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    <title>Orthopaedics</title>
    <link>http://repub.eur.nl/res/org/9795/</link>
    <description>List of Publications</description>
    <language>en</language>
    <image>
      <url>http://repub.eur.nl/static-eur/img/logo.png</url>
      <title>RePub, Erasmus University Rotterdam</title>
      <link>http://repub.eur.nl</link>
    </image>
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      <title>Epidemiology and health-care utilisation of wrist fractures in older adults in The Netherlands, 1997-2009 (Article)</title>
      <link>http://repub.eur.nl/res/pub/39311/</link>
      <pubDate>2013-04-01T00:00:00Z</pubDate>
      <description>
        
        Introduction: Wrist fractures are common in older adults and are expected to increase because of ageing populations worldwide. The introduction of plate and screw fixation has changed the management of this trauma in many patients. For policymaking it is essential to gain insight into trends in epidemiology and healthcare utilisation. The purpose of this study was to determine trends in incidence, hospitalisation and operative treatment of wrist fractures. Methods: A population-based study of patients aged 50 years and older using the Dutch National Injury Surveillance System and the National Hospital Discharge Registry. Data on emergency department visits, hospitalisations and operative treatment for wrist fractures within the period 1997-2009 were analysed. Results: In women, the age-standardised incidence rate of wrist fractures decreased from 497.2 per 100,000 persons (95% confidence interval, 472.3-522.1) in 1997 to 445.1 (422.8-467.4) in 2009 (P for trend &lt;0.001). In men, no significant trends were observed in the same time period. Hospitalisation rates increased from 30.1 (28.3-31.9) in 1997 to 78.9 (75.1-82.8) in 2009 in women (P &lt; 0.001), and from 6.4 (6.0-6.8) to 18.4 (17.3-19.5) in men (P &lt; 0.001). There was a strong increase in operative treatment of distal radius fractures, especially due to plate fixation techniques in all age groups. Conclusion: Incidence rates of wrist fractures decreased in women and remained stable in men, but hospitalisation rates strongly increased due to a steep rise in operative treatments. The use of plate and screw fixation techniques for distal radius fractures increased in all age groups. 
      </description>
      <author>Putter, C.E. de</author> <author>Selles, R.W.</author> <author>Polinder, S.</author> <author>Hartholt, K.A.</author> <author>Looman, C.W.N.</author> <author>Panneman, M.J.M.</author> <author>Verhaar, J.A.N.</author> <author>Hovius, S.E.R.</author> <author>Beeck, E.F. van</author>
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      <title>Image registration improves human knee cartilage T1 mapping with delayed gadolinium-enhanced MRI of cartilage (dGEMRIC) (Article)</title>
      <link>http://repub.eur.nl/res/pub/39232/</link>
      <pubDate>2013-01-01T00:00:00Z</pubDate>
      <description>
        
        Objectives: To evaluate the effect of automated registration in delayed gadolinium-enhanced MRI of cartilage (dGEMRIC) of the knee on the occurrence of movement artefacts on the T1 map and the reproducibility of region-of-interest (ROI)-based measurements. Methods: Eleven patients with early-stage knee osteoarthritis and ten healthy controls underwent dGEMRIC twice at 3 T. Controls underwent unenhanced imaging. ROIs were manually drawn on the femoral and tibial cartilage. T1 calculation was performed with and without registration of the T1-weighted images. Automated three-dimensional rigid registration was performed on the femur and tibia cartilage separately. Registration quality was evaluated using the square root Cramér-Rao lower bound (CRLBσ). Additionally, the reproducibility of dGEMRIC was assessed by comparing automated registration with manual slice-matching. Results: Automated registration of the T1-weighted images improved the T1 maps as the 90% percentile of the CRLBσwas significantly (P &lt; 0.05) reduced with a median reduction of 55.8ms (patients) and 112.9ms (controls). Manual matching and automated registration of the re-imaged T1 map gave comparable intraclass correlation coefficients of respectively 0.89/0.90 (patients) and 0.85/0.85 (controls). Conclusions: Registration in dGEMRIC reduces movement artefacts on T1 maps and provides a good alternative to manual slice-matching in longitudinal studies. Key Points: • Quantitative MRI is increasingly used for biomedical assessment of knee articular cartilage • Image registration leads to more accurate quantification of cartilage quality and damage • Movement artefacts in delayed gadolinium-enhanced MRI of cartilage (dGEMRIC) are reduced • Automated image registration successfully aligns baseline and follow-up dGEMRIC examinations • Reproducibility of dGEMRIC with registration is similar to that using manual slice-matching 
      </description>
      <author>Bron, E.E.</author> <author>Tiel, J. van</author> <author>Smit, H.A.</author> <author>Poot, D.H.J.</author> <author>Niessen, W.J.</author> <author>Krestin, G.P.</author> <author>Weinans, H.H.</author> <author>Oei, E.H.G.</author> <author>Kotek, G.</author> <author>Klein, S.</author>
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      <title>Comparing scaffold-free and fibrin-based adipose-derived stromal cell constructs for adipose tissue engineering: An in vitro and in vivo study (Article)</title>
      <link>http://repub.eur.nl/res/pub/39354/</link>
      <pubDate>2012-12-07T00:00:00Z</pubDate>
      <description>
        
