Abstract
Objectives: Disease flares in the post-coronavirus disease 2019 (COVID-19) vaccination period represent a prominent concern, though risk factors are poorly understood. We studied these flares among patients with idiopathic inflammatory myopathies (IIMs) and other autoimmune rheumatic diseases (AIRDs). Methods: The COVAD-1 and -2 global surveys were circulated in early 2021 and 2022, respectively, and we captured demographics, comorbidities, AIRDs details, COVID-19 infection history and vaccination details. Flares of IIMs were defined as (a) patient self-reported, (b) immunosuppression (IS) denoted, (c) clinical sign directed and (d) with >7.9-point minimal clinically significant improvement difference worsening of Patient-Reported Outcomes Measurement Information System (PROMIS) PROMISPF10a score. Risk factors of flares were analysed using regression models. Results: Of 15 165 total respondents, 1278 IIMs (age 63 years, 70.3% female, 80.8% Caucasians) and 3453 AIRDs were included. Flares of IIM were seen in 9.6%, 12.7%, 8.7% and 19.6% patients by definitions (a) to (d), respectively, with a median time to flare of 71.5 (10.7-235) days, similar to AIRDs. Patients with active IIMs pre-vaccination (OR 1.2; 95% CI 1.03, 1.6, P = 0.025) were prone to flares, while those receiving rituximab (OR 0.3; 95% CI 0.1, 0.7, P = 0.010) and AZA (OR 0.3, 95% CI 0.1, 0.8, P = 0.016) were at lower risk. Female gender and comorbidities predisposed to flares requiring changes in IS. Asthma (OR 1.62; 95% CI 1.05, 2.50, P = 0.028) and higher pain visual analogue score (OR 1.19; 95% CI 1.11, 1.27, P < 0.001) were associated with disparity between self-reported and IS-denoted flares. Conclusion: A diagnosis of IIMs confers an equal risk of flares in the post-COVID-19 vaccination period to AIRDs, with active disease, female gender and comorbidities conferring a higher risk. Disparity between patient- and physician-reported outcomes represents a future avenue for exploration.
Original language | English (US) |
---|---|
Pages (from-to) | 127-139 |
Number of pages | 13 |
Journal | Rheumatology (United Kingdom) |
Volume | 63 |
Issue number | 1 |
DOIs | |
State | Published - Jan 1 2024 |
Keywords
- COVID-19 vaccines
- disease exacerbation
- idiopathic inflammatory myopathies
- patient-reported outcomes
ASJC Scopus subject areas
- Rheumatology
- Pharmacology (medical)
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In: Rheumatology (United Kingdom), Vol. 63, No. 1, 01.01.2024, p. 127-139.
Research output: Contribution to journal › Article › peer-review
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TY - JOUR
T1 - Flares in IIMs and the timeline following COVID-19 vaccination
T2 - a combined analysis of the COVAD-1 and -2 surveys
AU - Naveen, R.
AU - Sen, Parikshit
AU - Griger, Zoltán
AU - Day, Jessica
AU - Joshi, Mrudula
AU - Nune, Arvind
AU - Nikiphorou, Elena
AU - Saha, Sreoshy
AU - Tan, Ai Lyn
AU - Shinjo, Samuel Katsuyuki
AU - Ziade, Nelly
AU - Velikova, Tsvetelina
AU - Milchert, Marcin
AU - Jagtap, Kshitij
AU - Parodis, Ioannis
AU - Gracia-Ramos, Abraham Edgar
AU - Cavagna, Lorenzo
AU - Kuwana, Masataka
AU - Knitza, Johannes
AU - Chen, Yi Ming
AU - Makol, Ashima
AU - Agarwal, Vishwesh
AU - Patel, Aarat
AU - Pauling, John D.
AU - Wincup, Chris
AU - Barman, Bhupen
AU - Zamora Tehozol, Erick Adrian
AU - Rojas Serrano, Jorge
AU - García-De La Torre, Ignacio
AU - Colunga-Pedraza, Iris J.
AU - Merayo-Chalico, Javier
AU - Chibuzo, Okwara Celestine
AU - Katchamart, Wanruchada
AU - Akarawatcharangura Goo, Phonpen
AU - Shumnalieva, Russka
AU - Hoff, Leonardo Santos
AU - El Kibbi, Lina
AU - Halabi, Hussein
AU - Vaidya, Binit
AU - Shaharir, Syahrul Sazliyana
AU - Hasan, A. T.M.Tanveer
AU - Dey, Dzifa
AU - Toro Gutiérrez, Carlos Enrique
AU - Caballero-Uribe, Carlo V.
AU - Lilleker, James B.
AU - Salim, Babur
AU - Gheita, Tamer
AU - Chatterjee, Tulika
AU - Distler, Oliver
AU - Saavedra, Miguel A.
