385 results on '"Lilleker, James B"'
Search Results
2. Flares of autoimmune rheumatic disease following COVID‐19 infection: Observations from the COVAD study
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Sandhu, Nimrat Kaur, Ravichandraan, Naveen, Nune, Arvind, Day, Jessica, Sen, Parikshit, Nikiphorou, Elena, Tan, Ai Lyn, Joshi, Mrudula, Saha, Sreoshy, Shinjo, Samuel Katsuyuki, Jagtap, Kshitij, Agarwal, Vishwesh, Ziade, Nelly, Velikova, Tsvetelina, Milchert, Marcin, Parodis, Ioannis, Gracia‐Ramos, Abraham Edgar, Cavagna, Lorenzo, Kuwana, Masataka, Knitza, Johannes, Makol, Ashima, Patel, Aarat, Pauling, John D, Wincup, Chris, Barman, Bhupen, Tehozol, Erick Adrian Zamora, Serrano, Jorge Rojas, La Torre, Ignacio García‐De, Colunga‐Pedraza, Iris J, Merayo‐Chalico, Javier, Okwara, Celestine Chibuzo, Katchamart, Wanruchada, Goo, Phonpen Akawatcharangura, Shumnalieva, Russka, Chen, Yi‐Ming, Hoff, Leonardo Santos, Kibbi, Lina El, Halabi, Hussein, Vaidya, Binit, Shaharir, Syahrul Sazliyana, Hasan, ATM Tanveer, Dey, Dzifa, Gutiérrez, Carlos Enrique Toro, Caballero‐Uribe, Carlo Vinicio, Lilleker, James B, Salim, Babur, Gheita, Tamer, Saavedra, Miguel A, Chatterjee, Tulika, Distler, Oliver, Group, COVAD Study, Chinoy, Hector, Agarwal, Vikas, Aggarwal, Rohit, and Gupta, Latika
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Biomedical and Clinical Sciences ,Immunology ,Autoimmune Disease ,Emerging Infectious Diseases ,Infectious Diseases ,Arthritis ,Coronaviruses ,Humans ,COVID-19 ,Rheumatic Diseases ,Autoimmune Diseases ,COVAD Study Group ,Arthritis & Rheumatology - Published
- 2024
3. Breakthrough SARS-CoV-2 infection in fully vaccinated patients with systemic lupus erythematosus: results from the COVID-19 Vaccination in Autoimmune Disease (COVAD) study
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Palazzo, Leonardo, Lindblom, Julius, Kihlgren Olsson, Emelie, Nikiphorou, Elena, Wincup, Chris, Saha, Sreoshy, Shaharir, Syahrul Sazliyana, Katchamart, Wanruchada, Akarawatcharangura Goo, Phonpen, Traboco, Lisa, Chen, Yi-Ming, Lilleker, James B., Nune, Arvind, Pauling, John D., Agarwal, Vishwesh, Dzifa, Dey, Toro Gutiérrez, Carlos Enrique, Caballero-Uribe, Carlo V., Chinoy, Hector, Agarwal, Vikas, Gupta, Latika, and Parodis, Ioannis
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- 2024
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4. Breakthrough SARS-CoV-2 infection and disease flares in patients with rheumatoid arthritis: result from COVAD e-survey study
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Santos, Cristiana Sieiro, Chen, Jun-Peng, Nikiphorou, Elena, Tseng, Chi-Wei, Gutiérrez, Carlos Enrique Toro, Tan, Ai Lyn, Nune, Arvind, Kadam, Esha, Kuwana, Masataka, Day, Jessica, Saha, Sreoshy, Velikova, Tsvetelina, Lilleker, James B., Caballero-Uribe, Carlo V., Sen, Parikshit, Chinoy, Hector, Aggarwal, Rohit, Agarwal, Vikas, Gupta, Latika, and Chen, Yi-Ming
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- 2024
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5. Adult idiopathic inflammatory myopathies
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Parker, Matthew JS, Lilleker, James B, and Chinoy, Hector
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- 2024
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6. Autoantibodies against a subunit of mitochondrial respiratory chain complex I in inclusion body myositis
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Notarnicola, Antonella, Hellstrom, Ceke, Horuluoglu, Begum, Pin, Elisa, Preger, Charlotta, Bonomi, Francesco, De Paepe, Boel, De Bleecker, Jan L., Van der Kooi, Anneke J., De Visser, Marianne, Sacconi, Sabrina, Machado, Pedro, Badrising, Umesh A., Rietveld, Anke, Pruijn, Ger, Rothwell, Simon, Lilleker, James B., Chinoy, Hector, Benveniste, Olivier, Svenungsson, Elisabet, Idborg, Helena, Jakobsson, Per-Johan, Nilsson, Peter, and Lundberg, Ingrid E.
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- 2024
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7. Correlates of breakthrough COVID-19 in vaccinated patients with systemic sclerosis: survival analysis from a multicentre international patient-reported survey
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Ahmed, Sakir, Gupta, Latika, Kuwana, Masataka, Pauling, John D., Day, Jessica, Ravichandran, Naveen, Joshi, Mrudula, Parodis, Ioannis, Sen, Parikshit, Jagtap, Kshitij, Nikiphorou, Elena, Saha, Sreoshy, Agarwal, Vishwesh, Chatterjee, Tulika, Lilleker, James B., Kardes, Sinan, Milchert, Marcin, Gheita, Tamer, Salim, Babur, Velikova, Tsvetelina, Gracia-Ramos, Abraham Edgar, Tan, Ai Lyn, Nune, Arvind, Cavagna, Lorenzo, Saavedra, Miguel A., Shinjo, Samuel Katsuyuki, Ziade, Nelly, Knitza, Johannes, Distler, Oliver, Wibowo, Suryo Anggoro Kusumo, Chinoy, Hector, Aggarwal, Rohit, Agarwal, Vikas, and Makol, Ashima
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- 2024
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8. Autoantibodies and damage in patients with idiopathic inflammatory myopathies: A longitudinal multicenter study from the MYONET international network
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Espinosa-Ortega, Fabricio, Lodin, Karin, Dastmalchi, Maryam, Vencovsky, Jiri, Diederichsen, Louise P, Shinjo, Samuel Katsuyuki, Danieli, Maria Giovanna, Selva-O'Callaghan, Albert, de Visser, Marianne, Griger, Zoltan, Ceribelli, Angela, Gómez-Martin, Diana, Andersson, Helena, Vázquez-Del Mercado, Mónica, Chinoy, Hector, Lilleker, James B, New, Paul, Krogh, Niels S, Lundberg, Ingrid E, and Alexanderson, Helene
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- 2024
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9. Utilising accessible and reproducible neurological assessments in clinical studies: Insights from use of the Neurological Impairment Scale in the multi-centre COVID-CNS study
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Alam, Ali M., Webb, Glynn W., Collie, Ceryce, Mariathasan, Sashini, Huang, Yun, Hilton, Orla, Shil, Rajish, Dodd, Katherine C., Lilleker, James B., Smith, Craig J., Easton, Ava, Tamborska, Arina, Thomas, Rhys H., Davies, Nicholas W.S., Jenkins, Thomas M., Zandi, Michael, Benjamin, Laura, Ellul, Mark A., Solomon, Tom, Pollak, Thomas A., Nicholson, Tim, Breen, Gerome, van Wamelen, Daniel J., Wood, Nicholas W., and Michael, Benedict D.
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- 2024
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10. Epidemiology of the idiopathic inflammatory myopathies
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Khoo, Thomas, Lilleker, James B., Thong, Bernard Yu-Hor, Leclair, Valérie, Lamb, Janine A., and Chinoy, Hector
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- 2023
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11. Long-term safety of COVID vaccination in individuals with idiopathic inflammatory myopathies: results from the COVAD study
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Doskaliuk, Bohdana, Ravichandran, Naveen, Sen, Parikshit, Day, Jessica, Joshi, Mrudula, Nune, Arvind, Nikiphorou, Elena, Saha, Sreoshy, Tan, Ai Lyn, Shinjo, Samuel Katsuyuki, Ziade, Nelly, Velikova, Tsvetelina, Milchert, Marcin, Jagtap, Kshitij, Parodis, Ioannis, Gracia-Ramos, Abraham Edgar, Cavagna, Lorenzo, Kuwana, Masataka, Knitza, Johannes, Chen, Yi Ming, Makol, Ashima, Agarwal, Vishwesh, Patel, Aarat, Pauling, John D., Wincup, Chris, Barman, Bhupen, Tehozol, Erick Adrian Zamora, Serrano, Jorge Rojas, La Torre, Ignacio García-De, Colunga-Pedraza, Iris J., Merayo-Chalico, Javier, Chibuzo, Okwara Celestine, Katchamart, Wanruchada, Goo, Phonpen Akarawatcharangura, Shumnalieva, Russka, Hoff, Leonardo Santos, Kibbi, Lina El, Halabi, Hussein, Vaidya, Binit, Shaharir, Syahrul Sazliyana, Hasan, A. T. M. Tanveer, Dey, Dzifa, Gutiérrez, Carlos Enrique Toro, Caballero-Uribe, Carlo V., Lilleker, James B., Salim, Babur, Gheita, Tamer, Chatterjee, Tulika, Distler, Oliver, Saavedra, Miguel A., Chinoy, Hector, Agarwal, Vikas, Aggarwal, Rohit, and Gupta, Latika
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- 2023
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12. High fatigue scores in patients with idiopathic inflammatory myopathies: a multigroup comparative study from the COVAD e-survey
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Grignaschi, Silvia, Kim, Minchul, Zanframundo, Giovanni, Ravichandran, Naveen, Lilleker, James B., Sen, Parikshit, Joshi, Mrudula, Agarwal, Vishwesh, Kardes, Sinan, Day, Jessica, Makol, Ashima, Milchert, Marcin, Gheita, Tamer, Salim, Babur, Velikova, Tsvetelina, Gracia-Ramos, Abraham Edgar, Parodis, Ioannis, Nikiphorou, Elena, Chatterjee, Tulika, Tan, Ai Lyn, Saavedra, Miguel A., Shinjo, Samuel Katsuyuki, Ziade, Nelly, Knitza, Johannes, Kuwana, Masataka, Nune, Arvind, Distler, Oliver, Chinoy, Hector, Cavagna, Lorenzo, Agarwal, Vikas, Aggarwal, Rohit, and Gupta, Latika
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- 2023
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13. Reply to: Current classification criteria underestimate the incidence of idiopathic inflammatory myopathies by ignoring subgroups
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Khoo, Thomas, Lilleker, James B., Thong, Bernard Yu-Hor, Leclair, Valérie, Lamb, Janine A., and Chinoy, Hector
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- 2024
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14. Addressing ethnic disparities in neurological research in the United Kingdom: An example from the prospective multicentre COVID-19 Clinical Neuroscience Study
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van Wamelen, Daniel J., Rota, Silvia, Hartmann, Monika, Martin, Naomi H., Alam, Ali M., Thomas, Rhys H., Dodd, Katherine C., Jenkins, Thomas, Smith, Craig J., Zandi, Michael S., Easton, Ava, Carr, Georgina, Benjamin, Laura A., Lilleker, James B., Saucer, David, Coles, Alasdair J., Wood, Nicholas, Ray Chaudhuri, K., Breen, Gerome, and Michael, Benedict Daniel
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- 2024
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15. Patient global assessment and inflammatory markers in patients with idiopathic inflammatory myopathies – A longitudinal study
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Lodin, Karin, Espinosa-Ortega, Fabricio, Dastmalchi, Maryam, Vencovsky, Jiri, Andersson, Helena, Chinoy, Hector, Lilleker, James B., Shinjo, Samuel Katsuyuki, Maurer, Britta, Griger, Zoltan, Ceribelli, Angela, Torres-Ruiz, Jiram, Mercado M., Vazquez-Del, Leonard, Dag, Alexanderson, Helene, and Lundberg, Ingrid E.
