Sex-specific association between schizophrenia polygenic risk and subclinical schizophrenia-related traits

多基因风险评分 精神分裂症(面向对象编程) 联想(心理学) 亚临床感染 临床心理学 心理学 遗传关联 精神科 医学 遗传学 生物 内科学 基因型 单核苷酸多态性 基因 心理治疗师
作者
Patricia Mas-Bermejo,Sergi Papiol,Pilar Torrecilla,Valeria Lavín,Thomas R. Kwapil,Neus Barrantes‐Vidal,Araceli Rosa
出处
期刊:Progress in Neuro-psychopharmacology & Biological Psychiatry [Elsevier BV]
卷期号:136: 111161-111161 被引量:7
标识
DOI:10.1016/j.pnpbp.2024.111161
摘要

BACKGROUND: According to the dimensional view of psychiatric disorders, psychosis is expressed as a continuum in the general population. However, the investigation of the putative genetic aetiological continuity between its clinical and subclinical phenotypes has yielded mixed results. We aimed to replicate previous findings regarding the association of polygenic risk for schizophrenia with subclinical traits (i.e., schizotypy traits and psychotic-like experiences), and to examine the role of sex in this association in a large nonclinical sample. METHODS: The Multidimensional Schizotypy Scale and the Community Assessment of Psychic Experiences were assessed in 919 nonclinical participants. Polygenic Risk Scores for schizophrenia (SZ-PRSs) were computed using the PRS-CS method based on the latest genome-wide association study of schizophrenia. Summary statistics derived from the total GWAS sample and stratified by sex were used. Linear regression analyses tested the associations of the SZ-PRSs with the psychometric variables, both in the total sample and by sex. RESULTS: No associations were found between the SZ-PRSs and the positive, negative or disorganized dimensions of schizotypy in the total sample. Likewise, no associations were found with psychotic-like experiences. However, the sex-stratified analyses revealed a male-specific association with positive schizotypy. Similar results were obtained with the PRSs derived from the sex-stratified summary statistics. DISCUSSION: Our results are consistent with the lack of clear evidence of an association between SZ common genetic risk and its subclinical phenotypes. Nevertheless, the male-specific association found suggests that this PRS might explain better the male phenotype, as reported in previous studies. Future studies should put a focus on the role of sex in this association to unravel its sex specificities.

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