AU - Chinoy, Hector
AU - Agarwal, Vikas
AU - Aggarwal, Rohit
AU - Gupta, Latika
AU - Kardes, Sinan
AU - Andreoli, Laura
AU - Lini, Daniele
AU - Screiber, Karen
AU - Vince, Melinda Nagy
AU - Singh, Yogesh Preet
AU - Ranjan, Rajiv
AU - Jain, Avinash
AU - Pandya, Sapan C.
AU - Pilania, Rakesh Kumar
AU - Sharma, Aman
AU - Manesh Manoj, M.
AU - Gupta, Vikas
AU - Kavadichanda, Chengappa G.
AU - Patro, Pradeepta Sekhar
AU - Ajmani, Sajal
AU - Phatak, Sanat
AU - Goswami, Rudra Prosad
AU - Chowdhury, Abhra Chandra
AU - Mathew, Ashish Jacob
AU - Shenoy, Padnamabha
AU - Asranna, Ajay
AU - Bommakanti, Keerthi Talari
AU - Shukla, Anuj
AU - Pande, Arunkumar R.
AU - Chandwar, Kunal
AU - Ghodke, Akanksha
AU - Boro, Hiya
AU - Fazal, Zoha Zahid
AU - Cansu, Döndü Üsküdar
AU - Ylldlrlm, Reşit
AU - Gasparyan, Armen Yuri
AU - Del Papa, Nicoletta
AU - Sambataro, Gianluca
AU - Fabiola, Atzeni
AU - Govoni, Marcello
AU - Parisi, Simone
AU - Bocci, Elena Bartoloni
AU - Sebastiani, Gian Domenico
AU - Fusaro, Enrico
AU - Sebastiani, Marco
AU - Quartuccio, Luca
AU - Franceschini, Franco
AU - Sainaghi, Pier Paolo
AU - Orsolini, Giovanni
AU - De Angelis, Rossella
AU - Danielli, Maria Giovanna
AU - Venerito, Vincenzo
AU - Grignaschi, Silvia
AU - Giollo, Alessandro
AU - Alluno, Alessia
AU - Ioannone, Florenzo
AU - Fornaro, Marco
AU - Traboco, Lisa S.
AU - Wibowo, Suryo Anggoro Kusumo
AU - Loarce-Martos, Jesús
AU - Prieto-González, Sergio
AU - Gonzalez, Raquel Aranega
AU - Yoshida, Akira
AU - Nakashima, Ran
AU - Sato, Shinji
AU - Kimura, Naoki
AU - Kaneko, Yuko
AU - Gono, Takahisa
AU - Tomaras, Stylianos
AU - Proft, Fabian Nikolai
AU - Holzer, Marie Therese
AU - Gromova, Margarita Aleksandrovna
AU - Aharonov, Or
AU - Griger, Zoltán
AU - Hmamouchi, Ihsane
AU - El Bouchti, Imane
AU - Baba, Zineb
AU - Giannini, Margherita
AU - Maurier, François
AU - Campagne, Julien
AU - Meyer, Alain
AU - Langguth, Daman
AU - Limaye, Vidya
AU - Needham, Merrilee
AU - Srivastav, Nilesh
AU - Hudson, Marie
AU - Landon-Cardinal, Océane
AU - Zuleta, Wilmer Gerardo Rojas
AU - Arbeláez, Álvaro
AU - Cajas, Javier
AU - Silva, José António Pereira
AU - Fonseca, João Eurico
AU - Zimba, Olena
AU - Bohdana, Doskaliuk
AU - Ima-Edomwonyi, Uyi
AU - Dedeke, Ibukunoluwa
AU - Airenakho, Emorinken
AU - Madu, Nwankwo Henry
AU - Yerima, Abubakar
AU - Olaosebikan, Hakeem
AU - Becky, A.
AU - Koussougbo, Oruma Devi
AU - Palalane, Elisa
AU - So, Ho
AU - Ugarte-Gil, Manuel Francisco
AU - Chinchay, Lyn
AU - Bernaola, José Proaño
AU - Pimentel, Victorio
AU - Fathi, Hanan Mohammed
AU - Mohammed, Reem Hamdy A.
AU - Harifi, Ghita
AU - Fuentes-Silva, Yurilís
AU - Cabriza, Karoll
AU - Losanto, Jonathan
AU - Colaman, Nelly
AU - Cachafeiro-Vilar, Antonio
AU - Bautista, Generoso Guerra
AU - Ho, Enrique Julio Giraldo
AU - González, Raúl
AU - Nunez, Lilith Stange
AU - Cristian Vergara, M.
AU - Báez, Jossiell Then
AU - Alonzo, Hugo
AU - Pastelin, Carlos Benito Santiago
AU - Salinas, Rodrigo García
AU - Obiols, Alejandro Quiñónez
AU - Chávez, Nilmo
AU - Ordóñez, Andrea Bran
AU - Llerena, Gil Alberto Reyes
AU - Sierra-Zorita, Radames
AU - Arrieta, Dina
AU - Hidalgo, Eduardo Romero
AU - Saenz, Ricardo
AU - Idania Escalante, M.
