Association Between VKORC1 Gene Polymorphisms and Osteopenia and Osteoporosis: A Systematic Review and Meta-Analysis
Ştefan Cristian Vesa, Vlad-Mihai Ichim, Silvina Iluț, Stefano Miglietta, Mihai Lupu, Camelia Alexandra Coada, Antonia Eugenia Macarie, Ovidiu Chiroban, Anca Dana Buzoianu, Octavia Sabin

TL;DR
This study finds a modest link between genetic variations in the VKORC1 gene and conditions like osteopenia and osteoporosis, suggesting a potential role in bone health.
Contribution
The study provides the first meta-analysis on the association between VKORC1 gene polymorphisms and bone health conditions.
Findings
VKORC1 risk alleles showed a significant association with osteopenia/osteoporosis (OR = 1.16, 95% CI = 1.01–1.35).
The most studied variants were rs9923231 and rs9934438.
There was no significant heterogeneity among the included studies (I2 = 0%).
Abstract
Background and Objectives: The vitamin K epoxide reductase complex subunit 1 (VKORC1) plays a central role in the vitamin K cycle, which is essential for γ-carboxylation of multiple bone-related proteins. Genetic variants in VKORC1 may influence bone mineral density (BMD) and osteoporosis risk. Materials and Methods: A systematic review and meta-analysis were conducted to evaluate the association between VKORC1 polymorphisms and osteopenia and osteoporosis. Relevant studies were identified through PubMed, Scopus, and Web of Science databases. Data on study characteristics, genotypes, BMD measurement, ethnicity, sex, and menopausal status were extracted. Results: Six studies comprising 7335 participants were included. All studies assessed BMD using dual-energy X-ray absorptiometry (DXA). The mean participant age ranged from 41.9 to 63.7 years. The VKORC1 variants most frequently studied,…
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Taxonomy
TopicsVitamin K Research Studies · Eicosanoids and Hypertension Pharmacology · Pharmacogenetics and Drug Metabolism
