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Alpha1-antitrypsin deficiency in Greece: Focus on rare variants.
Papiris, S A; Veith, M; Papaioannou, A I; Apollonatou, V; Ferrarotti, I; Ottaviani, S; Tzouvelekis, A; Tzilas, V; Rovina, N; Stratakos, G; Gerogianni, I; Daniil, Z; Kolilekas, L; Dimakou, K; Pitsidianakis, G; Tzanakis, N; Tryfon, S; Fragopoulos, F; Antonogiannaki, E M; Lazaratou, A; Fouka, E; Papakosta, D; Emmanouil, P; Anagnostopoulos, N; Karampitsakos, T; Vlami, K; Kallieri, M; Lyberopoulos, P; Loukides, S; Bouros, D; Bush, A; Balduyck, M; Lombard, C; Cottin, V; Mornex, J F; Vogelmeier, C F; Greulich, T; Manali, E D.
Afiliación
  • Papiris SA; 2nd Pulmonary Medicine Department, Medical School, General University Hospital "Attikon", National and Kapodistrian University of Athens, Greece 1 Rimini Street, Haidari 12462, Greece. Electronic address: papiris@otenet.gr.
  • Veith M; Department of Medicine, Pulmonary and Critical Care Medicine, Member of the German Center for Lung Research (DZL), UKGM, Marburg, Germany.
  • Papaioannou AI; 2nd Pulmonary Medicine Department, Medical School, General University Hospital "Attikon", National and Kapodistrian University of Athens, Greece 1 Rimini Street, Haidari 12462, Greece.
  • Apollonatou V; 2nd Pulmonary Medicine Department, Medical School, General University Hospital "Attikon", National and Kapodistrian University of Athens, Greece 1 Rimini Street, Haidari 12462, Greece.
  • Ferrarotti I; Center for Diagnosis of Inherited Alpha1-antitrypsin Deficiency, Department of Internal Medicine and Therapeutics, Pneumonology Unit, Fondazione IRCCS Policlinico San Matteo, Università di Pavia, Pavia, Italy.
  • Ottaviani S; Center for Diagnosis of Inherited Alpha1-antitrypsin Deficiency, Department of Internal Medicine and Therapeutics, Pneumonology Unit, Fondazione IRCCS Policlinico San Matteo, Università di Pavia, Pavia, Italy.
  • Tzouvelekis A; Department of Respiratory Medicine, General Hospital of Patras, University of Patras, Greece.
  • Tzilas V; 5th Pulmonary Department, Athens Chest Hospital "Sotiria", Athens Greece.
  • Rovina N; 1st Department of Pulmonary Medicine and Intensive Care Unit, Medical School, National and Kapodistrian University of Athens, Athens 115 27, Greece.
  • Stratakos G; 1st Respiratory Medicine Department of the National, Kapodistrian University of Athens, Athens, Greece.
  • Gerogianni I; Department of Respiratory Medicine, Faculty of Medicine, School of Health Sciences, University of Thessaly, Larissa Greece.
  • Daniil Z; Department of Respiratory Medicine, Faculty of Medicine, School of Health Sciences, University of Thessaly, Larissa Greece.
  • Kolilekas L; 7thPulmonary Department, Athens Chest Hospital "Sotiria", Athens Greece.
  • Dimakou K; 5th Pulmonary Department, Athens Chest Hospital "Sotiria", Athens Greece.
  • Pitsidianakis G; Department of Thoracic Medicine, University Hospital, University of Crete, Heraklion, Crete 71110, Greece.
  • Tzanakis N; Department of Thoracic Medicine, University Hospital, University of Crete, Heraklion, Crete 71110, Greece.
  • Tryfon S; General Hospital "G. Papanikolaou", Thessaloniki, Greece.
  • Fragopoulos F; Pulmonary Department, General Hospital of Nicosia, Cyprus.
  • Antonogiannaki EM; 4th Pulmonary Department, Athens Chest Hospital "Sotiria", Athens Greece.
  • Lazaratou A; 2nd Pulmonary Medicine Department, Medical School, General University Hospital "Attikon", National and Kapodistrian University of Athens, Greece 1 Rimini Street, Haidari 12462, Greece.
  • Fouka E; A Department of Pulmonary Medicine, Aristotle University of Thessaloniki, "G. Papanikolaou" Hospital, Exochi, Thessaloniki, Greece.
  • Papakosta D; A Department of Pulmonary Medicine, Aristotle University of Thessaloniki, "G. Papanikolaou" Hospital, Exochi, Thessaloniki, Greece.
  • Emmanouil P; Mediterraneo Hospital, Glyfada, Greece.
  • Anagnostopoulos N; 1st Respiratory Medicine Department of the National, Kapodistrian University of Athens, Athens, Greece.
  • Karampitsakos T; Department of Respiratory Medicine, General Hospital of Patras, University of Patras, Greece.
  • Vlami K; 2nd Pulmonary Medicine Department, Medical School, General University Hospital "Attikon", National and Kapodistrian University of Athens, Greece 1 Rimini Street, Haidari 12462, Greece.
  • Kallieri M; 2nd Pulmonary Medicine Department, Medical School, General University Hospital "Attikon", National and Kapodistrian University of Athens, Greece 1 Rimini Street, Haidari 12462, Greece.
  • Lyberopoulos P; 2nd Pulmonary Medicine Department, Medical School, General University Hospital "Attikon", National and Kapodistrian University of Athens, Greece 1 Rimini Street, Haidari 12462, Greece.
