CDKL5 deficiency disorder: Relationship between genotype, epilepsy, cortical visual impairment, and development

被引:109
作者
Demarest, Scott T. [1 ,2 ,3 ,4 ,5 ]
Olson, Heather E. [6 ]
Moss, Angela [2 ]
Pestana-Knight, Elia [7 ,8 ,9 ]
Zhang, Xiaoming [7 ,8 ,9 ]
Parikh, Sumit [9 ,10 ]
Swanson, Lindsay C. [6 ]
Riley, Katherine D. [6 ]
Bazin, Grace A. [6 ]
Angione, Katie [1 ,3 ]
Niestroj, Lisa-Marie [11 ]
Lai, Dennis [7 ,9 ,11 ,12 ,13 ,14 ]
Juarez-Colunga, Elizabeth [2 ,15 ]
Benke, Tim A. [1 ,3 ,4 ,5 ,16 ,17 ]
机构
[1] Childrens Hosp Colorado, Aurora, CO USA
[2] Adult & Child Consortium Hlth Outcomes Res & Deli, Aurora, CO USA
[3] Univ Colorado, Sch Med, Aurora, CO USA
[4] Colorado Sch Publ Hlth, Dept Pediat, Aurora, CO USA
[5] Colorado Sch Publ Hlth, Dept Neurol, Aurora, CO USA
[6] Boston Childrens Hosp, Dept Neurol, Div Epilepsy & Clin Neurophysiol, Boston, MA USA
[7] Cleveland Clin, Epiiepsy Ctr, Neurol Inst, Cleveland, OH 44106 USA
[8] Lerner Res Inst, Dept Neurol, Cleveland, OH USA
[9] Lerner Res Inst, Gen Med Inst, Cleveland, OH USA
[10] Lerner Res Inst, Dept Neurogenet, Cleveland, OH USA
[11] Univ Cologne, Cologne Ctr Genom, Cologne, Germany
[12] Cleveland Clin Childrens, Cleveland, OH USA
[13] Stanley Ctr Psychiat Res, Cambridge, MA USA
[14] Broad Inst Massachusetts, Inst Technol & Harvard, Cambridge, MA USA
[15] Colorado Sch Publ Hlth, Dept Biostat & Informat, Aurora, CO USA
[16] Colorado Sch Publ Hlth, Dept Pharmacol, Aurora, CO USA
[17] Colorado Sch Publ Hlth, Dept Otolaryngol, Aurora, CO USA
关键词
CDKL5 deficiency disorder; cortical visual impairment; hypermotor-tonic-spasms sequence; hypsarrhythmia; spasms; FUNCTIONAL ABILITIES; INFANTILE SPASMS; MUTATIONS; PHENOTYPE; CHILDREN; ONSET; HYPSARRHYTHMIA; VARIANTS; FEATURES;
D O I
10.1111/epi.16285
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective The cyclin-dependent kinase like 5 (CDKL5) gene is a known cause of early onset developmental and epileptic encephalopathy, also known as CDKL5 deficiency disorder (CDD). We sought to (1) provide a description of seizure types in patients with CDD, (2) provide an assessment of the frequency of seizure-free periods and cortical visual impairment (CVI), (3) correlate these features with genotype and gender, and (4) correlate these features with developmental milestones. Methods This is a cohort study of patients with CDD. Phenotypic features were explored and correlated with gene variant grouping and gender. A developmental score was created based on achieving seven primary milestones. Phenotypic variables were correlated with the developmental score to explore markers of better developmental outcomes. Multivariate linear regression was used to account for age at last visit. Results Ninety-two patients with CDD were seen during the enrollment period. Eighteen were male (19%); median age at last visit was 5 years (interquartile range = 2.0-11.0). Eighty-one percent of patients developed epileptic spasms, but only 47% of those also had hypsarrhythmia. Previously described hypermotor-tonic-spasms sequence was seen in only 24% of patients, but 56% of patients had seizures with multiple phases (often tonic and spasms). Forty-three percent of patients experienced a seizure-free period ranging from 1 to >12 months, but only 6% were still seizure-free at the last visit. CVI was present in 75% of all CDD patients. None of these features was associated with genotype group or gender. CVI was correlated with reduced milestone achievement after adjusting for age at last visit and a history of hypsarrhythmia. Significance The most common seizure types in CDD are epileptic spasms (often without hypsarrhythmia) and tonic seizures that may cluster together. CVI is a common feature in CDD and is correlated with achieving fewer milestones.
引用
收藏
页码:1733 / 1742
页数:10
相关论文
共 35 条
[1]   CDKL5-Related Disorders: From Clinical Description to Molecular Genetics [J].
Bahi-Buisson, N. ;
Bienvenu, T. .