        Success of adipose tissue engineering for soft tissue repair has been limited by insufficient adipogenic differentiation, an unfavorable host response, and insufficient vascularization. In this study, we examined how scaffold-free spheroid and fibrin-based environments impact these parameters in human adipose-derived stromal cell (ASC)-based adipose constructs. ASCs were differentiated in spheroids or fibrin-based constructs. After 7 days, conditioned medium was collected and spheroids/fibrin-based constructs were either harvested or implanted subcutaneously in athymic mice. Following 7 days of implantation, the number of blood vessels in fibrin-based constructs was significantly higher than in spheroids (93 ± 45 vs. 23 ± 11 vessels/mm2) and the inflammatory response to fibrin-based constructs was less severe. The reasons for these results were investigated further in vitro. We found that ASCs in fibrin-based constructs secreted significantly higher levels of the angiogenic factors VEGF and HGF and lower levels of the inflammatory cytokine IL-8. Furthermore, ASCs in fibrin-based constructs secreted significantly higher levels of leptin and showed a 2.5-fold upregulation of the adipogenic transcription factor PPARG and a fourfold to fivefold upregulation of the adipocyte-specific markers FABP4, perilipin, and leptin. These results indicate that fibrin-based ASC constructs are potentially more suitable for ASC-based adipose tissue reconstruction than scaffold-free spheroids. 
      </description>
      <author>Verseijden, F.</author> <author>Posthumus-van Sluijs, S.J.</author> <author>Neck, J.W. van</author> <author>Hofer, S.O.P</author> <author>Hovius, S.E.R.</author> <author>Osch, G.J.V.M. van</author>
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      <title>Re-displacement of stable distal both-bone forearm fractures in children: A randomised controlled multicentre trial (Article)</title>
      <link>http://repub.eur.nl/res/pub/39238/</link>
      <pubDate>2012-12-04T00:00:00Z</pubDate>
      <description>
        
        Introduction: Displaced metaphyseal both-bone fractures of the distal forearm are generally reduced and stabilised by an above-elbow cast (AEC) with or without additional pinning. The purpose of this study was to find out if re-displacement of a reduced stable metaphyseal both-bone fracture of the distal forearm in a child could be prevented by stabilisation with Kirschner wires. Methods: Consecutive children aged &lt;16 years with a displaced metaphyseal both-bone fracture of the distal forearm (n = 128) that was stable after reduction were randomised to AEC with or without percutaneous fixation with Kirschner wires. The primary outcome was re-displacement of the fracture. Results: A total of 67 children were allocated to fracture reduction and AEC and 61 to reduction of the fracture, fixation with Kirschner wires and AEC. The follow-up rate was 96% with a mean follow-up of 7.1 months. Fractures treated with additional pinning showed less re-displacement (8% vs. 45%), less limitation of pronation and supination (mean limitation 6.9 (±9.4)° vs. 14.3 (±13.6)°) but more complications (14 vs. 1). Conclusions: Pinning of apparent stable both-bone fractures of the distal forearm in children might reduce fracture re-displacement. The frequently seen complications of pinning might be reduced by a proper surgical technique. 
      </description>
      <author>Colaris, J.W.</author> <author>Allema, J.H.</author> <author>Biter, L.U.</author> <author>Vries, M.R. de</author> <author>Ven, C.P. van de</author> <author>Bloem, R.M.</author> <author>Kerver, A.J.H.</author> <author>Reijman, M.</author> <author>Verhaar, J.A.N.</author>
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      <title>Interleukin-6 is elevated in synovial fluid of patients with focal cartilage defects and stimulates cartilage matrix production in an in vitro regeneration model (Article)</title>
      <link>http://repub.eur.nl/res/pub/38411/</link>
      <pubDate>2012-12-03T00:00:00Z</pubDate>
      <description>
        
        Introduction: This study aimed to determine whether, as in osteoarthritis, increased levels of interleukin-6 (IL-6) are present in the synovial fluid of patients with symptomatic cartilage defects and whether this IL-6 affects cartilage regeneration as well as the cartilage in the degenerated knee.Methods: IL-6 concentrations were determined by ELISA in synovial fluid and in conditioned media of chondrocytes regenerating cartilage. Chondrocytes were obtained from donors with symptomatic cartilage defects, healthy and osteoarthritic donors. The effect of IL-6 on cartilage regeneration and on metabolism of the resident cartilage in the knee was studied by both inhibition of endogenous IL-6 and addition of IL-6, in a regeneration model and in osteoarthritic explants in the presence of synovial fluid, respectively. Readout parameters were DNA and glycosaminoglycan (GAG) content and release. Differences between controls and IL-6 blocked or supplemented samples were determined by univariate analysis of variance using a randomized block design.Results: Synovial fluid of patients with symptomatic cartilage defects contained more IL-6 than synovial fluid of healthy donors (P = 0.001) and did not differ from osteoarthritic donors. IL-6 production of osteoarthritic chondrocytes during cartilage regeneration was higher than that of healthy and defect chondrocytes (P &lt; 0.001). Adding IL-6 increased GAG production by healthy chondrocytes and decreased GAG release by osteoarthritic chondrocytes (P &lt; 0.05). Inhibition of IL-6 present in osteoarthritic synovial fluid showed a trend towards decreased GAG content of the explants (P = 0.06).Conclusions: Our results support a modest anabolic role for IL-6 in cartilage matrix production. Targeting multiple cytokines, including IL-6, may be effective in improving cartilage repair in symptomatic cartilage defects and osteoarthritis. 
      </description>
      <author>Tsuchida, A.I.</author> <author>Beekhuizen, M.</author> <author>Rutgers, M.</author> <author>Osch, G.J.V.M. van</author> <author>Bekkers, J.E.J.</author> <author>Bot, A.G.J.</author> <author>Geurts, T.B.P.</author> <author>Dhert, W.J.A.</author> <author>Saris, D.B.F.</author> <author>Creemers, L.B.</author>
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      <title>Synovial inflammation, immune cells and their cytokines in osteoarthritis: A review (Article)</title>
      <link>http://repub.eur.nl/res/pub/39296/</link>
      <pubDate>2012-12-01T00:00:00Z</pubDate>
      <description>
        
