Department of Clinical Epidemiology, Shengjing Hospital of China Medical University, No. 36, San Hao Street, Heping District, Shenyang, Liaoning Province, 110004, China.
Department of Epidemiology and Biostatistics, School of Public Health, China Medical University, No.77 Puhe Road, Shenyang North New Area, Shenyang, 110122, Liaoning Province, China.
BMC Public Health. 2024 May 27;24(1):1406. doi: 10.1186/s12889-024-18879-y.
No study has concentrated on the association of LE8 with cancer risk and death. We aim to examine the association of LE8 with death and cancer.
A total of 94733 adults aged 51.42 ± 12.46 years and 77551 participants aged 54.09±12.06 years were enrolled in longitudinal and trajectory analysis respectively. Baseline LE8 was divided into three groups based on the American Heart Association criteria and three trajectory patterns by latent mixture models. We reviewed medical records and clinical examinations to confirm incident cancer during the period from 2006 to 2020. Death information was collected from provincial vital statistics offices. Cox models were used.
12807 all-cause deaths and 5060 cancers were documented during a 14-year follow-up. Relative to participants with high LE8 at baseline, participants with lower levels of LE8 have a significantly increased risk of mortality and incident cancer. All these risks have an increasing trend with LE8 level decreasing. Meanwhile, the trajectory analysis recorded 7483 all-cause deaths and 3037 incident cancers after approximately 10 years. The associations of LE8 with death and cancer were identical to the longitudinal study. In the subtype cancer analysis, LE8 has a strong effect on colorectal cancer risk. Moreover, the cut point is 56.67 in the association between LE8 and death, while the cut point altered to 64.79 in the association between LE8 and incident cancers. These associations were enhanced among younger adults.
There was a significant association of LE8 with death and cancer risk, especially for the young population.
目前尚无研究集中探讨 LE8 与癌症风险和死亡之间的关系。本研究旨在探讨 LE8 与死亡和癌症的相关性。
共有 94733 名年龄为 51.42±12.46 岁的成年人和 77551 名年龄为 54.09±12.06 岁的参与者分别纳入纵向和轨迹分析。根据美国心脏协会的标准,将基线 LE8 分为三组,并通过潜在混合模型将三种轨迹模式进行分组。我们查阅了病历和临床检查记录,以确认 2006 年至 2020 年期间发生的癌症。死亡信息由省级生命统计办公室收集。采用 Cox 模型进行分析。
在 14 年的随访期间,共记录到 12807 例全因死亡和 5060 例癌症。与基线时 LE8 水平较高的参与者相比,LE8 水平较低的参与者死亡和癌症发病的风险显著增加。随着 LE8 水平的降低,这些风险呈上升趋势。同时,经过大约 10 年的时间,轨迹分析记录到 7483 例全因死亡和 3037 例癌症发病。LE8 与死亡和癌症的相关性与纵向研究相同。在亚组癌症分析中,LE8 与结直肠癌风险具有较强的相关性。此外,LE8 与死亡的关联中切点为 56.67,而 LE8 与癌症发病的关联中切点变为 64.79。这些相关性在年轻人群中更为明显。
LE8 与死亡和癌症风险显著相关,尤其是在年轻人群中。