MOLECULAR SYNDROMOLOGY, 2011, 2 (3-5) :137-152
[2]   Key clinical features to identify girls with CDKL5 mutations [J].
Bahi-Buisson, Nadia ;
Nectoux, Juliette ;
Rosas-Vargas, Haydee ;
Milh, Mathieu ;
Boddaert, Nathalie ;
Girard, Benoit ;
Cances, Claude ;
Ville, Dorothee ;
Afenjar, Alexandra ;
Rio, Marlene ;
Heron, Delphine ;
Morel, Marie Ange N'Guyen ;
Arzimanoglou, Alexis ;
Philippe, Christophe ;
Jonveaux, Philippe ;
Chelly, Jamel ;
Bienvenu, Thierry .
BRAIN, 2008, 131 :2647-2661
[3]   The three stages of epilepsy in patients with CDKL5 mutations [J].
Bahi-Buisson, Nadia ;
Kaminska, Anna ;
Boddaert, Nathalie ;
Rio, Marlene ;
Afenjar, Alexandra ;
Gerard, Marion ;
Giuliano, Fabienne ;
Motte, Jacques ;
Heron, Delphine ;
Morel, Marie Ange N'Guyen ;
Plouin, Perrine ;
Richelme, Christian ;
des Portes, Vincent ;
Dulac, Olivier ;
Philippe, Christophe ;
Chiron, Catherine ;
Nabbout, Rima ;
Bienvenu, Thierry .
EPILEPSIA, 2008, 49 (06) :1027-1037
[4]   Recurrent mutations in the CDKL5 gene: Genotype-phenotype relationships [J].
Bahi-Buisson, Nadia ;
Villeneuve, Nathalie ;
Caietta, Emilie ;
Jacquette, Aurelia ;
Maurey, Helene ;
Matthijs, Gert ;
Van Esch, Hilde ;
Delahaye, Andree ;
Moncla, Anne ;
Milh, Mathieu ;
Zufferey, Flore ;
Diebold, Bertrand ;
Bienvenu, Thierry .
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2012, 158A (07) :1612-1619
[5]   Complete remission of childhood-onset epilepsy: stability and prediction over two decades [J].
Berg, Anne T. ;
Rychlik, Karen ;
Levy, Susan R. ;
Testa, Francine M. .
BRAIN, 2014, 137 :3213-3222
[6]   Vision Assessments and Interventions for Infants 0-2 Years at High Risk for Cerebral Palsy: A Systematic Review [J].
Chorna, Olena D. ;
Guzzetta, Andrea ;
Maitre, Nathalie L. .
PEDIATRIC NEUROLOGY, 2017, 76 :3-13
[7]   The impact of hypsarrhythmia on infantile spasms treatment response: Observational cohort study from the National Infantile Spasms Consortium [J].
Demarest, Scott T. ;
Shellhaas, Renee A. ;
Gaillard, William D. ;
Keator, Cynthia ;
Nickels, Katherine C. ;
Hussain, Shaun A. ;
Loddenkemper, Tobias ;
Patel, Anup D. ;
Saneto, Russell P. ;
Wirrell, Elaine ;
Fernandez, Ivan Sanchez ;
Chu, Catherine J. ;
Grinspan, Zachary ;
Wusthoff, Courtney J. ;
Joshi, Sucheta ;
Mohamed, Ismail S. ;
Stafstrom, Carl E. ;
Stack, Cynthia V. ;
Yozawitz, Elissa ;
Bluvstein, Judith S. ;
Singh, Rani K. ;
Knupp, Kelly G. .
EPILEPSIA, 2017, 58 (12) :2098-2103
[8]   Seizure variables and their relationship to genotype and functional abilities in the CDKL5 disorder [J].
Fehr, Stephanie ;
Wong, Kingsley ;
Chin, Richard ;
Williams, Simon ;
de Klerk, Nick ;
Forbes, David ;
Krishnaraj, Rahul ;
Christodoulou, John ;
Downs, Jenny ;
Leonard, Helen .
NEUROLOGY, 2016, 87 (21) :2206-2213
[9]   Functional Abilities in Children and Adults with the CDKL5 Disorder [J].
Fehr, Stephanie ;
Downs, Jenny ;
Ho, Gladys ;
de Klerk, Nick ;
Forbes, David ;
Christodoulou, John ;
Williams, Simon ;
Leonard, Helen .
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2016, 170 (11) :2860-2869
[10]   There is variability in the attainment of developmental milestones in the CDKL5 disorder [J].
Fehr, Stephanie ;
Leonard, Helen ;
Ho, Gladys ;
Williams, Simon ;
de Klerk, Nick ;
Forbes, David ;
Christodoulou, John ;
Downs, Jenny .
JOURNAL OF NEURODEVELOPMENTAL DISORDERS, 2015, 7