Huibert J. Dinant
University of Amsterdam
Network
Latest external collaboration on country level. Dive into details by clicking on the dots.
Publication
Featured researches published by Huibert J. Dinant.
Annals of the Rheumatic Diseases | 1997
Carola J. E. Kaandorp; Huibert J. Dinant; M.A.F.J. van de Laar; H J Moens; A P. A Prins; B A C Dijkmans
OBJECTIVES To determine the incidence and sources of bacterial arthritis in the Amsterdam health district and the maximum percentage of cases that theoretically would be preventable. METHODS Patients with bacterial arthritis diagnosed between 1 October 1990 and 1 October 1993 were prospectively reported to the study centre by all 12 hospitals serving the district. Data were gathered on previous health status, source of infection, and microorganisms involved. RESULTS 188 episodes of bacterial arthritis were found in 186 patients. Most of the 38 children were previously healthy. Fifty per cent of the adults were 65 years or older. Of the adults 84% had an underlying disease, in 59% a joint disorder. Joint surgery constituted the largest part of direct infections (33%) and skin defects were the most important source of haematogenous infections (67%). Infection of joints containing prosthetic or osteosynthetic material by a known haematogenous source occurred 15 times (8%).Staphylococcus aureus was the causative organism in 44% of all positive cultures. CONCLUSION The incidence of bacterial arthritis was 5.7 per 100 000 inhabitants per year. Preventive measures directed to patients with prosthetic joints or osteosynthetic material, and a known haematogenous source would have prevented at most 8% of all cases.
Annals of the Rheumatic Diseases | 2008
Carla A. Wijbrandts; Marcel G. W. Dijkgraaf; Maarten C. Kraan; Marjolein Vinkenoog; Tjm Smeets; Huibert J. Dinant; Koen Vos; Willem F. Lems; Gerrit-Jan Wolbink; D Sijpkens; Ben A. C. Dijkmans; P P Tak
Objective: To determine whether the heterogeneous clinical response to tumour necrosis factor (TNF)α blocking therapy in rheumatoid arthritis (RA) can be predicted by TNFα expression in the synovium before initiation of treatment. Methods: Prior to initiation of infliximab treatment, arthroscopic synovial tissue biopsies were obtained from 143 patients with active RA. At week 16, clinical response was evaluated using the 28-joint Disease Activity Score (DAS28). Immunohistochemistry was used to analyse the cell infiltrate as well as the expression of various cytokines, adhesion molecules and growth factors. Stained sections were evaluated by digital image analysis. Student t tests were used to compare responders (decrease in DAS28 ⩾1.2) with non-responders (decrease in DAS28 <1.2) and multivariable regression was used to identify the independent predictors of clinical response. Results: Synovial tissue analysis confirmed our hypothesis that the baseline level of TNFα expression is a significant predictor of response to TNFα blocking therapy. TNFα expression in the intimal lining layer and synovial sublining were significantly higher in responders than in non-responders (p = 0.047 and p = 0.008, respectively). The numbers of macrophages, macrophage subsets and T cells (all able to produce TNFα) were also significantly higher in responders than in non-responders. The expression of interleukin (IL)1β, IL6, IL18, IL10, E-selectin, intercellular adhesion molecule (ICAM)-1, vascular cell adhesion molecule (VCAM)-1, vascular endothelial growth factor (VEGF) and basic fibroblast growth factor (bFGF) was not associated with response to anti-TNFα treatment. Conclusion: The effects of TNFα blockade are in part dependent on synovial TNFα expression and infiltration by TNFα producing inflammatory cells. Clinical response cannot be predicted completely, indicating involvement of other as yet unknown mechanisms.
