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Perspective

PredictAAT: Accounting for Inflammation in the Diagnosis of Alpha 1 Antitrypsin Deficiency

Pages 619-622 | Received 27 Jul 2020, Accepted 10 Aug 2020, Published online: 30 Aug 2020

Figures & data

Figure 1. AAT level distribution according to genotype (PI*MM, PI*MS and PI*MZ) in those with (dashed lines) and without (solid lines) the presence of inflammation, defined as CRP ≥5 mg/L and <5 mg/dL, respectively.

Reproduced from Sanders, Ponte and Kueppers. COPD 2018;15:10-16 [Citation6]

Figure 1. AAT level distribution according to genotype (PI*MM, PI*MS and PI*MZ) in those with (dashed lines) and without (solid lines) the presence of inflammation, defined as CRP ≥5 mg/L and <5 mg/dL, respectively.Reproduced from Sanders, Ponte and Kueppers. COPD 2018;15:10-16 [Citation6]

Figure 2. Changes in AAT levels of serum following the intravenous injection of 0.2 ml typhoid-paratyphoid vaccine (arrow) in the genetically different individuals. Homozygotes for common gene: solid line, heterozygotes for AATD gene: dashed line, homozygotes for deficiency gene: dotted line. At the right: standard error of the method.

Reproduced from Kueppers, Humangenetik 1968;6:207-14 [Citation14]

Figure 2. Changes in AAT levels of serum following the intravenous injection of 0.2 ml typhoid-paratyphoid vaccine (arrow) in the genetically different individuals. Homozygotes for common gene: solid line, heterozygotes for AATD gene: dashed line, homozygotes for deficiency gene: dotted line. At the right: standard error of the method.Reproduced from Kueppers, Humangenetik 1968;6:207-14 [Citation14]

Table 1. Comparison of observed and adjusted AAT levels calculated using the algorithm in the Sanders et al. cohort [Citation6].