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  1. Article ; Online: Novel Therapies in Takayasu Arteritis

    Francesca Regola / Martina Uzzo / Paola Toniati / Barbara Trezzi / Renato Alberto Sinico / Franco Franceschini

    Frontiers in Medicine, Vol

    2022  Volume 8

    Abstract: Takayasu Arteritis (TAK) is a large-vessel vasculitis that preferentially involves the aorta and its primary branches. Cardiac involvement is frequent in TAK and is a major determinant of the patient's outcome. Glucocorticoids (GC) are the mainstay of ... ...

    Abstract Takayasu Arteritis (TAK) is a large-vessel vasculitis that preferentially involves the aorta and its primary branches. Cardiac involvement is frequent in TAK and is a major determinant of the patient's outcome. Glucocorticoids (GC) are the mainstay of therapy for TAK, with high doses of GC effective to induce remission. However, relapses are common and lead to repeated and prolonged GC treatments with high risk of related adverse events. Potential GC toxicity is a major concern, especially because patients with TAK are young and need to be treated for several years, often for the whole life. Conventional immunosuppressive drugs are used in patients with severe manifestations but present some limitations. New therapeutic approaches are needed for patients with refractory disease or contraindications to conventional therapies. Fortunately, major progress has been made in understanding TAK pathogenesis, leading to the development of targeted biotherapies. In particular, IL-6 and TNF-α pathways seems to be the most promising therapeutic targets, with emerging data on Tocilizumab and TNF inhibitors. On the other hand, new insights on JAK-Inhibitors, Rituximab, Ustekinumab and Abatacept have been explored in recent studies. This review summarizes the emerging therapies used in TAK, focusing on the most recent studies on biologics and analyzing their efficacy and safety.
    Keywords Takayasu Arteritis ; novel therapies ; bDMARDs ; biologics ; heart ; Medicine (General) ; R5-920
    Subject code 616
    Language English
    Publishing date 2022-01-01T00:00:00Z
    Publisher Frontiers Media S.A.
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  2. Article ; Online: Endothelial Dysfunction in Systemic Lupus Erythematosus and Systemic Sclerosis

    Liala Moschetti / Silvia Piantoni / Enrico Vizzardi / Edoardo Sciatti / Mauro Riccardi / Franco Franceschini / Ilaria Cavazzana

    Frontiers in Medicine, Vol

    A Common Trigger for Different Microvascular Diseases

    2022  Volume 9

    Abstract: This review describes the complex interplay between inflammation, vasculopathy and fibrosis that involve the heart and peripheral small vessels, leading to endothelial stiffness, vascular damage, and early aging in patients with systemic lupus ... ...

    Abstract This review describes the complex interplay between inflammation, vasculopathy and fibrosis that involve the heart and peripheral small vessels, leading to endothelial stiffness, vascular damage, and early aging in patients with systemic lupus erythematosus and systemic sclerosis, which represents two different models of vascular dysfunction among systemic autoimmune diseases. In fact, despite the fact that diagnostic methods and therapies have been significantly improved in the last years, affected patients show an excess of cardiovascular mortality if compared with the general population. In addition, we provide a complete overview on the new techniques which are used for the evaluation of endothelial dysfunction in a preclinical phase, which could represent a new approach in the assessment of cardiovascular risk in these patients.
    Keywords endothelial dysfunction ; systemic lupus erythematosus ; systemic sclerosis ; microvascular disease ; techniques of assessment ; Medicine (General) ; R5-920
    Subject code 610
    Language English
    Publishing date 2022-04-01T00:00:00Z
    Publisher Frontiers Media S.A.
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  3. Article ; Online: Rheumatoid factor isotypes in rheumatoid arthritis diagnosis and prognosis

    Nicola Bizzaro / Franco Franceschini / Maria Infantino / Carlo Selmi / Gian Domenico Sebastiani / Francesca Motta / Davide Giavarina / Boaz Palterer

    RMD Open, Vol 9, Iss

    a systematic review and meta-analysis

    2023  Volume 3

    Abstract: Objective The first biomarker associated with the rheumatoid arthritis is rheumatoid factor (RF) and since the earliest reports a role has been proposed in the diagnosis and in the prediction of clinical features and outcome. The study of RF isotypes has ...

