{"title":"精神分裂症和双相情感障碍的多基因责任与教育程度和认知老化的关系。","authors":"Chi-Shin Wu, Chia-Lin Hsu, Mei-Chen Lin, Mei-Hsin Su, Yen-Feng Lin, Chia-Yen Chen, Po-Chang Hsiao, Yi-Jiun Pan, Pei-Chun Chen, Yen-Tsung Huang, Shi-Heng Wang","doi":"10.1038/s41398-024-03182-6","DOIUrl":null,"url":null,"abstract":"<p><p>To elucidate the specific and shared genetic background of schizophrenia (SCZ) and bipolar disorder (BPD), this study explored the association of polygenic liabilities for SCZ and BPD with educational attainment and cognitive aging. Among 106,806 unrelated community participants from the Taiwan Biobank, we calculated the polygenic risk score (PRS) for SCZ (PRS<sub>SCZ</sub>) and BPD (PRS<sub>BPD</sub>), shared PRS between SCZ and BPD (PRS<sub>SCZ+BPD</sub>), and SCZ-specific PRS (PRS<sub>SCZvsBPD</sub>). Based on the sign-concordance of the susceptibility variants with SCZ/BPD, PRS<sub>SCZ</sub> was split into PRS<sub>SCZ_concordant</sub>/PRS<sub>SCZ_discordant</sub>, and PRS<sub>BPD</sub> was split into PRS<sub>BPD_concordant</sub>/PRS<sub>BPD_discordant</sub>. Ordinal logistic regression models were used to estimate the association with educational attainment. Linear regression models were used to estimate the associations with cognitive aging (n = 27,005), measured by the Mini-Mental State Examination (MMSE), and with MMSE change (n = 6194 with mean follow-up duration of 3.9 y) in individuals aged≥ 60 years. PRS<sub>SCZ,</sub> PRS<sub>BPD</sub>, and PRS<sub>SCZ+BPD</sub> were positively associated with educational attainment, whereas PRS<sub>SCZvsBPD</sub> was negatively associated with educational attainment. PRS<sub>SCZ</sub> was negatively associated with MMSE, while PRS<sub>BPD</sub> was positively associated with MMSE. The concordant and discordant parts of polygenic liabilities have contrasting association, PRS<sub>SCZ_concordant</sub> and PRS<sub>BPD_concordant</sub> mainly determined these effects mentioned above<sub>.</sub> PRS<sub>SCZvsBPD</sub> predicted decreases in the MMSE scores. Using a large collection of community samples, this study provided evidence for the contrasting effects of polygenic architecture in SCZ and BPD on educational attainment and cognitive aging and suggested that SCZ and BPD were not genetically homogeneous.</p>","PeriodicalId":23278,"journal":{"name":"Translational Psychiatry","volume":"14 1","pages":"472"},"PeriodicalIF":5.8000,"publicationDate":"2024-11-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11569198/pdf/","citationCount":"0","resultStr":"{\"title\":\"Association of polygenic liabilities for schizophrenia and bipolar disorder with educational attainment and cognitive aging.\",\"authors\":\"Chi-Shin Wu, Chia-Lin Hsu, Mei-Chen Lin, Mei-Hsin Su, Yen-Feng Lin, Chia-Yen Chen, Po-Chang Hsiao, Yi-Jiun Pan, Pei-Chun Chen, Yen-Tsung Huang, Shi-Heng Wang\",\"doi\":\"10.1038/s41398-024-03182-6\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>To elucidate the specific and shared genetic background of schizophrenia (SCZ) and bipolar disorder (BPD), this study explored the association of polygenic liabilities for SCZ and BPD with educational attainment and cognitive aging. Among 106,806 unrelated community participants from the Taiwan Biobank, we calculated the polygenic risk score (PRS) for SCZ (PRS<sub>SCZ</sub>) and BPD (PRS<sub>BPD</sub>), shared PRS between SCZ and BPD (PRS<sub>SCZ+BPD</sub>), and SCZ-specific PRS (PRS<sub>SCZvsBPD</sub>). Based on the sign-concordance of the susceptibility variants with SCZ/BPD, PRS<sub>SCZ</sub> was split into PRS<sub>SCZ_concordant</sub>/PRS<sub>SCZ_discordant</sub>, and PRS<sub>BPD</sub> was split into PRS<sub>BPD_concordant</sub>/PRS<sub>BPD_discordant</sub>. Ordinal logistic regression models were used to estimate the association with educational attainment. Linear regression models were used to estimate the associations with cognitive aging (n = 27,005), measured by the Mini-Mental State Examination (MMSE), and with MMSE change (n = 6194 with mean follow-up duration of 3.9 y) in individuals aged≥ 60 years. PRS<sub>SCZ,</sub> PRS<sub>BPD</sub>, and PRS<sub>SCZ+BPD</sub> were positively associated with educational attainment, whereas PRS<sub>SCZvsBPD</sub> was negatively associated with educational attainment. PRS<sub>SCZ</sub> was negatively associated with MMSE, while PRS<sub>BPD</sub> was positively associated with MMSE. The concordant and discordant parts of polygenic liabilities have contrasting association, PRS<sub>SCZ_concordant</sub> and PRS<sub>BPD_concordant</sub> mainly determined these effects mentioned above<sub>.