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Trace Elements

Dr.Aws Hassan

MRCP UK


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Trace Elements

-a naturally occurring, homogeneous, 
inorganic substance required in humans 
in amounts less than 100 mg/day

Essential nutrients in trace amounts


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Assessment of trace mineral status is difficult and 
requires specialized analytical instruments (atomic 
absorption spectrometry

Serum measurements are complicated by 
associated disease states that affect levels of 
circulating binding proteins (e.g., albumin)

Diagnosis is dependent on high degree of suspicion, 
careful inspection for signs and symptoms, thorough 
understanding of predisposing causes and resolution 
of symptoms with therapeutic trial.


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Copper


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Copper Metabolism

Intestinal absorption/membrane translocation 
mediated by specific transporters

Copper circulates bound to ceruloplasmin

Relative tissue distribution of copper reflects levels 
of cuproenzymes

Excretion occurs via transport of copper into bile 
and elimination in feces 


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Copper: Biochemical Functions

Essential catalytic cofactor for many cuproenzymes
including:

Cu, Zn-superoxide dismutase (antioxidant)

Cytochrome C oxidase (ATP synthesis, neurologic function)

Ceruloplasmin (6 atoms per molecule)

Functions to oxidize Fe

+2 

to Fe

+3

for binding to transferrin.  

Congenital absence of this protein leads to tissue iron 
accumulation and iron overload syndrome 
(hemochromatosis)


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Copper Physiology/Deficiency

Acquired deficiency is rare. Causes include:

High intake of Zinc

Renal dialysis patients

Use of copper chelating agents (penicillamine)

Manifestations:

Hypochromic microcytic anemia

Neutropenia

Hypopigmentation of hair and skin

Structural abnormalities in connective tissue (hair, teeth, bone 
demineralization, vascular system with arterial aneurysms with risk 
of hemorrhage and thrombosis)

Fetal and neonatal deprivation leads to neurologic dysfunction

Reduced levels of circulating copper and ceruloplasmin


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Food Sources

-organ meats, seafood, nuts, seeds, 
cereals, whole grains, cocoa


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Iodine


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Iodine

-body normally has 20-30 mg of iodine 
and more than 75% is in the thyroid 
gland

-the rest is in the mammary gland, 
gastric mucosa, and blood

-

it’s only function is related to thyroid 

hormone


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Iodine

Required for synthesis of thyroid hormone

Thyroxine (T

4

– 4 atoms of iodine per molecule

Triiodothyronine (T

3

– 3 atoms of iodine per molecule

Thyroxine


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Absorption and 

Excretion

-iodine is absorbed in the form of iodide
-occurs both as free and protein-bound iodine 
in circulation
-iodine is stored in the thyroid where it is used 
for the synthesis of T3 and T4 
-the hormone is degraded in target cells and 
in the liver and the iodine is conserved if 
needed
-excretion is primarily via urine
-small amts from bile are excreted in the 
feces


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Food Sources

-foods of marine origin (seaweed), 
processed foods, iodized salt


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Deficiency

-goiter

—enlargement of the thyroid 

gland 

-deficiency may be absolute

—in areas 

of deficiency, or relative

—adolescence, 

pregnancy, lactation

-goiters are more prevalent in women 
and with increased age


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-goitrogens occurring naturally in foods can 
cause goiter by blocking absorption or 
utilization of iodine (cabbage, peanuts, 
soybeans)

-***severe deficiency during gestation and 
early postnatal growth:  cretinism

—mental 

deficiency, quadriplegia, deaf mutism, 
dysarthria, shuffling gait, short stature, 
hypothyroidism.


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Endemic Cretinism

Note normal man and 
three adult women with 
cretinism:

Short stature

Protuberant abdomen

Low IQ


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(IDD)

Iodine deficiency is the most 

common nutrient deficiency in the 

world!


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Iodine Excess and Toxicity

Humans are remarkably tolerant to high 
iodine intakes

In iodine deficiency, repletion must be done 
slowly to prevent hyperthyroidism

Paradoxical goiter (enlarged thyroid as a 
result of very high intakes of iodine)

Occurs in Japan and China with high intake of 
seaweed (50,000 - 80,000 

mg/day)


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Toxicity

-iodine has wide margin of safety


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Goiter

Endemic to parts 
of S. America and 
India

Sporadic cases in 
U.S.

