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Do any of your patients present clinically with one or more
of the following symptoms or conditions?
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Exhaustion |
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Weight Gain/Loss |
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Food Intolerances |
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Alcohol Intolerance |
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Allergies |
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Sinus Problems |
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Anxiety |
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Blood Sugar Imbalances |
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Depression |
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Digestive Disorders |
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Diminished Sex Drive
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Dizziness upon Standing |
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Dry and Thin Skin |
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Excessive Hunger |
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Craving for Sweets |
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Hair Loss |
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Headaches |
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Immune Deficiency |
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Inability to Concentrate |
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Parasite Infections |
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Bacterial Infections |
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Fungal Infections |
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General Pain |
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Inflammation |
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Chronic illness |
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Irritability |
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Liver Disorders |
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Thyroid Disorders |
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Pancreatic Disorders |
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Low blood pressure |
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Low Body Temperature |
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Mood Swings |
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Pain in the Neck |
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Pain in the Shoulders |
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Low Back Pain |
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Heart Palpitations |
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Poor memory |
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PMS |
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Sleep Disorders |
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Weakness |
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Difficulty Building
Muscle |
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If they do, this is an indication that they may be suffering
from adrenal insufficiency typically driven by one or more
chronic stressors.
There are a number of sources
of stress that may become chronic in nature
(refer to the
chart entitled “Chronic Stress Response").
The two, walnut-size adrenal glands are the command
post of the endocrine system and the glands are located in
the small of the back just above the kidneys and underneath
the last (twelfth) rib. These small but powerful glands are
strategically located in the body near the aorta and vena
cava to quickly receive information from the anterior pituitary
via the release of Adrenocorticotropic Hormone (ACTH). The
adrenals are also in close proximity to critical organs that
the adrenal hormones act upon including the liver, pancreas,
kidneys, and others.
The adrenal glands are divided into two parts: the outer
cortex, which consists of three main rings and the inner medulla.
The very thin outer ring of the cortex is the zona glomerulosa
which secretes aldosterone, the middle ring is the zona fasciculate
which primarily secretes cortisol, and the inner ring is the
zona reticularis which primarily produces androgens, including
DHEA and its metabolites. Despite the diminutive size of the
adrenal glands, they are involved in regulating virtually
every aspect of body function.
The adrenal hormones cortisol and DHEA have genetic influence
on the body, they penetrate cells and enter the nucleus, where
DNA is unlocked and transcribed. Cortisol is the main hormone
that directs immune function and its levels are tremendously
valuable in assessing overall health. Cortisol and DHEA are
also involved in carbohydrate, protein and fat metabolism;
eicosanoid modulation; detoxification capacity; endocrine
function; and the health of muscle, bone and neural tissues,
etc. (Please refer to the chart titled "Physiological
Aspects of Cortisol & DHEA").
Maintaining physiological balance is an important aspect
of vibrant health, and nowhere is this more evident when it
comes to cortisol. The production of too much cortisol can
literally burn up the body, and insufficient cortisol production
causes the body's internal machinery to malfunction, especially
at the cellular level.
The adrenal glands produce both cortisol and DHEA in the
adrenal cortex under the stimulation of adrenocorticotropic
hormone (ACTH), which is released by the pituitary gland.
ACTH acts like a whip on the adrenals. It is in many ways
similar to a jockey whipping a horse to make it run faster.
If the jockey ignores the clues that his horse is fatigued
and keeps whipping it, the horse will keep running until it
collapses in total exhaustion or death. In the case of the
human body, if we allow stress levels to become chronic and
out of control, we can sooner or later expect the same result.
Optimal adrenal function exists when the ratio of cortisol
to DHEA is in proper balance. This is why measuring this ratio
is the best way to both evaluate adrenal function and determine
the effects stress is having on overall health. When cortisol
levels are elevated and DHEA is low we are considered to be
in a Chronic Stress Response. When this happens we are losing
(or have already lost) our ability to modulate bodily functions
and are on the road to further hormone, immune, and metabolic
breakdown.
For example, if cortisol levels are too high at night, rather
than getting the rest and recovery necessary to maintain optimal
physical repair and psychic regeneration, the body will be
in a catabolic state (high nighttime cortisol levels inhibit
the release of growth hormone necessary to repair and rebuild
body tissues). This high cortisol will also have a negative
effect on brain function, memory, learning and mood. This
is especially true if this condition is ongoing (chronic in
nature).
We all have noticed individuals who have excess fat around
their hips, thighs or waist and yet they do not seem to be
particularly overweight. In fact, these people may be slender
except for those "problem" areas. More than making
them uncomfortable wearing a bathing suit in public, this
unsightly accumulation of fat is a telltale sign of adrenal
dysfunction and hormone imbalance, specifically an elevated
ratio of cortisol to DHEA.
