Literature DB >> 27836958

European Respiratory Society guidelines for the diagnosis of primary ciliary dyskinesia.

Jane S Lucas1,2, Angelo Barbato3, Samuel A Collins4,2, Myrofora Goutaki5,6, Laura Behan4,2, Daan Caudri7,8, Sharon Dell9,10, Ernst Eber11, Estelle Escudier12,13, Robert A Hirst14, Claire Hogg15, Mark Jorissen16, Philipp Latzin6, Marie Legendre12,13, Margaret W Leigh17, Fabio Midulla18, Kim G Nielsen19, Heymut Omran20, Jean-Francois Papon21,22, Petr Pohunek23, Beatrice Redfern24, David Rigau25, Bernhard Rindlisbacher26, Francesca Santamaria27, Amelia Shoemark15, Deborah Snijders3, Thomy Tonia5, Andrea Titieni20, Woolf T Walker4,2, Claudius Werner20, Andrew Bush15, Claudia E Kuehni5.   

Abstract

The diagnosis of primary ciliary dyskinesia is often confirmed with standard, albeit complex and expensive, tests. In many cases, however, the diagnosis remains difficult despite the array of sophisticated diagnostic tests. There is no "gold standard" reference test. Hence, a Task Force supported by the European Respiratory Society has developed this guideline to provide evidence-based recommendations on diagnostic testing, especially in light of new developments in such tests, and the need for robust diagnoses of patients who might enter randomised controlled trials of treatments. The guideline is based on pre-defined questions relevant for clinical care, a systematic review of the literature, and assessment of the evidence using the GRADE (Grading of Recommendations, Assessment, Development and Evaluation) approach. It focuses on clinical presentation, nasal nitric oxide, analysis of ciliary beat frequency and pattern by high-speed video-microscopy analysis, transmission electron microscopy, genotyping and immunofluorescence. It then used a modified Delphi survey to develop an algorithm for the use of diagnostic tests to definitively confirm and exclude the diagnosis of primary ciliary dyskinesia; and to provide advice when the diagnosis was not conclusive. Finally, this guideline proposes a set of quality criteria for future research on the validity of diagnostic methods for primary ciliary dyskinesia.
Copyright ©ERS 2017.

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Year:  2017        PMID: 27836958      PMCID: PMC6054534          DOI: 10.1183/13993003.01090-2016

Source DB:  PubMed          Journal:  Eur Respir J        ISSN: 0903-1936            Impact factor:   16.671


  117 in total

1.  Systematic Analysis of CCNO Variants in a Defined Population: Implications for Clinical Phenotype and Differential Diagnosis.

Authors:  Israel Amirav; Julia Wallmeier; Niki T Loges; Tabea Menchen; Petra Pennekamp; Huda Mussaffi; Revital Abitbul; Avraham Avital; Lea Bentur; Gerard W Dougherty; Elias Nael; Moran Lavie; Heike Olbrich; Claudius Werner; Chris Kintner; Heymut Omran
Journal:  Hum Mutat       Date:  2016-02-04       Impact factor: 4.878

2.  Management of primary ciliary dyskinesia in European children: recommendations and clinical practice.

Authors:  Marie-Pierre F Strippoli; Thomas Frischer; Angelo Barbato; Deborah Snijders; Elisabeth Maurer; Jane S A Lucas; Ernst Eber; Bulent Karadag; Petr Pohunek; Zorica Zivkovic; Amparo Escribano; Chris O'Callaghan; Andrew Bush; Claudia E Kuehni
Journal:  Eur Respir J       Date:  2012-01-26       Impact factor: 16.671

3.  Nasal NO: normal values in children age 6 through to 17 years.

Authors:  V M D Struben; M H Wieringa; C J Mantingh; C Bommeljé; M Don; L Feenstra; J C de Jongste
Journal:  Eur Respir J       Date:  2005-09       Impact factor: 16.671

4.  A new tool improves diagnostic test performance for transmission em evaluation of axonemal dynein arms.

Authors:  W Keith Funkhouser; Marc Niethammer; Johnny L Carson; Kimberlie A Burns; Michael R Knowles; Margaret W Leigh; Maimoona A Zariwala; William K Funkhouser
Journal:  Ultrastruct Pathol       Date:  2013-08-19       Impact factor: 1.094

5.  CCDC39 is required for assembly of inner dynein arms and the dynein regulatory complex and for normal ciliary motility in humans and dogs.

