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Early-Onset Psychosis and Child and Adolescent Schizophrenia

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Early-Onset Psychosis and Child and Adolescent Schizophrenia Scandinavian Journal of Child and Adolescent Psychiatry and Psychology Vol. 4(1):1-3 (2016) – Special Issue Editorial Open Access Early-Onset Psychosis and Child and Adolescent Schizophrenia Sune Bo* & Ulrik Helt Haahr Psychiatric Research Unit, Region Zealand, Denmark *Corresponding Author: [email protected] “Our lives disconnect and reconnect, we move on, and phenotypic characteristics include positive later we may again touch one another, again bounce away. symptoms (e.g., hallucinations, delusional thoughts), This is the felt shape of a human life, neither simply linear negative symptoms (e.g., apathy, lack of emotions, nor wholly disjunctive nor endlessly bifurcating, but rather poor or absent social functioning), bizarre behavior, this bouncey-castle sequence of bumpings-into and and a range of cognitive dysfunctions, including tumblings-apart.” ― Salman Rushdie, The Ground Beneath Her Feet disorganized thoughts, difficulty concentrating and completing tasks, reduced memory, and deficits in We are excited to introduce this special issue of the processing of information. These symptoms have SJCAPP about early-onset psychosis (EOP) and been found in cross-cultural studies conducted by the schizophrenia in children and adolescents. Several World Health Organization since the International years ago, an editorial in Nature described Pilot Study in Schizophrenia was initiated during the schizophrenia as “the worst disease affecting 1960s; this study proved that schizophrenia and its mankind” (1). We know that approximately 1% of related symptomatology are found worldwide, the world’s population is directly affected by this although the course and outcomes of the illness may debilitating psychiatric disorder at some point during vary (7). their lives (2). Every year, more than 5,000 new Schizophrenia affects more than just mental health. articles about schizophrenia spectrum disorders and Patients who are diagnosed with schizophrenia die 12 psychosis are added to PubMed (3). Schizophrenia to 15 years earlier than the average population (8), remains one of the most mysterious and severe and current studies have indicated that the mortality mental disorders. It has a complex and heterogenic difference continues to increase, mainly as a result of symptomatology that causes enormous suffering to suicide. The incidence rates for schizophrenia peak patients and their relatives, and it is generally around the age of 22 years (9), but one third of the considered a costly burden on society, although its individuals who will develop the disorder do so true financial cost is somewhat difficult to estimate before they are 18 years old (10). Schizophrenia that (4,5). In the Diagnostic and Statistical Manual of Mental appears in children and adolescents is accepted to be Disorders, Fifth Edition (DSM-5), schizophrenia is clinically and biologically coherent with adult-onset defined as: “…a disorder that lasts for at least 6 schizophrenia (AOS). However, there are some months and includes at least one month of active- differences. Patients with early-onset schizophrenia phase symptoms (i.e., two [or more] of the following: (EOS) display a more severe clinical prognosis and a delusions, hallucinations, disorganized speech, greater neurodegenerative trajectory, and they seem grossly disorganized or catatonic behavior, negative to be less responsive to treatment as compared with symptoms)” (6). The DSM-5 further states that “no patients with AOS. Schizophrenia that emerges in single symptom is pathognomonic of schizophrenia” patients before they are 18 years old is divided into (6). Across different diagnostic systems, there seems two groups: 1) EOS, with an onset between the ages to exist a general understanding that schizophrenia is of 13 and 17 years and prevalence rates of 1 to 2 per a heterogeneous syndrome composed of various 1,000 population; and 2) very EOS, which begins symptoms with different pathogeneses and before the age of 13 years and which has a prevalence etiologies. However, there is also consensus that the that is estimated at 1 per 10,000 population (11). The 1 EOP and Child and Adolescent Schizophrenia modern construct of EOS differs significantly from self-supporting, with some possibility of residual that used during much of the twentieth century. Until symptoms (28). A 25-year follow-up study that the early 1970s, children who would now be evaluated profoundly disabled patients with diagnosed within the autism spectrum would have schizophrenia with an average of 16 years of been diagnosed with schizophrenia, and widespread schizophrenic symptoms and an average total uncertainty existed regarding the validity of a