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. 2021 Feb 1;8:621590. doi: 10.3389/fmed.2021.621590

Table 1.

Clinical and demographic characteristics.

SLE aPS/PT positive SLE aPS/PT negative
(N = 18) % (N = 34) %
Age
Years (mean ±SD) 47.5 ± 11.5 44.8 ± 13.5
Female
(N; %) 14 77.8 28 82.4
aPS/PT IgG
Positive (N; %) 11 61.1
Titer (mean ±SD; median [range]) 99.8 ± 77.8; 121 [12–229]
aPS/PT IgM
Positive (N; %) 16 88.9
Titer (mean ±SD; median [range]) 126.2 ± 150.8; 131 [8–518]
Lupus anti-coagulant
Positive (N; %) 5 27.8 12 35.3
SLE manifestation
Skin (N; %) 6 33.3 8 23.5
Joints (N; %) 17 94.4 28 82.4
Hematological (N; %) 3 16.7 6 17.6
Lupus Nephritis* (N; %) 8 44.4 11 32.4
Sierositis (N; %) 4 22.2 7 20.6
Follow-up**
Years (mean ±SD; median [range]) 3.7 ± 1.2 3.9 ± 1.1
SLE disease duration
Years (mean ±SD; median [range]) 15.7 ± 8.1 19.7 ± 7.2
Therapy**
Hydroxychloroquine (N; %) 17 94.4 33 97.1
Prednisone <7.5 mg/die*** (N; %) 14 77.8 22 64.7
Cyclophosphamide (N; %) 2 11.1 2 5.9
Mycophenolate (N; %) 3 16.7 3 8.8
Azathioprine (N; %) 6 33.3 10 29.4
Methotrexate (N; %) 3 16.7 5 14.7
Rituximab (N; %) 5 27.8 10 29.4
Belimumab (N; %) 3 16.7 5 14.7
Thrombotic risk factors
Arterial hypertension (N; %) 7 38.9 10 29.4
Hyperlipidemia (N; %) 2 11.1 5 14.7
Smoking habit (N; %) 3 16.7 5 14.7
Diabetes (N; %) 0 0.0 0 0.0
Hormone replacement therapy (N; %) 0 0.0 0 0.0
Inherited thrombophilia (N; %) 0 0.0 0 0.0
*

Biopsy-proven.

**

After aPS/PT testing.

***

For at least 80% of the observation time.

No statistical difference was observed between the two groups.

S.D., standard deviation; N., number; aPS/PT, anti-phosphatidylserine/prothrombin; Ig, immunoglobulins; SLE, Systemic Lupus Erythematosus.