Iron Metabolism and M/H Anemias Flashcards

1
Q

Primary function of iron in the body

A

Oxygen transport

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2
Q

6 iron compartments of the body (largest to smallest) (%)

A
  1. Hb (~67% of TBI)
  2. Storage (~27%)
  3. Myoglobin (~3.5%)
  4. Labile pool (~2.2%)
  5. Tissue iron department (~0.2%)
  6. Transport compartment (~0.08%); smallest but most active
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3
Q

6 iron compartments of the body (forms of iron)

A
  1. Hb → Hb molecule
  2. Storage → ferritin
  3. Myoglobin → myoglobin molecule
  4. Labile pool → Fe bound to cell membrane
  5. Tissue iron department → Fe in cytochromes and intracellular enzymes
  6. Transport compartment → Fe bound to transferrin
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4
Q

4 factors that influence iron absorption

A
  1. Amount and type of iron accessible from food
  2. Functional state of GI mucosa and pancreas
  3. Current iron stores
  4. Erythropoietic needs
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5
Q

3 conditions that result in an increased need for iron

A
  • Growth periods
  • Blood loss
  • Diversion of iron to the fetus
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6
Q

Anatomic site at which iron is absrobed most efficiently

A

Duodenum of intestinal mucosa

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7
Q

Function of transferrin

A

Transports iron to nRBCs in BM

- iron is reduced to ferrous state and proceeds to mitochondria for insertion into protoporphyrin ring

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8
Q

Organelle that contains iron in erythrocyte precursors

A

Mitocondria

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9
Q

What is being measured

- Serum iron

A

Amount of iron (bound to transferrin) in serum/plasma

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10
Q

What is being measured

- TIBC

A

Amount of iron that transferrin can bind

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11
Q

What is being measured

- Serum ferritin

A

BM iron stores

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12
Q

What is being measured

- BM macrophage iron

A

Iron held by RE cells (“erythroblastic island”)

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13
Q

What is being measured

- BM sideroblasts

A

nRBCs that contain iron

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14
Q

What is being measured

- ZPP (zinc protoporphyrin) or FEP (free erythrocyte protoporphyrin)

A

Availability of insufficient iron to developing nRBCs; erythrocyte protoporphyrin accumulates in cell

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15
Q

Relationship b/w serum ferritin and bone marrow iron stores in healthy individual

A

↑ serum ferritin, ↓ TIBC

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16
Q

Peripheral smear RBC morphology that would prompt the ordering of iron studies

A

?

17
Q

Iron deficiency anemia (IDA)

- Causes

A

↓ dietary intake
- infants–“milk anemia”
- children–“fast food diet lacking iron”
- adults–poor diet, GI bleeds, pregnancy
↑ loss of iron
Malabsorption

18
Q

Iron deficiency anemia (IDA)

- Clinical signs and symptoms

A

Classic: pallor, fatigue, lethargy, shortness of breath

More specific: koilonychia, heart mumur, cravings for non-food items

19
Q

Iron deficiency anemia (IDA)

- RBC count and/or Hb

A
  • RBC may be normal initially…↓ in stage 3

- ↓ H&H (Hb

20
Q

Iron deficiency anemia (IDA)

- PLT count

A

Increased, esp. w/ blood loss

21
Q

Iron deficiency anemia (IDA)

- RBC morphology

A
  • Hypochromia
  • Microcytes
  • Aniso
  • Some poik, varies
22
Q

Iron deficiency anemia (IDA)

- MCV

A

Decreased

23
Q

Iron deficiency anemia (IDA)

- MCHC

A

Decreased

24
Q

Iron deficiency anemia (IDA)

- RDW

A

Increased

25
Q

Iron deficiency anemia (IDA)

- Retic count

A

Slight to moderately increased (esp after blood loss and in response to iron therapy)

26
Q

Iron deficiency anemia (IDA)

- Treatment

A

Supplemental iron (ferrous sulfate)

27
Q

Pathology/mechanism for iron deficiency anemia

A
  • Decreased dietary intake
  • Increased loss of iron
  • Malabsorption
28
Q

Pathology/mechanism for anemia of chronic inflammation

A

BM macrophages fail to give up Fe to developing RBC precursors; RBCs develop iron deficient

29
Q

Pathology/mechanism for sideroblastic anemia

A

Group of disorders characterized by accumulation of iron in the mitochondria of nRBCs…“gets trapped”
- due to defect in heme synthesis (porphyria)

30
Q

Why shouldn’t long-term iron therapy be given to a patient w/ anemia of chronic inflammation?

A

Keep building up in the BM macrophages??

31
Q

Reasons for presence of “ringed sideroblasts” upon BM iron exam of patient w/ lead poisoning

A

Due to iron overload caused by decresed survival of RBCs w/ inclusions and ineffective erythropoiesis

32
Q

Characteristic RBC histogram appearance one would expect to see in a patient w/ siderblastic anemia (esp. hereditary form)

A

pic

33
Q

Color of skin w/ excess iron

A

Bronze diabetes

34
Q

Major form in which iron is stored in the liver

A

Ferritin

35
Q

Disease of iron metabolism characterized by excess deposition of iron in tissues; may be inherited or may develop from complication of hemolytic anemia, such as B-thalassemia major

A

Hemochromatosis

36
Q

APR that’s incrased in inflammation; as a result iron absorption is decreased and iron release from mcrophages is blocked

A

Hepcidin

37
Q

nRBC precursor w/ “rings of iron”

A

Ringed sideroblast

38
Q

BM erythrocyte precursor w/ excessive iron granules (siderotic granules); visible w/ Prussian blue staining

A

Sideroblast

39
Q

Nonnucleated RBC visible w/ Prussian blue staining

A

Siderocyte