    Abstract Objective The first biomarker associated with the rheumatoid arthritis is rheumatoid factor (RF) and since the earliest reports a role has been proposed in the diagnosis and in the prediction of clinical features and outcome. The study of RF isotypes has further attempted to improve diagnostic accuracy and identify specific subgroups of patients. The main objective of this study is to provide an analysis of the literature on the role of RF isotypes in the diagnosis and prognosis of rheumatoid arthritis (RA).Methods We performed a systematic literature review and meta-analysis on the role of RF isotypes in RA (only in English, from PubMed, search terms: “rheumatoid factor isotypes”, “diagnosis”, “prognosis” and “rheumatoid arthritis”, last search 31 July 2022, two independent assessment of quality and biases, results included in tables and in the meta-analysis).Results Thirty-six articles were examined (7517 patients). Testing all RF isotypes with latex test or nephelometry allows for the highest sensitivity (68.6%, 95% CI 66.2% to 71.0%); nonetheless, the determination of IgA isotype provides the highest specificity (91.4%, 95% CI 90.8% to 92.0%) and the highest positive likelihood ratio (7.7, 95% CI 5.7 to 10.4). When testing IgM isotype the highest diagnostic OR (21.7, 95% CI 16.1 to 29.3) is reached. When analysing anti-citrullinated protein antibodies, RF isotype determination increases diagnostic accuracy. On the other hand, these do not provide relevant prognostic information, as results are conflicting.Conclusions Testing RF allows the highest sensitivity, while IgA isotype the highest specificity and positive likelihood ratio for RA diagnosis. On the other hand, determination of RF isotypes dose not allow prognostic information, as data are limited and heterogeneous.
    Keywords Medicine ; R
    Subject code 610
    Language English
    Publishing date 2023-09-01T00:00:00Z
    Publisher BMJ Publishing Group
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  4. Article ; Online: Diastolic dysfunction in rheumatoid arthritis

    Ilaria Cavazzana / Enrico Vizzardi / Franco Franceschini

    Monaldi Archives for Chest Disease, Vol 89, Iss

    a usual travel-mate?

    2019  Volume 3

    Abstract: A high rate of left ventricular diastolic dysfunction (LVDD) has been described in rheumatoid arthritis (RA), compared with general population. A prospective study demonstrated that LVDD occurred in 24% in one year of follow-up in RA patients without ... ...

    Abstract A high rate of left ventricular diastolic dysfunction (LVDD) has been described in rheumatoid arthritis (RA), compared with general population. A prospective study demonstrated that LVDD occurred in 24% in one year of follow-up in RA patients without cardiac disease. Older age, higher systolic arterial pressure and lower E/A ratio are considered predictive factors. In addition, in RA, LVDD is known to be the only risk factor for the development of cardiovascular (CV) events, also in absence of classical CV risk factors. Some occasional reports suggest that early and aggressive treatment of RA could influence the evolution of LVDD and, accordingly, modify the rate of CV events. Therefore, a correct assessment of diastolic function should be considered of pivotal importance in the routine follow-up of RA patients.
    Keywords diastolic dysfunction ; rheumatoid arthritis ; cardiovascular events ; Medicine ; R
    Language English
    Publishing date 2019-09-01T00:00:00Z
    Publisher PAGEPress Publications
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  5. Article ; Online: Novel Targets for Drug Use in Eosinophilic Granulomatosis With Polyangiitis

    Martina Uzzo / Francesca Regola / Barbara Trezzi / Paola Toniati / Franco Franceschini / Renato Alberto Sinico

    Frontiers in Medicine, Vol

    2021  Volume 8

    Abstract: Eosinophilic Granulomatosis with Polyangiitis (EGPA) is a rare autoimmune disease characterized by medium and small vessels inflammation. Cardiac vasculitic involvement is one of the most severe manifestations with a significant impact on patients' long- ... ...

