5 results on '"Huscher, Dörte"'
Search Results
2. Brief Report: Pulmonary Function Tests: High Rate of False-Negative Results in the Early Detection and Screening of Scleroderma-Related Interstitial Lung Disease.
- Author
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Suliman, Yossra A., Dobrota, Rucsandra, Huscher, Dörte, Nguyen-Kim, Thi D. L., Maurer, Britta, Jordan, Suzana, Speich, Rudolf, Frauenfelder, Thomas, and Distler, Oliver
- Subjects
INTERSTITIAL lung diseases ,ACADEMIC medical centers ,DIAGNOSTIC errors ,LONGITUDINAL method ,MEDICAL screening ,MULTIVARIATE analysis ,RESEARCH funding ,PULMONARY function tests ,SYSTEMIC scleroderma ,TOMOGRAPHY ,LOGISTIC regression analysis ,BLIND experiment ,EARLY diagnosis ,DATA analysis software ,DESCRIPTIVE statistics ,DISEASE complications ,DIAGNOSIS - Abstract
Objective Validated methods for the screening and early diagnosis of systemic sclerosis (SSc; scleroderma)-related interstitial lung disease (ILD) are needed. The aim of this study was to evaluate the performance of pulmonary function tests (PFTs) compared with that of high-resolution computed tomography (HRCT) of the chest for the detection of SSc-related ILD in clinical practice, and to identify predictors of lung involvement that is functionally occult but significant on HRCT. Methods Prospectively enrolled patients with SSc were assessed according to the European League Against Rheumatism (EULAR)/EULAR Scleroderma Trial and Research standards. The assessment included PFTs and HRCT. The HRCT images were evaluated in a blinded manner by 2 experienced radiologists. The performance parameters of PFTs for the diagnosis of SSc-related ILD were calculated. Predictors of significant ILD as determined by HRCT in patients with normal forced vital capacity (FVC) values were identified through logistic regression. Results Among the 102 patients, 64 (63.0%) showed significant ILD on HRCT, while only 27 (26.0%) had an FVC <80% of predicted, and 54 (53.0%) had a decrease in the results of at least 1 PFT. Forty (62.5%) of 64 patients with significant ILD on HRCT had a normal FVC value, translating into a high false-negative rate. Notably, 5 of 40 patients with a normal FVC value had severe, functionally occult lung fibrosis; in 2 of these patients, the results of all of the PFTs were within normal limits. Patients with normal FVC values despite evidence of fibrosis on HRCT more frequently had anti-Scl-70 antibodies and diffuse SSc and less frequently had anticentromere antibodies (ACAs) compared with patients with both normal FVC values and normal HRCT results. Conclusion The derived evidence-based data reveal a high risk of missing significant SSc-related ILD when relying solely on PFTs. More comprehensive screening algorithms for early detection are warranted. In particular, additional imaging investigations for the early detection of SSc-related ILD should be considered in ACA-negative patients with normal FVC values. [ABSTRACT FROM AUTHOR]
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- 2015
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3. Evaluation of Histologic, Serologic, and Clinical Changes in Response to Abatacept Treatment of Primary Sjögren's Syndrome: A Pilot Study.
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Adler, Sabine, Körner, Meike, Förger, Frauke, Huscher, Dörte, Caversaccio, Marco-Domenico, and Villiger, Peter M.
- Abstract
Objective To prospectively evaluate histopathologic, blood cellular, serologic, and clinical changes in response to abatacept treatment in patients with primary Sjögren's syndrome (SS). Methods Blood, saliva, and minor salivary gland biopsy samples were obtained before and after the last of 8 doses of abatacept in 11 primary SS patients. The histologic data evaluated the numbers of lymphocytic foci and B and T cell subtypes (CD20+, CD3+, CD4+, and CD8+). The numbers of FoxP3+ regulatory T cells were measured and the FoxP3:CD3 ratio was calculated. Histologic data were compared with results from peripheral blood and with changes in saliva secretion. Results The numbers of lymphocytic foci decreased significantly ( P = 0.041). Numbers of local FoxP3+ T cells decreased significantly in percentage of total lymphocytic infiltrates ( P = 0.037). In the peripheral blood, B cells increased ( P = 0.038). This was due to an expansion of the naive B cell pool ( P = 0.034). When adjusting for disease duration, an increase was also noted for total lymphocytes ( P = 0.044) and for CD4 cells ( P = 0.009). Gamma globulins decreased significantly ( P = 0.005), but IgG reduction did not reach significance. Adjusted for disease duration, saliva production increased significantly ( P = 0.029). Conclusion CTLA-4Ig treatment significantly reduces glandular inflammation in primary SS, induces several cellular changes, and increases saliva production. Remarkably, this increase in saliva production is significantly influenced by disease duration. [ABSTRACT FROM AUTHOR]
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- 2013
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4. The Relationship Between Plasma Microparticles and Disease Manifestations in Patients With Systemic Sclerosis.
