Similarities of Clinical Manifestations in Sibling Patients with Psychotic Disorder.
- Author:
Yeon Ho JOO
1
;
Jee Young AHN
;
Jong Hoon KIM
;
Yong Sik KIM
Author Information
1. Department of Psychiatry, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Korea.
- Publication Type:Original Article
- Keywords:
Psychosis;
Sibling patients;
Diagnosis similarities;
Symptom similarities
- MeSH:
Age of Onset;
Bipolar Disorder;
Delusions;
Diagnosis;
Diagnostic and Statistical Manual of Mental Disorders;
Hallucinations;
Humans;
Phenotype;
Psychotic Disorders*;
Schizophrenia;
Siblings*
- From:Journal of Korean Neuropsychiatric Association
2003;42(3):314-321
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
OBJECTIVES: To explore the possibilities of finding a heritable phenotype(s) in patients with psychosis, we examined the similarities of clinical variables between psychotic sibling patients who share the half of genetic information. METHODS: We recruited a group of sibling patients, whose diagnoses were schizophrenia, schizoaffective disorder and bipolar disorder and confirmed the diagnosis using SCID-RV(Structured Clinical Interview for DSM-IV, Research Version). Using 30 sets of sibling patients, we examined concordances or similarities of diagnosis, diagnostic subtypes, clinical symptoms, and longitudinal outcomes. RESULTS: There were significant concordances in terms of age of onset, auditory hallucination persisted for more than 7 years, general level of functioning. No significant similarities or concordances were found in diagnosis, diagnostic subtypes, delusion, negative symptom, and thought disorder between sibling patients. CONCLUSION: Above mentioned similarities have the possibilities of genetically determined phenotypes that could be used in the future genetic studies. Concordance of hallucination persisted for more than 7 years, not the presence or absence of auditory hallucination between sibling patients suggests that it is more important to examine longitudinal patterns of symptoms than to merely examine the presence of symptoms at specific cross-sectional time points in terms of genetic studies.
