98%
921
2 minutes
20
Objective: To investigate the relationship of susceptibility loci in chromosomes 1q21-25 and 6p21-25 and schizophrenia subtypes in Chinese population.
Methods: A genomic scan and parametric and non-parametric analyses were performed on 242 individuals from 36 schizophrenia pedigrees, including 19 paranoid schizophrenia and 17 undifferentiated schizophrenia pedigrees, from Henan province of China using 5 microsatellite markers in the chromosome region 1q21-25 and 8 microsatellite markers in the chromosome region 6p21-25, which were the candidates of previous studies. All affected subjects were diagnosed and typed according to the criteria of the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition, Text Revised (DSM-IV-TR; American Psychiatric Association, 2000). All subjects signed informed consent.
Results: In chromosome 1, parametric analysis under the dominant inheritance mode of all 36 pedigrees showed that the maximum multi-point heterogeneity Log of odds score method (HLOD) score was 1.33 (α = 0.38). The non-parametric analysis and the single point and multi-point nonparametric linkage (NPL) scores suggested linkage at D1S484, D1S2878, and D1S196. In the 19 paranoid schizophrenias pedigrees, linkage was not observed for any of the 5 markers. In the 17 undifferentiated schizophrenia pedigrees, the multi-point NPL score was 1.60 (P= 0.0367) at D1S484. The single point NPL score was 1.95(P= 0.0145) and the multi-point NPL score was 2.39 (P= 0.0041) at D1S2878. Additionally, the multi-point NPL score was 1.74 (P= 0.0255) at D1S196. These same three loci showed suggestive linkage during the integrative analysis of all 36 pedigrees. In chromosome 6, parametric linkage analysis under the dominant and recessive inheritance and the non-parametric linkage analysis of all 36 pedigrees and the 17 undifferentiated schizophrenia pedigrees, linkage was not observed for any of the 8 markers. In the 19 paranoid schizophrenias pedigrees, parametric analysis showed that under recessive inheritance mode the maximum single-point HLOD score was 1.26 (α = 0.40) and the multi-point HLOD was 1.12 (α = 0.38) at D6S289 in the chromosome 6p23. In nonparametric analysis, the single-point NPL score was 1.52 (P= 0.0402) and the multi-point NPL score was 1.92 (P= 0.0206) at D6S289.
Conclusion: Susceptibility genes correlated with undifferentiated schizophrenia pedigrees from D1S484, D1S2878, D1S196 loci, and those correlated with paranoid schizophrenia pedigrees from D6S289 locus are likely present in chromosome regions 1q23.3 and 1q24.2, and chromosome region 6p23, respectively.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.3760/cma.j.issn.1003-9406.2011.03.004 | DOI Listing |
Indian J Psychiatry
August 2025
Epidemiology, School of Public Health, SRM University, Sikkim, India.
Background: The role of sex chromosomes in transmission of schizophrenia may be revealed by studies of phenotypic characteristics.
Aim: To explore variations in dermatoglyphic parameters between probands with schizophrenia and their respective affected gender-matched parents, with unaffected controls.
Methods: The difference of the absolute finger ridge counts (AFRC) and occurrence of identical finger patterns between the male probands and their affected fathers (n = 12) was compared with that of female probands and their affected mothers (n = 15).
Lancet Psychiatry
August 2025
National Centre for Register-Based Research, Aarhus University, Aarhus V, Denmark; Centre for Integrated Register-Based Research, Aarhus University, CIRRAU, Aarhus V, Denmark; The Lundbeck Foundation Initiative for Integrative Psychiatric Research, iPSYCH, Aarhus V, Denmark.
Background: Relative risk estimates of familial aggregation of many types of mental disorders are available, but absolute risk estimates of familial aggregation of mental disorders remain sparse. The proportion of individuals who develop a mental disorder in the absence of the same disorder in a relative (non-familial cases) has not been examined. We aimed to create comprehensive risk estimates of the familial aggregation of mental disorders.
View Article and Find Full Text PDFInt J Mol Sci
May 2025
School of Biological Sciences, University of the Punjab, Lahore 54000, Pakistan.
Psychosis constitutes a cardinal component of schizophrenia and affects nearly fifty percent of those with bipolar disorder. We sought to molecularly characterize psychosis segregating in consanguineous families. Participants from eight multiplex families were evaluated using standardized testing tools.
View Article and Find Full Text PDFMol Psychiatry
August 2025
Center for Neuropsychiatric Research, National Health Research Institutes, Zhunan, Taiwan.
Whether delaying fatherhood leads to more mutations, thereby resulting in adverse psychiatric outcomes in offspring, remains under debate. No study has directly examined the role of de novo mutations (DNMs) between paternal age and offspring psychiatric outcomes. This study aimed to explore the association between paternal age, the number of DNMs, and age at onset of schizophrenia by sequencing the whole genome of multiplex schizophrenia families.
View Article and Find Full Text PDFJ Psychopathol Clin Sci
April 2025
Department of Psychology, University of Pittsburgh.
Individuals with schizophrenia have poorer performance and often differing patterns of brain activation compared to controls on a variety of cognitive tasks, including those that require inhibition of responses and shifting to new responses. This study sought to examine the degree to which performance on a task developed to measure cognitive flexibility, the Penn Conditional Exclusion Test (PCET), and its related brain activation, as assessed on functional magnetic resonance imaging, may reflect schizophrenia genetic risk using an extended pedigree design. A total of 455 participants (27 schizophrenia probands, 170 of their first- to fourth-degree relatives, and 258 unrelated controls) completed similar versions of the PCET, both outside and inside a magnetic resonance imaging scanner.
View Article and Find Full Text PDF