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- 2024
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16. Systemic sclerosis and COVID-19 vaccine safety: short-term insights from the global COVID-19 vaccination in autoimmune disease (COVAD) survey
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Naveen, R., Thakare, Darpan R., Kuwana, Masataka, Pauling, John D., Day, Jessica, Joshi, Mrudula, Parodis, Ioannis, Sen, Parikshit, Jagtap, Kshitij, Nikiphorou, Elena, Saha, Sreoshy, Agarwal, Vishwesh, Chatterjee, Tulika, Lilleker, James B., Kardes, Sinan, Milchert, Marcin, Gheita, Tamer, Salim, Babur, Velikova, Tsvetelina, Gracia-Ramos, Abraham Edgar, Tan, Ai Lyn, Nune, Arvind, Cavagna, Lorenzo, Saavedra, Miguel A., Shinjo, Samuel Katsuyuki, Ziade, Nelly, Knitza, Johannes, Distler, Oliver, Chinoy, Hector, Aggarwal, Rohit, Gupta, Latika, Agarwal, Vikas, and Makol, Ashima
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- 2023
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17. Improved outcomes with early immunosuppression in patients with immune-checkpoint inhibitor induced myasthenia gravis, myocarditis and myositis: a case series
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Weaver, Jamie MJ, Dodd, Katie, Knight, Tom, Chaudhri, Mehek, Khera, Raj, Lilleker, James B, Roberts, Mark, Lorigan, Paul, and Cooksley, Tim
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- 2023
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18. COVID-19 severity and vaccine breakthrough infections in idiopathic inflammatory myopathies, other systemic autoimmune and inflammatory diseases, and healthy controls: a multicenter cross-sectional study from the COVID-19 Vaccination in Autoimmune Diseases (COVAD) survey
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Hoff, Leonardo Santos, Ravichandran, Naveen, Shinjo, Samuel Katsuyuki, Day, Jessica, Sen, Parikshit, Junior, Jucier Gonçalves, Lilleker, James B., Joshi, Mrudula, Agarwal, Vishwesh, Kardes, Sinan, Kim, Minchul, Milchert, Marcin, Makol, Ashima, Gheita, Tamer, Salim, Babur, Velikova, Tsvetelina, Gracia-Ramos, Abraham Edgar, Parodis, Ioannis, O’Callaghan, Albert Selva, Nikiphorou, Elena, Tan, Ai Lyn, Chatterjee, Tulika, Cavagna, Lorenzo, Saavedra, Miguel A., Ziade, Nelly, Knitza, Johannes, Kuwana, Masataka, Nune, Arvind, Distler, Oliver, Cansu, Döndü Üsküdar, Traboco, Lisa, Wibowo, Suryo Angorro Kusumo, Tehozol, Erick Adrian Zamora, Serrano, Jorge Rojas, La Torre, Ignacio García-De, Wincup, Chris, Pauling, John D., Chinoy, Hector, Agarwal, Vikas, Aggarwal, Rohit, and Gupta, Latika
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- 2023
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19. COVAD survey 2 long-term outcomes: unmet need and protocol
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Fazal, Zoha Zahid, Sen, Parikshit, Joshi, Mrudula, Ravichandran, Naveen, Lilleker, James B., Agarwal, Vishwesh, Kardes, Sinan, Kim, Minchul, Day, Jessica, Makol, Ashima, Milchert, Marcin, Gheita, Tamer, Salim, Babur, Velikova, Tsvetelina, Gracia-Ramos, Abraham Edgar, Parodis, Ioannis, Nikiphorou, Elena, Tan, Ai Lyn, Chatterjee, Tulika, Cavagna, Lorenzo, Saavedra, Miguel A., Shinjo, Samuel Katsuyuki, Ziade, Nelly, Selva-O’Callaghan, Albert, Nune, Arvind, Knitza, Johannes, Kuwana, Masataka, Gutiérrez, Carlos-Enrique Toro, Caballero-Uribe, Carlo Vinicio, Dey, Dzifa, Distler, Oliver, Chinoy, Hector, Agarwal, Vikas, Aggarwal, Rohit, and Gupta, Latika
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- 2022
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20. Zilucoplan in immune-mediated necrotising myopathy: a phase 2, randomised, double-blind, placebo-controlled, multicentre trial
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Amato, Anthony A., Benveniste, Olivier, Biliciler, Suur, Chinoy, Hector, Dimachkie, Mazen M., Edmundson, Christyn, Freimer, Miriam, Geraci, Anthony, Hussain, Yessar, Machado, Pedro, Mammen, Andrew L., Mozaffar, Tahseen, Soltanzadeh, Payam, Suresh, Niraja, van der Kooi, Anneke, Allenbach, Yves, Appleby, Matthew, Barohn, Richard J, Champtiaux, Nicolas, Doughty, Christopher, Farias, Jerrica, Farmakidis, Constantine, Habib, Ali A., Karam, Chafic, Lilleker, James, Lorusso, Samantha, Pasnoor, Mamatha, Pinal-Fernandez, Iago, Querin, Giorgia, Raaphorst, Joost, Ransley, George, Saba, Sami, Sheikh, Kazim, Snedden, Andrew, Statland, Jeffrey, Vu, Tuan, Mammen, Andrew L, Amato, Anthony A, Dimachkie, Mazen M, Lilleker, James B, Boroojerdi, Babak, Vanderkelen, Mark, Delicha, Eumorphia Maria, Koendgen, Harold, Farzaneh-Far, Ramin, Duda, Petra W, and Sayegh, Camil
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- 2023
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21. SARS-CoV-2 vaccination and new-onset myasthenia gravis: A report of 7 cases and review of the literature
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Ramdas, Sithara, Hum, Ryan Malcolm, Price, Abigail, Paul, Anna, Bland, Jeremy, Burke, Georgina, Farrugia, Maria, Palace, Jacqueline, Storrie, Alice, Ho, Pauline, Standing, Emma, Lilleker, James B., and Jungbluth, Heinz
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- 2022
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22. Adult idiopathic inflammatory myopathies
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Parker, Matthew JS., Lilleker, James B., and Chinoy, Hector
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- 2022
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23. COVID-19 vaccination in autoimmune disease (COVAD) survey protocol
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Sen, Parikshit, Gupta, Latika, Lilleker, James B., Aggarwal, Vishwesh, Kardes, Sinan, Milchert, Marcin, Gheita, Tamer, Salim, Babur, Velikova, Tsvetelina, Gracia-Ramos, Abraham Edgar, Parodis, Ioannis, O’Callaghan, Albert Selva, Nikiphorou, Elena, Tan, Ai Lyn, Cavagna, Lorenzo, Saavedra, Miguel A., Shinjo, Samuel Katsuyuki, Ziade, Nelly, Knitza, Johannes, Kuwana, Masataka, Cagnotto, Giovanni, Nune, Arvind, Distler, Oliver, Chinoy, Hector, Aggarwal, Vikas, and Aggarwal, Rohit
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- 2022
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24. Perspectives on glucocorticoid usage in patients with adult inflammatory myopathy
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Loarce-Martos, Jesús, Lilleker, James B., Alder, Eve, Goode, Jo, and Chinoy, Hector
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- 2021
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25. COVID-19 severity, breakthrough infections and vaccine safety in young individuals with autoimmune diseases: insights from the COVAD study.
