Probiotic Intake May Protect from All-Cause Mortality and Especially Cardiovascular Mortality in People Without Diabetes

医学 糖尿病前期 糖尿病 混淆 危险系数 比例危险模型 血糖性 死亡风险 内科学 死亡率 置信区间 疾病 低风险 全国健康与营养检查调查 人口学 益生菌 死因 2型糖尿病 生理学 流行病学 环境卫生 血糖负荷 肠道菌群 代谢综合征 相对风险
作者
Yuan Zhou,Qian Zhang,Xinfang Du,Ying Song,Yongping Liu
出处
期刊:Current Nutrition & Food Science [Bentham Science Publishers]
卷期号:22 (4): 307-318
标识
DOI:10.2174/0115734013423814251127064733
摘要

Introduction: This study examined the association between probiotic/prebiotic intake and all-cause and cause-specific mortality among American adults stratified by glycemic status. Methods: We included participants with probiotic/prebiotic intake and follow-up data from NHANES 1999-2016. Mortality was linked to the National Death Index. Cox proportional hazards models with three levels of covariate adjustment were used to estimate hazard ratios (HRs) and 95% confidence intervals (CIs). Stratified analyses assessed result stability. Results: Among 13,604 adults (6,886 non-diabetic, 4,210 prediabetic, 2,508 diabetic), probiotic intake in the non-diabetic group was associated with reduced all-cause mortality (HR (95% CI) 0.68 (0.52, 0.88), P = 0.003) and cardiovascular disease (CVD) mortality (HR (95% CI) 0.43 (0.25, 0.71), P < 0.001). Yogurt consumption alone was similarly associated with lower all-cause (HR (95% CI) 0.70 (0.54, 0.90), P = 0.005) and CVD mortality (HR (95% CI) 0.45 (0.26, 0.78), P = 0.005). No significant associations were found in prediabetic or diabetic groups. Discussion: The protective association was observed only in non-diabetic individuals and may be partially mediated by socioeconomic and clinical factors. The lack of association in dysglycemic groups may be attributed to advanced metabolic dysregulation, concomitant medications, and gut microbiota alterations. Residual confounding cannot be excluded. Conclusion: Probiotic intake is associated with lower all-cause and CVD mortality in nondiabetic adults, but not in those with prediabetes or diabetes. These findings suggest population- specific effects and highlight the need for further clinical trials to establish causality.
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