Research Article
Comparisons of CVID and IgGSD: Referring Physicians, Autoimmune Conditions, Pneumovax Reactivity, Immunoglobulin Levels, Blood Lymphocyte Subsets, and HLA-A and -B Typing in 432 Adult Index Patients
Table 2
Autoimmune conditions in 432 adult CVID/IgGSD index patients1.
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CVID, common variable immunodeficiency; IgGSD, IgG subclass deficiency. These autoimmune conditions were diagnosed before referral for CVID/IgGSD evaluation. Comparisons were made with Pearson’s test or Fischer’s exact test, as appropriate. Some patients had two or more autoimmune conditions. 2Hypothyroidism of unreported cause was reported in 11 CVID patients (32.4%) and 52 IgGSD patients (13.1%) (). 3Crohn’s disease (3), ulcerative colitis (3), and pernicious anemia (3). 4ANA, antinuclear antibody. Titers of 1 : 80 or greater unexplained by other conditions were defined as positive. 5Warm-reacting IgG autoantibody. 6Arthritis interpreted as autoimmune but not otherwise specified. 7Cutaneous psoriasis (3), erythema nodosum (2), vitiligo (2), alopecia areata (1), and Behcet’s syndrome (1). 8Antiphospholipid syndrome (2), anticardiolipin antibody (1), and lupus anticoagulant (2). |