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      Mental health and periodontal and peri‐implant diseases

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          Abstract

          Mental health disorders, particularly depression and anxiety, affect a significant number of the global population. Several pathophysiological pathways for these disorders have been identified, including the hypothalamic‐pituitary‐adrenal axis, autonomic nervous system, and the immune system. In addition, life events, environmental factors, and lifestyle affect the onset, progression, and recurrence of mental health disorders. These may all overlap with periodontal and/or peri‐implant disease. Mental health disorders are associated with more severe periodontal disease and, in some cases, poorer healing outcomes to nonsurgical periodontal therapy. They can result in behavior modification, such as poor oral hygiene practices, tobacco smoking, and alcohol abuse, which are also risk factors for periodontal disease and, therefore, may have a contributory effect. Stress has immunomodulatory effects regulating immune cell numbers and function, as well as proinflammatory cytokine production. Stress markers such as cortisol and catecholamines may modulate periodontal bacterial growth and the expression of virulence factors. Stress and some mental health disorders are accompanied by a low‐grade chronic inflammation that may be involved in their relationship with periodontal disease and vice versa. Although the gut microbiome interacting with the central nervous system (gut‐brain axis) is thought to play a significant role in mental illness, less is understood about the role of the oral microbiome. The evidence for mental health disorders on implant outcomes is lacking, but may mainly be through behaviourial changes. Through lack of compliance withoral hygiene and maintenance visits, peri‐implant health can be affected. Increased smoking and risk of periodontal disease may also affect implant outcomes. Selective serotonin reuptake inhibitors have been linked with higher implant failure. They have an anabolic effect on bone, reducing turnover, which could account for the increased loss.

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          The role of inflammation in depression: from evolutionary imperative to modern treatment target.

          Crosstalk between inflammatory pathways and neurocircuits in the brain can lead to behavioural responses, such as avoidance and alarm, that are likely to have provided early humans with an evolutionary advantage in their interactions with pathogens and predators. However, in modern times, such interactions between inflammation and the brain appear to drive the development of depression and may contribute to non-responsiveness to current antidepressant therapies. Recent data have elucidated the mechanisms by which the innate and adaptive immune systems interact with neurotransmitters and neurocircuits to influence the risk for depression. Here, we detail our current understanding of these pathways and discuss the therapeutic potential of targeting the immune system to treat depression.
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            Global burden of disease attributable to mental and substance use disorders: findings from the Global Burden of Disease Study 2010

            The Lancet, 382(9904), 1575-1586
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              Introduction to the human gut microbiota

              The human gastrointestinal (GI) tract harbours a complex and dynamic population of microorganisms, the gut microbiota, which exert a marked influence on the host during homeostasis and disease. Multiple factors contribute to the establishment of the human gut microbiota during infancy. Diet is considered as one of the main drivers in shaping the gut microbiota across the life time. Intestinal bacteria play a crucial role in maintaining immune and metabolic homeostasis and protecting against pathogens. Altered gut bacterial composition (dysbiosis) has been associated with the pathogenesis of many inflammatory diseases and infections. The interpretation of these studies relies on a better understanding of inter-individual variations, heterogeneity of bacterial communities along and across the GI tract, functional redundancy and the need to distinguish cause from effect in states of dysbiosis. This review summarises our current understanding of the development and composition of the human GI microbiota, and its impact on gut integrity and host health, underlying the need for mechanistic studies focusing on host–microbe interactions.
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                Author and article information

                Contributors
                idarby@unimelb.edu.au
                Journal
                Periodontol 2000
                Periodontol 2000
                10.1111/(ISSN)1600-0757
                PRD
                Periodontology 2000
                John Wiley and Sons Inc. (Hoboken )
                0906-6713
                1600-0757
                01 August 2022
                October 2022
                : 90
                : 1 ( doiID: 10.1111/prd.v90.1 )
                : 106-124
                Affiliations
                [ 1 ] Centre for Rural Dentistry and Oral Health Charles Sturt University Orange New South Wales Australia
                [ 2 ] Periodontics, Melbourne Dental School The University of Melbourne Melbourne Victoria Australia
                Author notes
                [*] [* ] Correspondence

                Ivan Darby, Periodontics, Melbourne Dental School, University of Melbourne, 720 Swanston Street, Carlton, Melbourne 3053, VIC, Australia.

                Email: idarby@ 123456unimelb.edu.au

                Author information
                https://orcid.org/0000-0002-6457-5327
                Article
                PRD12452
                10.1111/prd.12452
                9804456
                35913583
                bc9857e4-e8c8-42d0-a733-2d08fd84b842
                © 2022 The Authors. Periodontology 2000 published by John Wiley & Sons Ltd.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.

                History
                Page count
                Figures: 5, Tables: 0, Pages: 19, Words: 15388
                Categories
                Review Article
                Review Articles
                Custom metadata
                2.0
                October 2022
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.2.3 mode:remove_FC converted:31.12.2022

                alzheimer disease,anxiety disorder,bipolar,depression,gut‐brain axis,mental health,microbiome,mood (affective) disorder,peri‐implant disease,periodontal disease,schizophrenia,stress,substance use disorder

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