Miller Amanda J, Theou Olga, McMillan Miranda, Howlett Susan E, Tennankore Karthik K, Rockwood Kenneth
Department of Nephrology.
Division of Geriatric Medicine, and.
J Gerontol A Biol Sci Med Sci. 2017 Mar 1;72(3):376-381. doi: 10.1093/gerona/glw114.
Frailty represents an age-related state of increased risk of adverse health outcomes, reflecting some combination of increased damage and compromised repair processes. Our objectives were to establish whether frailty is associated with dysnatremia (a deviation of serum sodium from normal values), to determine whether frailty explains the previously established association between age and dysnatremia and to assay the impact of each on mortality.
The relationship between age, frailty, and dysnatremia was investigated across the adult life course in 8,911 respondents from the 2003-2004 and 2005-2006 cross-sectional National Health and Nutrition Examination Survey, on whom both laboratory and mortality data were available. A frailty index (FI) was calculated for each respondent and related to dysnatremia (serum sodium values outside a 136-144 mmol/L reference range).
Dysnatremia was significantly related to both age and frailty; as the degree of frailty increased, so did the proportion with dysnatremia, for example, from 4.1% in those with FI less than 0.10, to 12.4% in those with FI 0.40 or more; p less than .001. Adjusted for frailty, the relationship between age and dysnatremia was no longer significant. In the age- and sex-adjusted Cox models, both frailty (hazard ratio [HR]: 1.05; 95% confidence interval [CI]: 1.04-1.05 for every 0.01 increase in FI) and dysnatremia (HR: 1.85; 95% CI: 1.51-2.26) were significant predictors of mortality; when hyponatremia was separated from hypernatremia in the Cox models, hypernatremia wasn't significant, but only 41 participants were identified as hypernatremic.
Increasing frailty is associated with dysnatremia and confounds the association between age and dysnatremia.
衰弱是一种与年龄相关的健康不良后果风险增加的状态,反映了损伤增加和修复过程受损的某种组合。我们的目标是确定衰弱是否与血钠异常(血清钠偏离正常值)相关,确定衰弱是否能解释先前确立的年龄与血钠异常之间的关联,并分析二者对死亡率的影响。
在2003 - 2004年和2005 - 2006年的横断面全国健康与营养检查调查的8911名受访者中,研究了整个成年期年龄、衰弱与血钠异常之间的关系,这些受访者均有实验室检查和死亡率数据。为每位受访者计算衰弱指数(FI),并将其与血钠异常(血清钠值超出136 - 144 mmol/L参考范围)相关联。
血钠异常与年龄和衰弱均显著相关;随着衰弱程度增加,血钠异常的比例也增加,例如,FI小于0.10者中为4.1%,FI为0.40或更高者中为12.4%;p < 0.001。校正衰弱因素后,年龄与血钠异常之间的关系不再显著。在年龄和性别校正的Cox模型中,衰弱(FI每增加0.01,风险比[HR]:1.05;95%置信区间[CI]:1.04 - 1.05)和血钠异常(HR:1.85;95% CI:1.51 - 2.26)均是死亡率的显著预测因素;在Cox模型中将低钠血症与高钠血症分开时,高钠血症不显著,但仅41名参与者被确定为高钠血症。
衰弱加剧与血钠异常相关,并混淆了年龄与血钠异常之间的关联。