Psychiatric and cognitive characteristics of individuals with Danon disease (LAMP2 gene mutation)

被引:20
|
作者
Yardeni, Maya [1 ]
Weisman, Omri [1 ,2 ]
Mandel, Hanna [3 ]
Weinberger, Ronnie [1 ]
Quarta, Giovanni [4 ]
Salazar-Mendiguchia, Joel [5 ,6 ]
Garcia-Pavia, Pablo [7 ]
Jose Lobato-Rodriguez, Maria [8 ]
Fajardo Simon, Lourdes [8 ]
Freimark, Dov [9 ,10 ]
Arad, Michael [9 ,10 ]
Gothelf, Doron [1 ,2 ,10 ]
机构
[1] Edmond & Lily Safra Childrens Hosp, Behav Neurogenet Ctr, Sheba Med Ctr, IL-52621 Tel Hashomer, Israel
[2] Tel Aviv Univ, Sagol Sch Neurosci, Tel Aviv, Israel
[3] Technion Israel Inst Technol, Childrens Hosp, Metab Unit, Rambam Hlth Care Campus, Haifa, Israel
[4] ASST Papa Giovanni XXIII, Cardiol Dept, Bergamo, Italy
[5] Bellvitge Univ Hosp, Heart Failure & Transplant Program, Cardiomyopathy Unit, Barcelona, Spain
[6] Hlth Code, Cardiovasc Genet, La Coruna, Spain
[7] Hosp Univ Puerta de Hierro Majadahonda, Dept Cardiol, Madrid, Spain
[8] Hosp Univ Puerta de Hierro Majadahonda, Madrid, Spain
[9] Sheba Med Ctr, Leviev Heart Ctr, Tel Hashomer, Israel
[10] Tel Aviv Univ, Sackler Sch Med, Tel Aviv, Israel
关键词
cardiomyopathy; cognition; Danon disease; IQ; LAMP2; psychiatric comorbidities; Wolff-Parkinson-White syndrome; CARDIOMYOPATHY; DEPRESSION; EFFICACY; BATTERY;
D O I
10.1002/ajmg.a.38320
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Danon disease (DD) is a rare X-linked disorder caused by loss-of-function mutations in the LAMP2 gene, which encodes lysosome-associated membrane protein. It is characterized by the triad of hypertrophic cardiomyopathy, myopathy, and intellectual disability. Whereas the molecular and pathophysiological mechanisms underlying this disorder have been previously reported and continue to be explored, the cognitive deficits and psychiatric comorbidities manifested in DD remain an understudied topic. We systematically assessed cognitive abilities and psychiatric comorbidities in 13 males and females. Most of the participants in our cohort (n=9; 75%) had an IQ score within the normal range, while only one participant had intellectual disability. Participants' performance on the Cognitive Neuropsychiatric Battery (CNB) showed only mildly impaired cognitive abilities in most modules, except in the executive functioning test, which was low compared to healthy controls. Of note, 69% of the participants met criteria for at least one psychiatric disorder, mainly mood and anxiety disorders, occurring alone or in combination in the same patient. The results of the present study challenge earlier reports suggesting that mental retardation is a core constituent in DD. Of importance, it underscores the need to refer Danon patients to psychiatric assessment.
引用
收藏
页码:2461 / 2466
页数:6
相关论文
共 50 条
  • [41] Novel Lamp-2 gene mutation and successful treatment with heart transplantation in a large family with Danon disease
    Echaniz-Laguna, A
    Mohr, M
    Epailly, E
    Nishino, I
    Charron, P
    Richard, P
    Guiraud-Chaumeil, C
    Tranchant, C
    MUSCLE & NERVE, 2006, 33 (03) : 393 - 397
  • [42] The c.65-2A>G splice site mutation is associated with a mild phenotype in Danon disease due to the transcription of normal LAMP2 mRNA
    Cetin, H.
    Woehrer, A.
    Rittelmeyer, I.
    Gencik, M.
    Zulehner, G.
    Zimprich, F.
    Stroebel, T.
    Zimprich, A.