        Objective: Although osteoarthritis (OA) is considered a non-inflammatory condition, it is widely accepted that synovial inflammation is a feature of OA. However, the role of immune cells and their cytokines in OA is largely unknown. This narrative systematic review summarizes the knowledge of inflammatory properties, immune cells and their cytokines in synovial tissues (STs) of OA patients. Design: Broad literature search in different databases was performed which resulted in 100 articles. Results: Of 100 articles 33 solely investigated inflammation in OA ST with or without comparison with normal samples; the remaining primarily focussed on rheumatoid arthritis (RA) ST. Studies investigating different severity stages or cellular source of cytokines were sparse. OA ST displayed mild/moderate grade inflammation when investigated by means of haematoxylin and eosin (H&amp;E) staining. Most frequently found cells types were macrophages, T cells and mast cells (MCs). Overall the number of cells was lower than in RA, although the number of MCs was as high as or sometimes even higher than in RA ST. Cytokines related to T cell or macrophage function were found in OA ST. Their expression was overall higher than in normal ST, but lower than in RA ST. Their cellular source remains largely unknown in OA ST. Conclusion: Inflammation is common in OA ST and characterized by immune cell infiltration and cytokine secretion. This inflammation seems quantitatively and qualitatively different from inflammation in RA. Further research is needed to clarify the role of inflammation, immune cells and their cytokines in the pathogenesis of OA. 
      </description>
      <author>Lange-Brokaar, B.J.E. de</author> <author>Ioan-Facsinay, A.</author> <author>Osch, G.J.V.M. van</author> <author>Zuurmond, A-M.</author> <author>Schoones, J.</author> <author>Toes, R.E.M.</author> <author>Huizinga, T.W.J.</author> <author>Kloppenburg, M.</author>
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      <title>Effect of arthritic synovial fluids on the expression of immunomodulatory factors by mesenchymal stem cells: An explorative in vitro study (Article)</title>
      <link>http://repub.eur.nl/res/pub/39299/</link>
      <pubDate>2012-12-01T00:00:00Z</pubDate>
      <description>
        
        Background:In diseased joints, the catabolic environment results in progressive joint damage. Mesenchymal stem cells (MSCs) can have immunomodulatory effects by secreting anti-inflammatory factors. To exert these effects, MSCs need to be triggered by proinflammatory cytokines. To explore the potential of MSCs as a treatment for diseased joints, we studied the effect of synovial fluid (SF) from donors with different joint diseases and donors without joint pathology on the immunomodulatory capacities of human MSCs in vitro. We hypothesized that SF of diseased joints influences the immunomodulatory effects of MSCs. Materials and Methods: MSCs were cultured in medium with SF of six osteoarthritis (OA) or six rheumatoid arthritis (RA) donors and three donors without joint pathology were used as control. Gene expressions of IL-6, HGF, TNFa, TGFb1, and indoleamine 2,3-dioxygenase (IDO) were analyzed. L-kynurenine concentration in conditioned medium (CM) by MSCs with SF was determined as a measure of IDO activity by MSCs. Furthermore, the effect of CM with SF on proliferation of activated lymphocytes was analyzed. Results: Addition of SF significantly up-regulated the mRNA expression of IL-6 and IDO in MSCs. SF(OA) induced significantly higher expression of IDO than SF(control), although no difference in IDO activity of the MSCs could be shown with a L-kynurenine assay. Medium conditioned by MSCs with SF(OA or RA) suppressed activated lymphocyte proliferation in vitro more than medium conditioned by MSCs without SF or with SF(control). Discussion: SF can influence the expression of genes involved in immunomodulation by MSCs and the effect on lymphocyte proliferation. We found indications for disease-specific differences between SFs but the variation between donors, even within one disease group was high. These data warrant further research to examine the potential application of MSC therapy in arthritic joints. 
      </description>
      <author>Leijs, M.J.C.</author> <author>Buul, G.M. van</author> <author>Lubberts, E.W.</author> <author>Bos, P.K.</author> <author>Verhaar, J.A.N.</author> <author>Hoogduijn, M.J.</author> <author>Osch, G.J.V.M. van</author>
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      <title>A guideline to medical photography: A perspective on digital photography in an orthopaedic setting (Article)</title>
      <link>http://repub.eur.nl/res/pub/39302/</link>
      <pubDate>2012-12-01T00:00:00Z</pubDate>
      <description>
        
