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本文引用的文献

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Correction: Genome-wide analysis reveals extensive genetic overlap between schizophrenia, bipolar disorder, and intelligence.更正:全基因组分析揭示了精神分裂症、双相情感障碍和智力之间广泛的遗传重叠。
Mol Psychiatry. 2020 Apr;25(4):914. doi: 10.1038/s41380-019-0456-7.
2
The Genetic Epidemiology of Treated Major Depression in Sweden.瑞典治疗性重度抑郁症的遗传流行病学。
Am J Psychiatry. 2018 Nov 1;175(11):1137-1144. doi: 10.1176/appi.ajp.2018.17111251. Epub 2018 Jul 19.
3
Sources of Parent-Offspring Resemblance for Major Depression in a National Swedish Extended Adoption Study.在一项全国性的瑞典扩展收养研究中,父母与子女在重度抑郁症方面的相似性来源。
JAMA Psychiatry. 2018 Feb 1;75(2):194-200. doi: 10.1001/jamapsychiatry.2017.3828.
4
Common adult psychiatric disorders in Swedish primary care where most mental health patients are treated.瑞典初级保健中常见的成人精神疾病,大多数心理健康患者在此接受治疗。
BMC Psychiatry. 2017 Jun 30;17(1):235. doi: 10.1186/s12888-017-1381-4.
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Heritability of personality: A meta-analysis of behavior genetic studies.人格的遗传性:行为遗传学研究的荟萃分析。
Psychol Bull. 2015 Jul;141(4):769-85. doi: 10.1037/bul0000017. Epub 2015 May 11.
6
Triparental families: a new genetic-epidemiological design applied to drug abuse, alcohol use disorders, and criminal behavior in a Swedish national sample.三亲家庭:一种应用于瑞典全国样本中药物滥用、酒精使用障碍和犯罪行为的新遗传流行病学设计。
Am J Psychiatry. 2015 Jun;172(6):553-60. doi: 10.1176/appi.ajp.2014.14091127. Epub 2015 Feb 20.
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An extended Swedish national adoption study of alcohol use disorder.一项关于酒精使用障碍的瑞典全国性扩展收养研究。
JAMA Psychiatry. 2015 Mar;72(3):211-8. doi: 10.1001/jamapsychiatry.2014.2138.
8
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs.基于全基因组 SNP 估算的五种精神障碍的遗传关系。
Nat Genet. 2013 Sep;45(9):984-94. doi: 10.1038/ng.2711. Epub 2013 Aug 11.
9
Fecundity of patients with schizophrenia, autism, bipolar disorder, depression, anorexia nervosa, or substance abuse vs their unaffected siblings.精神分裂症、自闭症、双相情感障碍、抑郁症、神经性厌食症或物质滥用患者与未受影响的兄弟姐妹的生育能力比较。
JAMA Psychiatry. 2013 Jan;70(1):22-30. doi: 10.1001/jamapsychiatry.2013.268.
10
Impact of diagnostic misclassification on estimation of genetic correlations using genome-wide genotypes.基于全基因组基因型估计遗传相关时诊断分类错误的影响。
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一项关于双相情感障碍疾病的瑞典全国领养研究及与精神分裂症和重度抑郁症的跨代家族关联性的延伸研究。

An Extended Swedish National Adoption Study of Bipolar Disorder Illness and Cross-Generational Familial Association With Schizophrenia and Major Depression.

机构信息

Virginia Institute for Psychiatric and Behavioral Genetics, Virginia Commonwealth University, Richmond.

Department of Psychiatry, Virginia Commonwealth University, Richmond.

出版信息

JAMA Psychiatry. 2020 Aug 1;77(8):814-822. doi: 10.1001/jamapsychiatry.2020.0223.

DOI:10.1001/jamapsychiatry.2020.0223
PMID:32186664
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7081154/
Abstract

IMPORTANCE

Information about how risk for bipolar disorder is transmitted across generations and how parental risk for bipolar disorder relates to their children's risk for schizophrenia and major depression is limited.

OBJECTIVE

To evaluate the sources of parent-offspring transmission of bipolar disorder and its familial cross-generational association with schizophrenia and major depression.

DESIGN, SETTING, AND PARTICIPANTS: Parents and offspring (born 1960-1990) from 4 family types were ascertained from Swedish national samples: intact (offspring, n = 2 175 259), not-lived-with biological father (n = 152 436), lived-with stepfather (n = 73 785), and adoptive (n = 15 624). Data analysis was conducted from October 28, 2019, to January 8, 2020.

EXPOSURES

Three sources of parent-offspring resemblance: genes plus rearing, genes only, and rearing only.

MAIN OUTCOMES AND MEASURES

Diagnosis of bipolar disorder, broad schizophrenia (ie, schizophrenia as a 3-level variable: unaffected, nonaffective psychosis, and schizophrenia) and major depression obtained from Swedish national registries. Parent-offspring resemblance was assessed primarily by tetrachoric correlation (ie, correlation of liability) and for key results, odds ratios (ORs) from logistic regression. Cross-generational associations of bipolar disorder with broad schizophrenia and major depression were assessed by their transmission from bipolar disorder in parents and transmission to bipolar disorder in offspring.

