TY - JOUR
T1 - Developmental and symptom profiles in early-onset psychosis
AU - Giannitelli, Marianna
AU - Levinson, Douglas F.
AU - Cohen, David
AU - Xavier, Jean
AU - Laurent-Levinson, Claudine
N1 - Funding Information:
Molecular Genetics of Schizophrenia (MGS) co-authors and funding sources are listed in Supplementary Information. This work was supported by the Centre de Référence des Maladies Rares à Expression Psychiatrique , Department of Child and Adolescent Psychiatry , Assistance Publique-Hôpitaux de Paris , Hôpital Pitié-Salpêtrière , Paris, France; by a NARSAD Junior Investigator Award (to C.L.L.); and by the Stanford Schizophrenia Genetics Research Fund (D.F.L.) and the Walter E. Nichols, M.D., Professorship (Stanford University School of Medicine; D.F.L.).
Funding Information:
Molecular Genetics of Schizophrenia (MGS) co-authors and funding sources are listed in Supplementary Information. This work was supported by the Centre de R?f?rence des Maladies Rares ? Expression Psychiatrique, Department of Child and Adolescent Psychiatry, Assistance Publique-H?pitaux de Paris, H?pital Piti?-Salp?tri?re, Paris, France; by a NARSAD Junior Investigator Award (to C.L.L.); and by the Stanford Schizophrenia Genetics Research Fund (D.F.L.) and the Walter E. Nichols, M.D., Professorship (Stanford University School of Medicine; D.F.L.).
Publisher Copyright:
© 2020 The Authors
PY - 2020/2
Y1 - 2020/2
N2 - Psychotic disorders in children are more heterogeneous than is captured by categorical diagnoses. In a new cohort of children and adolescents, we evaluated the relationships among age at onset (AAO), clinical symptoms and developmental impairments. Patients with schizophrenia and other “spectrum” psychotic diagnoses (N = 88; AAO 6–17, mean 12.6) were evaluated with diagnostic interviews, a new clinical scale (Lifetime Dimensions of Psychosis Scale-Child and Adolescent), and neuropsychological and medical evaluations. Key findings were replicated in an adult cohort of 2420 cases, including 127 with retrospective AAO<13. Factor and cluster analyses were carried out to identify clinical profiles. Five clinical factors were identified in each cohort: Positive, Bizarre Positive, Negative/Formal Thought Disorder, Depression and Mania. Earlier AAO predicted severity of bizarre positive symptoms in children and of bizarre and other symptoms in adults. Four clinical clusters in the child cohort were characterized by: more severe bizarre positive symptoms (N = 31); negative symptoms (N = 15); premorbid autism spectrum features and developmental delay (N = 12); and depressive symptoms with heterogeneous diagnoses and mild positive/negative symptoms (N = 25). Previous factor-analytic studies of childhood psychosis did not specifically consider bizarre positive symptoms. Here, bizarre positive symptoms emerged as clinical markers of severe, childhood-onset psychosis similar to adult schizophrenia. The four clusters are clinically meaningful and useful for treatment planning and potentially for biological research. Childhood-onset cases are rare and thus difficult to study, but additional, larger cohorts may be useful in dissecting the biological and developmental heterogeneity of psychotic disorders.
AB - Psychotic disorders in children are more heterogeneous than is captured by categorical diagnoses. In a new cohort of children and adolescents, we evaluated the relationships among age at onset (AAO), clinical symptoms and developmental impairments. Patients with schizophrenia and other “spectrum” psychotic diagnoses (N = 88; AAO 6–17, mean 12.6) were evaluated with diagnostic interviews, a new clinical scale (Lifetime Dimensions of Psychosis Scale-Child and Adolescent), and neuropsychological and medical evaluations. Key findings were replicated in an adult cohort of 2420 cases, including 127 with retrospective AAO<13. Factor and cluster analyses were carried out to identify clinical profiles. Five clinical factors were identified in each cohort: Positive, Bizarre Positive, Negative/Formal Thought Disorder, Depression and Mania. Earlier AAO predicted severity of bizarre positive symptoms in children and of bizarre and other symptoms in adults. Four clinical clusters in the child cohort were characterized by: more severe bizarre positive symptoms (N = 31); negative symptoms (N = 15); premorbid autism spectrum features and developmental delay (N = 12); and depressive symptoms with heterogeneous diagnoses and mild positive/negative symptoms (N = 25). Previous factor-analytic studies of childhood psychosis did not specifically consider bizarre positive symptoms. Here, bizarre positive symptoms emerged as clinical markers of severe, childhood-onset psychosis similar to adult schizophrenia. The four clusters are clinically meaningful and useful for treatment planning and potentially for biological research. Childhood-onset cases are rare and thus difficult to study, but additional, larger cohorts may be useful in dissecting the biological and developmental heterogeneity of psychotic disorders.
KW - Children
KW - Cluster analysis
KW - Factor analysis
KW - Psychopathology
KW - Schizophrenia
UR - http://www.scopus.com/inward/record.url?scp=85076862819&partnerID=8YFLogxK
U2 - 10.1016/j.schres.2019.10.028
DO - 10.1016/j.schres.2019.10.028
M3 - Article
C2 - 31874744
AN - SCOPUS:85076862819
SN - 0920-9964
VL - 216
SP - 470
EP - 478
JO - Schizophrenia Research
JF - Schizophrenia Research
ER -