        Purpose: Quality photographs are essential for clinical documentation, research, and publication in scientific journals and teaching. Oftentimes, non-ideal lighting and a sterile environment restrict the medical photographer, resulting in lower-quality photographs. This article aims to provide a clear and comprehensible guideline for medical photography in an orthopaedic setting. Methods: This article is based on extensive photographic involvement in operating and laboratory settings, in close collaboration with medical professionals from the Steadman Clinic (Vail, Colorado, USA), Gothenburg University (Göteborg, Sweden) and Erasmus MC (Rotterdam, the Netherlands). Background literature was searched through Google Scholar and PubMed. Results: Three relevant journal articles, and one book on medical photography, were used to write this paper. Seventeen Internet articles were used for background information. Conclusion: A relevant, up-to-date and comprehensive guideline to medical photography for medical professionals, with or without photographic experience, is provided. Level of evidence: Expert opinion, Level V. 
      </description>
      <author>Meijer, P.P.G. de</author> <author>Karlsson, J.</author> <author>LaPrade, R.F.</author> <author>Verhaar, J.A.N.</author> <author>Wijdicks, C.A.</author>
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      <title>Effects of new anti-adhesion polyvinyl alcohol gel on healing of colon anastomoses in rats (Article)</title>
      <link>http://repub.eur.nl/res/pub/39323/</link>
      <pubDate>2012-12-01T00:00:00Z</pubDate>
      <description>
        
        Background: Adhesions follow abdominal surgery with an incidence as high as 95%, resulting in invalidating complications such as bowel obstruction, female infertility, and chronic pain. Searches have been performed for a safe and effective adhesion barrier; however, such barriers have impaired anastomotic site healing. The primary aim of this study was to investigate the effect of a new adhesion barrier, polyvinyl alcohol gel, on healing of colonic anastomoses using a rat model. Methods: Thirty-two Wistar rats were divided in two groups. In all animals, an anastomosis was constructed in the ascending colon. The first group received no adhesion barrier, whereas in the second group, 2mL of polyvinyl alcohol gel (A-Part Gel®; Aesculap AG, Tuttlingen, Germany) was applied circularly around the anastomosis. All animals were sacrificed on the seventh post-operative day, and the abdomen was inspected for signs of anastomotic leakage. The anastomotic bursting pressure, the adhesions around the anastomosis, and the collagen content of the excised anastomosis were measured. Results: No significant differences were observed between the two groups in the incidence of anastomotic leakage, the anastomotic bursting pressure (p=0.08), or the collagen concentration (p=0.91). No significant reduction in amount of adhesions was observed in the rats receiving polyvinyl alcohol gel. Conclusions: This experimental study showed no significant differences in anastomotic leakage, anastomotic bursting pressure, or collagen content of the anastomosis when using the adhesion barrier polyvinyl alcohol around colonic anastomoses. The barrier did not prevent adhesion formation. 
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      <author>Slieker, J.</author> <author>Ditzel, M.</author> <author>Harlaar, J.J.</author> <author>Mulder, I.M.</author> <author>Deerenberg, E.</author> <author>Bastiaansen-Jenniskens, Y.M.</author> <author>Kleinrensink, G.J.</author> <author>Jeekel, J.</author> <author>Lange, J.F.</author>
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      <title>Cross-sectional and predictive associations between plasma adipokines and radiographic signs of early-stage knee osteoarthritis: Data from CHECK (Article)</title>
      <link>http://repub.eur.nl/res/pub/37393/</link>
      <pubDate>2012-11-01T00:00:00Z</pubDate>
      <description>
        
        Objective: To investigate cross-sectional and predictive associations of plasma adipokines with biochemical markers of systemic joint metabolism and radiographic signs of early-stage knee osteoarthritis (OA). Design: The adipokines pLeptin, pAdiponectin, and pResistin, the cartilage markers C-terminal telopeptide of type II collagen (uCTX-II), N-terminal propeptide of type IIA procollagen (sPIIANP), chondroitin sulfate 846 (sCS846), and cartilage oligomeric matrix protein (sCOMP), and the synovial markers hyaluronic acid (sHA) and N-terminal propeptide of type III procollagen (sPIIINP) were assessed by enzyme-linked immunosorbent assay or radioactive immunoassay in baseline samples of Cohort Hip and Cohort Knee (CHECK), a cohort of 1002 subjects with early-stage symptomatic knee and/or hip OA. Knee radiographs were obtained at baseline and after 2 and 5 years and scored according to Kellgren and Lawrence. Results: pLeptin showed positive associations with uCTX-II, sCOMP, sPIIANP, sHA, and sPIIINP, and with presence and progression of radiographic knee OA. Associations expectedly disappeared after adjustment for body mass index. pResistin showed positive associations with sPIIINP and present and incident radiographic knee OA that were largely independent of BMI. pAdiponectin showed positive associations with uCTX-II and sCOMP. Furthermore, pAdiponectin did not show associations with radiographic knee OA on itself, but associations of pResistin with present radiographic knee OA were stronger in higher pAdiponectin tertiles (P = 0.024 for interaction between pAdiponectin and pResistin). Although statistically significant, all associations were weak. Conclusions: Adipokines may have aggravating, although may be minor, structural effects in early-stage knee OA. 
      </description>
      <author>Spil, W.E. van</author> <author>Welsing, P.</author> <author>Kloppenburg, M.</author> <author>Bierma-Zeinstra, S.M.A.</author> <author>Bijlsma, J.W.J.</author> <author>Mastbergen, S.C.</author> <author>Lafeber, F.P.J.G.</author>
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      <title>Can one generate stable hyaline cartilage from adult mesenchymal stem cells? A developmental approach (Article)</title>
      <link>http://repub.eur.nl/res/pub/39287/</link>
      <pubDate>2012-11-01T00:00:00Z</pubDate>
      <description>
        
