PO.CL11.02 · 临床研究
肿瘤学中的自杀风险:一项病例对照研究中的性别与癌症类型差异
Suicide Risk in Oncology: Sex and Cancer Type Differences in a Case-Control Study
作者与单位 Authors & Affiliations
摘要 Abstract
中文摘要
背景:癌症患者的自杀风险可能因性别和癌症部位而异,反映出不同的生物学、社会心理及医疗系统路径。我们利用全州范围的链接死亡与临床数据,考察癌症病史及性别特异性癌症类型是否与死亡前自杀倾向及自杀死亡存在差异性关联。
方法:我们采用两步法研究,利用犹他州人群水平数据,将自杀死亡、癌症及电子健康记录进行链接。第一步,我们比较有既往癌症诊断与无癌症诊断的自杀死亡者(n=14,644)在自杀意念(SI)、自伤行为(SII)、既往自杀未遂(SA)、精神与医学合并症方面的差异。第二步,我们对自杀死亡者(病例;n=1,015)与在世对照(n=9,173)进行年龄与性别匹配的病例对照分析,以估计与任何癌症病史及特定癌症类型相关的自杀死亡的校正比值,并按性别分层。Logistic回归模型校正了既往自杀倾向、已诊断的精神与物质使用障碍(SUD)及慢性医学疾病负担。我们还刻画了首次记录的就诊类型(心理健康、SUD、慢性医学或癌症相关)的时间顺序。
结果:在自杀死亡者中,有任何癌症诊断史者较无癌症者具有更高的死亡前SA(OR=1.27,95% CI 1.09-1.49)、SII(OR=1.34,1.12-1.60)及SI(OR=1.29,1.07-1.56)的比值。女性死亡者的心理健康负担远高于男性(OR=7.90 vs 2.07)。在病例对照分析中,任何癌症病史与总体较低的自杀死亡比值相关,但这一汇总效应掩盖了按性别和癌症类型的异质性。在女性中,宫颈癌/发育异常在病例中较对照更多(OR=1.53,1.13-2.06),提示在性别特异性、身份显著的癌症中风险升高。在男性中,前列腺癌与自杀死亡呈负相关(OR=0.73,0.59-0.91)。心理健康和物质使用的首次就诊在两性病例中均更多,而慢性疾病就诊提示男性存在额外风险。
结论:本研究中,任何癌症诊断史与更高的死亡前自杀倾向相关,但总体自杀死亡比值较低,并存在重要的性别与癌症类型特异性差异。这些模式可能支持一种双路径模型,即社会心理/身份相关机制可能在患有性别特异性癌症的女性中占主导,而功能性或疾病负担路径可能在患有高负担癌症的男性中占主导。利用心理健康与物质使用就诊史、针对性别和癌症类型量身定制的自杀风险筛查,可能改善肿瘤学环境中的预防工作。
查看英文原文 English abstract
Background: Suicide risk among people with cancer may vary by sex and cancer site, reflecting different biological, psychosocial, and care-system pathways. We used statewide linked mortality and clinical data to examine whether cancer history and sex-specific cancer types differentially relate to pre-death suicidality and suicide mortality.
Methods: We conducted a two-step study using population-level data from Utah linking suicide mortality, cancer, and electronic health records. First, we compared suicide decedents with versus without a prior cancer diagnosis (n=14,644) on suicidal ideation (SI), self-injurious behavior (SI), prior suicide attempts (SA), psychiatric and medical comorbidities. Second, we performed an age-and sex-matched case-control analysis of suicide decedents (cases; n=1,015) and living controls (n=9,173) to estimate adjusted odds of suicide death associated with any cancer history and specific cancer types, stratified by sex. Logistic regression models adjusted for prior suicidality, diagnosed mental and substance use disorders (SUD), and chronic medical morbidity. We also characterized the temporal sequencing of first-recorded encounter types (mental health, SUD, chronic medical, or cancer-related).
Results: Among suicide decedents, those with any history of a cancer diagnosis had higher odds of pre-death SA (OR=1.27, 95% CI 1.09-1.49), SII (OR=1.34, 1.12-1.60), and SI (OR=1.29, 1.07-1.56) than decedents without cancer. Mental-health burden was substantially greater among female than male decedents (OR=7.90 vs 2.07). In case-control analyses, a history of any cancer was associated with lower overall odds of suicide death, but this aggregate effect masked heterogeneity by sex and cancer type. Among women, cervical cancer/dysplasia was over-represented in cases compared to controls (OR=1.53, 1.13-2.06), suggesting elevated risk in sex-specific, identity-salient cancers. Among men, prostate cancer was inversely associated with suicide death (OR=0.73, 0.59-0.91). First encounters for mental health and substance use were over-represented among cases of both sexes, while chronic-condition encounters suggest additional risk in men.
Conclusions: In this study, any history of a cancer diagnosis was linked to greater pre-death suicidality but lower overall odds of suicide death, with important sex-and cancer-type specific differences. Patterns may support a dual-pathway model in which psychosocial/identity-related mechanisms may predominate among women with sex-specific cancers, whereas functional or disease-burden pathways may predominate among men with high-burden cancers. Tailored, sex-and cancer-type-specific suicide risk screening that leverages mental health and substance use encounter history may improve prevention in oncology settings.
利益披露 Disclosure
B. M. Byrwa-Hill, None..
E. T. Monson, None..
E. DiBlasi, None..
H. Coon, None..
D. Chen, None..
M. J. Staley, None..
A. V. Bakian, None.