Clinical phenotypes of five patients with psychotic disorders carrying rare schizophrenia-associated loss-of-function variants

被引:2
|
作者
Cohen, Bruce M. [1 ,2 ]
Singh, Tarjinder [3 ,4 ,5 ]
Onguer, Dost [2 ,6 ]
Konstantin, Grace E. [6 ]
Gardner, Margaret E. [6 ]
机构
[1] McLean Hosp, Program Neuropsychiat Res, 115 Mill St, Belmont, MA 02478 USA
[2] Harvard Med Sch, 25 Shattuck St, Boston, MA 02115 USA
[3] Massachusetts Gen Hosp, Dept Med, Analyt & Translat Genet Unit, 185 Cambridge St, Boston, MA 02114 USA
[4] Stanley Ctr Psychiat Res, Broad Inst & Harvard, Cambridge, MA 02142 USA
[5] MIT, Broad Inst Harvard, Program Med & Populat Genet, Cambridge, MA 02139 USA
[6] McLean Hosp, Schizophrenia & Bipolar Disorder Res Program, 115 Mill St, Belmont, MA 02478 USA
关键词
Schizophrenia; Psychotic disorders; SCHEMA; Loss -of -function variants;
D O I
10.1016/j.schres.2022.11.006
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
The Schizophrenia Exome Meta-Analysis (SCHEMA) consortium identified 10 genes in which loss-of-function (LoF) variants are highly associated with schizophrenia (SZ). In a well-characterized sample of 988 patients with psychotic disorders, we investigated whether patients bearing a SCHEMA variant presented with unusual or unique signs, symptoms, or course of illness. We identified 5 patients who carried a LoF variant in a SCHEMA gene, each in a different gene. None of the patients with a SCHEMA variant had unique symptoms. However, compared to the average of patients in the sample, all of the patients with a SCHEMA variant had earlier onset of any mental illness and more hospitalizations. Also, among SCHEMA carriers, 80 % were treated with clozapine, 60 % with ECT, all with either clozapine or ECT and 40 % with both clozapine and ECT, compared to only 2 % treated with clozapine and 18 % treated with ECT in the comparison group of patients without SCHEMA variants. All 5 patients with a SCHEMA variant had polysubstance abuse, and all had attempted suicide. Fewer than half had such presentations in the group without SCHEMA variants. In this small sample, SCHEMA variants appear to be associated with earlier onset, less favorable response to standard first-line treatments, and more severe illness, but not unique presentations of illness.
引用
收藏
页码:100 / 103
页数:4
相关论文
共 50 条
  • [1] Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders
    Singh, Tarjinder
    Kurki, Mitja I.
    Curtis, David
    Purcell, Shaun M.
    Crooks, Lucy
    Mcrae, Jeremy
    Suvisaari, Jaana
    Chheda, Himanshu
    Blackwood, Douglas
    Breen, Gerome
    Pietilainen, Olli
    Gerety, Sebastian S.
    Ayub, Muhammad
    Blyth, Moira
    Cole, Trevor
    Collier, David
    Coomber, Eve L.
    Craddock, Nick
    Daly, Mark J.
    Danesh, John
    DiForti, Marta
    Foster, Alison
    Freimer, Nelson B.
    Geschwind, Daniel
    Johnstone, Mandy
    Joss, Shelagh
    Kirov, Georg
    Korkko, Jarmo
    Kuismin, Outi
    Holmans, Peter
    Hultman, Christina M.
    Iyegbe, Conrad
    Lonnqvist, Jouko
    Mannikko, Minna
    McCarroll, Steve A.
    McGuffin, Peter
    McIntosh, Andrew M.
    McQuillin, Andrew
    Moilanen, Jukka S.
    Moore, Carmel
    Murray, Robin M.
    Newbury-Ecob, Ruth
    Ouwehand, Willem
    Paunio, Tiina
    Prigmore, Elena
    Rees, Elliott
    Roberts, David
    Sambrook, Jennifer
    Sklar, Pamela
    St Clair, David
    NATURE NEUROSCIENCE, 2016, 19 (04) : 571 - +
  • [2] Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders
    Tarjinder Singh
    Mitja I Kurki
    David Curtis
    Shaun M Purcell
    Lucy Crooks
    Jeremy McRae
    Jaana Suvisaari
    Himanshu Chheda
    Douglas Blackwood
    Gerome Breen
    Olli Pietiläinen
    Sebastian S Gerety
    Muhammad Ayub
    Moira Blyth
    Trevor Cole
    David Collier
    Eve L Coomber
    Nick Craddock
    Mark J Daly
    John Danesh
    Marta DiForti
    Alison Foster
    Nelson B Freimer
    Daniel Geschwind
    Mandy Johnstone
    Shelagh Joss
    Georg Kirov
    Jarmo Körkkö
    Outi Kuismin
    Peter Holmans
    Christina M Hultman
    Conrad Iyegbe
    Jouko Lönnqvist
    Minna Männikkö
    Steve A McCarroll
    Peter McGuffin
    Andrew M McIntosh
    Andrew McQuillin
    Jukka S Moilanen
    Carmel Moore
    Robin M Murray
    Ruth Newbury-Ecob
    Willem Ouwehand
    Tiina Paunio
    Elena Prigmore
    Elliott Rees
    David Roberts
    Jennifer Sambrook
    Pamela Sklar
    David St Clair
    Nature Neuroscience, 2016, 19 : 571 - 577
  • [3] Excess of rare novel loss-of-function variants in synaptic genes in schizophrenia and autism spectrum disorders
    Kenny, E. M.
