Presentation on ITP

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    Presentation on

    ITPBy James Runco

    Everyone bleeds sometimes,

    I just bleed more.

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    ITP

    ITP stands for

    Idiopathic Thrombocytopenic Purpura

    but it is also frequently called:

    Immune Thrombocytopenic Purpura or

    Idiopathic Thrombocytopenia

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    Background Information

    There are three Basic types of blood cells

    made in the marrow of the bones each

    with their own specialized jobs.

    Red Blood Cells (Rbcs) Carry Oxygen

    White Blood Cells (Wbcs) Protect your body from infection

    Platelets (Plts) Help your help your body to heal injuries

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    This is a Picture of Normal Blood

    Cells

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    What ITP does.

    ITP is an autoimmune disease during which your

    bodys immune system attacks and destroys

    your platelets.

    The body releases auto-antibodies whichchemically tag its own cells as foreign

    White blood cells then seek out and destroy

    platelets as if they were fighting an infection

    This causes a rapid drop in the level of platelets in

    a persons body

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    More about ITP

    This Thrombocytopenia (lowered platelet level) is

    Idiopathic, (without known cause) and can be

    triggered at any time.

    Platelets are a specialized form of blood cells thatare absolutely essential for your blood to clot.

    When they are attacked by the White Blood cells it

    can be disastrous.

    Your body is left unable to mend any cuts or stop

    bleeding even from the smallest internal injuries

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    Symptoms of ITP

    Excessive bleeding with

    minor injuries

    Spontaneous bleeding from

    the mouth and nose

    Unexplainable orspontaneous bruising

    Excessive internal bleeding

    Disturbed sleep cycle/

    Insomnia Irregular appetite

    Depression

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    Depression and ITP Continued

    This L-Tryptophan is able to pass through

    the blood brain barrier, so its loss is the

    probable cause of the sleep/ eating

    irregularities.

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    This is Jane

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    Normal Platelet Counts

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    Thrombocytopenic Platelet Counts

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    This is Jane with ITP

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    Causes

    The exact causes of ITP are as yet unknown, butthere is currently research going on to try anddetermine what causes this disease.

    There are many theories, most state that ITP is amultifactorial disease with a strong geneticpredisposition.

    Researchers are currently looking for multiple

    instances of ITP in a family, and have found thatin some cases ITP can be passed from motherto child.

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    Moms and ITP

    There seems to be aconnection between ITPand pregnancy. Apreviously normal woman

    can sometimes developITP during a pregnancy.

    Pregnancies are much moredangerous for womenwith ITP, both because

    their platelet counts candrop and because of thebleeding involved withdelivery.

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    Theories

    Three most common theories for ITP are:

    The Microbial Trigger Theory

    The Molecular Mimicry Theory and

    The Free Radical Damage Theory

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    The Microbial Trigger Theory

    Links the destruction of platelets to a chemicalcalled interleuken 12 that is released when thebody is fighting a bacterial infection

    They believe that in some people thisinterleuken 12 can inadvertently activatedormant self reactive cells that then convinceyour body that a cell near the bacteria is alsopart of the infection

    If that cell is a specialized platelet then youwould develop ITP

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    The Molecular Mimicry Theory

    This theory says that someone can develop ITPwhen the bodies T helper cells recognize a viralor bacteria amino acid sequence that happensto occur on the surface of a platelet

    Normally T helpers that would target somaticcells are inhibited by other immune agents.

    If there is a malfunction in the production ofthese inhibiting agents then the self reactive T

    helper cells are free to target platelets fordestruction

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    Free Radical Damage Theory

    DNA is damaged by free radicals

    Free radicals are compounds that build up

    in the body, which need electrons in order

    to become stable

    If they steal these electrons from DNA

    they can cause mutations which could

    effect the immunes system, and possibly

    trigger ITP or other Autoimmune diseases.

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    Diagnosis

    ITP is often the Diagnosed by its symptoms. It isfrequently the diagnosis when all other blooddiseases are ruled out and there seems to bethe body mounting an attack against the

    plateletsThere are different forms of ITP. Some children

    experience a disease which is listed as ITPbecause it is thrombocytopenia with an unknownorigin. However it differs from adult and chronicchildhood ITP because many of these childhoodcases last only a matter of months and then gointo permanent remission.

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    ITP Statistics

    Approximately 200,000people in the US haveITP

    In Adults women arethree times more likely tohave ITP than men, but inchildren the statistics arefairly even

    The percentage rate ofITP cases is increasing.

    Each year there areapproximately 20,000new cases or about 10 to125 per million people.

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    Treatment

    In most cases ITP is not fatal and can be treated.

    There is a wide variety of treatment options, but with onlypartial success due to the unknown nature of thedisease.

    The most commonly excepted, and most successfultreatments for ITP involve the removal of the spleenbecause it is a site for autoantibody production.

    People are also very commonly given Prednisone which isan artificial steroid which can enhance plateletproduction

    For emergency case treatment (normally when platelets getbelow 20,000) They will administer IV G or intravenousgammaglobulin for several days, and they wait for countsto rebound

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    Sources

    Platelet Disorder Support Association

    www.ITPpeople.com

    Scripps Institute website

    http://seconde.scripps.edu/ltp

    Family Genetics.net

    www.familygenetics.net

    http://www.itppeople.com/http://seconde.scripps.edu/ltphttp://www.familygenetics.net/http://www.familygenetics.net/http://seconde.scripps.edu/ltphttp://www.itppeople.com/