AU - Calapaqui, Wendy
AU - Quezada, Ivonne
AU - Arredondo, Gabriela
N1 - Publisher Copyright: © 2023 The Author(s). Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved.
PY - 2024/1/1
Y1 - 2024/1/1
N2 - Objectives: Disease flares in the post-coronavirus disease 2019 (COVID-19) vaccination period represent a prominent concern, though risk factors are poorly understood. We studied these flares among patients with idiopathic inflammatory myopathies (IIMs) and other autoimmune rheumatic diseases (AIRDs). Methods: The COVAD-1 and -2 global surveys were circulated in early 2021 and 2022, respectively, and we captured demographics, comorbidities, AIRDs details, COVID-19 infection history and vaccination details. Flares of IIMs were defined as (a) patient self-reported, (b) immunosuppression (IS) denoted, (c) clinical sign directed and (d) with >7.9-point minimal clinically significant improvement difference worsening of Patient-Reported Outcomes Measurement Information System (PROMIS) PROMISPF10a score. Risk factors of flares were analysed using regression models. Results: Of 15 165 total respondents, 1278 IIMs (age 63 years, 70.3% female, 80.8% Caucasians) and 3453 AIRDs were included. Flares of IIM were seen in 9.6%, 12.7%, 8.7% and 19.6% patients by definitions (a) to (d), respectively, with a median time to flare of 71.5 (10.7-235) days, similar to AIRDs. Patients with active IIMs pre-vaccination (OR 1.2; 95% CI 1.03, 1.6, P = 0.025) were prone to flares, while those receiving rituximab (OR 0.3; 95% CI 0.1, 0.7, P = 0.010) and AZA (OR 0.3, 95% CI 0.1, 0.8, P = 0.016) were at lower risk. Female gender and comorbidities predisposed to flares requiring changes in IS. Asthma (OR 1.62; 95% CI 1.05, 2.50, P = 0.028) and higher pain visual analogue score (OR 1.19; 95% CI 1.11, 1.27, P < 0.001) were associated with disparity between self-reported and IS-denoted flares. Conclusion: A diagnosis of IIMs confers an equal risk of flares in the post-COVID-19 vaccination period to AIRDs, with active disease, female gender and comorbidities conferring a higher risk. Disparity between patient- and physician-reported outcomes represents a future avenue for exploration.
AB - Objectives: Disease flares in the post-coronavirus disease 2019 (COVID-19) vaccination period represent a prominent concern, though risk factors are poorly understood. We studied these flares among patients with idiopathic inflammatory myopathies (IIMs) and other autoimmune rheumatic diseases (AIRDs). Methods: The COVAD-1 and -2 global surveys were circulated in early 2021 and 2022, respectively, and we captured demographics, comorbidities, AIRDs details, COVID-19 infection history and vaccination details. Flares of IIMs were defined as (a) patient self-reported, (b) immunosuppression (IS) denoted, (c) clinical sign directed and (d) with >7.9-point minimal clinically significant improvement difference worsening of Patient-Reported Outcomes Measurement Information System (PROMIS) PROMISPF10a score. Risk factors of flares were analysed using regression models. Results: Of 15 165 total respondents, 1278 IIMs (age 63 years, 70.3% female, 80.8% Caucasians) and 3453 AIRDs were included. Flares of IIM were seen in 9.6%, 12.7%, 8.7% and 19.6% patients by definitions (a) to (d), respectively, with a median time to flare of 71.5 (10.7-235) days, similar to AIRDs. Patients with active IIMs pre-vaccination (OR 1.2; 95% CI 1.03, 1.6, P = 0.025) were prone to flares, while those receiving rituximab (OR 0.3; 95% CI 0.1, 0.7, P = 0.010) and AZA (OR 0.3, 95% CI 0.1, 0.8, P = 0.016) were at lower risk. Female gender and comorbidities predisposed to flares requiring changes in IS. Asthma (OR 1.62; 95% CI 1.05, 2.50, P = 0.028) and higher pain visual analogue score (OR 1.19; 95% CI 1.11, 1.27, P < 0.001) were associated with disparity between self-reported and IS-denoted flares. Conclusion: A diagnosis of IIMs confers an equal risk of flares in the post-COVID-19 vaccination period to AIRDs, with active disease, female gender and comorbidities conferring a higher risk. Disparity between patient- and physician-reported outcomes represents a future avenue for exploration.
KW - COVID-19 vaccines
KW - disease exacerbation
KW - idiopathic inflammatory myopathies
KW - patient-reported outcomes
UR - http://www.scopus.com/inward/record.url?scp=85180733005&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85180733005&partnerID=8YFLogxK
U2 - 10.1093/rheumatology/kead180
DO - 10.1093/rheumatology/kead180
M3 - Article
C2 - 37084267
AN - SCOPUS:85180733005
SN - 1462-0324
VL - 63
SP - 127
EP - 139
JO - Rheumatology (United Kingdom)
JF - Rheumatology (United Kingdom)
IS - 1
ER -