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Abstract
Background
Despite the overall safety and efficacy of COVID-19 vaccinations, rare cases of systemic autoimmune diseases (SAIDs) have been reported post-vaccination. This study used a global survey to analyze SAIDs in susceptible individuals' post-vaccination.
Methods
A cross-sectional study was conducted among participants with self-reported new-onset SAIDs using the COVID-19 Vaccination in Autoimmune Diseases (COVAD) 2 study dataset—a validated, patient-reported e-survey—to analyze the long-term safety of COVID-19 vaccines. Baseline characteristics of patients with new-onset SAIDs and vaccinated healthy controls (HCs) were compared after propensity score matching based on age and sex in a 1:4 ratio.
Results
Of 16 750 individuals, 74 (median age 52 years, 79.9% females, and 76.7% Caucasians) had new-onset SAID post-vaccination, mainly idiopathic inflammatory myopathies (IIMs) (n = 23, 31.51%), arthritis (n = 15; 20.53%), and polymyalgia rheumatica (PMR) (n = 12, 16.40%). Higher odds of new-onset SAIDs were noted among Caucasians (OR = 5.3; 95% CI = 2.9–9.7; p < .001) and Moderna vaccine recipients (OR = 2.7; 95% CI = 1.3–5.3; p = .004). New-onset SAIDs were associated with AID multimorbidity (OR = 1.4; 95% CI = 1.1–1.7; p < .001), mental health disorders (OR = 1.6; 95% CI = 1.3–1.9; p < .001), and mixed race (OR = 2.2; 95% CI = 1.2–4.2; p = .010), where those aged >60 years (OR = 0.6; 95% CI = 0.4–0.8; p = .007) and from high/medium human development index (HDI) countries (compared to very high HDI) reported fewer events than HCs.
Conclusion
This study reports a low occurrence of new-onset SAIDs following COVID-19 vaccination, primarily IIMs, PMR, and inflammatory arthritis. Identified risk factors included pre-existing AID multimorbidity, mental health diseases, and mixed race. Revaccination was well tolerated by most patients; therefore, we recommend continuing COVID-19 vaccination in the general population. However, long-term studies are needed to understand the autoimmune phenomena arising post-vaccination.
Characteristics of emerging new autoimmune diseases after COVID-19 vaccination: A sub-study by the COVAD group
Shumnalieva R;Ravichandran N;Hannah J;Javaid M;Darooka N;Roy D;Gonzalez DE;Velikova T;Milchert M;Kuwana M;Joshi M;Gracia-Ramos AE;Boyd P;Yaadav P;Cheng K;Kobert L;Cavagna L;Sen P;Day J;Makol A;Gutiérrez CET;Caballero-Uribe CV;Saha S;Parodis I;Dey D;Nikiphorou E;Distler O;Kadam E;Tan AL;Shinjo SK;Ziade N;Knitza J;Chinoy H;Aggarwal R;Agarwal V;Gupta L;Arvind Nune;Yi-Ming Chen;Aarat Patel;Chris Wincup;Bhupen Barman;Erick Adrian Zamora Tehozol;Jorge Rojas Serrano;Ignacio García-De La Torre;Iris J. Colunga-Pedraza;Javier Merayo-Chalico;Okwara Celestine Chibuzo;Leonardo Santos Hoff;Lina El Kibbi;Hussein Halabi;Binit Vaidya;A. T. M. Tanveer Hasan;James B. Lilleker;Babur Salim;Tamer Gheita;Miguel A. Saavedra;Sinan Kardes;Laura Andreoli;Daniele Lini;Karen Schreiber;Melinda Nagy Vince;Yogesh Preet Singh;Rajiv Ranjan;Avinash Jain;Sapan C. Pandya;Rakesh Kumar Pilania;Aman Sharma;Manesh Manoj M.;Vikas Gupta;Chengappa G. Kavadichanda;Pradeepta Sekhar Patro;Sajal Ajmani;Sanat Phatak;Rudra Prosad Goswami;Abhra Chandra Chowdhury;Ashish Jacob Mathew;Padnamabha Shenoy;Ajay Asranna;Keerthi Talari Bommakanti;Anuj Shukla;Arunkumar R. Pande;Kunal Chandwar;Akanksha Ghodke;Hiya Boro;Zoha Zahid Fazal;Döndü Üsküdar Cansu;Reşit Yıldırım;Armen Yuri Gasparyan;Nicoletta Del Papa;Gianluca Sambataro;Atzeni Fabiola;Marcello Govoni;Simone Parisi;Elena Bartoloni Bocci;Gian Domenico Sebastiani;Enrico Fusaro;Marco Sebastiani;Luca Quartuccio;Franco Franceschini;Pier Paolo Sainaghi;Giovanni Orsolini;Rossella De Angelis;Maria Giovanna Danielli;Vincenzo Venerito;Silvia Grignaschi;Alessandro