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The Capital Region of Denmark - a part of Copenhagen University Hospital

Protocol for the EARCO Registry: a pan-European observational study in patients with α1-antitrypsin deficiency

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  • Timm Greulich
  • Alan Altraja
  • Miriam Barrecheguren
  • Robert Bals
  • Jan Chlumsky
  • Joanna Chorostowska-Wynimko
  • Christian Clarenbach
  • Luciano Corda
  • Angelo Guido Corsico
  • Ilaria Ferrarotti
  • Cristina Esquinas
  • Caroline Gouder
  • Ana Hećimović
  • Aleksandra Ilic
  • Yavor Ivanov
  • Sabina Janciauskiene
  • Wim Janssens
  • Malcolm Kohler
  • Alvils Krams
  • Beatriz Lara
  • Ravi Mahadeva
  • Gerry McElvaney
  • Jean-François Mornex
  • Karen O'Hara
  • David Parr
  • Eava Piitulainen
  • Karin Schmid-Scherzer
  • Niels Seersholm
  • Robert A Stockley
  • Jan Stolk
  • Maria Sucena
  • Hanan Tanash
  • Alice Turner
  • Ruxandra Ulmeanu
  • Marion Wilkens
  • Arzu Yorgancioğlu
  • Ana Zaharie
  • Marc Miravitlles
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Rationale and objectives: Alpha-1 antitrypsin deficiency (AATD) is a genetic condition that leads to an increased risk of emphysema and liver disease. Despite extensive investigation, there remain unanswered questions concerning the natural history, pathophysiology, genetics and the prognosis of the lung disease in association with AATD. The European Alpha-1 Clinical Research Collaboration (EARCO) is designed to bring together researchers from European countries and to create a standardised database for the follow-up of patients with AATD.

Study design and population: The EARCO Registry is a non-interventional, multicentre, pan-European, longitudinal observational cohort study enrolling patients with AATD. Data will be collected prospectively without interference/modification of patient's management by the study team. The major inclusion criterion is diagnosed severe AATD, defined by an AAT serum level <11 µM (50 mg·dL-1) and/or a proteinase inhibitor genotype ZZ, SZ or compound heterozygotes or homozygotes of other rare deficient variants. Assessments at baseline and during the yearly follow-up visits include lung function testing (spirometry, body plethysmography and diffusing capacity of the lung), exercise capacity, blood tests and questionnaires (symptoms, quality of life and physical activity). To ensure correct data collection, there will be designated investigator staff to document the data in the case report form. All data will be reviewed by the EARCO database manager.

Summary: The EARCO Registry aims to understand the natural history and prognosis of AATD better with the goal to create and validate prognostic tools to support medical decision-making.

Original languageEnglish
JournalERJ Open Research
Issue number1
Publication statusPublished - 2 Mar 2020

ID: 61916079