Jack Nejand, Margherita Malanchini, Ivan Voronin, Thalia Eley, Kaili Rimfeld
{"title":"儿童对家庭环境的看法与整个童年期的一般心理病理学因素有何关联?","authors":"Jack Nejand, Margherita Malanchini, Ivan Voronin, Thalia Eley, Kaili Rimfeld","doi":"10.1101/2024.08.06.24311560","DOIUrl":null,"url":null,"abstract":"Background: Comorbidity and heterogeneity in psychiatric disorders may stem from a general psychopathology (p) factor influenced by both genetic and environmental factors. Although the relative contributions of these influences on psychopathology are established, the longitudinal associations between p-factor and specific environmental exposures across development are not well understood. Using a longitudinal genetically informative design, this study investigates the association between the home environment and p-factor across childhood. Methods: Data were obtained from the Twins Early Development Study (TEDS). Cross-lagged panel analyses were conducted separately to ascertain the direction of associations between parent-rated p, self-rated p, and self-rated home environment (chaos at home and parental discipline) at ages 9, 12, and 16 (N=6,213). Biometric autoregressive cross-lagged twin models were used to assess the aetiology of these associations, and MZ differences analyses were used to control for familial effects. Results: Both latent factors were stable over time, although twin-rated p-factor (r = 0.44-0.40) was more variable than parent-rated p-factor (r = 0.72-0.63). 'Home environment' was more variable than p-factor uniformly. Small, significant bi-directional associations were found between p-factor and home environment, with stronger cross-lagged paths from p-factor to home environment than vice versa. These longitudinal associations persisted over time, though attenuated for parent-rated p-factor. Genetic analyses revealed that bi-directional cross-lagged paths were largely explained by shared environmental factors, with a smaller proportion explained by genetic factors. This pattern of results was confirmed in MZ differences analyses. Conclusions: Our findings suggest a dynamic and bidirectional relationship between p-factor and the home environment across development, predominantly influenced by shared environmental factors. Changes in one can influence the other, highlighting the complexity of psychopathology's environmental influences. This underscores the need for further investigation into gene-environment interplay to inform approaches to psychopathology prevention and intervention.","PeriodicalId":501388,"journal":{"name":"medRxiv - Psychiatry and Clinical Psychology","volume":"25 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-08-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"How are children's perceptions of the home environment associated with a general psychopathology factor across childhood?\",\"authors\":\"Jack Nejand, Margherita Malanchini, Ivan Voronin, Thalia Eley, Kaili Rimfeld\",\"doi\":\"10.1101/2024.08.06.24311560\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Background: Comorbidity and heterogeneity in psychiatric disorders may stem from a general psychopathology (p) factor influenced by both genetic and environmental factors. Although the relative contributions of these influences on psychopathology are established, the longitudinal associations between p-factor and specific environmental exposures across development are not well understood. Using a longitudinal genetically informative design, this study investigates the association between the home environment and p-factor across childhood. Methods: Data were obtained from the Twins Early Development Study (TEDS). Cross-lagged panel analyses were conducted separately to ascertain the direction of associations between parent-rated p, self-rated p, and self-rated home environment (chaos at home and parental discipline) at ages 9, 12, and 16 (N=6,213). Biometric autoregressive cross-lagged twin models were used to assess the aetiology of these associations, and MZ differences analyses were used to control for familial effects. Results: Both latent factors were stable over time, although twin-rated p-factor (r = 0.44-0.40) was more variable than parent-rated p-factor (r = 0.72-0.63). 