c An enzyme immunoassay kit that detects serum IgA antibody reacting to glycopeptidolipid core antigen derived from Mycobacterium avium complex (MAC) was not useful for differentiating MAC pulmonary disease (PD) from Mycobacterium abscessus complex PD (MAB-PD). However, this assay could be useful for differentiating MAC-and MAB-PD from pulmonary tuberculosis. (This study has been registered at ClinicalTrials.gov under registration no. NCT00970801.) A n enzyme immunoassay (EIA) that detects serum immunoglobulin A (IgA) antibody reacting to the glycopeptidolipid (GPL) core antigen of Mycobacterium avium complex (MAC) was developed (1). This EIA kit was useful for rapid diagnosis of MAC pulmonary disease (MAC-PD) and for differentiating MAC-PD from pulmonary tuberculosis (PTB) (1-5).MAC, followed by Mycobacterium abscessus complex (MAB), is the most common etiologic organism in PD caused by nontuberculous mycobacteria (NTM-PD) in many countries, including the United States and South Korea (6-9). Because MAB also possesses GPL on its cell surface (10), there is a possibility of false-positive results in patients with MAB-PD. However, this EIA kit has not been evaluated in MAB-PD (1-5). The objective of this study was to evaluate the diagnostic performance of this EIA kit in patients with NTM-PD caused by MAB as well as by MAC.Serum samples were collected from patients with NTM-PD diagnosed between January 2008 and December 2011 at the Samsung Medical Center (a 1,950-bed referral hospital in Seoul, South Korea). The patients were enrolled in an institutional review board-approved observational cohort study investigating NTM-PD (ClinicalTrials.gov identifier NCT00970801). Informed consent was obtained from all participants. All patients met the diagnostic criteria for NTM-PD according to the guidelines of the American Thoracic Society (11).The study groups included 40 MAC-PD patients (20 M. avium and 20 M. intracellulare), 40 MAB-PD patients (20 M. abscessus sensu stricto and 20 M. massiliense), 20 culture-confirmed PTB patients, and 20 healthy controls. All patients were newly diagnosed and had not been treated for NTM lung disease at the time of collection of the serum samples.Serum IgA antibodies against the GPL core antigen were measured using the EIA kit (Tauns Laboratory Inc., Shizuoka, Japan) according to the manufacturer's instructions (2, 3). Results are given as arbitrary U/ml and reported as positive when the IgA titer was more than 0.7 U/ml (2, 3). The titers of each study group are presented as medians and interquartile ranges (IQR) and were compared using the Kruskal-Wallis test with post hoc paired comparisons using the Bonferroni method. We estimated the sensitivity, specificity, and positive predictive value (PPV) and negative predictive value (NPV) for a preset cutoff point (Ն0.7 U/ml) and the best cutoff point, which showed the highest Youden index ([sensitivity ϩ specificity] Ϫ 1) (12). The discriminative power of the EIA kit was assessed by calculating the area under the receiver operating charact...