Diagnostic test accuracy of anti-glycopeptidolipid-core IgA antibodies for Mycobacterium avium complex pulmonary disease: systematic review and meta-analysis

• Published in: Scientific reports Vol. 6; no. 1; p. 29325
• Main Authors: Shibata, Yuji, Horita, Nobuyuki, Yamamoto, Masaki, Tsukahara, Toshinori, Nagakura, Hideyuki, Tashiro, Ken, Watanabe, Hiroki, Nagai, Kenjiro, Nakashima, Kentaro, Ushio, Ryota, Ikeda, Misako, Narita, Atsuya, Kanai, Akinori, Sato, Takashi, Kaneko, Takeshi
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 04.07.2016; Nature Publishing Group
• Subjects: 692/53/2421; 692/699/255; Accuracy; Antibodies; Antibodies, Bacterial - blood; Antigens, Bacterial - immunology; Diagnostic Errors - prevention & control; Diagnostic tests; Diagnostic Tests, Routine - methods; Disease; Enzymes; Glycoconjugates - immunology; Humanities and Social Sciences; Humans; Immunoglobulin A - blood; Lung Diseases - diagnosis; Meta-analysis; multidisciplinary; Mycobacterium avium Complex - immunology; Mycobacterium avium-intracellulare Infection - diagnosis; Predictive Value of Tests; Reference Standards; Reproducibility of Results; Science; Sensitivity and Specificity; Systematic review; Tuberculosis; Japan
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/srep29325

Currently, an anti-glycopeptidolipid (GPL)-core IgA antibody assay kit for diagnosing Mycobacterium avium complex (MAC) is commercially available. We conducted this systematic review and meta-analysis to reveal the precise diagnostic accuracy of anti-GPL-core IgA antibodies for MAC pulmonary disease (MAC-PD). We systematically searched reports that could provide data for both sensitivity and specificity by anti-GPL-core IgA antibody for clinically diagnosed MAC-PD. Diagnostic test accuracy was estimated using the bivariate model. Of the 257 articles that we had found through primary search, we finally included 16 reports consisted of 1098 reference positive subjects and 2270 reference negative subjects. The diagnostic odds ratio was 24.8 (95% CI 11.6–52.8, I 2  = 5.5%) and the area under the hierarchical summary receiver operating characteristic curves was 0.873 (95% CI 0.837–0.913). With a cutoff value of 0.7 U/mL, the summary estimates of sensitivity and specificity were 0.696 (95% CI 0.621–0.761) and 0.906 (95% CI 0.836–0.951), respectively. The positive and negative likelihood ratios were 7.4 (95% CI 4.1–13.8) and 0.34 (95% CI 0.26–0.43), respectively. The demanding clinical diagnostic criteria may be a cause of false positive of the index test. The index test had good overall diagnostic accuracy and was useful to ruling in MAC-PD with the cutoff value.