Department of Medicine, Division of Gerontology/Geriatrics/Palliative Care, University of Alabama At Birmingham, 1313 13th Street S., Birmingham, AL, USA.
Integrative Center for Aging Research, University of Alabama At Birmingham, Birmingham, AL, USA.
Aging Clin Exp Res. 2021 Jun;33(6):1651-1658. doi: 10.1007/s40520-020-01684-z. Epub 2020 Sep 8.
Intestinal (i.e., "gut") permeability may be related to cardiovascular disease (CVD) risk, but biomarkers for gut permeability are limited and associations with CVD risk are unknown-particularly among older adults.
This cross-sectional study aimed to determine if serum biomarkers related to gut permeability [intestinal fatty acid-binding protein (iFABP)] and bacterial toxin clearing [cluster of differentiation 14 (CD14), lipopolysaccharide binding protein (LBP)] are associated with CVD risk among older adults.
Older adults (n = 74, 69.6 ± 6.5-years-old) were stratified by CVD risk category. One-way ANOVAs determined differences in each biomarker by risk category, and associations with risk score were evaluated with Pearson correlations.
LBP (p = 0.007), but not iFABP and CD14, was significantly different between CVD risk categories. Post-hoc tests indicated LBP was higher in moderate risk and high-moderate risk compared to the high risk category (p < 0.005). Evaluation of LBP and individual components in the risk score demonstrated a moderate, negative correlation of LBP with age and systolic blood pressure (r = - 0.335 and r = - 0.297) and a small positive correlation between LBP and total cholesterol and LDL cholesterol (r = 0.204 and r = 0.220).
DISCUSSION/CONCLUSION: Lower risk for CVD was associated with higher circulating concentrations of LBP, lower iFABP, and lower systemic inflammation in older adults. Further, there were small positive relationships between total and LDL cholesterol and circulating levels of LBP. These data suggest LBP may be a key component in reducing CVD risk in older adults.
肠道(即“肠道”)通透性可能与心血管疾病(CVD)风险有关,但肠道通透性的生物标志物有限,与 CVD 风险的关系尚不清楚 - 尤其是在老年人中。
这项横断面研究旨在确定与肠道通透性相关的血清生物标志物[肠脂肪酸结合蛋白(iFABP)]和细菌毒素清除[分化群 14(CD14),脂多糖结合蛋白(LBP)]是否与老年人的 CVD 风险相关。
将老年人(n=74,69.6±6.5 岁)按 CVD 风险类别分层。单向方差分析确定了每个生物标志物在风险类别之间的差异,并通过 Pearson 相关性评估了与风险评分的相关性。
LBP(p=0.007),而不是 iFABP 和 CD14,在 CVD 风险类别之间存在显著差异。事后检验表明,中度风险和中高风险组的 LBP 明显高于高风险组(p<0.005)。对 LBP 和风险评分中的单个成分进行评估表明,LBP 与年龄和收缩压呈中度负相关(r=-0.335 和 r=-0.297),与总胆固醇和 LDL 胆固醇呈小正相关(r=0.204 和 r=0.220)。
讨论/结论:较低的 CVD 风险与老年人循环中较高的 LBP 浓度、较低的 iFABP 和较低的全身性炎症相关。此外,总胆固醇和 LDL 胆固醇与循环 LBP 水平之间存在小的正相关关系。这些数据表明 LBP 可能是降低老年人 CVD 风险的关键因素。