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Table 1 Demographic and clinical characteristics of the study participants

From: Distinct genome-wide DNA methylation and gene expression signatures in classical monocytes from African American patients with systemic sclerosis

 

DNA methylation

Gene expression

Patients (n = 12)

Controls (n = 12)

Patients (n = 16)

Controls (n = 18)

Age at enrollment (mean ± SD)

52.17 ± 12.1

48.58 ± 15.6

51.75 ± 12.3

49.28 ± 13.9

Female, n (%)

12 (100%)

12 (100%)

16 (100%)

18 (100%)

dcSSc, n (%)

6 (50%)

NA

10 (62.5%)

NA

lcSSc, n (%)

5 (41.7%)

NA

4 (25%)

NA

ssSSc, n (%)

1 (8.3%)

NA

1 (6.25%)

NA

Raynaud’s Phenomenon, n (%)

12 (100%)

NA

16 (100%)

NA

Disease duration (mean ± SD)

11.08 ± 6.27

NA

8.88 ± 7.78

NA

mRSS (mean ± SD)a

13 ± 6.18

NA

13 ± 6.18

NA

ILD, n (%)

8 (66.7%)

NA

10 (62.5%)

NA

PH/PAH, n (%)

5 (41.7%)

NA

5 (31.3%)

NA

Overlap MCTD, n (%)

0 (0%)

NA

1 (6.25%)

NA

Overlap SLE, n (%)

0 (0%)

NA

1 (6.25%)

NA

Immunosuppressive medications, n (%)

8 (66.7%)

NA

12 (75%)

NA

Antihypertensive medications, n (%)

9 (75%)

NA

13 (81%)

NA

Smoker at enrollment, n (%)b

2 (16.7%)

0 (0%)

2 (12.5%)

2 (11.1%)

  1. Immunosuppressive medications include oral steroids, mycophenolate mofetil, or hydroxychloroquine; antihypertensive medications include diuretics, calcium channel blockers, alpha blockers, beta blockers, ACE inhibitors, or angiotensin receptor antagonists
  2. SSc systemic sclerosis, dcSSc diffuse cutaneous SSc, ssSSc sine SSc, mRSS modified Rodnan skin score, ILD interstitial lung disease, PH/PAH pulmonary hypertension/pulmonary arterial hypertension, MCTD mixed connective tissue disease, SLE systemic lupus erythematosus
  3. aAssessed for 4 patients with dcSSc within 3–18 months of enrolment
  4. bDisclosed for all participants except one control in the Gene Expression group