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. 2020 Sep 29;72(11):1897–1904. doi: 10.1002/art.41403

Table 3.

Baseline characteristics of SSc patients positive for anti–topo I IgG, stratified according to presence or absence of disease progression over 1 year of follow‐up*

Disease

progressors

(n = 23)

Disease

nonprogressors

(n = 58)

P
Demographic characteristics
Female sex 14 (61) 39 (67) 0.59
Age, mean ± SD years 55.3 ± 16.3 51.9 ± 13.9 0.21
Smoking (ever) 12 (52) 30 (52) 0.95
Disease duration
Since onset of first Raynaud’s symptom, median (IQR) years 3.8 (1.3–8.4) 5.6 (2.1–12.9) 0.21
Since onset of first non‐Raynaud’s symptom, median (IQR) years 1.9 (0.6–4.5) 3.5 (0.7–11.4) 0.07
Organ involvement
Diffuse cutaneous SSc 12 (52) 28 (48) 1.00
Modified Rodnan skin thickness score, median (IQR) 6 (2–19) 6 (3–13) 0.86
FVC%, mean ± SD 89 ± 26 89 ± 28 0.92
DLco%, mean ± SD 62 ± 18 64 ± 16 0.83
History of renal crisis 0 (0) 2 (4) 1.00
Digital ulcers 0 (0) 5 (9) 0.31
Pulmonary hypertension 2 (9) 2 (4) 0.59
History of immunosuppressive treatment
HSCT 0 (0) 7 (12) 0.18
CYC (ever) 4 (17) 16 (28) 0.34
MMF (ever) 1 (4) 0 (0) 0.28
Use of immunosuppressive treatment during 1‐year follow‐up
HSCT 0 (0) 0 (0)
CYC 11 (19) 5 (26) 0.52
MMF 1 (5) 6 (10) 0.67
Anti–topo I antibody characteristics
IgG level, median (IQR) AU/ml 813 (542–1,263) 396 (115–832) <0.01
IgA positivity 23 (100) 57 (98) 1.00
IgA level, median (IQR) AU/ml 9,898 (2,743–16,656) 2,045 (462–5,314) <0.01
IgM positivity 21 (91) 33 (57) 0.04
IgM level, median (IQR) AU/ml 1065 (869–3,853) 588 (223–1,610) 0.01
*

In 22 individuals, clinical follow‐up data were not available and they could not be classified as either disease progressors or disease nonprogressors. Except where indicated otherwise, values are the number (%) of patients. SSc = systemic sclerosis; anti–topo I = anti–topoisomerase I; IQR = interquartile range; FVC% = forced vital capacity % predicted; DLco% = diffusing capacity for carbon monoxide % predicted.

Immunosuppressive treatment includes the use of hematopoietic stem cell transplantation (HSCT), cyclophosphamide (CYC), or mycophenolate mofetil (MMF).