</sub> PRS<sub>SCZvsBPD</sub> predicted decreases in the MMSE scores. Using a large collection of community samples, this study provided evidence for the contrasting effects of polygenic architecture in SCZ and BPD on educational attainment and cognitive aging and suggested that SCZ and BPD were not genetically homogeneous.</p>\",\"PeriodicalId\":23278,\"journal\":{\"name\":\"Translational Psychiatry\",\"volume\":\"14 1\",\"pages\":\"472\"},\"PeriodicalIF\":5.8000,\"publicationDate\":\"2024-11-16\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11569198/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Translational Psychiatry\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1038/s41398-024-03182-6\",\"RegionNum\":1,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"PSYCHIATRY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Translational Psychiatry","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1038/s41398-024-03182-6","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PSYCHIATRY","Score":null,"Total":0}
Association of polygenic liabilities for schizophrenia and bipolar disorder with educational attainment and cognitive aging.
To elucidate the specific and shared genetic background of schizophrenia (SCZ) and bipolar disorder (BPD), this study explored the association of polygenic liabilities for SCZ and BPD with educational attainment and cognitive aging. Among 106,806 unrelated community participants from the Taiwan Biobank, we calculated the polygenic risk score (PRS) for SCZ (PRSSCZ) and BPD (PRSBPD), shared PRS between SCZ and BPD (PRSSCZ+BPD), and SCZ-specific PRS (PRSSCZvsBPD). Based on the sign-concordance of the susceptibility variants with SCZ/BPD, PRSSCZ was split into PRSSCZ_concordant/PRSSCZ_discordant, and PRSBPD was split into PRSBPD_concordant/PRSBPD_discordant. Ordinal logistic regression models were used to estimate the association with educational attainment. Linear regression models were used to estimate the associations with cognitive aging (n = 27,005), measured by the Mini-Mental State Examination (MMSE), and with MMSE change (n = 6194 with mean follow-up duration of 3.9 y) in individuals aged≥ 60 years. PRSSCZ, PRSBPD, and PRSSCZ+BPD were positively associated with educational attainment, whereas PRSSCZvsBPD was negatively associated with educational attainment. PRSSCZ was negatively associated with MMSE, while PRSBPD was positively associated with MMSE. The concordant and discordant parts of polygenic liabilities have contrasting association, PRSSCZ_concordant and PRSBPD_concordant mainly determined these effects mentioned above. PRSSCZvsBPD predicted decreases in the MMSE scores. Using a large collection of community samples, this study provided evidence for the contrasting effects of polygenic architecture in SCZ and BPD on educational attainment and cognitive aging and suggested that SCZ and BPD were not genetically homogeneous.
期刊介绍:
Psychiatry has suffered tremendously by the limited translational pipeline. Nobel laureate Julius Axelrod''s discovery in 1961 of monoamine reuptake by pre-synaptic neurons still forms the basis of contemporary antidepressant treatment. There is a grievous gap between the explosion of knowledge in neuroscience and conceptually novel treatments for our patients. Translational Psychiatry bridges this gap by fostering and highlighting the pathway from discovery to clinical applications, healthcare and global health. We view translation broadly as the full spectrum of work that marks the pathway from discovery to global health, inclusive. The steps of translation that are within the scope of Translational Psychiatry include (i) fundamental discovery, (ii) bench to bedside, (iii) bedside to clinical applications (clinical trials), (iv) translation to policy and health care guidelines, (v) assessment of health policy and usage, and (vi) global health. All areas of medical research, including — but not restricted to — molecular biology, genetics, pharmacology, imaging and epidemiology are welcome as they contribute to enhance the field of translational psychiatry.