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Alunno, Alessia, Carubbi, Francesco, Tan, Ai Lyn, Sen, Parikshit, Cavagna, Lorenzo, Joshi, Mrudula, Day, Jessica, Saha, Sreoshy, Gutiérrez, Carlos Enrique Toro, Caballero-Uribe, Carlo Vinicio, Distler, Oliver, Chinoy, Hector, Aggarwal, Rohit, Agarwal, Vikas, Gupta, Latika, COVAD Study Group, Nikiphorou, Elena, Nune, Arvind, Lilleker, James B., and Pauling, John D.
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BREAKTHROUGH infections ,YOUNG adults ,COVID-19 ,VACCINE safety ,COVID-19 vaccines - Abstract
Notwithstanding the wealth of literature on COVID-19, studies focusing on young adults with autoimmune diseases (AD) are lacking. To determine early (within 7 days) and late (after 7 days) anti-SARS-CoV-2 vaccine-related adverse events (AEs), post-vaccine disease flares, COVID-19 severity and breakthrough infections (B-INFs) in young people with rheumatic diseases (RMDs) and non-rheumatic autoimmune diseases (nr-ADs) compared to healthy controls (HC). Data were captured through the international COVID-19 vaccination in autoimmune diseases (COVAD) 1 and 2 questionnaires. Of 20,685 complete responses, we identified 6010 from patients aged 18–35 years (1692 RMD, 400 nrADs, 3918 HC) who received up to 4 vaccine doses. BNT162b2 was the most frequently administered vaccine and prior to vaccination, 7% of people with nrAD were taking immunosuppressants (IS) versus 80% in RMDs. Early mild AEs were more frequent in RMDs (93%) and nr-ADs (92%) compared to HC (85%). The frequency of late mild AEs was < 20% in all groups. Severe AEs were rare. SARS-CoV-2 infection rates were similar across all groups, however, RMD patients reported a single episode of infection more frequently than nrADs and HC, while nrADs reported multiple infections more frequently than RMD. Self-reported disease flares were reported by 10% or RMD and 7% of nrAD patients. Our study reinforces the safety of anti-SARS-CoV-2 vaccine also in young people with ADs, but it also highlights that among young individuals the number and clinical picture of SARS-CoV-2 infections is affected more by the type of AD rather than by coexisting IS therapy. [ABSTRACT FROM AUTHOR]
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- 2024
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26. P150 Diagnostic utility of anti-cN1A autoantibody testing in sporadic inclusion body myositis
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Al-Attar, Mariam, primary, Khoo, Thomas, additional, Lilleker, James B, additional, and Chinoy, Hector, additional
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- 2024
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27. 272nd ENMC international workshop: 10 Years of progress - revision of the ENMC 2013 diagnostic criteria for inclusion body myositis and clinical trial readiness. 16–18 June 2023, Hoofddorp, The Netherlands
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Lilleker, James B., primary, Naddaf, Elie, additional, Saris, Christiaan G.J., additional, Schmidt, Jens, additional, de Visser, Marianne, additional, Weihl, Conrad C., additional, Alexandersson, Helene, additional, Alfano, Lindsay, additional, Allenbach, Yves, additional, Badrising, Umesh, additional, Benveniste, Olivier, additional, Bhai, Salman, additional, De Bleecker, Jan, additional, Breeveld, Marie Christine, additional, Chinoy, Hector, additional, Diederichsen, Louise, additional, Dimachkie, Mazen, additional, Greenberg, Steven, additional, Johari, Mridul, additional, Lilleker, James, additional, Lindgren, Ulrika, additional, Lloyd, Tom, additional, Machado, Pedro, additional, Mozaffar, Tahseen, additional, Mischke, Roland, additional, Needham, Merrilee, additional, Nishino, Ichizo, additional, Oldfors, Anders, additional, Saris, Christiaan, additional, Stenzel, Werner, additional, Tasca, Giorgio, additional, and Weihl, Conrad, additional
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- 2024
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28. A protocol for a scoping review on the role of whole-body and dedicated body-part magnetic resonance imaging for assessment of adult and juvenile idiopathic inflammatory myopathies
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Essouma, Mickael, primary, de Araujo, Daniel Brito, additional, Day, Jessica, additional, Gupta, Latika, additional, Knight, Adina Kay, additional, Reed, Ann, additional, Naddaf, Elie, additional, Elias Sallum, Adriana Maluf, additional, Marrani, Edoardo, additional, Conticini, Edoardo, additional, Appenzeller, Simone, additional, Dimachkie, Mazen, additional, Abou, Tamima Mohamad, additional, Gibson, Daren, additional, Kirkhus, Eva, additional, van der Koi, Anneke J, additional, Lilleker, James B, additional, Lucchini, Matteo, additional, Machado, Pedro, additional, Riopel, Mary Anne, additional, Sanner, Helga, additional, Schiffenbauer, Adam, additional, Guimarães, Julio Brandão, additional, Saad-Magalhaes, Claudia, additional, O’Hanlon, Susan, additional, Omori, Clarissa Harumi, additional, Phaneuf, Susan, additional, Moghadam-Kia, Siamak, additional, Tolend, Mirkamal, additional, Ventura, Iazsmin Bauer, additional, Rider, Lisa G, additional, Christopher-Stine, Lisa, additional, Paik, Julie J, additional, Feldman, Brian, additional, Shinjo, Samuel Katsuyuki, additional, and Doria, Andrea Schwarz, additional
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- 2024
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29. Pitfalls in the diagnosis of myositis
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Chinoy, Hector and Lilleker, James B.
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- 2020
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30. 272nd ENMC international workshop: 10 Years of progress - revision of the ENMC 2013 diagnostic criteria for inclusion body myositis and clinical trial readiness. 16-18 June 2023, Hoofddorp, The Netherlands.
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Lilleker, James B. and Lilleker, James B.
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- Neurology - Radboud University Medical Center.
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- 2024
31. Impaired health-related quality of life in idiopathic inflammatory myopathies : a cross-sectional analysis from the COVAD-2 e-survey
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Yoshida, Akira, Li, Yuan, Maroufy, Vahed, Kuwana, Masataka, Sazliyana Shaharir, Syahrul, Makol, Ashima, Sen, Parikshit, Lilleker, James B, Agarwal, Vishwesh, Kadam, Esha, Akawatcharangura Goo, Phonpen, Day, Jessica, Milchert, Marcin, Chen, Yi-Ming, Dey, Dzifa, Velikova, Tsvetelina, Saha, Sreoshy, Edgar Gracia-Ramos, Abraham, Parodis, Ioannis, Nikiphorou, Elena, Tan, Ai Lyn, Nune, Arvind, Cavagna, Lorenzo, Toro Gutiérrez, Carlos Enrique, Caballero-Uribe, Carlo Vinicio, Saavedra, Miguel A, Shinjo, Samuel Katsuyuki, Ziade, Nelly, El Kibbi, Lina, Knitza, Johannes, Distler, Oliver, Chinoy, Hector, Agarwal, Vikas, Aggarwal, Rohit, Gupta, Latika, Yoshida, Akira, Li, Yuan, Maroufy, Vahed, Kuwana, Masataka, Sazliyana Shaharir, Syahrul, Makol, Ashima, Sen, Parikshit, Lilleker, James B, Agarwal, Vishwesh, Kadam, Esha, Akawatcharangura Goo, Phonpen, Day, Jessica, Milchert, Marcin, Chen, Yi-Ming, Dey, Dzifa, Velikova, Tsvetelina, Saha, Sreoshy, Edgar Gracia-Ramos, Abraham, Parodis, Ioannis, Nikiphorou, Elena, Tan, Ai Lyn, Nune, Arvind, Cavagna, Lorenzo, Toro Gutiérrez, Carlos Enrique, Caballero-Uribe, Carlo Vinicio, Saavedra, Miguel A, Shinjo, Samuel Katsuyuki, Ziade, Nelly, El Kibbi, Lina, Knitza, Johannes, Distler, Oliver, Chinoy, Hector, Agarwal, Vikas, Aggarwal, Rohit, and Gupta, Latika
- Abstract
OBJECTIVES: To investigate health-related quality of life in patients with idiopathic inflammatory myopathies (IIMs) compared with those with non-IIM autoimmune rheumatic diseases (AIRDs), non-rheumatic autoimmune diseases (nrAIDs) and without autoimmune diseases (controls) using Patient-Reported Outcome Measurement Information System (PROMIS) instrument data obtained from the second COVID-19 vaccination in autoimmune disease (COVAD-2) e-survey database. METHODS: Demographics, diagnosis, comorbidities, disease activity, treatments and PROMIS instrument data were analysed. Primary outcomes were PROMIS Global Physical Health (GPH) and Global Mental Health (GMH) scores. Factors affecting GPH and GMH scores in IIMs were identified using multivariable regression analysis. RESULTS: We analysed responses from 1582 IIM, 4700 non-IIM AIRD and 545 nrAID patients and 3675 controls gathered through 23 May 2022. The median GPH scores were the lowest in IIM and non-IIM AIRD patients {13 [interquartile range (IQR) 10-15] IIMs vs 13 [11-15] non-IIM AIRDs vs 15 [13-17] nrAIDs vs 17 [15-18] controls, P < 0.001}. The median GMH scores in IIM patients were also significantly lower compared with those without autoimmune diseases [13 (IQR 10-15) IIMs vs 15 (13-17) controls, P < 0.001]. Inclusion body myositis, comorbidities, active disease and glucocorticoid use were the determinants of lower GPH scores, whereas overlap myositis, interstitial lung disease, depression, active disease, lower PROMIS Physical Function 10a and higher PROMIS Fatigue 4a scores were associated with lower GMH scores in IIM patients. CONCLUSION: Both physical and mental health are significantly impaired in IIM patients, particularly in those with comorbidities and increased fatigue, emphasizing the importance of patient-reported experiences and optimized multidisciplinary care to enhance well-being in people with IIMs., Funding agency:National Institution for Health Research Manchester Biomedical Research Centre NIHR203308
