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NSG 533--ADVANCED PATHOPHYSIOLOGY Endocrine Disorders – 17 questions

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Compare and contrast type 1 and type 2 diabetes in regard to etiology, natural history, and pathogenesis. o Type 1 Diabetes  10% of the diabetic population  Usually occurs in adolescence or young adulthood  Can occur at any age  Pathophysiology:  Immune-mediated  Type 1 DM is a slowly progressive autoimmune T cell-mediated disease that occurs in genetically susceptible individuals  Causes destruction of pancreatic β-cell o Lymphocyte and macrophage infiltration of the islets resulting in inflammation (insulitis) and islet β-cell death o Production of autoantibodies against islet cells, insulin, glutamic acid decarboxylase (GAD) and other cytoplasmic proteins  Non-immune-mediated  No identified cause  Very small number of cases  Genetic Susceptibility  Concordance rate for type 1 DM is greater in monozygotic than dizygotic twins  In Caucasians, the risk in type 1 DM is 0.2-0.3%  If an individual has type 1 DM, the risk is approximately 5% among his/her siblings  Risk is 3% if mother has the disease  Risk is 6% if father has the disease  Risk is 30-50% for the identical twin of sibling with type 1 DM  The major genetic predisposition appears to be conferred by diabetogenic genes on the short arm of chromosome 6, either within or in close proximity to the MHC region, or the human leukocyte antigen (HLA) region  Autoimmunity  Evidence to strongly suggest autoimmunity o Presence of autoantibodies o Islet cell antibodies o Insulin autoantibodies o Clinical trials of immunosuppressive therapy (e.g. cyclosporine) demonstrated temporary preservation of Beta-cell function in newly diagnosed type 1 DM  Insulitis o “Lymphocyte-rich inflammatory infiltrate” noted in pancreas of those newly diagnosed o Consistent of other autoimmune processes and establishing a role of T-cell autoimmunity  Evidence of cell mediated immune process o Destruction of B-cells mediated by cytokines, produced by cells such as lymphocytes  Environmental  What environmental factor is the “triggering” event  Is it Viruses ???????? o Enteroviruses & H. pylori  Does the viral protein contain an amino acid sequence similar to a Beta cell protein? o This molecular mimicry initiates an immune response w/ destruction of B-cells  Does the virus damage a Beta -cell? o This initiates an immune response against antigens in virally altered B-cells with destruction of B-cells  Type 1 diabetes is the result of the human immune system mistaking the body’s beta cells, which produce insulin, for foreign cells and causing their destruction. Insulin is a protein that allows the transport of sugar into cells to provide energy. When sugar can’t get from the blood into the cells, the cells have no access to the glucose they need and cannot function correctly. The composition of our blood also gets off balance, with high blood sugar levels leading to detrimental effects on other organs of the body. Injecting synthetic insulin solves this problem because it keeps blood glucose levels in the right range and helps glucose reach our cells  Treatment:  Diet  Exercise  Insulin  Primarily associated with Type 1 Diabetes: Diabetic ketoacidosis (DKA) o Type 2 Diabetes  90% of the diabetic population  Usually occurs in midlife  Pathophysiology:  Insulin resistance (insulin normally binds to cell surface receptors)  The binding may be impaired  There may be less receptors  There may be post-receptor defects  Defect in pancreatic β-cell secretion  Treatment:  Diet  Exercise  Oral medications and/or insulin/incretins  Primarily associated with Type 2 Diabetes: Hyperglycemic Hyperosmolar (HHS)  Patients with type 2 diabetes make insulin, but the cells in the body cannot respond to it adequately so they cannot take up glucose. Later on, especially when treatment fails, type 2 diabetes is aggravated by exhausted beta cells, decreasing their insulin production resulting in further increases in blood sugar levels. Since beta cells aren’t killed off in type 2 diabetes, at least initially, blood sugar levels often become elevated at a slower rate than with type 1 diabetes. This means that someone can have high blood sugar for quite sometime without realizing it, and may only find out they have type 2 diabetes when complications of diabetes appear, such as damage to eyes, the kidney and nerves. Additionally, this means that treatment for type 2 diabetes varies from case to case. While insulin therapy is needed for some people with type 2 diabetes, others are able to use alternative medications. Lifestyle changes such as diet and exercise have also been known to help type 2 diabetes and are always recommended

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RUSH UNIVERSITY COLLEGE OF NURSING
NSG 533--ADVANCED PATHOPHYSIOLOGY
Endocrine Disorders – 17 questions

