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1.
J Am Dent Assoc ; 153(1): 14, 2022 01.
Article in English | MEDLINE | ID: covidwho-1597659
2.
Med Hypotheses ; 158: 110732, 2021 Nov 09.
Article in English | MEDLINE | ID: covidwho-1508043

ABSTRACT

The immune response elicited by vaccines is crucial in determining their eventual efficacy. The human microbiome, in particular, that of the gut has been demonstrated to influence the immunogenicity of vaccines delivered by both the oral and non-oral routes. There is a significant overlap between the microflora of the mouth and that recovered from the gut, with certain periodontopathogens playing key roles in influencing the gut microflora. The present paper hypothesized that the oral microflora may play a role in the eventual immunogenicity and efficacy of vaccines.

3.
Expert Rev Proteomics ; 18(8): 707-717, 2021 08.
Article in English | MEDLINE | ID: covidwho-1380972

ABSTRACT

INTRODUCTION: Active matrix metalloproteinase (aMMP)-8 utilized in point-of-care testing (POCT) is regarded as a potential biomarker for periodontal and peri-implant diseases. Various host and microbial factors eventually influence the expression, degranulation, levels and activation of aMMP-8. The type of oral fluids (saliva, mouthrinse, gingival crevicular, and peri-implant sulcular fluids [GCF/PISF], respectively) affect the analysis. AREAS COVERED: With this background, we aimed to review here the recent studies on practical, inexpensive, noninvasive and quantitative mouthrinse and GCF/PISF chair-side POCT lateral flow aMMP-8 immunoassays (PerioSafe and ImplantSafe/ORALyzer) and how they help to detect, predict, monitor the course, treatment and prevention of periodontitis and peri-implantitis. The correlations of aMMP-8 POCT to other independent and catalytic activity assays of MMP-8 are also addressed. EXPERT OPINION: The mouthrinse aMMP-8 POCT can also detect prediabetes/diabetes and tissue destructive oral side-effects due to the head and neck cancers' radiotherapy. Chlorhexidine and doxycycline can inhibit collagenolytic human neutrophil and GCF aMMP-8. Furthermore, by a set of case-series we demonstrate the potential of mouthrinse aMMP-8 POCT to real-time/online detect periodontitis as a potential risk disease for coronavirus disease 2019 (COVID-19). The clinical interdisciplinary utilization of aMMP-8 POCT requires additional oral, medical, and interdisciplinary studies.


Subject(s)
COVID-19/enzymology , Matrix Metalloproteinase 8/metabolism , Pandemics , SARS-CoV-2 , Biomarkers/analysis , Biomarkers/metabolism , COVID-19/complications , Diabetes Mellitus/diagnosis , Diabetes Mellitus/enzymology , Doxycycline/therapeutic use , Humans , Immunoassay/methods , Matrix Metalloproteinase 8/analysis , Mouthwashes , Oral Hygiene , Peri-Implantitis/diagnosis , Peri-Implantitis/enzymology , Periodontitis/complications , Periodontitis/diagnosis , Periodontitis/enzymology , Point-of-Care Testing , Radiotherapy/adverse effects , Risk Factors , COVID-19 Drug Treatment
4.
Clin Oral Investig ; 26(2): 1361-1374, 2022 Feb.
Article in English | MEDLINE | ID: covidwho-1375646

