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      Automation and deep (machine) learning in temporomandibular joint disorder radiomics: A systematic review

      1 , 1
      Journal of Oral Rehabilitation
      Wiley

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          Abstract

          Objective

          This review aimed to systematically analyse the influence of clinical variables, diagnostic parameters and the overall image acquisition process on automation and deep learning in TMJ disorders.

          Methods

          Articles were screened in late 2022 according to a predefined eligibility criteria adhering to the PRISMA protocol. Eligible studies were extracted from databases hosted by MEDLINE, EBSCOHost, Scopus, PubMed and Web of Science. Critical appraisals were performed on individual studies following Nature Medicine's MI‐CLAIM checklist while a combined appraisal of the image acquisition procedures was conducted using Cochrane's GRADE approach.

          Results

          Twenty articles were included for full review following eligibility screening. The average experience possessed by the clinical operators within the eligible studies was 13.7 years. Bone volume, trabecular number and separation, and bone surface‐to‐volume ratio were clinical radiographic parameters while disc shape, signal intensity, fluid collection, joint space narrowing and arthritic changes were successful parameters used in MRI‐based deep machine learning. Entropy was correlated to sclerosis in CBCT and was the most stable radiomic parameter in MRI while contrast was the least stable across thermography and MRI. Adjunct serum and salivary biomarkers, or clinical questionnaires only marginally improved diagnostic outcomes through deep learning. Substantial data was classified as unusable and subsequently discarded owing to a combination of suboptimal image acquisition and data augmentation procedures. Inadequate identification of the participant characteristics and multiple studies utilising the same dataset and data acquisition procedures accounted for serious risks of bias.

          Conclusion

          Deep‐learned models diagnosed osteoarthritis as accurately as clinicians from 2D and 3D radiographs but, in comparison, performed poorly when detecting disc disorders from MRI datasets. Complexities in clinical classification criteria; non‐standardised diagnostic parameters; errors in image acquisition; cognitive, contextual or implicit biases were influential variables that generally affected analyses of inflammatory joint changes and disc disorders.

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          Most cited references44

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          Plasma Hsp90 levels in patients with systemic sclerosis and relation to lung and skin involvement: a cross-sectional and longitudinal study

          Our previous study demonstrated increased expression of Heat shock protein (Hsp) 90 in the skin of patients with systemic sclerosis (SSc). We aimed to evaluate plasma Hsp90 in SSc and characterize its association with SSc-related features. Ninety-two SSc patients and 92 age-/sex-matched healthy controls were recruited for the cross-sectional analysis. The longitudinal analysis comprised 30 patients with SSc associated interstitial lung disease (ILD) routinely treated with cyclophosphamide. Hsp90 was increased in SSc compared to healthy controls. Hsp90 correlated positively with C-reactive protein and negatively with pulmonary function tests: forced vital capacity and diffusing capacity for carbon monoxide (DLCO). In patients with diffuse cutaneous (dc) SSc, Hsp90 positively correlated with the modified Rodnan skin score. In SSc-ILD patients treated with cyclophosphamide, no differences in Hsp90 were found between baseline and after 1, 6, or 12 months of therapy. However, baseline Hsp90 predicts the 12-month change in DLCO. This study shows that Hsp90 plasma levels are increased in SSc patients compared to age-/sex-matched healthy controls. Elevated Hsp90 in SSc is associated with increased inflammatory activity, worse lung functions, and in dcSSc, with the extent of skin involvement. Baseline plasma Hsp90 predicts the 12-month change in DLCO in SSc-ILD patients treated with cyclophosphamide.
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            Diagnostic Criteria for Temporomandibular Disorders (DC/TMD) for Clinical and Research Applications: recommendations of the International RDC/TMD Consortium Network* and Orofacial Pain Special Interest Group†.

