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. 2021 Apr 8;8(1):e000446. doi: 10.1136/lupus-2020-000446

Table 1.

Demographic and clinical characteristics of the Hopkins Lupus Cohort analytical cohort (N=1168)

 N (%)
Women 1085 (92.9)
Race
 White 643 (55.1)
 Black African Ancestry 460 (39.4)
 Other 65 (5.6)
History of seropositive status
 ANA+ 1075 (92.0)
 Anti-dsDNA+ 591 (50.6)
 ANA+ or anti-dsDNA+ 1093 (93.6)
Current smoker at cohort entry 202 (17.3)
Past smoker at cohort entry 465 (39.8)
Adjusted mean SELENA-SLEDAI <3 in background period 641 (54.9)
SLE therapies* ever prescribed in observation period
 Oral prednisone (any dose) 702 (60.1)
 Oral prednisone >7.5 mg/day 428 (36.6)
 HCQ 759 (65.0)
 NSAID 447 (38.3)
 Immunosuppressants† 262 (22.4)
Obesity in observation period (BMI >27.8 for men and BMI >27.3 for women) 604 (51.7)
Hypertension in observation period (SBP ≥140 or DBP ≥90 mm Hg) 652 (55.8)
Diabetes therapy with oral hypoglycaemic agent or insulin 118 (10.1)
Median (range)
Age at cohort entry‡, years 36 (11–77)
Age at SLE diagnosis§, years 31(5–75)
Age at last assessment in follow-up period, years 46 (20–85)
Adjusted mean SELENA-SLEDAI in background period 3 (0–16)
Disease duration from SLE diagnosis to cohort entry, years 2 (0–39)
Disease duration from SLE diagnosis to last assessment, years 11 (2–48)
Follow-up time from cohort entry to last assessment, years 7 (2–23)

*Categories not mutually exclusive.

†Leflunomide, mycophenolate, cyclophosphamide, tacrolimus, azathioprine, methotrexate or rituximab (biologic).

‡Less than 2% of cohort enrolled <18 years of age.

§Less than 5% of cohort diagnosed with SLE <18 years of age.

ANA, antinuclear antibodies; BMI, body mass index in kg/m2; DBP, diastolic blood pressure; dsDNA, double-stranded DNA; HCQ, hydroxychloroquine; NSAID, non-steroidal anti-inflammatory drug; SBP, systolic blood pressure; SELENA-SLEDAI, Safety of Estrogens in Lupus Erythematosus National Assessment-SLE Disease Activity Index; SLE, systemic lupus erythematosus.