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. 2020 Oct 13;15(10):e0240522. doi: 10.1371/journal.pone.0240522

Table 1. Characteristics of adults with IgGSD with and without subnormal IgG2 (<117 mg/dL)a.

Characteristic Subnormal IgG2 (n = 18) No subnormal IgG2 (n = 218) Value of p
Women, % (n) 94.4 (17) 79.4 (173) 0.2110
Mean age, y (± 1 SD) 52 ± 11 50 ± 13 0.4455
Upper respiratory tract infection, % (n) 94.4 (17) 93.6 (204) ~1.0000
Lower respiratory tract infection, % (n) 77.8 (14) 81.7 (178) 0.7522
Upper and lower respiratory tract infection, % (n) 72.2 (13) 77.1 (168) 0.5761
Autoimmune condition(s), % (n) 44.4 (8)b 47.2 (103)c ~1.0000
Atopy, % (n) 44.4 (8)d 28.0 (61)e 0.1767
Other allergy, % (n) 61.1 (11) 45.2 (99) 0.2260
Frequent/severe respiratory tract infection in first-degree relatives, % (n) 22.2 (4) 40.8 (89) 0.1391
Subnormal IgG (<700 mg/dL), % (n) 66.7 (12) 37.2 (81) 0.0218
Subnormal IgG1 (<422 mg/dL), % (n) 50.0 (9) 68.3 (149) 0.1235
Median IgG2, mg/dL (range) 105 (83, 116) 257 (117, 644) <0.0001
Subnormal IgG3 (<41 mg/dL), % (n) 94.4 (17) 67.4 (147) 0.0155
Subnormal IgG4 (<1 mg/dL), % (n) 5.6 (1) 5.0 (11) ~1.0000
Subnormal IgA (<70 mg/dL) 33.3 (6)f 4.1 (9)g 0.0003
Subnormal IgM (<40 mg/dL) 0 23.4 (51) 0.0156

a Abbreviations: IgGSD, immunoglobulin G subclass deficiency; IgG1, immunoglobulin G1; IgG2, immunoglobulin G2; IgG3, immunoglobulin G3; IgG4, immunoglobulin G4; SD, standard deviation. No patient had monoclonal gammopathy detected by serum electrophoresis and immunofixation.

b Eight patients (44.4%) had an autoimmune condition(s): rheumatoid arthritis (4); autoimmune/Hashimoto thyroiditis (3); lupus (2); Sjögren syndrome (2); anticardiolipin antibody syndrome (1); and positive anti-nuclear antibody ≥1:80 without greater specificity (1). Three patients (16.7%) had two or more autoimmune conditions.

c One hundred and three patients (47.2%) had an autoimmune condition(s): autoimmune/Hashimoto thyroiditis (39); rheumatoid arthritis (20); Sjögren syndrome (20); systemic lupus erythematosus (20); inflammatory arthritis not otherwise specified (6); psoriatic arthritis (6); ankylosing spondylitis (5); Graves disease (4); psoriasis (4); Raynaud phenomenon (4); Crohn disease (3); pernicious anemia (3); positive anti-nuclear antibody ≥1:80 without greater specificity (3); undifferentiated connective tissue disorder (3); autoimmune diabetes (2); Behçet disease (2); multiple sclerosis (2); ulcerative colitis (2); anti-cardiolipin antibody syndrome (1); autoimmune hemolytic anemia (1); autoimmune uveitis (1); glutamic acid decarboxylase autoantibody (1); Guillain-Barré syndrome (1); myasthenia gravis (1); and polymyalgia rheumatica (1). Forty-two patients (19.3%) had two or more autoimmune conditions.

d Seven patients had allergic asthma. One other patient had allergic rhinitis.

e Sixty-one patients had atopy (52 allergic asthma; 15 allergic rhinitis; 3 allergic dermatitis). Each of eight patients had two (or three) subtypes of atopy.

f The lowest IgA level observed in this subgroup was 32 mg/dL. Four of these 18 patients had both subnormal IgG and subnormal IgA.

g The lowest IgA level observed in this subgroup was 3 mg/dL. None of these 218 patients had both subnormal IgG and subnormal IgA.