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- 2024
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32. Gender differences in patient experience in idiopathic inflammatory myopathies : Sub analysis from the COVAD dataset
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Yoshida, Akira, Kim, Minchul, Kuwana, Masataka, Ravichandran, Naveen, Makol, Ashima, Sen, Parikshit, Lilleker, James B., Agarwal, Vishwesh, Kardes, Sinan, Day, Jessica, Milchert, Marcin, Joshi, Mrudula, Gheita, Tamer, Salim, Babur, Velikova, Tsvetelina, Gracia-Ramos, Abraham Edgar, Parodis, Ioannis, Nikiphorou, Elena, Chatterjee, Tulika, Tan, Ai Lyn, Nune, Arvind, Cavagna, Lorenzo, Saavedra, Miguel A., Shinjo, Samuel Katsuyuki, Ziade, Nelly, Knitza, Johannes, Distler, Oliver, Chinoy, Hector, Agarwal, Vikas, Aggarwal, Rohit, Gupta, Latika, Yoshida, Akira, Kim, Minchul, Kuwana, Masataka, Ravichandran, Naveen, Makol, Ashima, Sen, Parikshit, Lilleker, James B., Agarwal, Vishwesh, Kardes, Sinan, Day, Jessica, Milchert, Marcin, Joshi, Mrudula, Gheita, Tamer, Salim, Babur, Velikova, Tsvetelina, Gracia-Ramos, Abraham Edgar, Parodis, Ioannis, Nikiphorou, Elena, Chatterjee, Tulika, Tan, Ai Lyn, Nune, Arvind, Cavagna, Lorenzo, Saavedra, Miguel A., Shinjo, Samuel Katsuyuki, Ziade, Nelly, Knitza, Johannes, Distler, Oliver, Chinoy, Hector, Agarwal, Vikas, Aggarwal, Rohit, and Gupta, Latika
- Abstract
OBJECTIVES: We aimed to investigate gender-based differences in idiopathic inflammatory myopathies (IIMs), with a particular focus on patient-reported outcomes, utilizing data obtained through the international COVID-19 vaccination in autoimmune disease (COVAD) e-survey. METHODS: Patient-reported outcomes including fatigue, pain, and physical function were extracted from the COVAD database and compared between genders, adjusting for demographics and IIM subgroups by multivariable analysis. Inclusion body myositis (IBM) was analysed separately because of substantial differences in outcomes. RESULTS: 1197 complete responses from patients with IIMs as of 31 August 2021 were analysed. Seventy percent were women. Women were younger (58 [48-68] vs. 69 [58-75] years old, median [IQR], p < 0.001) and more likely to suffer from autoimmune multimorbidity, defined as three or more autoimmune diseases in an individual patient (11.4% vs. 2.8%, p < 0.001). In non-IBM IIMs, fatigue visual analogue scale scores were higher in women (5 [3-7] vs. 4 [2-6], median [IQR], p = 0.004), whereas no significant gender-based differences were noted in IBM. Multivariable analysis in non-IBM IIMs revealed women, residence in high-income countries, overlap myositis, and autoimmune multimorbidity were independently associated with increased fatigue. CONCLUSIONS: Women with IIMs suffer from autoimmune multimorbidity and experience increased fatigue compared to men.
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- 2024
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33. Global disparities in the treatment of idiopathic inflammatory myopathies : results from an international online survey study
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Ziade, Nelly, Aoude, Marc, Hmamouchi, Ihsane, Naveen, R., Lilleker, James B., Sen, Parikshit, Joshi, Mrudula, Agarwal, Vishwesh, Kardes, Sinan, Day, Jessica, Makol, Ashima, Milchert, Marcin, Gheita, Tamer, Salim, Babur, Velikova, Tsvetelina, Edgar Gracia-Ramos, Abraham, Parodis, Ioannis, Nikiphorou, Elena, Chatterjee, Tulika, Tan, Ai Lyn, Saavedra, Miguel A., Shinjo, Samuel Katsuyuki, Knitza, Johannes, Kuwana, Masataka, Nune, Arvind, Cavagna, Lorenzo, Distler, Oliver, Chinoy, Hector, Agarwal, Vikas, Aggarwal, Rohit, Gupta, Latika, Ziade, Nelly, Aoude, Marc, Hmamouchi, Ihsane, Naveen, R., Lilleker, James B., Sen, Parikshit, Joshi, Mrudula, Agarwal, Vishwesh, Kardes, Sinan, Day, Jessica, Makol, Ashima, Milchert, Marcin, Gheita, Tamer, Salim, Babur, Velikova, Tsvetelina, Edgar Gracia-Ramos, Abraham, Parodis, Ioannis, Nikiphorou, Elena, Chatterjee, Tulika, Tan, Ai Lyn, Saavedra, Miguel A., Shinjo, Samuel Katsuyuki, Knitza, Johannes, Kuwana, Masataka, Nune, Arvind, Cavagna, Lorenzo, Distler, Oliver, Chinoy, Hector, Agarwal, Vikas, Aggarwal, Rohit, and Gupta, Latika
- Abstract
OBJECTIVES: We aimed to explore current practice and interregional differences in the treatment of idiopathic inflammatory myopathies (IIMs). We triangulated these observations considering countries' Gross National Income (GNI), disease subtypes, and symptoms using patient-reported information. METHODS: A cross-sectional ancillary analysis of the "COVID-19 vaccination in auto-immune disease" (COVAD) e-survey containing demographic characteristics, IIM subtypes (dermatomyositis (DM), polymyositis (PM), inclusion-body myositis (IBM), anti-synthetase syndrome (ASSD), immune-mediated necrotizing myopathy (IMNM), overlap myopathies (OM)), current symptoms (surrogate for organ involvement), and treatments (corticosteroids (CS), immunomodulators (IM), i.e., antimalarials, immunosuppressants (IS), intravenous immunoglobulins (IVIG), biological treatments, and targeted-synthetic small molecules). Treatments were presented descriptively according to continents, GNI, IIM, and organ involvement, and associated factors were analyzed using multivariable binary logistic regressions. RESULTS: Of 18,851 respondents from 94 countries, 1,418 with IIM were analyzed (age 61 years, 62.5% females). DM (32.4%), IBM (24.5%), and OM (15.8%) were the most common subtypes. Treatment categories included IS (49.4%), CS (38.5%), IM (13.8%), and IVIG (9.4%). Notably, treatments varied across regions, GNI categories (IS mostly used in higher-middle income, IM in lower-middle income, IVIG and biologics largely limited to high-income countries), IIM subtypes (IS and CS associated with ASSD, IM with OM and DM, IVIG with IMNM, and biological treatments with OM and ASSD) and disease manifestations (IS and CS with dyspnea). Most inter-regional treatment disparities persisted after multivariable analysis. CONCLUSION: We identified marked regional treatment disparities in a global cohort of IIM. These observations highlight the need for international consensus-driven management guidelines considering patie, Funding agency:National Institution for Health Research Manchester Biomedical Research Centre Funding Scheme
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- 2024
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34. Impaired health-related quality of life in idiopathic inflammatory myopathies : a cross-sectional analysis from the COVAD-2 e-survey
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Yoshida, Akira; https://orcid.org/0000-0003-3590-1637, Li, Yuanfang; https://orcid.org/0000-0002-2646-3260, Maroufy, Vahed, Kuwana, Masataka; https://orcid.org/0000-0001-8352-6136, Sazliyana Shaharir, Syahrul, Makol, Ashima; https://orcid.org/0000-0002-8748-898X, Sen, Parikshit; https://orcid.org/0000-0002-1630-6026, Lilleker, James B; https://orcid.org/0000-0002-9230-4137, Agarwal, Vishwesh; https://orcid.org/0000-0002-0986-8354, Kadam, Esha; https://orcid.org/0000-0002-8739-4502, Akawatcharangura Goo, Phonpen, Day, Jessica; https://orcid.org/0000-0001-8528-4361, Milchert, Marcin; https://orcid.org/0000-0002-0943-8768, Chen, Yi-Ming, Dey, Dzifa; https://orcid.org/0000-0002-3339-5112, Velikova, Tsvetelina; https://orcid.org/0000-0002-0593-1272, Saha, Sreoshy; https://orcid.org/0000-0001-6745-9770, Edgar Gracia-Ramos, Abraham; https://orcid.org/0000-0003-1842-2554, Parodis, Ioannis; https://orcid.org/0000-0002-4875-5395, Nikiphorou, Elena; https://orcid.org/0000-0001-6847-3726, Tan, Ai Lyn; https://orcid.org/0000-0002-9158-7243, Nune, Arvind; https://orcid.org/0000-0002-3849-614X, Cavagna, Lorenzo; https://orcid.org/0000-0003-3292-1528, Toro Gutiérrez, Carlos Enrique, Caballero-Uribe, Carlo Vinicio; https://orcid.org/0000-0002-9845-8620, Saavedra, Miguel A; https://orcid.org/0000-0003-0687-9944, Shinjo, Samuel Katsuyuki; https://orcid.org/0000-0002-3682-4517, Ziade, Nelly; https://orcid.org/0000-0002-4479-7678, El Kibbi, Lina, Knitza, Johannes; https://orcid.org/0000-0001-9695-0657, Distler, Oliver; https://orcid.org/0000-0002-0546-8310, Chinoy, Hector; https://orcid.org/0000-0001-6492-1288, Agarwal, Vikas; https://orcid.org/0000-0002-4508-1233, Aggarwal, Rohit; https://orcid.org/0000-0001-7531-8038, Gupta, Latika; https://orcid.org/0000-0003-2753-2990, COVAD Study Group, Yoshida, Akira; https://orcid.org/0000-0003-3590-1637, Li, Yuanfang; https://orcid.org/0000-0002-2646-3260, Maroufy, Vahed, Kuwana, Masataka; https://orcid.org/0000-0001-8352-6136, Sazliyana Shaharir, Syahrul, Makol, Ashima; https://orcid.org/0000-0002-8748-898X, Sen, Parikshit; https://orcid.org/0000-0002-1630-6026, Lilleker, James B; https://orcid.org/0000-0002-9230-4137, Agarwal, Vishwesh; https://orcid.org/0000-0002-0986-8354, Kadam, Esha; https://orcid.org/0000-0002-8739-4502, Akawatcharangura Goo, Phonpen, Day, Jessica; https://orcid.org/0000-0001-8528-4361, Milchert, Marcin; https://orcid.org/0000-0002-0943-8768, Chen, Yi-Ming, Dey, Dzifa; https://orcid.org/0000-0002-3339-5112, Velikova, Tsvetelina; https://orcid.org/0000-0002-0593-1272, Saha, Sreoshy; https://orcid.org/0000-0001-6745-9770, Edgar Gracia-Ramos, Abraham; https://orcid.org/0000-0003-1842-2554, Parodis, Ioannis; https://orcid.org/0000-0002-4875-5395, Nikiphorou, Elena; https://orcid.org/0000-0001-6847-3726, Tan, Ai Lyn; https://orcid.org/0000-0002-9158-7243, Nune, Arvind; https://orcid.org/0000-0002-3849-614X, Cavagna, Lorenzo; https://orcid.org/0000-0003-3292-1528, Toro Gutiérrez, Carlos Enrique, Caballero-Uribe, Carlo Vinicio; https://orcid.org/0000-0002-9845-8620, Saavedra, Miguel A; https://orcid.org/0000-0003-0687-9944, Shinjo, Samuel Katsuyuki; https://orcid.org/0000-0002-3682-4517, Ziade, Nelly; https://orcid.org/0000-0002-4479-7678, El Kibbi, Lina, Knitza, Johannes; https://orcid.org/0000-0001-9695-0657, Distler, Oliver; https://orcid.org/0000-0002-0546-8310, Chinoy, Hector; https://orcid.org/0000-0001-6492-1288, Agarwal, Vikas; https://orcid.org/0000-0002-4508-1233, Aggarwal, Rohit; https://orcid.org/0000-0001-7531-8038, Gupta, Latika; https://orcid.org/0000-0003-2753-2990, and COVAD Study Group
