W1_10 Nutritional diseases 1 Flashcards

1
Q

How do celiac disease and crohn’s disease affect malnutrition?

A

They are malabsorption syndromes

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2
Q

What is PEM?

A

Protein-energy malnutrition

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3
Q

How prevalent is PEM?

A

Affects 25% of children in 3rd world countries

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4
Q

How much does a malnourished child weigh, as a percentage of normal?

A

80%

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5
Q

What is kwashiorkor?

A

Protein deficiency, but caloric is maintained. Affects the visceral protein compartment. Person has metabolic issues

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6
Q

What is marasmus?

A

Protein and energy deficiency. Affects the somatic compartment and the person thins. Weight 60% of normal. Decreased leptin because less fat.

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7
Q

What is kwashiorkor?

A

Weight 60-80% of normal. Hypoalbuminenia and edema. Flaky paint skin lesions. Hair changes.

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8
Q

What is cachexia?

A

PEM, secondary to chronic illness, such as cancer or AIDS. Looks like marasmus, but moreso due to increased BMR than lack of eating.

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9
Q

Name a few cytokines that can cause cachexia.

A

TNF, IL-2, IL-6, PIF (proteolysis inducing factor)

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10
Q

What endocrine effects does anorexia nervosa have?

A

Gonadal function, thyroid, calcium metabolism, dehydration, electrolyte abnormalities

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11
Q

Name 3 complications of bulimia

A

electrolyte imbalances (hypokalemia)
pulmonary aspiration
esophageal/gastric cardia tears/rupture

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12
Q

Where does leptin come from?

A

adipose tissue

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13
Q

where does adiponectin come from?

A

adipose tissue

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14
Q

where does ghrelin come from?

A

stomach

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15
Q

POMC and CART are what kind of signalling?

A

anorexigenic

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16
Q

neuropeptide Y and AgRP are what kind of signalling?

A

orexigenic

17
Q

which neuropeptide pathway does leptin stimulate in the arcuate nucleus?

A

POMC and CART

18
Q

what does adiponectin do?

A

fatty acid to muscle for oxidation;
decrease fatty acids to liver;
decrease glucose production in liver

19
Q

whcih neuropeptide pathway does ghrelin stimulate?

A

NPY and AgRP

20
Q

how do insulin conditions relate to cancer?

A

activated cell growth pathways;
increase IGF-1 expression (then HIF-1 and VEGF);
increased androgen in adrenals/ovaries;
increased conversion of androgens to estrogens