Copper
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| Copper |
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Copper is a mineral that occurs naturally in many foods, including vegetables,
legumes, nuts, grains and fruits, as well as shellfish, avocado, and beef
(organs such as liver). Because copper is found in the earth's crust, most of
the world's surface water and ground water used for drinking purposes contains
small amounts of copper.
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Copper is involved in numerous biochemical reactions in human cells. Copper is
a component of multiple enzymes, is involved with the regulation of gene
expression, mitochondrial function/cellular metabolism, connective tissue
formation, as well as the absorption, storage, and metabolism of iron. Copper
levels are tightly regulated in the body.
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Copper toxicity is rare in the general population. Wilson's disease is a
genetic disorder in which the body cannot rid itself of copper, resulting in
deposition in organs and serious consequences such as liver failure and
neurologic damage. Obstruction of bile flow, contamination of dialysis
solution (in patients receiving hemodialysis for kidney failure), Indian
childhood cirrhosis, and idiopathic copper toxicosis are other rare causes of
potentially dangerous excess copper levels. Such individuals should be
followed closely by a physician and nutritionist.
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Copper deficiency can occur in infants fed only cow-milk formulas (which are
relatively low in copper content), premature/low-birth weight infants, infants
with prolonged diarrhea or malnutrition, individuals with malabsorption
syndromes (including celiac disease, sprue, or short bowel syndrome), cystic
fibrosis, in the elderly, or those receiving intravenous total parenteral
nutrition (TPN) or other restrictive diets.
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Medicinal use of copper compounds dates to Hippocrates in 400 B.C. Bacterial
growth is inhibited on copper's surface, and hospitals historically installed
copper-alloy doorknobs and push-panels as a measure to prevent transmission of
infectious disease.
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Copper 7, copper acetate, copper amino acid chelates, copper citrate, copper
gluconate, copper glycinate, copper intrauterine device, copper sebecate,
copper sulfate, copper T, Cu, Cu IUD, cuivre, cupric oxide, cupric sulfate,
cuprum, CuSO4, elemental copper, inorganic copper, organic copper.
These uses have been tested in humans or animals. Safety
and effectiveness have not always been proven. Some of these conditions are
potentially serious, and should be evaluated by a qualified healthcare provider.
| Uses based on scientific evidence |
Grade* |
| Copper deficiency
Copper deficiency may occur in infants fed only cow-milk formulas (which
are relatively low in copper content), premature/low-birth weight
infants, infants with prolonged diarrhea or malnutrition, individuals
with malabsorption syndromes (including celiac disease, sprue, or short
bowel syndrome), cystic fibrosis, in the elderly, or those receiving
intravenous total parenteral nutrition (TPN) or other restrictive diets.
Such individuals may require supplementation with copper (and other
trace elements).
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| Age-related macular degeneration
There is not enough scientific evidence available to determine if copper
plays a role in this disorder.
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C |
| Alzheimer's disease prevention
Conflicting study results report that copper intake may either increase
or decrease the risk of developing Alzheimer's disease. Additional
research is needed before a recommendation can be made.
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| Arthritis
The use of copper bracelets in the treatment of arthritis has a long
history of traditional use, with many anecdotal reports of
effectiveness. There are research reports suggesting that copper
salicylate may reduce arthritis symptoms more effectively than either
copper or aspirin alone. Further study is needed before a recommendation
can be made.
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| Cancer
Preliminary research reports that lowering copper levels theoretically
may arrest the progression of cancer by inhibiting blood vessel growth
(angiogenesis). Copper intake has not been identified as a risk factor
for the development or progression of cancer.
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| Cardiovascular disease prevention /
atherosclerosis
The effects of copper intake or blood copper levels on cholesterol,
atherosclerosis (cholesterol plaques in arteries), or coronary artery
disease remain unclear. Studies in humans are mixed, and further
research is needed in this area.
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| Childhood growth promotion
Severe copper deficiency may retard growth. Adequate intake of
micronutrients including copper and other vitamins may promote growth as
measured by length gains.
