通过整合电子健康记录和多基因风险来识别精神分裂症的可修改并发症
Tess Vessels1, Nicholas Strayer2, Karmel W Choi3,4
1Division of Genetic Medicine, Department of Medicine, Vanderbilt Genetics Institute, Vanderbilt University Medical Center, Nashville TN.
由于伴随疾病,精神分裂症患者的预期寿命缩短. 这项研究确定了缺乏共同遗传风险的并发症,表明它们可能可以通过治疗或生活方式改变进行修改,从而有可能改善患者的治疗结果.
科学领域:
- 遗传学和基因组学 遗传学和基因组学
- 精神病学和心理健康 精神病学和心理健康
- 计算生物学 计算生物学
背景情况:
- 精神分裂症患者经历了显著的并发症,导致预期寿命减少10-20年.
- 识别可修改的并发症对于改善这一群体的过早死亡率至关重要.
- 共享遗传风险可能会掩盖主要受到治疗,行为或环境影响的并发症.
结论:
- 这项研究验证了基于EHR的精神分裂症并发症数据在不同人群中的稳定性.
- 识别独立于共享遗传风险的并发症突出了干预目标.
- 对这些可修改的并发症的因果途径的进一步研究可以显著改善患者的治疗结果和寿命.
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