RESULTS

The study population included 2 417 104 individuals of 4 family types (51.8% male and 48.2% female; median age, 41 [range, 25-60] years). For bipolar disorder to bipolar disorder transmission, tetrachoric correlations for 3 types of parent-offspring relationships were statistically homogeneous across family type and mothers and fathers for genes plus rearing (0.25; 95% CI, 0.24-0.26), genes only (0.22; 95% CI, 0.18-0.26), and rearing only (0.07; 95% CI, -0.01 to 0.15). Parallel ORs were 5.20 (95% CI, 4.91-5.50), 3.66 (95% CI, 2.97-4.51), and 1.63 (95% CI, 0.96-2.78). Best-estimate, cross-disorder tetrachoric correlations for 3 types of parent-offspring relationships for bipolar disorder and broad schizophrenia were 0.12 (95% CI, 0.11-0.13) for genes plus rearing, 0.12 (95% CI, 0.09-0.14) for genes only, and -0.03 (95% CI, -0.11 to 0.04) for rearing only, with parallel ORs of 1.95 (95% CI, 1.93-1.97), 2.04 (95% CI, 1.75-2.38), and 0.76 (95% CI, 0.43-1.35). For bipolar disorder and major depression, the parallel tetrachoric correlations were 0.09 (95% CI, 0.07-0.10) for genes plus rearing, 0.04 (95% CI, 0.01-0.07) for genes only, and 0.05 (95% CI, 0.01-0.08) for rearing only; parallel ORs were 1.53 (95% CI, 1.50-1.57), 1.23 (95% CI, 1.13-1.34), and 1.25 (95% CI, 1.09-1.42). Heritability for bipolar disorder was estimated at 0.44 (95% CI, 0.36-0.48). Genetic correlations were estimated at 0.572 (95% CI, 0.560-0.589) between bipolar disorder and broad schizophrenia and 0.302 (95% CI, 0.001-0.523) between bipolar disorder and major depression.

CONCLUSIONS AND RELEVANCE

The findings of this study suggest that genes are largely responsible for bipolar disorder transmission across generations, although modest rearing effects are also likely present. Cross-generational transmission between bipolar disorder and broad schizophrenia appears to be entirely genetic with a moderate genetic correlation; for bipolar disorder and major depression, transmission appears to result equally from genes and rearing with a modest genetic correlation.

摘要

重要性

关于双相情感障碍风险在代际间如何传递,以及父母的双相情感障碍风险与子女患精神分裂症和重度抑郁症的风险之间的关系,相关信息有限。

目的

评估双相情感障碍的父母-子女来源及其与精神分裂症和重度抑郁症的家族跨代关联。

设计、设置和参与者:从瑞典全国样本中确定了 4 种家庭类型的父母和子女(1960-1990 年出生):完整家庭(子女,n=2175259)、与生物学父亲无同住(n=152436)、与继父同住(n=73785)和收养(n=15624)。数据分析于 2019 年 10 月 28 日至 2020 年 1 月 8 日进行。

暴露情况

亲子相似的三个来源:基因加养育、仅基因和仅养育。

主要结果和措施

从瑞典国家登记处获得双相情感障碍、广泛精神分裂症(即精神分裂症作为 3 级变量:未受影响、非情感性精神病和精神分裂症)和重度抑郁症的诊断。亲子相似性主要通过四次相关(即易感性的相关)进行评估,对于关键结果,使用来自逻辑回归的优势比(OR)。通过双相情感障碍在父母中的传递和在子女中的传递,评估双相情感障碍与广泛精神分裂症和重度抑郁症之间的跨代关联。

结果

该研究人群包括 2417104 名来自 4 种家庭类型的个体(51.8%为男性,48.2%为女性;中位年龄为 41[范围为 25-60]岁)。对于双相情感障碍到双相情感障碍的传递,三种亲子关系的四次相关在家庭类型和母亲和父亲之间在基因加养育(0.25;95%置信区间,0.24-0.26)、仅基因(0.22;95%置信区间,0.18-0.26)和仅养育(0.07;95%置信区间,-0.01 至 0.15)方面是统计学同质的。平行 OR 分别为 5.20(95%置信区间,4.91-5.50)、3.66(95%置信区间,2.97-4.51)和 1.63(95%置信区间,0.96-2.78)。对于亲子关系的三种类型,最佳估计的双相情感障碍和广泛精神分裂症的跨障碍四次相关为基因加养育的 0.12(95%置信区间,0.11-0.13)、仅基因的 0.12(95%置信区间,0.09-0.14)和仅养育的-0.03(95%置信区间,-0.11 至 0.04),平行 OR 分别为 1.95(95%置信区间,1.93-1.97)、2.04(95%置信区间,1.75-2.38)和 0.76(95%置信区间,0.43-1.35)。对于双相情感障碍和重度抑郁症,基因加养育的平行四次相关为 0.09(95%置信区间,0.07-0.10)、仅基因的 0.04(95%置信区间,0.01-0.07)和仅养育的 0.05(95%置信区间,0.01-0.08);平行 OR 分别为 1.53(95%置信区间,1.50-1.57)、1.23(95%置信区间,1.13-1.34)和 1.25(95%置信区间,1.09-1.42)。双相情感障碍的遗传度估计为 0.44(95%置信区间,0.36-0.48)。遗传相关性估计为双相情感障碍与广泛精神分裂症之间的 0.572(95%置信区间,0.560-0.589)和双相情感障碍与重度抑郁症之间的 0.302(95%置信区间,0.001-0.523)。

结论和相关性

这项研究的结果表明,基因在很大程度上负责双相情感障碍的代际传递,尽管可能存在适度的养育影响。双相情感障碍与广泛精神分裂症之间的跨代传递似乎完全是遗传的,遗传相关性中度;对于双相情感障碍和重度抑郁症,传递似乎同样来自基因和养育,遗传相关性适度。