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Guiducci, Serena, Distler, Jörg H. W., Jüngel, Astrid, Huscher, Dörte, Huber, Lars C., Michel, Beat A., Gay, Renate E., Pisetsky, David S., Gay, Steffen, Matucci-Cerinic, Marco, and Distler, Oliver
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SYSTEMIC scleroderma ,COLLAGEN diseases ,DEMYELINATION ,MYELIN sheath diseases ,VIRUS diseases - Abstract
The article presents a study that aims to analyze the profile of microparticles in the blood of patients with systemic sclerosis (SSc) and healthy controls. Result of the study shows that the total number of microparticles was strongly increased in patients with SSc compared with healthy controls. It is concluded that the number of microparticles from different cellular increased in the blood of SSc patients.
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- 2008
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5. Transgenic disruption of glucocorticoid signaling in mature osteoblasts and osteocytes attenuates K/BxN mouse serum-induced arthritis in vivo.
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Buttgereit F, Zhou H, Kalak R, Gaber T, Spies CM, Huscher D, Straub RH, Modzelewski J, Dunstan CR, and Seibel MJ
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- 11-beta-Hydroxysteroid Dehydrogenase Type 2 genetics, 11-beta-Hydroxysteroid Dehydrogenase Type 2 metabolism, Adrenocorticotropic Hormone blood, Animals, Arthritis pathology, Autoimmune Diseases pathology, Body Weight physiology, Bone and Bones metabolism, Corticosterone blood, Cytokines blood, Disease Models, Animal, Joints pathology, Male, Mice, Mice, Transgenic, Osteoblasts pathology, Osteocytes pathology, Arthritis metabolism, Arthritis prevention & control, Autoimmune Diseases metabolism, Autoimmune Diseases prevention & control, Glucocorticoids metabolism, Osteoblasts metabolism, Osteocytes metabolism, Signal Transduction physiology
- Abstract
Objective: Endogenous glucocorticoids (GCs) modulate numerous biologic systems involved in the initiation and maintenance of arthritis. Bone cells play a critical role in the progression of arthritis, and some of the effects of GCs on inflammation may be mediated via these cells. The aim of this study was to investigate the impact of osteoblast-targeted disruption of GC signaling on joint inflammation, cartilage damage, and bone metabolism in the K/BxN mouse serum transfer model of autoimmune arthritis., Methods: Intracellular GC signaling was disrupted in osteoblasts through transgenic overexpression of 11beta-hydroxysteroid dehydrogenase type 2 under the control of a type I collagen promoter. Arthritis was induced in 5-week-old male transgenic mice and their wild-type (WT) littermates, and paw swelling was assessed daily until the mice were killed. The mice were examined by histology, histomorphometry, and microfocal computed tomography, and serum was analyzed for cytokines, adrenocorticotropic hormone, and corticosterone., Results: Acute arthritis developed in both transgenic and WT mice treated with K/BxN mouse serum. However, the arthritis and local inflammatory activity were significantly attenuated in transgenic mice, as judged by clinical and histologic indices of inflammation and cartilage damage. Bone turnover and bone volume remained unchanged in arthritic transgenic mice, while WT mice exhibited stimulated bone resorption, suppressed osteoblast activity, and significantly reduced bone volume, compatible with the known effects of active inflammation on bone. Circulating levels of proinflammatory cytokines tended to be lower in arthritic transgenic mice than in control transgenic mice., Conclusion: Disruption of GC signaling in osteoblasts significantly attenuates K/BxN mouse serum-induced autoimmune arthritis in mice. These data suggest that osteoblasts modulate the immune-mediated inflammatory response via a GC-dependent pathway.
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- 2009
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