        Chondrogenically differentiating bone marrow-derived mesenchymal stem cells (BMSCs) display signs of chondrocyte hypertrophy, such as production of collagen type X, MMP13 and alkaline phosphatase (ALPL). For cartilage reconstructions this is undesirable, as terminally differentiated cartilage produced by BMSCs mineralizes when implanted in vivo. Terminal differentiation is not restricted to BMSCs but is also encountered in chondrogenic differentiation of adipose-derived mesenchymal stem cells (MSCs) as well as embryonic stem cells, which by definition should be able to generate all types of tissues, including stable cartilage. Therefore, we propose that the currently used culture conditions may drive the cells towards terminal differentiation. In this manuscript we aim to review the literature, supplemented by our own data to answer the question, is it possible to generate stable hyaline cartilage from adult MSCs? We demonstrate that recently published methods for inhibiting terminal differentiation (through PTHrP, MMP13 or blocking phosphorylation of Smad1/5/8) result in cartilage formation with reduction of hypertrophic markers, although this does not reach the low level of stable chondrocytes. A set of hypertrophy markers should be included in future studies to characterize the phenotype more precisely. Finally, we used what is currently known in developmental biology about the differential development of hyaline and terminally differentiated cartilage to provide thought and insights to change current culture models for creating hyaline cartilage. Inhibiting terminal differentiation may not result in stable hyaline cartilage if the right balance of signals has not been created from the start of culture onwards. 
      </description>
      <author>Hellingman, C.A.</author> <author>Koevoet, W.</author> <author>Osch, G.J.V.M. van</author>
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      <title>Mesenchymal stem cells secrete factors that inhibit inflammatory processes in short-term osteoarthritic synovium and cartilage explant culture (Article)</title>
      <link>http://repub.eur.nl/res/pub/39233/</link>
      <pubDate>2012-10-01T00:00:00Z</pubDate>
      <description>
        
        Objective: Mesenchymal stem cells (MSCs) are promising candidates for osteoarthritis (OA) therapies, although their mechanism of action remains unclear. MSCs have recently been discovered to secrete anti-inflammatory cytokines and growth factors. We studied the paracrine effects of MSCs on OA cartilage and synovial explants in vitro. Design: MSC-conditioned medium was prepared by stimulating primary human MSCs with tumour necrosis factor alpha (TNFα) and (50. ng/ml each). Human synovium and cartilage explants were cultured in MSC-conditioned medium or in control medium, containing the same amount of added TNFα and IFNγ but not incubated with MSCs. Explants were analyzed for gene expression and the production of nitric oxide (NO). The presence of the inhibitor of nuclear factor kappa B alpha (IκBa) was assessed by Western blot analysis. Results: Synovial explants exposed to MSC-conditioned medium showed decreased gene expression of interleukin-1 beta (IL-1β), matrix metalloproteinase (MMP). 1 and MMP13, while suppressor of cytokine signaling (SOCS). 1 was upregulated. In cartilage, expression of IL-1 receptor antagonist (IL-1RA) was upregulated, whereas a disintegrin and metalloproteinase with thrombospondin motifs (ADAMTS). 5 and collagen type II alpha 1 (COL2A1) were downregulated. MSC-conditioned medium reduced NO production in cartilage explants and the presence of IκBa was increased in synoviocytes and chondrocytes treated with MSC-conditioned medium. Conclusions: In an inflammatory environment, MSCs secrete factors which cause multiple anti-inflammatory effects and influence matrix turnover in synovium and cartilage explants. Thereby, the presented data encourage further study of MSCs as a treatment for joint diseases. 
      </description>
      <author>Buul, G.M. van</author> <author>Villafuertes, E.</author> <author>Bos, P.K.</author> <author>Waarsing, J.H.</author> <author>Kops, N.</author> <author>Narcisi, R.</author> <author>Weinans, H.H.</author> <author>Verhaar, J.A.N.</author> <author>Bernsen, M.R.</author> <author>Osch, G.J.V.M. van</author>
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      <title>TGFβ inhibition during expansion phase increases the chondrogenic re-differentiation capacity of human articular chondrocytes (Article)</title>
      <link>http://repub.eur.nl/res/pub/39305/</link>
      <pubDate>2012-10-01T00:00:00Z</pubDate>
      <description>
        