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| Immune system function
Copper is involved in the development of immune cells and immune
function in the body. Severe copper deficiency appears to have adverse
effects on immune function, although the exact mechanism is not clear.
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| Marasmus
Copper deficiency may occur in this condition, and supplementation with
copper may play a role in the nutritional treatment of infants with this
condition. Infants with marasmus should be managed by a qualified
healthcare professional.
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| Menkes' kinky-hair disease
Menkes' kinky-hair disease is a rare disorder of copper
transport/absorption. Copper supplementation may be helpful in this
disease, although further research is necessary before a clear
management recommendation can be made.
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| Osteoporosis / osteopenia
Osteopenia and other abnormalities of bone development related to copper
deficiency may occur in copper-deficient low-birth weight infants and
young children. Supplementation with copper may be helpful in the
treatment and/or prevention of osteoporosis, although early human
evidence is conflicting. The effects of copper deficiency or copper
supplementation on bone metabolism and age-related osteoporosis require
further research before clear conclusions can be drawn.
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| Plaque prevention
A preliminary study suggests that rinsing with a copper solution is
effective in plaque reduction. Further research is required before
recommendations can be made.
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| Schizophrenia
Some studies of schizophrenic patients report high blood copper levels
with low urinary copper (suggesting that copper is being retained), and
low blood zinc levels. In some of these cases, zinc was observed to be
helpful as an anti-anxiety agent. The role of copper supplementation is
not clear.
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| Sideroblastic anemia
Copper deficiency is one of the causes of sideroblastic anemia that
should be considered when evaluating this condition, particularly when
the anemia is unresponsive to iron therapy alone. This anemia appears to
be caused by defective iron mobilization due to decreased ceruloplasmin
activity.
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| Systemic lupus erythematosus (SLE)
A preliminary study suggests that copper offers no benefit to
individuals with SLE. Further research is required before
recommendations can be made.
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| Trimethylaminuria (TMAU)
Trimethylaminuria (TMAU) is a metabolic disorder characterized by the
inability to oxidize and convert dietary-derived trimethylamine (TMA) to
trimethylamine N-oxide (TMAO). Preliminary evidence suggests that the
use of copper chlorophyllin results in a reduced urinary free TMA
concentration and normalization of TMAO. Further research is required in
this field before recommendations can be made.
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| Neural-tube defect prevention
The risk of neural-tube defects is decreased in women who take folic
acid and multivitamins during the periconception period. Supplementation
with trace-elements alone such as copper does not appear to prevent
these defects.
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D |
*Key to grades
A: Strong scientific evidence for this use;
B: Good scientific evidence for this use;
C: Unclear scientific evidence for this use;
D: Fair scientific evidence against this use;
F: Strong scientific evidence against this use.
Grading rationale
Uses based on tradition or theory
The below uses are based on tradition or scientific theories. They often
have not been thoroughly tested in humans, and safety and effectiveness have
not always been proven. Some of these conditions are potentially serious, and
should be evaluated by a qualified healthcare provider.
Aflatoxin toxicity, allergies, anemia, antibacterial, antioxidant, athletic
performance, bone diseases (growth), bone healing, bronchitis, cancer, cataracts
(prevention/progression), cognition, cystic fibrosis, decreasing cadmium
absorption, depression, fatigue, fetal development, hematopoiesis (stimulation
of blood cell production), Hodgkin's disease, hypercholesterolemia (high
cholesterol), hyperactivity, hypertension (high blood pressure), infertility,
learning disabilities, muscle ache, muscle cramps, optic nerve damage (ethambutol-induced),
oral deodorant,Pasteurellainfection, phenylketonuria, pneumonia,
premenstrual syndrome, psoriasis, rheumatic heart disease, senility, skin
problems (stretch marks), stomach ulcer, toxicity (pyrrolizidine alkaloid),
vitiligo, weight gain, wound healing.