ABSTRACT

OBJECTIVES: The study aimed to clinically assess the association between periodontitis and COVID-19-related outcomes. MATERIAL AND METHODS: Data pertaining to patient demographics, medical history, blood parameters, periodontal clinical examination and aMMP-8 point-of-care diagnostics (both site-level and patient-level) was recorded for eighty-two COVID-19-positive patients. COVID-19-related outcomes such as COVID-19 pneumonia, death/survival, types of hospital admission and need of assisted ventilation were also assessed. RESULTS: Males were predominantly afflicted with COVID-19, with advanced age exhibiting a greater association with the presence of periodontitis. Higher severity of periodontitis led to 7.45 odds of requiring assisted ventilation, 36.52 odds of hospital admission, 14.58 odds of being deceased and 4.42 odds of COVID-19-related pneumonia. The aMMP-8 mouthrinse kit was slightly more sensitive but less specific than aMMP-8 site-specific tests. CONCLUSIONS: Based on the findings of the present study, periodontitis seems to be related to poorer COVID-19-related outcomes. However, within the constraints of this work, a direct causality may not be established. Periodontitis, by means of skewing the systemic condition for a number of comorbidities, may eventually influence COVID-19 outcomes in an indirect manner. CLINICAL RELEVANCE: The study is the first to clinically, and by means of a validated point-of-care diagnostic methodology, assess the association between periodontal health and COVID-19-related outcomes. Assessment of the periodontal status of individuals can aid in the identification of risk groups during the pandemic along with reinforcing the need to maintain oral hygiene and seeking periodontal care.


Subject(s)
COVID-19 , Periodontitis , Humans , Male , Matrix Metalloproteinase 8 , Pandemics , Periodontitis/epidemiology , SARS-CoV-2
5.
Evid Based Dent ; 22(2): 72-73, 2021 01.
Article in English | MEDLINE | ID: covidwho-1281703

ABSTRACT

Data sources PubMed/Medline, Biomed Central, Embase, Thai Journals and the Cochrane library.Study selection Reports or studies dealing with the craniomaxillofacial (CMF) manifestations of COVID-19 were selected.Data extraction and synthesis The reviewers extracted data from the included studies; however, being a meta-narrative review, it was not deemed fit to contact authors for unpublished work, conduct a meta-analysis, search for unpublished data or search for studies in languages different from English, German, French and Thai. The primary variable for prediction was set as the COVID-19 infection, with the primary outcome variable being manifestation in the CMF region. Parameters of a clinical, demographic, investigative and therapeutic nature were the other included variables. Subsequently, the reports and abstracted data were reviewed for study design, author names, country, size of the sample, level of evidence, signs/symptoms, treatment undertaken and investigations conducted. Studies exhibiting the highest level of evidence were included eventually. As deemed appropriate, uni/bivariate and descriptive statistics were applied.Results Cumulatively, 101 publications were included in the meta-narrative after due screening, the data of which was further divided into five groups of: 1) nose/paranasal sinus/skull base; 2) mouth/throat; 3) periorbital/ocular tissue; 4) skin; and 5) ear.Conclusions The majority of data pertaining to CMF manifestations of COVID-19 qualifies as a low level of evidence. With the exception of taste/smell dysfunction, most CMF manifestations are nonspecific and can be diagnosed by CMF surgeons and dentists, which underscores their role in battling the pandemic.


Subject(s)
COVID-19 , Humans , Pandemics , SARS-CoV-2
6.
J Int Med Res ; 49(5): 3000605211016996, 2021 May.
Article in English | MEDLINE | ID: covidwho-1241091

ABSTRACT

INTRODUCTION: The current gold standard for detection of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) RNA involves subjecting nasopharyngeal or oropharyngeal swabs to reverse transcription quantitative PCR (RT-qPCR). However, both sample types need to be collected by trained professionals. Using self-collected buccal swabs as an alternative could simplify and accelerate diagnosis of coronavirus disease 2019 (COVID-19). OBJECTIVE: To assess self-collected buccal swab samples as an alternative method for SARS-CoV-2 detection in patients with COVID-19. METHODS: Buccal swab samples were self-collected by 73 patients with COVID-19. Total RNA was extracted using Qiagen kits. RNA encoding the SARS-CoV-2 Env protein and human RNase P as an internal control was amplified using the TRUPCR® SARS-CoV-2 RT-qPCR kit version 2.1 and a Bio-Rad CFX96 Real-Time Detection System. RESULT: The sensitivity of RT-qPCR from buccal swabs was 58.9% (43/73; 95% confidence interval [CI] 46.77%-70.27%) and that of RT-qPCR from saliva was 62.90% (39/62; 95% CI 49.69%-74.84%) taking positive SARS-CoV-2 RT-qPCR from nasopharyngeal swabs as the gold standard. CONCLUSION: Self-collected buccal swabs are promising alternatives to nasopharyngeal or oropharyngeal swabs for SARS CoV-2 detection.


