diabeties 2 Flashcards
what are the causes of type 2 diabeties
Type II diabetes is characterised by reduced insulin secretion and insulin resistance.
Insulin resistance means that ‘normal’ biological effects of insulin (i.e. inhibition of hepatic glucose output, skeletal muscle uptake of glucose, suppression of lipolysis) are not observed at physiologically-relevant insulin concentrations.
Relative insulin deficiency results from pancreatic beta-cell dysfunction:
At Type II diabetes diagnosis, a 50% reduction in beta-cell mass is common.
Further beta cell loss (4%) can occur post-diagnosis.
It is still not fully understood the events that lead to insulin insensitivity and beta-cell dysfunction in Type II diabetes.
relationship between insulin sensitivity and insulin secretion
One model proposes that, as insulin sensitivity falls, insulin secretion increases to compensate. When max. insulin secretion is reached, secretion declines and blood glucose levels rise as the individual develops impaired glucose tolerance and, eventually diabetes
Both insulin resistance and beta-cell dysfunction (e.g. reduction in beta cell mass) occur early but can often be reversed through lifestyle inventions
people with type ii diabetes - secrete more or less insulin
People with Type II diabetes secrete less insulin daily
They lose the early phase insulin release in response to glucose but compensate for this by an exaggerated second phase response
This exaggerated second phase response can cause hypoglycaemia 3-4 hours after a meal
what are the symptoms of type ii diabetes
Gradual and insidious onset of illness (months-years), or asymptomatic:
Almost one third of people are diagnosed by chance (!) as a result of routine screening or a diabetes-related complication.
Increased thirst and hunger.
Increased frequency of urination (especially at night).
Fatigue.
Blurred vision.
Infection.
Hyperosmolar Hyperglycaemic State (HHS):
what is Hyperosmolar Hyperglycaemic State (HHS):
Hyperosmolar Hyperglycaemic State (HHS): a medical emergency involving hyperglycaemia, dehydration and uraemia.
Used to be called HONK is a presenting feature for up to 25% cases (especially in middle-aged, elderly and Afro-Caribbean individuals).
how can type ii diabetes be prevented
Type II diabetes can be prevented (or at least delayed) by lifestyle intervention
Lifestyle interventions can significantly reduce incidence of diabetes:
reduce weight,
reduce fat intake,
increase dietary fibre, and,
exercise
Lifestyle interventions not easy as type II diabetes can be asymptomatic for up to a decade before complications become apparent
how is type ii diabetes screened? / testing
As Type II diabetes can be prevented (or delayed) and many people with Type II diabetes are undiagnosed, or have already developed complications by diagnosis, screening programmes are essential.
Universal screening is not practical: screening programmes should focus on those at risk.
Screening tests could include random blood glucose levels (OGTT), or fasting blood glucose levels and HbA1c levels.
higher the bmi higher the risk of diabetes .. true or false?
true
why is screening programmes imperative?
Diabetic complications (macrovascular and microvascular) can develop in asymptomatic diabetics
diabetes is commonly diagnosed by cardiac units treating a patient following a heart attack
20% people with newly diagnosed diabetes have retinopathy
Good management of type II diabetes is needed to prevent these complications
what are the treatment goals for type ii diabetes
Preserve life.
Alleviate symptoms.
Achieve good glycaemic control to avoid long-term complications.
Avoid iatrogenic side effects (i.e. hypoglycaemia).
how can type ii diabetes be managed?
Lifestyle interventions (first line)
Diet and weight loss
Exercise,
Education
Then add drug treatments:
Oral hypoglycaemic agents
Insulins
what are the advice given to people with type ii diabetes
Successful lifestyle modification and maintaining good glycaemic control is key to avoiding diabetic complications:
People with diabetes have increased mortality and morbidity risk.
Diabetic retinopathy is the most common cause of blindness in people of working age.
Diabetics have 2-3 fold higher risk of CVD.
16% of patients requiring kidney replacement are diabetic.
Erectile dysfunction affects 50% of diabetic men.
15% of diabetics will develop foot ulcers, and due to impaired wound healing and infection: 5-15% of these people will require amputations.
Remember: education about complications can improve compliance.
when is oral hypolycaemic agent added?
If diet and exercise alone fails, oral hypoglycaemic agents are added
what does oral hypoglycaemic agents require
Oral hypoglycaemic agents require some residual capacity to be effective
what are the categories for oral hypoglycaemics?
Categories of oral hypoglycaemics are used:
Insulin sensitisers
Insulin secretagogues
Inhibitors of glucose absorption from GI tract
Inhibitors of renal glucose uptake
what is the mechanism of action of blood glucose lowering medicines?
- drug classes and location
- LIVER - biguanides and thiazolidineodiones reduces glucose production
-SMALL intestine - alpha- glucosidase inhibitors slow down absorption of sucrose and starch
-PANCREAS - GLP-1 (incretins) improve response to glucose levels
insulin secretogogues: sulphonylureas and megiltitnides increase insulin production
-SKELETAL MUSCLE and ADIPOSE TISSUE - thiazolidinediones and biguanides reduce insulin resistance
what is insulin sensitisers and examples?
Enhance the effect of endogenous circulating insulin, increasing the sensitivity of peripheral tissues to insulin and decreasing glucose production in liver
Biguanide, metformin, and thiazolidinediones (“glitazones”) are insulin sensitisers
what is the drug class of metformin, aims, common side effects and cautions.
moa
Metformin is the only biguanide currently available and is the “first line” treatment for type II diabetes
Typically will reduce HbA1c by 1.5-2%
Suppresses appetite, helps achieve weight loss and has a cardio-protective effect (reduced mortality and morbidity)
Common side effects (e.g. abdominal pain, nausea, diarrhoea) minimised by gradual increases to reach therapeutic dose or by modified release formulations
Metformin cannot be used in patients with renal impairment, cardiac failure or liver failure as it is associated with lactic acidosis (potentially fatal)
moa : It activates energy sensor AMP kinase which promotes cellular energy uptake
what is the mode of action of thiazoldinediones?
Bind to peroxisome proliferator-activated receptor-gamma (PPAR-gamma) and, through regulation of gene transcription, enhance glucose and fatty acid uptake and utilisation in adipocytes, reduce secretion of cytokines that inhibit insulin action
Reduced availability of fatty acids in muscle improves insulin sensitivity
Reduce hepatic glucose output
how long can thiaxolidinediones take to show maximal effects?
Can take up to 3 months to see maximal effect as have indirect effect on blood glucose but, once achieved, effect is comparable to metformin and sulphonylureas
what can glitazones increase the risk of? - pioglitazone
Link between the “glitazones” and increase risk of cardiovascular disease
Pioglitazone associated with increased risk of heart failure (especially when combined with insulin) and bladder cancer. (Should not be used in patients with history of these conditions)
Associated with fluid retention (precipitating heart failure)
Induces weight gain but weight gain is limited to hips and thighs (a “lower risk” pattern of distribution) and intraabdominal fat is reduced
what is insulin secretagogues
Stimulate insulin release from the pancreas
Aim to restore early phase insulin release and return plasma insulin levels to pre-prandial levels rapidly to avoid post-meal hypoglycaemia
Sulphonylureas and meglitinides are insulin secretogogues
what is the moa of Both sulphonylureas and meglitinides
close K+ ATP channel but do so by binding to different (but related receptors)
name a short acting Sulphonylureas
gliclazide or tolbutamide