PT  - JOURNAL ARTICLE
AU  - R.A. Stockley
AU  - E.J. Campbell
TI  - Alpha‐1‐antitrypsin genotyping with mouthwash specimens
AID  - 10.1183/09031936.01.17303560
DP  - 2001 Mar 01
TA  - European Respiratory Journal
PG  - 356--359
VI  - 17
IP  - 3
4099  - http://erj.ersjournals.com/content/17/3/356.short
4100  - http://erj.ersjournals.com/content/17/3/356.full
SO  - Eur Respir J2001 Mar 01; 17
AB  - α1‐antitrypsin (α1‐AT) deficiency is diagnosed as a two-stage procedure (concentration and phenotype). However the latter does not provide clues to the presence of null genes without family studies and obtaining blood from patients at a distance often proves difficult. The aim of the study was to assess the feasibility of genotyping α1‐AT using buccal cells.Mouthwash specimens were sent by 84 patients (with a variety of phenotypes of α1‐antitrypsin) through the post. Deoxyribonucleic acid (DNA) was isolated from buccal cells in each sample and subjected to polymerase chain reaction (PCR) using a genotyping kit to detect the S and Z alleles.Eighty-three of 84 samples received were suitable for amplification. The specific primers successfully identified the S and Z alleles in each case. However, five of the 35 samples obtained from patients thought to be Z allele homozygotes were found to be heterozygotes for another severe deficiency allele.These data confirm the feasibility of “at distance” testing for α1‐antitrypsin deficiency alleles using buccal cells from mouthwash samples. The results raise the possibility that other deficiency alleles are more common than has previously been suspected.This project was part of the ADAPT programme funded through a noncommercial grant by Bayer Corporation USA. Asta/Zeneca Diagnostics provided reagents.