An elevated cortisol to DHEA ratio will also interfere with
the surface integrity of the body's mucosal linings that act
as its first-line immune defense. This mucosal barrier is
primarily under the direction of the adrenal glands, specifically
cortisol and DHEA. Cortisol and DHEA systemically modulate
the production and turnover of specialized immune cells called
immunocytes (also known as plasmacytes) that produce the secretory
antibodies that protect us. The primary antibody of defense
is secretory IgA (sIgA). When cortisol is elevated and DHEA
is low, suppression of these mucosal immune cells occurs,
compromising our first-line immune defense, resulting in low
sIgA output.
The longer a person is in a state of chronic stress (high
ratio of cortisol to DHEA), the more compromised his or her
first line of immune defense will be and the greater the risk
for opportunistic infections and allergic reactions to foods.
This could ultimately lead to cancer, cardiovascular disease
as well as autoimmune disease, a variety of degenerative diseases
and accelerated aging.
In a Chronic Stress Response all body functions have become
compromised due to prolonged hormone, immune and metabolic
breakdown that can lead like falling dominoes to a cascade
of chronic degenerative diseases from which the weakened body
has a reduced chance to recover.
Adrenal exhaustion progresses in three stages (please refer
to the chart titled Progression of Stages in Adrenal Exhaustion).
Stage I is distinguished by an increase in output of ACTH
by the anterior pituitary gland, increased adrenocortical
stimulation, increased cortisol output and an increased probability
of pregnenolone steal and decreased DHEA. (Please refer to
the chart titled Steroidal
Hormone Principal Pathways). When in a Chronic Stress
Response, pregnenolone, the common precursor to cortisol,
DHEA and other hormones is preferentially diverted to cortisol
production at the expense of the rest of the steroidal hormones
(follow the small arrows on the chart). Generally in Stage
I cortisol increases and DHEA and its metabolites decrease
or an imbalance occurs especially between testosterone and
estrogen.
Stage II Adrenal Exhaustion is marked by the transition from
increased to decreased cortisol output. This stage is characterized
by continuing high levels of ACTH and thus: adrenocortical
stimulation, normal total cortisol output, low or borderline
low morning, noon or afternoon cortisol levels, normal nighttime
cortisol level, and an increased probability of pregnenolone
steal and a further decrease in DHEA. This is a transitional
phase in which although ACTH stimulation remains high or even
increases, the adrenal output of cortisol declines due to
the adrenal fatigue associated with continued hyper stimulation.
Stage III Adrenal Exhaustion is an advanced stage of adrenal
exhaustion characterized by decreased total cortisol output.
This stage is characterized by continuing high levels of ACTH
and thus adrenocortical stimulation, low total cortisol output,
and increased probability of a low nighttime cortisol level
and pregnenolone steal and even further decrease in DHEA.
The adrenal glands are now exhausted to the point that even
though there is ongoing hyperstimulation (high ACTH); they
continue to lose their capacity and reserve to produce enough
cortisol. The eventual result is a crash of the hypothalamic-pituitary-adrenal
axis (HPAA) in which essential neuroendocrine feedback loops
are unable to return the system to homeostasis. (To understand
more about the Stages of Adrenal Exhaustion refer to BioHealth
Diagnostics' "Adrenal and Metabolic Interpretive Guide".)
BioHealth Diagnostics' Functional Adrenal Stress Profile
(BHD #201) and Functional Adrenal Stress Profile plus V (BHD
#205) are tests that have been specifically developed to assess
the level of your patients' adrenal function. Both the BHD
#201 and BHD #205 assess the free fraction of the hormones
that they measure; this is the biologically active portion
of the hormone that does work at the cellular level. Since
cortisol levels ideally fluctuate according to a daily circadian,
peaking in the morning and decrementing to a low at bedtime
only to rise again over night, four time-specific saliva samples
are collected during a "normal" day (morning, noon,
afternoon and nighttime).
On the BHD #201, four time-specific cortisol readings are
reported along with a single average of two DHEA-S levels,
one taken on the noon sample and one on the afternoon sample.
The BHD #205 includes the levels on the #201 plus morning
estradiol, estriol and testosterone as well as bedtime progesterone
and melatonin. (Please refer to Technical Bulletin "Functional
Adrenal Profiles: BHD 201-205" for more details on
these tests). The "Adrenal and Metabolic Interpretive
Guide" provides sample treatment protocols for a wide
variety of sample tests that fall into the Stage I, II or
III categories.

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