Prevalence of Congenital Ocular Anomalies in 15 Countries of Europe: Results From the Medikeye Study

被引:2
作者
Dubucs, Charlotte [1 ,2 ,3 ]
Caillet, Anthony [1 ]
Fremont, Felix [4 ,5 ]
Delteil, Laurane [1 ]
N'Go, Van [1 ]
Neville, Amanda Julie [6 ]
Ballardini, Elisa [7 ,8 ]
Dolk, Helen [9 ]
Loane, Maria [10 ]
Garne, Ester [11 ]
Khoshnood, Babak [12 ]
Lelong, Nathalie [12 ]
Rissmann, Anke [13 ]
O'Mahony, Mary [14 ]
Pierini, Anna [15 ]
Gatt, Miriam [16 ]
Bergman, Jorieke [17 ]
Krawczynski, Maciej Robert [18 ]
Bielenska, Anna Latos [18 ]
de Garibay, Luis Javier Echevarria Gonzalez [19 ]
Cavero-Carbonell, Clara [20 ]
Addor, Marie-Claude [21 ]
Tucker, David [22 ]
Jordan, Sue [23 ]
Den Hond, Elly [24 ]
Nelen, Vera [24 ]
Barisic, Ingeborg [25 ]
Rouget, Florence [26 ]
Randrianaivo, Hanitra [27 ]
Hoareau, Jonathan [27 ]
Perthus, Isabelle [28 ]
Hurault-Delarue, Caroline [1 ]
Courtade-Saidi, Monique [2 ,3 ]
Damase-Michel, Christine [1 ,29 ]
机构
[1] Univ Toulouse, Unite Pharmacoepidemiol, UMR, CERPOP, Toulouse, France
[2] IUCT Oncopole, Dept Anat & Cytol Pathol, Toulouse, France
[3] Fac St, Dept MMP, Toulouse, France
[4] CHU Toulouse Purpan, Hop Pierre Paul Riquet, Serv Ophtalmol, Toulouse, France
[5] Clin Honore Cave, Montauban, France
[6] Univ Ferrara, Osped Univ Ferrara, Ctr Clin & Epidemiol Res, Cona, Italy
[7] Univ Hosp Ferrara, Neonatal Intens Care Unit, IMER Registry, Emilia Romagna Registry Birth Defects, Ferrara, Italy
[8] Univ Ferrara, Dept Med Sci, Ferrara, Italy
[9] Ulster Univ, Sch Med, Belfast, North Ireland
[10] Ulster Univ, Inst Nursing & Hlth Res, Belfast, North Ireland
[11] Univ Hosp Southern Denmark, Lillebaelt Hosp, Dept Paediat & Adolescent Med, Kolding, Denmark
[12] Hop St Vincent De Paul, INSERM, U953, Paris, France
[13] Otto von Guericke Univ, Med Fac, Malformat Monitoring Ctr Saxony Anhalt, Magdeburg, Germany
[14] St Finbarrs Hosp, Dept Publ Hlth, Cork, Ireland
[15] CNR, Inst Clin Physiol, Unit Epidemiol Rare Dis & CA, Pisa, Italy
[16] Directorate Hlth Informat & Res, Malta CA Register, Pieta, Malta
[17] Univ Groningen, Univ Med Ctr Groningen, Dept Genet, Groningen, Netherlands
[18] Poznan Univ Med Sci, Dept Med Genet, Poznan, Poland
[19] Basque Govt, Vitoria, Spain
[20] Fdn Promot Hlth & Biomed Res Valencian Reg, Rare Dis Res Unit, Valencia, Spain
[21] Ctr Hosp Univ Vaudois CHUV, Univ Ctr Pediat Surg Western Switzerland, Lausanne, Switzerland
[22] Singleton Hosp, Publ Hlth Wales Microbiol, Swansea, W Glam, Wales
[23] Swansea Univ, Fac Med Hlth & Life Sci, Swansea, Wales
[24] Prov Inst Hyg, Antwerp, Belgium
[25] Univ Zagreb, Ctr Excellence Reprod & Regenerat Med, Med Sch, Zagreb, Croatia
[26] Univ Hosp, Dept Neonatol, Rennes, France
[27] Univ Reunion St Pierre, Unit Congenital Malformat, St Clotilde Register Reunion Isl CHU REUN, REMACOR Med Sch, F-59037 Reunion, France
[28] CHU Estaing, Ctr Etud Malformat Congenitales Auvergne, Genet Med, Clermont Ferrand, France
[29] Univ Toulouse, Fac Med, CHU Toulouse, Serv Pharmacol Clin, F-31000 Toulouse, France
关键词
congenital ocular anomalies; descriptive epidemiological study; epidemiology; Europe; ocular defect; GENETICS; CATARACT; GLAUCOMA;
D O I
10.1002/bdr2.2414
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
BackgroundCongenital ocular anomalies (COA) are among the most common causes of visual impairment in children in high-income countries. The aim of the study is to describe the prevalence of the various COA recorded in European population-based registries of CA (EUROCAT) participating in the EUROmediCAT consortium.MethodsData from 19 EUROmediCAT registries and one healthcare database (EFEMERIS) were included in this descriptive epidemiological study. Cases of COA included live births, FD from 20 weeks gestational age (GA), and termination of pregnancy for fetal anomaly.ResultsThe prevalence of total COA was 3.47/10,000 births (95% CI [3.61-3.82]), ranging from 1.41 to 13.46/10,000 depending on the registry. Among COA cases, congenital lens anomalies were the most frequent anomalies (31%), of which over half were single ocular anomalies (presenting with only one ocular anomaly). An/microphthalmia was the second most frequent COA (24%) of which three-quarters were multiply malformed (associated to extraocular major anomalies). Among single COA cases, 58 were prenatally diagnosed (4%), of which, 58% were diagnosed in the second trimester. Known genetic causes of COA explained 2.5%-25% of COA depending on their class.ConclusionsThis is the first European study describing COA. The detailed prevalence data offered in this study could improve screening and early diagnosis of different classes of COA. As COA are rare, epidemiological surveillance of large populations and accurate clinical descriptions are essential.