        Objective: Autologous chondrocyte implantation is a cell-based treatment to repair articular cartilage defects, relying on the availability of expanded (de-differentiated) chondrocytes. Unfortunately, the expansion process causes several phenotypical changes, requiring re-establishment of the native chondrogenic phenotype to sustain proper repair. Among other proteins, transforming growth factor-β (TGFβ) is known to influence the chondrogenic re-differentiation of human articular chondrocytes (HACs) and their matrix deposition. Thus we investigated the effects of TGFβ-depletion during the expansion phase. Design: HACs were isolated from articular cartilage and expanded in the canonical serum-supplemented medium [fetal calf serum (FCS)] or in a chemically-defined (CD) medium, with or without anti-TGFβ antibody administration. The re-differentiation potential of the cells was assessed by pellet cultures, gene expression analysis and histology. Results: Cell proliferation proceeded more rapidly in CD-medium than in FCS-medium; it was not affected by the use of anti-TGFβ antibody but was further increased by addition of exogenous TGFβ1, via increased p-Smad1/5/8. Conversely, in FCS-medium, addition of anti-TGFβ antibody decreased both proliferation and p-Smad1/5/8 level. Challenging either FCS- or CD-medium with anti-TGFβ antibody during expansion enhanced chondrogenesis in the subsequent pellet cultures. Moreover, TGFβ-depletion during expansion in CD-medium inhibited mRNA expression of hypertrophic markers, collagen type-X (COL10) and matrix metalloproteinase-13 (MMP-13). Interestingly, the TGFβ1 level detected by enzyme-linked immunosorbent sandwich assay (ELISA) during cell expansion was correlated with COL10 mRNA expression after re-differentiation. Conclusion: TGFβ-depletion during expansion improves the re-differentiation capacity of chondrocytes and inhibits hypertrophy. These results indicate the importance of the expansion medium composition to improve chondrogenic re-differentiation and to inhibit hypertrophy. 
      </description>
      <author>Narcisi, R.</author> <author>Signorile, L.</author> <author>Verhaar, J.A.N.</author> <author>Giannoni, P.</author> <author>Osch, G.J.V.M. van</author>
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      <title>No positive bone healing after using platelet rich plasma in a skeletal defect. An observational prospective cohort study
 (Article)</title>
      <link>http://repub.eur.nl/res/pub/39309/</link>
      <pubDate>2012-10-01T00:00:00Z</pubDate>
      <description>
        
        Purpose
Platelet rich plasma (PRP) is derived from the patient’s own blood. The activated blood platelets release a cocktail of growth factors, some of which are thought to initiate and stimulate repair. We compared two groups to investigate whether the use of PRP mixed with bone chips improves bone healing in patients with a skeletal defect.

Methods
In total, 41 patients were observed. One group underwent a high tibial osteotomy with the addition of PRP and bone chips in the open wedge. The other group underwent the same procedure without the addition of PRP. Six patients had to be excluded because of insufficient data or they were lost to follow-up. Bone healing was studied using computed tomography scanning. The blood was sequestered and PRP was produced using a blood cell separator with a PRP software program (Electa, Sorin Group, Mirandola, Italy).

Results
Analysis focused on the remaining 35 patients. At baseline, there were no differences between the two groups for age, sex and side of operation. At one week postoperatively, the bone density under (p = 0.02) and above the wedge was significantly lower in the PRP group than the control group (p = 0.24). At six weeks postoperatively, no significant differences between the treatment groups were found. At 12 weeks, the PRP group had significantly lower bone density under the wedge compared to the control group (p = 0.01).

Conclusions
We found that patients with a skeletal defect did not benefit from the application of PRP mixed with an allograft regarding bone healing.

      </description>
      <author>Peerbooms, J.C.</author> <author>Colaris, J.W.</author> <author>Appeldorn, M. van</author> <author>Bruijn, D.J.</author> <author>Oudsten, B.L. den</author> <author>Gosens, T.</author>
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      <title>De harde les van metaal-op-metaalheupprothesen  (Article)</title>
      <link>http://repub.eur.nl/res/pub/39349/</link>
      <pubDate>2012-10-01T00:00:00Z</pubDate>
      <description>
        
        Een toename van de concentratie van kobalt in het bloed blijkt niet ongevaarlijk. In dit nummer van het Tijdschrift schrijven Dijkman et al. dat een toxische concentratie kan leiden tot hypothyreoïdie, polyneuropathie, aantasting van oog- en gehoorzenuwen en cardiomyopathie.1 Daarnaast is er nog de onzekerheid over de langetermijngevolgen van een verhoogde, maar niet-toxische kobaltconcentratie in het bloed.

Geen wonder dat er wereldwijd veel aandacht is voor deze mogelijke gevolgen van plaatsing van metaal-op-metaalheupprothesen (MoM-prothese) met grote kop, de heupprothese van de laatste generatie.2 Deze prothesen zijn in opzet bedoeld voor jonge patiënten. De kop en kom zijn beide van metaal in tegenstelling tot de traditionele heupprothese, waarbij de kom van plastic (polyethyleen) is.