    Abstract Eosinophilic Granulomatosis with Polyangiitis (EGPA) is a rare autoimmune disease characterized by medium and small vessels inflammation. Cardiac vasculitic involvement is one of the most severe manifestations with a significant impact on patients' long-term prognosis: anyway, a specific therapeutic approach for heart involvement in EGPA has not been explored yet. Current regimen consists of a long-term therapy with high dose of glucocorticoids, causing the well-known related-adverse events; immunosuppressive drugs are used in patients with severe manifestations, with some limitations. New therapeutic approaches are needed for patients with refractory disease or contraindications to conventional therapies. The quest for the ideal therapy is going toward a more and more personalized approach: on the one hand, efforts are made to use already existing therapies in the most appropriate way; on the other hand, new insights into EGPA pathogenesis allow the discovery of new targets, as demonstrated by mepolizumab and rituximab, targeting eosinophils, and B-cell compartments. This review summarizes the emerging therapies used in EGPA, focusing on the most recent studies on biologics and analyzing their efficacy and safety.
    Keywords Eosinophilic Granulomatosis with Polyangiitis ; heart involvement ; novel therapies ; biologics ; rituximab ; mepolizumab ; Medicine (General) ; R5-920
    Subject code 610
    Language English
    Publishing date 2021-11-01T00:00:00Z
    Publisher Frontiers Media S.A.
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  6. Article ; Online: The 2016 classification criteria for primary Sjogren’s syndrome

    Franco Franceschini / Ilaria Cavazzana / Laura Andreoli / Angela Tincani

    BMC Medicine, Vol 15, Iss 1, Pp 1-

    what’s new?

    2017  Volume 3

    Abstract: Abstract New 2016 ACR/EULAR classification criteria for primary Sjogren’s syndrome (SS) have been developed and endorsed by the ACR. The newly proposed criteria include simple-to-perform items. Two important points of the new criteria should be ... ...

    Abstract Abstract New 2016 ACR/EULAR classification criteria for primary Sjogren’s syndrome (SS) have been developed and endorsed by the ACR. The newly proposed criteria include simple-to-perform items. Two important points of the new criteria should be considered. Firstly, they indicate that either salivary gland biopsy or anti-Ro must be positive in order to corroborate the inflammatory and autoimmune nature of the disease. Secondly, the criteria recognize the systemic nature of SS, namely that patients without salivary or ocular glandular symptoms, but with extraglandular manifestations and B cell activation markers were also included in the SS classification. Additionally, the new criteria modified some technical points. The ocular staining score threshold was increased to 5 due to the higher specificity. The immunological profile includes only anti-Ro antibodies, while positivity for antinuclear antibodies and rheumatoid factor or isolated anti-La was excluded due to a lack of specificity. The 2016 ACR/EULAR criteria are suitable for early identification of SS, providing patients with the opportunity of enrollment in clinical trials for new specific treatment. Although validation has been successful, the real life application of these criteria will test their performance.
    Keywords Sjogren’s syndrome ; Classification criteria ; ACR ; EULAR ; Anti-Ro/SSA ; Anti-La/SSB ; Medicine ; R
    Subject code 710
    Language English
    Publishing date 2017-03-01T00:00:00Z
    Publisher BMC
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  7. Article ; Online: Production of anti-PF4 antibodies in antiphospholipid antibody-positive patients is not affected by COVID-19 vaccination

    Angela Tincani / Pier Luigi Meroni / Maria Orietta Borghi / Franco Franceschini / Maria Gerosa / Caterina Bodio / Giuliana Martini / Andrea Lombardi / Alessandra Bandera / Marco Cattaneo / Paola Adele Lonati / Mariangela Scavone / Elisa Pesce / Gianmarco Podda / Sergio Abrignani / Renata Grifantini