引用
收藏
页数:16
相关论文
共 35 条
[1]   The genetics of primary open-angle glaucoma: A review [J].
Allingham, R. Rand ;
Liu, Yutao ;
Rhee, Douglas J. .
EXPERIMENTAL EYE RESEARCH, 2009, 88 (04) :837-844
[2]   The Lancet Global Health Commission on Global Eye Health: vision beyond 2020 [J].
Burton, Matthew J. ;
Ramke, Jacqueline ;
Marques, Ana Patricia ;
Bourne, Rupert R. A. ;
Congdon, Nathan ;
Jones, Iain ;
Tong, Brandon A. M. Ah ;
Arunga, Simon ;
Bachani, Damodar ;
Bascaran, Covadonga ;
Bastawrous, Andrew ;
Blanchet, Karl ;
Braithwaite, Tasanee ;
Buchan, John C. ;
Cairns, John ;
Cama, Anasaini ;
Chagunda, Margarida ;
Chuluunkhuu, Chimgee ;
Cooper, Andrew ;
Crofts-Lawrence, Jessica ;
Dean, William H. ;
Denniston, Alastair K. ;
Ehrlich, Joshua R. ;
Emerson, Paul M. ;
Evans, Jennifer R. ;
Frick, Kevin D. ;
Friedman, David S. ;
Furtado, Joao M. ;
Gichangi, Michael M. ;
Gichuhi, Stephen ;
Gilbert, Suzanne S. ;
Gurung, Reeta ;
Habtamu, Esmael ;
Holland, Peter ;
Jonas, Jost B. ;
Keane, Pearse A. ;
Keay, Lisa ;
Khanna, Rohit C. ;
Khaw, Peng Tee ;
Kuper, Hannah ;
Kyari, Fatima ;
Lansingh, Van C. ;
Mactaggart, Islay ;
Mafwiri, Milka M. ;
Mathenge, Wanjiku ;
McCormick, Ian ;
Morjaria, Priya ;
Mowatt, Lizette ;
Muirhead, Debbie ;
Murthy, Gudlavalleti V. S. .
LANCET GLOBAL HEALTH, 2021, 9 (04) :E489-E551
[3]  
Campbell Carrie Lahnstein, 2003, Optometry, V74, P417
[4]  
Campbell H, 2002, J Cancer Epidemiol Prev, V7, P21, DOI 10.1080/14766650252962649
[5]   Epidemiology of anophthalmia and microphthalmia: Prevalence and patterns in Texas, 1999-2009 [J].
Chambers, Tiffany M. ;
Agopian, A. J. ;
Lewis, Richard A. ;
Langlois, Peter H. ;
Danysh, Heather E. ;
Weber, Kari A. ;
Shaw, Gary M. ;
Mitchell, Laura E. ;
Lupo, Philip J. .
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2018, 176 (09) :1810-1818
[6]   Risk factors for primary congenital glaucoma in the National Birth Defects Prevention Study [J].
Forestieri, Nina E. ;
Desrosiers, Tania A. ;
Freedman, Sharon F. ;
Aylsworth, Arthur S. ;
Voltzke, Kristin ;
Olshan, Andrew F. ;
Meyer, Robert E. .
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2019, 179 (09) :1846-1856
[7]   Epidemiology of septo-optic dysplasia with focus on prevalence and maternal age - A EUROCAT study [J].
Garne, Ester ;
Rissmann, Anke ;
Addor, Marie-Claude ;
Barisic, Ingeborg ;
Bergman, Jorieke ;
Braz, Paula ;
Cavero-Carbonell, Clara ;
Draper, Elizabeth S. ;
Gatt, Miriam ;
Haeusler, Martin ;
Klungsoyr, Kari ;
Kurinczuk, Jennifer J. ;
Lelong, Nathalie ;
Luyt, Karen ;
Lynch, Catherine ;
O'Mahony, Mary T. ;
Mokoroa, Olatz ;
Nelen, Vera ;
Neville, Amanda J. ;
Pierini, Anna ;
Randrianaivo, Hanitra ;
Rankin, Judith ;
Rouget, Florence ;
Schaub, Bruno ;
Tucker, David ;
Verellen-Dumoulin, Christine ;
Wellesley, Diana ;
Wiesel, Awi ;
Zymak-Zakutnia, Nataliia ;
Lanzoni, Monica ;
Morris, Joan K. .
EUROPEAN JOURNAL OF MEDICAL GENETICS, 2018, 61 (09) :483-488
[8]   Paper 5: Surveillance of Multiple Congenital Anomalies: Implementation of a Computer Algorithm in European Registers for Classification of Cases [J].
Garne, Ester ;
Dolk, Helen ;
Loane, Maria ;
Wellesley, Diana ;
Barisic, Ingeborg ;
Calzolari, Elisa ;
Densem, James .
BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY, 2011, 91 :S44-S50
[9]   Genetics of syndromic ocular coloboma: CHARGE and COACH syndromes [J].
George, Aman ;
Cogliati, Tiziana ;
Brooks, Brian P. .
EXPERIMENTAL EYE RESEARCH, 2020, 193
[10]   Ocular coloboma: a reassessment in the age of molecular neuroscience [J].
Gregory-Evans, CY ;
Williams, MJ ;
Halford, S ;
Gregory-Evans, K .
JOURNAL OF MEDICAL GENETICS, 2004, 41 (12) :881-891