Hypopituitarism

From: Traumatic Brain Injury, Panhypopituitarism and Hormonal Evaluations as a Standard of Care
<a href="http://www.nevadaosteopathic.org/attachments/article/33/Clearfield%20Panhypopituitarism%20and%20TBI.pdf">http://www.nevadaosteopathic.org/attachments/article/33/Clearfield%20Panhypopituitarism%20and%20TBI.pdf</a>

Symptoms of Hypopituitarism are (almost) identical to TBI symptoms:

TBI vs. Hypopituitarism

TBI

Fatigue (100%)

Depression w Anxiety/Panic (50-77%)

Difficulty Concentrating Memory impairment

Decreased Libido; Sexual Dysfunction

Insomnia Faulty Judgement, Slow Thinking Irritability w emotional outburst

Substance Abuse

<a href="http://www.bcftbi.org/about-tbi/behavior.asp">http://www.bcftbi.org/about-tbi/behavior.asp</a>

Hypopituitarism

Fatigue, Lethargy Depression w Panic

Difficulty Concentrating

Memory Impairment

Decreased Libido, Sexual Dysfunction

Insomnia

Faulty Judgement Emotional Outbursts

Substance Abuse https://www.pituitaryinjuryfoundation.org/about/

Fatigue, Lethargy Depression w Panic

Difficulty Concentrating

Memory Impairment

Decreased Libido, Sexual Dysfunction

Insomnia

Faulty Judgement Emotional Outbursts

Substance Abuse https://www.pituitaryinjuryfoundation.org/about/

Fom: 'Chronic Fatigue Syndrome, A Roadmap for Testing and Treatment' <a href="https://sites.google.com/site/cfstestingandtreatmentroadmap/home">https://sites.google.com/site/cfstestingandtreatmentroadmap/home</a>
Note that hypopituitarism will occur in up to 30% of people who sustain a moderate or severe traumatic brain injury (TBI), and can sometimes occur even in mild TBI cases. Hypopituitarism can have symptoms very close to those of ME/CFS.<a href="http://www.dailymail.co.uk/health/article-2631263/How-doctors-failing-spot-brain-injury-30-000-cases-chronic-fatigue.html#ixzz322IbpZZe" target="_blank" rel="nofollow">1</a> Thus there is a real danger of misdiagnosing such symptoms ME/CFS when the true cause is hypopituitarism.

Physical trauma such as a road accident or a fall can precipitate fibromyalgia and ME/CFS,<a href="http://www.investinme.org/Documents/PDFdocuments/CanadianDefinitionME-CFS.pdf" target="blank" rel="nofollow">1</a> particularly if a head or neck injury is sustained (such as whiplash or concussion).

Fibromyalgia or ME/CFS can appear immediately after an accident, or begin to develop over the subsequent months.<a href="http://www.ncbi.nlm.nih.gov/pubmed/11123046" target="blank" rel="nofollow">1</a> <a href="http://wayback.archive.org/web/20150715020811/http://www.meassociation.org.uk/2010/10/2134" target="blank" rel="nofollow">2</a>One study found fibromyalgia was 13 times more likely to occur following neck injury compared to lower extremity injury.<a href="http://www.ncbi.nlm.nih.gov/pubmed/9082932" target="blank" rel="nofollow">1</a>However, another study of 264 whiplash patients found no evidence of a greater incidence of fibromyalgia.<a href="http://www.ncbi.nlm.nih.gov/pubmed/26509044" target="blank" rel="nofollow">1</a>

A concussion can precipitate a condition similar to ME/CFS called <a href="http://www.nhs.uk/Conditions/Concussion/Pages/Complications.aspx" target="blank" rel="nofollow">post-concussion syndrome</a> (PCS). A concussion is a mild traumatic brain injury typically caused by a blow to the head, resulting in short-lived initial symptoms such as loss of consciousness or disturbances in vision (such as "seeing stars"). Most cases of PCS will resolve within six months, but 1 in 10 cases will persist for more than a year.
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From: 'Pre existing conditions' <a href="http://forums.phoenixrising.me/index.php?threads/pre-existing-conditions.33345/">http://forums.phoenixrising.me/index.php?threads/pre-existing-conditions.33345/</a>
It may be worthwhile to see an endocrinologist to discuss the effects of your concussion. If it turns out that the concussion has caused some damage to the pituitary, then hormone replacement of the hormones that aren't being produced would be in order.

