Fernando Rivadeneira
Professor Translational Skeletal Genomics
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About
Professor Fernando Rivadeneira is a faculty member in Translational Skeletal Genomics at Erasmus MC, Netherlands. His research areas include genomic studies of facial traits, fracture risk, muscle phenotyping, and bone health assessment. Recent publications highlight his work on bone mineral density and its associations with dementia and cardiovascular health.
Articles (20)
Year:
2025
Observational studies have reported inconsistent associations between bone mineral density (BMD) and coronary artery calcification (CAC). We examined the observational association of BMD with CAC in 2 large population-based studies and evaluated the evidence for a potential causal relation between BMD and CAC using polygenic risk scores (PRS), 1- and 2-sample Mendelian randomization (MR) approaches. Our study populations comprised 1414 individuals (mean age 69.9 yr, 52.0% women) from the Rotterdam Study and 2233 individuals (mean age 56.5 yr, 50.9% women) from the Framingham Heart Study with complete information on CAC and BMD measurements at the total body (TB-), lumbar spine (LS-), and femoral neck (FN-). We used linear regression models to evaluate the observational association between BMD and CAC. Subsequently, we compared the mean CAC across PRSBMD quintile groups at different skeletal sites. In addition, we used the 2-stage least squares regression and the inverse variance weighted (IVW) model as primary methods for 1- and 2-sample MR to test evidence for a potentially causal association. We did not observe robust associations between measured BMD levels and CAC. These results were consistent with a uniform random distribution of mean CAC across PRSBMD quintile groups (P-value > .05). Moreover, neither 1- nor 2-sample MR supported the possible causal association between BMD and CAC. Our results do not support the contention that lower BMD is (causally) associated with an increased CAC risk. These findings suggest that previously reported epidemiological associations of BMD with CAC are likely explained by unmeasured confounders or shared etiology, rather than by causal pathways underlying both osteoporosis and vascular calcification processes.
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2024
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2024
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2024
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2024
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2024
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2024
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2024
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2024
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2024
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2023
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2022
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2022
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2022
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2022
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2022
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2021
Collaborators (30)
Xianjing LIU
Erasmus University Rotterdam
Lies Lahousse
Professor at Ghent University
Ghent University
Randall T. Loder
Indiana University School of Medicine
Ivan Duran
Professor
University of Malaga
André G Uitterlinden
Erasmus University Rotterdam
Pirro Hysi
King's College London
Melissa Kacena
Professor, Vice Chair for Research
Indiana University School of Medicine
Antonio Maurizi
University of L'Aquila
Vincent W. V. Jaddoe
-
José A. Riancho
Universidad de Cantabria
Liesbeth Vandenput
Professor
Australian Catholic University
Enwu Liu
Flinders University
G V Roshchupkin
Erasmus University Medical Center
Roberto Civitelli
Professor of medicine
Washington University in St. Louis
Mohsen Ghanbari
Associate Professor and Principal Investigator
Erasmus MC
Emma Duncan
King’s College London
Henning Tiemeier
Professor of Maternal and Child Health
Harvard T.H. Chan School of Public Health
Raquel Rabionet
Professor Agregat
University of Barcelona
Jose Da Silva
Full Professor of Rheumatology
University of Coimbra
Guy Brusselle
Head of Department
Ghent University Hospital
Kaitlin Wade
Senior Lecturer of Epidemiology
University of Bristol
Neelam Hassan
University of Bristol
Annemieke JMH Verkerk
assistant professor, molecular biologist
Erasmus MC
Carolina Medina-Gomez
-
Eleni Douni
Agricultural University of Athens
Luba M Pardo
Erasmus University Medical Center
Tjeerd van Staa
The University of Manchester
Dylan Bergen
University of Bristol
Sara R. A. Wijnant
Universiteit Gent
Kathleen Curran
Prof.
Dublin City University
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