    CLINICAL GENETICS, 2016, 90 (04) : 366 - 371
  • [43] LAMP2 exon-copy number variations in Danon disease heterozygote female probands: Infrequent or underdetected?
    Majer, Filip
    Piherova, Lenka
    Reboun, Martin
    Stara, Veronika
    Pelak, Ondrej
    Norambuena, Patricia
    Stranecky, Viktor
    Krebsova, Alice
    Vlaskova, Hana
    Dvorakova, Lenka
    Kmoch, Stanislav
    Kalina, Tomas
    Kubanek, Milos
    Sikora, Jakub
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2018, 176 (11) : 2430 - 2434
  • [44] Identification and functional analysis of a novel de novo missense mutation located in the initiation codon of LAMP2 associated with early onset female Danon disease
    Wang, Yongxiang
    Bai, Ming
    Zhang, Piyi
    Peng, Yu
    Chen, Zixian
    He, Zhiyu
    Xu, Jin
    Zhu, Youqi
    Yan, Dongdong
    Wang, Runqing
    Zhang, Zheng
    MOLECULAR GENETICS & GENOMIC MEDICINE, 2023, 11 (09):
  • [45] Danon disease is an underdiagnosed cause of advanced heart failure in young female patients: a LAMP2 flow cytometric study
    Gurka, Jiri
    Piherova, Lenka
    Majer, Filip
    Chaloupka, Anna
    Zakova, Daniela
    Pelak, Ondrej
    Krebsova, Alice
    Peichl, Petr
    Krejci, Jan
    Freiberger, Tomas
    Melenovsky, Vojtech
    Kautzner, Josef
    Kalina, Tomas
    Sikora, Jakub
    Kubanek, Milos
    ESC HEART FAILURE, 2020, 7 (05): : 2534 - 2543
  • [46] Danon disease: intrafamilial phenotypic variability related to a novel LAMP-2 mutation
    Cottinet, Sarah-Louise
    Bergemer-Fouquet, Anne-Marie
    Toutain, Annick
    Sabourdy, Frederique
    Maakaroun-Vermesse, Zoha
    Levade, Thierry
    Chantepie, Alain
    Labarthe, Francois
    JOURNAL OF INHERITED METABOLIC DISEASE, 2011, 34 (02) : 515 - 522
  • [47] Extension of the clinical spectrum of Danon's disease. A novel missense mutation in the splice variant B of the LAMP2 gene leads to myopathy, with mild cardiac abnormalities, and no evident mental retardation
    van der Kooi, Anneke J.
    Rozemuller, Annemieke
    van Doorn, Pieter A.
    Wokke, John H. J.
    van Langen, Irene M.
    Deprez, Ronald H. Lekanne Dit
    Dekker, Lucas R. C.
    de Visser, Marianne
    NEUROMUSCULAR DISORDERS, 2006, 16 : S109 - S110
  • [48] Familial X-linked cardiomyopathy (Danon disease): diagnostic confirmation by mutation analysis of the LAMP2gene
    Christian Balmer
    Diana Ballhausen
    Nils U. Bosshard
    Beat Steinmann
    Eugen Boltshauser
    Urs Bauersfeld
    Andrea Superti-Furga
    European Journal of Pediatrics, 2005, 164 : 509 - 514
  • [49] Familial X-linked cardiomyopathy (Danon disease):: diagnostic confirmation by mutation analysis of the LAMP2gene
    Balmer, C
    Ballhausen, D
    Bosshard, NU
    Steinmann, B
    Boltshauser, E
    Bauersfeld, U
    Superti-Furga, A
    EUROPEAN JOURNAL OF PEDIATRICS, 2005, 164 (08) : 509 - 514
  • [50] Novel LAMP-2 Mutation in a Family With Danon Disease Presenting With Hypertrophic Cardiomyopathy
    Dougu, Nobuhiro
    Joho, Shuji
    Shan, Lishen
    Shida, Takuya
    Matsuki, Akira
    Uese, Keiichiro
    Hirono, Keiichi
    Ichida, Fukiko
    Tanaka, Kortaro
    Nishino, Ichizo
    Inoue, Hiroshi
    CIRCULATION JOURNAL, 2009, 73 (02) : 376 - 380