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      Is there any association between the presence of biomarkers and apical periodontitis? A systematic review

      systematic-review

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          Abstract

          This systematic review aimed to verify whether there is evidence of an association between apical periodontitis and the presence of systemic biomarkers. This study adhered to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses - PRISMA. For this, the acronym PECO was used; population (P) of adult humans exposed (E) to the presence of apical periodontitis, compared (C) to adult humans without apical periodontitis, and the outcome (O) of the presence of biomarkers was observed. The articles were searched in PubMed, Scopus, Web of Science, LILACS, Cochrane Library, OpenGray, and Google Scholar grey databases. Subsequently, studies were excluded based on title, abstract, and full article reading, following the eligibility criteria. The methodological quality of the selected studies was evaluated using the Newcastle-Ottawa qualifier. After exclusion, 656 studies were identified, resulting in 17 final articles that were divided into case-control, cross-sectional, and cohort studies. Eight studies were considered to have a low risk of bias, one had a medium risk of bias, and eight had a high risk of bias. In addition, 12 articles evaluated biomarkers in blood plasma, four evaluated them in saliva, and only one evaluated them in gingival crevicular fluid. The results of these studies indicated an association between apical periodontitis and the systemic presence of biomarkers. These markers are mainly related to inflammation, such as interleukins IL-1, IL-2, and IL-6, oxidative markers, such as nitric oxide and superoxide anions, and immunoglobulins IgG and IgM.

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          https://www.crd.york.ac.uk/prospero/, identifier (CRD42023493959).

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          Most cited references68

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          Cytokines in Inflammatory Disease

          This review aims to briefly discuss a short list of a broad variety of inflammatory cytokines. Numerous studies have implicated that inflammatory cytokines exert important effects with regard to various inflammatory diseases, yet the reports on their specific roles are not always consistent. They can be used as biomarkers to indicate or monitor disease or its progress, and also may serve as clinically applicable parameters for therapies. Yet, their precise role is not always clearly defined. Thus, in this review, we focus on the existing literature dealing with the biology of cytokines interleukin (IL)-6, IL-1, IL-33, tumor necrosis factor-alpha (TNF-α), IL-10, and IL-8. We will briefly focus on the correlations and role of these inflammatory mediators in the genesis of inflammatory impacts (e.g., shock, trauma, immune dysregulation, osteoporosis, and/or critical illness).
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            Local and systemic mechanisms linking periodontal disease and inflammatory comorbidities

            Periodontitis, a major inflammatory disease of the oral mucosa, is epidemiologically associated with other chronic inflammation-driven disorders, including cardio-metabolic, neurodegenerative and autoimmune diseases and cancer. Emerging evidence from interventional studies indicates that local treatment of periodontitis ameliorates surrogate markers of comorbid conditions. The potential causal link between periodontitis and its comorbidities is further strengthened by recent experimental animal studies establishing biologically plausible and clinically consistent mechanisms whereby periodontitis could initiate or aggravate a comorbid condition. This multi-faceted ‘mechanistic causality’ aspect of the link between periodontitis and comorbidities is the focus of this Review. Understanding how certain extra-oral pathologies are affected by disseminated periodontal pathogens and periodontitis-associated systemic inflammation, including adaptation of bone marrow haematopoietic progenitors, may provide new therapeutic options to reduce the risk of periodontitis-associated comorbidities.
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              COSMOS-E: Guidance on conducting systematic reviews and meta-analyses of observational studies of etiology

              Background To our knowledge, no publication providing overarching guidance on the conduct of systematic reviews of observational studies of etiology exists. Methods and findings Conducting Systematic Reviews and Meta-Analyses of Observational Studies of Etiology (COSMOS-E) provides guidance on all steps in systematic reviews of observational studies of etiology, from shaping the research question, defining exposure and outcomes, to assessing the risk of bias and statistical analysis. The writing group included researchers experienced in meta-analyses and observational studies of etiology. Standard peer-review was performed. While the structure of systematic reviews of observational studies on etiology may be similar to that for systematic reviews of randomised controlled trials, there are specific tasks within each component that differ. Examples include assessment for confounding, selection bias, and information bias. In systematic reviews of observational studies of etiology, combining studies in meta-analysis may lead to more precise estimates, but such greater precision does not automatically remedy potential bias. Thorough exploration of sources of heterogeneity is key when assessing the validity of estimates and causality. Conclusion As many reviews of observational studies on etiology are being performed, this document may provide researchers with guidance on how to conduct and analyse such reviews.
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                Author and article information

                Contributors
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                Journal
                Front Immunol
                Front Immunol
                Front. Immunol.
                Frontiers in Immunology
                Frontiers Media S.A.
                1664-3224
                22 May 2024
                2024
                : 15
                : 1366954
                Affiliations
                [1] 1 Laboratory of Functional and Structural Biology, Institute of Biological Sciences, Federal University of Pará , Belém-Pará, Brazil
                [2] 2 Department of Preventive and Social Dentistry, Faculty of Dentistry, Federal University of Uberlândia , Uberlândia, Minas Gerais, Brazil
                [3] 3 Department of Pediatric Dentistry and Orthodontics, School of Dentistry, Federal University of Rio de Janeiro , Rio de Janeiro, Brazil
                [4] 4 School of Dentistry, Faculty of Medicine and Dentistry, University of Alberta , Edmonton, AB, Canada
                [5] 5 Health Science Institute, Federal University of Pará , Belém-Pará, Brazil
                Author notes

                Edited by: Francisco W. G. Paula-Silva, University of São Paulo, Brazil

                Reviewed by: Krzysztof Guzik, Jagiellonian University, Poland

                Nadya Marouf, Hamad Medical Corporation, Qatar

                *Correspondence: Rafael Rodrigues Lima, rafalima@ 123456ufpa.br
                Article
                10.3389/fimmu.2024.1366954
                11150667
                38840914
                2687fcd8-f152-4ab2-88ba-62ba98afebce
                Copyright © 2024 Matos-Sousa, Chemelo, Frazão, Bittencourt, Moura, Mesquita, Marañón-Vásquez, Fagundes, Paranhos, Maia, Monteiro and Lima

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 07 January 2024
                : 15 April 2024
                Page count
                Figures: 7, Tables: 5, Equations: 0, References: 68, Pages: 19, Words: 7996
                Funding
                The author(s) declare financial support was received for the research, authorship, and/or publication of this article. RL is a Conselho Nacional de Desenvolvimento Cientifico e Tecnológico (CNPq) researcher who has earned grants numbered 312275/2021-8. This study was financed in part by Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - Brazil (CAPES) – Finance Code 001. The APC was supported by the Federal University of Pará’s Pró-Reitoria de Pesquisa e Pós-graduaço (PROPESP-UFPA).
                Categories
                Immunology
                Systematic Review
                Custom metadata
                Inflammation

                Immunology
                apical periodontitis,biomarkers,inflammatory markers,systemic biomarkers,and endodontic infection

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