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. 2018 Nov 28;196(1):39–51. doi: 10.1111/cei.13242

Table 1.

Background information of enrolled subjects

Variables pSS (n = 11) Non‐SS (n = 5) P‐value
Age (years), median (IQR) 61 (57–65) 52 (40–68) 0·65a
Female, n (%) 11 (100%) 5 (100%) 1b
Xerostomia, n (%) 10 (90·9%) 3 (60%) 0·21b
Xerophthalmia, n (%) 6 (54·5%) 3 (60%) 1b
Schirmer test positivity, n (%) 4 (36·4%) 2 (40%) 0·84b
Saxon test positivity, n (%) 9 (81·8%) 3 (60%) 0·35b
Anti‐SS‐A/Ro antibody positivity, n (%) 11 (100%) 0 (0%) <0·001b
Anti‐SS‐B/La antibody positivity, n (%) 4 (36·3%) 0 (0%) 0·12b
ANA positivity, n (%) 11 (100%) 0 (0%) <0·001b
RF positivity, n (%) 7 (63·6%) 4 (80%) 0·51b
Serum IgG, mg/dl, median (IQR) 2140 (1550–2550) 1047 (656–1246) 0·009a
LSG biopsy, focus score 6·9 (4–19·2) 0 0·0019a
ESSDAI score, median (IQR) 6 (4–6) n.a. n.a.

P‐values < 0·05 were considered significant.

Non‐SS = these subjects were classified as non‐SS sicca control subjects based on the American–European Consensus Group (AECG) classification criteria.

ANA = anti‐nuclear antibody; ESSDAI = European League Against Rheumatism Sjögren's Syndrome Disease Activity Index; IgG = immunoglobulin G; IQR = interquartile range; LSG = labial salivary gland; n.a. = not assessed; pSS = primary Sjögren's syndrome; RF = rheumatoid factor.

a

Mann–Whitney U‐test.

b

Fisher's exact test.