I researched traumatic brain injury (TBI) and how it affects hormones because I had a whiplash injury shortly before developing ME/CFS. I just recently shared some of these articles with my primary doc and endocrinologist. Here are some of the articles I found:

<a class="externalLink" href="https://www.ghc.org/redirector.jhtml?url=http%3A%2F%2Fwww.eje-online.org%2Fcontent%2F152%2F5%2F679.full" target="blank" rel="nofollow">http://www.eje-online.org/content/152/5/679.full</a>
Hypopituitarism after traumatic brain injury

I think the article is saying that hypopituitarism is common even with mild concussion.

A low T4 in the absence of elevated TSH indicates secondary hypothyroidism. TSH deficiency has been found in TBI patients evaluated by assessing either basal hormone levels (1–22%)or response to TRH stimulation (4.5%). A previous series demonstrated a very high occurrence of thyrotropin deficiency among TBI patients with hypopituitarism, suggesting TBI as an important cause of otherwise unexplained central hypothyroidism.

<a class="externalLink" href="https://www.ghc.org/redirector.jhtml?url=http%3A%2F%2Fwww.hormones.gr%2F177%2Farticle%2Farticle.html" target="blank" rel="nofollow">http://www.hormones.gr/177/article/article.html</a>
Title: Endocrine evaluation of patients after brain injury: what else is needed to define specific clinical recommendations?

<a class="externalLink" href="http://pituitary.mgh.harvard.edu/NCBV11I2.htm" target="blank" rel="nofollow">http://pituitary.mgh.harvard.edu/NCBV11I2.htm</a>
<a class="externalLink" href="http://pituitary.mgh.harvard.edu/NCBV11I2.htm" target="blank" rel="nofollow">Brain Injury and Pituitary Dysfunction
</a>
<a class="externalLink" href="http://www.ncbi.nlm.nih.gov/pubmed/15253797" target="blank" rel="nofollow">http://www.ncbi.nlm.nih.gov/pubmed/15253797</a>
<a class="externalLink" href="http://www.ncbi.nlm.nih.gov/pubmed/15253797" target="blank" rel="nofollow">Occurrence of pituitary dysfunction following traumatic brain injury
</a>
<a class="externalLink" href="http://drbobseiler.com/wp-content/uploads/2010/09/article_05-44_gaab.pdf" target="blank" rel="nofollow">http://drbobseiler.com/wp-content/uploads/2010/09/article_05-44_gaab.pdf</a>
Reduced reactivity and enhanced negative feedback sensitivity of the hypothalamus-pituitary-adrenal axis in chronic whiplash-associated disorder

Here's a good outline discussing hypopitutiarism:
<a class="externalLink" href="http://www.merckmanuals.com/home/hormonal_and_metabolic_disorders/pituitary_gland_disorders/hypopituitarism.html" target="blank" rel="nofollow">http://www.merckmanuals.com/home/ho...ituitary_gland_disorders/hypopituitarism.html</a>
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From: 'Hypopituitarism Signs and Symptoms!' <a href="http://forums.prohealth.com/forums/index.php?threads/hypopituitarism-signs-and-symptoms.127623/">http://forums.prohealth.com/forums/index.php?threads/hypopituitarism-signs-and-symptoms.127623/</a>

Hypopituitarism is loss of function in an endocrine gland due to failure of the pituitary gland to secrete hormones which stimulate that gland's function. The pituitary gland is located at the base of the brain. Patients diagnosed with hypopituitarism may be deficient in one single hormone, several hormones, or have complete pituitary failure.

Description 

The pituitary is a pea-sized gland located at the base of the brain, and surrounded by bone. The hypothalamus, another endocrine organ in the brain, controls the function of the pituitary gland by providing "hormonal orders." In turn, the pituitary gland regulates the many hormones that control various functions and organs within the body. The posterior pituitary acts as a sort of storage area for the hypothalamus and passes on hormones that control function of the muscles and kidneys. The anterior pituitary produces its own hormones which help to regulate several endocrine functions.

In hypopituitarism, something interferes with the production and release of these hormones, thus affecting the function of the target gland. Commonly affected hormones may include:

Gonadotropin deficiency 

Gonadotropin deficiency involves two distinct hormones affecting the reproductive system. Luteinizing hormone (LH) stimulates the testes in men and the ovaries in women. This deficiency can affect fertility in men and women and menstruation in women. Follicle-stimulating hormone (FSH) has similar effects to LH.

