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  1. Article ; Online: Vasculitic neuropathy-related disability, pain, quality of life, and autonomic symptoms: A survey of 312 patients.

    Collins, Michael P / Hadden, Robert D M / Luqmani, Raashid A

    Rheumatology (Oxford, England)

    2024  

    Abstract: Objectives: To assess self-reported symptoms of neuropathy, disability, pain, health-related quality of life (HR-QOL), and autonomic dysfunction in patients with vasculitis.: Methods: Patients with vasculitis (with or without neuropathy) were invited ...

    Abstract Objectives: To assess self-reported symptoms of neuropathy, disability, pain, health-related quality of life (HR-QOL), and autonomic dysfunction in patients with vasculitis.
    Methods: Patients with vasculitis (with or without neuropathy) were invited by Vasculitis UK to complete an anonymous online survey.
    Results: 312 patients (71% female) responded. Median age was 61-70 years. Median duration of vasculitis was 4 years (<2 months to > 15 years). Vasculitic types included granulomatosis with polyangiitis (34%), unspecified ANCA-associated vasculitis (13%), microscopic polyangiitis (11%), eosinophilic granulomatosis with polyangiitis (11%), giant cell arteritis (10%), non-systemic vasculitic neuropathy (2%), and other (19%). Many patients reported foot/hand symptoms suggestive of neuropathy, including numbness (64%), pain (54%), or weakness (40%). 242 patients (78%) met our definition of probable vasculitic neuropathy: diagnosis of neuropathy by vasculitis team OR numbness OR weakness in feet/hands. Only 52% had been formally diagnosed with neuropathy. Compared with 70 patients without neuropathy, neuropathy patients had greater disability measured by the inflammatory Rasch-built Overall Disability Scale (centile mean 63.1 (SD 17.3) vs 75.2 (16.7); p< 0.0001), Inflammatory Neuropathy Cause and Treatment scale (median 2 (IQR 1-4) vs 0.5 (0-2); p< 0.0001), and modified Rankin scale (median 2 (IQR 1-3) vs 2 (1-2); p= 0.0002); greater pain on an 11-point rating scale (mean 4.6 (SD 2.6) vs 3.5 (2.8); p= 0.0009); and poorer HR-QOL on the EQ5D-3L (summary index mean 0.58 (SD 0.29) vs 0.69 (0.28); p<0.0001). Two-thirds reported autonomic symptoms (not associated with neuropathy).
    Conclusion: Neuropathy is common and associated with significant disability, pain, and impaired HR-QOL in patients with systemic vasculitis.
    Language English
    Publishing date 2024-01-30
    Publishing country England
    Document type Journal Article
    ZDB-ID 1464822-2
    ISSN 1462-0332 ; 1462-0324
    ISSN (online) 1462-0332
    ISSN 1462-0324
    DOI 10.1093/rheumatology/keae038
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Re: Nair et al. Consensus statement on the processing, interpretation and reporting of temporal artery biopsy for arteritis.

    Taze, Dilek / Chakrabarty, Aruna / Mackie, Sarah / Luqmani, Raashid / Cid, Maria C / Morgan, Ann W / Griffin, Kathryn

    Cardiovascular pathology : the official journal of the Society for Cardiovascular Pathology

    2024  Volume 70, Page(s) 107621

    Language English
    Publishing date 2024-02-14
    Publishing country United States
    Document type Letter
    ZDB-ID 1134600-0
    ISSN 1879-1336 ; 1054-8807
    ISSN (online) 1879-1336
    ISSN 1054-8807
    DOI 10.1016/j.carpath.2024.107621
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  3. Article ; Online: The role of neutrophils in rheumatic disease-associated vascular inflammation.

    Wang, Lihui / Luqmani, Raashid / Udalova, Irina A

    Nature reviews. Rheumatology

    2022  Volume 18, Issue 3, Page(s) 158–170

    Abstract: Vascular pathologies underpin and intertwine autoimmune rheumatic diseases and cardiovascular conditions, and atherosclerosis is increasingly recognized as the leading cause of morbidity in conditions such as systemic lupus erythematosus (SLE), ... ...

