Cited by 119Bone health and osteoporosis researchGenetic Associations and EpidemiologyBone Metabolism and Diseases

Evaluating the cardiovascular safety of sclerostin inhibition using evidence from meta-analysis of clinical trials and human genetics

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Bovijn, Jonas, Krebs, Kristi, Chen, Chia-Yen, Boxall, Ruth, Censin, Jenny C., Ferreira, Teresa, Pulit, Sara L., Glastonbury, Craig A. +12 more·2020·Science Translational Medicine

Abstract

SOST variants that mimic therapeutic inhibition of sclerostin for osteoporosis are associated with higher risk of cardiovascular disease.

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Crossref · 10.1126/scitranslmed.aay6570

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References 122 · Cited by 119

Research works printed but not linked: 2

  1. [24]UCB EVENITY (romosozumab) receives positive CHMP opinion for the treatment of severe osteoporosis in postmenopausal women at high risk of fracture 2019 www.ucb.com/stories-media/Press-Releases/article/EVENITY-romosozumab-Receives-Positive-CHMP-Opinion-for-the-Treatment-of-Severe-Osteoporosis-in-Postmenopausal-Women-at-High-Risk-of-Fracture
  2. [72]McGregor TL Hunt KA Nioi P Mason D Ticau S Pelosi M Perry L Finer S Griffiths C MacArthur D Trembath RC Deep phenotyping of a healthy human HAO1 knockout informs therapeutic development for primary hyperoxaluria type 1 bioRxiv 2019 1 18 524256 [Preprint

Authors
Bovijn, J., Krebs, K., Chen, C.-Y., Boxall, R., Censin, J. C., Ferreira, T., Pulit, S. L., Glastonbury, C. A., Laber, S., Millwood, I. Y., Lin, K., Li, L., Chen, Z., Milani, L., Smith, G. D., Walters, R. G., Mägi, R., Neale, B. M., Lindgren, C. M., & Holmes, M. V.
Affiliations
  • Centre for Human Genetics (GB)
  • University of Tartu (EE)
  • Broad Institute (US)
  • University of Oxford (GB)
  • Peking University (CN)
  • University of Bristol (GB)
  • John Radcliffe Hospital (GB)
Corresponding author
  • Bovijn, Jonas
  • Krebs, Kristi
  • Chen, Chia-Yen
  • Boxall, Ruth
  • Walters, Robin G.
  • Mägi, Reedik
  • Neale, Benjamin M.
  • Lindgren, Cecilia M.
  • Holmes, Michael V.
Venue
Science Translational Medicine
Published
2020-06-24
Volume
12
Issue
549
ISSN
  • 1946-6234 (ISSN-L)
  • 1946-6242
OpenAlex
W3035249131
Cited by
119
References
122
Citations by year
2026: 17 · 2025: 20 · 2024: 12 · 2023: 22 · 2022: 16 · 2021: 24 · 2020: 8
FWCI
3.42
Type
journal article
Language
en
Licence
other-oa
Locations
  • Science Translational Medicine (publishedVersion)
  • PubMed (publishedVersion)
  • Explore Bristol Research (publishedVersion, other-oa)
  • Europe PMC (PubMed Central) (acceptedVersion)
  • PubMed Central (acceptedVersion)
Funders
  • National Institutes of Health
  • Li Ka Shing Foundation
  • Wellcome
  • Medical Research Council
  • British Heart Foundation
  • Estonian Research Council
  • Nederlandse Organisatie voor Wetenschappelijk Onderzoek
  • John Fell Fund, University of Oxford
  • NIHR Oxford Biomedical Research Centre
Topics
  • Health Sciences › Medicine › Orthopedics and Sports Medicine › Bone health and osteoporosis research
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bone Metabolism and Diseases
Keywords
sclerostin inhibition, romosozumab, cardiovascular safety, genetic variants, myocardial infarction, coronary revascularization, major adverse cardiovascular events, type 2 diabetes, systolic blood pressure, abdominal obesity, osteoporosis, fracture risk, bone metabolism
MeSH terms
Human Genetics, Humans, Osteoporosis, Bone Density, Bone Density Conservation Agents, Fractures, Bone

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