α1-antitrypsin deficiency (AATD) remains the only readily identified genetic cause of chronic obstructive pulmonary disease (COPD). Furthermore, there is growing evidence that even a moderate deficiency increases the risk of lung disease among smokers. Despite these facts, the uptake of testing for AATD in at-risk populations remains low for many reasons, and a lack of clarity among clinicians regarding the most appropriate diagnostic techniques presents a major deterrent.
This 2019 guide for α1-antitrypsin deficiency testing addresses the benefits of A1AT diagnosis, the technical basis of the available diagnostic methods. AAT phenotyping by isolectric focusing is part of the available diagnostic methods and it allows detection of multiple variants of AAT in one assay.
The topics covered should equip clinicians with the core knowledge required to confidently assess patients for AATD and increase the number of AATD testing.
Alpha 1-Antitrypsin (A1AT) Phenotype Testing
The gold standard assay for the alpha 1-antitrypsin (A1AT) phenotype testing.
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