Caregiver perspectives on patient-focused drug development for Phelan-McDermid syndrome

被引:5
作者
Gizzo, Luciana [1 ]
Bliss, Geraldine [2 ]
Palaty, Chrystal [3 ]
Kolevzon, Alexander [4 ]
机构
[1] Univ New England, Coll Osteopath Med, Biddeford, ME USA
[2] CureSHANK, Beverly Hills, CA USA
[3] Metaphase Hlth Res Consulting Inc, Vancouver, BC, Canada
[4] Icahn Sch Med Mt Sinai, Seaver Autism Ctr Res & Treatment, Dept Psychiat, One Gustave L Levy Pl,Box 1230, New York, NY 10029 USA
关键词
Phelan-McDermid syndrome; PMS; SHANK3; Autism spectrum disorder; ASD; Drug development; Caregiver perspective;
D O I
10.1186/s13023-024-03141-w
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background Phelan-McDermid syndrome (PMS) is a neurodevelopmental disorder caused by SHANK3 haploinsufficiency with clinical manifestations that can be devastating and profoundly affect quality of life.Results The Externally Led Patient-Focused Drug Development (EL-PFDD) meeting was an opportunity for families affected by PMS to share with the Food and Drug Administration (FDA) how symptoms impact their lives and how treatments could be most meaningful. The Voice of the Patient report serves as a summary of this meeting to influence upcoming drug development and clinical trials. The purpose of this report is to provide a clinical perspective on the results of the EL-PFDD meeting to amplify the voice of these caregivers to the scientific community.Conclusions Caregivers prioritize an improved quality of life for their loved ones characterized by improved cognitive function, improved communication, increased independence, and reduced risk of regression. With these caregiver priorities in mind, this report provides the FDA and the scientific community with a clear understanding of which aspects of PMS should influence the development of future therapeutics.
引用
收藏
页数:8
相关论文
共 24 条
[1]  
[Anonymous], 2021, Lake Forest
[2]   Subacute Neuropsychiatric Syndrome in Girls With SHANK3 Mutations Responds to Immunomodulation [J].
Bey, Alexandra L. ;
Gorman, Mark P. ;
Gallentine, William ;
Kohlenberg, Teresa M. ;
Frankovich, Jennifer ;
Jiang, Yong-hui ;
Van Haren, Keith .
PEDIATRICS, 2020, 145 (02)
[3]  
Bliss G, 2023, Phelan-McDermid syndrome voice of the patient report
[4]   Sleep Disturbances in Individuals With Phelan-McDermid Syndrome: Correlation With Caregivers' Sleep Quality and Daytime Functioning [J].
Bro, Della ;
O'Hara, Ruth ;
Primeau, Michelle ;
Hanson-Kahn, Andrea ;
Hallmayer, Joachim ;
Bernstein, Jonathan A. .
SLEEP, 2017, 40 (02)
[5]   Efficacy and Safety of Q10 Ubiquinol With Vitamins B and E in Neurodevelopmental Disorders: A Retrospective Chart Review [J].
Cucinotta, Francesca ;
Ricciardello, Arianna ;
Turriziani, Laura ;
Mancini, Arianna ;
Keller, Roberto ;
Sacco, Roberto ;
Persico, Antonio M. .
FRONTIERS IN PSYCHIATRY, 2022, 13
[6]   Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders [J].
Durand, Christelle M. ;
Betancur, Catalina ;
Boeckers, Tobias M. ;
Bockmann, Juergen ;
Chaste, Pauline ;
Fauchereau, Fabien ;
Nygren, Gudrun ;
Rastam, Maria ;
Gillberg, I. Carina ;
Anckarsater, Henrik ;
Sponheim, Eili ;
Goubran-Botros, Hany ;
Delorme, Richard ;
Chabane, Nadia ;
Mouren-Simeoni, Marie-Christine ;
de Mas, Philippe ;
Bieth, Eric ;
Roge, Bernadette ;
Heron, Delphine ;
Burglen, Lydie ;
Gillberg, Christopher ;
Leboyer, Marion ;
Bourgeron, Thomas .
NATURE GENETICS, 2007, 39 (01) :25-27
[7]   Psychiatric illness and regression in individuals with Phelan-McDermid syndrome [J].
Kohlenberg, Teresa M. ;
Trelles, M. Pilar ;
McLarney, Brittany ;
Betancur, Catalina ;
Thurm, Audrey ;
Kolevzon, Alexander .
JOURNAL OF NEURODEVELOPMENTAL DISORDERS, 2020, 12 (01)
[8]   Clinical trial of insulin-like growth factor-1 in Phelan-McDermid syndrome [J].
Kolevzon, A. ;
Breen, M. S. ;
Siper, P. M. ;
Halpern, D. ;
Frank, Y. ;
Rieger, H. ;
Weismann, J. ;
Trelles, M. P. ;
Lerman, B. ;
Rapaport, R. ;
Buxbaum, J. D. .
MOLECULAR AUTISM, 2022, 13 (01)
[9]   Neuropsychiatric decompensation in adolescents and adults with Phelan-McDermid syndrome: a systematic review of the literature [J].
Kolevzon, Alexander ;
Delaby, Elsa ;
Berry-Kravis, Elizabeth ;
Buxbaum, Joseph D. ;
Betancur, Catalina .
MOLECULAR AUTISM, 2019, 10 (01)
[10]   A pilot controlled trial of insulin-like growth factor-1 in children with Phelan-McDermid syndrome [J].
Kolevzon, Alexander ;
Bush, Lauren ;
Wang, A. Ting ;
Halpern, Danielle ;
Frank, Yitzchak ;
Grodberg, David ;
Rapaport, Robert ;
Tavassoli, Teresa ;
Chaplin, William ;
Soorya, Latha ;
Buxbaum, Joseph D. .
MOLECULAR AUTISM, 2014, 5