Evaluating the role of common risk variation in the recurrence risk of schizophrenia in multiplex schizophrenia families.
Autor: | Ahangari M; Virginia Institute for Psychiatric and Behavioral Genetics, Virginia Commonwealth University, Richmond, VA, USA.; Integrative Life Sciences PhD Program, Virginia Commonwealth University, Richmond, VA, USA., Gentry AE; Virginia Institute for Psychiatric and Behavioral Genetics, Virginia Commonwealth University, Richmond, VA, USA., Nguyen TH; Virginia Institute for Psychiatric and Behavioral Genetics, Virginia Commonwealth University, Richmond, VA, USA.; Department of Psychiatry, Virginia Commonwealth University, Richmond, VA, USA., Kirkpatrick R; Virginia Institute for Psychiatric and Behavioral Genetics, Virginia Commonwealth University, Richmond, VA, USA.; Department of Psychiatry, Virginia Commonwealth University, Richmond, VA, USA., Verrelli BC; Center for Biological Data Science, Virginia Commonwealth University, Richmond, VA, USA., Bacanu SA; Virginia Institute for Psychiatric and Behavioral Genetics, Virginia Commonwealth University, Richmond, VA, USA.; Department of Psychiatry, Virginia Commonwealth University, Richmond, VA, USA., Kendler KS; Virginia Institute for Psychiatric and Behavioral Genetics, Virginia Commonwealth University, Richmond, VA, USA.; Department of Psychiatry, Virginia Commonwealth University, Richmond, VA, USA.; Department of Human and Molecular Genetics, Virginia Commonwealth University, Richmond, VA, USA., Webb BT; GenOmics, Bioinformatics, and Translational Research Center, Biostatistics and Epidemiology Division, RTI, Richmond, VA, USA., Riley BP; Virginia Institute for Psychiatric and Behavioral Genetics, Virginia Commonwealth University, Richmond, VA, USA. Brien.Riley@vcuhealth.org.; Department of Psychiatry, Virginia Commonwealth University, Richmond, VA, USA. Brien.Riley@vcuhealth.org.; Department of Human and Molecular Genetics, Virginia Commonwealth University, Richmond, VA, USA. Brien.Riley@vcuhealth.org. |
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Jazyk: | angličtina |
Zdroj: | Translational psychiatry [Transl Psychiatry] 2022 Jul 21; Vol. 12 (1), pp. 291. Date of Electronic Publication: 2022 Jul 21. |
DOI: | 10.1038/s41398-022-02060-3 |
Abstrakt: | Multiplex families have higher recurrence risk of schizophrenia compared to the families of sporadic cases, but the source of this increased recurrence risk is unknown. We used schizophrenia genome-wide association study data (N = 156,509) to construct polygenic risk scores (PRS) in 1005 individuals from 257 multiplex schizophrenia families, 2114 ancestry-matched sporadic cases, and 2205 population controls, to evaluate whether increased PRS can explain the higher recurrence risk of schizophrenia in multiplex families compared to ancestry-matched sporadic cases. Using mixed-effects logistic regression with family structure modeled as a random effect, we show that SCZ PRS in familial cases does not differ significantly from sporadic cases either with, or without family history (FH) of psychotic disorders (All sporadic cases p = 0.90, FH+ cases p = 0.88, FH- cases p = 0.82). These results indicate that increased burden of common schizophrenia risk variation as indexed by current SCZ PRS, is unlikely to account for the higher recurrence risk of schizophrenia in multiplex families. In the absence of elevated PRS, segregation of rare risk variation or environmental influences unique to the families may explain the increased familial recurrence risk. These findings also further validate a genetically influenced psychosis spectrum, as shown by a continuous increase of common SCZ risk variation burden from unaffected relatives to schizophrenia cases in multiplex families. Finally, these results suggest that common risk variation loading are unlikely to be predictive of schizophrenia recurrence risk in the families of index probands, and additional components of genetic risk must be identified and included in order to improve recurrence risk prediction. (© 2022. The Author(s).) |
Databáze: | MEDLINE |
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