Authors:  Anne-Christine Merveille; Erica E Davis; Anita Becker-Heck; Marie Legendre; Israel Amirav; Géraldine Bataille; John Belmont; Nicole Beydon; Frédéric Billen; Annick Clément; Cécile Clercx; André Coste; Rachelle Crosbie; Jacques de Blic; Stephane Deleuze; Philippe Duquesnoy; Denise Escalier; Estelle Escudier; Manfred Fliegauf; Judith Horvath; Kent Hill; Mark Jorissen; Jocelyne Just; Andreas Kispert; Mark Lathrop; Niki Tomas Loges; June K Marthin; Yukihide Momozawa; Guy Montantin; Kim G Nielsen; Heike Olbrich; Jean-François Papon; Isabelle Rayet; Gilles Roger; Miriam Schmidts; Henrique Tenreiro; Jeffrey A Towbin; Diana Zelenika; Hanswalter Zentgraf; Michel Georges; Anne-Sophie Lequarré; Nicholas Katsanis; Heymut Omran; Serge Amselem
Journal:  Nat Genet       Date:  2010-12-05       Impact factor: 38.330

6.  Zebrafish Ciliopathy Screen Plus Human Mutational Analysis Identifies C21orf59 and CCDC65 Defects as Causing Primary Ciliary Dyskinesia.

Authors:  Christina Austin-Tse; Jan Halbritter; Maimoona A Zariwala; Renée M Gilberti; Heon Yung Gee; Nathan Hellman; Narendra Pathak; Yan Liu; Jennifer R Panizzi; Ramila S Patel-King; Douglas Tritschler; Raqual Bower; Eileen O'Toole; Jonathan D Porath; Toby W Hurd; Moumita Chaki; Katrina A Diaz; Stefan Kohl; Svjetlana Lovric; Daw-Yang Hwang; Daniela A Braun; Markus Schueler; Rannar Airik; Edgar A Otto; Margaret W Leigh; Peadar G Noone; Johnny L Carson; Stephanie D Davis; Jessica E Pittman; Thomas W Ferkol; Jeffry J Atkinson; Kenneth N Olivier; Scott D Sagel; Sharon D Dell; Margaret Rosenfeld; Carlos E Milla; Niki T Loges; Heymut Omran; Mary E Porter; Stephen M King; Michael R Knowles; Iain A Drummond; Friedhelm Hildebrandt
Journal:  Am J Hum Genet       Date:  2013-10-03       Impact factor: 11.025

7.  Rapid diagnosis of primary ciliary dyskinesia: cell culture and soft computing analysis.

Authors:  Massimo Pifferi; Andrew Bush; Francesca Montemurro; Giovanni Pioggia; Martina Piras; Gennaro Tartarisco; Maria Di Cicco; Iolanda Chinellato; Angela M Cangiotti; Attilio L Boner
Journal:  Eur Respir J       Date:  2012-08-16       Impact factor: 16.671

8.  Mutations in DNAH5 account for only 15% of a non-preselected cohort of patients with primary ciliary dyskinesia.

Authors:  M Failly; L Bartoloni; A Letourneau; A Munoz; E Falconnet; C Rossier; M M de Santi; F Santamaria; O Sacco; C D DeLozier-Blanchet; R Lazor; J-L Blouin
Journal:  J Med Genet       Date:  2009-04       Impact factor: 6.318

9.  RPGR mutations might cause reduced orientation of respiratory cilia.

Authors:  Zuzanna Bukowy-Bieryłło; Ewa Ziętkiewicz; Niki Tomas Loges; Mariana Wittmer; Maciej Geremek; Heike Olbrich; Manfred Fliegauf; Katarzyna Voelkel; Ewa Rutkiewicz; Jonathan Rutland; Lucy Morgan; Andrzej Pogorzelski; James Martin; Eric Haan; Wolfgang Berger; Heymut Omran; Michał Witt
Journal:  Pediatr Pulmonol       Date:  2012-08-06

10.  Primary ciliary dyskinesia associated with normal axoneme ultrastructure is caused by DNAH11 mutations.

Authors:  Georg C Schwabe; Katrin Hoffmann; Niki Tomas Loges; Daniel Birker; Colette Rossier; Margherita M de Santi; Heike Olbrich; Manfred Fliegauf; Mike Failly; Uta Liebers; Mirella Collura; Gerhard Gaedicke; Stefan Mundlos; Ulrich Wahn; Jean-Louis Blouin; Bodo Niggemann; Heymut Omran; Stylianos E Antonarakis; Lucia Bartoloni
Journal:  Hum Mutat       Date:  2008-02       Impact factor: 4.878

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  119 in total

Review 1.  Genetic Basis for Congenital Heart Disease: Revisited: A Scientific Statement From the American Heart Association.

Authors:  Mary Ella Pierpont; Martina Brueckner; Wendy K Chung; Vidu Garg; Ronald V Lacro; Amy L McGuire; Seema Mital; James R Priest; William T Pu; Amy Roberts; Stephanie M Ware; Bruce D Gelb; Mark W Russell
Journal:  Circulation       Date:  2018-11-20       Impact factor: 29.690

2.  Mutations in DNAH17, Encoding a Sperm-Specific Axonemal Outer Dynein Arm Heavy Chain, Cause Isolated Male Infertility Due to Asthenozoospermia.

