Latent Class Analysis Identifies Distinct Phenotypes of Systemic Lupus Erythematosus Predictive of Flares after mRNA COVID-19 Vaccination: Results from the Coronavirus National Vaccine Registry for ImmuNe Diseases SINGapore (CONVIN-SING)
Tao Ming Sim,
Manjari Lahiri,
Margaret Ma,
Peter Pak-Moon Cheung,
Anselm Mak,
Warren Fong,
Stanley Angkodjojo,
Chuanhui Xu,
Kok Ooi Kong,
Thaschawee Arkachaisri,
Kee Fong Phang,
Teck Choon Tan,
Qai Ven Yap,
Yiong Huak Chan,
Melonie Sriranganathan,
Tyng Yu Chuah,
Nur Emillia Roslan,
Yih Jia Poh,
Annie Law,
Amelia Santosa,
Sen Hee Tay
Affiliations
Tao Ming Sim
Yong Loo Lin School of Medicine, National University of Singapore, Singapore 117599, Singapore
Manjari Lahiri
Division of Rheumatology, Department of Medicine, National University Hospital, 1E Kent Ridge Road, Level 10, NUHS Tower Block, Singapore 119228, Singapore
Margaret Ma
Division of Rheumatology, Department of Medicine, National University Hospital, 1E Kent Ridge Road, Level 10, NUHS Tower Block, Singapore 119228, Singapore
Peter Pak-Moon Cheung
Division of Rheumatology, Department of Medicine, National University Hospital, 1E Kent Ridge Road, Level 10, NUHS Tower Block, Singapore 119228, Singapore
Anselm Mak
Division of Rheumatology, Department of Medicine, National University Hospital, 1E Kent Ridge Road, Level 10, NUHS Tower Block, Singapore 119228, Singapore
Warren Fong
Department of Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 117597, Singapore
Stanley Angkodjojo
Rheumatology Service, Department of General Medicine, Sengkang General Hospital, Singapore 544886, Singapore
Chuanhui Xu
Department of Rheumatology, Allergy and Immunology, Tan Tock Seng Hospital, Singapore 308433, Singapore
Kok Ooi Kong
Department of Rheumatology, Allergy and Immunology, Tan Tock Seng Hospital, Singapore 308433, Singapore
Thaschawee Arkachaisri
Duke-NUS Medical School, Singapore 169857, Singapore
Kee Fong Phang
Department of Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 117597, Singapore
Teck Choon Tan
Division of Rheumatology, Department of General Medicine, Khoo Teck Puat Hospital, Singapore 768828, Singapore
Qai Ven Yap
Biostatistics Unit, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 117599, Singapore
Yiong Huak Chan
Biostatistics Unit, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 117599, Singapore
Melonie Sriranganathan
Division of Rheumatology, Department of Medicine, Changi General Hospital, Singapore 529889, Singapore
Tyng Yu Chuah
Rheumatology Service, Department of General Medicine, Sengkang General Hospital, Singapore 544886, Singapore
Nur Emillia Roslan
Rheumatology Service, Department of General Medicine, Sengkang General Hospital, Singapore 544886, Singapore
Yih Jia Poh
Department of Rheumatology and Immunology, Singapore General Hospital, Singapore 169608, Singapore
Annie Law
Department of Rheumatology and Immunology, Singapore General Hospital, Singapore 169608, Singapore
Amelia Santosa
Division of Rheumatology, Department of Medicine, National University Hospital, 1E Kent Ridge Road, Level 10, NUHS Tower Block, Singapore 119228, Singapore
Sen Hee Tay
Division of Rheumatology, Department of Medicine, National University Hospital, 1E Kent Ridge Road, Level 10, NUHS Tower Block, Singapore 119228, Singapore
We recently reported that messenger ribonucleic acid (mRNA) coronavirus disease 2019 (COVID-19) vaccination was associated with flares in 9% of patients with systemic lupus erythematosus (SLE). Herein, we focused our analysis on patients from a multi-ethnic Southeast Asian lupus cohort with the intention of identifying distinct phenotypes associated with increased flares after mRNA COVID-19 vaccination. Methods: Six hundred and thirty-three SLE patients from eight public healthcare institutions were divided into test and validation cohorts based on healthcare clusters. Latent class analysis was performed based on age, ethnicity, gender, vaccine type, past COVID-19 infection, interruption of immunomodulatory/immunosuppressive treatment for vaccination, disease activity and background immunomodulatory/immunosuppressive treatment as input variables. Data from both cohorts were then combined for mixed effect Cox regression to determine which phenotypic cluster had a higher risk for time to first SLE flare, adjusted for the number of vaccine doses. Results: Two clusters were identified in the test (C1 vs. C2), validation (C1′ vs. C2′) and combined (C1″ vs. C2″) cohorts, with corresponding clusters sharing similar characteristics. Of 633 SLE patients, 88.6% were female and there was multi-ethnic representation with 74.9% Chinese, 14.2% Malay and 4.6% Indian. The second cluster (C2, C2′ and C2″) was smaller compared to the first. SLE patients in the second cluster (C2 and C2′) were more likely to be male, non-Chinese and younger, with higher baseline disease activity. The second cluster (C2″) had more incident flares (hazard ratio = 1.4, 95% confidence interval 1.1–1.9, p = 0.014) after vaccination. A higher proportion of patients in C2″ had immunomodulatory/immunosuppressive treatment interruption for vaccination as compared to patients in C1″ (6.6% vs. 0.2%) (p < 0.001). Conclusion: We identified two distinct phenotypic clusters of SLE with different patterns of flares following mRNA COVID-19 vaccination. Caution has to be exercised in monitoring for post-vaccination flares in patients with risk factors for flares such as non-Chinese ethnicity, young age, male gender and suboptimal disease control at the time of vaccination.