab has been shown to have a possible cardiovascular signal, and therefore post-market surveillance of this therapy will be vital.

Indexed as

Bone Density Conservation AgentsCalciumDietary SupplementsDiphosphonatesFemaleHormone Replacement TherapyHumansIncidenceMenopauseOsteoporosisPlaque, AtheroscleroticProduct Surveillance, PostmarketingRisk AssessmentSelective Estrogen Receptor ModulatorsStrokeVenous ThromboembolismBone Density Conservation AgentsCalciumDiphosphonatesSelective Estrogen Receptor ModulatorsVitamin D

Identifiers

PMID32725307
PMCPMC7536167
OpenAlexW3037592394

What OpenQuestion holds

Textmetadata
LicenceTDM
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.