    Cormican, P.
    Furlong, S.
    Kenny, E. Heron G.
    Fahey, C.
    Kelleher, E.
    Ennis, S.
    Tropea, D.
    Anney, R.
    Corvin, P.
    Donohoe, G.
    Gallagher, L.
    Gill, M.
    Morris, D. W.
    MOLECULAR PSYCHIATRY, 2014, 19 (08) : 872 - 879
  • [4] Excess of rare novel loss-of-function variants in synaptic genes in schizophrenia and autism spectrum disorders
    E M Kenny
    P Cormican
    S Furlong
    E Heron
    G Kenny
    C Fahey
    E Kelleher
    S Ennis
    D Tropea
    R Anney
    A P Corvin
    G Donohoe
    L Gallagher
    M Gill
    D W Morris
    Molecular Psychiatry, 2014, 19 : 872 - 879
  • [5] Pulmonary hypertension in patients carrying FLNA loss-of-function variants
    Stourm, Laura
    Grynblat, Julien
    Savale, Laurent
    Lacoste-Palasset, Thomas
    Jais, Xavier
    Coulet, Florence
    Levy, Marilyne
    Bonnet, Damien
    Meyrignac, Olivier
    Sitbon, Olivier
    Goupil, Francois
    Humbert, Marc
    Gagnadoux, Frederic
    Montani, David
    EUROPEAN RESPIRATORY JOURNAL, 2024, 64
  • [6] Clinical phenotypes of patients with GABRG2 loss-of-function and gain-of-function variants
    Rossi, A.
    Lin, S. X.
    Moller, R. S.
    Gardella, E.
    Absalom, N. L.
    Ahring, P. K.
    Rubboli, G.
    EPILEPSIA, 2023, 64 : 32 - 33
  • [7] Rare Heterozygous Loss-of-Function Variants in the Human GLP-1 Receptor Are Not Associated With Cardiometabolic Phenotypes
    Melchiorsen, Josefine U.
    Sorensen, Kimmie, V
    Bork-Jensen, Jette
    Kizilkaya, Husun S.
    Gasbjerg, Laerke S.
    Hauser, Alexander S.
    Rungby, Jorgen
    Sorensen, Henrik T.
    Vaag, Allan
    Nielsen, Jens S.
    Pedersen, Oluf
    Linneberg, Allan
    Hartmann, Bolette
    Gjesing, Anette P.
    Holst, Jens J.
    Hansen, Torben
    Rosenkilde, Mette M.
    Grarup, Niels
    JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2023, 108 (11): : 2821 - 2833
  • [8] Secondary Findings of Loss-of-function Variants in FLNC Are Associated With Arrhythmogenic Cardiomyopathy Phenotypes in a General Clinical Population
    Haggerty, Christopher M.
    Kelly, Melissa
    Tichnell, Crystal
    Murray, Brittney
    Sturm, Amy C.
    Fornwalt, Brandon
    James, Cynthia
    CIRCULATION, 2020, 142
  • [9] Ophthalmic phenotypes associated with biallelic loss-of-function PCDH12 variants
    Mattioli, Francesca
    Voisin, Norine
    Preiksaitiene, Egle
    Kozlovskaja, Irina
    Kucinskas, Vaidutis
    Reymond, Alexandre
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2021, 185 (04) : 1275 - 1281
  • [10] Heterozygous loss-of-function variants significantly expand the phenotypes associated with loss of GDF11
    Ravenscroft, Thomas A.
    Phillips, Jennifer B.
    Fieg, Elizabeth
    Bajikar, Sameer S.
    Peirce, Judy
    Wegner, Jeremy
    Luna, Alia A.
    Fox, Eric J.
    Yan, Yi-Lin
    Rosenfeld, Jill A.
    Zirin, Jonathan
    Kanca, Oguz
    Benke, Paul J.
    Cameron, Eric S.
    Strehlow, Vincent
    Platzer, Konrad
    Abou Jamra, Rami
    Klockner, Chiara
    Osmond, Matthew
    Licata, Thomas
    Rojas, Samantha
    Dyment, David
    Chong, Josephine S. C.
    Lincoln, Sharyn
    Stoler, Joan M.
    Postlethwait, John H.
    Wangler, Michael F.
    Yamamoto, Shinya
    Krier, Joel
    Westerfield, Monte
    Bellen, Hugo J.
    GENETICS IN MEDICINE, 2021, 23 (10) : 1889 - 1900