- Abstract
OBJECTIVES To investigate health-related quality of life in patients with idiopathic inflammatory myopathies (IIMs) compared with those with non-IIM autoimmune rheumatic diseases (AIRDs), non-rheumatic autoimmune diseases (nrAIDs) and without autoimmune diseases (controls) using Patient-Reported Outcome Measurement Information System (PROMIS) instrument data obtained from the second COVID-19 vaccination in autoimmune disease (COVAD-2) e-survey database. METHODS Demographics, diagnosis, comorbidities, disease activity, treatments and PROMIS instrument data were analysed. Primary outcomes were PROMIS Global Physical Health (GPH) and Global Mental Health (GMH) scores. Factors affecting GPH and GMH scores in IIMs were identified using multivariable regression analysis. RESULTS We analysed responses from 1582 IIM, 4700 non-IIM AIRD and 545 nrAID patients and 3675 controls gathered through 23 May 2022. The median GPH scores were the lowest in IIM and non-IIM AIRD patients {13 [interquartile range (IQR) 10-15] IIMs vs 13 [11-15] non-IIM AIRDs vs 15 [13-17] nrAIDs vs 17 [15-18] controls, P < 0.001}. The median GMH scores in IIM patients were also significantly lower compared with those without autoimmune diseases [13 (IQR 10-15) IIMs vs 15 (13-17) controls, P < 0.001]. Inclusion body myositis, comorbidities, active disease and glucocorticoid use were the determinants of lower GPH scores, whereas overlap myositis, interstitial lung disease, depression, active disease, lower PROMIS Physical Function 10a and higher PROMIS Fatigue 4a scores were associated with lower GMH scores in IIM patients. CONCLUSION Both physical and mental health are significantly impaired in IIM patients, particularly in those with comorbidities and increased fatigue, emphasizing the importance of patient-reported experiences and optimized multidisciplinary care to enhance well-being in people with IIMs.
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- 2024
35. Global disparities in the treatment of idiopathic inflammatory myopathies: results from an international online survey study
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Ziade, Nelly; https://orcid.org/0000-0002-4479-7678, Aoude, Marc, Hmamouchi, Ihsane, Naveen, R; https://orcid.org/0000-0003-2014-3925, Lilleker, James B; https://orcid.org/0000-0002-9230-4137, Sen, Parikshit; https://orcid.org/0000-0002-1630-6026, Joshi, Mrudula; https://orcid.org/0000-0001-7312-351X, Agarwal, Vishwesh; https://orcid.org/0000-0002-0986-8354, Kardes, Sinan; https://orcid.org/0000-0002-6311-8634, Day, Jessica; https://orcid.org/0000-0001-8528-4361, Makol, Ashima; https://orcid.org/0000-0002-8748-898X, Milchert, Marcin; https://orcid.org/0000-0002-0943-8768, Gheita, Tamer; https://orcid.org/0000-0002-1155-9729, Salim, Babur; https://orcid.org/0000-0001-8430-9299, Velikova, Tsvetelina; https://orcid.org/0000-0002-0593-1272, Edgar Gracia-Ramos, Abraham; https://orcid.org/0000-0003-1842-2554, Parodis, Ioannis; https://orcid.org/0000-0002-4875-5395, Nikiphorou, Elena; https://orcid.org/0000-0001-6847-3726, Chatterjee, Tulika; https://orcid.org/0000-0001-8844-851X, Tan, Ai Lyn; https://orcid.org/0000-0002-9158-7243, Saavedra, Miguel A; https://orcid.org/0000-0003-0687-9944, Shinjo, Samuel Katsuyuki; https://orcid.org/0000-0002-3682-4517, Knitza, Johannes; https://orcid.org/0000-0001-9695-0657, Kuwana, Masataka; https://orcid.org/0000-0001-8352-6136, Nune, Arvind; https://orcid.org/0000-0002-3849-614X, Cavagna, Lorenzo; https://orcid.org/0000-0003-3292-1528, Distler, Oliver; https://orcid.org/0000-0002-0546-8310, Chinoy, Hector; https://orcid.org/0000-0001-6492-1288, Agarwal, Vikas; https://orcid.org/0000-0002-4508-1233, Aggarwal, Rohit; https://orcid.org/0000-0001-7531-8038, et al, Ziade, Nelly; https://orcid.org/0000-0002-4479-7678, Aoude, Marc, Hmamouchi, Ihsane, Naveen, R; https://orcid.org/0000-0003-2014-3925, Lilleker, James B; https://orcid.org/0000-0002-9230-4137, Sen, Parikshit; https://orcid.org/0000-0002-1630-6026, Joshi, Mrudula; https://orcid.org/0000-0001-7312-351X, Agarwal, Vishwesh; https://orcid.org/0000-0002-0986-8354, Kardes, Sinan; https://orcid.org/0000-0002-6311-8634, Day, Jessica; https://orcid.org/0000-0001-8528-4361, Makol, Ashima; https://orcid.org/0000-0002-8748-898X, Milchert, Marcin; https://orcid.org/0000-0002-0943-8768, Gheita, Tamer; https://orcid.org/0000-0002-1155-9729, Salim, Babur; https://orcid.org/0000-0001-8430-9299, Velikova, Tsvetelina; https://orcid.org/0000-0002-0593-1272, Edgar Gracia-Ramos, Abraham; https://orcid.org/0000-0003-1842-2554, Parodis, Ioannis; https://orcid.org/0000-0002-4875-5395, Nikiphorou, Elena; https://orcid.org/0000-0001-6847-3726, Chatterjee, Tulika; https://orcid.org/0000-0001-8844-851X, Tan, Ai Lyn; https://orcid.org/0000-0002-9158-7243, Saavedra, Miguel A; https://orcid.org/0000-0003-0687-9944, Shinjo, Samuel Katsuyuki; https://orcid.org/0000-0002-3682-4517, Knitza, Johannes; https://orcid.org/0000-0001-9695-0657, Kuwana, Masataka; https://orcid.org/0000-0001-8352-6136, Nune, Arvind; https://orcid.org/0000-0002-3849-614X, Cavagna, Lorenzo; https://orcid.org/0000-0003-3292-1528, Distler, Oliver; https://orcid.org/0000-0002-0546-8310, Chinoy, Hector; https://orcid.org/0000-0001-6492-1288, Agarwal, Vikas; https://orcid.org/0000-0002-4508-1233, Aggarwal, Rohit; https://orcid.org/0000-0001-7531-8038, and et al
- Abstract
OBJECTIVES We aimed to explore current practice and interregional differences in the treatment of idiopathic inflammatory myopathies (IIMs). We triangulated these observations considering countries' Gross National Income (GNI), disease subtypes, and symptoms using patient-reported information. METHODS A cross-sectional ancillary analysis of the "COVID-19 vaccination in auto-immune disease" (COVAD) e-survey containing demographic characteristics, IIM subtypes (dermatomyositis (DM), polymyositis (PM), inclusion-body myositis (IBM), anti-synthetase syndrome (ASSD), immune-mediated necrotizing myopathy (IMNM), overlap myopathies (OM)), current symptoms (surrogate for organ involvement), and treatments (corticosteroids (CS), immunomodulators (IM), i.e., antimalarials, immunosuppressants (IS), intravenous immunoglobulins (IVIG), biological treatments, and targeted-synthetic small molecules). Treatments were presented descriptively according to continents, GNI, IIM, and organ involvement, and associated factors were analyzed using multivariable binary logistic regressions. RESULTS Of 18,851 respondents from 94 countries, 1,418 with IIM were analyzed (age 61 years, 62.5% females). DM (32.4%), IBM (24.5%), and OM (15.8%) were the most common subtypes. Treatment categories included IS (49.4%), CS (38.5%), IM (13.8%), and IVIG (9.4%). Notably, treatments varied across regions, GNI categories (IS mostly used in higher-middle income, IM in lower-middle income, IVIG and biologics largely limited to high-income countries), IIM subtypes (IS and CS associated with ASSD, IM with OM and DM, IVIG with IMNM, and biological treatments with OM and ASSD) and disease manifestations (IS and CS with dyspnea). Most inter-regional treatment disparities persisted after multivariable analysis. CONCLUSION We identified marked regional treatment disparities in a global cohort of IIM. These observations highlight the need for international consensus-driven management guidelines considering patient-c
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- 2024
36. Insights into the knowledge, attitude and practices for the treatment of idiopathic inflammatory myopathy from a cross-sectional cohort survey of physicians
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Gupta, Latika, Muhammed, Hafis, Naveen, R., Kharbanda, Rajat, Gangadharan, Harikrishnan, Misra, Durga P., Lilleker, James B., Chinoy, Hector, and Agarwal, Vikas
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- 2020
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37. Therapeutic plasma exchange in neurological disorders: Experience from a tertiary neuroscience centre
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Das, Joyutpal, Chauhan, Vanisha D., Mills, Daniel, Johal, Nicholas J., Tan, Maevis, Matthews, Rachael, Keh, Ryan, Lilleker, James B., Gosal, David, and Sharaf, Nazar
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- 2019
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38. Comparison of clinical features between patients with anti-synthetase syndrome and dermatomyositis: results from the MYONET registry.
