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德国老年人群大样本队列中代谢、炎症及氧化应激标志物与总发病率和多种疾病共病的关联

Associations of metabolic, inflammatory and oxidative stress markers with total morbidity and multi-morbidity in a large cohort of older German adults.

作者信息

Schöttker Ben, Saum Kai-Uwe, Jansen Eugène H J M, Holleczek Bernd, Brenner Hermann

机构信息

Division of Clinical Epidemiology and Aging Research, German Cancer Research Center, Heidelberg, Germany Network Aging Research, University of Heidelberg, Heidelberg, Germany.

Division of Clinical Epidemiology and Aging Research, German Cancer Research Center, Heidelberg, Germany.

出版信息

Age Ageing. 2016 Jan;45(1):127-35. doi: 10.1093/ageing/afv159. Epub 2015 Nov 11.

Abstract

BACKGROUND

imbalances in metabolic, inflammatory and redox homeostasis play an important role in the leading theories of age-related morbidity, but no large-scale epidemiological study has been conducted so far assessing their associations with total morbidity and multi-morbidity in the same model.

METHODS

analyses were conducted in 2,547 participants of an established population-based cohort study from Germany. The participants' median age was 70 years (range: 57-84) and 51.9% were women. End points were total somatic morbidity and multi-morbidity, assessed by the Cumulative Illness Rating Scale-Geriatric version.

RESULTS

overall, 251 study participants had multi-morbidity (9.9%). Except for the redox marker 'total thiol levels of proteins', all other assessed metabolic (obesity, diabetes, dyslipidaemia and hypertension), inflammatory (C-reactive protein) and oxidative stress markers (derivatives of reactive oxygen metabolites) were significantly associated with total somatic morbidity and multi-morbidity if assessed individually. If modelled jointly, effect estimates were attenuated but remained statistically significant for the outcome 'total morbidity' and for low weight, obesity, insufficiently controlled diabetes and derivatives of reactive oxygen metabolites with respect to the outcome 'multi-morbidity'.

CONCLUSIONS

results from this large sample of older adults support hypotheses that relate imbalances in metabolic, inflammatory and redox homeostasis to age-related morbidity. Despite over adjustment for closely related metabolic, inflammatory and oxidative stress conditions in the full model, independent associations of the markers with total morbidity and/or multi-morbidity were observed. Therefore, adverse metabolic, inflammatory and oxidative stress conditions may all play important roles in the pathogenesis of age-related morbidity, which should be investigated further in future longitudinal studies.

摘要

背景

代谢、炎症和氧化还原稳态失衡在与年龄相关的发病机制的主流理论中起着重要作用,但迄今为止尚未进行大规模流行病学研究,在同一模型中评估它们与总发病率和多种疾病并存的关联。

方法

对来自德国一项既定的基于人群的队列研究的2547名参与者进行分析。参与者的年龄中位数为70岁(范围:57 - 84岁),51.9%为女性。终点指标为总躯体发病率和多种疾病并存情况,通过累积疾病评定量表 - 老年版进行评估。

结果

总体而言,251名研究参与者患有多种疾病(9.9%)。除氧化还原标志物“蛋白质总硫醇水平”外,所有其他评估的代谢指标(肥胖、糖尿病、血脂异常和高血压)、炎症指标(C反应蛋白)和氧化应激标志物(活性氧代谢产物衍生物)单独评估时均与总躯体发病率和多种疾病并存显著相关。如果联合建模,效应估计值会减弱,但对于“总发病率”这一结果以及低体重、肥胖、控制不佳的糖尿病和活性氧代谢产物衍生物与“多种疾病并存”这一结果而言,仍具有统计学意义。

结论

来自大量老年人样本的结果支持了将代谢、炎症和氧化还原稳态失衡与年龄相关发病机制联系起来的假设。尽管在完整模型中对密切相关的代谢、炎症和氧化应激状况进行了过度调整,但仍观察到这些标志物与总发病率和/或多种疾病并存之间的独立关联。因此,不良的代谢、炎症和氧化应激状况可能在与年龄相关的发病机制中均起重要作用,未来的纵向研究应进一步对此进行调查。

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