      </description>
      <author>Verhaar, J.A.N.</author>
    </item> <item>
      <title>Reliability and validity of diagnosing acetabular labral lesions with magnetic resonance arthrography (Article)</title>
      <link>http://repub.eur.nl/res/pub/39313/</link>
      <pubDate>2012-09-19T00:00:00Z</pubDate>
      <description>
        
        Background: Arthroscopic surgery of the hip is being increasingly used to diagnose and treat various abnormalities, including acetabular labral tears. Magnetic resonance arthrography has been suggested as the imaging test of choice for the evaluation of the acetabular labrum. There is substantial variability in the previously reported accuracy of magnetic resonance arthrography for diagnosing labral lesions. Interobserver reliability has not been established previously. The purpose of this study was to establish the interobserver reliability and the validity of magnetic resonance arthrography for detecting lesions of the acetabular labrum in a retrospective case series. Methods: Two radiologists independently assessed the acetabular labrum on magnetic resonance arthrograms of ninety-five hips in ninety-three patients who underwent hip arthroscopy for a suspected acetabular labral lesion. Magnetic resonance arthrography findings were compared with the gold standard, which was defined as the assessment of the labrum during the hip arthroscopy. Results: At arthroscopy, ninety-one labral lesions were identified in the ninety-five hips. The interobserver reliability of detecting labral lesions with magnetic resonance arthrography was fair (kappa = 0.268). Magnetic resonance arthrography, as interpreted by observers A and B, showed a sensitivity of 86% and 86%, specificity of 75% and 50%, negative predictive value of 19% and 13%, and positive predictive value of 99% and 98%, respectively. Conclusions: Because of its limited reliability and the high prevalence of labral lesions, magnetic resonance arthrography provides a limited complementary benefit in the detection of labral lesions in patients with a high clinical suspicion of labral pathology. When there is a high clinical suspicion of a labral lesion, magnetic resonance arthrography has a poor negative predictive value and cannot be used to rule out a labral lesion. Physicians should critically consider whether the findings on a magnetic resonance arthrogram will alter the treatment strategy for an individual patient with a clinical suspicion of labral pathology. Copyright 
      </description>
      <author>Reurink, G.</author> <author>Jansen, S.P.L.</author> <author>Bisselink, J.M.</author> <author>Vincken, P.W.J.</author> <author>Weir, A.</author> <author>Moen, M.H.</author>
    </item> <item>
      <title>Computer-assisted surgery is not more accurate or precise than conventional arthroscopic ACL reconstruction: A prospective randomized clinical trial (Article)</title>
      <link>http://repub.eur.nl/res/pub/38731/</link>
      <pubDate>2012-09-05T00:00:00Z</pubDate>
      <description>
        
        Background: Accurate and precise tunnel placement is critical to the success of anterior cruciate ligament (ACL) reconstruction. A new development, computer-assisted surgery, aids in placement of the ACL bone tunnels during surgery. Our hypothesis was that computer-assisted ACL reconstruction would allow more accurate and precise tunnel placement compared with conventional surgery. Methods: In a prospective, double-blind, randomized clinical study, 100 patients eligible for ACL reconstruction with a transtibial technique were stratified by surgeon and randomized to either conventional or computer-assisted surgery. Measurement of femoral and tibial tunnel placement with use of three-dimensional computed tomography (CT) was used as the primary outcome to compare conventional ACL surgery with computer-assisted surgery. Results: The placement of the femoral tunnel did not differ between groups (mean, 39.7% of the proximal-distal distance on the intracondylar axis [Blumensaat line] in the conventional group compared with 39.0% in the computer-assisted surgery group; p = 0.70). The anterior-posterior positioning of the tibial tunnel on the tibial plateau also did not differ significantly (38.9% in the conventional group compared with 38.2% in the computer-assisted surgery group; p = 0.58). There was no significant difference in the precision of either the femoral or the tibial tunnel placement between the two groups. Conclusions: There was no significant difference in either the accuracy or the precision of tunnel placement between conventional and computer-assisted ACL reconstruction. Level of Evidence: Therapeutic Level I. See Instructions for Authors for a complete description of levels of evidence. Copyright 
      </description>
      <author>Meuffels, D.E.</author> <author>Reijman, M.</author> <author>Verhaar, J.A.N.</author>
    </item> <item>
      <title>Re-sprains during the first 3 months after initial ankle sprain are related to incomplete recovery: An observational study (Article)</title>
      <link>http://repub.eur.nl/res/pub/39304/</link>
      <pubDate>2012-09-01T00:00:00Z</pubDate>
      <description>
        
