Austin Gregory L, Weiskopf Jennifer R, Czwornog Jennifer L
Division of Gastroenterology and Hepatology.
Department of Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO.
J Clin Gastroenterol. 2018 Sep;52(8):691-695. doi: 10.1097/MCG.0000000000000921.
Proton pump inhibitor (PPI) use has been associated with cardiovascular disease, chronic kidney disease, and dementia. Prior studies did not account for key confounders and little is known about the association of PPIs with serum biomarkers of inflammation, insulin resistance, cardiovascular risk, and renal function. Our aims were to investigate differences in these biomarkers between PPI users and nonusers.
Our data are from the National Health and Nutrition Examination Survey (NHANES), a complex cross-sectional multistage probability sample of the US civilian population. We used data on 5189 eligible adults aged 18 to 85 years. Appropriate survey commands were used and potential confounding variables (including BMI, duration of PPI use, use of other non-PPI medications, and health behaviors) were included in multivariable regression models assessing biomarker outcomes.
PPI use was associated with differences in mean (±SE) fasting low-density lipoprotein (LDL) (by 11.7±3.7 mg/dL; P=0.006), and apolipoprotein B (by 7.6±2.6 mg/dL; P=0.01). PPI use was not associated with significant differences in total cholesterol (P=0.13), high-density lipoprotein (P=0.27), triglycerides (P=0.70), c-reactive protein (P=0.52), the homeostatic model assessment-insulin resistance (P=0.48), hemoglobin A1c (P=0.39), or homocysteine (P=0.87). PPI use was associated with a decrease in blood urea nitrogen (by 1.0±0.3 mg/dL; P=0.008) but not creatinine (P=0.38) or uric acid (P=0.34).
PPI was not associated with clinically significant differences in serum biomarkers of inflammation, insulin resistance, cardiovascular risk, and renal function. Rather, increasing BMI was strongly associated with PPI use and clinically significant differences in these biomarkers.
质子泵抑制剂(PPI)的使用与心血管疾病、慢性肾脏病及痴呆有关。既往研究未考虑关键混杂因素,关于PPI与炎症、胰岛素抵抗、心血管风险及肾功能的血清生物标志物之间的关联知之甚少。我们的目的是调查PPI使用者与非使用者在这些生物标志物方面的差异。
我们的数据来自美国国家健康与营养检查调查(NHANES),这是一项针对美国平民人口的复杂横断面多阶段概率样本。我们使用了5189名年龄在18至85岁之间的符合条件成年人的数据。使用了适当的调查指令,并将潜在的混杂变量(包括体重指数、PPI使用时长、其他非PPI药物的使用及健康行为)纳入评估生物标志物结果的多变量回归模型。
使用PPI与空腹低密度脂蛋白(LDL)均值(±标准误)差异有关(相差11.7±3.7mg/dL;P = 0.006),以及载脂蛋白B(相差7.6±2.6mg/dL;P = 0.01)。使用PPI与总胆固醇(P = 0.13)、高密度脂蛋白(P = 0.27)、甘油三酯(P = 0.70)、C反应蛋白(P = 0.52)、稳态模型评估胰岛素抵抗(P = 0.48)、糖化血红蛋白(P = 0.39)或同型半胱氨酸(P = 0.87)的显著差异无关。使用PPI与血尿素氮降低有关(相差1.0±0.3mg/dL;P = 0.008),但与肌酐(P = 0.38)或尿酸(P = 0.34)无关。
PPI与炎症、胰岛素抵抗、心血管风险及肾功能的血清生物标志物的临床显著差异无关。相反,体重指数增加与PPI使用及这些生物标志物的临床显著差异密切相关。