Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
Department of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
World Psychiatry. 2015 Oct;14(3):333-8. doi: 10.1002/wps.20251.
Obsessive-compulsive disorder (OCD) often co-occurs with anorexia nervosa (AN), a comorbid profile that complicates the clinical management of both conditions. This population-based study aimed to examine patterns of comorbidity, longitudinal risks, shared familial risks and shared genetic factors between OCD and AN at the population level. Participants were individuals with a diagnosis of OCD (N=19,814) or AN (N=8,462) in the Swedish National Patient Register between January 1992 and December 2009; their first-, second- and third-degree relatives; and population-matched (1:10 ratio) unaffected comparison individuals and their relatives. Female twins from the population-based Swedish Twin Register (N=8,550) were also included. Females with OCD had a 16-fold increased risk of having a comorbid diagnosis of AN, whereas males with OCD had a 37-fold increased risk. Longitudinal analyses showed that individuals first diagnosed with OCD had an increased risk for a later diagnosis of AN (risk ratio, RR=3.6), whereas individuals first diagnosed with AN had an even greater risk for a later diagnosis of OCD (RR=9.6). These longitudinal risks were about twice as high for males than for females. First- and second-degree relatives of probands with OCD had an increased risk for AN, and the magnitude of this risk tended to increase with the degree of genetic relatedness. Bivariate twin models revealed a moderate but significant degree of genetic overlap between self-reported OCD and AN diagnoses (ra =0.52, 95% CI: 0.26-0.81), but most of the genetic variance was disorder-specific. The moderately high genetic correlation supports the idea that this frequently observed comorbid pattern is at least in part due to shared genetic factors, though disorder-specific factors are more important. These results have implications for current gene-searching efforts and for clinical practice.
强迫症 (OCD) 常与神经性厌食症 (AN) 共病,这种共病特征使这两种疾病的临床管理复杂化。本项基于人群的研究旨在人群水平上研究 OCD 和 AN 之间的共病模式、纵向风险、共同的家族风险和共同的遗传因素。参与者是瑞典国家患者登记处 1992 年 1 月至 2009 年 12 月期间被诊断为 OCD(N=19814)或 AN(N=8462)的个体;他们的一级、二级和三级亲属;以及人群匹配(1:10 比例)的未受影响的对照个体及其亲属。还纳入了来自基于人群的瑞典双胞胎登记处的女性双胞胎(N=8550)。患有 OCD 的女性患 AN 的共病诊断风险增加了 16 倍,而患有 OCD 的男性则增加了 37 倍。纵向分析表明,首次被诊断为 OCD 的个体随后诊断为 AN 的风险增加(风险比,RR=3.6),而首次被诊断为 AN 的个体随后诊断为 OCD 的风险更高(RR=9.6)。这些纵向风险对于男性比女性高出近两倍。OCD 患者的一级和二级亲属患 AN 的风险增加,且这种风险的程度随着遗传关系程度的增加而增加。双变量双胞胎模型显示,自我报告的 OCD 和 AN 诊断之间存在中度但显著的遗传重叠(ra=0.52,95%CI:0.26-0.81),但大多数遗传变异是特定于疾病的。中度高的遗传相关性支持这样一种观点,即这种经常观察到的共病模式至少部分归因于共同的遗传因素,尽管特定于疾病的因素更为重要。这些结果对当前的基因搜索工作和临床实践具有启示意义。