        Question: What are prognostic factors for incomplete recovery, instability, re-sprains and pain intensity 12 months after patients consult primary care practitioners for acute ankle sprains? Design: Observational study. Participants: One hundred and two patients who consulted their general practitioner or an emergency department for an acute ankle sprain were included in the study. Outcome measures: Possible prognostic factors were assessed at baseline and at 3 months follow-up. Outcome measures assessed at 12 months follow-up were self-reported recovery, instability, re-sprains and pain intensity. Results: At 3 months follow-up, 65% of the participants reported instability and 24% reported one or more re-sprains. At 12 months follow-up, 55% still reported instability and more than 50% regarded themselves not completely recovered. None of the factors measured at baseline could predict the outcome at 12 months follow-up. Additionally, prognostic factors from the physical examination of the non-recovered participants at 3 months could not be identified. However, among the non-recovered participants at 3 months follow-up, re-sprains and self-reported pain at rest at 3 months were related to incomplete recovery at 12 months. Conclusion: A physical examination at 3 months follow-up for the non-recovered ankle sprain patient seems to have no additional value for predicting outcome at 12 months. However, for the non-recovered patients at 3 months follow-up, self-reported pain at rest and re-sprains during the first 3 months of follow-up seem to have a prognostic value for recovery at 12 months. 
      </description>
      <author>Middelkoop, M. van</author> <author>Rijn, R.M. van</author> <author>Verhaar, J.A.N.</author> <author>Koes, B.W.</author> <author>Bierma-Zeinstra, S.M.A.</author>
    </item> <item>
      <title>Course of back complaints in older adults: a systematic literature review (Article)</title>
      <link>http://repub.eur.nl/res/pub/39317/</link>
      <pubDate>2012-09-01T00:00:00Z</pubDate>
      <description>
        
        BACKGROUND: Back pain is a common musculoskeletal complaint seen in older people. It is important to get an insight in the course of back complaints and to identify factors associated with a chronic course.

AIM: To describe the course of acute and subacute back complaints in older people (≥ 45 years) and to identify prognostic factors for developing chronic back complaints.

DESIGN: Systematic review of the literature.

METHODS: A database search was conducted in MEDLINE, EMBASE, Cochrane library, CINAHL, PsycINFO and PEDro. Cohort studies or randomized controlled trials reporting on the course of acute or subacute back complaints in older people were included. The percentage of patients that developed chronic back complaints was calculated, if possible.

RESULTS: The search yielded 9293 potentially relevant articles. Of these, 5 studies met all inclusion criteria. At 3 months follow-up 37-40% of the patients still had back complaints. At 12 months follow-up, the percentage ranged from 26-45%. Older age was frequently reported as a prognostic factor for developing chronic back complaints of the whole study population. No prognostic factors could be retrieved for patients aged 45 years and older.

CONCLUSIONS: At 3 and 12 month follow-up, about 40% of the older people still reported back complaints. However, the heterogeneity of the studies made comparisons difficult. In order to get a clear insight in the course of back complaints in the older adult patients and to indentify prognostic factors for developing chronic back complaints in older people, high quality prospective cohort studies are needed.

CLINICAL REHABILITATION IMPACT: More than one-third of the older patients with back pain still experience complaints after 3 and 12 months.


      </description>
      <author>Scheele, J.</author> <author>Luijsterburg, P.A.J.</author> <author>Bierma-Zeinstra, S.M.A.</author> <author>Koes, B.W.</author>
    </item> <item>
      <title>Association between spinal morning stiffness and lumbar disc degeneration: the Rotterdam Study
 (Article)</title>
      <link>http://repub.eur.nl/res/pub/39322/</link>
      <pubDate>2012-09-01T00:00:00Z</pubDate>
      <description>
        
        Objective
To explore the associations between spinal morning stiffness and lumbar disc degeneration (LDD).

Design
Data from a cross-sectional general population-based study (Rotterdam Study-I) were used. Intervertebral disc spaces and osteophytes of people aged ≥55 years were scored on lumbar lateral radiographs (L1-2 through L5-S1 was scored). Logistic regression analysis was used to explore associations between spinal morning stiffness and two definitions of LDD (i.e., ‘narrowing’ and ‘osteophytes’). Spinal morning stiffness combined with low back pain and its association with LDD was also analyzed. Similar analyses were performed for knee and hip pain, morning stiffness in the legs, and radiographic knee and hip osteoarthritis (OA) in order to compare these associations with those of LDD. All analyses were adjusted for age, gender, and body mass index (BMI).

Results
Lumbar lateral radiographs were scored for 2,819 participants. Both definitions of LDD were associated with spinal morning stiffness: adjusted odds ratio (aOR) 1.3; 95% confidence interval (CI): 1.1–1.6 for ‘osteophytes’ and aOR 1.8; 95% CI: 1.4–2.2 for ‘narrowing’. Both the odds ratios increased when spinal morning stiffness was combined with low back pain: aOR 1.5; 95% CI: 1.1–2.0 for ‘osteophytes’ and aOR 2.5; 95% CI: 1.9–3.4 for ‘narrowing’. When morning stiffness in the legs was combined with knee or hip pain, the associations with radiographic knee or hip OA were: aOR 3.0; 95% CI: 2.1–4.1 for knee OA and aOR 3.1; 95% CI: 1.9–5.0 for hip OA.

Conclusions
Reported spinal morning stiffness is associated with LDD. The associations increased when we combined spinal morning stiffness with low back pain. The magnitude of the association for the definition ‘narrowing’ is similar to the association between morning stiffness in the legs and knee or hip OA.


      </description>
      <author>Scheele, J.</author> <author>Schepper, E.I.T. de</author> <author>Meurs, J.B.J. van</author> <author>Hofman, A.</author> <author>Koes, B.W.</author> <author>Luijsterburg, P.A.J.</author> <author>Bierma-Zeinstra, S.M.A.</author>
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