Table 1.
Baseline characteristics
Continue methotrexate (n=127) | Suspend methotrexate (n=127) | ||
---|---|---|---|
Age, years | 59·2 (11·0) | 59·0 (11·9) | |
<40 years | 8 (6%) | 8 (6%) | |
40–64 years | 73 (57%) | 73 (57%) | |
≥65 years | 46 (36%) | 46 (36%) | |
Sex | |||
Male | 47 (37%) | 52 (41%) | |
Female | 80 (63%) | 75 (59%) | |
BMI, kg/m2 | 29·0 (6·5) | 30·3 (5·6) | |
Ethnicity | |||
White | 120 (94%) | 118 (93%) | |
Other | 7 (6%) | 8 (6%) | |
Missing data | 0 | 1 (1%) | |
Smoking status | |||
Never smoked | 67 (53%) | 68 (54%) | |
Ex-smoker | 46 (36%) | 49 (39%) | |
Current smoker | 14 (11%) | 10 (8%) | |
Serum creatinine concentration, μmol/L | 71·7 (14·8) | 75·8 (13·2) | |
Type of immune-mediated inflammatory disease | |||
Rheumatic disease (with or without skin disease) | 101 (80%) | 102 (80%) | |
Skin disease alone | 26 (20%) | 25 (20%) | |
Immune-mediated inflammatory disease* | |||
Rheumatoid arthritis | 68 (54%) | 62 (49%) | |
Psoriasis with arthritis | 24 (19%) | 28 (22%) | |
Psoriasis without arthritis | 15 (12%) | 19 (15%) | |
Seronegative (axial) spondyloarthritis | 3 (2%) | 1 (1%) | |
Reactive arthritis | 0 | 0 | |
Atopic eczema | 6 (5%) | 6 (5%) | |
Polymyalgia rheumatica | 2 (2%) | 3 (2%) | |
Systemic lupus erythematosus | 2 (2%) | 0 | |
Other rheumatic disease | 6 (5%) | 9 (7%) | |
Other skin disease | 6 (5%) | 3 (2%) | |
Methotrexate use | |||
Weekly dose ≤5 mg | 55 (43%) | 51 (40%) | |
Weekly dose >15 mg | 72 (57%) | 76 (60%) | |
Median dose | 20 (15–20) | 20 (15–20) | |
Oral administration | 79 (62%) | 75 (59%) | |
Subcutaneous administration | 48 (38%) | 52 (41%) | |
Folic acid supplementation | |||
Yes | 124 (98%) | 125 (98%) | |
No | 2 (2%) | 2 (2%) | |
Missing data | 1 (1%) | 0 | |
Hydroxychloroquine | |||
Yes | 21 (17%) | 26 (20%) | |
No | 106 (83%) | 101 (80%) | |
Median dose | 200 (200–200) | 200 (200–400) | |
Concomitant systemic medications* | |||
Non-steroidal anti-inflammatory drugs | 22 (17%) | 23 (18%) | |
Oral glucocorticoid | 3 (2%) | 2 (2%) | |
Insulin | 3 (2%) | 1 (1%) | |
Missing data | 1 (1%) | 0 | |
Parenteral glucocorticoid in past 3 months | |||
Intra-articular glucocorticoid | 0 | 2 (2%) | |
Intramuscular glucocorticoid | 1 (1%) | 3 (2%) | |
None | 125 (98%) | 122 (96%) | |
Missing data | 1 (1%) | 0 | |
Current use of topical glucocorticoid | |||
Yes | 17 (13%) | 20 (16%) | |
No | 110 (87%) | 107 (84%) | |
Comorbidities* | |||
Diabetes | 16 (13%) | 10 (8%) | |
Hypertension | 30 (24%) | 28 (22%) | |
Ischaemic heart disease | 1 (1%) | 3 (2%) | |
Congestive cardiac failure | 0 | 0 | |
Asthma | 18 (14%) | 16 (13%) | |
Chronic obstructive pulmonary disease | 3 (2%) | 5 (4%) | |
High cholesterol | 12 (9%) | 16 (13%) | |
Stroke (including transient ischaemic attack) | 2 (2%) | 3 (2%) | |
None of the above | 71 (56%) | 77 (61%) | |
Primary COVID-19 vaccination type | |||
mRNA (BNT162b2 or mRNA-1273) | 42 (33%) | 43 (34%) | |
Viral vector (AZD1222) | 85 (67%) | 82 (65%) | |
Combination | 0 | 2 (2%) | |
Days between two doses | 76 (11·0) | 76 (12·0) | |
COVID-19 disease history | |||
COVID-19 disease leading to hospitalisation | 1 (1%) | 3 (2%) | |
COVID-19 disease without hospitalisation | 16 (13%) | 21 (17%) | |
No COVID-19 disease | 110 (87%) | 103 (81%) | |
COVID-19 booster vaccine | |||
BNT162b2 | 106 (83%) | 102 (80%) | |
AZD1222 | 6 (5%) | 4 (3%) | |
mRNA-1273 | 13 (10%) | 18 (14%) | |
None | 2 (2%) | 3 (2%) | |
Booster as 3rd dose† | 124 (99%) | 124 (100%) | |
Booster as 4th dose† | 1 (1%) | 0 | |
Days between previous vaccination and booster | 189·9 (31·0) | 195·4 (22·1) |
Data are n (%), mean (SD), or median (IQR).
Participants can have more than one category.
Percentages are of those who received a booster vaccine.