Thyroid stimulating hormone deficiency 

Thyroid stimulating hormone (TSH) is involved in stimulation of the thyroid gland. A lack of stimulation in the gland leads to hypothyroidism.

Adrenocorticotopic hormone deficiency 

Also known as corticotropin, adrenocorticotopic hormone (ACTH) stimulates the adrenal gland to produce a hormone similar to cortisone, called cortisol. The loss of this hormone can lead to serious problems.

Growth hormone deficiency 

Growth hormone (GH) regulates the body's growth. Patients who lose supply of this hormone before physical maturity will suffer impaired growth. Loss of the hormone can also affect adults.

Other hormone deficiencies 

Prolactin stimulates the female breast to produce milk. A hormone produced by the posterior pituitary, antidiuretic hormone (ADH), controls the function of the kidneys. When this hormone is deficient, diabetes insipidus can result. However, patients with hypopituitarism rarely suffer ADH deficiency, unless the hypopituitarism is the result of hypothalamus disease.

Multiple hormone deficiencies 

Deficiency of a single pituitary hormone occurs less commonly than deficiency of more than one hormone. Sometimes referred to as progressive pituitary hormone deficiency or partial hypopituitarism, there is usually a predictable order of hormone loss. Generally, growth hormone is lost first, then luteinizing hormone deficiency follows. The loss of follicle-stimulating hormone, thyroid stimulating hormone and adrenocorticotopic hormones follow much later. The progressive loss of pituitary hormone secretion is usually a slow process, which can occur over a period of months or years. Hypopituitarism does occasionally start suddenly with rapid onset of symptoms.

Panhypopituitarism 

This condition represents the loss 0of all hormones released by the anterior pituitary gland. Panhypopituitarism is also known as complete pituitary failure. 

Causes & symptoms 

There are three major mechanisms which lead to the development of hypopituitarism. The first involves decreased release of hypothalamic hormones that stimulate pituitary function. The cause of decreased hypothalamic function may be congenital or acquired through interference such as tumors, inflammation, infection, mass lesions or interruption of blood supply. A second category of causes is any event or mass which interrupts the delivery of hormones from the hypothalamus. These may include particular tumors and aneurysms. Damage to the pituitary stalk from injury or surgery can also lead to hypopituitarism.

The third cause of hypopituitarism is damage to the pituitary gland cells. Destroyed cells can not produce the pituitary hormones that would normally be secreted by the gland. Cells may be destroyed by a number of tumors and diseases. Hypopituitarism is often caused by tumors, the most common of which is pituitary adenoma. 

Symptoms of hypopituitarism vary with the affected hormones and severity of deficiency. Frequently, patients have had years of symptoms that were nonspecific until a major illness or stress occurred. Overall symptoms may include fatigue, sensitivity to cold, weakness, decreased appetite, weight loss and abdominal pain. Low blood pressure, headache and visual disturbances are other associated symptoms. 

Gonadotropin deficiency 

Symptoms specific to this hormone deficiency include decreased interest in sex for women and infertility in women and men. Women may also have premature cessation of menstruation, hot flashes, vaginal dryness and pain during intercourse. Women who are postmenopausal will not have obvious symptoms such as these and may first present with headache or loss of vision. Men may also suffer sexual dysfunction as a result of gonadotropin deficiency. In acquired gonadotropin deficiency, both men and women may notice loss of body hair.

Thyroid stimulating hormone deficiency 

Intolerance to cold, fatigue, weight gain, constipation and pale, waxy and dry skin indicate thyroid hormone deficiency.

Adrenocorticotopic hormone deficiency 

Symptoms of ACTH deficiency include fatigue, weakness, weight loss and low blood pressure. Nausea, pale skin and loss of pubic and armpit hair in women may also indicate deficiency of ACTH.

Growth hormone deficiency 

In children, growth hormone deficiency will result in short stature and growth retardation. Symptoms such as obesity and skin wrinkling may or may not show in adults and normal release of growth hormone normally declines with age.

Other hormone deficiencies 

Prolactin deficiency is rare and is the result of partial or generalized anterior pituitary failure. When present, the symptom is absence of milk production in women. There are no known symptoms for men. ADH deficiency may produce symptoms of diabetes insipidus, such as excessive thirst and frequent urination. 

