Nutritional Anaemias Flashcards

1
Q

Define anaemia.

A

WHO: a condition in which the amount of haemoglobin and consequently the oxygen-carrying capacity of RBCs is insufficient to meet the body’s physiologic needs.

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2
Q

Name the nutritional causes of microcytic and macrocytic anaemia.

A
  • Microcytic - iron deficiency
  • Macrocytic - B12/folate deficiency
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3
Q

Outline the absorption and distribution of iron.

A
  • Iron is absorbed from duodenum via enterocytes into plasma, where it binds to transferrin.
  • Transported via transferrin to bone marrow to make RBCs.
  • Excess iron absorbed is stored as ferritin.
  • The hormone hepcidin decreases absorption from the duodenum and release from macrophages and iron-storing hepatocytes - this process is driven by ferroportin (iron channel) internalisation and regulated by negative feedback mechanisms.
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4
Q

What happens to ferritin and transferrin during a state of iron deficiency?

A
  • Ferritin stores are depleted.
  • Increased transferrin levels, but low saturation.
  • Transferrin saturation calculated by ratio of serum iron to total iron binding capacity (TIBC).
  • In iron deficiency, TIBC is very high compared to serum iron > low saturation.
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5
Q

Name the main causes of iron deficiency anaemia (IDA).

A

Not enough in:

  • Poor diet
  • Malabsorption
  • Increased physiological needs

Losing too much:

  • Blood loss - menstruation, GI tract loss, parasites
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6
Q

What tests are likely to diagnose iron deficiency anaemia at an earlier stage and why?

A
  • IDA initially normocytic and normochromic.
  • FBC will show microcytic RBCs and low Hb but not until later on.
  • Ferritin levels fall before other markers, so ferritin test is good for early diagnosis.
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7
Q

A patient presents with moderate anaemia, microcytic and hypochromic erythrocytes, reticulocytopenia and a ferritin level of 8. What is the diagnosis and why?

A
  • Microcytic and hypochromic RBCs consistent with iron deficiency anaemia.
  • Reticulocytopenia - reduced reticulocyte count indicates poor erythrocyte production from the bone marrow.
  • Ferritin < 20, 8 is very low - severe depletion of iron stores - confirms iron deficiency.
  • High TIBC and low transferrin saturation would corroborate the findings.
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8
Q

What is the most common cause of iron deficiency anaemia in adult men and postmenopausal women?

A
  • Blood loss from the GI tract
  • Menstrual blood loss is the most common cause in premenopausal women
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9
Q

Describe the common signs and symptoms of iron deficiency anaemia.

A
  • Symptoms - fatigue, lethargy, dizziness
  • Signs - pallor of mucous membranes, bounding pulse, systolic flow murmurs, smooth tongue, koilonychias
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10
Q

Outline the different causes of megaloblastic and nonmegaloblastic macrocytic anaemia.

A
  • Megaloblastic - caused by B12/folate deficiency or drug-related interference with B12/folate metabolism.
  • Nonmegaloblastic - alcoholism, liver disease, hypothyroidism, myelodysplastic syndromes, reticulocytosis.
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11
Q

In B12/folate deficiency, which of these nutrients is likely to be depleted from the body’s stores more quickly and why?

A
  • B12: 2-3mg stored over 2-4 years, easy to obtain sufficient amounts from animal and dairy products.
  • Folate: 10-12mg stored over 3-4 months, found in vegetables and animal liver and harder to obtain in diet.
  • Folate stores depleted quicker because required daily intake is higher, stores are short-term, harder to obtain in typical Western diet and cooking produces 60-90% loss.
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12
Q

Outline the role of vitamin B12 (cobalamin) and folic acid (folate) in erythrocyte production.

A
  • Both important for final RBC maturation and DNA synthesis.
  • Both needed for thymidine triphosphate synthesis.
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13
Q

Describe the characteristic changes seen on a peripheral blood smear in B12/folate deficiency anaemia.

A
  • Changes are megaloblastic.
  • Macroovalocytes - large oval RBCs.
  • Hypersegmented neutrophils.
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14
Q

Describe the main causes of folate deficiency.

A
  • Increased demand - pregnancy/breast feeding, growth spurts, haemolysis/rapid cell turnover, disseminated cancer, urinary loss.
  • Decreased intake - poor diet, elderly, chronic alcohol intake.
  • Decreased absorption - medication (folate antagonists), coeliac, jejunal resection, tropical sprue.
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15
Q

How is folate absorbed and stored?

A
  • Absorbed in the jejunum.
  • Body stores enough folate for 3-5 months.
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16
Q

Outline the cellular role of vitamin B12 (cobalamin).

A
  • Essential co-factor for methylation in DNA and cell metabolism.
  • Co-factor in metabolism of methylmalonic acid (MMA) - thus high MMA may indicate B12 deficiency.
  • Co-factor in homocysteine metabolism - producing methionine.
17
Q

Describe the absorption and transport of vitamin B12.

A
  • Absorbed in the terminal ileum - requires intrinsic factor (IF) which is made in gastric parietal cells.
  • Transcobalamin I and II transport vitB12 to tissues.
18
Q

What is pernicious anaemia?

A
  • Anaemia caused by impaired vitB12 absorption.
  • Intrinsic factor/IF receptor deficiency.
  • May be congenital or autoimmune - e.g. anti-parietal cell antibodies.
  • Most common cause of vitB12 deficiency anaemia.
19
Q

Outline the clinical consequences of vitamin B12 deficiency.

A
  • Brain - cognition, depression, psychosis.
  • Neurology - myelopathy, ataxia, sensory changes.
  • Infertility.
  • Cardiomyopathy.
  • Tongue - glossitis.
  • Blood - pancytopenia.