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Hum, Ryan Malcolm, Lilleker, James B, Lamb, Janine A, Oldroyd, Alexander G S, Wang, Guochun, Wedderburn, Lucy R, Diederichsen, Louise P, Schmidt, Jens, Danieli, Maria Giovanna, Oakley, Paula, Griger, Zoltan, Phuong, Thuy Nguyen Thi, Kodishala, Chanakya, Mercado, Monica Vazquez-Del, Andersson, Helena, Paepe, Boel De, Bleecker, Jan L De, Maurer, Britta, McCann, Liza, and Pipitone, Nicolo
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DERMATOMYOSITIS , *DIFFERENTIAL diagnosis , *RESEARCH funding , *RAYNAUD'S disease , *SKIN diseases , *MYOSITIS , *EXFOLIATIVE dermatitis , *AUTOANTIBODIES , *EXANTHEMA , *INTERSTITIAL lung diseases , *ANTISYNTHETASE syndrome , *ARTHRITIS , *COMPARATIVE studies , *TUMORS , *DISEASE complications , *SYMPTOMS , *ADULTS - Abstract
Objectives To compare clinical characteristics, including the frequency of cutaneous, extramuscular manifestations and malignancy, between adults with anti-synthetase syndrome (ASyS) and DM. Methods Using data regarding adults from the MYONET registry, a cohort of DM patients with anti-Mi2/-TIF1γ/-NXP2/-SAE/-MDA5 autoantibodies, and a cohort of ASyS patients with anti-tRNA synthetase autoantibodies (anti-Jo1/-PL7/-PL12/-OJ/-EJ/-Zo/-KS) were identified. Patients with DM sine dermatitis or with discordant dual autoantibody specificities were excluded. Sub-cohorts of patients with ASyS with or without skin involvement were defined based on presence of DM-type rashes (heliotrope rash, Gottron's papules/sign, violaceous rash, shawl sign, V-sign, erythroderma, and/or periorbital rash). Results In total 1054 patients were included (DM, n = 405; ASyS, n = 649). In the ASyS cohort, 31% (n = 203) had DM-type skin involvement (ASyS-DMskin). A higher frequency of extramuscular manifestations, including Mechanic's hands, Raynaud's phenomenon, arthritis, interstitial lung disease and cardiac involvement differentiated ASyS-DMskin from DM (all P < 0.001), whereas higher frequency of any of four DM-type rashes—heliotrope rash (n = 248, 61% vs n = 90, 44%), violaceous rash (n = 166, 41% vs n = 57, 9%), V-sign (n = 124, 31% vs n = 28, 4%), and shawl sign (n = 133, 33% vs n = 18, 3%)—differentiated DM from ASyS-DMskin (all P < 0.005). Cancer-associated myositis (CAM) was more frequent in DM (n = 67, 17%) compared with ASyS (n = 21, 3%) and ASyS-DMskin (n = 7, 3%) cohorts (both P < 0.001). Conclusion DM-type rashes are frequent in patients with ASyS; however, distinct clinical manifestations differentiate these patients from classical DM. Skin involvement in ASyS does not necessitate increased malignancy surveillance. These findings will inform future ASyS classification criteria and patient management. [ABSTRACT FROM AUTHOR]
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- 2024
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39. Gender differences in patient experience in idiopathic inflammatory myopathies: Subanalysis from the COVAD dataset.
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Yoshida, Akira, Kim, Minchul, Kuwana, Masataka, Ravichandran, Naveen, Makol, Ashima, Sen, Parikshit, Lilleker, James B., Agarwal, Vishwesh, Kardes, Sinan, Day, Jessica, Milchert, Marcin, Joshi, Mrudula, Gheita, Tamer, Salim, Babur, Velikova, Tsvetelina, Gracia-Ramos, Abraham Edgar, Parodis, Ioannis, Nikiphorou, Elena, Chatterjee, Tulika, and Tan, Ai Lyn
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INCLUSION body myositis ,PATIENT experience ,IDIOPATHIC diseases ,FATIGUE (Physiology) ,VISUAL analog scale ,CANCER fatigue - Abstract
Objectives: We aimed to investigate the gender-based differences in idiopathic inflammatory myopathies (IIMs), with a particular focus on patient-reported outcomes, utilizing the data obtained through the international COVID-19 vaccination in autoimmune disease e-survey. Methods: Patient-reported outcomes including fatigue, pain, and physical function were extracted from the COVID-19 vaccination in autoimmune disease database and compared between genders, adjusting for demographics and IIM subgroups by multivariable analysis. Inclusion body myositis (IBM) was analysed separately because of the substantial differences in outcomes. Results: A total of 1197 complete responses from patients with IIMs as of 31 August 2021 were analysed. Seventy percent were women. Women were younger (58 [48–68] vs. 69 [58–75] years old, median [interquartile range], P < .001) and were more likely to suffer from autoimmune multimorbidity, defined as three or more autoimmune diseases in an individual patient (11.4% vs. 2.8%, P < .001). In non-IBM IIMs, fatigue visual analogue scale scores were higher in women (5 [3–7] vs. 4 [2–6], median [interquartile range], P = .004), whereas no significant gender-based differences were noted in IBM. Multivariable analysis in non-IBM IIMs revealed that women, residence in high-income countries, overlap myositis, and autoimmune multimorbidity were independently associated with increased fatigue. Conclusions: Women with IIMs suffer from autoimmune multimorbidity and experience increased fatigue compared to men. [ABSTRACT FROM AUTHOR]
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- 2024
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40. Cardiac involvement in inflammatory myopathies and inherited muscle diseases
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Lilleker, James B., Roberts, Mark, and Diederichsen, Louise
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- 2020
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41. Pain in individuals with idiopathic inflammatory myopathies, other systemic autoimmune rheumatic diseases, and without rheumatic diseases: A report from the COVAD study
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Shinjo, Samuel Katsuyuki, Kim, Minchul, Hoff, Leonardo Santos, Missé, Rafael Giovani, Sen, Parikshit, Naveen, R., Day, Jessica, Cordeiro, Rafael Alves, Júnior, Jucier Gonçalves, Chatterjee, Tulika, Lilleker, James B., Agarwal, Vishwesh, Kardes, Sinan, Milchert, Marcin, Gheita, Tamer, Salim, Babur, Velikova, Tsvetelina, Gracia‐ramos, Abraham Edgar, Parodis, Ioannis, O'callaghan, Albert Selva, Nikiphorou, Elena, Makol, Ashima, Tan, Ai Lyn, Cavagna, Lorenzo, Saavedra, Miguel A., Ziade, Nelly, Knitza, Johannes, Kuwana, Masataka, Nune, Arvind, Distler, Oliver, Chinoy, Hector, Agarwal, Vikas, Aggarwal, Rohit, Gupta, Latika, Institut Català de la Salut, [Shinjo SK, Missé RG] Division of Rheumatology, Faculdade de Medicina FMUSP, Universidade de Sao Paulo, Sao Paulo, Brazil. [Kim M] Center for Outcomes Research, Department of Internal Medicine, University of Illinois College of Medicine Peoria, Peoria, Illinois, USA. [Hoff LS] School of Medicine, Universidade Potiguar (UnP), Natal, Brazil. [Sen P] Maulana Azad Medical College, New Delhi, India. [Naveen R] Department of Clinical Immunology and Rheumatology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, India. [O'Callaghan AS] Servei de Medicina Interna, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Universitat Autònoma de Barcelona, Bellaterra, Spain, and Vall d'Hebron Barcelona Hospital Campus
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Malalties autoimmunitàries ,Immune System Diseases::Autoimmune Diseases [DISEASES] ,enfermedades del sistema inmune::enfermedades autoinmunes [ENFERMEDADES] ,aminoácidos, péptidos y proteínas::proteínas::proteínas sanguíneas::inmunoproteínas::inmunoglobulinas::anticuerpos::autoanticuerpos [COMPUESTOS QUÍMICOS Y DROGAS] ,Virus Diseases::RNA Virus Infections::Nidovirales Infections::Coronaviridae Infections::Coronavirus Infections [DISEASES] ,Autoanticossos ,functional status ,Musculoskeletal Diseases::Muscular Diseases::Myositis [DISEASES] ,COVID-19 (Malaltia) ,Amino Acids, Peptides, and Proteins::Proteins::Blood Proteins::Immunoproteins::Immunoglobulins::Antibodies::Autoantibodies [CHEMICALS AND DRUGS] ,Rheumatology ,rheumatic diseases ,virosis::infecciones por virus ARN::infecciones por Nidovirales::infecciones por Coronaviridae::infecciones por Coronavirus [ENFERMEDADES] ,autoimmune diseases ,pain ,Músculs - Inflamació ,myositis ,enfermedades musculoesqueléticas::enfermedades musculares::miositis [ENFERMEDADES] - Abstract
