Table 1.

Baseline characteristics of the study sample from the BRASS cohort by smoking status. Total sample size was 659 after 3 patients were excluded for lack of smoking status.

Smoking Status
CharacteristicsNever, n = 353Past, n = 250Current, n = 56p
Age, yrs, mean ± SD54.6 ± 14.361.2 ± 11.054.5 ± 11.4< 0.001
Sex (female), %83.082.478.60.72
Race (white), %93.197.289.10.02
Education (high school graduate or higher), %67.357.355.40.02
Smoking pack-yrs019.2 ± 21.429.6 ± 22.1< 0.001
Alcohol consumption, g/day4.8 ± 10.17.7 ± 14.96.2 ± 11.10.02
DAS28-CRP33.97 ± 1.564.07 ± 1.504.45 ± 1.480.06
MHAQ0.41 ± 0.450.40 ± 0.460.56 ± 0.530.13
Disease duration, yrs14.8 ± 12.215.7 ± 12.214.9 ± 12.30.63
HLA-SE carrier, %61.566.067.90.42
BMI, kg/m2, mean ± SD26.2 ± 5.627.3 ± 5.226.9 ± 6.10.004
Anti-CCP–positive, %64.471.871.70.13
Prednisone, %29.730.030.40.99
Methotrexate, %47.052.042.90.33
Antimalarial, %17.614.016.10.50
Other DMARD, %17.619.219.60.85
Biologic DMARD, %37.740.835.70.66
NSAID, %63.563.266.10.92
  • Some measurements were missing at baseline (race, n = 653; education, n = 656; and anti-CCP, n = 649). P values were based on Kruskal-Wallis test for continuous variables or chi-squared test for categorical variables. DAS28-CRP3: Disease Activity Score using 28 joints with high-sensitivity C-reactive protein; MHAQ: Modified Health Assessment Questionnaire; BMI: body mass index; DMARD: disease-modifying antirheumatic drug (biologic DMARD refers to all kinds of anti-tumor necrosis factor, anti-interleukin 1, or anti-B cell agents); NSAID: nonsteroidal antiinflammatory drug; anti-CCP: anticyclic citrullinated peptide.