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      Systemic versus local adipokine expression differs in a combined obesity and osteoarthritis mouse model

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          Abstract

          Osteoarthritis (OA) is a degenerative joint disease characterized by cartilage loss and reduced joint function. OA risk factors are age and obesity. Many adipokines are altered by obesity but also OA although systemic adipokine regulation in OA is not always clear. Therefore, metabolic effects of diet-induced obesity on OA development as well as the influence of obesity and OA progression on systemic vs. local adipokine expression in joints were compared. C57Bl/6-mice fed with HFD (high fat diet) or normal diet prior to destabilization of the medial meniscus (DMM) were sacrificed 4/6/8 weeks after surgery. Sera were evaluated for adiponectin, leptin, visfatin, cytokines. Liver grading and staging for non-alcoholic steatohepatitis (NASH) was performed and crown-like structures (CLS) in adipose tissue measured. OA progression was scored histologically. Adipokine-expressing cells and types were evaluated by immunohistochemistry. Time-dependent changes in DMM-progression were reflected by increased systemic adiponectin levels in DMM especially combined with HFD. While HFD increased serum leptin, DMM reduced systemic leptin significantly. OA scores correlated with bodyweight, leptin and hepatic scoring. Locally, increased numbers of adiponectin- and leptin-producing fibroblasts were observed in damaged menisci but visfatin was not changed. Local adipokine expression was independent from systemic levels, suggesting different mechanisms of action.

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          Design and validation of a histological scoring system for nonalcoholic fatty liver disease.

          Nonalcoholic fatty liver disease (NAFLD) is characterized by hepatic steatosis in the absence of a history of significant alcohol use or other known liver disease. Nonalcoholic steatohepatitis (NASH) is the progressive form of NAFLD. The Pathology Committee of the NASH Clinical Research Network designed and validated a histological feature scoring system that addresses the full spectrum of lesions of NAFLD and proposed a NAFLD activity score (NAS) for use in clinical trials. The scoring system comprised 14 histological features, 4 of which were evaluated semi-quantitatively: steatosis (0-3), lobular inflammation (0-2), hepatocellular ballooning (0-2), and fibrosis (0-4). Another nine features were recorded as present or absent. An anonymized study set of 50 cases (32 from adult hepatology services, 18 from pediatric hepatology services) was assembled, coded, and circulated. For the validation study, agreement on scoring and a diagnostic categorization ("NASH," "borderline," or "not NASH") were evaluated by using weighted kappa statistics. Inter-rater agreement on adult cases was: 0.84 for fibrosis, 0.79 for steatosis, 0.56 for injury, and 0.45 for lobular inflammation. Agreement on diagnostic category was 0.61. Using multiple logistic regression, five features were independently associated with the diagnosis of NASH in adult biopsies: steatosis (P = .009), hepatocellular ballooning (P = .0001), lobular inflammation (P = .0001), fibrosis (P = .0001), and the absence of lipogranulomas (P = .001). The proposed NAS is the unweighted sum of steatosis, lobular inflammation, and hepatocellular ballooning scores. In conclusion, we present a strong scoring system and NAS for NAFLD and NASH with reasonable inter-rater reproducibility that should be useful for studies of both adults and children with any degree of NAFLD. NAS of > or =5 correlated with a diagnosis of NASH, and biopsies with scores of less than 3 were diagnosed as "not NASH."
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            Osteoarthritis.

            Osteoarthritis is a major source of pain, disability, and socioeconomic cost worldwide. The epidemiology of the disorder is complex and multifactorial, with genetic, biological, and biomechanical components. Aetiological factors are also joint specific. Joint replacement is an effective treatment for symptomatic end-stage disease, although functional outcomes can be poor and the lifespan of prostheses is limited. Consequently, the focus is shifting to disease prevention and the treatment of early osteoarthritis. This task is challenging since conventional imaging techniques can detect only quite advanced disease and the relation between pain and structural degeneration is not close. Nevertheless, advances in both imaging and biochemical markers offer potential for diagnosis and as outcome measures for new treatments. Joint-preserving interventions under development include lifestyle modification and pharmaceutical and surgical modalities. Some show potential, but at present few have proven ability to arrest or delay disease progression.
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              Osteoarthritis: a disease of the joint as an organ.

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                Author and article information

                Contributors
                e.neumann@kerckhoff-klinik.de
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                20 August 2021
                20 August 2021
                2021
                : 11
                : 17001
                Affiliations
                [1 ]GRID grid.8664.c, ISNI 0000 0001 2165 8627, Department of Rheumatology and Clinical Immunology, Campus Kerckhoff, , Justus-Liebig-University of Giessen, ; Bad Nauheim, Germany
                [2 ]GRID grid.5330.5, ISNI 0000 0001 2107 3311, Department of Medicine 3, Rheumatology and Immunology, , Friedrich Alexander University Erlangen-Nuremberg and Universitätsklinikum, ; Erlangen, Germany
                [3 ]GRID grid.8664.c, ISNI 0000 0001 2165 8627, Institute of Veterinary Pathology, , Justus-Liebig-University of Giessen, ; Giessen, Germany
                [4 ]GRID grid.8664.c, ISNI 0000 0001 2165 8627, Institute of Veterinary Physiology and Biochemistry, , Justus-Liebig-University of Giessen, ; Giessen, Germany
                [5 ]GRID grid.8664.c, ISNI 0000 0001 2165 8627, Department of Gastroenterology, , Justus-Liebig-University of Giessen, ; Giessen, Germany
                [6 ]GRID grid.8664.c, ISNI 0000 0001 2165 8627, Department of Rheumatology and Clinical Immunology, Campus Kerckhoff, , Justus-Liebig-University of Giessen, ; Benekestr. 2-8, 61231 Bad Nauheim, Germany
                Article
                96545
                10.1038/s41598-021-96545-8
                8379250
                34417537
                b06118ee-03d1-4d57-87f9-d19523de76c7
                © The Author(s) 2021

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 27 May 2020
                : 2 August 2021
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100001659, Deutsche Forschungsgemeinschaft;
                Award ID: 3811/6, -/5
                Award ID: CRC1811-A01
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100002347, Bundesministerium für Bildung und Forschung;
                Award ID: METARTHROS, project 01EC1407B
                Award ID: METARTHROS, project 01EC1407B
                Award Recipient :
                Funded by: Justus-Liebig-Universität Gießen (3114)
                Categories
                Article
                Custom metadata
                © The Author(s) 2021

                Uncategorized
                immunology,rheumatology
                Uncategorized
                immunology, rheumatology

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