Giollo;Alessia Alluno;Florenzo Ioannone;Marco Fornaro;Lisa S. Traboco;Suryo Anggoro Kusumo Wibowo;Jesús Loarce-Martos;Sergio Prieto-González;Raquel Aranega Gonzalez;Ran Nakashima;Shinji Sato;Naoki Kimura;Yuko Kaneko;Takahisa Gono;Stylianos Tomaras;Fabian Nikolai Proft;Marie-Therese Holzer;Margarita Aleksandrovna Gromova;Or Aharonov;Zoltán Griger;Ihsane Hmamouchi;Imane El Bouchti;Zineb Baba;Margherita Giannini;François Maurier;Julien Campagne;Alain Meyer;Daman Langguth;Vidya Limaye;Merrilee Needham;Nilesh Srivastav;Marie Hudson;Océane Landon-Cardinal;Wilmer Gerardo Rojas Zuleta;Álvaro Arbeláez;Javier Cajas;José António Pereira Silva;João Eurico Fonseca;Olena Zimba;Uyi Ima-Edomwonyi;Ibukunoluwa Dedeke;Emorinken Airenakho;Nwankwo Henry Madu;Abubakar Yerima;Hakeem Olaosebikan;Becky A.;Oruma Devi Koussougbo;Elisa Palalane;Ho So;Manuel Francisco Ugarte-Gil;Lyn Chinchay;José Proaño Bernaola;Victorio Pimentel;Hanan Mohammed Fathi;Reem Hamdy A. Mohammed;Ghita Harifi;Yurilís Fuentes-Silva;Karoll Cabriza;Jonathan Losanto;Nelly Colaman;Antonio Cachafeiro-Vilar;Generoso Guerra Bautista;Enrique Julio Giraldo Ho;Lilith Stange Nunez;Cristian Vergara M;Jossiell Then Báez;Hugo Alonzo;Carlos Benito Santiago Pastelin;Rodrigo García Salinas;Alejandro Quiñónez Obiols;Nilmo Chávez;Andrea Bran Ordóñez;Gil Alberto Reyes Llerena;Radames Sierra-Zorita;Dina Arrieta;Eduardo Romero Hidalgo;Ricardo Saenz;Idania Escalante M;Wendy Calapaqui;Ivonne Quezada;Gabriela Arredondo;Akira Yoshida;Keina Yomono;John D Pauling;Tulika Chatterjee;Wanruchada Katchamart;Phonpen Akarawatcharangura Goo;Vishwesh Agarwal.
2024-01-01
Abstract
Abstract
Background
Despite the overall safety and efficacy of COVID-19 vaccinations, rare cases of systemic autoimmune diseases (SAIDs) have been reported post-vaccination. This study used a global survey to analyze SAIDs in susceptible individuals' post-vaccination.
Methods
A cross-sectional study was conducted among participants with self-reported new-onset SAIDs using the COVID-19 Vaccination in Autoimmune Diseases (COVAD) 2 study dataset—a validated, patient-reported e-survey—to analyze the long-term safety of COVID-19 vaccines. Baseline characteristics of patients with new-onset SAIDs and vaccinated healthy controls (HCs) were compared after propensity score matching based on age and sex in a 1:4 ratio.
Results
Of 16 750 individuals, 74 (median age 52 years, 79.9% females, and 76.7% Caucasians) had new-onset SAID post-vaccination, mainly idiopathic inflammatory myopathies (IIMs) (n = 23, 31.51%), arthritis (n = 15; 20.53%), and polymyalgia rheumatica (PMR) (n = 12, 16.40%). Higher odds of new-onset SAIDs were noted among Caucasians (OR = 5.3; 95% CI = 2.9–9.7; p < .001) and Moderna vaccine recipients (OR = 2.7; 95% CI = 1.3–5.3; p = .004). New-onset SAIDs were associated with AID multimorbidity (OR = 1.4; 95% CI = 1.1–1.7; p < .001), mental health disorders (OR = 1.6; 95% CI = 1.3–1.9; p < .001), and mixed race (OR = 2.2; 95% CI = 1.2–4.2; p = .010), where those aged >60 years (OR = 0.6; 95% CI = 0.4–0.8; p = .007) and from high/medium human development index (HDI) countries (compared to very high HDI) reported fewer events than HCs.
Conclusion
This study reports a low occurrence of new-onset SAIDs following COVID-19 vaccination, primarily IIMs, PMR, and inflammatory arthritis. Identified risk factors included pre-existing AID multimorbidity, mental health diseases, and mixed race. Revaccination was well tolerated by most patients; therefore, we recommend continuing COVID-19 vaccination in the general population. However, long-term studies are needed to understand the autoimmune phenomena arising post-vaccination.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11379/599971
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