  • Loukides S; 2nd Pulmonary Medicine Department, Medical School, General University Hospital "Attikon", National and Kapodistrian University of Athens, Greece 1 Rimini Street, Haidari 12462, Greece.
  • Bouros D; Iatriko Medical Center, Athens, Greece; School of Medicine, National and Kapodistrian University of Athens, Athens Greece.
  • Bush A; Paediatrics and Paediatric Respirology, Imperial College, Imperial Centre for Paediatrics and Child Health, Royal Brompton Harefield NHS Foundation Trust, London, United Kingdom.
  • Balduyck M; laboratoire de Biochimie et Biologie Moléculaire (HMNO), Centre de Biologie Pathologie, Faculté de pharmacie et EA 7364 RADEME, Laboratoire de Biochimie et Biologie Moléculaire, CHU de Lille, Université de Lille, Lille, France.
  • Lombard C; Laboratoire d'Immunologie, Centre Hospitalier Lyon-Sud, Hospices Civils de Lyon and Université Claude Bernard-Lyon 1, Lyon, France.
  • Cottin V; Service de pneumologie, Centre National Coordinateur de Référence des Maladies Pulmonaires Rares, Hôpital Louis Pradel, Hospices Civils de Lyon, Université de Lyon, Université Claude Bernard Lyon 1, UMR754 INRA, IVPC, Lyon, France.
  • Mornex JF; Service de pneumologie, Centre National Coordinateur de Référence des Maladies Pulmonaires Rares, Hôpital Louis Pradel, Hospices Civils de Lyon, Université de Lyon, Université Claude Bernard Lyon 1, UMR754 INRA, IVPC, Lyon, France.
  • Vogelmeier CF; Department of Medicine, Pulmonary and Critical Care Medicine, Member of the German Center for Lung Research (DZL), UKGM, Marburg, Germany.
  • Greulich T; Department of Medicine, Pulmonary and Critical Care Medicine, Member of the German Center for Lung Research (DZL), UKGM, Marburg, Germany.
  • Manali ED; 2nd Pulmonary Medicine Department, Medical School, General University Hospital "Attikon", National and Kapodistrian University of Athens, Greece 1 Rimini Street, Haidari 12462, Greece.
Pulmonology ; 30(1): 43-52, 2024.
Article en En | MEDLINE | ID: mdl-36797151
PURPOSE: A1Antitrypsin deficiency (AATD) pathogenic mutations are expanding beyond the PI*Z and PI*S to a multitude of rare variants. AIM: to investigate genotype and clinical profile of Greeks with AATD. METHODS: Symptomatic adult-patients with early-emphysema defined by fixed airway obstruction and computerized-tomography scan and lower than normal serum AAT levels were enrolled from reference centers all over Greece. Samples were analyzed in the AAT Laboratory, University of Marburg-Germany. RESULTS: Included are 45 adults, 38 homozygous or compound heterozygous for pathogenic variants and 7 heterozygous. Homozygous were 57.9% male, 65.8% ever-smokers, median (IQR) age 49.0(42.5-58.5) years, AAT-levels 0.20(0.08-0.26) g/L, FEV1(%predicted) 41.5(28.8-64.5). PI*Z, PI*Q0, and rare deficient allele's frequency was 51.3%, 32.9%,15.8%, respectively. PI*ZZ genotype was 36.8%, PI*Q0Q0 21.1%, PI*MdeficientMdeficient 7.9%, PI*ZQ0 18.4%, PI*Q0Mdeficient 5.3% and PI*Zrare-deficient 10.5%. Genotyping by Luminex detected: p.(Pro393Leu) associated with MHeerlen (M1Ala/M1Val); p.(Leu65Pro) with MProcida; p.(Lys241Ter) with Q0Bellingham; p.(Leu377Phefs*24) with Q0Mattawa (M1Val) and Q0Ourem (M3); p.(Phe76del) with MMalton (M2), MPalermo (M1Val), MNichinan (V) and Q0LaPalma (S); p.(Asp280Val) with PLowell (M1Val); PDuarte (M4), YBarcelona (p.Pro39His). Gene-sequencing (46.7%) detected Q0GraniteFalls, Q0Saint-Etienne, Q0Amersfoort(M1Ala), MWürzburg, NHartfordcity and one novel-variant (c.1A>G) named Q0Attikon.Heterozygous included PI*MQ0Amersfoort(M1Ala), PI*MMProcida, PI*Mp.(Asp280Val), PI*MOFeyzin. AAT-levels were significantly different between genotypes (p = 0.002). CONCLUSION: Genotyping AATD in Greece, a multiplicity of rare variants and a diversity of rare combinations, including unique ones were observed in two thirds of patients, expanding knowledge regarding European geographical trend in rare variants. Gene sequencing was necessary for genetic diagnosis. In the future the detection of rare genotypes may add to personalize preventive and therapeutic measures.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Deficiencia de alfa 1-Antitripsina Límite: Adult / Female / Humans / Male / Middle aged País/Región como asunto: Europa Idioma: En Revista: Pulmonology Año: 2024 Tipo del documento: Article Pais de publicación: España

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Deficiencia de alfa 1-Antitripsina Límite: Adult / Female / Humans / Male / Middle aged País/Región como asunto: Europa Idioma: En Revista: Pulmonology Año: 2024 Tipo del documento: Article Pais de publicación: España