Arthritis & Rheumatism | 2008
Rogier M. Thurlings; Carla A. Wijbrandts; Reina E. Mebius; Tineke Cantaert; Huibert J. Dinant; Tineke van der Pouw-Kraan; Cornelis L. Verweij; Dominique Baeten; Paul P. Tak
OBJECTIVE To investigate the relationship between lymphoid neogenesis in the synovium of patients with rheumatoid arthritis (RA) and characteristics of inflammation and disease severity. METHODS Arthroscopic synovial biopsy was performed in 103 patients with active RA (Disease Activity Score 28-joint assessment >or=3.2) who had not received treatment with biologic agents. Sections were stained and assessed by digital image analysis. Lymphocyte aggregates were counted and graded for size (1-3). Synovial lymphoid neogenesis was defined as the presence of grade 2 or 3 aggregates and subclassified based on the presence of follicular dendritic cells (FDCs). RESULTS Lymphoid neogenesis was present in 31% of the RA synovial tissues, whereas an additional 25% contained only grade 1 aggregates. FDCs were present in 28% of the samples with lymphoid neogenesis, corresponding to 8% of the total RA cohort. Histologically, synovia with lymphoid neogenesis showed increased infiltration by T and B lymphocytes, plasma cells, and macrophages, and increased expression of tumor necrosis factor alpha and lymphotoxin beta compared with samples without lymphoid neogenesis. Patients with lymphoid neogenesis also had higher C-reactive protein levels, erythrocyte sedimentation rates, and leukocyte and thrombocyte counts, but exhibited no increase in the severity of clinical signs and symptoms. Of importance, there was no relationship between the presence of lymphoid neogenesis and IgM rheumatoid factor or anti-citrullinated protein antibodies. The presence of lymphocyte aggregates with FDCs did not define a specific clinical phenotype compared with lymphocyte aggregates without FDCs. CONCLUSION These findings indicate that synovial lymphoid neogenesis is associated with more severe synovial and systemic inflammation, but this is not confined to a specific clinical subset of RA.
Arthritis & Rheumatism | 2001
Catharina E. Jacobi; Mattanja Triemstra; Ines Rupp; Huibert J. Dinant; Geertrudis A.M. van den Bos
OBJECTIVE To quantify the utilization of health care by rheumatoid arthritis (RA) patients and to estimate the contribution of patient characteristics to the explanation of the use of care, in order to evaluate whether those in need of care actually receive care. METHODS A questionnaire survey and a clinical examination were conducted among patients with RA referred to a rheumatology center. Health care utilization was assessed for medical care, allied health care, psychosocial care, and home care. The influence of sociodemographic variables and clinical and health characteristics on health care utilization was assessed by means of logistic regression. RESULTS Multivariate analyses showed that, for all types of services, disease-related factors explained most of the utilization. However, some sociodemographic variables (age, sex, and living situation) were also related to the utilization of care. CONCLUSION Most patients received the care they needed. However, for the elderly with RA, problems in access to allied health care and psychosocial care exist.
Arthritis Care and Research | 2004
Ines Rupp; Hendriek C. Boshuizen; Catharina E. Jacobi; Huibert J. Dinant; Geertrudis A.M. van den Bos
Scandinavian Journal of Rheumatology | 2006
Ines Rupp; Hendriek C. Boshuizen; Huibert J. Dinant; Catharina E. Jacobi; G. A. M. van den Bos
Arthritis & Rheumatism | 2003
Catharina E. Jacobi; Geert D. Mol; Hendriek C. Boshuizen; Ines Rupp; Huibert J. Dinant; Geertrudis A.M. van den Bos
Arthritis & Rheumatism | 2006
M. van der Esch; M. Steultjens; Dirk L. Knol; Huibert J. Dinant; Jacqueline M. Dekker
Rheumatology | 2003
Catharina E. Jacobi; B. van den Berg; Hendriek C. Boshuizen; Ines Rupp; Huibert J. Dinant; G. A. M. van den Bos
The Journal of Rheumatology | 2004
Ines Rupp; Hendriek C. Boshuizen; Catharina E. Jacobi; Huibert J. Dinant; Geertrudis A.M. van den Bos