disability of 10 years found that 68% of these schizophrenia diagnosis in children and adolescents subjects were free of schizophrenic symptoms and (12). With the introduction of the DSM-III and the that 45% were free of all psychiatric symptoms at 25 International Statistical Classification of Diseases and years (29). Related Health Problems, 9th Revision, the specific Specifically, studies of EOS show that the disease criteria that were used to define childhood and displays strong associations with poor premorbid adolescent schizophrenia were removed: the same functioning and a reduction in normative criteria have since been used to diagnose development (30), and this diminution seems to be schizophrenia in children, adolescents, and adults. more severe in patients with EOS as compared with With the alignment of the defining criteria, AOS. In addition, studies have shown that, in about prospective studies have demonstrated good validity 20% of adolescents who have been diagnosed with of the diagnosis for children and adolescents; youths schizophrenia, clear language and motor who are diagnosed with schizophrenia display high developmental delays are present; these delays are stability with regard to the phenotypical expression only found in about 10% of patients with AOS (31). of the disorder into adulthood (13). Studies of Research has also reported a substantial difference in neuropsychological functions and brain structure in the premorbid intelligence quotients of patients with people with schizophrenia have shown the same EOS as compared with those with AOS, with degenerative patterns, regardless of the patient’s age patients with EOS scoring roughly 10 to 15 points at the onset of the disorder (14). lower (30). Patients with EOS generally have more The discrete developmental trajectories of negative symptoms, more severely incoherent schizophrenia remain obscure, but recent research thoughts, and a more profoundly disordered sense of has enhanced our understanding of the disorder and self, whereas AOS is associated with more severe of the underlying etiological factors (3,15,16). Gene- positive symptomatology, such as paranoid delusions environment studies have emphasized genetic factors (32). As compared with the relatively high remission that affect an individual’s vulnerability to the rates for patients with AOS, only 12% of patients development of schizophrenia, and twin studies have with EOS are in full remission at discharge. In several shown that the syndrome has heritability rates of prospective follow-up studies, patients with EOS approximately 80% (17,18). There has been a have displayed a chronically disabling course of substantial effort from those supporting the medical illness and severely impaired functioning well into disease model to demonstrate that schizophrenia has adulthood (13,33). a biological origin. This stance is supported by Important EOS predictors of diminished studies that have demonstrated a genetic functioning point to premorbid cognitive and social predisposition for schizophrenia among family deficiencies (33), long periods of untreated psychosis, members, twins, adoptees, and offspring of twins and a long first psychotic episode (34). (19). Other studies have shown that schizophrenia is This special issue of SJCAPP addresses several of associated with structural brain abnormalities (20) the issues just described, and the two included and with biochemical imbalances that are mostly commentaries build further on these ideas. In the associated with the functioning of the dopaminergic first commentary, Aggernæs connects the four system (21). articles included in this issue, and she describes the Epidemiological studies also indicate that growing evidence of a shared genetic risk for autism, environmental factors affect the rate of attention-deficit/hyperactivity disorder, and schizo- schizophrenia (8;22-24), including adverse phrenia. She emphasizes the importance of the experiences in childhood (25). Living in urbanized thorough assessment of the patient in addition to the communities raises the risk of schizophrenia (26), need for intervention during the first psychotic and the tendency to develop schizophrenia is higher episode and the prodromal phase. Nordgaard and among certain ethnic groups as compared with colleagues also address this in their commentary, and native-born individuals (27). they discuss the need for more specific instruments With respect to long-term prognosis, longitudinal for the assessment of clinically high-risk patients. studies that have followed patients with Patients who experience their first episode of schizophrenia for more than 25 years have suggested psychosis need to be treated early and optimally to that approximately 35% of patients recover fully and decrease morbidity and to improve the outcomes of that another 35% function
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