    RMD Open, Vol 8, Iss

    2022  Volume 1

    Keywords Medicine ; R
    Language English
    Publishing date 2022-02-01T00:00:00Z
    Publisher BMJ Publishing Group
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  8. Article ; Online: Revisão do gênero Appula (Coleoptera, Cerambycidae, Cerambycinae, Elaphidiini) Revision of the genus Appula (Coleoptera, Cerambycidae, Cerambycinae, Elaphidiini)

    André Franco Franceschini

    Iheringia: Série Zoologia, Vol 92, Iss 1, Pp 5-

    2002  Volume 40

    Abstract: A taxonomic revision of the genus Appula Thomson, 1864 is presented. Three new species are described: from Brazil, A. diamantinensis (Pará, Mato Grosso) and A. santarensis (Pará); from Peru and Brazil (Mato Grosso, Goiás, Mato Grosso do Sul), A. eduardae. ...

    Abstract A taxonomic revision of the genus Appula Thomson, 1864 is presented. Three new species are described: from Brazil, A. diamantinensis (Pará, Mato Grosso) and A. santarensis (Pará); from Peru and Brazil (Mato Grosso, Goiás, Mato Grosso do Sul), A. eduardae. Seven species are redescribed. Illustrations and key to the species are added. Male and female genitalia are studied for the first time for the Appula species.
    Keywords Appula ; Cerambycidae ; Elaphidiini ; Neotropical ; Taxonomy ; Zoology ; QL1-991
    Language English
    Publishing date 2002-01-01T00:00:00Z
    Publisher Fundação Zoobotânica do Rio Grande do Sul
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  9. Article ; Online: Glucocorticoid tapering and associated outcome in patients with newly diagnosed systemic lupus erythematosus

    Carlo Alberto Scirè / Alessandra Bortoluzzi / Fabrizio Conti / Andrea Doria / Micaela Fredi / Marcello Govoni / Chiara Tani / Marta Mosca / Alberto Cauli / Matteo Piga / Alberto Floris / Florenzo Iannone / Luca Iaccarino / Greta Carrara / Franco Franceschini / Anna Zanetti / Francesca Romana Spinelli / Francesca Bellisai / Roberto D'Alessandro /
    Elisabetta Chessa / Gian Domenico Sebastiani / Immacolata Prevete / Laura Coladonato

    RMD Open, Vol 8, Iss

    the real-world GULP prospective observational study

    2022  Volume 2

    Abstract: Objective A subanalysis of the multicentre Early Lupus inception cohort was performed to investigate the real-world Glucocorticoids (GCs) Use in newly diagnosed systemic lupus erythematosus (SLE) Patients (GULP).Methods Patients starting prednisone (PDN) ...

    Abstract Objective A subanalysis of the multicentre Early Lupus inception cohort was performed to investigate the real-world Glucocorticoids (GCs) Use in newly diagnosed systemic lupus erythematosus (SLE) Patients (GULP).Methods Patients starting prednisone (PDN) ≥5 mg/day and concomitant hydroxychloroquine or immunosuppressant within 12 months of SLE classification were enrolled. Core set variables were recorded at baseline and every 6 months, including changes in PDN dose, European Consensus Lupus Activity Measurement (ECLAM) and Systemic Lupus International Collaborating Clinics damage index. Regression models analysed predictors of tapering PDN<5 mg/day at any time and outcomes associated with different patterns of GCs tapering.Results The GULP study included 127 patients with SLE; 73 (57.5%) tapered and maintained PDN <5 mg/day, and 17 (13.4%) discontinued PDN within a 2-year follow-up. Renal involvement (HR: 0.41; p=0.009) and lower C3 serum levels (HR: 1.04; p=0.025) predicted a lack of PDN tapering below 5 mg/day. High ECLAM scores were associated with a greater probability of increasing PDN dose (OR: 1.6; p=0.004), independently of daily intake. Disease relapse rate did not statistically differ (p=0.706) between patients tapering PDN <5 mg/day (42/99, 42.4%) and those tapering PDN without dropping below 5 mg/day (13/28, 46.4%). Every month on PDN <5 mg/day associated with lower damage accrual (IRR: 0.96; p=0.007), whereas never tapering PDN <5 mg/day associated with a higher risk of developing GC-related damage (OR 5.9; p=0.014).Conclusion Tapering PDN <5 mg/day was achieved and maintained in half of newly diagnosed patients with SLE and may represent a good balance between the need to prevent damage accrual and the risk of disease relapse.
    Keywords Medicine ; R
    Subject code 610
    Language English
    Publishing date 2022-10-01T00:00:00Z
    Publisher BMJ Publishing Group
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  10. Article ; Online: Autoantibody status according to multiparametric assay accurately estimates connective tissue disease classification and identifies clinically relevant disease clusters

