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      Association between periodontal disease and osteoporosis in postmenopausal women: A systematic review and meta-analysis

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          Abstract

          Objective

          To evaluate the relationship between periodontitis and postmenopausal osteoporosis.

          Methods

          This research was carried out according to the principles laid down by the PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) guideline statement. We searched the Web of Science, Embase, PubMed, The Cochrane Library, CNKI, VIP, and WanFang databases from inception to July 1, 2023 to collect all relevant publications, with no restrictions on publication date or Languages. Cochrane's tool for assessing RoB was used to evaluate the RoB for RCTs. The Newcastle-Ottawa Scale was used to assess the RoB for cohort studies and case-control studies. Mean differences (MD) with 95 % confidence intervals (CI) were used for analysis of continuous data. Heterogeneity was measured using the I 2 statistic. Revman 5.4 software was used for the meta-analysis.

          Results

          28 observational studies with 19611 patients, including 5813 cases in the postmenopausal osteoporosis group and 13798 cases in the non-osteoporosis group. The studies showed that the degrees of clinical attachment loss (CAL), probing depth (PD), gingival recession (GR), simplified oral hygiene index (OHIS), and percentage of sites with bleeding on probing (BOP) in the postmenopausal osteoporosis group were higher than those in the non-osteoporosis group[CAL(MD = 0.89(mm), 95 % CI [0.48,1.30], p < 0.00001), PD (MD = 0.27(mm), 95 % CI [0.13, 0.41], p = 0.0001), GR (MD = 0.28(mm), 95 % CI [0.20, 0.35], p < 0.00001), OHIS (MD = 1.32,95 % CI [1.12,1.51], p < 0.00001), BOP(MD = 12.71(%), 95 % CI [3.24,22.18], p = 0.009)]. Eleven studies found that bone mineral density (BMD) in the postmenopausal osteoporosis group was lower than that in non-osteoporosis group (MD = −0.41(U/cm 2), 95 % CI [-0.77,-0.05], p = 0.03). The combined analysis results of the studies in the two groups showed that there were no significant differences in the loss of alveolar crestal height (ACH)[(MD = −1.76(%),95%CI [-3.64,0.12], p = 0.07)].

          Conclusion

          Postmenopausal osteoporosis patients are more likely to suffer from periodontitis, and the condition is easily aggravated.

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          Most cited references62

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          Bias in meta-analysis detected by a simple, graphical test

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            The Simplified Oral Hygiene Index

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              Interaction between bone and immune cells: Implications for postmenopausal osteoporosis

              Postmenopausal osteoporosis is a systemic disease characterized by the loss of bone mass and increased bone fracture risk largely resulting from significantly reduced levels of the hormone estrogen after menopause. Besides the direct negative effects of estrogen-deficiency on bone, indirect effects of altered immune status in postmenopausal women might contribute to ongoing bone destruction, as postmenopausal women often display a chronic low-grade inflammatory phenotype with altered cytokine expression and immune cell profile. In this context, it was previously shown that various immune cells interact with osteoblasts and osteoclasts either via direct cell-cell contact, or more likely via paracrine mechanisms. For example, specific subtypes of T lymphocytes express TNFα, which was shown to increase osteoblast apoptosis and to indirectly stimulate osteoclastogenesis via B cell-produced receptor-activator of NF-κB ligand (RANKL), thereby triggering bone loss during postmenopausal osteoporosis. Th17 cells release interleukin-17 (IL-17), which directs mesenchymal stem cell differentiation towards the osteogenic lineage, but also indirectly increases osteoclast differentiation. B lymphocytes are a major regulator of osteoclast formation via granulocyte colony-stimulating factor secretion and the RANKL/osteoprotegerin system under estrogen-deficient conditions. Macrophages might act differently on bone cells dependent on their polarization profile and their secreted paracrine factors, which might have implications for the development of postmenopausal osteoporosis, because macrophage polarization is altered during disease progression. Likewise, neutrophils play an important role during bone homeostasis, but their over-activation under estrogen-deficient conditions contributes to osteoblast apoptosis via the release of reactive oxygen species and increased osteoclastogenesis via RANKL signaling. Furthermore, mast cells might be involved in the development of postmenopausal osteoporosis, because they store high levels of osteoclastic mediators, including IL-6 and RANKL, in their granules and their numbers are greatly increased in osteoporotic bone. Additionally, bone fracture healing is altered under estrogen-deficient conditions with the increased presence of pro-inflammatory cytokines, including IL-6 and Midkine, which might contribute to healing disturbances. Consequently, in addition to the direct negative influence of estrogen-deficiency on bone, immune cell alterations contribute to the pathogenesis of postmenopausal osteoporosis.
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                Author and article information

                Contributors
                Journal
                Heliyon
                Heliyon
                Heliyon
                Elsevier
                2405-8440
                20 October 2023
                November 2023
                20 October 2023
                : 9
                : 11
                : e20922
                Affiliations
                [a ]The First School of Clinical Medicine, Lanzhou University, Lanzhou, 730000, China
                [b ]Stomatology Center of Gansu Provincial Hospital, Lanzhou, 730000, China
                [c ]Department of Clinical Skills Training Center, The First School of Clinical Medicine, The First Hospital of Lanzhou University, Lanzhou, 730000, China
                [d ]School of Stomatology Lanzhou University, Lanzhou, 730000, China
                [e ]Department of Stomatology, Affiliated Hospital of Northwest University for Nationalities, Lanzhou, 730000, China
                [f ]Radiology of Gansu Provincial Hospital, Lanzhou, 730000, China
                Author notes
                []Corresponding author. Department of School of Stomatology Lanzhou University, The First School of Clinical Medicine, Lanzhou University, Lanzhou, 730000, Gansu Province, China. lzukqwj@ 123456126.com
                [∗∗ ]Corresponding author. Department of Stomatology Center of Gansu Provincial Hospita, Lanzhou, 730000, Gansu Province, China. 769358966@ 123456qq.com
                [1]

                These authors contributed equally to this work.

                Article
                S2405-8440(23)08130-6 e20922
                10.1016/j.heliyon.2023.e20922
                10618781
                37920517
                a48fcd09-24a9-4f79-9c12-5e62f7b350e1
                © 2023 The Authors

                This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                : 17 February 2023
                : 23 September 2023
                : 11 October 2023
                Categories
                Review Article

                periodontal diseases,perimenopausal bone loss,meta-analysis

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