Estimation of health risks associated with dietary cadmium exposure

In much of the world, currently employed upper limits of tolerable intake and acceptable excretion of cadmium (Cd) (E-Cd/E-cr) are 0.83 mu g/kg body weight/day and 5.24 mu g/g creatinine, respectively. These figures were derived from a risk assessment model that interpreted beta(2)-microglobulin (beta(2)MG) excretion > 300 mu g/g creatinine as a critical endpoint. However, current evidence suggests that Cd accumulation reduces glomerular filtration rate at values of E-Cd/E-cr much lower than 5.24 mu g/g creatinine. Low E-Cd/E-cr has also been associated with increased risks of kidney disease, type 2 diabetes, osteoporosis, cancer, and other disorders. These associations have cast considerable doubt on conventional guidelines. The goals of this paper are to evaluate whether these guidelines are low enough to minimize associated health risks reliably, and indeed whether permissible intake of a cumulative toxin like Cd is a valid concept. We highlight sources and levels of Cd in the human diet and review absorption, distribution, kidney accumulation, and excretion of the metal. We present evidence for the following propositions: excreted Cd emanates from injured tubular epithelial cells of the kidney; Cd excretion is a manifestation of current tissue injury; reduction of present and future exposure to environmental Cd cannot mitigate injury in progress; and Cd excretion is optimally expressed as a function of creatinine clearance rather than creatinine excretion. We comprehensively review the adverse health effects of Cd and urine and blood Cd levels at which adverse effects have been observed. The cumulative nature of Cd toxicity and the susceptibility of multiple organs to toxicity at low body burdens raise serious doubt that guidelines concerning permissible intake of Cd can be meaningful.

Automated summary

In most parts of the world, the currently accepted upper limits of cadmium (Cd) intake and excretion are 0.83 μg/kg body weight/day and 5.24 μg/g creatinine, respectively. However, recent evidence suggests that even lower levels of Cd accumulation can lead to reduced kidney function and increased risks of various diseases. This raises doubts about the reliability and validity of conventional guidelines for Cd exposure.