Myositis; Pain; Rheumatic diseases Miositis; Dolor; Enfermedades reumáticas Miositis; Dolor; Malalties reumàtiques Objectives To compare pain intensity among individuals with idiopathic inflammatory myopathies (IIMs), other systemic autoimmune rheumatic diseases (AIRDs), and without rheumatic disease (wAIDs). Methods Data were collected from the COVID-19 Vaccination in Autoimmune Diseases (COVAD) study, an international cross-sectional online survey, from December 2020 to August 2021. Pain experienced in the preceding week was assessed using numeral rating scale (NRS). We performed a negative binomial regression analysis to assess pain in IIMs subtypes and whether demographics, disease activity, general health status, and physical function had an impact on pain scores. Results Of 6988 participants included, 15.1% had IIMs, 27.9% had other AIRDs, and 57.0% were wAIDs. The median pain NRS in patients with IIMs, other AIRDs, and wAIDs were 2.0 (interquartile range [IQR] = 1.0–5.0), 3.0 (IQR = 1.0–6.0), and 1.0 (IQR = 0–2.0), respectively (P
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42. Idiopathic inflammatory myopathies
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Parker, Matthew J.S., Lilleker, James B., Roberts, Mark E., and Chinoy, Hector
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- 2018
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43. Gender differences in patient experience in idiopathic inflammatory myopathies: Sub analysis from the COVAD dataset
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Yoshida, Akira, primary, Kim, Minchul, additional, Kuwana, Masataka, additional, Ravichandran, Naveen, additional, Makol, Ashima, additional, Sen, Parikshit, additional, Lilleker, James B, additional, Agarwal, Vishwesh, additional, Kardes, Sinan, additional, Day, Jessica, additional, Milchert, Marcin, additional, Joshi, Mrudula, additional, Gheita, Tamer, additional, Salim, Babur, additional, Velikova, Tsvetelina, additional, Gracia-Ramos, Abraham Edgar, additional, Parodis, Ioannis, additional, Nikiphorou, Elena, additional, Chatterjee, Tulika, additional, Tan, Ai Lyn, additional, Nune, Arvind, additional, Cavagna, Lorenzo, additional, Saavedra, Miguel A, additional, Shinjo, Samuel Katsuyuki, additional, Ziade, Nelly, additional, Knitza, Johannes, additional, Distler, Oliver, additional, Chinoy, Hector, additional, Agarwal, Vikas, additional, Aggarwal, Rohit, additional, and Gupta, Latika, additional
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- 2023
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44. Line blot immunoassays in idiopathic inflammatory myopathies: retrospective review of diagnostic accuracy and factors predicting true positive results
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To, Fergus, Ventín-Rodríguez, Clara, Elkhalifa, Shuayb, Lilleker, James B., and Chinoy, Hector
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- 2020
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45. Systemic sclerosis and COVID-19 vaccine safety: short-term insights from the global COVID-19 vaccination in autoimmune disease (COVAD) survey
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Naveen, R, Thakare, Darpan R, Kuwana, Masataka, Pauling, John D, Day, Jessica, Joshi, Mrudula, Parodis, Ioannis, Sen, Parikshit, Jagtap, Kshitij, Nikiphorou, Elena, Saha, Sreoshy, Agarwal, Vishwesh, Chatterjee, Tulika, Lilleker, James B, Kardes, Sinan, Milchert, Marcin, Gheita, Tamer, Salim, Babur, Velikova, Tsvetelina, Gracia-Ramos, Abraham Edgar, Tan, Ai Lyn, Nune, Arvind, Cavagna, Lorenzo, Saavedra, Miguel A, Shinjo, Samuel Katsuyuki, Ziade, Nelly, Knitza, Johannes, Distler, Oliver, Chinoy, Hector, COVAD Study Group, et al, and University of Zurich
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10051 Rheumatology Clinic and Institute of Physical Medicine ,610 Medicine & health - Published
- 2023
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46. Can machine learning unravel the complex IIM spectrum?
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Lilleker, James B. and Chinoy, Hector
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- 2020
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47. COVID-19 Vaccination-Related Delayed Adverse Events among Patients with Systemic Lupus Erythematosus
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Dey, Mrinalini, Doskaliuk, Bohdana, Lindblom, Julius, Nikiphorou, Elena, Wincup, Chris, Fathima, Madiha, Saha, Sreoshy, Shaharir, Syahrul Sazliyana, Katchamart, Wanruchada, Goo, Phonpen Akarawatcharangura, Traboco, Lisa, Chen, Yi-Ming, Kadam, Esha, Lilleker, James B., Nune, Arvind, Pauling, John D., Agarwal, Vishwesh, Dey, Dzifa, Toro Gutierrez, Carlos Enrique, Caballero, Carlo Vinicio, Chinoy, Hector, Aggarwal, Rohit, Agarwal, Vikas, Gupta, Latika, Parodis, Ioannis, Dey, Mrinalini, Doskaliuk, Bohdana, Lindblom, Julius, Nikiphorou, Elena, Wincup, Chris, Fathima, Madiha, Saha, Sreoshy, Shaharir, Syahrul Sazliyana, Katchamart, Wanruchada, Goo, Phonpen Akarawatcharangura, Traboco, Lisa, Chen, Yi-Ming, Kadam, Esha, Lilleker, James B., Nune, Arvind, Pauling, John D., Agarwal, Vishwesh, Dey, Dzifa, Toro Gutierrez, Carlos Enrique, Caballero, Carlo Vinicio, Chinoy, Hector, Aggarwal, Rohit, Agarwal, Vikas, Gupta, Latika, and Parodis, Ioannis
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BACKGROUND: The safety profile of COVID-19 vaccination is well documented, but hesitancy among people with immune-mediated inflammatory diseases, often immunocompromised, remains high, partially due to a scarcity of data on safety over a longer term. We herein aimed to assess delayed adverse events (DAEs) occurring >7 days after COVID-19 vaccination in systemic lupus erythematosus (SLE) versus other rheumatic autoimmune diseases (rAIDs), non-rheumatic AIDs (nrAIDs), and healthy controls (HCs). METHODS: Self-reported data were captured within the COVID-19 Vaccination in Autoimmune Diseases (COVAD)-2 online survey, which comprised >150 centres and responses from 106 countries, between February and June 2022. Logistic regression analysis adjusting for important confounders (age, sex, ethnicity) was used to compare groups. RESULTS: Of 7203 eligible individuals, 882 (12.2%) patients had SLE, 3161 (43.9%) patients had rAIDs, 426 (5.9%) patients had nrAIDs, and 2734 (38.0%) were HCs. SLE patients had a median age of 39 years (IQR: 31-50); 93.7% were women. SLE patients reported, more frequently, major DAEs (OR: 1.6; 95% CI: 1.2-2.0; p = 0.001) and hospitalisation (OR: 2.2; 95% CI: 1.4-3.4; p < 0.001) compared to HCs, severe rashes (OR: 2.4; 95% CI: 1.3-4.2; p = 0.004) compared to people with rAIDS, and hospitalisation (OR: 2.3; 95% CI: 1.1-4.9; p = 0.029) as well as several minor DAEs compared to people with nrAIDs. Differences were observed between vaccines in terms of frequency of major DAEs and hospitalisations, with the latter seen more frequently in patients receiving the Moderna vaccine. People with SLE with no autoimmune multimorbidity less frequently reported overall minor DAEs compared to SLE patients with comorbid nrAIDs (OR: 0.5; 95% CI: 0.3-1.0; p = 0.036). CONCLUSION: Hospitalisations post-vaccination were more frequent in SLE patients than in HCs. Monitoring of SLE patients following COVID-19 vaccination can help in identifying DAEs early, informing, IP is supported by grants from the Swedish Rheumatism Association (R-969696), King Gustaf V's 80-year Foundation (FAI-2020-0741), Swedish Society of Medicine (SLS-974449), Nyckel-fonden (OLL-974804), Professor Nanna Svartz Foundation (2021-00436), Ulla and Roland Gustafsson Foundation (2021-26), Region Stockholm (FoUI-955483), and Karolinska Institutet.