The below doses are based on scientific research,
publications, traditional use, or expert opinion. Many herbs and supplements
have not been thoroughly tested, and safety and effectiveness may not be proven.
Brands may be made differently, with variable ingredients, even within the same
brand. The below doses may not apply to all products. You should read product
labels, and discuss doses with a qualified healthcare provider before starting
therapy.
Adults (18 years and older):
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The U.S. Recommended Daily Allowance (RDA) is 900 micrograms for adults; 1,000
micrograms for pregnant women; 1,300 micrograms for nursing women; and 890
micrograms for adolescents 14-18 years old. Surveys suggest that most
Americans consume less than the RDA for copper each day. Up to 10,000
micrograms daily appears to be safe for consumption in adults. Vegan diets
appear to provide adequate amounts of copper.
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In a number of clinical trials copper doses of 2-10 milligrams by mouth were
safely used in patients. For plaque inhibition, a 1.1mM copper rinse has been
used for four days. The appropriate application of ointment preparations
containing copper in concentrations up to 20% has also been studied with no
apparent toxic effects.
Children (younger than 18 years):
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The U.S. Recommended Daily Allowance (RDA) for children is 890 micrograms for
adolescents 14-18 years old; 700 micrograms for children 9-13 years old; 440
micrograms for children 4-8 years old; 340 micrograms for children 1-3 years
old; 220 micrograms for infants 7-12 months old; and 200 micrograms for
infants 0-6 months old. Surveys suggest that most Americans consume less than
the RDA for copper each day. Up to 3,000-5,000 micrograms daily appears to be
safe for consumption in children.
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Copper deficiency may occur in infants fed only cow-milk formulas (which are
relatively low in copper content) or synthetic low lactose diets,
premature/low-birth weight infants, infants with prolonged diarrhea or
malnutrition, malabsorption syndromes (including celiac disease, sprue, or
short bowel syndrome), cystic fibrosis, or during intravenous total parenteral
nutrition (TPN) or other restrictive diets. Such situations may merit copper
supplementation (and other trace elements), which should be under the
supervision of a healthcare professional. In the United States, copper is not
available in infant supplements.
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Management of marasmus should be under the supervision of a healthcare
professional, although 20-80 micrograms per kilogram per day of copper sulfate
supplementation by mouth has been reported as safe.
The U.S. Food and Drug Administration does not strictly
regulate herbs and supplements. There is no guarantee of strength, purity or
safety of products, and effects may vary. You should always read product labels.
If you have a medical condition, or are taking other drugs, herbs, or
supplements, you should speak with a qualified healthcare provider before
starting a new therapy. Consult a healthcare provider immediately if you
experience side effects.
Allergies
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Insufficient available evidence.
Side Effects and Warnings
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Copper toxicity is rare in the general population. Excess copper consumption
may lead to liver, kidney, or neurologic damage. Excess dosing may lead to
toxic symptoms including weakness, abdominal pain, nausea, vomiting, and
diarrhea, with more serious signs of acute toxicity including liver damage,
kidney failure, pleural damage, coma, and death. Other medical problems
associated with copper toxicity in studies or anecdotally include anxiety,
depression, fatigue, learning disabilities, memory lapses, diminished
concentration, insomnia, seizure, delirium, stuttering, hyperactivity,
arthralgias, myalgias, hypertension, gingivitis, dermatitis, discoloration of
skin/hair, preeclampsia, postpartum psychosis, weight gain, or transaminitis.
Acute copper poisoning has occurred through the contamination of beverages by
storage in copper containing containers as well as from contaminated water
supplies. In the U.S., the health-based guideline for a maximum water copper
concentration of 1.3 milligrams per liter has been enforced by the
Environmental Protection Agency.
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Genetic disorders affecting copper metabolism such as Wilson's disease, Indian
childhood cirrhosis, or idiopathic copper toxicosis place individuals at risk
of adverse effects of chronic copper toxicity at significantly lower intake
levels. Trientine is a copper-chelating agent used in the management of
Wilson's disease. Penicillamine has also been used to bind copper and enhance
its elimination in Wilson's disease. Zinc in therapeutic dosages has been used
to inhibit copper absorption in patients with Wilson's disease. Animal
research suggests that supplementation with taurine may reduce toxic effects
of copper when given in combination, although it is not clear if this is the
case in humans.