Subject(s)
COVID-19 , SARS-CoV-2 , Humans , Nasopharynx , RNA, Viral/genetics , Saliva , Specimen Handling
7.
Br Dent J ; 228(10): 736, 2020 05.
Article in English | MEDLINE | ID: covidwho-1019800
8.
Injury ; 51(10): 2325, 2020 10.
Article in English | MEDLINE | ID: covidwho-665343
9.
Injury ; 51(10): 2326-2328, 2020 Oct.
Article in English | MEDLINE | ID: covidwho-614086

ABSTRACT

The oral & maxillofacial region and by that virtue surgery of the same is correlated to an increased risk of the transfer of the SARS CoV-2. In times of a pandemic it is imperative to institute a protocol based management of maxillofacial injuries based on currently available literature which is suggestive, simplistic, executable and amenable to modifications should the rapidly changing situation demand the same. The author, in the present study conducted a review of literature to undertake the task of forming a simplistic protocol which is readily applicable for the management of maxillofacial injuries which would not only provide the clinician guidance on what to do now but caution towards the future implications of his/her present decision.


Subject(s)
Coronavirus Infections/epidemiology , Delivery of Health Care/methods , Maxillofacial Injuries/therapy , Pneumonia, Viral/epidemiology , Triage/standards , Betacoronavirus , COVID-19 , Humans , Pandemics , SARS-CoV-2
10.
Med Hypotheses ; 144: 109968, 2020 Nov.
Article in English | MEDLINE | ID: covidwho-548596

ABSTRACT

NETosis, being an alternative form of cell death is the creation of web-like chromatin decondensates by suitably primed neutrophils as a response to stimulus aimed at containing and eliminating the same. In certain situations, it causes more harm than benefit in the form of bystander damage directly or via activation of autoimmune mechanisms. Such pathophysiology finds evidence in both Periodontal disease and COVID-19. Coupled with impaired removal, NETs have been implicated in both these disease forms to promote a state of inflammation and be a source of constant harm to the tissues involved. This potentially forms groundwork to implicate Periodontal disease as predisposing towards adverse COVID-19 related outcomes.


Subject(s)
COVID-19/immunology , Extracellular Traps/immunology , Periodontal Diseases/immunology , SARS-CoV-2/physiology , Bronchoalveolar Lavage Fluid/cytology , Bronchoalveolar Lavage Fluid/immunology , COVID-19/complications , COVID-19/physiopathology , Humans , Models, Immunological , Neutrophils/physiology , Pandemics , Periodontal Diseases/physiopathology , Respiratory Distress Syndrome/etiology , Respiratory Distress Syndrome/immunology
11.
Med Hypotheses ; 144: 109908, 2020 Nov.
Article in English | MEDLINE | ID: covidwho-436322

ABSTRACT

COVID-19 is now recognized as a pandemic throughout the world, leading to a scramble in order to gather knowledge as well as evidence regarding the 'novel' corona virus which causes this disease. Chemokines are a family of cytokines which are chemotactic in nature and cause the recruitment of cells of inflammation. Periodontitis has long been attributed to having its pathophysiology rooted in a cytokine response. The recent COVID-19 pandemic has been reported to have adverse outcomes related to the establishment of a cytokine storm, many of the components of which are common with the cytokine expression profile of periodontitis. This communication explores the connection between COVID-19 and periodontal disease through their cytokine connection to form a translational basis for recommending maintenance of oral hygiene in the COVID era and to red flag patients with periodontitis as having an increased risk of exhibiting COVID related adverse outcomes.


Subject(s)
COVID-19/complications , Cytokines/metabolism , Periodontitis/complications , COVID-19/blood , COVID-19/immunology , Chemokines , Comorbidity , Humans , Inflammation , Models, Theoretical , Periodontitis/blood , Periodontitis/virology , Treatment Outcome
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