Iron metabolism/Anemias Flashcards

1
Q

What are the major ways to control iron balance? Is there a way to excrete iron? How much iron is there in one RBC?

A
  1. Dietary uptake
  2. Release of iron from macrophages and liver

NO MECHANISM FOR IRON EXCRETION

RBC contains 1 mg of iron/mL

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2
Q

What foods inhibits iron adsorption and what foods increase iron adsorption?

A

Inhibit
Oxalates - ex. spinach, tea
Phylates - ex. soy, almond
Calcium - ex. milk
Antacids
Polyphenols
Tannins - ex. coffee, tea

Increase
Alcohol
Red meat
Vit C and A
Fresh fruit and juice

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3
Q

Where does iron absorption occur? What are the 3 steps in iron absorption. Describe and explain.

A

Occurs in enterocyte (intestinal epithelial cells)

  1. Transfer of iron within cytosol of enterocyte
    - Once within cytoplasm, iron is shuttled by a small MW transport peptides which retains the iron redox state
    - Iron can be stored as ferritin or transported through the basolateral membrane and into circulation through ferroportin
  2. Transfer of iron from cytosol to plasma
    - Major pathway:
    a. transport of Fe2+ across basolateral surface via FERROPORTIN
    b. Fe2+ oxidized to Fe3+ by HEPHAESTIN
    c. Fe3+ binds to TRANSFERRIN (Tf) and is transported to various tissue/cells
    - Minor pathway:
    a. Fe2+ directly transported into plasma via a transmembrane iron transporter
    b. CERULOPLASMIN oxidizes it into Fe3+ and is bound by Tf
  3. Iron uptake into plasma into tissues
    - Transferrin receptor 1 (TFR1) is expressed on cell surface and is responsible for taking up Tf-bound iron
    - Involve receptor mediated endocytosis
    - Vesicles acidified and iron is released from Tf
    - ApoTf recycled back to cell surface
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4
Q

What are the different pathways in the regulation of iron absorption? Describe and explain.

A
  1. Hepcidin pathway
    Hepcidin -> produced by liver and regulates iron absorption by binding to ferroportin
    - Naturally tries to inhibit iron absorption to prevent bacteria from utilizing iron as bacteria needs iron for growth
    - Plays a role in anemia of chronic inflammation
  2. Intracellular regulation of iron metabolism
    The synthesis of transferiin receptor (TfR), ferritin and DMT1 is regulated post-transcriptionally
    - mRNA for each of these proteins contain 1 or several IRON RESPONSE ELEMENTS (IREs)

In iron depeleted cells:
- Iron regulatory protein (IRP) binds to 5’ IRE which prevents the initiation of translation and inhibits ferritin synthesis
- IRP binds to 3’ IRE of TfR which stablizes mRNA and increases translation

When iron is high in cells:
- Efficient translation of ferritin mRNA and ferritin synthesis proceeds
- TfR mRNA is destabilized which reduces translation of TfR

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5
Q

What are the two forms of iron storage? Where are they found?

A

Ferritin
- 48000 MW
- Highest conc in LIVER, SPLEEN, BM

Hemosiderin
- Denatured form of ferritin
- If cells overloaded with iron, hemosiderin accumulates in the lysosomes (mainly found in MACROPHAGES)

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6
Q

Difference between absorption of heme vs non-heme iron.

A

Heme absorption - well absorbed (ex. meat)
Iron uptake not regulated
~ 10% of total iron intake

Non-heme absorption - less well absorbed (ex. nuts)
Iron uptake tightly regulated
~ 90% of iron in diet

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7
Q

What is the process of heme absorption?

A
  1. Heme iron is taken up by endocytosis
  2. Fe(2+) is liberated from heme within endosome/lysosome by Heme Oxygenase (HO) that cleaves porphyric ring
  3. Proceed similar to non-heme absorption
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8
Q

What is the process of non-heme absorption?

A
  1. Enterocytes are incapable of binding and absorbing Fe(3+), ferro-reductase reduced Fe(3+) to Fe(2+)
  2. Fe(2+) bound and transported into the enterocyte by divalent metal transporter (DMT-1) channels
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9
Q

What are the different proteins involved in iron metabolism and regulation? State their names and functions.