 Compare and contrast type 1 and type 2 diabetes in regard to etiology, natural history, and pathogenesis.
o Type 1 Diabetes
 10% of the diabetic population
 Usually occurs in adolescence or young adulthood
 Can occur at any age
 Pathophysiology:
 Immune-mediated
 Type 1 DM is a slowly progressive autoimmune T cell-mediated disease that occurs in
genetically susceptible individuals
 Causes destruction of pancreatic β-cell
o Lymphocyte and macrophage infiltration of the islets resulting in inflammation
(insulitis) and islet β-cell death
o Production of autoantibodies against islet cells, insulin, glutamic acid
decarboxylase (GAD) and other cytoplasmic proteins
 Non-immune-mediated
 No identified cause
 Very small number of cases
 Genetic Susceptibility
 Concordance rate for type 1 DM is greater in monozygotic than dizygotic twins
 In Caucasians, the risk in type 1 DM is 0.2-0.3%
 If an individual has type 1 DM, the risk is approximately 5% among his/her siblings
 Risk is 3% if mother has the disease
 Risk is 6% if father has the disease
 Risk is 30-50% for the identical twin of sibling with type 1 DM
 The major genetic predisposition appears to be conferred by diabetogenic genes on
the short arm of chromosome 6, either within or in close proximity to the MHC
region, or the human leukocyte antigen (HLA) region
 Autoimmunity
 Evidence to strongly suggest autoimmunity
o Presence of autoantibodies
o Islet cell antibodies
o Insulin autoantibodies
o Clinical trials of immunosuppressive therapy (e.g. cyclosporine) demonstrated
temporary preservation of Beta-cell function in newly diagnosed type 1 DM
 Insulitis
o “Lymphocyte-rich inflammatory infiltrate” noted in pancreas of those newly
diagnosed
o Consistent of other autoimmune processes and establishing a role of T-cell
autoimmunity
 Evidence of cell mediated immune process
o Destruction of B-cells mediated by cytokines, produced by cells such as
lymphocytes
 Environmental
 What environmental factor is the “triggering” event

,  Is it Viruses ????????
o Enteroviruses & H. pylori
 Does the viral protein contain an amino acid sequence similar to a Beta cell protein?
o This molecular mimicry initiates an immune response w/ destruction of B-cells
 Does the virus damage a Beta -cell?
o This initiates an immune response against antigens in virally altered B-cells
with destruction of B-cells
 Type 1 diabetes is the result of the human immune system mistaking the body’s beta cells,
which produce insulin, for foreign cells and causing their destruction. Insulin is a protein that
allows the transport of sugar into cells to provide energy. When sugar can’t get from the blood
into the cells, the cells have no access to the glucose they need and cannot function correctly.
The composition of our blood also gets off balance, with high blood sugar levels leading to
detrimental effects on other organs of the body. Injecting synthetic insulin solves this problem
because it keeps blood glucose levels in the right range and helps glucose reach our cells
 Treatment:
 Diet
 Exercise
 Insulin
 Primarily associated with Type 1 Diabetes: Diabetic ketoacidosis (DKA)
o Type 2 Diabetes
 90% of the diabetic population
 Usually occurs in midlife
 Pathophysiology:
 Insulin resistance (insulin normally binds to cell surface receptors)
 The binding may be impaired
 There may be less receptors
 There may be post-receptor defects
 Defect in pancreatic β-cell secretion
 Treatment:
 Diet
 Exercise
 Oral medications and/or insulin/incretins
 Primarily associated with Type 2 Diabetes: Hyperglycemic Hyperosmolar (HHS)
 Patients with type 2 diabetes make insulin, but the cells in the body cannot respond to it
adequately so they cannot take up glucose. Later on, especially when treatment fails, type 2
diabetes is aggravated by exhausted beta cells, decreasing their insulin production resulting in
further increases in blood sugar levels. Since beta cells aren’t killed off in type 2 diabetes, at
least initially, blood sugar levels often become elevated at a slower rate than with type 1
diabetes. This means that someone can have high blood sugar for quite sometime without
realizing it, and may only find out they have type 2 diabetes when complications of diabetes
appear, such as damage to eyes, the kidney and nerves. Additionally, this means that treatment
for type 2 diabetes varies from case to case. While insulin therapy is needed for some people
with type 2 diabetes, others are able to use alternative medications. Lifestyle changes such as
diet and exercise have also been known to help type 2 diabetes and are always recommended

, for those with the disease.




 List the classic symptoms of diabetes mellitus. (Type 1)
o Polydipsia (increased thirst)
 Because of elevated blood glucose levels, water is osmotically attracted from body cells,
resulting in intracellular dehydration and hypothalamic stimulation of thirst
 As fluid from the body tissues is reduced and runs through osmosis into the bloodstream
there is a call for more fluids to avoid dehydration at the cellular level. This means that
your brain gets the signal to drink more water as the body feels thirsty.
 The excessive sugar buildup in the body is dumped into the kidney and body needs more urine
to get rid of the sugar. This means that the diabetic person needs to drink more fluids to flush
out the sugar that is deposited in the kidneys and so they tend to feel extra thirsty. So both
reasons increase the level of thirst in a diabetic person to higher than that of a healthy person.
o Polyuria (frequent urination)
 Hyperglycemia acts as an osmotic diuretic; the amount of glucose filtered by the glomeruli of
the kidneys exceeds the amount that can be reabsorbed by the renal tubules; glycosuria results,
accompanied by large amounts of water lost in the urine
 Polyuria happens because as the blood sugar level in the body rises there is an increase in the
osmosis rate of the blood. This results in the drawing out the fluid from the tissues into the
bloodstream. This does not help decrease the blood sugar level but does dilute it to a level
where it is acceptable to the rest of the body’s cells.
 Now all this excess fluid in the bloodstream is cleaned out by the kidneys. This results in the
bladder becoming full with urine and so you need to go empty the bladder to relieve the
pressure you feel by urinating.
o Polyphagia (increased hunger)
 Depletion of cellular stores of carbohydrates, fats, and protein results in cellular starvation and a
corresponding increase in hunger
 Body thinks its starving because it is unable to use glucose stores
o Weight loss

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