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Incidence of cancer in patients with schizophrenia and their first-degree relatives: A population-based study in Sweden

机译:精神分裂症患者及其一级亲属的癌症发病率:瑞典一项基于人群的研究

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ContextPrevious studies of the association between schizophrenia and cancer have produced conflicting results, probably because of the failure to control for confounding factors.ObjectiveTo test if the possible association between schizophrenia and cancer is genetic by investigating the incidence of cancer in patients with schizophrenia and their relatives.DesignRetrospective cohort study with follow-up between 1965 and 2008. Estimated smoking rates were used to adjust the incidence rates of smoking-related cancers.ParticipantsThe entire Swedish population.Main outcome measuresRisk of overall cancer and 34 site-/type-specific cancers.ResultsA total of 59 233 patients in Sweden with schizophrenia were identified, of whom 6137 developed cancer during the study period, giving a decreased standardized incidence ratio (SIR) of 0.79 (95% CI 0.77-0.81). The decrease was more pronounced (SIR 0.40, 95% CI 0.38-0.43) before the first diagnosis of schizophrenia. The overall risk was significantly reduced among their unaffected parents (SIR 0.96, 95% CI 0.94-0.98) and siblings (SIR 0.92, 95% CI 0.89-0.96). Sex-stratified analyses indicated different incidence rates between males and females, with female patients having higher cancer risks than the general population.ConclusionsThe significantly decreased incidences of cancers in patients diagnosed with schizophrenia and their unaffected relatives suggest that familiar/genetic factors contributing to schizophrenia may protect against the development of cancer, especially for those cancer sites observed in both settings. The increased risk of breast, cervical, and endometrial cancers after the first diagnosis of schizophrenia could be attributed to nongenetic factors such as antipsychotics administration, which may justify preventive medical screening.
机译:先前关于精神分裂症与癌症之间关系的研究可能产生矛盾的结果,可能是由于无法控制混杂因素。目的通过调查精神分裂症患者及其亲属的癌症发病率来检验精神分裂症与癌症之间的可能联系是否是遗传的设计回顾性队列研究,并于1965年至2008年进行了跟踪研究。估计吸烟率用于调整与吸烟有关的癌症的发生率。研究对象是整个瑞典人口。主要结果指标是总体癌症和34种针对特定部位/类型的癌症的风险。结果在瑞典共鉴定出59 233例精神分裂症患者,其中6 137例在研究期间患了癌症,标准化发生率(SIR)降低了0.79(95%CI 0.77-0.81)。在首次诊断为精神分裂症之前,下降更为明显(SIR 0.40,95%CI 0.38-0.43)。未患病父母(SIR 0.96,95%CI 0.94-0.98)和兄弟姐妹(SIR 0.92,95%CI 0.89-0.96)的总体风险显着降低。性别分层分析表明,男性和女性之间的发病率不同,女性患者的癌症风险比普通人群高。结论诊断为精神分裂症的患者及其未受影响的亲属的癌症发病率显着下降表明,导致精神分裂症的熟悉/遗传因素可能可以防止癌症的发展,特别是对于在两种情况下都观察到的那些癌症部位。首次诊断为精神分裂症后,乳腺癌,宫颈癌和子宫内膜癌的风险增加可能归因于非遗传因素,例如抗精神病药物的使用,这可能证明进行预防性医学筛查是合理的。

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