Carriere Isabelle, Dupuy Anne-Marie, Lacroux Annie, Cristol Jean-Paul, Delcourt Cécile
Inserm, U888, Montpellier, France.
J Am Geriatr Soc. 2008 May;56(5):840-6. doi: 10.1111/j.1532-5415.2008.01677.x. Epub 2008 Apr 9.
To determine whether malnutrition and biomarkers of inflammation predict all-cause, cancer, and cardiovascular mortality in healthy elderly subjects.
Population-based study, prospective cohort.
Sète, on the French Mediterranean coast.
Five hundred and fifty-three men and 888 women aged 60 and older from the Pathologies Oculaires Liées à l'Age cohort free of known comorbidities.
Plasma levels of cholesterol, albumin, transthyretin (TTR), C-reactive protein (CRP), and alpha 1-acid glycoprotein (AAG) were measured at baseline. To investigate the risks of 5-year (early) and 5- to 9-year (late) mortality, hazard ratios (HR) were evaluated using Cox models.
In men, early death was associated with high CRP and AAG and low albumin and TTR. In women, early death was associated with high AAG, low TTR and low cholesterol. For late death, the only significant association was with CRP in men. A synergistic effect was observed between biomarkers of inflammation and malnutrition. In men, the adjusted HR of early death was 4.98 (95% confidence interval (CI)=2.25-11.01) for both CRP in the highest quartile and albumin in the lowest. In men, this risk was greatest for both AAG in the highest quartile and TTR in the lowest (HR=6.86, 95% CI=3.20-14.71). In women, this risk was greatest for both AAG in the highest quartile and TTR in the lowest (HR=4.64, 95% CI=1.79-12.05). Cancer mortality was greater for high CRP and AAG and for low albumin and TTR in men but not in women.
Biomarkers of inflammation and malnutrition together predict early mortality. In healthy elderly subjects, TTR and AAG could be helpful in identifying elderly subjects at higher risk of death.
确定营养不良和炎症生物标志物是否能预测健康老年受试者的全因死亡率、癌症死亡率和心血管死亡率。
基于人群的前瞻性队列研究。
法国地中海沿岸的塞特。
来自“与年龄相关的眼部疾病”队列的553名男性和888名60岁及以上的女性,无已知合并症。
在基线时测量血浆胆固醇、白蛋白、转甲状腺素蛋白(TTR)、C反应蛋白(CRP)和α1-酸性糖蛋白(AAG)水平。为了研究5年(早期)和5至9年(晚期)死亡率的风险,使用Cox模型评估风险比(HR)。
在男性中,早期死亡与高CRP和AAG以及低白蛋白和TTR有关。在女性中,早期死亡与高AAG、低TTR和低胆固醇有关。对于晚期死亡,唯一显著的关联是男性中的CRP。在炎症生物标志物和营养不良之间观察到协同效应。在男性中,最高四分位数的CRP和最低四分位数的白蛋白同时存在时,早期死亡的校正HR为4.98(95%置信区间(CI)=2.25-11.01)。在男性中,最高四分位数的AAG和最低四分位数的TTR同时存在时,这种风险最大(HR=6.86,95%CI=3.20-14.71)。在女性中,最高四分位数的AAG和最低四分位数的TTR同时存在时,这种风险最大(HR=4.64,95%CI=1.79-12.05)。男性中高CRP和AAG以及低白蛋白和TTR的癌症死亡率更高,但女性并非如此。
炎症和营养不良的生物标志物共同预测早期死亡率。在健康老年受试者中,TTR和AAG有助于识别死亡风险较高的老年受试者。