- Ortega, Victor E;
- Li, Xingnan;
- O’Neal, Wanda K;
- Lackey, Lela;
- Ampleford, Elizabeth;
- Hawkins, Gregory A;
- Grayeski, Philip J;
- Laederach, Alain;
- Barjaktarevic, Igor;
- Barr, R Graham;
- Cooper, Christopher;
- Couper, David;
- Han, MeiLan K;
- Kanner, Richard E;
- Kleerup, Eric C;
- Martinez, Fernando J;
- Paine, Robert;
- Peters, Stephen P;
- Pirozzi, Cheryl;
- Rennard, Stephen I;
- Woodruff, Prescott G;
- Hoffman, Eric A;
- Meyers, Deborah A;
- Bleecker, Eugene R;
- Alexis, Neil E;
- Anderson, Wayne H;
- Arjomandi, Mehrdad;
- Bateman, Lori A;
- Bhatt, Surya P;
- Boucher, Richard C;
- Bowler, Russell P;
- Christenson, Stephanie A;
- Comellas, Alejandro P;
- Criner, Gerard J;
- Crystal, Ronald G;
- Curtis, Jeffrey L;
- Doerschuk, Claire M;
- Dransfield, Mark T;
- Freeman, Christine M;
- Galban, Craig;
- Hansel, Nadia N;
- Hastie, Annette T;
- Huang, Yvonne;
- Kaner, Robert J;
- Krishnan, Jerry A;
- LaVange, Lisa M;
- Lazarus, Stephen C;
- Moore, Wendy C;
- Paulin, Laura;
- Putcha, Nirupama;
- Oelsner, Elizabeth C;
- Raman, Sanjeev;
- Tashkin, Donald P;
- Wells, J Michael;
- Wise, Robert A
Rationale: The role of PI (protease inhibitor) type Z heterozygotes and additional rare variant genotypes in the gene encoding alpha-1 antitrypsin, SERPINA1 (serpin peptidase inhibitor, clade A, member 1), in determining chronic obstructive pulmonary disease risk and severity is controversial.Objectives: To comprehensively evaluate the effects of rare SERPINA1 variants on lung function and emphysema phenotypes in subjects with significant tobacco smoke exposure using deep gene resequencing and alpha-1 antitrypsin concentrations.Methods: DNA samples from 1,693 non-Hispanic white individuals, 385 African Americans, and 90 Hispanics with ≥20 pack-years smoking were resequenced for the identification of rare variants (allele frequency < 0.05) in 16.9 kB of SERPINA1.Measurements and Main Results: White PI Z heterozygotes confirmed by sequencing (MZ; n = 74) had lower post-bronchodilator FEV1 (P = 0.007), FEV1/FVC (P = 0.003), and greater computed tomography-based emphysema (P = 0.02) compared with 1,411 white individuals without PI Z, S, or additional rare variants denoted as VR. PI Z-containing compound heterozygotes (ZS/ZVR; n = 7) had lower FEV1/FVC (P = 0.02) and forced expiratory flow, midexpiratory phase (P = 0.009). Nineteen white heterozygotes for five non-S/Z coding variants associated with lower alpha-1 antitrypsin had greater computed tomography-based emphysema compared with those without rare variants. In African Americans, a 5' untranslated region insertion (rs568223361) was associated with lower alpha-1 antitrypsin and functional small airway disease (P = 0.007).Conclusions: In this integrative deep sequencing study of SERPINA1 with alpha-1 antitrypsin concentrations in a heavy smoker and chronic obstructive pulmonary disease cohort, we confirmed the effects of PI Z heterozygote and compound heterozygote genotypes. We demonstrate the cumulative effects of multiple SERPINA1 variants on alpha-1 antitrypsin deficiency, lung function, and emphysema, thus significantly increasing the frequency of SERPINA1 variation associated with respiratory disease in at-risk smokers.