Lichtenstein Paul, Yip Benjamin H, Björk Camilla, Pawitan Yudi, Cannon Tyrone D, Sullivan Patrick F, Hultman Christina M
Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
Lancet. 2009 Jan 17;373(9659):234-9. doi: 10.1016/S0140-6736(09)60072-6.
Whether schizophrenia and bipolar disorder are the clinical outcomes of discrete or shared causative processes is much debated in psychiatry. We aimed to assess genetic and environmental contributions to liability for schizophrenia, bipolar disorder, and their comorbidity.
We linked the multi-generation register, which contains information about all children and their parents in Sweden, and the hospital discharge register, which includes all public psychiatric inpatient admissions in Sweden. We identified 9 009 202 unique individuals in more than 2 million nuclear families between 1973 and 2004. Risks for schizophrenia, bipolar disorder, and their comorbidity were assessed for biological and adoptive parents, offspring, full-siblings and half-siblings of probands with one of the diseases. We used a multivariate generalised linear mixed model for analysis of genetic and environmental contributions to liability for schizophrenia, bipolar disorder, and the comorbidity.
First-degree relatives of probands with either schizophrenia (n=35 985) or bipolar disorder (n=40 487) were at increased risk of these disorders. Half-siblings had a significantly increased risk (schizophrenia: relative risk [RR] 3.6, 95% CI 2.3-5.5 for maternal half-siblings, and 2.7, 1.9-3.8 for paternal half-siblings; bipolar disorder: 4.5, 2.7-7.4 for maternal half-siblings, and 2.4, 1.4-4.1 for paternal half-siblings), but substantially lower than that of the full-siblings (schizophrenia: 9.0, 8.5-11.6; bipolar disorder: 7.9, 7.1-8.8). When relatives of probands with bipolar disorder were analysed, increased risks for schizophrenia existed for all relationships, including adopted children to biological parents with bipolar disorder. Heritability for schizophrenia and bipolar disorder was 64% and 59%, respectively. Shared environmental effects were small but substantial (schizophrenia: 4.5%, 4.4%-7.4%; bipolar disorder: 3.4%, 2.3%-6.2%) for both disorders. The comorbidity between disorders was mainly (63%) due to additive genetic effects common to both disorders.
Similar to molecular genetic studies, we showed evidence that schizophrenia and bipolar disorder partly share a common genetic cause. These results challenge the current nosological dichotomy between schizophrenia and bipolar disorder, and are consistent with a reappraisal of these disorders as distinct diagnostic entities.
精神分裂症和双相情感障碍是由离散的还是共同的致病过程导致的临床结果,这在精神病学领域备受争议。我们旨在评估遗传因素和环境因素对精神分裂症、双相情感障碍及其共病易感性的影响。
我们将包含瑞典所有儿童及其父母信息的多代登记册与包含瑞典所有公立精神病住院患者信息的医院出院登记册相链接。我们在1973年至2004年间超过200万个核心家庭中识别出9009202名独特个体。对患有其中一种疾病的先证者的生物学父母、养子女、后代、全同胞和半同胞的精神分裂症、双相情感障碍及其共病风险进行了评估。我们使用多元广义线性混合模型分析遗传因素和环境因素对精神分裂症、双相情感障碍及其共病易感性的影响。
患有精神分裂症(n = 35985)或双相情感障碍(n = 40487)的先证者的一级亲属患这些疾病的风险增加。半同胞的风险显著增加(精神分裂症:母系半同胞的相对风险[RR]为3.6,95%可信区间为2.3 - 5.5;父系半同胞为2.7,1.9 - 3.8;双相情感障碍:母系半同胞为4.5,2.7 - 7.4;父系半同胞为2.4,1.4 - 4.1),但远低于全同胞(精神分裂症:9.0,8.5 - 11.6;双相情感障碍:7.9,7.1 - 8.8)。在分析患有双相情感障碍的先证者的亲属时,所有亲属关系患精神分裂症的风险均增加,包括患有双相情感障碍的生物学父母领养的孩子。精神分裂症和双相情感障碍的遗传度分别为64%和59%。两种疾病的共同环境影响虽小但显著(精神分裂症:4.5%,4.4% - 7.4%;双相情感障碍:3.4%,2.3% - 6.2%)。疾病之间的共病主要(63%)归因于两种疾病共有的加性遗传效应。
与分子遗传学研究相似,我们有证据表明精神分裂症和双相情感障碍部分共享一个共同的遗传病因。这些结果挑战了目前精神分裂症和双相情感障碍之间的疾病分类二分法,并且与将这些疾病重新评估为不同的诊断实体相一致。