A

Transferrin - Transports iron in plasma

DMT1 - transport ferrous iron from gut lumen into enterocyte

Duodenal cytochrome b (DCYTB) - reduces Fe3+ to Fe2+ that can be transported by DMT1

TfR1 - delivers iron from plasma into erythroid precursors in the bone marrow and other cells in the body

Ferritin - major iron storage protein

Hepcidin - regulates iron absorption and release of iron from macrophages

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10
Q

*What happens when there is an increase or decrease in hepcidin production in the liver?

A

Increase hepcidin -> hepcidin binds and inhibits ferroportin which blocks iron export into the blood circulation

Decreased hepcidin -> ferroportin is free to export iron from enterocytes and macrophages which increases iron absorption and recycling

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11
Q

Is excess iron good or bad? Why?

A

Bad - If the capacity of ferritin to store iron is exceeded, iron is stored in liver cells and other tissues which can take up non-Tf-bound iron from the plasma, causing significant damage

  1. Unbound (free) iron is toxic, because it catalyzes the generation of potent free-radical species via the Fenton and Haber-Weiss reactions
  2. Iron can produce abundant quantities of hydroxyl radical (OH) from less reactive oxygen species
  3. Hydroxyl radical (OH) cause irreversible oxidative damage to DNA, lipids and proteins a.k.a oxidative stress
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12
Q

How can body iron content accumulate?

A
  1. Increased intestinal iron absorption
  2. Ineffective erythropoiesis
  3. Iron is injected into the body
  4. Liver disease
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13
Q

What is Hereditary Hemochromatosis? What is it, why does it happen and what are the clinical manifestations? What can we do to treat this disease?

A

Hereditary Hemochromatosis is a disorder of excess iron that is caused by increased intestinal iron absorption.
- autosomal recessive disorder
- disrupts the body’s regulation of iron that results in toxic accumulation of iron in vital organs

Cause - Genetic mutation in genes responsible for regulating Hepcidin
- Mutations: HFE Cys282Tyr and His63Ap

CM - occur in 5th decade or later
- High transferrin saturation (>45% men, 55% women)
- High ferritin

Treatment
- Phlebotomy
- Donate blood if meet all other criteria

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14
Q

What is anemia? What causes anemia?

A

Anemia is a condition in which there is reduced proportion of RBCs

Causes
1. Too little iron
2. Too little Hb
3. Too little RBCs
-> decreased production
-> increased destruction
-> loss of RBC like bleeding

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15
Q

What are useful blood indices used for the classification of anemia?

A

MCV = Mean Cell Volume
Measurement of size and volume of RBC
High MCV = large RBC cell size
Low MCV = Small RBC cell size

Reticulocytes = Immature RBCs
Helps to determine whether anemia is due to production/destruction
Low reticulocyte = production prob
High reticulocyte = increased destruction/blood loss

Other cell counts - neutrophils, platelets

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16
Q

What are the classifications of anemia?

A

Normocytic - Normal MCV
Microcytic - Low MCV
Macrocytic - High MCV

17
Q

What are the subcategories of normocytic anemia?

A

Increased Reticulocyte
- Within RBCs
- Outside RBCs

Decreased or normal reticulocyte

18
Q

What are the various disorders of normocytic (hemolytic) anemia due to problems within RBCs? (Increased reticulocyte)

A
  1. Hereditary Spherocytosis
    - Inherited defects caused by mutations in RBC membrane cytoskeleton
    - Spherocytes are formed
  2. Hereditary Elliptocytosis
    - Can be detected by blood smear examination showing >25% elliptocytes
    - Heterogenous group of disorders caused by various mutations in genes affecting RBC cytoskeleton and membrane protein integrity
    - Asymptomatic, some demonstrate hemolytic anemia and splenomegaly
  3. RBC Enzyme Defect
    - G6PD DEFICIENCY (“Fava Beans” hemolysis)
    -> failure to generate adequate NADPH
    -> erythrocytes susceptible to oxidation of Hb by oxidant radicals like h2o2
    - PK DEFICIENCY
    -> caused by a defect in glycolytic RBC metabolism
    -> lack of ATP
    -> incr RBC destruction
  4. Sickle cell anemia
19
Q

What are the various disorders of normocytic (hemolytic) anemia due to problems outside RBCs? (Increased reticulocyte)

A

Immune hemolytic anemia
1. Autoimmune hemolytic anemia (AIHA)
2. Alloimmune

Non-immune hemolytic anemia
1. Thrombotic thrombocytopenic purpura (TTP)
2. Hemolytic uremic syndrome
Causes FRAGMENTATION HEMOLYSIS

20
Q

What is autoimmune hemolytic anemia (AIHA)? What are the 2 subgroups of AIHA?