    Micaela Fredi / Nicola Bizzaro / Margherita Zen / Chiara Baldini / Ilaria Cavazzana / Roberto Giacomelli / Valeria Riccieri / Marco Fornaro / Franco Franceschini / Roberto Gerli / Anna Ghirardello / Paola Migliorini / Maurizio Benucci / Maria Infantino / Mariangela Manfredi / Elena Bartoloni / Antonella Fioravanti / Amelia Rigon / Silvia Piantoni /
    Onelia Bistoni / Francesca Bellisai / Carlo Perricone / Giacomo Cafaro / Danilo Villalta / Stefania Masneri / Paola Parronchi / Boaz Palterer / Stefania Del Rosso / Fabiana Topini / Manuela Sebastiano / Emirena Garrafa / Sara Cheleschi / Maria-Romana Bacarelli / Marilina Tampoia / Daniele Cammelli / Luisa Arcarese / Patrizia Rovere Querini / Valentina Canti

    RMD Open, Vol 9, Iss

    2023  Volume 3

    Abstract: Objective Assessment of circulating autoantibodies represents one of the earliest diagnostic procedures in patients with suspected connective tissue disease (CTD), providing important information for disease diagnosis, identification and prediction of ... ...

    Abstract Objective Assessment of circulating autoantibodies represents one of the earliest diagnostic procedures in patients with suspected connective tissue disease (CTD), providing important information for disease diagnosis, identification and prediction of potential clinical manifestations. The purpose of this study was to evaluate the ability of multiparametric assay to correctly classify patients with multiple CTDs and healthy controls (HC), independent of clinical features, and to evaluate whether serological status could identify clusters of patients with similar clinical features.Methods Patients with systemic lupus erythematosus (SLE), systemic sclerosis (SSc), Sjogren’s syndrome (SjS), undifferentiated connective tissue disease (UCTD), idiopathic inflammatory myopathies (IIM) and HC were enrolled. Serum was tested for 29 autoantibodies. An XGBoost model, exclusively based on autoantibody titres was built and classification accuracy was evaluated. A hierarchical clustering model was subsequently developed and clinical/laboratory features compared among clusters.Results 908 subjects were enrolled. The classification model showed a mean accuracy of 60.84±4.05% and a mean area under the receiver operator characteristic curve of 88.99±2.50%, with significant discrepancies among groups. Cluster analysis identified four clusters (CL). CL1 included patients with typical features of SLE. CL2 included most patients with SjS, along with some SLE and UCTD patients with SjS-like features. CL4 included anti-Jo1 patients only. CL3 was the largest and most heterogeneous, including all the remaining subjects, overall characterised by low titre or lower-prevalence autoantibodies.Conclusion Extended multiparametric autoantibody assay allowed an accurate classification of CTD patients, independently of clinical features. Clustering according to autoantibody titres is able to identify clusters of CTD subjects with similar clinical features, independently of their final diagnosis.
    Keywords Medicine ; R
    Subject code 610 ; 616
    Language English
    Publishing date 2023-08-01T00:00:00Z
    Publisher BMJ Publishing Group
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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