    Abstract Vascular pathologies underpin and intertwine autoimmune rheumatic diseases and cardiovascular conditions, and atherosclerosis is increasingly recognized as the leading cause of morbidity in conditions such as systemic lupus erythematosus (SLE), rheumatoid arthritis and antineutrophil cytoplasmic antibody-associated vasculitis. Neutrophils, important cells in the innate immune system, exert their functional effects in tissues via a variety of mechanisms, including the generation of neutrophil extracellular traps and the production of reactive oxygen species. Neutrophils have been implicated in the pathogenesis of several rheumatic diseases, and can also intimately interact with the vascular system, either through modulating endothelial barriers at the blood-vessel interface, or through associations with platelets. Emerging data suggest that neutrophils also have an important role maintaining homeostasis in individual organs and can protect the vascular system. Furthermore, studies using high-dimensional omics technologies have advanced our understanding of neutrophil diversity, and immature neutrophils are receiving new attention in rheumatic diseases including SLE and systemic vasculitis. Developments in genomic, imaging and organoid technologies are beginning to enable more in-depth investigations into the pathophysiology of vascular inflammation in rheumatic diseases, making now a good time to re-examine the full scope of roles of neutrophils in these processes.
    MeSH term(s) Extracellular Traps ; Humans ; Inflammation/pathology ; Lupus Erythematosus, Systemic ; Neutrophils ; Rheumatic Diseases/pathology
    Language English
    Publishing date 2022-01-17
    Publishing country United States
    Document type Journal Article ; Review
    ZDB-ID 2491532-4
    ISSN 1759-4804 ; 1759-4790
    ISSN (online) 1759-4804
    ISSN 1759-4790
    DOI 10.1038/s41584-021-00738-4
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: Preface.

    Luqmani, Raashid Ahmed / Jayne, David

    Best practice & research. Clinical rheumatology

    2018  Volume 32, Issue 1, Page(s) 1–2

    Language English
    Publishing date 2018-09-22
    Publishing country Netherlands
    Document type Editorial ; Introductory Journal Article
    ZDB-ID 2052323-3
    ISSN 1532-1770 ; 1521-6942
    ISSN (online) 1532-1770
    ISSN 1521-6942
    DOI 10.1016/j.berh.2018.11.001
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  5. Article: Updates on the diagnosis and monitoring of giant cell arteritis.

    Monti, Sara / Schäfer, Valentin Sebastian / Muratore, Francesco / Salvarani, Carlo / Montecucco, Carlomaurizio / Luqmani, Raashid

    Frontiers in medicine

    2023  Volume 10, Page(s) 1125141

    Abstract: This mini-review offers a critical appraisal of the currently employed imaging or histopathological tools to diagnose and monitor giant cell arteritis (GCA). An overview of the most updated evidence and current application of color duplex ultrasonography ...

    Abstract This mini-review offers a critical appraisal of the currently employed imaging or histopathological tools to diagnose and monitor giant cell arteritis (GCA). An overview of the most updated evidence and current application of color duplex ultrasonography (US), temporal artery biopsy (TAB), 18-fluorodeoxyglucose [18F] FDG-PET/CT, magnetic resonance imaging, and computed tomography angiography is provided. The main limitations of each tool, and the most relevant research developments are discussed. The review highlights the complementary value of the available modalities to ensure a correct diagnosis of GCA, and to provide valuable prognostic information. Novel evidence is accumulating to support the role of imaging, and particularly US, as a monitoring tool for the disease, opening new perspectives for the future management of large vessel vasculitis.
    Language English
    Publishing date 2023-02-23
    Publishing country Switzerland
    Document type Journal Article ; Review
    ZDB-ID 2775999-4
    ISSN 2296-858X
    ISSN 2296-858X
    DOI 10.3389/fmed.2023.1125141
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Comment on: Diagnosis of giant cell arteritis: reply.

    Ponte, Cristina / Martins-Martinho, Joana / Ahmed Luqmani, Raashid

    Rheumatology (Oxford, England)

    2020  Volume 59, Issue 11, Page(s) e119–e121

    MeSH term(s) Giant Cell Arteritis/diagnosis ; Humans ; Polymyalgia Rheumatica ; Temporal Arteries
    Keywords covid19
    Language English
    Publishing date 2020-09-04
    Publishing country England
    Document type Journal Article ; Comment
    ZDB-ID 1464822-2
    ISSN 1462-0332 ; 1462-0324
    ISSN (online) 1462-0332
    ISSN 1462-0324
    DOI 10.1093/rheumatology/keaa439
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article: A computerised system to evaluate patients with rheumatic diseases.