            The original Research Diagnostic Criteria for Temporomandibular Disorders (RDC/TMD) Axis I diagnostic algorithms have been demonstrated to be reliable. However, the Validation Project determined that the RDC/TMD Axis I validity was below the target sensitivity of ≥ 0.70 and specificity of ≥ 0.95. Consequently, these empirical results supported the development of revised RDC/TMD Axis I diagnostic algorithms that were subsequently demonstrated to be valid for the most common pain-related TMD and for one temporomandibular joint (TMJ) intra-articular disorder. The original RDC/TMD Axis II instruments were shown to be both reliable and valid. Working from these findings and revisions, two international consensus workshops were convened, from which recommendations were obtained for the finalization of new Axis I diagnostic algorithms and new Axis II instruments. Through a series of workshops and symposia, a panel of clinical and basic science pain experts modified the revised RDC/TMD Axis I algorithms by using comprehensive searches of published TMD diagnostic literature followed by review and consensus via a formal structured process. The panel's recommendations for further revision of the Axis I diagnostic algorithms were assessed for validity by using the Validation Project's data set, and for reliability by using newly collected data from the ongoing TMJ Impact Project-the follow-up study to the Validation Project. New Axis II instruments were identified through a comprehensive search of the literature providing valid instruments that, relative to the RDC/TMD, are shorter in length, are available in the public domain, and currently are being used in medical settings. The newly recommended Diagnostic Criteria for TMD (DC/TMD) Axis I protocol includes both a valid screener for detecting any pain-related TMD as well as valid diagnostic criteria for differentiating the most common pain-related TMD (sensitivity ≥ 0.86, specificity ≥ 0.98) and for one intra-articular disorder (sensitivity of 0.80 and specificity of 0.97). Diagnostic criteria for other common intra-articular disorders lack adequate validity for clinical diagnoses but can be used for screening purposes. Inter-examiner reliability for the clinical assessment associated with the validated DC/TMD criteria for pain-related TMD is excellent (kappa ≥ 0.85). Finally, a comprehensive classification system that includes both the common and less common TMD is also presented. The Axis II protocol retains selected original RDC/TMD screening instruments augmented with new instruments to assess jaw function as well as behavioral and additional psychosocial factors. The Axis II protocol is divided into screening and comprehensive self report instrument sets. The screening instruments' 41 questions assess pain intensity, pain-related disability, psychological distress, jaw functional limitations, and parafunctional behaviors, and a pain drawing is used to assess locations of pain. The comprehensive instruments, composed of 81 questions, assess in further detail jaw functional limitations and psychological distress as well as additional constructs of anxiety and presence of comorbid pain conditions. The recommended evidence-based new DC/TMD protocol is appropriate for use in both clinical and research settings. More comprehensive instruments augment short and simple screening instruments for Axis I and Axis II. These validated instruments allow for identification of patients with a range of simple to complex TMD presentations.
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              GRADE guidelines: a new series of articles in the Journal of Clinical Epidemiology.

              The "Grades of Recommendation, Assessment, Development, and Evaluation" (GRADE) approach provides guidance for rating quality of evidence and grading strength of recommendations in health care. It has important implications for those summarizing evidence for systematic reviews, health technology assessment, and clinical practice guidelines. GRADE provides a systematic and transparent framework for clarifying questions, determining the outcomes of interest, summarizing the evidence that addresses a question, and moving from the evidence to a recommendation or decision. Wide dissemination and use of the GRADE approach, with endorsement from more than 50 organizations worldwide, many highly influential (http://www.gradeworkinggroup.org/), attests to the importance of this work. This article introduces a 20-part series providing guidance for the use of GRADE methodology that will appear in the Journal of Clinical Epidemiology. Copyright © 2011 Elsevier Inc. All rights reserved.
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                Author and article information

                Contributors
                (View ORCID Profile)
                (View ORCID Profile)
                Journal
                Journal of Oral Rehabilitation
                J of Oral Rehabilitation
                Wiley
                0305-182X
                1365-2842
                June 2023
                March 09 2023
                June 2023
                : 50
                : 6
                : 501-521
                Affiliations
                [1 ] Adelaide Dental School The University of Adelaide Adelaide South Australia Australia
                Article
                10.1111/joor.13440
                36843391
                4e7b014f-8f87-4f74-a180-5d187cf968a9
                © 2023

                http://creativecommons.org/licenses/by/4.0/

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