Files
reflector/server/evaluate/reference_texts/ref_sample_3.txt
Gokul Mohanarangan bb983194f8 update folder structure
2023-08-10 12:24:07 +05:30

971 lines
18 KiB
Plaintext

learning medicine is hard work osmosis
makes it easy it takes our lectures and
notes to create a personalized study
plan with exclusive videos practice
questions and flashcards and so much
more try it free today
in diabetes mellitus your body has
trouble moving glucose which is the type
of sugar from your blood into your cells
this leads to high levels of glucose in
your blood and not enough of it in your
cells and remember that your cells need
glucose as a source of energy so not
letting the glucose enter means that the
cells star for energy despite having
glucose right on their doorstep in
general the body controls how much
glucose is in the blood relative to how
much gets into the cells with two
hormones insulin and glucagon insulin is
used to reduce blood glucose levels and
glucagon is used to increase blood
glucose levels both of these hormones
are produced by clusters of cells in the
pancreas called islets of langerhans
insulin is secreted by beta cells in the
center of these islets and glucagon is
secreted by alpha cells in the periphery
of the islets insulin reduces the amount
of glucose in the blood by binding to
insulin receptors embedded in the cell
membrane of various insulin responsive
tissues like muscle cells in adipose
tissue when activated the insulin
receptors cause vesicles containing
glucose transporter that are inside the
cell to fuse with the cell membrane
allowing glucose to be transported into
the cell glucagon does exactly the
opposite it raises the blood glucose
levels by getting the liver to generate
new molecules of glucose from other
molecules and also break down glycogen
into glucose so that I can all get
dumped into the blood diabetes mellitus
is diagnosed when blood glucose levels
get too high and this is seen among 10
percent of the world population there
are two types of diabetes type 1 and
type 2 and the main difference between
them is the underlying mechanism that
causes the blood glucose levels to rise
about 10% of people with diabetes have
type 1 and the remaining 90% of people
with diabetes have type 2 let's start
with type 1 diabetes mellitus sometimes
just called type 1 diabetes in this
situation the body doesn't make enough
insulin the reason this happens is that
in type 1 diabetes there's a type 4
hypersensitivity response or a cell
mediated immune response where a
person's own T cells at
the pancreas as a quick review remember
that the immune system has T cells that
react to all sorts of antigens which are
usually small peptides polysaccharides
or lipids and that some of these
antigens are part of our own body cells
it doesn't make sense to allow T cells
that will attack our own cells to hang
around until there's this process to
eliminate them called self tolerance in
type 1 diabetes there's a genetic
abnormality that causes a loss of self
tolerance among T cells that
specifically target the beta cell
antigens losing self tolerance means
that these T cells are allowed to
recruit other immune cells and
coordinate an attack on these beta cells
losing beta cells means less insulin and
less insulin means that glucose piles up
in the blood because it can't enter the
body's cells one really important group
of genes involved in regulation of the
immune response is the human leukocyte
antigen system or HLA system even though
it's called a system it's basically this
group of genes on chromosome 6 that
encode the major histocompatibility
complex or MHC which is a protein that's
extremely important in helping the
immune system recognize foreign
molecules as well as maintaining self
tolerance MHC is like the serving
platter that antigens are presented to
the immune cells on interestingly people
with type 1 diabetes often have specific
HLA genes in common with each other one
called
HLA dr3 and another called HLA dr4 but
this is just a genetic clue right
because not everyone with HLA dr3 and
HLA dr4 develops diabetes in diabetes
mellitus type 1 destruction of beta
cells usually starts early in life but
sometimes up to 90% of the beta cells
are destroyed before symptoms crop up
for clinical symptoms of uncontrolled
diabetes that all sound similar our
polyphagia glycosuria polyuria and
polydipsia let's go through them one by
one even though there's a lot of glucose
in the blood it cannot get into the
cells which leaves cells starved for
energy so in response adipose tissue
