Nickel, 24 Hour, Urine
Detecting nickel toxicity in patients exposed to nickel carbonyl
Clinical Information Discusses physiology, pathophysiology, and general clinical aspects, as they relate to a laboratory test
Nickel (Ni) is a silvery white metal that is widely distributed in the earth's crust. Nickel is essential for the catalytic activity of some plant and bacterial enzymes but its role in humans has not been defined. Elemental Ni may be essential for life at very low concentrations and is virtually nontoxic.
Nickel is commonly used in industry. It is a pigment in glass, ceramics, and fabric dyes; is converted in the Mond process to nickel carbonyl, Ni(CO)4, and used as a catalyst in petroleum refining and in the plastics industry, is frequently employed in the production of metal alloys (which are popular for their anticorrosive and hardness properties) in nickel-cadmium rechargeable batteries, and is used as a catalyst in hydrogenation of oils.
Ni(CO)4, a liquid with low vapor pressure, is one of the most toxic chemicals known to man. Ni(CO)4 is absorbed after inhalation, readily crosses all biological membranes, and noncompetitively inhibits ATP-ase and RNA polymerase. Breathing the vapors of Ni(CO)4 binds avidly to hemoglobin with resultant inability to take up oxygen. The affinity for hemoglobin is higher than carbon monoxide. The binding to hemoglobin is the main transport mechanism for spreading Ni(CO)4 throughout the body. Urine is the specimen of choice for the determination of Ni exposure via inhalation.
Patients undergoing dialysis are exposed to Ni and accumulate Ni in blood and other organs; there appears to be no adverse health effects from this exposure. Hypernickelemia has been observed in patients undergoing renal dialysis. At the present time, this is considered to be an incidental finding as no correlation with toxic events has been identified. Routine monitoring of patients undergoing dialysis is currently not recommended.
Breathing dust high in Ni content has been associated with development of neoplasms of the respiratory system and nasal sinuses. Most reactions to Ni are localized skin sensitivity and allergic skin disorders that occur on contact with nickel-containing alloys. These reactions do not correlate to blood concentrations; patients experiencing skin sensitivity reactions to nickel are likely to have normal circulating concentrations of Ni.
Reference Values Describes reference intervals and additional information for interpretation of test results. May include intervals based on age and sex when appropriate. Intervals are Mayo-derived, unless otherwise designated. If an interpretive report is provided, the reference value field will state this.
0-17 years: not established
> or =18 years: <3.6 mcg/24h
Values of 3.6 mcg/24-hour specimen and higher represent possible environmental or occupational exposure.
Nickel (Ni) concentrations above 50 mcg/24-hour specimen are of concern, suggesting excessive exposure.
Clinical concern about Ni toxicity should be limited to patients with potential for exposure to toxic Ni compounds such as nickel carbonyl. Hypernickelemia, in the absence of exposure to that specific form of Ni, may be an incidental finding or could be due to specimen contamination.
Cautions Discusses conditions that may cause diagnostic confusion, including improper specimen collection and handling, inappropriate test selection, and interfering substances
Specimen collection procedures for Ni require special collection containers, rigorous attention to ultraclean specimen collection and handling procedures, and analysis in an ultraclean facility. Unless all of these procedures are followed, increased urinary Ni results may be an incidental and misleading finding.
High concentrations of gadolinium and iodine are known to interfere with most metals tests. If either gadolinium- or iodine-containing contrast media has been administered, a specimen should not be collected for 96 hours.
This test cannot determine the source compound (eg, Ni sulfate) responsible for the exposure.
Clinical Reference Provides recommendations for further in-depth reading of a clinical nature
1. Moreno ME, Acosta-Saavedra LC, Meza-Figueroa D, et al: Biomonitoring of metal in children living in a mine tailings zone in Southern Mexico: A pilot study. Int J Hyg Environ Hlth 2010;213:252-258
2. Schulz C, Angerer J, Ewers U, et al: Revised and new reference values for environmental pollutants in urine or blood of children in Germany derived from the German Environmental Survey on Children 2003-2006 (GerES IV). Int J Hyg Environ Health 2009;212:637-647