Johnson Richard J, Segal Mark S, Sautin Yuri, Nakagawa Takahiko, Feig Daniel I, Kang Duk-Hee, Gersch Michael S, Benner Steven, Sánchez-Lozada Laura G
Division of Nephrology and Department of Medicine, University of Florida, Gainesville, FL, USA.
Am J Clin Nutr. 2007 Oct;86(4):899-906. doi: 10.1093/ajcn/86.4.899.
Currently, we are experiencing an epidemic of cardiorenal disease characterized by increasing rates of obesity, hypertension, the metabolic syndrome, type 2 diabetes, and kidney disease. Whereas excessive caloric intake and physical inactivity are likely important factors driving the obesity epidemic, it is important to consider additional mechanisms. We revisit an old hypothesis that sugar, particularly excessive fructose intake, has a critical role in the epidemic of cardiorenal disease. We also present evidence that the unique ability of fructose to induce an increase in uric acid may be a major mechanism by which fructose can cause cardiorenal disease. Finally, we suggest that high intakes of fructose in African Americans may explain their greater predisposition to develop cardiorenal disease, and we provide a list of testable predictions to evaluate this hypothesis.
目前,我们正经历一场以肥胖、高血压、代谢综合征、2型糖尿病和肾脏疾病发病率上升为特征的心脏肾脏疾病流行。虽然热量摄入过多和缺乏身体活动可能是推动肥胖流行的重要因素,但考虑其他机制也很重要。我们重新审视一个古老的假说,即糖,尤其是过量的果糖摄入,在心脏肾脏疾病流行中起关键作用。我们还提供证据表明,果糖独特的诱导尿酸升高的能力可能是果糖导致心脏肾脏疾病的主要机制。最后,我们认为非裔美国人中高果糖摄入量可能解释了他们患心脏肾脏疾病的更大易感性,并且我们提供了一系列可检验的预测来评估这一假说。