A

Caused by auto-Ab-mediated destruction

Classified into 2 primary subgroups based on optimal temperatures at which Ab bind:
1. Warm AIHA - involves IgG Ab that react with RBC membrane at normal body temp
2. Cold AIHA - involves IgM Ab that bind to polysaccharides on RBC surface at low temp and then cause lysis on rewarming
- Can see “clumps” of RBC under microscope

21
Q

What is alloimmune hemolytic anemia? What test used to diagnose? Describe the test.

A

Ab against a non-self Ag

Direct antiglobulin test (DAT)
1. Determines whether there is any Ab and/or complement binding to a patient’s RBC
2. Anti-human globulin reagent is added directly to patient’s washed RBCs
3. The occurrence of agglutination means that patient’s RBCs have Abs (self/non-self) binding to its surface

22
Q

What is thrombotic thrombocytopenic purpura (TTP) and hemolytic uremic syndrome (HUS) caused by?

A

TTP - Life threatening disease characterized by deficiency in ADAMTS13 enzyme

HUS - Caused by shiga toxin-producing E.coli and shigella, usually from ingestion of uncooked ground meat

23
Q

What is a disorder that causes decreased reticulocytes (or normal) in normocytic anemia?

A

Aplastic anemia - a.k.a bone marrow failure
- Reduced cellularity and less production of RBC, WBC and platelets in BM

24
Q

What are the causes of microcytic anemia?

A

TAILS
T - Thalassemia*
A - Anemia of chronic inflammation*
I - Iron deficiency*
L - Lead poisoning
S - Sideroblastic anemia

25
Q

What is thalassemia?

A

Mutation of single globin gene/deletion of 1 or more globin genes which lead to unstable globin chain hence, damages/deforms RBC

Example of hemoglobinopathies that result in hemolytic anemia

26
Q

What is the pathophysiology of anemia of chronic inflammation?

A

Inflammatory cytokines (IL-6) cause an incr in hepcidin production in the liver. Hepcidin leads to inhibition of ferroportin. Results in:
1. Decreased intestinal absorption of iron
2. Inhibits export of iron from body tissues into plasma
3. Decreased release of iron from iron-recycling macrophages in spleen and liver
Decr iron in plasma -> decr prod of RBCs

2nd most common anemia worldwide

Develops in the context of systemic inflammation

Disorder of IRON DISTRIBUTION

27
Q

What are the clinical manifestations of iron deficiency anemia? What is the diagnostic testing for iron deficiency anemia?

A
  1. Elliptocyte
  2. Fatigue, headache, exercise intolerance, weakness

FERRITIN

28
Q

What are the causes of macrocytic anemia? Name the categories.

A
  1. Megaloblastic - inhibition of DNA synthesis
  2. Non-megaloblastic
    Myelodysplastic syndrome
    - Ineffective hematopoiesis + dysplasia (abnormal development)
    - Increase risk to development to acute myeloid leukemia
    - BM cellularity is usually normal/increased due to ineffecient hematopoiesis
29
Q

How are Anemia of Chronic Disease and Iron deficiency anemia similar and different from each other?

A

Similarity:
- Both have low iron levels in the plasma

Differences:
- Iron binding capacity is low in ACD
- Serum ferritin is high in ACD)
- C-reactive protein is high in ACD

30
Q

Why do people with chronic hemolytic anemia (e.g. hereditary spherocytosis, thalassemias) do not develop iron deficiency?

A
  1. Because iron is recycled efficiently
  2. Increased GI absorption
  3. Subset of patients also get transfused

However may dvlp folate deficiency

31
Q

What iron level do you expect in a patient with myelodysplastic syndrome?

A

Increased bc:
1. Ineffective erythropoiesis leads to decreased production of mature RBC
2. Leads to increased iron absorption mediated by suppressed hepcidin and upregulation of ferroportin
3. Increaased RBC transfusion requirements