Multiple hormone deficiencies 

Patients with multiple hormone deficiencies will show symptoms of one or more specific hormone deficiencies or some of the generalized symptoms listed above.

Panhypopituitarism 

The absence of any pituitary function should show symptoms of one or all of the specific hormone deficiencies. In addition to those symptoms, patients may have dry, pale skin that is finely textured. The face may appear finely wrinkled and contain a disinterested expression.

Diagnosis 

Once the diagnosis of a single hormone deficiency is made, it is strongly recommended that tests for other hormone deficiencies be conducted.

Gonadotropin deficiency 

The detection of low levels of gonadotropin can be accomplished through simple blood tests which measure luteinizing hormone and follicle-stimulating hormone, simultaneously with gonadal steroid levels. The combination of results can indicate to a physician if the cause of decreased hormone levels or function belongs to hypopituitarism or some sort of primary gonadal failure. Diagnosis will vary among men and women. 

Thyroid stimulating hormone deficiency 

Laboratory tests measuring thyroid function can help determine a diagnosis of TSH deficiency. The commonly used tests are T4 and TSH measurement done simultaneously to determine the reserve, or pool, of thyroid-stimulating hormone. 

Adrenocorticotopic hormone deficiency 

An insulin tolerance test may be given to determine if cortisol levels rise when hypoglycemia is induced. If they do not rise, there is insufficient reserve of cortisol, indicating an ACTH deficiency. If the insulin tolerance test is not safe for a particular patient, a glucagon test offers similar results. A CRH (corticotropin-releasing hormone) test may also be given. It involves injection of CRH to measure, through regularly drawn blood samples, a resulting rise in ACTH and cortisol. Other tests which stimulate ACTH may be ordered.

Growth hormone deficiency 

Growth hormone deficiency is measured through the use of insulin-like growth factor I tests, which measure growth factors that are dependent on growth hormones. Sleep and exercise studies may also be used to test for growth hormone deficiency, since these activities are known to stimulate growth hormone secretion. Several drugs also induce secretion of growth hormone and may be given to measure hormone response. The standard test for growth hormone deficiency is the insulin-induced hypoglycemia test. This test does carry some risk from the induced hypoglycemia. Other tests include an arginine infusion test, clonidine test and growth-hormone releasing hormone test.

Other hormone deficiencies 

If a test calculates normal levels of prolactin, deficiency of the hormone is eliminated as a diagnosis. A TRH (thyrotropin-releasing hormone) simulation test can determine prolactin levels. A number of tests are available to detect ADH levels and to determine diagnosis of diabetes insipidus.

Multiple and general hypopituitarism tests 

Physicians should be aware that nonspecific symptoms can indicate deficiency of one or more hormones and should conduct a thorough clinical history. In general, diagnosis of hypopituitarism can be accomplished with a combination of dynamic tests and simple blood tests, as well as imaging exams. Most of these tests can be conducted in an outpatient lab or radiology facility. Magnetic resonance imaging (MRI) exams with gadolinium contrast enhancement are preferred imaging exams to study the region of the hypothalamus and pituitary gland. When MRI is not available, a properly conducted 

Panhypopituitarism 

The insulin-induced hypoglycemia, or insulin tolerance test, which is used to determine specific hormone deficiencies, is an excellent test to diagnose panhypopituitarism. This test can reveal levels of growth hormone, ACTH (cortisol) and prolactin deficiency. The presence of insufficient levels of all of these hormones is a good indication of complete pituitary failure. Imaging studies and clinical history are also important.

Treatment 

Treatment differs widely, depending on the age and sex of the patient, severity of the deficiency, the number of hormones involved, and even the underlying cause of the hypopituitarism. Immediate hormone replacement is generally administered to replace the specific deficient hormone. Patient education is encouraged to help patients manage the impact of their hormone deficiency on daily life. For instance, certain illnesses, accidents or surgical procedures may have adverse complications due to hypopituitarism.

Gonadotropin deficiency 

Replacement of gonadal steroids is common treatment for LH and FSH deficiency. Estrogen for women and testosterone for men will be prescribed in the lowest effective dosage possible, since there can be complications to this therapy. To correct women's loss of libido, small doses of androgens may be prescribed. To restore fertility in men, regular hormone injections may be required. Male and female patients whose hypopituitarism results from hypothalamic disease may be successfully treated with a hypothalamic releasing hormone (GnRH), which can restore gonadal function and fertility.

