Predictors of granulomatous lymphocytic interstitial lung disease in common variable immunodeficiency

Publication date: Available online 20 February 2017
Source:Annals of Allergy, Asthma & Immunology
Author(s): Stella Hartono, Megan S. Motosue, Shakila Khan, Vilmarie Rodriguez, Vivek N. Iyer, Rohit Divekar, Avni Y. Joshi
BackgroundA subset of patients with common variable immunodeficiency (CVID) develop granulomatous lymphocytic interstitial lung disease (GLILD), which is associated with early mortality.ObjectiveTo determine a set of clinical and/or laboratory parameters that correlate with GLILD.MethodsA retrospective, nested case-control (patients with CVID diagnosed with GLILD compared with patients with CVID without a diagnosis of GLILD) medical record review was undertaken at Mayo Clinic, Rochester, MN. Network and univariate analysis was used to identify clinical and laboratory parameters at the time of diagnosis that are associated with GLILD.ResultsTwenty-six cases with radiologic evidence of GLILD were included in this study. Eighteen cases (69%) cases had coexistent splenomegaly with lower IgA levels (P = .04) compared with the controls. Patients with low IgA levels (<13 mg/dL) also had percentage expansion of low CD21 B cells (CD21low >5%) (P = .007). Univariate analysis revealed that splenomegaly (odds ratio [OR], 17.3; 95% confidence interval [CI], 3.9–74.5), history of immune thrombocytopenic purpura (ITP) or autoimmune hemolytic anemia (AIHA) (OR, 4.8; 95% CI, 1.1–20.2), low IgA level (OR, 3.6; 95% CI, 1.2–11.9), and percentage expansion of CD21low (OR, 5.8; 95% CI, 1.6–24.7) were independently associated with GLILD. Logistic regression analysis revealed that splenomegaly, history of ITP or AIHA, low IgA level, and percentage expansion of CD21low B cells are highly sensitive in predicting presence of GLILD (area under the receiver operating curve of 0.86).ConclusionPresence of splenomegaly, history of ITP or AIHA, low serum IgA level, and percentage expansion of CD21low B cells may be useful to identify a group of patients at high risk for development of GLILD.



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