    Luqmani, Raashid / O'Neill, Lorraine / David, Joel

    Future healthcare journal

    2019  Volume 6, Issue Suppl 1, Page(s) 80–81

    Language English
    Publishing date 2019-07-30
    Publishing country England
    Document type Journal Article
    ZDB-ID 3016427-8
    ISSN 2514-6653 ; 2514-6645
    ISSN (online) 2514-6653
    ISSN 2514-6645
    DOI 10.7861/futurehosp.6-1-s80
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  8. Article ; Online: Disease assessment in systemic vasculitis.

    Luqmani, Raashid Ahmed

    Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association

    2015  Volume 30 Suppl 1, Page(s) i76–82

    Abstract: The anti-neutrophil cytoplasm antibody-associated vasculitides are complex multi-system disorders with many overlapping clinical features. Their outcome has been transformed by effective immunosuppression, preventing death in over 70% of cases. The ... ...

    Abstract The anti-neutrophil cytoplasm antibody-associated vasculitides are complex multi-system disorders with many overlapping clinical features. Their outcome has been transformed by effective immunosuppression, preventing death in over 70% of cases. The quality of survival is affected by the disease course, which is characterized by a significant likelihood of relapse in 38%, chronic effects from the disease and its treatment, as well as emerging or worsening comorbidity, all of which contribute to the patient's clinical condition and outcome. Whilst imaging and laboratory testing including histology are important aspects of diagnosis, they are of limited value in assessing response to therapy or subsequent disease course. We have developed standardized validated clinical methods to quantify disease activity and damage; we are developing effective measures of patient experience to complement these procedures. This approach provides a rational basis for clinical management as well as being essential in the conduct of clinical trials and studies in vasculitis, by providing reproducible definitions of relapse, remission and response to therapy for patients with systemic vasculitis. Clinical assessment remains the current gold standard for evaluating disease progress, but requires regular training to ensure standardization. The development of biomarkers in future may produce a more accurate description of disease and identify potential targets for therapy as well as predictors of response to drugs.
    MeSH term(s) Antibodies, Antineutrophil Cytoplasmic/analysis ; Biomarkers/analysis ; Humans ; Systemic Vasculitis/diagnosis ; Systemic Vasculitis/metabolism
    Chemical Substances Antibodies, Antineutrophil Cytoplasmic ; Biomarkers
    Language English
    Publishing date 2015-04
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 90594-x
    ISSN 1460-2385 ; 0931-0509
    ISSN (online) 1460-2385
    ISSN 0931-0509
    DOI 10.1093/ndt/gfv002
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  9. Article: Vasculitis: an update.

    Luqmani, Raashid A

    British journal of hospital medicine (London, England : 2005)

    2014  Volume 75, Issue 8, Page(s) 432–439

    Abstract: The systemic vasculitides are uncommon but serious diseases. Early recognition can be difficult because they mimic many conditions. Aggressive immunosuppression is toxic but effective; a targeted approach with biological agents may improve the outcome. ...

    Abstract The systemic vasculitides are uncommon but serious diseases. Early recognition can be difficult because they mimic many conditions. Aggressive immunosuppression is toxic but effective; a targeted approach with biological agents may improve the outcome.
    MeSH term(s) Anti-Inflammatory Agents/therapeutic use ; Diagnosis, Differential ; Humans ; Immunologic Factors/therapeutic use ; Prognosis ; Vasculitis/diagnosis ; Vasculitis/etiology ; Vasculitis/therapy
    Chemical Substances Anti-Inflammatory Agents ; Immunologic Factors
    Language English
    Publishing date 2014-08
    Publishing country England
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ISSN 1750-8460
    ISSN 1750-8460
    DOI 10.12968/hmed.2014.75.8.432
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  10. Article ; Online: Reply.

    Ponte, Cristina / Grayson, Peter C / Gribbons, Katherine Bates / Robson, Joanna C / Suppiah, Ravi / Judge, Andrew / Watts, Richard A / Luqmani, Raashid A / Merkel, Peter A

    Arthritis & rheumatology (Hoboken, N.J.)

    2023  Volume 75, Issue 6, Page(s) 1077–1080

    Language English
    Publishing date 2023-03-21
    Publishing country United States
    Document type Letter ; Comment
    ZDB-ID 2756371-6
    ISSN 2326-5205 ; 2326-5191
    ISSN (online) 2326-5205
    ISSN 2326-5191
    DOI 10.1002/art.42448
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