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超越风险窗口?荷兰双相情感障碍后代研究:22年随访

Beyond the Window of Risk? The Dutch Bipolar Offspring Study: 22-Year Follow-Up.

作者信息

Helmink Fleur G L, Mesman Esther, Hillegers Manon H J

机构信息

Erasmus MC Sophia Children's Hospital, Rotterdam, the Netherlands.

Erasmus MC Sophia Children's Hospital, Rotterdam, the Netherlands.

出版信息

J Am Acad Child Adolesc Psychiatry. 2025 May;64(5):593-601. doi: 10.1016/j.jaac.2024.05.024. Epub 2024 Jun 6.

Abstract

OBJECTIVE

Adolescent offspring of parents with bipolar disorder (BD) are at high risk to develop BD and other psychopathology, yet how this risk continues into middle adulthood remains unknown. This study aimed to determine the window of risk for BD and other psychopathology in offspring of parents with BD followed from adolescence into adulthood.

METHOD

This study reported on the 22-year follow-up assessment of the Dutch Bipolar Offspring Study, a fixed cohort study of 140 participants established in 1997. Offspring (n = 100; mean [SD] age = 38.28 [2.74] years) of parents with bipolar I disorder or bipolar II disorder were assessed at baseline and 1-, 5-, 12-, and 22-year follow-up.

RESULTS

No new BD onsets occurred since the 12-year follow-up (lifetime prevalence = 11%-13%; bipolar I disorder = 4%; bipolar II disorder = 7%). Lifetime prevalence of any mood disorder was 65%; for major depressive disorder, prevalence was 36%; and for recurrent mood episodes, prevalence was 37%. Prevalence of major depressive disorder more than doubled in the past decade. Point prevalence of any psychopathology peaked between 20 and 25 years (38%-46%), subsiding to 29% to 35% per year after age 30. Overall, 71% of offspring contacted mental health services since the last assessment.

CONCLUSION

The risk for homotypic transmission of BD in offspring of parents with BD is highest during adolescence. The heterotypic risk for mood disorder onset and recurrences continues over the life course. Severe mood disorders are often preceded by milder psychopathology, emphasizing the need for early identification and interventions. This study allows for better understanding of the onset and course of mood disorders and specific windows of risk in a familial high-risk population.

PLAIN LANGUAGE SUMMARY

This longitudinal study followed 100 offspring of parents with bipolar disorder, finding that they are at increased risk to develop mood and other disorders themselves. The window of risk, in terms of age of onset for mood disorders is still unclear. The 22-year follow-up of the Dutch Bipolar Offspring Study shows the highest risk for occurences of bipolar disorder was during late adolescence (11-13%) while the risk for onset and recurrences of other mood disorders continues into middle adulthood (65% and 37%, respectively).

摘要

目的

双相情感障碍(BD)患者的青春期后代患BD及其他精神病理学疾病的风险很高,但这种风险如何持续到中年仍不清楚。本研究旨在确定BD患者后代从青春期到成年期患BD及其他精神病理学疾病的风险窗口期。

方法

本研究报告了荷兰双相情感障碍后代研究的22年随访评估结果,该研究是一项固定队列研究,于1997年招募了140名参与者。对患有双相I型障碍或双相II型障碍的父母的后代(n = 100;平均[标准差]年龄 = 38.28 [2.74]岁)在基线以及1年、5年、12年和22年随访时进行评估。

结果

自12年随访以来未出现新的BD发病病例(终生患病率 = 11%-13%;双相I型障碍 = 4%;双相II型障碍 = 7%)。任何情绪障碍的终生患病率为65%;重度抑郁症的患病率为36%;复发性情绪发作的患病率为37%。在过去十年中,重度抑郁症的患病率增加了一倍多。任何精神病理学疾病的时点患病率在20至25岁之间达到峰值(38%-46%),30岁以后每年降至29%至35%。总体而言,自上次评估以来,71%的后代曾联系过心理健康服务机构。

结论

BD患者后代中BD同型传播的风险在青春期最高。情绪障碍发作和复发的异型风险在整个生命过程中持续存在。严重情绪障碍之前通常有较轻的精神病理学症状,这强调了早期识别和干预的必要性。本研究有助于更好地理解情绪障碍的发病和病程以及家族高危人群中的特定风险窗口期。

通俗易懂的总结

这项纵向研究跟踪了100名双相情感障碍患者的后代,发现他们自身患情绪及其他疾病的风险增加。就情绪障碍发病年龄而言,风险窗口期仍不明确。荷兰双相情感障碍后代研究的22年随访显示,双相情感障碍发病的最高风险出现在青春期后期(11-13%),而其他情绪障碍发作和复发的风险持续到中年期(分别为65%和37%)。

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