TY - JOUR
T1 - Time trends of variability in disease activity in systemic lupus erythematosus
AU - Li, Ning
AU - Hoi, Alberta
AU - Luo, Shue-Fen
AU - Wu, Yeong-Jian Jan
AU - Louthrenoo, Worawit
AU - Golder, Vera
AU - Sockalingam, Sargunan
AU - Cho, Jiacai
AU - Lateef, Aisha
AU - O'Neill, Sean
AU - Lau, Chak Sing
AU - Hamijoyo, Laniyati
AU - Nikpour, Mandana
AU - Oon, Shereen
AU - Hao, Yanjie
AU - Chan, Madelynn
AU - Li, Zhanguo
AU - Navarra, Sandra
AU - Zamora, Leonid
AU - Katsumata, Yasuhiro
AU - Harigai, Masayoshi
AU - Goldblatt, Fiona
AU - Bae, Sang Cheol
AU - Zhang, Zhuoli
AU - Takeuchi, Tsutomu
AU - Kikuchi, Jun
AU - Ng, Kristine
AU - Tugnet, Nicola
AU - Tanaka, Yoshiya
AU - Ohkubo, Naoaki
AU - Chen, Yi Hsing
AU - Basnayake, B. M.D.B.
AU - Law, Annie
AU - Kumar, Sunil
AU - Tee, Cherica
AU - Tee, Michael Lucas
AU - Choi, Jiyoon
AU - Kandane-Rathnayake, Rangi
AU - Morand, Eric
N1 - Publisher Copyright:
© Author(s) (or their employer(s)) 2025.
PY - 2025/2/12
Y1 - 2025/2/12
N2 - Objective Disease activity both between and within patients with SLE is highly variable, yet factors driving this variability remain unclear. This study aimed to identify predictors of variability in SLE disease activity over time. Methods We analysed data from 2930 patients with SLE across 13 countries, collected over 38 754 clinic visits between 2013 and 2020. Clinic visit records were converted to panel data with 1-year intervals. The time-adjusted mean disease activity, termed AMS, was calculated. The yearly change in AMS, denoted as î "AMSt, was regressed onto AMSt-1 and other potential predictors using random-effects models. Some variables were split into a person-mean component to assess between-patient differences and a demeaned component to assess within-patient variability. Results Overall, variability in SLE disease activity exhibited stabilisation over time. A significant inverse relationship emerged between a patient's disease activity in a given year and variability in disease activity in the subsequent year: a 1-point increase in person-mean disease activity was associated with a 0.27-point decrease (95% CI -0.29 to -0.26, p<0.001) in subsequent variability. Additionally, a 1-point increase in within-patient disease activity variability was associated with a 0.56-point decrease (95% CI -0.57 to -0.55, p<0.001) in the subsequent year. Furthermore, each 1-point increase in the annual average time-adjusted mean Physician Global Assessment was associated with a 0.08-point decrease (90% CI -0.13 to -0.03, p=0.002) in disease activity variability for the following year. Prednisolone dose and the duration of activity in specific organ systems exhibited negative and positive associations, respectively, with disease activity variability in the subsequent year. Patients from less affluent countries displayed greater disease activity variability compared with those from wealthier nations. Conclusion Disease activity tends to be less variable among patients with higher or more variable disease activity in the previous year. Within-patient variability in disease activity has a stronger impact on subsequent fluctuations than differences between individual patients.
AB - Objective Disease activity both between and within patients with SLE is highly variable, yet factors driving this variability remain unclear. This study aimed to identify predictors of variability in SLE disease activity over time. Methods We analysed data from 2930 patients with SLE across 13 countries, collected over 38 754 clinic visits between 2013 and 2020. Clinic visit records were converted to panel data with 1-year intervals. The time-adjusted mean disease activity, termed AMS, was calculated. The yearly change in AMS, denoted as î "AMSt, was regressed onto AMSt-1 and other potential predictors using random-effects models. Some variables were split into a person-mean component to assess between-patient differences and a demeaned component to assess within-patient variability. Results Overall, variability in SLE disease activity exhibited stabilisation over time. A significant inverse relationship emerged between a patient's disease activity in a given year and variability in disease activity in the subsequent year: a 1-point increase in person-mean disease activity was associated with a 0.27-point decrease (95% CI -0.29 to -0.26, p<0.001) in subsequent variability. Additionally, a 1-point increase in within-patient disease activity variability was associated with a 0.56-point decrease (95% CI -0.57 to -0.55, p<0.001) in the subsequent year. Furthermore, each 1-point increase in the annual average time-adjusted mean Physician Global Assessment was associated with a 0.08-point decrease (90% CI -0.13 to -0.03, p=0.002) in disease activity variability for the following year. Prednisolone dose and the duration of activity in specific organ systems exhibited negative and positive associations, respectively, with disease activity variability in the subsequent year. Patients from less affluent countries displayed greater disease activity variability compared with those from wealthier nations. Conclusion Disease activity tends to be less variable among patients with higher or more variable disease activity in the previous year. Within-patient variability in disease activity has a stronger impact on subsequent fluctuations than differences between individual patients.
KW - Lupus Erythematosus, Systemic
KW - Outcome Assessment, Health Care
KW - Severity of Illness Index
UR - https://www.scopus.com/pages/publications/85218155489
U2 - 10.1136/lupus-2024-001335
DO - 10.1136/lupus-2024-001335
M3 - Article
C2 - 39939124
AN - SCOPUS:85218155489
SN - 2053-8790
VL - 12
JO - Lupus Science and Medicine
JF - Lupus Science and Medicine
IS - 1
M1 - e001335
ER -