starts breaking down fat called
lipolysis
and muscle tissue starts breaking down
proteins both of which results in weight
loss for someone with uncontrolled
diabetes this catabolic state leaves
people feeling hungry
also known as poly fascia Faiza means
eating and poly means a lot now with
high glucose levels that means that when
blood gets filtered through the kidneys
some of it starts to spill into the
urine called glycosuria glyco surfers to
glucose and urea the urine since glucose
is osmotically active water tends to
follow it resulting in an increase in
urination or polyuria poly again refers
to a lot and urea again refers to urine
finally because there's so much
urination people with uncontrolled
diabetes become dehydrated and thirsty
or polydipsia poly means a lot and dip
SIA means thirst even though people with
diabetes are not able to produce their
own insulin they can still respond to
insulin so treatment involves lifelong
insulin therapy to regulate their blood
glucose levels and basically enable
their cells to use glucose
one really serious complication with
type 1 diabetes is called diabetic
ketoacidosis or DKA to understand it
let's go back to the process of
lipolysis where fat is broken down into
free fatty acids after that happens the
liver turns the fatty acids into ketone
bodies like Osito acetic acid in beta
hydroxy butyrate acid a seed of acetic
acid is a keto acid because it has a
ketone group in a carboxylic acid group
beta hydroxy rhetoric acid on the other
hand even though it's still one of the
ketone bodies isn't technically a keto
acid since its ketone group has been
reduced to a hydroxyl group these ketone
bodies are important because they can be
used by cells for energy but they also
increase the acidity of the blood which
is why it's called ketoacidosis and the
blood becoming really acidic can have
major effects throughout the body
individuals can develop custom all
respiration which is a deep and labored
breathing as the body tries to move
carbon dioxide out of the blood in an
effort to reduce its acidity cells also
have a transporter that exchanges
hydrogen ions or protons for potassium
when the blood gets acidic it's by
definition loaded with protons that get
sent into cells while potassium gets
sent into the fluid outside cells
another thing to keep in mind is that in
addition to helping glucose enter cells
insulin stimulates the sodium potassium
ATPase --is which help potassium get
into the cells and so without insulin
more potassium stays in the fluid
outside cells both of these mechanisms
lead to increased potassium in the fluid
outside cells which quickly makes it
into the blood and causes hyperkalemia
the potassium is then excreted so over
time even though the blood potassium
levels remain high over all stores of
potassium in the body which include
potassium inside cells starts to run low
individuals will also have a high anion
gap which reflects a large difference in
the unmeasured negative and positive
ions in the serum largely due to the
build-up of ketoacids
diabetic ketoacidosis can happen even in
people who have already been diagnosed
with diabetes and currently have some
sort of insulin therapy
in states of stress like an infection
the body releases epinephrine which in
turn stimulates the release of glucagon
too much glucagon can tip the delicate
hormonal balance of glucagon and insulin
in favor of elevating blood sugars and
can lead to a cascade of events we just
described increased glucose in the blood
loss of glucose in the urine loss of
water dehydration and in parallel and
need for alternative energy generation
of ketone bodies and ketoacidosis
interestingly both ketone bodies break
down into acetone and escape as a gas by
getting breathed out the lungs which
gives us sweet fruity smell to a
person's breath in general though that's
the only sweet thing about this illness
which also causes nausea vomiting and if
severe mental status changes and acute
cerebral edema
treatment of a DKA episode involves
giving plenty of fluids which helps with
dehydration insulin which helps lower
blood glucose levels and replacement of
electrolytes like potassium all of which
help to reverse the acidosis now let's
switch gears and talk about type 2
diabetes which is where the body makes
insulin but the tissues don't respond as
well to it the exact reason why cells
don't respond isn't fully understood
essentially the body's providing the
normal amount of insulin but the cells
don't move their glucose transporters to
their membrane in response which
remember is needed for the glucose to
