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Periodontitis and osteoporosis: a two-sample Mendelian randomization analysis
Wu, Jiale; Yao, Lihui; Liu, Yuchen; Zhang, ShuaiShuai; Wang, Kan.
  • Wu, Jiale; Peking University School of Medicine, Hospital of Stomatology. Department of Oral and Maxillofacial Surgery. CN
  • Yao, Lihui; The First Affiliated Hospital of Zhengzhou University. Department of Stomatology. Zhengzhou. CN
  • Liu, Yuchen; Peking University School of Medicine, Hospital of Stomatology. Department of Oral and Maxillofacial Surgery. CN
  • Zhang, ShuaiShuai; The First Affiliated Hospital of Zhengzhou University. Department of Stomatology. Zhengzhou. CN
  • Wang, Kan; Peking University School of Medicine, Hospital of Stomatology. Department of Oral and Maxillofacial Surgery. CN
Braz. j. med. biol. res ; 57: e12951, fev.2024. tab, graf
Article Dans Anglais | LILACS-Express | LILACS | ID: biblio-1550148
ABSTRACT
Abstract The incidences of periodontitis and osteoporosis are rising worldwide. Observational studies have shown that periodontitis is associated with increased risk of osteoporosis. We performed a Mendelian randomization (MR) study to genetically investigate the causality of periodontitis on osteoporosis. We explored the causal effect of periodontitis on osteoporosis by MR analysis. A total of 9 single nucleotide polymorphisms (SNP) were related to periodontitis. The primary approach in this MR analysis was the inverse variance-weighted (IVW) method. Simple median, weighted median, and penalized weighted median were used to analyze sensitivity. The fixed-effect IVW model and random-effect IVW model showed no significant causal effect of genetically predicted periodontitis on the risk of osteoporosis (OR=1.032; 95%CI 0.923-1.153; P=0.574; OR=1.032; 95%CI 0.920-1.158; P=0.588, respectively). Similar results were observed in simple mode (OR=1.031; 95%CI 0.780-1.361, P=0.835), weighted mode (OR=1.120; 95%CI 0.944-1.328, P=0.229), simple median (OR=1.003; 95%CI 0.839-1.197, P=0.977), weighted median (OR=1.078; 95%CI 0.921-1.262, P=0.346), penalized weight median (OR 1.078; 95%CI 0.919-1.264, P=0.351), and MR-Egger method (OR=1.360; 95%CI 0.998-1.853, P=0.092). There was no heterogeneity in the IVW and MR-Egger analyses (Q=7.454, P=0.489 and Q=3.901, P=0.791, respectively). MR-Egger regression revealed no evidence of a pleiotropic influence through genetic variants (intercept -0.004; P=0.101). The leave-one-out sensitivity analysis indicated no driven influence of any individual SNP on the association between periodontitis and osteoporosis. The Mendelian randomization analysis did not show a significant detrimental effect of periodontitis on the risk of osteoporosis.


Texte intégral: Disponible Indice: LILAS (Amériques) langue: Anglais Texte intégral: Braz. j. med. biol. res Thème du journal: Biologie / Médicament Année: 2024 Type: Article Pays d'affiliation: Chine Institution/Pays d'affiliation: Peking University School of Medicine, Hospital of Stomatology/CN / The First Affiliated Hospital of Zhengzhou University/CN

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Texte intégral: Disponible Indice: LILAS (Amériques) langue: Anglais Texte intégral: Braz. j. med. biol. res Thème du journal: Biologie / Médicament Année: 2024 Type: Article Pays d'affiliation: Chine Institution/Pays d'affiliation: Peking University School of Medicine, Hospital of Stomatology/CN / The First Affiliated Hospital of Zhengzhou University/CN