Human Growth Hormone Warnings
Normal
use of Human Growth Hormone in low dosages is generally
considered safe. Documented
risks of HGH supplementation are few and uncommon.
This is evidenced by the fact that HGH therapy is
primarily used for children with growth disorders. What
parent or doctor would incur a high risk of bodily harm to a
child just to add a few inches of height? However, Human Growth
Hormone is a pharmaceutical, and as such, carries the risk of
certain side effects that have been reported during treatment
often enough to be considered non coincidental.
Below is a list of the rarest, but more serious possible
side effects of HGH.
Rare but Serious Side Effects
Slipped
Capital Femoral Epiphysis (SCFE) is a condition which
brings on hip
pain as a result of the separation of the head of the femur
from the shaft. Incidence in patients treated with Human Growth
Hormone may be about 1 in 1000. Slipped Capital Femoral
Epiphysis usually requires casting or surgical pinning to
reverse.
Pseudotumor
Cerebri
(also known as Benign Intracranial Hypertension) is
signified by symptoms such as severe headaches,
papilledema, nausea, and visual changes. Incidence of this rare
side effect from HGH use is also perhaps 1 in 1000. Every single
known case has been reversed, usually by temporary
discontinuation or reduced dose of Human Growth Hormone.
Pancreatitis
has been reported in a few patients receiving HGH, but a causal
relationship seemed unlikely yet possible.
Children
or adults being treated with Human Growth Hormone occasionally
experience joint pains.
Fluid
retention and edema in early months of treatment is rare in
children but a bit more common and occasionally more severe in
adults. It by and large disappears with temporary interruption
of HGH treatment.
Carpal
tunnel syndrome
has also sometimes occurred in adults being
treated with HGH, most probably due to a combination of tissue
growth and fluid retention which exerting pressure on the
securely confined nerve and tendon tissue contained in the
wrists.
A
small but controlled study of HGH given to severely ill adults
in an intensive
care unit (ICU) setting for the purpose of increasing
strength and reducing the muscle wasting of critical illness
such as AIDS showed a higher mortality rate for the patients who
received Human Growth Hormone. The reason is unknown, but HGH is
now rarely used in ICU patients unless they have severe growth
hormone deficiency.
More Common but Less Serious Side
Effects
Below
is a list of HGH side effects that were reported more often by
individuals taking Human Growth Hormone.
Proponents of HGH supplementation argue that most of the
more common side effects are of questionable harm.
Human
Growth Hormone therapy has been known to decrease insulin
sensitivity. This side effect does not seem to be very
problematic for most people but it is possible to envision
situations that would make this an undesirable effect, such as
the presence of obesity or pre-existing diabetes.
When
HGH is given to children and adults who are not deficient, IGF1
levels may be raised above normal. Though no adverse effects are
obvious, extended periods of extremely high IGF1 levels occur in
a condition called Acromegaly, which causes overgrowth of
certain facial bones and the connective tissues of the body. A
small amount of evidence suggests that higher IGF1 levels in
older adults (not receiving HGH) are associated with a slightly
higher risk of certain cancers;
however, a causal relationship has not been established.
When
HGH is given to a child in high doses for several years, it has
been known to subtly affect the facial
bone structure. It rarely is recognized as a change by
patients and parents and even less often causes problems.
Extremely Rare but Extremely Serious
Side Effects
The
serious problems listed below have only been linked to the use
of Human Growth Hormone in one or two cases.
It is important to note that a true risk has yet to be
confirmed by research studies.
Type
2 diabetes has been reported in a few adolescents treated with
GH. IT is still uncertain whether a causal association is
present because the prevalence of adolescent type 2 diabetes in
general is rising so rapidly in most countries around the world
that we no longer have reliable incidence statistics for
diabetes in the untreated adolescent population.
Leukemia
is the most common childhood cancer, occurring in about 1 in
40,000 children each year. Because leukocytes have HGH
receptors, leukemia cases have been watchfully counted since
recombinant Human Growth Hormone was introduced. Even though a
few children with no risk factors who were treated with HGH have
developed leukemia, the numbers have been no more than would be
expected in a similarly sized group of children not being
treated with HGH. For a variety of reasons, it has been harder
to achieve the same level of reassurance for children who do
have a higher leukemia risk. These are primarily children who
became HGH deficient as a result of treatment for leukemia or a
brain tumor. Available statistics are reassuring, but numbers
are not large enough to exclude any magnification of risk.
Several
cases of colon cancer were found in a research study of lifelong
health and mortality of a group of middle-aged British adults
who suffered from severe HGH deficiency since childhood. All had
been treated as children with cadaver Growth Hormone. This
association has yet to be confirmed and even if it were, it
would need to be established whether the HGH treatment in
childhood or the untreated HGH deficient state in adult life
represented the true association. Furthermore, since cadaver HGH
has not been used for several decades, it is even more unlikely
that this side effect should occur with present day treatments.
Both obesity and elevated levels of IGF-1 have been
associated with colon cancer.
Finally,
in any discussion of side effects, the well-documented
experience with Creutzfeldt-Jacob disease 20 years after cadaver
HGH treatment reminds us that side effects of an apparently safe
treatment may be unforeseeable and long-delayed.
This is the case not only for Human Growth Hormone but
also for any pharmaceutical or supplement that has risen in the
last 20 years.
HGH is Not For Everyone
Though
there are undisputed benefits to supplementing with Human Growth
Hormone for anti-aging and/or weight loss, there are some people
who should not take HGH. For
certain people, Human Growth Hormone would be an inappropriate
treatment or supplement because risks or contraindications would
be greater than the benefits from HGH therapy.
Below is a list of people who should not take Human
Growth Hormone.
Children
and teenagers whose bones have finished growing should not take
HGH for the purpose of increasing height.
Human
Growth Hormone should not be used in Diabetes patients who
suffer from related retinopathy (eye disease).
HGH
should not be used in patients with cancer or who are being
treated for cancer. Growth Hormone deficiency can be caused by
the presence of brain tumors. As such, the presence of these
brain tumors should be ruled out before HGH treatment is
started. Human Growth Hormone should not be used if it is shown
that a previous brain tumor has come back or is getting larger.
HGH
should not be used in patients who are critically ill after open
heart surgery or abdominal (stomach) surgery, are severely hurt,
or have severe breathing problems.
Growth
hormone should not be used in children with Prader-Willi
syndrome who are very overweight or have severe breathing
problems.
Other Safety Considerations
Dosage
of diabetes medicines may need to be adjusted during HGH
treatment. Doctors should monitor patients carefully if Human Growth Hormone
is given along with gluco corticoid therapy and/or
other drugs that are processed by the body in the same way.
In
childhood cancer survivors, treatment with Human Growth Hormone
may increase the risk of a new tumor, particularly certain
benign brain tumors. This risk may be greater in patients who
were treated with cranial radiation.
A
small number of patients treated with HGH have experienced
increased pressure in the brain. This can cause headaches and
problems with vision. Treatment should be stopped and reassessed
in these rare cases. Patients with Turner syndrome and
Prader-Willi syndrome may be at higher risk of developing
increased pressure in the brain.
Thyroid
function should be monitored regularly during HGH therapy.
Thyroid hormone replacement therapy should be started or
adjusted if needed.
Patients
treated with HGH should be checked regularly if they are
receiving standard hormone replacement therapy to treat a lack
of more than one hormone.
Human
Growth Hormone should only be used during pregnancy if clearly
needed. It should be used with caution in nursing mothers
because it is not known whether growth hormone is present in
human milk.
A
different site should be used each day for growth hormone
injections. This can help to prevent skin problems such as
lumpiness or soreness.
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