get into the cells these cells therefore
have insulin resistance some risk
factors for insulin resistance are
obesity lack of exercise and
hypertension the exact mechanisms are
still being explored for example in
excess of adipose tissue or fat is
thought to cause the release of free
fatty acids in so-called edible kinds
which are signaling molecules that can
cause inflammation which seems related
to insulin resistance
however many people that are obese are
not diabetic so genetic factors probably
play a major role as well we see this
when we look at twin studies as well
we're having a twin with type-2 diabetes
increases the risk of developing type 2
diabetes completely independently of
other environmental risk factors in type
2 diabetes since tissues don't respond
as well to normal levels of insulin the
body ends up producing more insulin in
order to get the same effect and move
glucose out of the blood
they do this through beta cell
hyperplasia an increased number of beta
cells and beta cell hypertrophy where
they actually grow in size all in this
attempt to pump out more insulin this
works for a while and by keeping insulin
levels higher than normal blood glucose
levels can be kept normal called normal
glycemia now along with insulin beta
cells also secrete islet amyloid
polypeptide or amylin so while beta
cells are cranking out insulin they also
secrete an increased amount of amylin
over time Emlyn builds up and aggregates
in the islets this beta cell
compensation though is not sustainable
and over time those maxed out beta cells
get exhausted and they become
dysfunctional and undergo hypo trophy
and get smaller as well as hypoplasia
and die off as beta cells are lost in
insulin levels decrease glucose levels
in the blood start to increase in
patients develop hyperglycemia which
leads to similar clinical signs that we
mentioned before like Paul aphasia
glycosuria polyuria polydipsia but
unlike type 1 diabetes there's generally
some circulating insulin in type 2
diabetes from the beta cells that are
trying to compensate for the insulin
resistance this means that the insulin
glucagon balances such that diabetic
ketoacidosis does not usually develop
having said that a complication called
hyperosmolar hyperglycemic state or HHS
is much more common in type 2 diabetes
than type 1 diabetes and it causes
increased plasma osmolarity due to
extreme dehydration and concentration of
the blood to help understand this
remember that glucose is a polar
molecule that cannot passively diffuse
across cell membranes which means that
it acts as a solute so when levels of
glucose are super high in the blood
meaning it's a hyperosmolar State water
starts to leave the body cells and enter
the blood vessels leaving the cells were
relatively dry in travailed rather than
plump and juicy blood vessels that are
full of water lead to increased
urination and total body dehydration and
this is a very serious situation because
the dehydration of the body's cells and
in particular the brain can cause a
number of symptoms including mental
status changes in HHS you can sometimes
see mild ketone emia and acidosis but
not to the extent that it's seen in DKA
and in DKA you can see some hyper
osmolarity so there's definitely overlap
between these two syndromes
besides type 1 and type 2 diabetes there
are also a couple other subtypes of
diabetes mellitus gestational diabetes
is when pregnant women have increased
blood glucose which is particularly
during the third trimester although
ultimately unknown the cause is thought
to be related to pregnancy hormones that
interfere with insulins action on
insulin receptors also sometimes people
can develop drug-induced diabetes which
is where medications have side effects
that tend to increase blood glucose
levels the mechanism for both of these
is thought to be related to insulin
resistance like type 2 diabetes rather
than an autoimmune destruction process
like in type 1 diabetes diagnosing type
1 or type 2 diabetes is done by getting
a sense for how much glucose is floating
around in the blood and has specific
standards that the World Health
Organization uses very commonly a
fasting glucose test is taken where the
person doesn't eat or drink except the
water that's okay for a total of eight
hours and then has their blood tested
for glucose levels levels of 100
milligrams per deciliter to 120
five milligrams per deciliter indicates
pre-diabetes and 126 milligrams per
deciliter or higher indicates diabetes a
non fasting a random glucose test can be