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Copper-T devices are a type of intrauterine devices (IUD) used for birth
control which have been linked to the development of anemia and increased risk
of pelvic infection in some users. Copper released from the IUDs may cause
hormonal changes and alter the menstrual cycle in women. Other common side
effects include pain/cramps, abnormal bleeding, and device expulsion. In some
cases, pelvic inflammatory disease (PID) or anemia may develop.
Pregnancy and Breastfeeding
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Pregnancy: It is unclear if copper supplementation is necessary during
pregnancy to maintain adequate levels. Copper is potentially unsafe when used
orally in higher doses than the RDA. Animal studies suggest that trace metal
aberrations, including copper, may be related to disturbed fetal growth or
teratogenicity, particularly in the setting of diabetic pregnancy.
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Breastfeeding: Copper is potentially unsafe when used orally in higher doses
than the RDA. Copper is present in breast milk.
Most herbs and supplements have not been thoroughly
tested for interactions with other herbs, supplements, drugs, or foods. The
interactions listed below are based on reports in scientific publications,
laboratory experiments, or traditional use. You should always read product
labels. If you have a medical condition, or are taking other drugs, herbs, or
supplements, you should speak with a qualified healthcare provider before
starting a new therapy.
Interactions with Drugs
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Antacids may interfere with copper absorption.
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Several human studies indicate that taking certain antipsychotics (haloperidol
and risperidone), nifedipine, or oral contraceptives may alter copper levels
in the body, although clinical significance is unknown. Copper levels should
be monitored by a qualified healthcare professional.
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Ethambutol (Myambutol®), and its metabolite, chelate copper resulting in
depleted levels. Copper chelation in the retina may contribute to ethambutol-induced
optic neuropathy. Whether supplemental copper can prevent this adverse effect
is not clear.
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Penicillamine (Cuprimine®, Depen®) is used to bind copper and enhance its
elimination in Wilson's disease. Because it dramatically increases the urinary
excretion of copper, individuals taking penicillamine for reasons other than
copper overload may have an increased requirement for copper.
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Trientine (Syprine®, Trien®) is a copper-chelating agent used in the
management of Wilson's disease.
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Levels of copper may be reduced after Zidovudine (Retrovir®, AZT), although
there is some evidence that this may be beneficial in HIV/AIDS patients, and
therefore copper supplements may not be advisable.
Interactions with Herbs and Dietary Supplements
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Several herbs and supplements, such as boron, vitamin C, selenium, molybdenum
and manganese may alter (decrease or increase) copper levels in the body.
Although copper may increase the concentration of cadmium in tissues based on
animal research, cadmium supplementation does not appear to significantly
alter copper levels. Calcium or rapeseed oilmeal may alter the metabolism of
copper.
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Long-term, high-copper intake may cause decreases in plasma concentrations of
folate.
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Animal studies suggest that low copper levels may result in decreased serum
dehydroepiandrosterone (DHEA) levels, although it is unclear if increased
copper intake increases DHEA levels.
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Adequate copper nutritional status appears to be necessary for normal iron
metabolism, transport, and red blood cell formation. High iron intake may
interfere with copper absorption. Copper deficiency is associated with
retention of iron in the liver.
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Animal research suggests that supplementation with taurine may reduce toxic
effects of copper when given in combination, although it is not clear if this
is the case in humans.
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High levels of supplemental zinc intake over extended periods of time may
result in decreased copper absorption in the intestines or copper deficiency
possibly due to increased synthesis of the intestinal cell protein
metallothionein which binds some metals. This may be the mechanism by which
zinc induces sideroblastic anemia. However, some animal research suggests that
high dietary zinc may not interfere with tissue or plasma concentrations of
copper.