'Home environment' was more variable than p-factor uniformly. Small, significant bi-directional associations were found between p-factor and home environment, with stronger cross-lagged paths from p-factor to home environment than vice versa. These longitudinal associations persisted over time, though attenuated for parent-rated p-factor. Genetic analyses revealed that bi-directional cross-lagged paths were largely explained by shared environmental factors, with a smaller proportion explained by genetic factors. This pattern of results was confirmed in MZ differences analyses. Conclusions: Our findings suggest a dynamic and bidirectional relationship between p-factor and the home environment across development, predominantly influenced by shared environmental factors. Changes in one can influence the other, highlighting the complexity of psychopathology's environmental influences. This underscores the need for further investigation into gene-environment interplay to inform approaches to psychopathology prevention and intervention.\",\"PeriodicalId\":501388,\"journal\":{\"name\":\"medRxiv - Psychiatry and Clinical Psychology\",\"volume\":\"25 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-08-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"medRxiv - Psychiatry and Clinical Psychology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1101/2024.08.06.24311560\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"medRxiv - Psychiatry and Clinical Psychology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1101/2024.08.06.24311560","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
背景:精神疾病的共存性和异质性可能源于受遗传和环境因素影响的一般精神病理学(p)因子。虽然这些影响因素对精神病理学的相对贡献已经确定,但人们对 p 因子与整个发育过程中特定环境暴露之间的纵向关联还不甚了解。本研究采用纵向遗传信息设计,调查了儿童期家庭环境与p因子之间的关系。研究方法数据来自双胞胎早期发育研究(TEDS)。分别进行了交叉滞后面板分析,以确定9、12和16岁时父母评定的p、自我评定的p和自我评定的家庭环境(家庭混乱和父母管教)之间的关联方向(N=6,213)。采用生物自回归交叉滞后双胞胎模型来评估这些关联的病因,并采用 MZ 差异分析来控制家族效应。研究结果两个潜因子随着时间的推移都很稳定,但双胞胎评定的p因子(r = 0.44-0.40)比父母评定的p因子(r = 0.72-0.63)更具可变性。家庭环境 "比 p 因子的变化更大。在 p 因素与家庭环境之间发现了微小而重要的双向联系,p 因素与家庭环境之间的交叉滞后路径比反向滞后路径更强。这些纵向关联随着时间的推移而持续存在,但父母评定的 p 因子则有所减弱。遗传分析表明,双向交叉滞后路径主要由共同的环境因素解释,遗传因素解释的比例较小。这种结果模式在 MZ 差异分析中得到了证实。结论我们的研究结果表明,在整个成长过程中,P因子与家庭环境之间存在动态的双向关系,主要受共同环境因素的影响。其中一个因素的变化会影响另一个因素,这凸显了精神病理学环境影响的复杂性。这强调了进一步研究基因-环境相互作用的必要性,从而为心理病理学预防和干预方法提供依据。
How are children's perceptions of the home environment associated with a general psychopathology factor across childhood?
Background: Comorbidity and heterogeneity in psychiatric disorders may stem from a general psychopathology (p) factor influenced by both genetic and environmental factors. Although the relative contributions of these influences on psychopathology are established, the longitudinal associations between p-factor and specific environmental exposures across development are not well understood. Using a longitudinal genetically informative design, this study investigates the association between the home environment and p-factor across childhood. Methods: Data were obtained from the Twins Early Development Study (TEDS). Cross-lagged panel analyses were conducted separately to ascertain the direction of associations between parent-rated p, self-rated p, and self-rated home environment (chaos at home and parental discipline) at ages 9, 12, and 16 (N=6,213). Biometric autoregressive cross-lagged twin models were used to assess the aetiology of these associations, and MZ differences analyses were used to control for familial effects. Results: Both latent factors were stable over time, although twin-rated p-factor (r = 0.44-0.40) was more variable than parent-rated p-factor (r = 0.72-0.63). 'Home environment' was more variable than p-factor uniformly. Small, significant bi-directional associations were found between p-factor and home environment, with stronger cross-lagged paths from p-factor to home environment than vice versa. These longitudinal associations persisted over time, though attenuated for parent-rated p-factor. Genetic analyses revealed that bi-directional cross-lagged paths were largely explained by shared environmental factors, with a smaller proportion explained by genetic factors. This pattern of results was confirmed in MZ differences analyses. Conclusions: Our findings suggest a dynamic and bidirectional relationship between p-factor and the home environment across development, predominantly influenced by shared environmental factors. Changes in one can influence the other, highlighting the complexity of psychopathology's environmental influences. This underscores the need for further investigation into gene-environment interplay to inform approaches to psychopathology prevention and intervention.