done at any time with 200 milligrams per
deciliter or higher being a red flag for
diabetes another test is called an oral
glucose tolerance test where person is
given glucose and then blood samples are
taken at time intervals to figure out
how well it's being cleared from the
blood the most important interval being
two hours later levels of 140 milligrams
per deciliter to 199 milligrams per
deciliter indicate pre-diabetes
and 200 or above indicates diabetes
another thing to know is that when blood
glucose levels get high the glucose can
also stick to proteins that are floating
around in the blood or in cells so that
brings us to another type of test that
can be done which is the hba1c test
which tests for the proportion of
hemoglobin in red blood cells that has
glucose stuck to it called glycated
hemoglobin hba1c levels of 5.7% 26.4%
indicate pre-diabetes
and 6.5 percent or higher indicates
diabetes this proportion of glycated
hemoglobin doesn't change day to day so
it gives a sense for whether the blood
glucose levels have been high over the
past two to three months finally we have
the c-peptide test which tests for
byproducts of insulin production if the
level of c-peptide is low or absent it
means the pancreas is no longer
producing enough insulin and the glucose
cannot enter the cells
for type one diabetes insulin is the
only treatment option for type 2
diabetes on the other hand lifestyle
changes like weight loss and exercise
along with a healthy diet and an oral
anti-diabetic medication like metformin
in several other classes can sometimes
be enough to reverse some of that
insulin resistance and keep blood sugar
levels in check however if oral
anti-diabetic medications fail type 2
diabetes can also be treated with
insulin something to bear in mind is
that insulin treatment comes with a risk
of hypoglycemia especially if insulin is
taken without a meal symptoms of
hypoglycemia can be mild like weakness
hunger and shaking but they can progress
to a loss of consciousness in seizures
in severe cases in mild cases drinking
juices or eating candy or sugar might be
enough to bring blood sugar up but in
severe cases intravenous glucose should
be given as soon as possible
the FDA has also recently approved
intranasal glucagon as a treatment for
severe hypoglycemia all right now over
time high glucose levels can cause
damage to tiny blood vessels while the
micro vasculature in arterioles a
process called hyaline
arteriolosclerosis is where the walls of
the arterioles develop hyaline deposits
which are deposits of proteins and these
make them hard and inflexible in
capillaries the basement membrane can
thicken and make it difficult for oxygen
to easily move from the capillary to the
tissues causing hypoxia
one of the most significant effects is
that diabetes increases the risk of
medium and large arterial wall damage
and subsequent atherosclerosis which can
lead to heart attacks and strokes which
are major causes of morbidity and
mortality for patients with diabetes in
the eyes diabetes can lead to
retinopathy and evidence of that can be
seen on a fundus copic exam that shows
cotton-wool spots or flare hemorrhages
and can eventually cause blindness in
the kidneys the a ferrant and efferent
arterioles as well as the glomerulus
itself can get damaged which can lead to
an F Radek syndrome that slowly
diminishes the kidneys ability to filter
blood over time and can ultimately lead
to dialysis diabetes can also affect the
function of nerves causing symptoms like
a decrease in sensation in the toes and
fingers sometimes called a stocking
glove distribution as well as causes the
autonomic nervous system to malfunction
and that system controls a number of
body functions
everything from sweating to passing gas
finally both the poor blood supply and
nerve damage can lead to ulcers
typically on the feet that don't heal
quickly and can get pretty severe and
need to be amputated these are some of
the complications of uncontrolled
diabetes which is why it's important to
diagnose and control diabetes through a
healthy lifestyle medications to reduce
insulin resistance and even insulin
therapy if beta cells have been
exhausted while type 1 diabetes cannot
be prevented type 2 diabetes can in fact
many people with diabetes can control
their blood sugar levels really
effectively and live a full and active
life without any of the complications
thanks for watching if you're interested
in a deeper dive on this topic take a
look at as Moses org where we have
flashcards questions and other awesome
tools to help you learn medicine
you