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48. Safety and tolerance of vaccines against SARS-CoV-2 infection in systemic lupus erythematosus : results from the COVAD study
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R., Naveen, Nikiphorou, Elena, Joshi, Mrudula, Sen, Parikshit, Lindblom, Julius, Agarwal, Vishwesh, Lilleker, James B., Tan, Ai Lyn, Salim, Babur, Ziade, Nelly, Velikova, Tsvetelina, Edgar Gracia-Ramos, Abraham, Kuwana, Masataka, Day, Jessica, Makol, Ashima, Distler, Oliver, Chinoy, Hector, Traboco, Lisa S., Kusumo Wibowo, Suryo Anggoro, Zamora Tehozol, Erick Adrian, Serrano, Jorge Rojas, La Torre, Ignacio García-De, Aggarwal, Rohit, Gupta, Latika, Agarwal, Vikas, Parodis, Ioannis, R., Naveen, Nikiphorou, Elena, Joshi, Mrudula, Sen, Parikshit, Lindblom, Julius, Agarwal, Vishwesh, Lilleker, James B., Tan, Ai Lyn, Salim, Babur, Ziade, Nelly, Velikova, Tsvetelina, Edgar Gracia-Ramos, Abraham, Kuwana, Masataka, Day, Jessica, Makol, Ashima, Distler, Oliver, Chinoy, Hector, Traboco, Lisa S., Kusumo Wibowo, Suryo Anggoro, Zamora Tehozol, Erick Adrian, Serrano, Jorge Rojas, La Torre, Ignacio García-De, Aggarwal, Rohit, Gupta, Latika, Agarwal, Vikas, and Parodis, Ioannis
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OBJECTIVE: To determine COVID-19 vaccine-related adverse events (AEs) in the seven-day post-vaccination period in patients with SLE versus autoimmune rheumatic diseases (AIRDs), non-rheumatic autoimmune diseases (nrAIDs), and healthy controls (HC). METHODS: Data were captured through the COVID-19 Vaccination in Autoimmune Diseases (COVAD) questionnaire (March-December 2021). Multivariable regression models accounted for age, gender, ethnicity, vaccine type, and background treatment. RESULTS: Among 9462 complete respondents, 583 (6.2%) were SLE patients (mean age: 40.1 years; 94.5% females; 40.5% Asian; 42.9% Pfizer-recipients). Minor AEs were reported by 83.0% of SLE patients, major by 2.6%, hospitalisation by 0.2%.AE and hospitalisation frequencies were similar between patients with active and inactive SLE. Rashes were more frequent in SLE patients versus HC (OR; 95% CI: 1.2; 1.0-1.5), chills less frequent in SLE versus AIRDs (0.6; 0.4-0.8) and nrAIDs (0.5; 0.3-0.8), and fatigue less frequent in SLE versus nrAIDs (0.6; 0.4-0.9). Pfizer-recipients reported higher overall AE (2.2; 1.1-4.2) and injection site pain (2.9; 1.6-5.0) frequencies than recipients of other vaccines, Oxford/AstraZeneca-recipients more body ache, fever, chills (OR: 2.5-3.0), Moderna-recipients more body ache, fever, chills, rashes (OR: 2.6-4.3). Hospitalisation frequencies were similar across vaccine types. AE frequencies were similar across treatment groups, although chills were less frequent in antimalarial users versus non-users (0.5; 0.3-0.9). CONCLUSION: While COVID-19 vaccination-related AEs were reported by four-fifths of SLE patients, those were mostly minor and comparable to AEs reported by healthy individuals, providing reassurance regarding COVID-19 vaccination safety in SLE., Funding agencies:Professor Nanna Svartz Foundation 2020-00368Ulla and Roland Gustafsson Foundation
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- 2023
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49. COVID-19 vaccination in autoimmune diseases (COVAD) Study : vaccine safety and tolerance in rheumatoid arthritis
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R., Naveen, Parodis, Ioannis, Joshi, Mrudula, Sen, Parikshit, Lindblom, Julius, Agarwal, Vishwesh, Lilleker, James B., Tan, Ai Lyn, Nune, Arvind, Shinjo, Samuel Katsuyuki, Salim, Babur, Ziade, Nelly, Velikova, Tsvetelina, Edgar Gracia-Ramos, Abraham, Saavedra, Miguel A., Day, Jessica, Makol, Ashima, Distler, Oliver, Chinoy, Hector, Agarwal, Vikas, Aggarwal, Rohit, Gupta, Latika, Nikiphorou, Elena, R., Naveen, Parodis, Ioannis, Joshi, Mrudula, Sen, Parikshit, Lindblom, Julius, Agarwal, Vishwesh, Lilleker, James B., Tan, Ai Lyn, Nune, Arvind, Shinjo, Samuel Katsuyuki, Salim, Babur, Ziade, Nelly, Velikova, Tsvetelina, Edgar Gracia-Ramos, Abraham, Saavedra, Miguel A., Day, Jessica, Makol, Ashima, Distler, Oliver, Chinoy, Hector, Agarwal, Vikas, Aggarwal, Rohit, Gupta, Latika, and Nikiphorou, Elena
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OBJECTIVES: The COVID-19 vaccination in autoimmune diseases (COVAD) study aimed to assess short-term COVID-19 vaccination-related adverse events (AEs) in rheumatoid arthritis (RA) patients. METHODS: An online self-reported questionnaire (March-December 2021) was used to capture data related to COVID-19 vaccination-related AEs in RA, other autoimmune rheumatic diseases (AIRDs) (excluding RA and inflammatory myositis), non-rheumatic autoimmune diseases (nrAIDs), and healthy controls (HCs). Descriptive and multivariable regression analyses were performed. RESULTS: Of the 9462 complete respondents, 14.2% (n = 1347) had been diagnosed with RA who had a mean (standard deviation) age of 50.7 (13.7) years, and 74.2% were women, and 49.3% were Caucasian. In total, 76.9% and 4.2% of patients with RA reported minor and major AEs, respectively. Patients with active and inactive RA had similar AE and hospitalization frequencies. Overall, AEs were reported more frequently by BNT162b2 and mRNA-1273 recipients and less frequently by BBV152 recipients compared with the rest. Major AE and hospitalization frequencies were similar across recipients of different vaccines. Patients receiving methotrexate and hydroxychloroquine reported fewer minor AEs than those patients not on them. Compared with HCs and patients with other AIRDs, patients with RA reported similar total AEs, overall minor AEs, and hospitalizations. Compared with nrAIDs, patients with RA reported lower frequencies of overall AEs, minor AEs (both OR = 0.7; 95%CI = 0.5-0.9), and injection site pain (OR = 0.6; 95%CI = 0.5-0.8) with similar major AE and hospitalization frequencies. CONCLUSION: Despite the differences in AE frequency across different COVID-19 vaccines, all were well tolerated in patients with RA and were comparable to HCs providing reassurance to the safety of COVID-19 vaccination., Funding agency:National Institution for HealthResearch Manchester Biomedical Research Centre Funding Scheme
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- 2023
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50. Impaired physical function in patients with idiopathic inflammatory myopathies : results from the multicentre COVAD patient-reported e-survey
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Yoshida, Akira, Kim, Minchul, Kuwana, Masataka, Naveen, R., Makol, Ashima, Sen, Parikshit, Lilleker, James B., Agarwal, Vishwesh, Kardes, Sinan, Day, Jessica, Milchert, Marcin, Joshi, Mrudula, Gheita, Tamer, Salim, Babur, Velikova, Tsvetelina, Edgar Gracia-Ramos, Abraham, Parodis, Ioannis, O'Callaghan, Albert Selva, Nikiphorou, Elena, Chatterjee, Tulika, Tan, Ai Lyn, Nune, Arvind, Cavagna, Lorenzo, Saavedra, Miguel A., Shinjo, Samuel Katsuyuki, Ziade, Nelly, Knitza, Johannes, Distler, Oliver, Chinoy, Hector, Agarwal, Vikas, Aggarwal, Rohit, Gupta, Latika, Yoshida, Akira, Kim, Minchul, Kuwana, Masataka, Naveen, R., Makol, Ashima, Sen, Parikshit, Lilleker, James B., Agarwal, Vishwesh, Kardes, Sinan, Day, Jessica, Milchert, Marcin, Joshi, Mrudula, Gheita, Tamer, Salim, Babur, Velikova, Tsvetelina, Edgar Gracia-Ramos, Abraham, Parodis, Ioannis, O'Callaghan, Albert Selva, Nikiphorou, Elena, Chatterjee, Tulika, Tan, Ai Lyn, Nune, Arvind, Cavagna, Lorenzo, Saavedra, Miguel A., Shinjo, Samuel Katsuyuki, Ziade, Nelly, Knitza, Johannes, Distler, Oliver, Chinoy, Hector, Agarwal, Vikas, Aggarwal, Rohit, and Gupta, Latika
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OBJECTIVES: The assessment of physical function is fundamental in the management of patients with idiopathic inflammatory myopathies (IIMs). We aimed to investigate the physical function of patients with IIMs compared with those with non-IIM autoimmune rheumatic diseases (AIRDs) utilizing Patient-Reported Outcome Measurement Information System (PROMIS) Physical Function (PF) data obtained in the COVAD study, an international self-reported e-survey assessing the safety of COVID-19 vaccines in AIRDs. METHODS: Demographics, AIRD diagnosis, disease activity, and PROMIS PF short form-10a data were extracted from the COVAD database. PROMIS PF-10a scores were compared between disease categories and stratified by disease activity. Factors affecting PROMIS PF-10a scores other than disease activity were identified by multivariable regression analysis in patients with inactive disease. RESULTS: 1057 IIM patients, 3635 non-IIM AIRD patients, and 3981 healthy controls (HCs) responded to the COVAD e-survey from April to August 2021. Using a binomial regression model, the predicted mean of PROMIS PF-10a scores was significantly lower in IIM patients compared with non-IIM AIRD patients or HCs (36.3 [95% confidence interval (CI) 35.5-37.1] vs 41.3 [95%CI 40.2-42.5] vs 46.2 [95%CI 45.8-46.6], P < 0.001), irrespective of disease activity. The independent factors for lower PROMIS PF-10a scores in patients with inactive disease were older age, female, longer disease duration, and a diagnosis of inclusion body myositis or polymyositis. CONCLUSION: Physical function is significantly impaired in IIMs compared with non-IIM AIRDs or HCs, even in patients with inactive disease. Our study highlights a critical need for better strategies to minimize functional disability in patients with IIMs., Funding agency:National Institution for Health Research Manchester Biomedical Research Centre Funding Scheme
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- 2023
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