Selenium 
deficiency 
(needed to 
convert T4 to T3)


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Goiter - Complications

Usually 
asymptomatic
Acute pain from 
thyroidal 
hemorrhage
Dysphagia (trouble 
swallowing)
Dyspnea (trouble 
breathing)


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Chromium


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Chromium--Functions

-required for normal lipid and CHO 

metabolism and for the fxn of insulin

-?can supplementation raise HDL


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Absorption and 

Excretion

-10-25% absorption in its trivalent form
-amount absorbed remains constant at 
dietary intakes >40 ug (micrograms) at which 
point excretion in urine is proportional to 
intake
-increased intake of simple sugar, strenuous 
exercise, or physical trauma also increase 
urinary excretion
-both chromium and Fe are carried by Tf, 
however albumin can also assume this role


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Food Sources

-cereals, meats, poultry, fish, beer 


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Deficiency

-altered CHO metabolism, impaired glucose 
tolerance, glycosuria, fasting hyperglycemia, 
increased insulin levels and decreased insulin 
binding
-impaired growth, peripheral neuropathy, 
negative nitrogen balance
-increased chromium losses in stress
-hyperglycemia and wt loss reverse with IV 
supplementation in TPN


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Toxicity

-chronic renal failure


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Cobalt


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Cobalt

-most stored with vitamin B12

-component of B12

—cobalamin

-

essential for maturation of RBC’s and 

normal function of all cells


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Absorption and 

Excretion

-shared with Fe

-absorption is increased in pts with 
deficient Fe intake, portal cirrhosis with 
Fe overload, and hemochromatosis

-excretion is mainly thru the urine

-small amts in feces, hair, sweat


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Sources and Intakes

-microorganisms are able to synthesize 
B12

-***humans must obtain B12 and cobalt 
from animal foods such as organ and 
muscle meat

-***takes a long time to become 
deficient

—happens in vegetarians


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Deficiency

-related to vit B12 deficiency

-**macrocytic anemia

-genetic defect:  pernicious anemia

-tx:  massive doses

-discussed in the vitamin lecture


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Toxicity

-polycythemia

-hyperplasia of BM

-reticulocytosis

-increased blood volume


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Selenium


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Selenium

-glutathione peroxidase
-acts with other antioxidants and free 
radical scavengers
-overlaps with vit E for antioxidant 
effects
-fxn with vit E to protect cell and 
organelle membranes from oxidative 
damage


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Selenium 

– Biochemical Functions

Serves as a catalytic component in enzymes 
and proteins

Iodothyronine 5

’- deiodinase 

Thioredoxin reductase 

Glutathione peroxidase (destroys hydrogen 
peroxide)


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Selenium 

– Metabolism

Selenium is stored in the body as 
selenocysteine in selenoproteins

Excreted in urine and in breath as dimethyl 
selenide with a garlic-like odor


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Relationship of glutathione peroxidase,
selenium, and vitamin E

GSH peroxidase
contains selenocysteine


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Absorption and 

Excretion

-upper segment of the small intestine
-increased absorption with deficiency
-status is measured by measuring 
selenium or glutathione peroxidase in 
plasma, platelets, and RBC

’s or 

selenium levels in whole blood or urine
-RBC selenium is an indicator of long-
term status


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Food Sources

Food content tends to follow Se content of soil 

richest food sources are organ meats and sea 
foods, followed by  cereals and grains, dairy 
products, fruits and vegetables

Se content of grains can vary by 10,000 fold

Requirements determined based on serum 
glutathione peroxidase activity


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Selenium Deficiency Diseases

Major problem in livestock

Human deficiency is rare except in areas with low 
Se content in soil

Keshan disease occurs in Keshan China: endemic 
cardiomyopathy and muscle weakness (due to oxidized 
lipids)

Aggressive supplementation has eliminated disease

Iatrogenic deficiency

TPN without supplemental Se


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Selenium Toxicity

Range of dietary Se intake without 
toxicity is narrow
Acute selenium poisoning can result 
in cardiorespiratory collapse (gram 
amounts)
Chronic toxicity (selenosis) changes 
in nail structure and loss of hair 
(intakes ~6x UL)
Hair and nail brittleness


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Selenium and Cancer Prevention

Epidemiologic evidence indicates low intakes of 
Se are associated with higher risk of prostate 
cancer

Prospective study of Se supplementation 
demonstrated 42% reduction in cancer incidence

Small sample size and other confounding factors 
have diminished enthusiasm for the results of 
these studies


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Molybendum


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Molybendum

-relationship with copper and sulfate
-cofactor of many enzymes involved in 
the catabolism of sulfur AA, purines and 
pyridines
-Toxicity:  gout-like syndrome, 
reproductive SE

’s

-Deficiency:  increased risk with co-
existing copper deficiency, TPN


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Silicon, Vanadium, 

Arsenic, Boron

-see handouts posted on the web

-will not be on the exam!!!




رفعت المحاضرة من قبل: Ismail AL Jarrah
المشاهدات: لقد قام 4 أعضاء و 84 زائراً بقراءة هذه المحاضرة








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