Thyroid stimulating hormone deficiency 

In patients who have hypothyroidism, the function of the adrenal glands will be tested and treated with steroids before administering thyroid hormone replacement.

Adrenocorticotopic hormone deficiency 

Hydrocortisone or cortisone in divided doses may be given to replace this hormone deficiency. Most patients require 20 mg or less of hydrocortisone per day.

Growth hormone deficiency 

It is essential to treat children suffering from growth hormone deficiency. The effectiveness of growth hormone therapy in adults, particularly elderly adults, is not as well documented. It is thought to help restore normal muscle to fat ratios. Growth hormone is an expensive and cautiously prescribed treatment. 

Treatment of multiple deficiencies and panhypopituitarism 

The treatment of hypopituitarism is usually very straightforward, but must normally continue for the remainder of the patient's life. Some patients may receive treatment with GnRH, the hypothalamic hormone. In most cases, treatment will be based on the specific deficiency demonstrated. Patients with hypopituitarism should be followed regularly to measure treatment effectiveness and to avoid overtreatment with hormone therapy. If the cause of the disorder is a tumor or lesion, radiation or surgical removal are treatment options. Successful removal may reverse the hypopituitarism. However, even after removal of the mass, hormone replacement therapy may still be necessary.

Prognosis 

The prognosis for most patients with hypopituitarism is excellent. As long as therapy is continued, many experience normal life spans. However, hypopituitarism is usually a permanent condition and prognosis depends on the primary cause of the disorder. It can be potentially life threatening, particularly when acute hypopituitarism occurs as a result of a large pituitary tumor. Morbidity from the disease has increased, although the cause is not known. It is possible that increased morbidity and death are due to overtreatment with hormones. Any time that recovery of pituitary function can occur is preferred to lifelong hormone therapy.

Prevention 

There is no known prevention of hypopituitarism, except for prevention of damage to the pituitary/hypothalamic area from injury.

Terms: 
Adenoma 
A benign (not threatening or cancerous) tumor that originates in a gland. 
Androgen 
A hormone that usually stimulates the sex hormones of the male. 
Congenital 
Present at birth. 
Diabetes insipidus 
A disorder originating in the pituitary gland which is characterized by excessive thirst and urination. 
Endocrine 
Refers to the system of internal secretion of substances into the body system from glands. 
Hypoglycemia 
Abnormal decrease of sugar in the blood. 
Hypothyroidism 
Deficient activity of the thyroid gland and resulting loss of energy. 
 
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From: 'Hypopituitarism after traumatic brain injury.' <a href="https://www.ncbi.nlm.nih.gov/pubmed/15879352">https://www.ncbi.nlm.nih.gov/pubmed/15879352</a>

Traumatic brain injury (TBI) is one of the main causes of death and disability in young adults, with consequences ranging from physical disabilities to long-term cognitive, behavioural, psychological and social defects. Post-traumatic hypopituitarism (PTHP) was recognized more than 80 years ago, but it was thought to be a rare occurrence. Recently, clinical evidence has demonstrated that TBI may frequently cause hypothalamic-pituitary dysfunction, probably contributing to a delayed or hampered recovery from TBI. Changes in pituitary hormone secretion may be observed during the acute phase post-TBI, representing part of the acute adaptive response to the injury. Moreover, diminished pituitary hormone secretion, caused by damage to the pituitary and/or hypothalamus, may occur at any time after TBI. PTHP is observed in about 40% of patients with a history of TBI, presenting as an isolated deficiency in most cases, and more rarely as complete pituitary failure. The most common alterations appear to be gonadotropin and somatotropin deficiency, followed by corticotropin and thyrotropin deficiency. Hyper- or hypoprolactinemia may also be present. Diabetes insipidus may be frequent in the early, acute phase post-TBI, but it is rarely permanent. Severity of TBI seems to be an important risk factor for developing PTHP; however, PTHP can also manifest after mild TBI. Accurate evaluation and long-term follow-up of all TBI patients are necessary in order to detect the occurrence of PTHP, regardless of clinical evidence for pituitary dysfunction. In order to improve outcome and quality of life of TBI patients, an adequate replacement therapy is of paramount importance.
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"In Spring 2008, I eventually had dynamic testing (the glucagon test) and was diagnosed with inflammation of the pituitary gland. This had caused severe deficiency of the Adult Growth Hormone and hypocortisolaemia, which is secondary hypoadrenalism caused by a lack of ACTH from the pituitary."