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队列研究考察了梅奥诊所生物样本库参与者中神经酰胺水平与多种疾病风险之间的关联。

Cohort study examining associations between ceramide levels and risk of multimorbidity among persons participating in the Mayo Clinic Biobank.

机构信息

Division of Epidemiology, Department of Quantitative Health Sciences, Mayo Clinic, Rochester, Minnesota, USA

Robert and Arlene Kogod Center on Aging, Mayo Clinic, Rochester, Minnesota, USA.

出版信息

BMJ Open. 2023 Apr 21;13(4):e069375. doi: 10.1136/bmjopen-2022-069375.

Abstract

OBJECTIVE

Ceramides have been associated with several ageing-related conditions but have not been studied as a general biomarker of multimorbidity (MM). Therefore, we determined whether ceramide levels are associated with the rapid development of MM.

DESIGN

Retrospective cohort study.

SETTING

Mayo Clinic Biobank.

PARTICIPANTS

1809 persons in the Mayo Clinic Biobank ≥65 years without MM at the time of enrolment, and with ceramide levels assayed from stored plasma.

PRIMARY OUTCOME MEASURE

Persons were followed for a median of 5.7 years through their medical records to identify new diagnoses of 20 chronic conditions. The number of new conditions was divided by the person-years of follow-up to calculate the rate of accumulation of new chronic conditions.

RESULTS

Higher levels of C18:0 and C20:0 were associated with a more rapid rate of accumulation of chronic conditions (C18:0 z score RR: 1.30, 95% CI: 1.10 to 1.53; C20:0 z score RR: 1.26, 95% CI: 1.07 to 1.49). Higher C18:0 and C20:0 levels were also associated with an increased risk of hypertension and coronary artery disease.

CONCLUSIONS

C18:0 and C20:0 were associated with an increased risk of cardiometabolic conditions. When combined with biomarkers specific to other diseases of ageing, these ceramides may be a useful component of a biomarker panel for predicting accelerated ageing.

摘要

目的

神经酰胺与多种与衰老相关的疾病有关,但尚未作为多种疾病(MM)的一般生物标志物进行研究。因此,我们确定神经酰胺水平是否与 MM 的快速发展有关。

设计

回顾性队列研究。

地点

梅奥诊所生物库。

参与者

1809 名年龄在 65 岁以上的梅奥诊所生物库成员,在入组时没有 MM,并且其储存的血浆中可检测到神经酰胺水平。

主要观察指标

通过医疗记录对参与者进行中位随访 5.7 年,以确定 20 种慢性疾病的新诊断。将新疾病的数量除以随访的人年数,以计算新慢性疾病的累积速度。

结果

C18:0 和 C20:0 水平越高,慢性疾病累积速度越快(C18:0 z 分数 RR:1.30,95%CI:1.10 至 1.53;C20:0 z 分数 RR:1.26,95%CI:1.07 至 1.49)。较高的 C18:0 和 C20:0 水平也与高血压和冠状动脉疾病的风险增加有关。

结论

C18:0 和 C20:0 与心血管代谢疾病的风险增加有关。当与特定于其他衰老疾病的生物标志物结合使用时,这些神经酰胺可能是预测加速衰老的生物标志物组合的有用组成部分。

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