健康和生活方式风险因素的社会决定因素调节妇女健康结果的遗传易感性。

Q2 Computer Science
Lindsay A Guare, Jagyashila Das, Lannawill Caruth, Shefali Setia-Verma
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引用次数: 0

摘要

妇女的健康状况受到遗传和环境因素的影响。单独了解这些因素及其相互作用对于实施预防性、个体化医疗至关重要。然而,由于遗传和环境暴露,特别是健康的社会决定因素(SDoH)与种族和血统相关,没有仔细考虑这些措施的风险模型可能会加剧健康差距。我们在“我们所有人”研究项目中重点研究了七种女性健康疾病:乳腺癌、宫颈癌、子宫内膜异位症、卵巢癌、子痫前期、子宫癌和子宫肌瘤。我们从公开可用的权重计算了多基因风险评分(PRSs),并测试了PRSs对各自表型的影响以及遗传风险对诊断年龄的任何影响。接下来,我们测试了环境风险因素(BMI、生活方式和SDoH)对诊断年龄的影响。最后,我们通过分层逻辑回归研究了环境暴露对遗传风险调节的影响,比较了不同类型环境变量的效应大小。在7种条件下的12组权重中,有9组与其各自的表型显著正相关。在时间-事件分析中,PRSs与诊断时的不同年龄无关。最高环境风险组比中、低风险组更早得到诊断。例如,高BMI组的乳腺癌、卵巢癌、子宫癌和子宫肌瘤的诊断分别明显早于低BMI组和中BMI组)。在环境风险最高的人群中,PRS回归系数往往最大,表明对遗传风险的易感性增加。本研究的优势包括我们所有人研究队列的多样性,对SDoH主题的考虑,以及对关键风险因素及其相互关系的检查。这些因素共同强调了整合遗传和环境数据以开发更精确的风险模型、加强个性化医疗并最终减少健康差距的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Social Determinants of Health and Lifestyle Risk Factors Modulate Genetic Susceptibility for Women's Health Outcomes.

Women's health conditions are influenced by both genetic and environmental factors. Understanding these factors individually and their interactions is crucial for implementing preventative, personalized medicine. However, since genetics and environmental exposures, particularly social determinants of health (SDoH), are correlated with race and ancestry, risk models without careful consideration of these measures can exacerbate health disparities. We focused on seven women's health disorders in the All of Us Research Program: breast cancer, cervical cancer, endometriosis, ovarian cancer, preeclampsia, uterine cancer, and uterine fibroids. We computed polygenic risk scores (PRSs) from publicly available weights and tested the effect of the PRSs on their respective phenotypes as well as any effects of genetic risk on age at diagnosis. We next tested the effects of environmental risk factors (BMI, lifestyle measures, and SDoH) on age at diagnosis. Finally, we examined the impact of environmental exposures in modulating genetic risk by stratified logistic regressions for different tertiles of the environment variables, comparing the effect size of the PRS. Of the twelve sets of weights for the seven conditions, nine were significantly and positively associated with their respective phenotypes. None of the PRSs was associated with different ages at diagnoses in the time-to-event analyses. The highest environmental risk group tended to be diagnosed earlier than the low and medium-risk groups. For example, the cases of breast cancer, ovarian cancer, uterine cancer, and uterine fibroids in highest BMI tertile were diagnosed significantly earlier than the low and medium BMI groups, respectively). PRS regression coefficients were often the largest in the highest environment risk groups, showing increased susceptibility to genetic risk. This study's strengths include the diversity of the All of Us study cohort, the consideration of SDoH themes, and the examination of key risk factors and their interrelationships. These elements collectively underscore the importance of integrating genetic and environmental data to develop more precise risk models, enhance personalized medicine, and ultimately reduce health disparities.

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