Authors:  Marjorie Whitfield; Lucie Thomas; Emilie Bequignon; Alain Schmitt; Laurence Stouvenel; Guy Montantin; Sylvie Tissier; Philippe Duquesnoy; Bruno Copin; Sandra Chantot; Florence Dastot; Catherine Faucon; Anne Laure Barbotin; Anne Loyens; Jean-Pierre Siffroi; Jean-François Papon; Estelle Escudier; Serge Amselem; Valérie Mitchell; Aminata Touré; Marie Legendre
Journal:  Am J Hum Genet       Date:  2019-06-06       Impact factor: 11.025

3.  A Novel Homozygous Nonsense HYDIN Gene Mutation p.(Arg951*) in Primary Ciliary Dyskinesia.

Authors:  Antony Terance Benjamin; Ram Ganesh; Balan Louis Gaspar; Jane Lucas; Claire Jackson; Marie Legendre; Rahma Mani; Estelle Escudier
Journal:  Indian J Pediatr       Date:  2019-05-14       Impact factor: 1.967

4.  Summary for Clinicians: Diagnosis of Primary Ciliary Dyskinesia.

Authors:  Michael G O'Connor; Anne Griffiths; Narayan P Iyer; Adam J Shapiro; Kevin C Wilson; Carey C Thomson
Journal:  Ann Am Thorac Soc       Date:  2019-02

5.  Proof of Concept: Very Rapid Tidal Breathing Nasal Nitric Oxide Sampling Discriminates Primary Ciliary Dyskinesia from Healthy Subjects.

Authors:  Mathias G Holgersen; June K Marthin; Kim G Nielsen
Journal:  Lung       Date:  2019-02-14       Impact factor: 2.584

Review 6.  Seeing cilia: imaging modalities for ciliary motion and clinical connections.

Authors:  Jacelyn E Peabody; Ren-Jay Shei; Brent M Bermingham; Scott E Phillips; Brett Turner; Steven M Rowe; George M Solomon
Journal:  Am J Physiol Lung Cell Mol Physiol       Date:  2018-03-01       Impact factor: 5.464

7.  Ciliary Feature Counter: A program for the Quantitative Assessment of Cilia to Diagnose Primary Ciliary Dyskinesia.

Authors:  Andreia L Pinto; Ranjit K Rai; Claire Hogg; Thomas Burgoyne
Journal:  Diagnostics (Basel)       Date:  2020-07-28

8.  Mutations in C11orf70 Cause Primary Ciliary Dyskinesia with Randomization of Left/Right Body Asymmetry Due to Defects of Outer and Inner Dynein Arms.

Authors:  Inga M Höben; Rim Hjeij; Heike Olbrich; Gerard W Dougherty; Tabea Nöthe-Menchen; Isabella Aprea; Diana Frank; Petra Pennekamp; Bernd Dworniczak; Julia Wallmeier; Johanna Raidt; Kim G Nielsen; Maria C Philipsen; Francesca Santamaria; Laura Venditto; Israel Amirav; Huda Mussaffi; Freerk Prenzel; Kaman Wu; Zeineb Bakey; Miriam Schmidts; Niki T Loges; Heymut Omran
Journal:  Am J Hum Genet       Date:  2018-05-03       Impact factor: 11.025

9.  C11orf70 Mutations Disrupting the Intraflagellar Transport-Dependent Assembly of Multiple Axonemal Dyneins Cause Primary Ciliary Dyskinesia.

Authors:  Mahmoud R Fassad; Amelia Shoemark; Pierrick le Borgne; France Koll; Mitali Patel; Mellisa Dixon; Jane Hayward; Charlotte Richardson; Emily Frost; Lucy Jenkins; Thomas Cullup; Eddie M K Chung; Michel Lemullois; Anne Aubusson-Fleury; Claire Hogg; David R Mitchell; Anne-Marie Tassin; Hannah M Mitchison
Journal:  Am J Hum Genet       Date:  2018-05-03       Impact factor: 11.025

10.  Diagnosis of Primary Ciliary Dyskinesia. An Official American Thoracic Society Clinical Practice Guideline.

Authors:  Adam J Shapiro; Stephanie D Davis; Deepika Polineni; Michele Manion; Margaret Rosenfeld; Sharon D Dell; Mark A Chilvers; Thomas W Ferkol; Maimoona A Zariwala; Scott D Sagel; Maureen Josephson; Lucy Morgan; Ozge Yilmaz; Kenneth N Olivier; Carlos Milla; Jessica E Pittman; M Leigh Anne Daniels; Marcus Herbert Jones; Ibrahim A Janahi; Stephanie M Ware; Sam J Daniel; Matthew L Cooper; Lawrence M Nogee; Billy Anton; Tori Eastvold; Lynn Ehrne; Elena Guadagno; Michael R Knowles; Margaret W Leigh; Valery Lavergne
Journal:  Am J Respir Crit Care Med       Date:  2018-06-15       Impact factor: 21.405

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