Department of Biobehavioral Health, Pennsylvania State University, 219 Biobehavioral Health Building, University Park, PA, 16802, USA.
Department of Anthropology, Pennsylvania State University, University Park, PA, USA.
Eur J Nutr. 2023 Jun;62(4):1681-1690. doi: 10.1007/s00394-023-03105-z. Epub 2023 Feb 15.
Suboptimal hydration has been linked to a variety of adverse health outcomes. Few studies have examined the impact of hydration status on immune function, a plausible physiological mechanism underlying these associations. Therefore, we tested how variation in hydration status was associated with circulating pro-inflammatory cytokine levels and ex vivo lipopolysaccharide (LPS)-stimulated pro-inflammatory cytokine production.
Blood samples were obtained from a community sample of healthy middle-to-older-aged adults (N = 72). These samples were used to assess serum osmolality, a biomarker of hydration status, and markers of immune function including circulating pro-inflammatory cytokines and stimulated pro-inflammatory cytokine production after 4 and 24 h of incubation with LPS. Multiple linear regressions were used to test the association between serum osmolality (as a continuous variable) and markers of immune function at baseline and after 4 and 24 h adjusting for age, sex, and BMI. These models were re-estimated with serum osmolality dichotomized at the cut-off for dehydration (> 300 mOsm/kg).
While not significantly associated with circulating cytokines (B = - 0.03, p = 0.09), serum osmolality was negatively associated with both 4 h (B = - 0.05, p = 0.048) and 24 h (B = - 0.05, p = 0.03) stimulated cytokine production when controlling for age, sex, and BMI. Similarly, dehydration was associated with significantly lower cytokine production at both 4 h (B = - 0.54, p = 0.02) and 24 h (B = - 0.51, p = 0.02) compared to adequate hydration.
These findings suggest that dehydration may be associated with suppressed immune function in generally healthy middle-to-older aged community-dwelling adults. Further longitudinal research is needed to more clearly define the role of hydration in immune function.
水分摄入不足与多种健康不良后果有关。很少有研究探讨水合状态对免疫功能的影响,而免疫功能是这些关联的一种合理生理机制。因此,我们测试了水合状态的变化如何与循环促炎细胞因子水平和体外脂多糖 (LPS) 刺激的促炎细胞因子产生相关。
从健康的中老年社区样本中采集血样(N=72)。这些样本用于评估血清渗透压,这是水合状态的生物标志物,以及循环促炎细胞因子和 LPS 孵育 4 和 24 小时后刺激的促炎细胞因子产生的免疫功能标志物。使用多元线性回归测试血清渗透压(作为连续变量)与基线以及 4 和 24 小时后的免疫功能标志物之间的关联,调整年龄、性别和 BMI。这些模型使用血清渗透压在脱水(>300 mOsm/kg)临界点上的二分法重新进行估计。
虽然血清渗透压与循环细胞因子没有显著相关(B=-0.03,p=0.09),但在控制年龄、性别和 BMI 后,血清渗透压与 4 小时(B=-0.05,p=0.048)和 24 小时(B=-0.05,p=0.03)刺激的细胞因子产生均呈负相关。同样,与充足水合相比,脱水与 4 小时(B=-0.54,p=0.02)和 24 小时(B=-0.51,p=0.02)的细胞因子产生明显降低相关。
这些发现表明,脱水可能与一般健康的中老年社区居民的免疫功能抑制有关。需要进一步的纵向研究来更清楚地定义水合作用在免疫功能中的作用。